You need to break the cycle of the physiologic obstruction. They are obstructed both at the sphincter level and in the aganglionic segment. And you have to break that cycle by getting a tube across it and then a lumen of that tube then to allow for egress of that stool because it's the stasis that's the problem. It's the stasis, the bacterial overgrowth. That overgrowth leads to translocation and that's where the sepsis comes in.
A few key tips to irrigation for those listening to me, an irrigation is instilling a, a small aloquat of saline, usually warm saline. Somewhere between 20 and 40 mLs um at a time. And it's infusing, instilling it in and getting it removed, whether that be by withdrawing from, with a catheter, so that you evacuate that saline and not just infuse it into the lumen of the colon, I think is important.
The overriding principle in this patient population is the overriding principle of bowel preservation, right? The small intestine can be shortened in some of these patients. Some of these patients have nutritional concerns, not immediately, but long term. In general, I think the theme should be preserve all bowel.
We typically get at about the 24-hour mark, give or take a few hours, a cross table lateral to see what does the gas column look like in this patient? Is there a low gas column that looks like it's almost touching the skin or is it pretty high up? And that might dictate what your next steps might be.
the most important thing that kind of keeps showing up is the fact that we really need to define what your own institution has for tolerance and to kind of stay on the protocol and then really just look at the infant condition as you continue to go is the most important thing
they must see submucosa. And if you send them a biopsy without submucosa, our pathologist will say, hey, where's the submucosa? Because you want to make sure, again, that you don't find ganglion cells in the seromuscular layer and hypertrophic nerves in the submucosal layer.
Gastroschisis and sutureless abdominal wall closure
StatementMany patients who underwent sutureless repair were done in more recent cohorts and tended towards less interventions.Open
QuotationI think it was probably what we were expecting, I think, for a couple of reasons. One, due to the heterogeneity of this disease, you know, especially with gastroschisis, a lot of the patients that were able to undergo, you know, especially a primary repair, they probably had more favorable bowel. And then those patients, you know, theoretically would have less hospital stay and theoretically feed faster and things like that.Open
StatementDue to the heterogeneity of gastroschisis, patients able to undergo primary repair probably had more favorable bowel and theoretically would have less hospital stay and feed faster.Open
QuotationMoreover, too, if you think about just the way that we close a sutured repair, you mobilize flaps from the skin and flaps from the fascia. So there's always, you know, redness around the incision, bruising around the incision. And so, you know, even that tissue manipulation is going to put you at higher risk for a potential infection or calling it erythema infection.Open
StatementThe finding of increased antibiotics needed after sutured repair was expected due to tissue manipulation.Open
StatementIn sutured repair, mobilizing flaps from the skin and fascia causes redness and bruising around the incision, which puts patients at higher risk for potential infection.Open
StatementThe consortium is working on operationalizing protocolization of gastroschisis closure across member institutions for a more prospective study with long-term follow-up.Open
StatementThe next phase of the study is examining the same patients over several years of follow-up to assess growth and umbilical hernia repair rates.Open
Update Course 2022 - UPDATES IN GASTROSCHISIS FEEDING PROTOCOLS - Jason Fraser, Beth Rymeski, and Steven Lee
StatementJason Fraser's institution starts feeding immediately after dressing placement as long as the baby is not sick, not having horrible output, and not vomiting.Open
Quotationwe start feeding essentially you have to put the dressing on uh as long as the baby's not sick not having horrible output not puking or anything like thatOpen
StatementFraser's institution does not intubate gastroschisis babies for reduction.Open
Quotationwe don't innovate our babies at all so we put the dressing plastic dressing on and as long as the kid's not you know has voluminous output we'll try to start start feedings on itOpen
Quotationif you try to just keep pushing and pushing pushing the baby kind of can squirm and stuff but if you go slow if you empty out the stomach if you kind of squish out the colon a little bit and you go slow you give the baby some sweeties the nurses are there to kind of relax the baby you have a couple people that that are there doing it you go slow you slowly kind of push things in you stretch out the belly a little bitOpen
StatementAwake reduction can be successful if performed slowly, with stomach emptying, colon decompression, oral sucrose, and gradual abdominal wall stretching.Open
StatementCincinnati Children's feeding protocol is based on patient tolerance and data from resource-limited settings where TPN is unavailable and feeding is mandatory.Open
Quotationit's really just based upon patient tolerance and it's kind of based upon some of the data that's out there from the rest of the world where they don't have tpn and so they just you have to feed the kid if the kid does okay then they keep goingOpen
Quotationa lot of the inconclusivity from the the study showed that you know most likely due to the fact that there was lots of different feeding protocols that were used uh across our member institutionsOpen
StatementThe multi-institutional study showed inconclusive results due to significant variation in feeding protocols across institutions.Open
StatementThe reduction in surgical site infections with protocol feeding was likely due to decreased care variability rather than the feeding protocol itself.Open
Quotationthe ssi thing was probably just because patients that were fed via protocol were cared for via protocol and so that they actually had less variability and less uh less changes uh in the way that these these patients are not you know look forOpen
StatementCincinnati Children's average gastroschisis length of stay was 49 days before protocol implementation, which was astronomically higher than comparable NICUs in their cooperative network.Open
Quotationour length of stay for gastroschisis and cincinnati was astronomically higher than like any other nick micu in the cooperative network that we worked with so we sat down we're like what is going on here so our average length of stay was 49 daysOpen
StatementCincinnati Children's has seen a decrease in time from first feed to full feeds but has not yet reduced the time from admission to first feed (except in 2020).Open
StatementAfter implementing a feeding protocol, Cincinnati Children's reduced gastroschisis length of stay by 10 days over two years.Open
Quotationwe instituted this uh a feeding protocol we spent a lot of time trying to get people to follow it and and making some adjustments and over two years we dropped the length of stay by 10 days and the mix of patients is not differentOpen
StatementCincinnati Children's gastroschisis protocol includes prenatal care coordination with obstetricians and neonatologists, with surgery continuing to follow patients throughout hospitalization.Open
Quotationthe most important thing that kind of keeps showing up is the fact that we really need to define what your own institution has for tolerance and to kind of stay on the protocol and then really just look at the infant condition as you continue to go is the most important thingOpen
StatementThe most important aspects of gastroschisis feeding are defining institutional tolerance criteria, adhering to protocol, and continuously evaluating the infant's condition.Open
StatementFor significant feeding intolerance, Cincinnati Children's protocol calls for stopping feeds for six hours, though this is not clearly evidence-based.Open
Quotationyes you can have a protocol yes you know you need to follow it but the most really you really need to continually evaluate the patient as they continue to go to make sure that you know yes your protocol is working but also to the patient does okay throughoutOpen
StatementOne recent Cincinnati Children's gastroschisis patient who was primarily reduced on day of life zero was discharged at approximately two weeks and remained well at two-week follow-up, though this is an outlier on the faster end.Open
StatementCincinnati Children's current average gastroschisis length of stay is 30 to 34 days.Open
StatementCincinnati Children's has not seen any aspirations with their early aggressive feeding approach, though they acknowledge they are still early in implementation and continue to monitor data.Open
StatementAt Cincinnati Children's, approximately two-thirds of gastroschisis cases cannot be reduced immediately and are placed in a silo for gradual reduction followed by sutureless closure, with feeds started after closure.Open
Jason's statements about Anorectal Malformation129 statements
The Colorectal Quiz Episode 1: ARM - Low Bulbar Fistula
QuotationI always worry about a missed presacral mass.Open
StatementCross-table lateral X-ray should be obtained at approximately 24 hours of life to assess the air column position relative to the perineal skin, with the baby positioned prone to allow air to rise to the buttocks.Open
StatementThe cross-table lateral film should include a marker at the expected anal location to allow measurement of the distance between the air column and the perineal skin.Open
StatementWell-formed buttocks, visible sphincter mechanism location, and well-developed sacrum together predict good prognosis for continence.Open
QuotationWell, I have two answers for you, Mark. I think if I was sitting in a hotel room, being examined by a bunch of board examiners, my answer would likely be a diverting stoma in real life, which is what we're discussing here.Open
StatementThe surgeon should never attempt posterior sagittal approach blind; imaging must confirm that the first structure encountered will be the air pocket of the distal rectum.Open
QuotationIt goes without saying and, and one of our, I think one of our big teaching points is you should never try to go in blind.Open
QuotationWe both agree that probably in real life, we would have done a primary posterior sagittal approach on this patient, and we would have found the rectum, and we could have made that rectum reach the perineum and done our anoplasty. How do we handle this? Because I didn't know that there was a fistula there. This is troublesome.Open
QuotationYou can see this fistula is very close to the rectum. And if you're going to dissect that free, and along the urethra, um, it's important to make sure that you know that those two structures are not very far apart, and getting that into that proper plane is very important.Open
StatementA bulbar fistula is located at the elbow of the urethra, using anatomic nomenclature based on the urethral location.Open
QuotationThe reason why Doctor Levitt or Mark is saying that. It's a bulbar fistula, it's at the elbow. You can see it's at the elbow of the urethra. And tell us that the uh the nomenclature we like to use is an anatomic pure anatomic nomenclature saying that it's a bulbar fistula.Open
Colorectal Quiz Episode 2: When to redo a PSARP
StatementFor anorectoplasty, if you don't get it perfect, you might not have the best outcomes, which separates it from other surgical procedures.Open
QuotationHow many patients, Jason, have you seen on laxatives that comes with an anus in the wrong place? How many patients have you seen having had a cecostomy with perfect anatomy? That's the real frustrating one. Right? A lot.Open
QuotationI can tell you, the family doesn't really care how technically elegant is your analplasty. What they care about is whether that analplasty that you make is going to work. And is the child going to be clean and in normal underwear and just like all the other kids?Open
StatementThe family doesn't really care how technically elegant is your analplasty. What they care about is whether that analplasty that you make is going to work and is the child going to be clean and in normal underwear.Open
StatementThe higher the malformation, the worse the prognosis.Open
StatementA sacrum ratio of 0.7 or greater usually means normal or close to normal sphincters and good muscle tone, indicating that spine innervation of that area is probably good.Open
StatementPatients can come with associated spinal anomaly, most commonly tethered cord, but the worst is a myelomeningocele, and those patients have much more trouble with continence.Open
StatementIt's amazingly common to have a mislocated anus, either because the surgeon misses where the center is during laparoscopic pull-through or opens the PSARP incision first.Open
StatementA key pitfall is opening the PSARP incision first; instead, mark the sphincters first, then open the PSARP so you don't get confused when placing the anoplasty in the correct location.Open
QuotationA key pitfall is not do that. Mark the sphincters first, then open the PSARP because then you don't get confused at the end when you're trying to place the anoplasty in the correct location.Open
StatementIn higher malformations such as a bladder neck fistula in a boy, the sphincter complex isn't always where you think it's going to be and is sometimes more anterior than anticipated.Open
StatementAn alternative approach for borderline cases is to let the child take their car out for a ride first and see how it works—if it drives well, stay with that anatomy; if not, then consider the redo.Open
Colorectal Quiz Episode 13: Newborn ARM Part 2
QuotationMy conversation with the family often involves that this will keratinize and look like a normal peroneal body over time.Open
StatementPerineal groove with mucosal lining will keratinize and look like normal perineal body over timeOpen
StatementSurgical intervention for perineal groove is indicated only if secreting mucus, causing irritation, or developing ulcersOpen
StatementVestibular fistula is very common in females and needs formal repair with hole transposed to center of sphincterOpen
StatementFor vestibular fistula diagnosed in newborn period, options are primary repair if baby is well, or allow stooling through fistula for couple months then elective repair without stomaOpen
StatementPatients diagnosed with vestibular fistula at 6-12 months who have dilated rectosigmoid need diversion as first step, then repairOpen
StatementPurpose of diversion in ARM repair is to avoid perineal body dehiscenceOpen
StatementTo evaluate for vestibular fistula, pull labia towards examiner with both hands to visualize vaginal opening and urethraOpen
Colorectal Quiz Episode 14: ARM Newborn Part 3
StatementCross-table lateral films can be obtained early and then around 24 hours later in cases where there is no evidence of fistula on exam.Open
StatementIf the air column stops at about the 4th sacral vertebral body with a large distance between the air column and the sphincter marker, the patient should be considered for diversion and distal colostogram to delineate anatomy.Open
Quotationif you look at the film on the left, the air column stops at about the 4th sacral vertebral body, give or take a little bit. And so, what, and you could see where the marker is or the BB is, uh, where the, where the sphincter complex appears to be located. There's a large distance between those.Open
StatementWhen the air column is very close to where the anticipated anal opening should be located, primary anoplasty may be performed.Open
Quotationthe air column is very close to where the anticipated anal opening should be located. And this is a case where you could take your barley bush, potentially, and make a nick, uh, a scratch, and, and do your anoplasty.Open
StatementWhether to perform primary anoplasty in cases with close air column depends on individual surgeon comfort and the level of post-operative care available at the institution.Open
Quotationthat common wall or, or that wall between the rectum and the urethra is a lot closer and a lot longer. Of a common wall, then I think some people anticipate.Open
StatementThe common wall between the rectum and the urethra is closer and longer than some people anticipate.Open
StatementA patient at 24 hours with no obvious fistula and cross-table lateral showing air column not very distal needs a colostomy.Open
The Colorectal Quiz Episode 23: Hirschsprung Disease - The Soiling Patient...
QuotationCan I scare you for a moment? Can we talk scientifically for one minute? I know this is crazy.Open
StatementThe dentate (or pectinate) line is the transition from squamous epithelium to columnar epithelium, located about 2/3 of the way up the anal canal.Open
StatementBlood supply changes occur at the dentate line (splanchnic versus systemic), and there is also innervation in that area.Open
StatementThe nerves located at the dentate line region tell you gas, liquid, solid; how hard, how long, and how tight to squeeze.Open
QuotationI talk about that dentate line in the area where the nerves are located that tell you gas, liquid, solid. How hard do I need to squeeze, how long do I have to squeeze for, how tight do I have to squeeze?Open
StatementPreserving the dentate line region is key because injury to that region affects a patient's ability to be continent.Open
StatementIn children with anorectal malformation, Hirschsprung disease, spinal conditions, or combinations thereof, the ability to sense stool in the rectum or neorectum region is critical to success; the right consistency and bulk of stool is very important.Open
StatementIf clinicians make stool too soft or too loose with medications, they put a child on the edge of having control or not and throw them over that edge, preventing success.Open
QuotationAnd if we make it too soft or too loose, we're putting a child or a person who is on the teeter of having control or not, and you throw them over that edge, and, and you just won't be successful.Open
StatementA Hirschsprung patient with missing dentate line and intact muscle should be able to achieve continence, similar to an anorectal malformation anastomosis (rectum or colon mucosa to skin).Open
QuotationI mean, it makes sense that they should if the muscle is intact, right, because this is no different than an anorectal malformation, anastomosis. That's right. But it's, it's, it's rectum or colon mucosa to skin.Open
StatementPatients with no dentate line and patulous sphincters who are soiling develop severe skin irritation from sitting in pull-ups or diapers.Open
QuotationThat is a patient with no dentate line and pattula sphincters, and you clearly see with the skin changes around that, that this patient has really struggled and has been soiling and, and, and sitting in, in pull-ups or a diaper, really causing severe skin irritation.Open
QuotationThis, this is, these are the harder patients to take care of, and the trick that I use is you have to constipate them. And then if they're able to empty with continence on their own, then great. If they're not, then you have to mechanically help them empty.Open
StatementFor hypermotile patients (stooling 7-8 times a day), the approach is to constipate them first, then figure out how to empty them in a time-controlled fashion.Open
QuotationBut it, it's, it's like, it sounds counterintuitive, but at least the way I treat these patients, I constipate them, and then I empty them.Open
StatementWhether hypermotile patients can empty on their own versus needing mechanical emptying to maintain social continence depends on their sphincter function.Open
QuotationBut that's how I sort of explain it to the families. It sounds weird, but we're gonna constipate you, and then we have to figure out how to empty you in a time-controlled fashion.Open
StatementSome Hirschsprung patients who have a good operation have super strong sphincters that just need a little relaxation to allow passage of stool until they learn proper sphincter coordination for evacuation.Open
StatementBotox helps train sphincters in Hirschsprung patients; anorectal manometry can provide objective data showing resting pressures are usually on the higher end of normal, and some patients need extra relaxation to allow them to go.Open
StatementNutrition in Hirschsprung patients is very important; some patients are very sensitive to certain foods, particularly lactose.Open
StatementPaying attention to diet (whether breastfed infants or older children) is important because lactose is particularly problematic in some Hirschsprung patients.Open
QuotationNone. We have to get it right the first time.Open
StatementEvery Hirschsprung patient should be able to do well; they might need help and might need mechanical evacuations or Botox, but all should be able to get on the right track.Open
QuotationAnd if you don't get it right, you gotta use these techniques and this algorithm to figure out what's wrong, cause we could get every patient doing well. They might need help, and they might need mechanical evacuations, Botox, etc. but we could, we all should be able to get these patients on the right track.Open
Colorectal Quiz Episode 28: Female ARM Management - Perineal Fistula
StatementWhen neurologic anomalies are found in anorectal malformation patients, gynecological anomalies are more likely, especially on the same side.Open
Quotationwhen you do find neurologic anomalies. That leads to more likely gynecological anomalies as well, especially on the same side.Open
Colorectal Quiz Episode 29: Female ARM-Post Op Management
StatementDr. Fisher's protocol for perineal body primary repair (no stoma) is 5-7 days NPO on D10 via midline catheter (not PICC line) until the repair is confirmed healed.Open
QuotationJust because it's published doesn't mean it works.Open
QuotationMy only concern is what's the continence rate of your patients?Open
QuotationI guess my question is somewhere around 20% required a redo either local or total operation. Most just like local, but what did a functional out in the end of the game, all the parents want is their kid pooping in the potty. And we don't know that answer.Open
QuotationThat's a very valid point. So what you're saying, wait, wait, Mark agreed with me.Open
QuotationAnd when I was working with Mark here, I know, especially in the older patients that we were doing redos on, used to teach me to make the anoplasty maybe a little larger.Open
Colorectal Quiz Episode 38: Transitional Care in Colorectal Surgery
StatementMRI with specific protocols and endorectal ultrasound can help determine whether the anoplasty is within the muscle complex.Open
StatementThe transition model includes joint clinic visits and collaborative operating, which is key to successful handoff.Open
StatementFreestanding children's hospitals face greater challenges than integrated hospitals because they are completely separate entities both physically and financially.Open
StatementIn Cincinnati, ARM patients still come to the colorectal center at the children's hospital whether they are 12 or 40 years old, partnering with an adult colorectal surgeon; collaborative operating occurs at the University of Cincinnati with adult colorectal surgeons, adult neurologists for urology, and pediatric urologists who have privileges at the university.Open
StatementAdult hospitals are much more adept and skilled at managing perioperative complications like pulmonary embolism or myocardial infarction; such events in a children's hospital lead to many meetings and potential for poor outcomes.Open
StatementPhysicians and surgeons are making progress on transition, but the greater struggle is providing intensive bowel management training for 35-year-old patients; pediatric centers are adept at bowel management for patients of any age, but currently adult patients requiring intensive outpatient bowel management are still being seen at children's hospitals.Open
StatementCross-table lateral X-ray should be obtained at approximately 24 hours of life to assess the air column position relative to the perineal skin.Open
StatementCross-table lateral is performed with the baby prone, positioning the buttock at the highest point where air will rise.Open
StatementA marker should be placed where the anus is thought to be appropriate on the cross-table lateral to allow measurements and inform operative approach.Open
StatementWell-formed buttocks, visible sphincter mechanism location, and well-developed sacrum together indicate likely good prognosis for continence.Open
Quotationyou should never try to go in blind. Right, we're going in with knowing that if we make a posterior sagittal incision right now, the first thing we're gonna hit is that air pocket, which is the distal rectum.Open
StatementWhen a fistula is very close to the rectum, it is important to identify the proper dissection plane between the two structures.Open
StatementA bulbar fistula is located at the elbow of the urethra, using anatomic nomenclature.Open
Colorectal Quiz: Episode 43
StatementAbout 60% of the time there is success with using a split appendix for both Malone and Mitrofanoff, but about 40% of the time you cannot make it work.Open
StatementThe longer the appendix, the less likely it will leak based on Poiseuille's law (flow through a tube based on radius to fourth power and length).Open
QuotationSo we plicate them all. And I haven't had a leakage in a long, long time, several years. So I think it's a very effective strategy.Open
StatementDr. Frischer and Levitt did 10 Malones in a row without plicating and five leaked, so they decided to plicate them all and have not had a leakage in several years.Open
StatementIf appendix is short and stumpy, it is best for the Malone and the Mitrofanoff should be made from small bowel.Open
StatementIf appendix is 7 centimeters or greater it can be split, requiring minimum 2 centimeters for the Malone and 5 centimeters minimum for the Mitrofanoff.Open
StatementIf appendix is 5 to 7 centimeters, that is not enough to share and should go for the Mitrofanoff because long term the Mitrofanovs do much better, requiring a neo-Malone.Open
StatementUsing a 10 French tube (not 8), leaving it in for a month, and cathing twice a day can minimize stenosis rate.Open
StatementLeaving indwelling tubes in Malones increases the amount of prolapse, likely due to pressure on the appendiceal base pushing up mucosa.Open
StatementUrologists almost never get stenosis of Mitrofanovs because they catheterize every four hours; applying this to Malones by cathing twice daily has reduced stenosis rate.Open
StatementFor lost Malone access, blow up a balloon on a Foley catheter to occlude the umbilicus and inject dye under pressure to find any micro hole tract.Open
Colorectal Quiz: Episode 40
StatementOptions for vaginal reconstruction when native vagina cannot reach include: dilating the existing introitus, opening the area and laying in a buccal graft, or waiting for tissue engineering options expected within 20 years or less.Open
QuotationI think it's going to be, there are people right now taking a few vaginal cells and growing them and hopeful, just like you said, Mark, we're going to have some great tissue engineering that will assist us and make this a easier and better procedure for our patients.Open
StatementIf a neovagina bridge is functioning well without problems, there may be no reason to remove it later.Open
Colorectal Quiz Episode 32: Anorectal Malformations And Cardiac Anomalies
QuotationDo you automatically get an echo on every one of your anorectal malformation babies?Open
StatementIn a cardiac patient with an external opening from ARM, the typical approach is to dilate as long as they're evacuating okay.Open
StatementFor perineal fistula or vestibular fistula in a female, one can consider just dilating with good evacuation and letting the cardiac situation play itself out.Open
StatementIn a blue baby with significant cardiac lesion requiring early surgery where patient isn't oxygenating well, there is concern about healing of an ARM repair.Open
QuotationMy concern would be if you're going to have a significant cardiac lesion that's going to likely require early surgery, you have a blue baby. You're having a lesion that a patient isn't oxygenating well. And then I worry about the healing of that repairOpen
StatementFor umbilical access in laparoscopy, dissect in with a mosquito, ensure you're in the peritoneum without touching any vessel before insufflation, and clear the line of air.Open
QuotationDissecting in with a mosquito, making sure you're in, not touching any vessel before you insufflate, and also clear the line of airOpen
QuotationI've seen teenagers and young adults with those beads that never went away. So, yeah, you've got to scrape that offOpen
StatementThe white beads along the raphe should be scraped off during repair, as they can persist into teenage years and young adulthood if left alone.Open
StatementFor a 50-50 perineal fistula (half within muscle complex, half anterior), leave the anterior wall as it's the danger zone, mobilize posteriorly to fill the anal sphincter, creating an 80-20 reconstruction.Open
Colorectal Quiz Episode 29: Female ARM
StatementDr. Frisher uses a midline catheter (not PICC line) with D10 until the repair is confirmed healed, typically five to seven days NPO.Open
StatementApproximately 20% of patients in the dilation study required a redo operation, either local or total, with most being local procedures.Open
StatementIn higher malformations such as bladder neck fistula in boys, the sphincter complex is sometimes more anterior than anticipatedOpen
StatementAlternative approach for borderline anatomy: let the child try their current anatomy first; if it works well, stay with it; if not, consider redoOpen
The Colorectal Quiz: Episode 1
StatementPre-sacral masses are rare in typical imperforate anus but occur in almost half of anal stenosis or rectal atresia cases, requiring MRIOpen
Quotationif it's an anal stenosis or a rectal atresia defect, then you need to be very worried about finding a pre-sacral mass. And almost half the time, you'll find one. And those patients will end up getting an MRI.Open
QuotationWe typically get at about the 24-hour mark, give or take a few hours, a cross table lateral to see what does the gas column look like in this patient? Is there a low gas column that looks like it's almost touching the skin or is it pretty high up? And that might dictate what your next steps might be.Open
StatementCross-table lateral x-ray should be obtained at approximately 24 hours of life to assess gas column height and guide surgical planningOpen
StatementWell-formed buttocks, good muscle, true sphincter mechanism area, and well-developed sacrum together indicate likely good prognosisOpen
StatementWith air column 8.8mm from skin, primary posterior sagittal anorectoplasty is a reasonable option based on imagingOpen
QuotationI have two answers for you, Mark. I think if I was sitting in a hotel room being examined by a bunch of board examiners, my answer would likely be a diverting stoma in real life, which is what we're discussing here. What would we do on a Tuesday afternoon? I think this air column is, if you're going to get this x-ray and base your decision-making on where the air column is and what's going on, I'm pretty apt to say I might perform a primary posterior sagittal anorectoplasty with this type of imaging in front of me.Open
StatementShould never try to go in blind—must know what structure will be encountered before making posterior sagittal incisionOpen
Quotationyou should never try to go in blind, right? We're going in with knowing that if we make a posterior sagittal incision right now, the first thing we're going to hit is that air pocket, which is the distal rectum.Open
StatementBulbar fistula nomenclature refers to anatomic location at the elbow of the urethraOpen
Quotationyou can see this fistula is very close to the rectum. And if you're going to dissect that free and along the urethra, it's important to make sure that you know that those two structures are not very far apart. And getting that into that proper plane is very important.Open
StatementFistula can be very close to rectum, making proper plane dissection along urethra importantOpen
QuotationThe reason why Dr. Levitt or Mark is saying that it's a bulbar fistula is it's at the elbow. You can see it's at the elbow of the urethra. And tell us that the nomenclature we like to use is an anatomic, pure anatomic nomenclature saying that it's a bulbar fistula.Open
Jason's statements about Anorectal Malformations & Cloacal Reconstruction7 statements
StatementCross-table lateral X-ray should be obtained at approximately 24 hours of life to assess the air column position relative to the perineal skin.Open
StatementCross-table lateral is performed with the baby prone, positioning the buttock at the highest point where air will rise.Open
StatementA marker should be placed where the anus is thought to be appropriate on the cross-table lateral to allow measurements and inform operative approach.Open
StatementWell-formed buttocks, visible sphincter mechanism location, and well-developed sacrum together indicate likely good prognosis for continence.Open
Quotationyou should never try to go in blind. Right, we're going in with knowing that if we make a posterior sagittal incision right now, the first thing we're gonna hit is that air pocket, which is the distal rectum.Open
StatementWhen a fistula is very close to the rectum, it is important to identify the proper dissection plane between the two structures.Open
StatementA bulbar fistula is located at the elbow of the urethra, using anatomic nomenclature.Open
Jason's statements about Anorectal Malformations & Cloacal Reconstruction7 statements
StatementCross-table lateral X-ray should be obtained at approximately 24 hours of life to assess the air column position relative to the perineal skin.Open
StatementCross-table lateral is performed with the baby prone, positioning the buttock at the highest point where air will rise.Open
StatementA marker should be placed where the anus is thought to be appropriate on the cross-table lateral to allow measurements and inform operative approach.Open
StatementWell-formed buttocks, visible sphincter mechanism location, and well-developed sacrum together indicate likely good prognosis for continence.Open
Quotationyou should never try to go in blind. Right, we're going in with knowing that if we make a posterior sagittal incision right now, the first thing we're gonna hit is that air pocket, which is the distal rectum.Open
StatementWhen a fistula is very close to the rectum, it is important to identify the proper dissection plane between the two structures.Open
StatementA bulbar fistula is located at the elbow of the urethra, using anatomic nomenclature.Open
QuotationThis is huge. This is why, this is real time, and we all know a book chapter takes five years to, three to five years to get published.Open
Colorectal Quiz Episode 18: Cloaca Part 2
StatementDuring cystoscopy it is important to look for cervices to understand Müllerian development (one vagina vs. two, presence of uterus) and to identify ureteral orifices, which in complex malformations may attach anomalously low to the bladder or bladder neck.Open
Colorectal Quiz: Episode 40
StatementOptions for vaginal reconstruction when native vagina cannot reach include: dilating the existing introitus, opening the area and laying in a buccal graft, or waiting for tissue engineering options expected within 20 years or less.Open
QuotationI think it's going to be, there are people right now taking a few vaginal cells and growing them and hopeful, just like you said, Mark, we're going to have some great tissue engineering that will assist us and make this a easier and better procedure for our patients.Open
StatementIf a neovagina bridge is functioning well without problems, there may be no reason to remove it later.Open
Jason's statements about Cloacal Exstrophy4 statements
StatementTwo major surgical decision points in cloacal exstrophy are: (1) whether the omphalocele is large or small enough to close the abdominal wall, and (2) the staging of the exstrophy procedure—whether to just bring bladder plates together in a multi-stage approach or to close the bladder and bring the symphysis pubis together.Open
QuotationThe overriding principle in this patient population is the overriding principle of bowel preservation, right? The small intestine can be shortened in some of these patients. Some of these patients have nutritional concerns, not immediately, but long term. In general, I think the theme should be preserve all bowel.Open
StatementThe overriding principle in cloacal exstrophy management is bowel preservation, as small intestine can be shortened and some patients have long-term nutritional concerns.Open
StatementOne reason for not performing early pull-through in cloacal exstrophy is concern about rash and managing a perineal stoma.Open
Jason's statements about Colorectal / ARM & Hirschsprung450 statements
QuotationI, I don't believe that a pure trans anal is necessarily less invasive. In other words, I believe that putting 3 incisions on the abdomen is actually less invasive in my hands, in my hands, certainly not in your guys' hands, but in my hands, I'm gonna be torquing in that anal canal much more than if I had done it laparoscopically and freed everything up from the abdominal approach.Open
StatementA pure transanal Hirschsprung dissection is not necessarily less invasive than laparoscopic approach; prolonged torquing in the anal canal may be more traumatic than three small abdominal incisions.Open
QuotationI, I don't believe that a pure trans anal is necessarily less invasive. In other words, I believe that putting 3 incisions on the abdomen is actually less invasive in my hands, in my hands, certainly not in your guys' hands, but in my hands, I'm gonna be torquing in that anal canal much more than if I had done it laparoscopically and freed everything up from the abdominal approach.Open
StatementA pure transanal Hirschsprung dissection is not necessarily less invasive than laparoscopic approach; prolonged torquing in the anal canal may be more traumatic than three small abdominal incisions.Open
StatementFor standard rectosigmoid Hirschsprung disease (6-10 cm up), transanal dissection can be completed in the same timeframe as laparoscopic mobilization if the surgeon knows the level from a good contrast study.Open
StatementFor standard rectosigmoid Hirschsprung disease (6-10 cm up), transanal dissection can be completed in the same timeframe as laparoscopic mobilization if the surgeon knows the level from a good contrast study.Open
StatementPost-Hirschsprung complications divide into two categories: obstructive symptoms (enterocolitis, failure to thrive, distention) and soiling issues (true incontinence vs pseudo-incontinence from constipation).Open
StatementPost-Hirschsprung complications divide into two categories: obstructive symptoms (enterocolitis, failure to thrive, distention) and soiling issues (true incontinence vs pseudo-incontinence from constipation).Open
StatementWorkup for post-Hirschsprung complications includes water-soluble contrast enema and exam under anesthesia looking for dentate line position, stricture, stretched sphincter, and twists; if no anatomic cause is found, perform biopsy.Open
StatementWorkup for post-Hirschsprung complications includes water-soluble contrast enema and exam under anesthesia looking for dentate line position, stricture, stretched sphincter, and twists; if no anatomic cause is found, perform biopsy.Open
StatementGoing only 0.5 cm above the dentate line in a newborn may result in 2.5-3 cm of aganglionic segment remaining when the child reaches 7 years old, creating an ultra-short segment Hirschsprung situation with constipation.Open
StatementFor Hirschsprung pull-through, dissection should start approximately 1 cm above the dentate line (defined as the transition from squamous to columnar epithelium, at the bottom of the anal columns).Open
StatementGoing only 0.5 cm above the dentate line in a newborn may result in 2.5-3 cm of aganglionic segment remaining when the child reaches 7 years old, creating an ultra-short segment Hirschsprung situation with constipation.Open
StatementFor Hirschsprung pull-through, dissection should start approximately 1 cm above the dentate line (defined as the transition from squamous to columnar epithelium, at the bottom of the anal columns).Open
StatementInjury to the dentate line during Hirschsprung pull-through can cause devastating fecal incontinence; it is better to risk leaving ultra-short segment aganglionosis (manageable with laxatives) than to injure the dentate line.Open
QuotationI want to ensure, because, and maybe we have a biased population in what we see, that I do not injure the dentate line because the patients who are rendered potentially fecally incontinent due to injury to the dentate line is a devastating injury for those patients.Open
StatementInjury to the dentate line during Hirschsprung pull-through can cause devastating fecal incontinence; it is better to risk leaving ultra-short segment aganglionosis (manageable with laxatives) than to injure the dentate line.Open
QuotationI want to ensure, because, and maybe we have a biased population in what we see, that I do not injure the dentate line because the patients who are rendered potentially fecally incontinent due to injury to the dentate line is a devastating injury for those patients.Open
StatementIn ulcerative colitis or FAP patients undergoing J-pouch creation, dissection goes right at the top of the columns, or even slightly lower if polyps are present in that region.Open
StatementIn ulcerative colitis or FAP patients undergoing J-pouch creation, dissection goes right at the top of the columns, or even slightly lower if polyps are present in that region.Open
StatementThe dentate line is variably defined in anatomic literature and textbooks; different sources point to different locations within the anal columns when labeling the dentate or pectinate line.Open
StatementThe dentate line is variably defined in anatomic literature and textbooks; different sources point to different locations within the anal columns when labeling the dentate or pectinate line.Open
StatementThe traditional teaching that newborn meconium is sterile and therefore anorectal malformation repair should be done in the newborn period (before dilations introduce bacteria) is questioned; some surgeons repair at any age with stool present and feed early postoperatively with similar complication rates.Open
StatementThe traditional teaching that newborn meconium is sterile and therefore anorectal malformation repair should be done in the newborn period (before dilations introduce bacteria) is questioned; some surgeons repair at any age with stool present and feed early postoperatively with similar complication rates.Open
StatementConservative postoperative management of anorectal malformation repair includes keeping the patient NPO for approximately one week with hyperalimentation (a 'medical colostomy'), though there is no data supporting this practice over early feeding.Open
StatementConservative postoperative management of anorectal malformation repair includes keeping the patient NPO for approximately one week with hyperalimentation (a 'medical colostomy'), though there is no data supporting this practice over early feeding.Open
QuotationI know there are a number of pediatric surgeons that will repair an anorectal malformation at whatever age with dirty stool and feed the child the day 1 or 2 days post-op when they recover from the anesthesia, and I'm sure that incidence of complication is probably similar.Open
QuotationI know there are a number of pediatric surgeons that will repair an anorectal malformation at whatever age with dirty stool and feed the child the day 1 or 2 days post-op when they recover from the anesthesia, and I'm sure that incidence of complication is probably similar.Open
StatementWhen vestibular fistula is discovered intraoperatively to have an absent vagina, management depends on prognosis for bowel control: if good prognosis, use graft (colon or small bowel) to create vagina and bring rectum down; if poor prognosis (sacral agenesis, tethered cord), use the rectum/fistula as vagina and bring proximal colon down as pull-through.Open
StatementWhen vestibular fistula is discovered intraoperatively to have an absent vagina, management depends on prognosis for bowel control: if good prognosis, use graft (colon or small bowel) to create vagina and bring rectum down; if poor prognosis (sacral agenesis, tethered cord), use the rectum/fistula as vagina and bring proximal colon down as pull-through.Open
StatementRectal prolapse workup should distinguish full-thickness prolapse from partial-thickness (mucosal) prolapse based on physical examination appearance.Open
StatementRectal prolapse workup should distinguish full-thickness prolapse from partial-thickness (mucosal) prolapse based on physical examination appearance.Open
StatementTesting for cystic fibrosis in children presenting with rectal prolapse is traditional teaching and a board exam answer, but in clinical practice rarely identifies new CF cases; most CF patients with prolapse are already diagnosed.Open
StatementTesting for cystic fibrosis in children presenting with rectal prolapse is traditional teaching and a board exam answer, but in clinical practice rarely identifies new CF cases; most CF patients with prolapse are already diagnosed.Open
StatementInitial management of rectal prolapse includes treating constipation and limiting toilet sitting time to 5 minutes; surgical intervention is considered after 6 months to 2 years of failed medical management.Open
StatementInitial management of rectal prolapse includes treating constipation and limiting toilet sitting time to 5 minutes; surgical intervention is considered after 6 months to 2 years of failed medical management.Open
StatementSclerosing agent injection for rectal prolapse has high recurrence rates; patients who fail this approach and require subsequent rectopexy have difficult reoperative dissection.Open
QuotationI can tell you when it recurs to re-operate on those patients is not going to matter at all.Open
QuotationI can tell you when it recurs to re-operate on those patients is not going to matter at all.Open
StatementSclerosing agent injection for rectal prolapse has high recurrence rates; patients who fail this approach and require subsequent rectopexy have difficult reoperative dissection.Open
StatementTransabdominal approaches for rectal prolapse (rectopexy with or without resection) have approximately 5% recurrence rate, compared to 15-20% recurrence for transanal approaches (transanal pull-through or Altmeier procedure).Open
StatementResection and rectopexy for rectal prolapse may be preferable when constipation control is difficult, but has higher complication rate compared to rectopexy alone.Open
StatementLaparoscopic rectopexy for rectal prolapse can be performed as same-day surgery or with next-day discharge in current practice.Open
StatementMesh erosion is a known complication of ventral mesh rectopexy, but the procedure can be effective for refractory rectal prolapse after multiple failed transabdominal repairs.Open
StatementVentral mesh rectopexy is a newer procedure popularized by the Cleveland Clinic for rectal prolapse; it involves placing mesh on the anterior rectum surface, elevating the rectum without posterior dissection, and tacking mesh to the sacral promontory.Open
StatementVentral mesh rectopexy is a newer procedure popularized by the Cleveland Clinic for rectal prolapse; it involves placing mesh on the anterior rectum surface, elevating the rectum without posterior dissection, and tacking mesh to the sacral promontory.Open
StatementMesh erosion is a known complication of ventral mesh rectopexy, but the procedure can be effective for refractory rectal prolapse after multiple failed transabdominal repairs.Open
StatementVentral mesh rectopexy aims to change the angle between rectum and anal canal; younger patients with rectal prolapse have a straighter rectum-to-anal-canal angle that becomes more acute with age.Open
StatementVentral mesh rectopexy aims to change the angle between rectum and anal canal; younger patients with rectal prolapse have a straighter rectum-to-anal-canal angle that becomes more acute with age.Open
Hirschsprung Disease: Update Course 2015
QuotationI recall having a full day of uh Hirschprung's webcast, and now I get 5 minutes.Open
QuotationI, every time that I do a primary trans anal, I get. I tighten up a little bit to make sure that I'm confident that I can do, and I have an exit strategy in mind if I get in troubleOpen
StatementThe safest approach to Hirschsprung surgery involves some form of biopsy (laparoscopic or full-thickness through umbilicus) prior to definitive pull-through.Open
StatementLeveling colostomy may be the safest approach when institutional pathology expertise in reading Hirschsprung biopsies is limited or unavailable.Open
StatementLeveling colostomy represents a three-stage procedure for Hirschsprung disease management.Open
QuotationBelinda and I talk about this a lot, and it's about a comfort level and how fit, I take, I watch the clock how long I'm doing a trans anal dissection because I do not want to be stretching on those sphincters for 4 hours trying to dig up in a dark hole when I could put a scope in.Open
StatementProlonged transanal dissection (approaching 4 hours) should prompt consideration of converting to laparoscopic approach to avoid excessive sphincter stretching.Open
StatementLaparoscopic mobilization with 3-millimeter ports can be completed in approximately 45 minutes for appropriate cases.Open
StatementStandard rectosigmoid Hirschsprung disease (6-10 centimeters proximal) can be completed transanally in approximately 2 hours when the level is known from a good contrast study.Open
StatementComplications after Hirschsprung surgery are divided into two categories: obstructive symptoms (including enterocolitis, failure to thrive, abdominal distention) and soiling issues.Open
StatementSoiling after Hirschsprung surgery is further classified into true incontinence and pseudo-incontinence.Open
StatementObstructive symptoms after Hirschsprung surgery require differentiation between anatomic problems and pathologic problems.Open
StatementTrue fecal incontinence after Hirschsprung surgery can result from injury to the sphincter or injury to the dentate line.Open
StatementPseudo-incontinence after Hirschsprung surgery may be caused by underlying constipation.Open
StatementWorkup for post-Hirschsprung complications includes water-soluble contrast enema and exam under anesthesia evaluating dentate line position, stricture, stretched sphincter, and anatomic twists.Open
Hirschsprung's Disease
QuotationMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementSome infants with Hirschsprung's disease do pass meconium.Open
QuotationMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementSome infants with Hirschsprung's disease do pass meconium.Open
StatementMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementThe classic finding on contrast enema is a transition zone in the rectosigmoid, but that transition zone can be located anywhere within the bowel.Open
StatementA rectosigmoid ratio of less than 1.0 is suggestive of Hirschsprung's disease, meaning the aganglionic bowel is contracted and narrow compared to the dilated ganglionated bowel more proximal.Open
StatementIn total colonic Hirschsprung's disease, a foreshortened or question mark colon can be seen on contrast enema.Open
StatementApproximately 10% of newborns with Hirschsprung's disease may lack the typical findings on a contrast enema.Open
StatementRectal biopsy is the true definitive diagnosis for Hirschsprung disease.Open
StatementTypical features on rectal biopsy include absence of ganglion cells, presence of hypertrophic nerves, abnormal pattern of cholinesterase staining, and an absence of calretinine staining.Open
StatementTo be considered an adequate biopsy, it must be taken from the rectum at least one centimeter above the dentate line and must include both mucosa and submucosal layers.Open
StatementSuction biopsy technique is typically used for patients less than six months of age.Open
StatementFull thickness biopsy technique should be considered for patients older than six months, or when a suction biopsy is inadequate.Open
QuotationThe three studies that should be considered for evaluating for Hirschsprung's disease include contrast enema, rectal biopsy, and possibly anorectal manometry.Open
QuotationThe second part of a diagnostic workup for Hirschsprung's disease, and most important, is the rectal biopsy. It is the true definitive diagnosis.Open
StatementApproximately 10% of newborns with Hirschsprung's disease may lack the typical findings on a contrast enema.Open
StatementThe classic finding on contrast enema is a transition zone in the rectosigmoid, but that transition zone can be located anywhere within the bowel.Open
StatementA rectosigmoid ratio of less than 1.0 is suggestive of Hirschsprung's disease, meaning the aganglionic bowel is contracted and narrow compared to the dilated ganglionated bowel more proximal.Open
StatementIn total colonic Hirschsprung's disease, a foreshortened or question mark colon can be seen on contrast enema.Open
StatementRectal biopsy is the true definitive diagnosis for Hirschsprung disease.Open
StatementTypical features on rectal biopsy include absence of ganglion cells, presence of hypertrophic nerves, abnormal pattern of cholinesterase staining, and an absence of calretinine staining.Open
StatementTo be considered an adequate biopsy, it must be taken from the rectum at least one centimeter above the dentate line and must include both mucosa and submucosal layers.Open
StatementSuction biopsy technique is typically used for patients less than six months of age.Open
StatementFull thickness biopsy technique should be considered for patients older than six months, or when a suction biopsy is inadequate.Open
QuotationThe three studies that should be considered for evaluating for Hirschsprung's disease include contrast enema, rectal biopsy, and possibly anorectal manometry.Open
QuotationThe second part of a diagnostic workup for Hirschsprung's disease, and most important, is the rectal biopsy. It is the true definitive diagnosis.Open
StatementAny patient with an absent RAIR must undergo a rectal biopsy for confirmation of the diagnosis.Open
StatementIn Hirschsprung's disease, anorectal manometry shows a lack of the rectoanal inhibitory reflex (RAIR).Open
StatementThe rectoanal inhibitory reflex may be absent in other conditions as well, and some children have a false positive test.Open
StatementThe rectoanal inhibitory reflex may be absent in other conditions as well, and some children have a false positive test.Open
StatementAny patient with an absent RAIR must undergo a rectal biopsy for confirmation of the diagnosis.Open
StatementIn Hirschsprung's disease, anorectal manometry shows a lack of the rectoanal inhibitory reflex (RAIR).Open
QuotationThere are three goals to the surgical management of Hirschsprung's disease. First, identify the extent of the aganglionic segment. Second, resect that segment. And third, restore the bowel to its continuity.Open
StatementThe three goals of surgical management are: identify the extent of the aganglionic segment, resect that segment, and restore the bowel to its continuity.Open
QuotationThere are three goals to the surgical management of Hirschsprung's disease. First, identify the extent of the aganglionic segment. Second, resect that segment. And third, restore the bowel to its continuity.Open
StatementThe three goals of surgical management are: identify the extent of the aganglionic segment, resect that segment, and restore the bowel to its continuity.Open
StatementA con of the Suave procedure is that the aganglionic cuff can become stiff enough to cause an obstruction or outlet obstruction.Open
StatementIn the Suave procedure, the actual anastomosis is performed within a cuff of aganglionic rectum.Open
StatementThe Suave procedure theoretically causes less injury to pelvic structures, nerves, urethra and vagina.Open
StatementThe Suave procedure involves performing a mucosectomy from a transanal approach slightly above the dentate line and pulling through the normal bowel.Open
StatementIn the Swenson procedure, it is very important to be cautious about injuring the urethra as it's quite close, especially in boys.Open
StatementIn the Swenson procedure, you pull down the aganglionic bowel and perform a full thickness anastomosis one to two centimeters above the dentate line, leaving the most minimal amount of aganglionic bowel possible.Open
StatementThe Suave procedure involves performing a mucosectomy from a transanal approach slightly above the dentate line and pulling through the normal bowel.Open
StatementIn the Suave procedure, the actual anastomosis is performed within a cuff of aganglionic rectum.Open
StatementThe Suave procedure theoretically causes less injury to pelvic structures, nerves, urethra and vagina.Open
StatementA con of the Suave procedure is that the aganglionic cuff can become stiff enough to cause an obstruction or outlet obstruction.Open
StatementIn the Swenson procedure, you pull down the aganglionic bowel and perform a full thickness anastomosis one to two centimeters above the dentate line, leaving the most minimal amount of aganglionic bowel possible.Open
StatementIn the Swenson procedure, it is very important to be cautious about injuring the urethra as it's quite close, especially in boys.Open
StatementA child with enterocolitis presents with abdominal distension, vomiting, fever, and change in bowel habits that could be either diarrhea or not passing stool at all.Open
QuotationWhen we treat these patients with enterocolitis, it is important to provide fluid resuscitation, digital rectal exam, and colonic irrigations.Open
QuotationHirschsprung's-associated enterocolitis is poorly understood and likely is an inflammatory condition secondary to bacterial overgrowth.Open
StatementFor enterocolitis, antibiotics including metronidazole or broad-spectrum antibiotics are added depending on the severity of presentation.Open
StatementTreatment of enterocolitis includes fluid resuscitation, digital rectal exam, and colonic irrigations.Open
StatementA child with enterocolitis presents with abdominal distension, vomiting, fever, and change in bowel habits that could be either diarrhea or not passing stool at all.Open
StatementHirschsprung's-associated enterocolitis is likely an inflammatory condition secondary to bacterial overgrowth.Open
QuotationWhen we treat these patients with enterocolitis, it is important to provide fluid resuscitation, digital rectal exam, and colonic irrigations.Open
QuotationHirschsprung's-associated enterocolitis is poorly understood and likely is an inflammatory condition secondary to bacterial overgrowth.Open
StatementFor enterocolitis, antibiotics including metronidazole or broad-spectrum antibiotics are added depending on the severity of presentation.Open
StatementTreatment of enterocolitis includes fluid resuscitation, digital rectal exam, and colonic irrigations.Open
StatementHirschsprung's-associated enterocolitis is likely an inflammatory condition secondary to bacterial overgrowth.Open
StatementAnatomic problems after pull-through can include a twist in the pull through, an obstructing cuff, a non-functioning Duhamel pouch, or a transition zone or continued aganglionic segment.Open
StatementFor patients not doing well after pull-through, if there is a stricture at the anastomosis, it needs to be addressed either through dilations or revising the pull through procedure.Open
StatementFor patients without anatomic problems after pull-through, treatment can include bowel management, Botox injection to relieve sphincter tone, or motility studies.Open
StatementFor patients with anatomic problems after pull-through, you typically have to revise the pull through.Open
StatementFor patients without anatomic problems after pull-through, treatment can include bowel management, Botox injection to relieve sphincter tone, or motility studies.Open
StatementFor patients not doing well after pull-through, if there is a stricture at the anastomosis, it needs to be addressed either through dilations or revising the pull through procedure.Open
StatementAnatomic problems after pull-through can include a twist in the pull through, an obstructing cuff, a non-functioning Duhamel pouch, or a transition zone or continued aganglionic segment.Open
StatementFor patients with anatomic problems after pull-through, you typically have to revise the pull through.Open
The Colorectal Quiz Episode 1: ARM - Low Bulbar Fistula
QuotationI always worry about a missed presacral mass.Open
StatementCross-table lateral X-ray should be obtained at approximately 24 hours of life to assess the air column position relative to the perineal skin, with the baby positioned prone to allow air to rise to the buttocks.Open
StatementThe cross-table lateral film should include a marker at the expected anal location to allow measurement of the distance between the air column and the perineal skin.Open
StatementWell-formed buttocks, visible sphincter mechanism location, and well-developed sacrum together predict good prognosis for continence.Open
QuotationWell, I have two answers for you, Mark. I think if I was sitting in a hotel room, being examined by a bunch of board examiners, my answer would likely be a diverting stoma in real life, which is what we're discussing here.Open
StatementThe surgeon should never attempt posterior sagittal approach blind; imaging must confirm that the first structure encountered will be the air pocket of the distal rectum.Open
QuotationIt goes without saying and, and one of our, I think one of our big teaching points is you should never try to go in blind.Open
QuotationWe both agree that probably in real life, we would have done a primary posterior sagittal approach on this patient, and we would have found the rectum, and we could have made that rectum reach the perineum and done our anoplasty. How do we handle this? Because I didn't know that there was a fistula there. This is troublesome.Open
QuotationYou can see this fistula is very close to the rectum. And if you're going to dissect that free, and along the urethra, um, it's important to make sure that you know that those two structures are not very far apart, and getting that into that proper plane is very important.Open
StatementA bulbar fistula is located at the elbow of the urethra, using anatomic nomenclature based on the urethral location.Open
QuotationThe reason why Doctor Levitt or Mark is saying that. It's a bulbar fistula, it's at the elbow. You can see it's at the elbow of the urethra. And tell us that the uh the nomenclature we like to use is an anatomic pure anatomic nomenclature saying that it's a bulbar fistula.Open
Colorectal Quiz Episode 2: When to redo a PSARP
StatementFor anorectoplasty, if you don't get it perfect, you might not have the best outcomes, which separates it from other surgical procedures.Open
StatementA lot of surgeons agree that oftentimes your first shot might be your only shot to give this patient a good outcome and the right anatomy.Open
QuotationHow many patients, Jason, have you seen on laxatives that comes with an anus in the wrong place? How many patients have you seen having had a cecostomy with perfect anatomy? That's the real frustrating one. Right? A lot.Open
QuotationI can tell you, the family doesn't really care how technically elegant is your analplasty. What they care about is whether that analplasty that you make is going to work. And is the child going to be clean and in normal underwear and just like all the other kids?Open
StatementThe family doesn't really care how technically elegant is your analplasty. What they care about is whether that analplasty that you make is going to work and is the child going to be clean and in normal underwear.Open
StatementThe higher the malformation, the worse the prognosis.Open
StatementA sacrum ratio of 0.7 or greater usually means normal or close to normal sphincters and good muscle tone, indicating that spine innervation of that area is probably good.Open
StatementPatients can come with associated spinal anomaly, most commonly tethered cord, but the worst is a myelomeningocele, and those patients have much more trouble with continence.Open
StatementIt's amazingly common to have a mislocated anus, either because the surgeon misses where the center is during laparoscopic pull-through or opens the PSARP incision first.Open
StatementA key pitfall is opening the PSARP incision first; instead, mark the sphincters first, then open the PSARP so you don't get confused when placing the anoplasty in the correct location.Open
QuotationA key pitfall is not do that. Mark the sphincters first, then open the PSARP because then you don't get confused at the end when you're trying to place the anoplasty in the correct location.Open
StatementIn higher malformations such as a bladder neck fistula in a boy, the sphincter complex isn't always where you think it's going to be and is sometimes more anterior than anticipated.Open
StatementAn alternative approach for borderline cases is to let the child take their car out for a ride first and see how it works—if it drives well, stay with that anatomy; if not, then consider the redo.Open
Colorectal Quiz Episode 3: Hirschsprung Disease
StatementIn Hirschsprung disease, the aganglionic rectum appears narrow due to spasm and inability to relax, while the ganglionated proximal bowel is dilated, creating the recto-sigmoid ratioOpen
StatementThree good biopsy specimens should be obtained for pathologic evaluationOpen
StatementQuick diff staining highlights ganglion cells better than standard H&E stainingOpen
StatementThe crypts are located above the dentate line, so optimal biopsy location is at least 1-2 cm above the dentate lineOpen
The Colorectal Quiz Episode 3.5: Proximal Hirschsprung Disease
QuotationYeah. And I think you could make guesses about this. But like you said, it's hard on a newborn film to really discern small and large bowel. And you can get fooled.Open
StatementIt is hard on a newborn film to really discern small and large bowel, and you can get fooled.Open
StatementA limited upper GI was performed and ruled out malrotation in this child.Open
StatementPatients with proximal Hirschsprung disease are at risk of perforation, usually in the cecum.Open
QuotationSo they were quick to point out that we're lucky this patient didn't show up with a perforation. And usually they perforate in the cecum.Open
StatementTo get a perforation, you need distension, and if you have a transition zone at the hepatic flexure, then all the pressure is in the right colon.Open
StatementA baby that doesn't have a competent ileosecal valve might be saved from perforation because pressure can decompress into the small bowel.Open
QuotationYou're obligated at some point, maybe after resuscitation, to get a rectal biopsy.Open
StatementYou are obligated at some point, maybe after resuscitation, to get a rectal biopsy in a patient with suspected Hirschsprung disease.Open
StatementProximal Hirschsprung disease and distal Hirschsprung disease require two different operative approaches.Open
QuotationTwo different operative approaches for the same disease because one is more proximal and more complicated and the other is more distal.Open
StatementWith proper laparoscopic dissection, the transanal portion of a primary Hirschsprung pull-through should take well under one hour.Open
QuotationPreviously, we used to do this transanally, it would take a few hours. Now, the transanal dissection should be usually way under 1 hour, especially in a primary pull-through point.Open
QuotationPreviously, we used to do this transanally, it would take a few hours. Now, the transanal dissection should be usually way under 1 hour, especially in a primary pull-through point.Open
StatementWith proper laparoscopic dissection, the transanal portion of a primary Hirschsprung pull-through should take well under one hour.Open
StatementFor distal Hirschsprung disease, only distal branches of the IMA need to be taken, but for left colon involvement, the IMA itself may need to be taken to achieve adequate reach.Open
StatementFor distal Hirschsprung disease, only distal branches of the IMA need to be taken, but for left colon involvement, the IMA itself may need to be taken to achieve adequate reach.Open
The Colorectal Quiz Episode 8: Motility Disorders Part 1
QuotationIt's saying that this is not a Monet, that is for certain.Open
StatementContrast studies are not great predictors of how patients will respond to medical or surgical management; normal-looking colons may not respond while abnormal-appearing colons may respond wellOpen
StatementWater-soluble contrast (not barium) is used for contrast enemas because it helps empty the colon and acts as a cleanout for patients starting new medical therapyOpen
QuotationI think back in the day, Mark, yeah, we, we didn't understand the sphincter and the major role it played.Open
StatementIn the past, surgeons did not understand the major role the sphincter played in many patientsOpen
The Colorectal Quiz Episode 10: Total Colonic Hirschsprung Disease Part 1
StatementThe age cutoff for switching from suction rectal biopsy to full-thickness biopsy is around 6 monthsOpen
QuotationMy cutoff is around 6 months when I switch from suction rectal biopsy to full thickness biopsy.Open
QuotationIf the patient is doing well and able to be managed with irrigations, would love to have my final diagnosis of Hirschprung's disease through the rectal biopsy before entering the abdomen.Open
StatementIf the patient is doing well and can be managed with irrigations, it is preferable to have final pathology diagnosis of Hirschsprung disease from rectal biopsy before entering the abdomenOpen
StatementStandard biopsy locations during operative mapping include rectosigmoid, proximal sigmoid around the left colon, splenic flexure/transverse colon, and right colon or hepatic flexure areaOpen
The Colorectal Quiz Episode 11: Total Colonic Hirschsprung's Part 2
StatementDr. Fisher waits until the child has good growth and more solid stool on table food diet, sometimes adding thickeners to achieve thicker stool consistency.Open
QuotationSo how do you get them to the point where they're having more solid stool, you know, when they're on more of a solid diet and table food diet, and maybe we even add some thickeners to their diet so that their stool becomes more thick.Open
StatementDr. Fisher uses a skin training technique where families take stool from the ostomy bag and place it in the diaper for 15-20 minutes to expose virgin buttock skin to stool before pull-through.Open
QuotationThe skin, the buttock skin, has not really seen or been exposed to stool.Open
QuotationAnd so I have the families put some stool in the diaper and expose that skin to stool for a little.Open
StatementFor patients with long-standing ileostomies and high output who are not growing well, checking urine sodium (which reflects total body sodium, not just blood sodium) is a key component for growth assessment.Open
QuotationBut the one thing that I learned checking a urine sodium, the total body sodium and not just the blood sodium, is a key component for these patients, which is obviously important in growth.Open
StatementDr. Fisher checks urine sodium a few weeks after ileostomy creation prior to discharge and again a month or two later.Open
StatementLow total body sodium can be treated with salt tablets or salt addition.Open
QuotationFor this case, I typically do an ileoanal anastomosis, a straight pull through, but there are a few other options.Open
StatementDr. Fisher typically performs an ileoanal anastomosis (straight pull-through) for total colonic Hirschsprung disease.Open
QuotationI talk to the families and I, I say it's a game time decision.Open
StatementDr. Fisher makes a game-time decision on whether to divert after ileoanal anastomosis based on anastomotic appearance, blood supply, tension, and nutritional optimization; if any concerns exist, he diverts and returns 6-8 weeks later to close the ileostomy.Open
StatementFamily comfort with rectal irrigations is an important consideration when planning surgery.Open
StatementDr. Fisher's first-line medication treatment is loperamide.Open
StatementLomotil (diphenoxylate-atropine) is a controlled substance in the United States.Open
StatementDr. Fisher gives Botox immediately when intestinal continuity is established.Open
QuotationI give the Botox immediately, um, when we have intestinal continuity, and I see the child at 2 weeks post-op just for a routine check.Open
StatementDr. Fisher sees the child at 2 weeks post-op for routine check (eating, growth, rash assessment) and does not check the anastomosis until 4 weeks.Open
QuotationI don't check the anastomosis until 4 weeks.Open
StatementAt 4 weeks in clinic, Dr. Fisher performs an anastomosis check using Hagar dilators to size to the appropriate size for the child's age.Open
StatementDr. Fisher starts with a 7 or 8 Hagar dilator in clinic and gently sizes up to resistance, not to stretch but to check size; for a child who had pull-through at around 10 months, the proper size should be 13 or 14 Hagar dilator.Open
QuotationMy conversation with the family often involves that this will keratinize and look like a normal peroneal body over time.Open
QuotationMy conversation with the family often involves that this will keratinize and look like a normal peroneal body over time.Open
StatementPerineal groove with mucosal lining will keratinize and look like normal perineal body over timeOpen
StatementPerineal groove with mucosal lining will keratinize and look like normal perineal body over timeOpen
StatementSurgical intervention for perineal groove is indicated only if secreting mucus, causing irritation, or developing ulcersOpen
StatementSurgical intervention for perineal groove is indicated only if secreting mucus, causing irritation, or developing ulcersOpen
StatementVestibular fistula is very common in females and needs formal repair with hole transposed to center of sphincterOpen
StatementVestibular fistula is very common in females and needs formal repair with hole transposed to center of sphincterOpen
StatementPurpose of diversion in ARM repair is to avoid perineal body dehiscenceOpen
StatementFor vestibular fistula diagnosed in newborn period, options are primary repair if baby is well, or allow stooling through fistula for couple months then elective repair without stomaOpen
StatementPurpose of diversion in ARM repair is to avoid perineal body dehiscenceOpen
StatementPatients diagnosed with vestibular fistula at 6-12 months who have dilated rectosigmoid need diversion as first step, then repairOpen
StatementFor vestibular fistula diagnosed in newborn period, options are primary repair if baby is well, or allow stooling through fistula for couple months then elective repair without stomaOpen
StatementPatients diagnosed with vestibular fistula at 6-12 months who have dilated rectosigmoid need diversion as first step, then repairOpen
StatementTo evaluate for vestibular fistula, pull labia towards examiner with both hands to visualize vaginal opening and urethraOpen
StatementTo evaluate for vestibular fistula, pull labia towards examiner with both hands to visualize vaginal opening and urethraOpen
Colorectal Quiz Episode 14: ARM Newborn Part 3
StatementCross-table lateral films can be obtained early and then around 24 hours later in cases where there is no evidence of fistula on exam.Open
StatementIf the air column stops at about the 4th sacral vertebral body with a large distance between the air column and the sphincter marker, the patient should be considered for diversion and distal colostogram to delineate anatomy.Open
Quotationif you look at the film on the left, the air column stops at about the 4th sacral vertebral body, give or take a little bit. And so, what, and you could see where the marker is or the BB is, uh, where the, where the sphincter complex appears to be located. There's a large distance between those.Open
Quotationthe air column is very close to where the anticipated anal opening should be located. And this is a case where you could take your barley bush, potentially, and make a nick, uh, a scratch, and, and do your anoplasty.Open
StatementWhen the air column is very close to where the anticipated anal opening should be located, primary anoplasty may be performed.Open
StatementWhether to perform primary anoplasty in cases with close air column depends on individual surgeon comfort and the level of post-operative care available at the institution.Open
Quotationthat common wall or, or that wall between the rectum and the urethra is a lot closer and a lot longer. Of a common wall, then I think some people anticipate.Open
StatementThe common wall between the rectum and the urethra is closer and longer than some people anticipate.Open
StatementA patient at 24 hours with no obvious fistula and cross-table lateral showing air column not very distal needs a colostomy.Open
Colorectal Quiz Episode 15: Bowel Management in Spinal Patients - Need for a UrologistPart 1
StatementSenna-induced perineal rash is thought to be a chemical burn rather than a true allergy, presenting with blistering.Open
Quotationit's almost like a chemical burn. The cause they're blistered usually.Open
StatementSenna rash is treated with silver sulfadiazine and resolves with time; some patients tolerate senna upon reintroduction.Open
QuotationWe treat it with silver sulfadiazine, and they've all gotten better with time.Open
StatementTiming senna doses in the early morning so that bowel movements occur during the day (when diapers are changed promptly) reduces the risk of senna rash.Open
Quotationwhat we've done is we timed the dose of Senna in these patients, usually in the early morning, so that they're pooping during the day. And their diapers changed rather quickly versus potentially being in a diaper over a long period of time at night.Open
StatementBisacodyl can be administered as an enema or suppository in infants.Open
QuotationIf there's one take-home message from this podcast, you just said itOpen
Quotationthat care coordination, collaboration with the urologist might be the most beneficial thing we could do for our patients.Open
Colorectal Quiz Episode 16: Bowel Management in Spinal Patients - Need for a Urologist Part 2
StatementWhen a 7 cm appendix is shared between urology and colorectal surgery, the urologist typically takes 6.25 cm leaving only 0.75 cm for colorectal useOpen
QuotationWhen you get that really short stumpy appendix, whether it be from splitting it, and the urologist, if I have a 7 centimeter appendix, the urologist takes 6.25 centimeters and I get 0.75.Open
StatementThe colorectal team benefits from using the appendix portion closer to the cecum which has a stronger blood supplyOpen
StatementA short appendiceal stump can be extended by suturing or using a laparoscopic non-cutting linear stapler along the cecal wall to add 2-3 cm of lengthOpen
StatementOne of the problems with Malone appendicostomy is leakageOpen
StatementThe longer the Malone channel, the less likely it is to leakOpen
QuotationThe longer the channel, the less likely that Malone's going to leak.Open
StatementExtending the Malone channel by 2-3 cm using suturing or stapling can be extremely helpful in preventing leakageOpen
StatementRectal irrigation using pressurized water systems made for patients with hand difficulties is an alternative to Malone and Mitrofanoff proceduresOpen
StatementColoplast makes a rectal irrigation device for self-administration of enemasOpen
StatementAt Cincinnati Children's, 99% of Malones are placed in the umbilicus and almost all Mitrofanoffs are in the right lower quadrant with a tunnel channel through the rectus to prevent leakageOpen
StatementThe primary determinant of orifice location is where the appendix reaches and its blood supplyOpen
StatementLaxity of the pelvic floor and anal canal is a huge issue in spinal patients, especially when doing retrograde enemasOpen
Colorectal Quiz Episode 17: Cloaca Part 1
QuotationThis is huge. This is why, this is real time, and we all know a book chapter takes five years to, three to five years to get published.Open
Colorectal Quiz Episode 18: Cloaca Part 2
StatementDuring cystoscopy it is important to look for cervices to understand Müllerian development (one vagina vs. two, presence of uterus) and to identify ureteral orifices, which in complex malformations may attach anomalously low to the bladder or bladder neck.Open
QuotationBut I think our management style now here at Cincinnati Children's has been to try to maximize medical therapy, understand the anatomic and functional issues, and then if we can't overcome those issues with medical management, resort to surgical intervention and potential resection.Open
StatementThe management approach at Cincinnati Children's is to maximize medical therapy and understand anatomic and functional issues before resorting to surgical intervention and potential resection.Open
QuotationI want to stress that we shouldn't resort to resection right away just because we have one abnormal finding.Open
StatementResection should not be performed immediately based on one abnormal finding; multiple factors must be considered.Open
QuotationOne, you have to ensure normal anatomy.Open
StatementThe first step in evaluating a patient with suspected motility disorder is to ensure normal anatomy, which can be assessed with contrast studies.Open
Colorectal Quiz Episode 19: Hirschsprung Disease - The Obstructed Patient Part 1
QuotationI think one key thing to talk about with all our listeners is when you do that exam, make sure you step to the side. A little bit funny, but a little bit, you don't wanna be in the way of what could be coming out.Open
StatementWhen performing initial rectal exam on a distended child with suspected enterocolitis, step to the side because there may be an explosive release of stool and gas.Open
StatementFor a patient with prior Hirschsprung diagnosis presenting sick, assume Hirschsprung-associated enterocolitis; treatment with rectal irrigations, IV fluids, and antibiotics will not cause harm even if the diagnosis is different (e.g., Crohn's disease, E. coli enterocolitis).Open
QuotationIf you have a patient that comes in with a diagnosis of Hirschprung's in the past and comes with, comes in sick, you have to assume it's Hirschprung's associated enterocolitis.Open
StatementFamilies should not undergo Hirschsprung pull-through surgery until they can demonstrate ability to perform rectal irrigations, and they should be discharged with supplies to perform irrigations at home.Open
StatementIn a logical workup, obtain the contrast study before going to the OR for rectal exam under anesthesia, as it may reveal findings that guide the surgical approach.Open
QuotationI think we all agree we get the contrast study before going to the operating room for a rectal examOpen
StatementA lateral view on contrast enema is important because it provides significant information about the presacral space and distal rectum anatomy.Open
The Colorectal Quiz Episode 20: Hirschsprung Disease Obstruction Part 2
StatementBotox is being studied to prevent enterocolitis with the theory of chemo-denervating nerves in the area instead of permanent stretch or anatomic destruction from surgeryOpen
QuotationIs now, let's say 3 centimeters, or 4, or 5. Well, is that the problem that this kid did well until that cuff got to a length, that's a ganglionic, and now it's causing obstructive problems.Open
StatementInitial treatment for obstructed Hirschsprung's patient must include rectal irrigation, done earlyOpen
StatementEvery institution should have a protocol for obstructed Hirschsprung's patients to ensure quick and efficient responseOpen
StatementSystematic workup for obstructed Hirschsprung's includes: resuscitation, imaging studies, and comprehensive rectal exam under anesthesiaOpen
The Colorectal Quiz Episode 21: The History of Hirschsprung Disease
StatementDoctor Martin developed the Martin procedure, an extended Duhamel procedure that leaves a longer aganglionic segment of rectum for long-segment Hirschsprung disease.Open
StatementIn 1977, Doctor Martin was the first to apply the endorectal pull-through technique used in Hirschsprung disease to the surgical treatment of ulcerative colitis, performing total proctocolectomy with ileoanal anastomosis.Open
StatementDoctor Martin's ulcerative colitis technique predated the J-pouch, which later modified his approach.Open
The Colorectal Quiz Episode 22: Hirschsprung Disease - the Soiling Patient Part 1
StatementPathology can change over time; cases exist where ganglion cells were present at pull-through but absent with hypertrophic nerves 7 years later when problems developed.Open
StatementSphincters should be assessed with the patient awake; examination under anesthesia makes it harder to assess sphincter function.Open
StatementDuring normal bowel movements, sphincters relax and the anus opens with some mucosal descent, but as soon as sphincters tighten, the mucosa retracts back in; prolapse at rest indicates damaged muscles and/or mucosa brought too low at anastomosis.Open
StatementIf terminal ileum cannot be intubated, gastroenterologists may treat presumptively and re-scope after a few months of treatment when inflammation has decreased.Open
StatementThe highest risk factors for lymphoma with biologic therapy are male gender, teenage age, and combination therapy with methotrexate.Open
StatementMale gender over the age of 10, and presence of a fistula are risk factors with much higher incidence of Crohn's disease being diagnosed in patients presenting with perianal lesions to the emergency room.Open
StatementIn pediatric patients, unlike adult patients, the first presenting factor for Crohn's disease can often be perianal disease.Open
QuotationI don't like to make holes when there aren't holes there.Open
QuotationThe thing that's going to heal first is the mucosa.Open
StatementThe mucosa heals first compared to skin in perianal disease, so leaving a mucosal opening without a seton risks recurrent abscess when biologics heal the mucosa.Open
StatementMaking a large cruciate incision and packing a perianal abscess in a child with undiagnosed Crohn's disease may result in non-healing and potentially require colostomy or ileostomy.Open
QuotationYou may have bought that kid a colostomy or ileostomy.Open
StatementHydrogen peroxide is preferred over methylene blue for identifying fistula tracts because it is neater; 3% hydrogen peroxide in a syringe with 16-20 gauge angiocath is used with a speculum in the anus.Open
StatementWhen a fistula opening cannot be found despite hydrogen peroxide testing, a seton should not be placed at that time to avoid creating a hole where there isn't one.Open
StatementSource control of infection must be achieved before starting immunosuppressive therapy including steroids and biologics.Open
StatementIf an abscess is not adequately drained, reimaging should be performed before giving biologics or steroids.Open
StatementBefore removing a seton, the bottom must look better, drainage must be better, the patient must be symptom-free, and they must have reached steady state of biologic (loading dose plus at least 3 more doses, typically 2-3 months from start).Open
StatementInflammatory markers including fecal calprotectin, ESR, and CRP should be checked before removing a seton to ensure systemic disease is under control.Open
StatementThe initial Remicade paper from 1998 or 1999 in the New England Journal of Medicine was on perianal disease and demonstrated improved healing time and improved length of time between recurrence when combination of seton and infliximab is used versus either separately.Open
Hirschsprung Disease in Brief
StatementHirschsprung disease is a congenital anomaly of the GI tract that results in a functional bowel obstruction.Open
QuotationMore than 95% of neonates pass meconium within the first 48 hours of life. And failure to pass meconium is typical of Hirschsprung's disease.Open
StatementFailure to pass meconium within the first 48 hours of life is typical of Hirschsprung's disease.Open
StatementMore than 95% of neonates pass meconium within the first 48 hours of life.Open
StatementUp to 10% of children with Hirschsprung's disease will have trisomy 21.Open
StatementHirschsprung disease is associated with Wordenberg syndrome and congenital central hyperventilation (Andine's curse).Open
StatementOnly 1 to 2% of patients with trisomy 21 have Hirschsprung's disease.Open
StatementThe RET gene is a predisposing genetic condition associated with Hirschsprung disease.Open
StatementAbout 10% of children with Hirschsprung disease will have a positive family history.Open
StatementThe three studies that should be considered for evaluating for Hirschsprung's disease include contrast enema, rectal biopsy, and possibly anorectal manometry.Open
QuotationThe classic finding is a transition zone in the rectosigmoid, but that transition zone really can be located anywhere within the bowel.Open
StatementThe classic finding on contrast enema is a transition zone in the rectosigmoid, but that transition zone can be located anywhere within the bowel.Open
StatementA rectosigmoid ratio of less than 1.0 is suggestive of Hirschsprung's disease.Open
StatementRectal biopsy is the true definitive diagnosis for Hirschsprung disease.Open
QuotationThe second part of a diagnostic workup for Hirschsprung's disease, and most important, is the rectal biopsy. It is the true definitive diagnosis.Open
QuotationTypical features on the biopsy include absence of ganglion cells, presence of hypertrophic nerves, abnormal pattern of colon esterase staining, and an absence of calretinine staining.Open
StatementTypical features on rectal biopsy include absence of ganglion cells, presence of hypertrophic nerves, abnormal pattern of colon esterase staining, and an absence of calretinine staining.Open
StatementTo be considered an adequate rectal biopsy, it must be taken from the rectum at least 1 cm above the dentate line and must include both mucosa and submucosal layers.Open
StatementSuction rectal biopsy technique is typically used for patients less than 6 months of age.Open
StatementFull thickness rectal biopsy technique should be considered for patients older than 6 months or when a suction biopsy is inadequate.Open
StatementAny patient with an absent RAIR must undergo a rectal biopsy for confirmation of the diagnosis.Open
QuotationThere are three goals to the surgical management of Hirschsprung disease. First, identify the extent of the aganglionic segment. Second, resect that segment. And third, restore the bowel to its continuity.Open
StatementThe three goals of surgical management of Hirschsprung disease are: identify the extent of the aganglionic segment, resect that segment, and restore the bowel to its continuity.Open
StatementThe Swensen technique is a full thickness dissection and anastomosis.Open
StatementThe Duamel procedure involves performing a pouch with an anastomosis of aganglionic and ganglionated bowel.Open
StatementThe Suave procedure is a mucosectomy where you leave a cuff of aganglionic bowel and bring the ganglionated bowel through that cuff of rectum and perform the anastomosis.Open
StatementThe three procedures for Hirschsprung disease (Swensen, Suave, Duamel) all involve a transanal approach of removing the aganglionic colon and pulling down healthy colon and sewing it to the anus.Open
StatementHirschsprung's associated enterocolitis is poorly understood and likely is an inflammatory condition secondary to bacterial overgrowth.Open
StatementA child with enterocolitis presents with abdominal distention, vomiting, fever, and change in bowel habits.Open
StatementEnterocolitis must be recognized as potential enterocolitis and treated urgently.Open
StatementTreatment for enterocolitis includes fluid resuscitation, digital rectal exam, and colonic irrigations.Open
StatementDepending on the severity of enterocolitis, broad-spectrum antibiotics are sometimes added, and patients are usually started on metronidazole.Open
QuotationHirschsprung's associated enterocolitis is poorly understood and likely is an inflammatory condition secondary to bacterial overgrowth.Open
The Colorectal Quiz Episode 23: Hirschsprung Disease - The Soiling Patient...
QuotationCan I scare you for a moment? Can we talk scientifically for one minute? I know this is crazy.Open
StatementThe dentate (or pectinate) line is the transition from squamous epithelium to columnar epithelium, located about 2/3 of the way up the anal canal.Open
StatementBlood supply changes occur at the dentate line (splanchnic versus systemic), and there is also innervation in that area.Open
QuotationI talk about that dentate line in the area where the nerves are located that tell you gas, liquid, solid. How hard do I need to squeeze, how long do I have to squeeze for, how tight do I have to squeeze?Open
StatementThe nerves located at the dentate line region tell you gas, liquid, solid; how hard, how long, and how tight to squeeze.Open
StatementPreserving the dentate line region is key because injury to that region affects a patient's ability to be continent.Open
StatementIn children with anorectal malformation, Hirschsprung disease, spinal conditions, or combinations thereof, the ability to sense stool in the rectum or neorectum region is critical to success; the right consistency and bulk of stool is very important.Open
StatementIf clinicians make stool too soft or too loose with medications, they put a child on the edge of having control or not and throw them over that edge, preventing success.Open
QuotationAnd if we make it too soft or too loose, we're putting a child or a person who is on the teeter of having control or not, and you throw them over that edge, and, and you just won't be successful.Open
QuotationI mean, it makes sense that they should if the muscle is intact, right, because this is no different than an anorectal malformation, anastomosis. That's right. But it's, it's, it's rectum or colon mucosa to skin.Open
StatementA Hirschsprung patient with missing dentate line and intact muscle should be able to achieve continence, similar to an anorectal malformation anastomosis (rectum or colon mucosa to skin).Open
StatementPatients with no dentate line and patulous sphincters who are soiling develop severe skin irritation from sitting in pull-ups or diapers.Open
QuotationThat is a patient with no dentate line and pattula sphincters, and you clearly see with the skin changes around that, that this patient has really struggled and has been soiling and, and, and sitting in, in pull-ups or a diaper, really causing severe skin irritation.Open
StatementFor hypermotile patients (stooling 7-8 times a day), the approach is to constipate them first, then figure out how to empty them in a time-controlled fashion.Open
QuotationThis, this is, these are the harder patients to take care of, and the trick that I use is you have to constipate them. And then if they're able to empty with continence on their own, then great. If they're not, then you have to mechanically help them empty.Open
StatementWhether hypermotile patients can empty on their own versus needing mechanical emptying to maintain social continence depends on their sphincter function.Open
QuotationBut it, it's, it's like, it sounds counterintuitive, but at least the way I treat these patients, I constipate them, and then I empty them.Open
QuotationBut that's how I sort of explain it to the families. It sounds weird, but we're gonna constipate you, and then we have to figure out how to empty you in a time-controlled fashion.Open
StatementSome Hirschsprung patients who have a good operation have super strong sphincters that just need a little relaxation to allow passage of stool until they learn proper sphincter coordination for evacuation.Open
StatementBotox helps train sphincters in Hirschsprung patients; anorectal manometry can provide objective data showing resting pressures are usually on the higher end of normal, and some patients need extra relaxation to allow them to go.Open
StatementNutrition in Hirschsprung patients is very important; some patients are very sensitive to certain foods, particularly lactose.Open
StatementPaying attention to diet (whether breastfed infants or older children) is important because lactose is particularly problematic in some Hirschsprung patients.Open
QuotationNone. We have to get it right the first time.Open
StatementEvery Hirschsprung patient should be able to do well; they might need help and might need mechanical evacuations or Botox, but all should be able to get on the right track.Open
QuotationAnd if you don't get it right, you gotta use these techniques and this algorithm to figure out what's wrong, cause we could get every patient doing well. They might need help, and they might need mechanical evacuations, Botox, etc. but we could, we all should be able to get these patients on the right track.Open
Colorectal Quiz Episode 28: Female ARM Management - Perineal Fistula
StatementWhen neurologic anomalies are found in anorectal malformation patients, gynecological anomalies are more likely, especially on the same side.Open
Quotationwhen you do find neurologic anomalies. That leads to more likely gynecological anomalies as well, especially on the same side.Open
Colorectal Quiz Episode 29: Female ARM-Post Op Management
StatementDr. Fisher's protocol for perineal body primary repair (no stoma) is 5-7 days NPO on D10 via midline catheter (not PICC line) until the repair is confirmed healed.Open
QuotationJust because it's published doesn't mean it works.Open
QuotationMy only concern is what's the continence rate of your patients?Open
QuotationI guess my question is somewhere around 20% required a redo either local or total operation. Most just like local, but what did a functional out in the end of the game, all the parents want is their kid pooping in the potty. And we don't know that answer.Open
QuotationThat's a very valid point. So what you're saying, wait, wait, Mark agreed with me.Open
QuotationAnd when I was working with Mark here, I know, especially in the older patients that we were doing redos on, used to teach me to make the anoplasty maybe a little larger.Open
Colorectal Quiz Episode 37: The Yancey-Soave story of the original surgical descriptions for Hirschsprung disease
StatementDr. Newman brought Dr. Yancey's story to the attention of the Hirschsprung interest group at APSA.Open
StatementA fellow at Children's National wrote an operative note describing a patient as status post a 'Yancey-Suave procedure,' indicating the terminology has become part of standard practice.Open
QuotationI was reading the operative note from one of my fellows who provided the history of the patient. I had to do a reoperation on the patient. And the history read that this five-year-old child is status post a Yancey Suave procedure in such and such date and had an asthmatic stricture.Open
Colorectal Quiz Episode 38: Transitional Care in Colorectal Surgery
StatementMRI with specific protocols and endorectal ultrasound can help determine whether the anoplasty is within the muscle complex.Open
StatementThe transition model includes joint clinic visits and collaborative operating, which is key to successful handoff.Open
StatementFreestanding children's hospitals face greater challenges than integrated hospitals because they are completely separate entities both physically and financially.Open
StatementIn Cincinnati, ARM patients still come to the colorectal center at the children's hospital whether they are 12 or 40 years old, partnering with an adult colorectal surgeon; collaborative operating occurs at the University of Cincinnati with adult colorectal surgeons, adult neurologists for urology, and pediatric urologists who have privileges at the university.Open
StatementAdult hospitals are much more adept and skilled at managing perioperative complications like pulmonary embolism or myocardial infarction; such events in a children's hospital lead to many meetings and potential for poor outcomes.Open
StatementPhysicians and surgeons are making progress on transition, but the greater struggle is providing intensive bowel management training for 35-year-old patients; pediatric centers are adept at bowel management for patients of any age, but currently adult patients requiring intensive outpatient bowel management are still being seen at children's hospitals.Open
StatementIn anorectal malformation patients with perforation, the sigmoid colon typically perforates with a linear, longitudinal tear along the taenia.Open
QuotationYou need to break the cycle of the physiologic obstruction. They are obstructed both at the sphincter level and in the aganglionic segment. And you have to break that cycle by getting a tube across it and then a lumen of that tube then to allow for egress of that stool because it's the stasis that's the problem. It's the stasis, the bacterial overgrowth. That overgrowth leads to translocation and that's where the sepsis comes in.Open
StatementThe pathophysiology of Hirschsprung enterocolitis involves physiologic obstruction at both the sphincter level and in the aganglionic segment, leading to stasis, bacterial overgrowth, translocation, and sepsis.Open
StatementCold saline used for irrigations in small children can significantly change the child's body temperature, so warm saline should be used.Open
StatementSawtoothing in the rectum on contrast enema represents hyperperistalsis and is very classic for Hirschsprung disease, particularly when associated with enterocolitis.Open
StatementIf a patient has recovered from enterocolitis and irrigations are going well with reliable family, it is reasonable to send them home for 1-2 months before definitive operation rather than operating at 2 weeks.Open
QuotationIf it was a reliable family and irrigations were going well, I probably would have sent them home for a couple, a month or two, and then brought them back for their definitive operation.Open
StatementLiterature from the PCPLC and Michael Rollins shows that delayed definitive surgery for Hirschsprung disease (around 3 months out) has similar outcomes, so it is okay to wait as long as patient receives good irrigations and is growing and healthy.Open
QuotationI agree with Mark. I would wait minimum four weeks from getting healthy after treating enterocolitis, maybe even longer before doing this. And I think there's good literature out there from the PCPLC and Michael Rollins on outcomes of Hirschsprung's disease and delayed treatment and delayed mepeter, wrong term. But just doing the definitive surgery, they looked at about three months out and had similar outcomes.Open
StatementIf mapping the colon without frozen section available, the entire colon should be mapped (left colon, transverse colon, and hepatic flexure/right colon) to avoid missing ganglionic segments.Open
QuotationI'm a fan of doing ileostomies in these cases where we need to divert and we have time and we're in a place where we're able to keep the patients hydrated well.Open
StatementIn settings where patients can be kept well hydrated with easy healthcare access, ileostomy is preferred over colostomy for diversion because colostomy mesentery becomes shortened and inflamed after division, making subsequent pull-through technically difficult with inadequate reach.Open
StatementWhen performing ileostomy for Hirschsprung diversion, frozen section should be done on the ileostomy to ensure it will function.Open
StatementCincinnati group is conducting a non-randomized study of Botox injection at the anal sphincter at time of ileostomy closure, with retrospective baseline comparison and prospective data collection currently in mid-30s patients; some patients in the protocol have still developed enterocolitis, so it is not 100% effective.Open
QuotationWe send the families home with the equipment to irrigate. That's a must, right? And also we teach how to irrigate before we do our pull through so that they are, and make the parents practice whether the child has enterocolitis or not pre-op so that they know how to do it.Open
StatementFamilies should be sent home with equipment to irrigate and taught how to irrigate before the pull-through so they can practice, ensuring they know the technique before discharge and avoiding catheter passage through fresh anastomosis post-op day 5.Open
Colorectal Quiz: Episode 43
StatementAbout 60% of the time there is success with using a split appendix for both Malone and Mitrofanoff, but about 40% of the time you cannot make it work.Open
StatementThe longer the appendix, the less likely it will leak based on Poiseuille's law (flow through a tube based on radius to fourth power and length).Open
StatementDr. Frischer and Levitt did 10 Malones in a row without plicating and five leaked, so they decided to plicate them all and have not had a leakage in several years.Open
QuotationSo we plicate them all. And I haven't had a leakage in a long, long time, several years. So I think it's a very effective strategy.Open
StatementIf appendix is short and stumpy, it is best for the Malone and the Mitrofanoff should be made from small bowel.Open
StatementIf appendix is 7 centimeters or greater it can be split, requiring minimum 2 centimeters for the Malone and 5 centimeters minimum for the Mitrofanoff.Open
StatementIf appendix is 5 to 7 centimeters, that is not enough to share and should go for the Mitrofanoff because long term the Mitrofanovs do much better, requiring a neo-Malone.Open
StatementUsing a 10 French tube (not 8), leaving it in for a month, and cathing twice a day can minimize stenosis rate.Open
StatementLeaving indwelling tubes in Malones increases the amount of prolapse, likely due to pressure on the appendiceal base pushing up mucosa.Open
StatementUrologists almost never get stenosis of Mitrofanovs because they catheterize every four hours; applying this to Malones by cathing twice daily has reduced stenosis rate.Open
StatementFor lost Malone access, blow up a balloon on a Foley catheter to occlude the umbilicus and inject dye under pressure to find any micro hole tract.Open
Colorectal Quiz: Episode 40
StatementOptions for vaginal reconstruction when native vagina cannot reach include: dilating the existing introitus, opening the area and laying in a buccal graft, or waiting for tissue engineering options expected within 20 years or less.Open
QuotationI think it's going to be, there are people right now taking a few vaginal cells and growing them and hopeful, just like you said, Mark, we're going to have some great tissue engineering that will assist us and make this a easier and better procedure for our patients.Open
StatementIf a neovagina bridge is functioning well without problems, there may be no reason to remove it later.Open
Colorectal Quiz Episode 32: Anorectal Malformations And Cardiac Anomalies
QuotationDo you automatically get an echo on every one of your anorectal malformation babies?Open
StatementFor perineal fistula or vestibular fistula in a female, one can consider just dilating with good evacuation and letting the cardiac situation play itself out.Open
StatementIn a cardiac patient with an external opening from ARM, the typical approach is to dilate as long as they're evacuating okay.Open
QuotationMy concern would be if you're going to have a significant cardiac lesion that's going to likely require early surgery, you have a blue baby. You're having a lesion that a patient isn't oxygenating well. And then I worry about the healing of that repairOpen
StatementIn a blue baby with significant cardiac lesion requiring early surgery where patient isn't oxygenating well, there is concern about healing of an ARM repair.Open
StatementFor umbilical access in laparoscopy, dissect in with a mosquito, ensure you're in the peritoneum without touching any vessel before insufflation, and clear the line of air.Open
QuotationDissecting in with a mosquito, making sure you're in, not touching any vessel before you insufflate, and also clear the line of airOpen
StatementThe white beads along the raphe should be scraped off during repair, as they can persist into teenage years and young adulthood if left alone.Open
QuotationI've seen teenagers and young adults with those beads that never went away. So, yeah, you've got to scrape that offOpen
StatementFor a 50-50 perineal fistula (half within muscle complex, half anterior), leave the anterior wall as it's the danger zone, mobilize posteriorly to fill the anal sphincter, creating an 80-20 reconstruction.Open
Colorectal Quiz Episode 29: Female ARM
StatementDr. Frisher uses a midline catheter (not PICC line) with D10 until the repair is confirmed healed, typically five to seven days NPO.Open
StatementApproximately 20% of patients in the dilation study required a redo operation, either local or total, with most being local procedures.Open
The Colorectal Quiz Episode 21: The History of Hirschsprung Disease
QuotationHe united us. Yeah. In a way. And he doesn't even know it.Open
StatementDr. Martin was the first surgeon-in-chief and pediatric surgeon at Cincinnati Children's Hospital.Open
StatementDr. Martin developed the Martin procedure, an expansion of the Duhamel for long-segment Hirschsprung disease, leaving a longer aganglionated segment of rectum and pulling through ganglionated bowel.Open
QuotationI think that's the who's who of Hirschsprung's right there.Open
QuotationI have a feeling we're going to have way more discussions about Hirschsprung disease because just because, because I think it's a fascinating disease that there are so many intricacies. You just mentioned dentorocolitis. We could talk forever about that.Open
The Colorectal Quiz Episode 4
Quotationthey must see submucosa. And if you send them a biopsy without submucosa, our pathologist will say, hey, where's the submucosa? Because you want to make sure, again, that you don't find ganglion cells in the seromuscular layer and hypertrophic nerves in the submucosal layer.Open
StatementFrozen section biopsy must include submucosa to avoid missing hypertrophic nerves in submucosal layer while finding ganglion cells in seromuscular layerOpen
StatementMesenteric dissection should stay close to bowel wall, not deep in mesentery, to reduce bleedingOpen
StatementMust preserve arcade along left colon and sigmoid to get enough length to reach pelvisOpen
QuotationYou need to be very careful of preserving that arcade along the left colon and sigmoid colon so you could get enough distance to reach the pelvis.Open
StatementResection margin should be approximately five centimeters above biopsy site where bowel looks goodOpen
StatementIn higher malformations such as bladder neck fistula in boys, the sphincter complex is sometimes more anterior than anticipatedOpen
StatementAlternative approach for borderline anatomy: let the child try their current anatomy first; if it works well, stay with it; if not, consider redoOpen
The Colorectal Quiz: Episode 1
StatementPre-sacral masses are rare in typical imperforate anus but occur in almost half of anal stenosis or rectal atresia cases, requiring MRIOpen
Quotationif it's an anal stenosis or a rectal atresia defect, then you need to be very worried about finding a pre-sacral mass. And almost half the time, you'll find one. And those patients will end up getting an MRI.Open
StatementCross-table lateral x-ray should be obtained at approximately 24 hours of life to assess gas column height and guide surgical planningOpen
QuotationWe typically get at about the 24-hour mark, give or take a few hours, a cross table lateral to see what does the gas column look like in this patient? Is there a low gas column that looks like it's almost touching the skin or is it pretty high up? And that might dictate what your next steps might be.Open
StatementWell-formed buttocks, good muscle, true sphincter mechanism area, and well-developed sacrum together indicate likely good prognosisOpen
StatementWith air column 8.8mm from skin, primary posterior sagittal anorectoplasty is a reasonable option based on imagingOpen
QuotationI have two answers for you, Mark. I think if I was sitting in a hotel room being examined by a bunch of board examiners, my answer would likely be a diverting stoma in real life, which is what we're discussing here. What would we do on a Tuesday afternoon? I think this air column is, if you're going to get this x-ray and base your decision-making on where the air column is and what's going on, I'm pretty apt to say I might perform a primary posterior sagittal anorectoplasty with this type of imaging in front of me.Open
StatementShould never try to go in blind—must know what structure will be encountered before making posterior sagittal incisionOpen
Quotationyou should never try to go in blind, right? We're going in with knowing that if we make a posterior sagittal incision right now, the first thing we're going to hit is that air pocket, which is the distal rectum.Open
StatementBulbar fistula nomenclature refers to anatomic location at the elbow of the urethraOpen
StatementFistula can be very close to rectum, making proper plane dissection along urethra importantOpen
Quotationyou can see this fistula is very close to the rectum. And if you're going to dissect that free and along the urethra, it's important to make sure that you know that those two structures are not very far apart. And getting that into that proper plane is very important.Open
QuotationThe reason why Dr. Levitt or Mark is saying that it's a bulbar fistula is it's at the elbow. You can see it's at the elbow of the urethra. And tell us that the nomenclature we like to use is an anatomic, pure anatomic nomenclature saying that it's a bulbar fistula.Open
Jason's statements about Congenital Diaphragmatic Hernia21 statements
QuotationI've seen it associated with congenital diaphragmatic hernias a few times, and I think that's when we have a high suspicion for it.Open
Quotation60% happen in the first year of life in the pediatric population, and so about 21% in the first month and over a third in the first year of life.Open
Statement60% of gastric volvulus cases in the pediatric population happen in the first year of life, with about 21% in the first month.Open
QuotationIf the child's like 4 months old, is it more likely, are you're more likely to have an acute problem or a chronic problem? So they're acute.Open
StatementIn a 4-month-old child with gastric volvulus, acute presentation is more likely than chronic.Open
QuotationThat's the big one, I think, right there. I think a little bit of bloody aspirate from the. Logo can't advance it. Funny looking stomach bubble on the X-ray.Open
StatementA little bit of bloody aspirate from the NG tube and a funny looking stomach bubble on X-ray are key findings in gastric volvulus.Open
StatementChronic gastric volvulus is more related to laxity of the gastric ligaments including gastrophrenic, gastrosplenic, gastrocolic, and gastrohepatic ligaments.Open
QuotationThose are more to do with the laxity of the gastric ligaments, and the stomach has ligamentous attachments basically surrounding the entire stomach from gastrophrenic, gastrosplenic, gastrocolic. And of course. Gastropatic ligament.Open
StatementOrganoaxial volvulus is the first and most common type of gastric volvulus.Open
QuotationThe first one, the first and most common is organoaxial volvulus.Open
StatementIn organoaxial volvulus, the stomach spins around an axis drawn between the GE junction and the pylorus, with the greater curvature flipping up and over to become more superior than the lesser curvature.Open
QuotationThey describe a line that's drawn on this diagram between the GE junction and the pylorus, and it's spinning around that axis. The greater curvature then sort of flips up and over and becomes more superior than the lesser curvature.Open
StatementIn mesenteroaxial volvulus, rotation occurs around a line through the middle of the stomach from lesser to greater curvature, with the stomach flipping behind and back over.Open
QuotationThen, and flip the stomach up and over that way, so it's going sort of behind. The stomach and back over it.Open
StatementIn gastric volvulus, when filled with contrast, the pylorus appears right next to or near the GE junction and above the body of the stomach.Open
QuotationWhen the pylorus is at, right next to the GE junction or near the GE junction, and above the body of the stomach.Open
StatementIn mesenteroaxial volvulus, the duodenum may fill above or superior to the GE junction because the pylorus has flipped up and over or behind and over the top of the stomach.Open
QuotationMesentero axial favulus. Again, this is the sort of pylorus flipping up and over or behind and over the top of the stomach, and then therefore, your pylorus is located all the way up here.Open
StatementWhen managing gastric volvulus found during CDH repair, viability of the stomach must always be checked, especially if chronically volvulized or volvulized for a couple of days, by looking at the serosa and blood flow.Open
QuotationAlso, you always want to check the viability of the stomach. So, right, if this is chronically volvulized or been volvulized for a couple of days, uh, at least looking at the cirrhosa and looking at the blood flow.Open
Jason's statements about Congenital Lung Lesions (CPAM)15 statements
StatementIn asymptomatic newborns with prenatally diagnosed lung lesions, most US practitioners obtain chest X-ray initially in NICUOpen
StatementCT angiography for congenital lung lesions is typically performed at 3-6 months in clinic rather than in NICU for asymptomatic patientsOpen
StatementCT angiography for congenital lung lesions is typically performed at 3-6 months in clinic rather than in NICU for asymptomatic patientsOpen
StatementWhen using energy devices for vessel control, leave enough remnant tissue so the vessel doesn't retract if seal fails, allowing purchase for clip or sutureOpen
StatementWhen using energy devices for vessel control, leave enough remnant tissue so the vessel doesn't retract if seal fails, allowing purchase for clip or sutureOpen
StatementObtain proximal control or partially cut across vessel with energy device to detect failure before complete divisionOpen
StatementObtain proximal control or partially cut across vessel with energy device to detect failure before complete divisionOpen
StatementWhen using staplers, visualize the stapler end, use appropriate staple size for tissue, and leave extra tissue around stapler edge for adequate coaptationOpen
StatementWhen using staplers, visualize the stapler end, use appropriate staple size for tissue, and leave extra tissue around stapler edge for adequate coaptationOpen
StatementNewborn with esophageal atresia, dextrocardia, and respiratory instability at birth suggests complex anatomy beyond typical EA/TEFOpen
StatementNewborn with esophageal atresia, dextrocardia, and respiratory instability at birth suggests complex anatomy beyond typical EA/TEFOpen
StatementEcho findings of mesocardia, hypoplastic pulmonary arteries, persistent left SVC, and dilated right ventricle indicate significant cardiac anomaliesOpen
StatementEcho findings of mesocardia, hypoplastic pulmonary arteries, persistent left SVC, and dilated right ventricle indicate significant cardiac anomaliesOpen
StatementEsophageal lung is rare congenital anomaly with approximately 30 reported cases where bronchus arises directly from esophagus rather than tracheaOpen
StatementEsophageal lung is rare congenital anomaly with approximately 30 reported cases where bronchus arises directly from esophagus rather than tracheaOpen
Jason's statements about Congenital Pulmonary Airway Malformation7 statements
StatementCT angiography for congenital lung lesions is typically performed at 3-6 months in clinic rather than in NICU for asymptomatic patientsOpen
StatementWhen using energy devices for vessel control, leave enough remnant tissue so the vessel doesn't retract if seal fails, allowing purchase for clip or sutureOpen
StatementObtain proximal control or partially cut across vessel with energy device to detect failure before complete divisionOpen
StatementWhen using staplers, visualize the stapler end, use appropriate staple size for tissue, and leave extra tissue around stapler edge for adequate coaptationOpen
StatementNewborn with esophageal atresia, dextrocardia, and respiratory instability at birth suggests complex anatomy beyond typical EA/TEFOpen
StatementEcho findings of mesocardia, hypoplastic pulmonary arteries, persistent left SVC, and dilated right ventricle indicate significant cardiac anomaliesOpen
StatementEsophageal lung is rare congenital anomaly with approximately 30 reported cases where bronchus arises directly from esophagus rather than tracheaOpen
Jason's statements about Constipation18 statements
The Colorectal Quiz Episode 8: Motility Disorders Part 1
QuotationIt's saying that this is not a Monet, that is for certain.Open
StatementContrast studies are not great predictors of how patients will respond to medical or surgical management; normal-looking colons may not respond while abnormal-appearing colons may respond wellOpen
StatementWater-soluble contrast (not barium) is used for contrast enemas because it helps empty the colon and acts as a cleanout for patients starting new medical therapyOpen
QuotationI think back in the day, Mark, yeah, we, we didn't understand the sphincter and the major role it played.Open
StatementIn the past, surgeons did not understand the major role the sphincter played in many patientsOpen
Colorectal Quiz Episode 16: Bowel Management in Spinal Patients - Need for a Urologist Part 2
QuotationWhen you get that really short stumpy appendix, whether it be from splitting it, and the urologist, if I have a 7 centimeter appendix, the urologist takes 6.25 centimeters and I get 0.75.Open
StatementWhen a 7 cm appendix is shared between urology and colorectal surgery, the urologist typically takes 6.25 cm leaving only 0.75 cm for colorectal useOpen
StatementThe colorectal team benefits from using the appendix portion closer to the cecum which has a stronger blood supplyOpen
StatementA short appendiceal stump can be extended by suturing or using a laparoscopic non-cutting linear stapler along the cecal wall to add 2-3 cm of lengthOpen
StatementOne of the problems with Malone appendicostomy is leakageOpen
StatementThe longer the Malone channel, the less likely it is to leakOpen
QuotationThe longer the channel, the less likely that Malone's going to leak.Open
StatementExtending the Malone channel by 2-3 cm using suturing or stapling can be extremely helpful in preventing leakageOpen
StatementRectal irrigation using pressurized water systems made for patients with hand difficulties is an alternative to Malone and Mitrofanoff proceduresOpen
StatementColoplast makes a rectal irrigation device for self-administration of enemasOpen
StatementAt Cincinnati Children's, 99% of Malones are placed in the umbilicus and almost all Mitrofanoffs are in the right lower quadrant with a tunnel channel through the rectus to prevent leakageOpen
StatementThe primary determinant of orifice location is where the appendix reaches and its blood supplyOpen
StatementLaxity of the pelvic floor and anal canal is a huge issue in spinal patients, especially when doing retrograde enemasOpen
Jason's statements about Crohn's Disease35 statements
Colorectal Quiz Episode 19: Hirschsprung Disease - The Obstructed Patient Part 1
QuotationI think one key thing to talk about with all our listeners is when you do that exam, make sure you step to the side. A little bit funny, but a little bit, you don't wanna be in the way of what could be coming out.Open
StatementWhen performing initial rectal exam on a distended child with suspected enterocolitis, step to the side because there may be an explosive release of stool and gas.Open
QuotationIf you have a patient that comes in with a diagnosis of Hirschprung's in the past and comes with, comes in sick, you have to assume it's Hirschprung's associated enterocolitis.Open
StatementFor a patient with prior Hirschsprung diagnosis presenting sick, assume Hirschsprung-associated enterocolitis; treatment with rectal irrigations, IV fluids, and antibiotics will not cause harm even if the diagnosis is different (e.g., Crohn's disease, E. coli enterocolitis).Open
StatementFamilies should not undergo Hirschsprung pull-through surgery until they can demonstrate ability to perform rectal irrigations, and they should be discharged with supplies to perform irrigations at home.Open
StatementIn a logical workup, obtain the contrast study before going to the OR for rectal exam under anesthesia, as it may reveal findings that guide the surgical approach.Open
QuotationI think we all agree we get the contrast study before going to the operating room for a rectal examOpen
StatementA lateral view on contrast enema is important because it provides significant information about the presacral space and distal rectum anatomy.Open
StatementIf terminal ileum cannot be intubated, gastroenterologists may treat presumptively and re-scope after a few months of treatment when inflammation has decreased.Open
StatementThe highest risk factors for lymphoma with biologic therapy are male gender, teenage age, and combination therapy with methotrexate.Open
StatementMale gender over the age of 10, and presence of a fistula are risk factors with much higher incidence of Crohn's disease being diagnosed in patients presenting with perianal lesions to the emergency room.Open
StatementIn pediatric patients, unlike adult patients, the first presenting factor for Crohn's disease can often be perianal disease.Open
QuotationI don't like to make holes when there aren't holes there.Open
StatementThe mucosa heals first compared to skin in perianal disease, so leaving a mucosal opening without a seton risks recurrent abscess when biologics heal the mucosa.Open
QuotationThe thing that's going to heal first is the mucosa.Open
StatementMaking a large cruciate incision and packing a perianal abscess in a child with undiagnosed Crohn's disease may result in non-healing and potentially require colostomy or ileostomy.Open
QuotationYou may have bought that kid a colostomy or ileostomy.Open
StatementHydrogen peroxide is preferred over methylene blue for identifying fistula tracts because it is neater; 3% hydrogen peroxide in a syringe with 16-20 gauge angiocath is used with a speculum in the anus.Open
StatementWhen a fistula opening cannot be found despite hydrogen peroxide testing, a seton should not be placed at that time to avoid creating a hole where there isn't one.Open
StatementSource control of infection must be achieved before starting immunosuppressive therapy including steroids and biologics.Open
StatementIf an abscess is not adequately drained, reimaging should be performed before giving biologics or steroids.Open
StatementBefore removing a seton, the bottom must look better, drainage must be better, the patient must be symptom-free, and they must have reached steady state of biologic (loading dose plus at least 3 more doses, typically 2-3 months from start).Open
StatementInflammatory markers including fecal calprotectin, ESR, and CRP should be checked before removing a seton to ensure systemic disease is under control.Open
StatementThe initial Remicade paper from 1998 or 1999 in the New England Journal of Medicine was on perianal disease and demonstrated improved healing time and improved length of time between recurrence when combination of seton and infliximab is used versus either separately.Open
Colorectal Quiz: Episode 43
StatementAbout 60% of the time there is success with using a split appendix for both Malone and Mitrofanoff, but about 40% of the time you cannot make it work.Open
StatementThe longer the appendix, the less likely it will leak based on Poiseuille's law (flow through a tube based on radius to fourth power and length).Open
StatementDr. Frischer and Levitt did 10 Malones in a row without plicating and five leaked, so they decided to plicate them all and have not had a leakage in several years.Open
QuotationSo we plicate them all. And I haven't had a leakage in a long, long time, several years. So I think it's a very effective strategy.Open
StatementIf appendix is short and stumpy, it is best for the Malone and the Mitrofanoff should be made from small bowel.Open
StatementIf appendix is 7 centimeters or greater it can be split, requiring minimum 2 centimeters for the Malone and 5 centimeters minimum for the Mitrofanoff.Open
StatementIf appendix is 5 to 7 centimeters, that is not enough to share and should go for the Mitrofanoff because long term the Mitrofanovs do much better, requiring a neo-Malone.Open
StatementUsing a 10 French tube (not 8), leaving it in for a month, and cathing twice a day can minimize stenosis rate.Open
StatementLeaving indwelling tubes in Malones increases the amount of prolapse, likely due to pressure on the appendiceal base pushing up mucosa.Open
StatementUrologists almost never get stenosis of Mitrofanovs because they catheterize every four hours; applying this to Malones by cathing twice daily has reduced stenosis rate.Open
StatementFor lost Malone access, blow up a balloon on a Foley catheter to occlude the umbilicus and inject dye under pressure to find any micro hole tract.Open
Jason's statements about Enterocolitis80 statements
QuotationI, I don't believe that a pure trans anal is necessarily less invasive. In other words, I believe that putting 3 incisions on the abdomen is actually less invasive in my hands, in my hands, certainly not in your guys' hands, but in my hands, I'm gonna be torquing in that anal canal much more than if I had done it laparoscopically and freed everything up from the abdominal approach.Open
StatementA pure transanal Hirschsprung dissection is not necessarily less invasive than laparoscopic approach; prolonged torquing in the anal canal may be more traumatic than three small abdominal incisions.Open
StatementFor standard rectosigmoid Hirschsprung disease (6-10 cm up), transanal dissection can be completed in the same timeframe as laparoscopic mobilization if the surgeon knows the level from a good contrast study.Open
StatementPost-Hirschsprung complications divide into two categories: obstructive symptoms (enterocolitis, failure to thrive, distention) and soiling issues (true incontinence vs pseudo-incontinence from constipation).Open
StatementWorkup for post-Hirschsprung complications includes water-soluble contrast enema and exam under anesthesia looking for dentate line position, stricture, stretched sphincter, and twists; if no anatomic cause is found, perform biopsy.Open
StatementFor Hirschsprung pull-through, dissection should start approximately 1 cm above the dentate line (defined as the transition from squamous to columnar epithelium, at the bottom of the anal columns).Open
StatementGoing only 0.5 cm above the dentate line in a newborn may result in 2.5-3 cm of aganglionic segment remaining when the child reaches 7 years old, creating an ultra-short segment Hirschsprung situation with constipation.Open
QuotationI want to ensure, because, and maybe we have a biased population in what we see, that I do not injure the dentate line because the patients who are rendered potentially fecally incontinent due to injury to the dentate line is a devastating injury for those patients.Open
StatementInjury to the dentate line during Hirschsprung pull-through can cause devastating fecal incontinence; it is better to risk leaving ultra-short segment aganglionosis (manageable with laxatives) than to injure the dentate line.Open
StatementIn ulcerative colitis or FAP patients undergoing J-pouch creation, dissection goes right at the top of the columns, or even slightly lower if polyps are present in that region.Open
StatementThe dentate line is variably defined in anatomic literature and textbooks; different sources point to different locations within the anal columns when labeling the dentate or pectinate line.Open
StatementThe traditional teaching that newborn meconium is sterile and therefore anorectal malformation repair should be done in the newborn period (before dilations introduce bacteria) is questioned; some surgeons repair at any age with stool present and feed early postoperatively with similar complication rates.Open
StatementConservative postoperative management of anorectal malformation repair includes keeping the patient NPO for approximately one week with hyperalimentation (a 'medical colostomy'), though there is no data supporting this practice over early feeding.Open
QuotationI know there are a number of pediatric surgeons that will repair an anorectal malformation at whatever age with dirty stool and feed the child the day 1 or 2 days post-op when they recover from the anesthesia, and I'm sure that incidence of complication is probably similar.Open
StatementWhen vestibular fistula is discovered intraoperatively to have an absent vagina, management depends on prognosis for bowel control: if good prognosis, use graft (colon or small bowel) to create vagina and bring rectum down; if poor prognosis (sacral agenesis, tethered cord), use the rectum/fistula as vagina and bring proximal colon down as pull-through.Open
StatementRectal prolapse workup should distinguish full-thickness prolapse from partial-thickness (mucosal) prolapse based on physical examination appearance.Open
StatementTesting for cystic fibrosis in children presenting with rectal prolapse is traditional teaching and a board exam answer, but in clinical practice rarely identifies new CF cases; most CF patients with prolapse are already diagnosed.Open
StatementInitial management of rectal prolapse includes treating constipation and limiting toilet sitting time to 5 minutes; surgical intervention is considered after 6 months to 2 years of failed medical management.Open
QuotationI can tell you when it recurs to re-operate on those patients is not going to matter at all.Open
StatementSclerosing agent injection for rectal prolapse has high recurrence rates; patients who fail this approach and require subsequent rectopexy have difficult reoperative dissection.Open
StatementVentral mesh rectopexy is a newer procedure popularized by the Cleveland Clinic for rectal prolapse; it involves placing mesh on the anterior rectum surface, elevating the rectum without posterior dissection, and tacking mesh to the sacral promontory.Open
StatementMesh erosion is a known complication of ventral mesh rectopexy, but the procedure can be effective for refractory rectal prolapse after multiple failed transabdominal repairs.Open
StatementVentral mesh rectopexy aims to change the angle between rectum and anal canal; younger patients with rectal prolapse have a straighter rectum-to-anal-canal angle that becomes more acute with age.Open
Hirschsprung Disease: Update Course 2015
QuotationI recall having a full day of uh Hirschprung's webcast, and now I get 5 minutes.Open
StatementThe safest approach to Hirschsprung surgery involves some form of biopsy (laparoscopic or full-thickness through umbilicus) prior to definitive pull-through.Open
QuotationI, every time that I do a primary trans anal, I get. I tighten up a little bit to make sure that I'm confident that I can do, and I have an exit strategy in mind if I get in troubleOpen
StatementLeveling colostomy may be the safest approach when institutional pathology expertise in reading Hirschsprung biopsies is limited or unavailable.Open
StatementLeveling colostomy represents a three-stage procedure for Hirschsprung disease management.Open
StatementProlonged transanal dissection (approaching 4 hours) should prompt consideration of converting to laparoscopic approach to avoid excessive sphincter stretching.Open
QuotationBelinda and I talk about this a lot, and it's about a comfort level and how fit, I take, I watch the clock how long I'm doing a trans anal dissection because I do not want to be stretching on those sphincters for 4 hours trying to dig up in a dark hole when I could put a scope in.Open
StatementLaparoscopic mobilization with 3-millimeter ports can be completed in approximately 45 minutes for appropriate cases.Open
StatementStandard rectosigmoid Hirschsprung disease (6-10 centimeters proximal) can be completed transanally in approximately 2 hours when the level is known from a good contrast study.Open
StatementComplications after Hirschsprung surgery are divided into two categories: obstructive symptoms (including enterocolitis, failure to thrive, abdominal distention) and soiling issues.Open
StatementSoiling after Hirschsprung surgery is further classified into true incontinence and pseudo-incontinence.Open
StatementObstructive symptoms after Hirschsprung surgery require differentiation between anatomic problems and pathologic problems.Open
StatementTrue fecal incontinence after Hirschsprung surgery can result from injury to the sphincter or injury to the dentate line.Open
StatementPseudo-incontinence after Hirschsprung surgery may be caused by underlying constipation.Open
StatementWorkup for post-Hirschsprung complications includes water-soluble contrast enema and exam under anesthesia evaluating dentate line position, stricture, stretched sphincter, and anatomic twists.Open
Hirschsprung's Disease
QuotationMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementSome infants with Hirschsprung's disease do pass meconium.Open
StatementMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementApproximately 10% of newborns with Hirschsprung's disease may lack the typical findings on a contrast enema.Open
StatementTypical features on rectal biopsy include absence of ganglion cells, presence of hypertrophic nerves, abnormal pattern of cholinesterase staining, and an absence of calretinine staining.Open
StatementRectal biopsy is the true definitive diagnosis for Hirschsprung disease.Open
StatementFull thickness biopsy technique should be considered for patients older than six months, or when a suction biopsy is inadequate.Open
StatementSuction biopsy technique is typically used for patients less than six months of age.Open
StatementTo be considered an adequate biopsy, it must be taken from the rectum at least one centimeter above the dentate line and must include both mucosa and submucosal layers.Open
QuotationThe second part of a diagnostic workup for Hirschsprung's disease, and most important, is the rectal biopsy. It is the true definitive diagnosis.Open
QuotationThe three studies that should be considered for evaluating for Hirschsprung's disease include contrast enema, rectal biopsy, and possibly anorectal manometry.Open
StatementThe classic finding on contrast enema is a transition zone in the rectosigmoid, but that transition zone can be located anywhere within the bowel.Open
StatementA rectosigmoid ratio of less than 1.0 is suggestive of Hirschsprung's disease, meaning the aganglionic bowel is contracted and narrow compared to the dilated ganglionated bowel more proximal.Open
StatementIn total colonic Hirschsprung's disease, a foreshortened or question mark colon can be seen on contrast enema.Open
StatementThe rectoanal inhibitory reflex may be absent in other conditions as well, and some children have a false positive test.Open
StatementAny patient with an absent RAIR must undergo a rectal biopsy for confirmation of the diagnosis.Open
StatementIn Hirschsprung's disease, anorectal manometry shows a lack of the rectoanal inhibitory reflex (RAIR).Open
QuotationThere are three goals to the surgical management of Hirschsprung's disease. First, identify the extent of the aganglionic segment. Second, resect that segment. And third, restore the bowel to its continuity.Open
StatementThe three goals of surgical management are: identify the extent of the aganglionic segment, resect that segment, and restore the bowel to its continuity.Open
StatementA con of the Suave procedure is that the aganglionic cuff can become stiff enough to cause an obstruction or outlet obstruction.Open
StatementThe Suave procedure theoretically causes less injury to pelvic structures, nerves, urethra and vagina.Open
StatementIn the Suave procedure, the actual anastomosis is performed within a cuff of aganglionic rectum.Open
StatementIn the Swenson procedure, it is very important to be cautious about injuring the urethra as it's quite close, especially in boys.Open
StatementThe Suave procedure involves performing a mucosectomy from a transanal approach slightly above the dentate line and pulling through the normal bowel.Open
StatementIn the Swenson procedure, you pull down the aganglionic bowel and perform a full thickness anastomosis one to two centimeters above the dentate line, leaving the most minimal amount of aganglionic bowel possible.Open
StatementHirschsprung's-associated enterocolitis is likely an inflammatory condition secondary to bacterial overgrowth.Open
StatementTreatment of enterocolitis includes fluid resuscitation, digital rectal exam, and colonic irrigations.Open
StatementFor enterocolitis, antibiotics including metronidazole or broad-spectrum antibiotics are added depending on the severity of presentation.Open
QuotationWhen we treat these patients with enterocolitis, it is important to provide fluid resuscitation, digital rectal exam, and colonic irrigations.Open
QuotationHirschsprung's-associated enterocolitis is poorly understood and likely is an inflammatory condition secondary to bacterial overgrowth.Open
StatementA child with enterocolitis presents with abdominal distension, vomiting, fever, and change in bowel habits that could be either diarrhea or not passing stool at all.Open
StatementFor patients not doing well after pull-through, if there is a stricture at the anastomosis, it needs to be addressed either through dilations or revising the pull through procedure.Open
StatementFor patients without anatomic problems after pull-through, treatment can include bowel management, Botox injection to relieve sphincter tone, or motility studies.Open
StatementFor patients with anatomic problems after pull-through, you typically have to revise the pull through.Open
StatementAnatomic problems after pull-through can include a twist in the pull through, an obstructing cuff, a non-functioning Duhamel pouch, or a transition zone or continued aganglionic segment.Open
Colorectal Quiz Episode 3: Hirschsprung Disease
StatementIn Hirschsprung disease, the aganglionic rectum appears narrow due to spasm and inability to relax, while the ganglionated proximal bowel is dilated, creating the recto-sigmoid ratioOpen
StatementQuick diff staining highlights ganglion cells better than standard H&E stainingOpen
StatementThree good biopsy specimens should be obtained for pathologic evaluationOpen
StatementThe crypts are located above the dentate line, so optimal biopsy location is at least 1-2 cm above the dentate lineOpen
The Colorectal Quiz Episode 22: Hirschsprung Disease - the Soiling Patient Part 1
StatementPathology can change over time; cases exist where ganglion cells were present at pull-through but absent with hypertrophic nerves 7 years later when problems developed.Open
StatementSphincters should be assessed with the patient awake; examination under anesthesia makes it harder to assess sphincter function.Open
StatementDuring normal bowel movements, sphincters relax and the anus opens with some mucosal descent, but as soon as sphincters tighten, the mucosa retracts back in; prolapse at rest indicates damaged muscles and/or mucosa brought too low at anastomosis.Open
Jason's statements about Esophageal Atresia8 statements
StatementIn asymptomatic newborns with prenatally diagnosed lung lesions, most US practitioners obtain chest X-ray initially in NICUOpen
StatementCT angiography for congenital lung lesions is typically performed at 3-6 months in clinic rather than in NICU for asymptomatic patientsOpen
StatementWhen using energy devices for vessel control, leave enough remnant tissue so the vessel doesn't retract if seal fails, allowing purchase for clip or sutureOpen
StatementObtain proximal control or partially cut across vessel with energy device to detect failure before complete divisionOpen
StatementWhen using staplers, visualize the stapler end, use appropriate staple size for tissue, and leave extra tissue around stapler edge for adequate coaptationOpen
StatementNewborn with esophageal atresia, dextrocardia, and respiratory instability at birth suggests complex anatomy beyond typical EA/TEFOpen
StatementEcho findings of mesocardia, hypoplastic pulmonary arteries, persistent left SVC, and dilated right ventricle indicate significant cardiac anomaliesOpen
StatementEsophageal lung is rare congenital anomaly with approximately 30 reported cases where bronchus arises directly from esophagus rather than tracheaOpen
Jason's statements about Etiologies (Gastroschisis/NEC/Atresia/Volvulus)55 statements
Gastroschisis and sutureless abdominal wall closure
StatementDue to the heterogeneity of gastroschisis, patients able to undergo primary repair probably had more favorable bowel and theoretically would have less hospital stay and feed faster.Open
QuotationI think it was probably what we were expecting, I think, for a couple of reasons. One, due to the heterogeneity of this disease, you know, especially with gastroschisis, a lot of the patients that were able to undergo, you know, especially a primary repair, they probably had more favorable bowel. And then those patients, you know, theoretically would have less hospital stay and theoretically feed faster and things like that.Open
StatementMany patients who underwent sutureless repair were done in more recent cohorts and tended towards less interventions.Open
StatementIn sutured repair, mobilizing flaps from the skin and fascia causes redness and bruising around the incision, which puts patients at higher risk for potential infection.Open
QuotationMoreover, too, if you think about just the way that we close a sutured repair, you mobilize flaps from the skin and flaps from the fascia. So there's always, you know, redness around the incision, bruising around the incision. And so, you know, even that tissue manipulation is going to put you at higher risk for a potential infection or calling it erythema infection.Open
StatementThe finding of increased antibiotics needed after sutured repair was expected due to tissue manipulation.Open
StatementThe consortium is working on operationalizing protocolization of gastroschisis closure across member institutions for a more prospective study with long-term follow-up.Open
StatementThe next phase of the study is examining the same patients over several years of follow-up to assess growth and umbilical hernia repair rates.Open
Neonatal Gastric Volvulus with Dr. Jason Frischer
QuotationI've seen it associated with congenital diaphragmatic hernias a few times, and I think that's when we have a high suspicion for it.Open
Statement60% of gastric volvulus cases in the pediatric population happen in the first year of life, with about 21% in the first month.Open
Quotation60% happen in the first year of life in the pediatric population, and so about 21% in the first month and over a third in the first year of life.Open
StatementIn a 4-month-old child with gastric volvulus, acute presentation is more likely than chronic.Open
QuotationIf the child's like 4 months old, is it more likely, are you're more likely to have an acute problem or a chronic problem? So they're acute.Open
QuotationThat's the big one, I think, right there. I think a little bit of bloody aspirate from the. Logo can't advance it. Funny looking stomach bubble on the X-ray.Open
StatementA little bit of bloody aspirate from the NG tube and a funny looking stomach bubble on X-ray are key findings in gastric volvulus.Open
StatementChronic gastric volvulus is more related to laxity of the gastric ligaments including gastrophrenic, gastrosplenic, gastrocolic, and gastrohepatic ligaments.Open
QuotationThose are more to do with the laxity of the gastric ligaments, and the stomach has ligamentous attachments basically surrounding the entire stomach from gastrophrenic, gastrosplenic, gastrocolic. And of course. Gastropatic ligament.Open
StatementOrganoaxial volvulus is the first and most common type of gastric volvulus.Open
QuotationThe first one, the first and most common is organoaxial volvulus.Open
StatementIn organoaxial volvulus, the stomach spins around an axis drawn between the GE junction and the pylorus, with the greater curvature flipping up and over to become more superior than the lesser curvature.Open
QuotationThey describe a line that's drawn on this diagram between the GE junction and the pylorus, and it's spinning around that axis. The greater curvature then sort of flips up and over and becomes more superior than the lesser curvature.Open
StatementIn mesenteroaxial volvulus, rotation occurs around a line through the middle of the stomach from lesser to greater curvature, with the stomach flipping behind and back over.Open
QuotationThen, and flip the stomach up and over that way, so it's going sort of behind. The stomach and back over it.Open
StatementIn gastric volvulus, when filled with contrast, the pylorus appears right next to or near the GE junction and above the body of the stomach.Open
QuotationWhen the pylorus is at, right next to the GE junction or near the GE junction, and above the body of the stomach.Open
StatementIn mesenteroaxial volvulus, the duodenum may fill above or superior to the GE junction because the pylorus has flipped up and over or behind and over the top of the stomach.Open
QuotationMesentero axial favulus. Again, this is the sort of pylorus flipping up and over or behind and over the top of the stomach, and then therefore, your pylorus is located all the way up here.Open
StatementWhen managing gastric volvulus found during CDH repair, viability of the stomach must always be checked, especially if chronically volvulized or volvulized for a couple of days, by looking at the serosa and blood flow.Open
QuotationAlso, you always want to check the viability of the stomach. So, right, if this is chronically volvulized or been volvulized for a couple of days, uh, at least looking at the cirrhosa and looking at the blood flow.Open
Update Course 2022 - UPDATES IN GASTROSCHISIS FEEDING PROTOCOLS - Jason Fraser, Beth Rymeski, and Steven Lee
StatementJason Fraser's institution starts feeding immediately after dressing placement as long as the baby is not sick, not having horrible output, and not vomiting.Open
Quotationwe start feeding essentially you have to put the dressing on uh as long as the baby's not sick not having horrible output not puking or anything like thatOpen
StatementFraser's institution does not intubate gastroschisis babies for reduction.Open
Quotationwe don't innovate our babies at all so we put the dressing plastic dressing on and as long as the kid's not you know has voluminous output we'll try to start start feedings on itOpen
StatementAwake reduction can be successful if performed slowly, with stomach emptying, colon decompression, oral sucrose, and gradual abdominal wall stretching.Open
Quotationif you try to just keep pushing and pushing pushing the baby kind of can squirm and stuff but if you go slow if you empty out the stomach if you kind of squish out the colon a little bit and you go slow you give the baby some sweeties the nurses are there to kind of relax the baby you have a couple people that that are there doing it you go slow you slowly kind of push things in you stretch out the belly a little bitOpen
StatementCincinnati Children's feeding protocol is based on patient tolerance and data from resource-limited settings where TPN is unavailable and feeding is mandatory.Open
Quotationit's really just based upon patient tolerance and it's kind of based upon some of the data that's out there from the rest of the world where they don't have tpn and so they just you have to feed the kid if the kid does okay then they keep goingOpen
StatementThe multi-institutional study showed inconclusive results due to significant variation in feeding protocols across institutions.Open
Quotationa lot of the inconclusivity from the the study showed that you know most likely due to the fact that there was lots of different feeding protocols that were used uh across our member institutionsOpen
StatementThe reduction in surgical site infections with protocol feeding was likely due to decreased care variability rather than the feeding protocol itself.Open
Quotationthe ssi thing was probably just because patients that were fed via protocol were cared for via protocol and so that they actually had less variability and less uh less changes uh in the way that these these patients are not you know look forOpen
StatementCincinnati Children's average gastroschisis length of stay was 49 days before protocol implementation, which was astronomically higher than comparable NICUs in their cooperative network.Open
Quotationour length of stay for gastroschisis and cincinnati was astronomically higher than like any other nick micu in the cooperative network that we worked with so we sat down we're like what is going on here so our average length of stay was 49 daysOpen
Quotationwe instituted this uh a feeding protocol we spent a lot of time trying to get people to follow it and and making some adjustments and over two years we dropped the length of stay by 10 days and the mix of patients is not differentOpen
StatementAfter implementing a feeding protocol, Cincinnati Children's reduced gastroschisis length of stay by 10 days over two years.Open
StatementCincinnati Children's has seen a decrease in time from first feed to full feeds but has not yet reduced the time from admission to first feed (except in 2020).Open
StatementCincinnati Children's gastroschisis protocol includes prenatal care coordination with obstetricians and neonatologists, with surgery continuing to follow patients throughout hospitalization.Open
StatementThe most important aspects of gastroschisis feeding are defining institutional tolerance criteria, adhering to protocol, and continuously evaluating the infant's condition.Open
Quotationthe most important thing that kind of keeps showing up is the fact that we really need to define what your own institution has for tolerance and to kind of stay on the protocol and then really just look at the infant condition as you continue to go is the most important thingOpen
StatementFor significant feeding intolerance, Cincinnati Children's protocol calls for stopping feeds for six hours, though this is not clearly evidence-based.Open
Quotationyes you can have a protocol yes you know you need to follow it but the most really you really need to continually evaluate the patient as they continue to go to make sure that you know yes your protocol is working but also to the patient does okay throughoutOpen
StatementOne recent Cincinnati Children's gastroschisis patient who was primarily reduced on day of life zero was discharged at approximately two weeks and remained well at two-week follow-up, though this is an outlier on the faster end.Open
StatementCincinnati Children's current average gastroschisis length of stay is 30 to 34 days.Open
StatementCincinnati Children's has not seen any aspirations with their early aggressive feeding approach, though they acknowledge they are still early in implementation and continue to monitor data.Open
StatementAt Cincinnati Children's, approximately two-thirds of gastroschisis cases cannot be reduced immediately and are placed in a silo for gradual reduction followed by sutureless closure, with feeds started after closure.Open
Jason's statements about Fecal Incontinence9 statements
Colorectal Quiz Episode 37: The Yancey-Soave story of the original surgical descriptions for Hirschsprung disease
StatementDr. Newman brought Dr. Yancey's story to the attention of the Hirschsprung interest group at APSA.Open
QuotationI was reading the operative note from one of my fellows who provided the history of the patient. I had to do a reoperation on the patient. And the history read that this five-year-old child is status post a Yancey Suave procedure in such and such date and had an asthmatic stricture.Open
StatementA fellow at Children's National wrote an operative note describing a patient as status post a 'Yancey-Suave procedure,' indicating the terminology has become part of standard practice.Open
The Colorectal Quiz Episode 21: The History of Hirschsprung Disease
QuotationHe united us. Yeah. In a way. And he doesn't even know it.Open
StatementDr. Martin developed the Martin procedure, an expansion of the Duhamel for long-segment Hirschsprung disease, leaving a longer aganglionated segment of rectum and pulling through ganglionated bowel.Open
StatementDr. Martin was the first surgeon-in-chief and pediatric surgeon at Cincinnati Children's Hospital.Open
QuotationI think that's the who's who of Hirschsprung's right there.Open
QuotationI have a feeling we're going to have way more discussions about Hirschsprung disease because just because, because I think it's a fascinating disease that there are so many intricacies. You just mentioned dentorocolitis. We could talk forever about that.Open
Jason's statements about Gastroschisis34 statements
Gastroschisis and sutureless abdominal wall closure
StatementMany patients who underwent sutureless repair were done in more recent cohorts and tended towards less interventions.Open
QuotationI think it was probably what we were expecting, I think, for a couple of reasons. One, due to the heterogeneity of this disease, you know, especially with gastroschisis, a lot of the patients that were able to undergo, you know, especially a primary repair, they probably had more favorable bowel. And then those patients, you know, theoretically would have less hospital stay and theoretically feed faster and things like that.Open
StatementDue to the heterogeneity of gastroschisis, patients able to undergo primary repair probably had more favorable bowel and theoretically would have less hospital stay and feed faster.Open
StatementThe finding of increased antibiotics needed after sutured repair was expected due to tissue manipulation.Open
StatementIn sutured repair, mobilizing flaps from the skin and fascia causes redness and bruising around the incision, which puts patients at higher risk for potential infection.Open
QuotationMoreover, too, if you think about just the way that we close a sutured repair, you mobilize flaps from the skin and flaps from the fascia. So there's always, you know, redness around the incision, bruising around the incision. And so, you know, even that tissue manipulation is going to put you at higher risk for a potential infection or calling it erythema infection.Open
StatementThe next phase of the study is examining the same patients over several years of follow-up to assess growth and umbilical hernia repair rates.Open
StatementThe consortium is working on operationalizing protocolization of gastroschisis closure across member institutions for a more prospective study with long-term follow-up.Open
Update Course 2022 - UPDATES IN GASTROSCHISIS FEEDING PROTOCOLS - Jason Fraser, Beth Rymeski, and Steven Lee
StatementJason Fraser's institution starts feeding immediately after dressing placement as long as the baby is not sick, not having horrible output, and not vomiting.Open
Quotationwe start feeding essentially you have to put the dressing on uh as long as the baby's not sick not having horrible output not puking or anything like thatOpen
StatementFraser's institution does not intubate gastroschisis babies for reduction.Open
Quotationwe don't innovate our babies at all so we put the dressing plastic dressing on and as long as the kid's not you know has voluminous output we'll try to start start feedings on itOpen
StatementAwake reduction can be successful if performed slowly, with stomach emptying, colon decompression, oral sucrose, and gradual abdominal wall stretching.Open
Quotationif you try to just keep pushing and pushing pushing the baby kind of can squirm and stuff but if you go slow if you empty out the stomach if you kind of squish out the colon a little bit and you go slow you give the baby some sweeties the nurses are there to kind of relax the baby you have a couple people that that are there doing it you go slow you slowly kind of push things in you stretch out the belly a little bitOpen
StatementCincinnati Children's feeding protocol is based on patient tolerance and data from resource-limited settings where TPN is unavailable and feeding is mandatory.Open
Quotationit's really just based upon patient tolerance and it's kind of based upon some of the data that's out there from the rest of the world where they don't have tpn and so they just you have to feed the kid if the kid does okay then they keep goingOpen
Quotationa lot of the inconclusivity from the the study showed that you know most likely due to the fact that there was lots of different feeding protocols that were used uh across our member institutionsOpen
StatementThe reduction in surgical site infections with protocol feeding was likely due to decreased care variability rather than the feeding protocol itself.Open
StatementThe multi-institutional study showed inconclusive results due to significant variation in feeding protocols across institutions.Open
Quotationthe ssi thing was probably just because patients that were fed via protocol were cared for via protocol and so that they actually had less variability and less uh less changes uh in the way that these these patients are not you know look forOpen
StatementCincinnati Children's average gastroschisis length of stay was 49 days before protocol implementation, which was astronomically higher than comparable NICUs in their cooperative network.Open
Quotationour length of stay for gastroschisis and cincinnati was astronomically higher than like any other nick micu in the cooperative network that we worked with so we sat down we're like what is going on here so our average length of stay was 49 daysOpen
StatementAfter implementing a feeding protocol, Cincinnati Children's reduced gastroschisis length of stay by 10 days over two years.Open
StatementCincinnati Children's has seen a decrease in time from first feed to full feeds but has not yet reduced the time from admission to first feed (except in 2020).Open
Quotationwe instituted this uh a feeding protocol we spent a lot of time trying to get people to follow it and and making some adjustments and over two years we dropped the length of stay by 10 days and the mix of patients is not differentOpen
StatementCincinnati Children's gastroschisis protocol includes prenatal care coordination with obstetricians and neonatologists, with surgery continuing to follow patients throughout hospitalization.Open
StatementThe most important aspects of gastroschisis feeding are defining institutional tolerance criteria, adhering to protocol, and continuously evaluating the infant's condition.Open
Quotationthe most important thing that kind of keeps showing up is the fact that we really need to define what your own institution has for tolerance and to kind of stay on the protocol and then really just look at the infant condition as you continue to go is the most important thingOpen
Quotationyes you can have a protocol yes you know you need to follow it but the most really you really need to continually evaluate the patient as they continue to go to make sure that you know yes your protocol is working but also to the patient does okay throughoutOpen
StatementFor significant feeding intolerance, Cincinnati Children's protocol calls for stopping feeds for six hours, though this is not clearly evidence-based.Open
StatementOne recent Cincinnati Children's gastroschisis patient who was primarily reduced on day of life zero was discharged at approximately two weeks and remained well at two-week follow-up, though this is an outlier on the faster end.Open
StatementCincinnati Children's current average gastroschisis length of stay is 30 to 34 days.Open
StatementCincinnati Children's has not seen any aspirations with their early aggressive feeding approach, though they acknowledge they are still early in implementation and continue to monitor data.Open
StatementAt Cincinnati Children's, approximately two-thirds of gastroschisis cases cannot be reduced immediately and are placed in a silo for gradual reduction followed by sutureless closure, with feeds started after closure.Open
Jason's statements about Hirschsprung disease236 statements
QuotationI, I don't believe that a pure trans anal is necessarily less invasive. In other words, I believe that putting 3 incisions on the abdomen is actually less invasive in my hands, in my hands, certainly not in your guys' hands, but in my hands, I'm gonna be torquing in that anal canal much more than if I had done it laparoscopically and freed everything up from the abdominal approach.Open
StatementA pure transanal Hirschsprung dissection is not necessarily less invasive than laparoscopic approach; prolonged torquing in the anal canal may be more traumatic than three small abdominal incisions.Open
QuotationI, I don't believe that a pure trans anal is necessarily less invasive. In other words, I believe that putting 3 incisions on the abdomen is actually less invasive in my hands, in my hands, certainly not in your guys' hands, but in my hands, I'm gonna be torquing in that anal canal much more than if I had done it laparoscopically and freed everything up from the abdominal approach.Open
StatementA pure transanal Hirschsprung dissection is not necessarily less invasive than laparoscopic approach; prolonged torquing in the anal canal may be more traumatic than three small abdominal incisions.Open
StatementFor standard rectosigmoid Hirschsprung disease (6-10 cm up), transanal dissection can be completed in the same timeframe as laparoscopic mobilization if the surgeon knows the level from a good contrast study.Open
StatementFor standard rectosigmoid Hirschsprung disease (6-10 cm up), transanal dissection can be completed in the same timeframe as laparoscopic mobilization if the surgeon knows the level from a good contrast study.Open
StatementPost-Hirschsprung complications divide into two categories: obstructive symptoms (enterocolitis, failure to thrive, distention) and soiling issues (true incontinence vs pseudo-incontinence from constipation).Open
StatementPost-Hirschsprung complications divide into two categories: obstructive symptoms (enterocolitis, failure to thrive, distention) and soiling issues (true incontinence vs pseudo-incontinence from constipation).Open
StatementWorkup for post-Hirschsprung complications includes water-soluble contrast enema and exam under anesthesia looking for dentate line position, stricture, stretched sphincter, and twists; if no anatomic cause is found, perform biopsy.Open
StatementWorkup for post-Hirschsprung complications includes water-soluble contrast enema and exam under anesthesia looking for dentate line position, stricture, stretched sphincter, and twists; if no anatomic cause is found, perform biopsy.Open
StatementFor Hirschsprung pull-through, dissection should start approximately 1 cm above the dentate line (defined as the transition from squamous to columnar epithelium, at the bottom of the anal columns).Open
StatementGoing only 0.5 cm above the dentate line in a newborn may result in 2.5-3 cm of aganglionic segment remaining when the child reaches 7 years old, creating an ultra-short segment Hirschsprung situation with constipation.Open
StatementGoing only 0.5 cm above the dentate line in a newborn may result in 2.5-3 cm of aganglionic segment remaining when the child reaches 7 years old, creating an ultra-short segment Hirschsprung situation with constipation.Open
StatementFor Hirschsprung pull-through, dissection should start approximately 1 cm above the dentate line (defined as the transition from squamous to columnar epithelium, at the bottom of the anal columns).Open
StatementInjury to the dentate line during Hirschsprung pull-through can cause devastating fecal incontinence; it is better to risk leaving ultra-short segment aganglionosis (manageable with laxatives) than to injure the dentate line.Open
QuotationI want to ensure, because, and maybe we have a biased population in what we see, that I do not injure the dentate line because the patients who are rendered potentially fecally incontinent due to injury to the dentate line is a devastating injury for those patients.Open
StatementInjury to the dentate line during Hirschsprung pull-through can cause devastating fecal incontinence; it is better to risk leaving ultra-short segment aganglionosis (manageable with laxatives) than to injure the dentate line.Open
QuotationI want to ensure, because, and maybe we have a biased population in what we see, that I do not injure the dentate line because the patients who are rendered potentially fecally incontinent due to injury to the dentate line is a devastating injury for those patients.Open
StatementIn ulcerative colitis or FAP patients undergoing J-pouch creation, dissection goes right at the top of the columns, or even slightly lower if polyps are present in that region.Open
StatementIn ulcerative colitis or FAP patients undergoing J-pouch creation, dissection goes right at the top of the columns, or even slightly lower if polyps are present in that region.Open
StatementThe dentate line is variably defined in anatomic literature and textbooks; different sources point to different locations within the anal columns when labeling the dentate or pectinate line.Open
StatementThe dentate line is variably defined in anatomic literature and textbooks; different sources point to different locations within the anal columns when labeling the dentate or pectinate line.Open
StatementThe traditional teaching that newborn meconium is sterile and therefore anorectal malformation repair should be done in the newborn period (before dilations introduce bacteria) is questioned; some surgeons repair at any age with stool present and feed early postoperatively with similar complication rates.Open
StatementThe traditional teaching that newborn meconium is sterile and therefore anorectal malformation repair should be done in the newborn period (before dilations introduce bacteria) is questioned; some surgeons repair at any age with stool present and feed early postoperatively with similar complication rates.Open
StatementConservative postoperative management of anorectal malformation repair includes keeping the patient NPO for approximately one week with hyperalimentation (a 'medical colostomy'), though there is no data supporting this practice over early feeding.Open
StatementConservative postoperative management of anorectal malformation repair includes keeping the patient NPO for approximately one week with hyperalimentation (a 'medical colostomy'), though there is no data supporting this practice over early feeding.Open
QuotationI know there are a number of pediatric surgeons that will repair an anorectal malformation at whatever age with dirty stool and feed the child the day 1 or 2 days post-op when they recover from the anesthesia, and I'm sure that incidence of complication is probably similar.Open
QuotationI know there are a number of pediatric surgeons that will repair an anorectal malformation at whatever age with dirty stool and feed the child the day 1 or 2 days post-op when they recover from the anesthesia, and I'm sure that incidence of complication is probably similar.Open
StatementWhen vestibular fistula is discovered intraoperatively to have an absent vagina, management depends on prognosis for bowel control: if good prognosis, use graft (colon or small bowel) to create vagina and bring rectum down; if poor prognosis (sacral agenesis, tethered cord), use the rectum/fistula as vagina and bring proximal colon down as pull-through.Open
StatementWhen vestibular fistula is discovered intraoperatively to have an absent vagina, management depends on prognosis for bowel control: if good prognosis, use graft (colon or small bowel) to create vagina and bring rectum down; if poor prognosis (sacral agenesis, tethered cord), use the rectum/fistula as vagina and bring proximal colon down as pull-through.Open
StatementRectal prolapse workup should distinguish full-thickness prolapse from partial-thickness (mucosal) prolapse based on physical examination appearance.Open
StatementRectal prolapse workup should distinguish full-thickness prolapse from partial-thickness (mucosal) prolapse based on physical examination appearance.Open
StatementTesting for cystic fibrosis in children presenting with rectal prolapse is traditional teaching and a board exam answer, but in clinical practice rarely identifies new CF cases; most CF patients with prolapse are already diagnosed.Open
StatementTesting for cystic fibrosis in children presenting with rectal prolapse is traditional teaching and a board exam answer, but in clinical practice rarely identifies new CF cases; most CF patients with prolapse are already diagnosed.Open
StatementInitial management of rectal prolapse includes treating constipation and limiting toilet sitting time to 5 minutes; surgical intervention is considered after 6 months to 2 years of failed medical management.Open
StatementInitial management of rectal prolapse includes treating constipation and limiting toilet sitting time to 5 minutes; surgical intervention is considered after 6 months to 2 years of failed medical management.Open
QuotationI can tell you when it recurs to re-operate on those patients is not going to matter at all.Open
QuotationI can tell you when it recurs to re-operate on those patients is not going to matter at all.Open
StatementSclerosing agent injection for rectal prolapse has high recurrence rates; patients who fail this approach and require subsequent rectopexy have difficult reoperative dissection.Open
StatementSclerosing agent injection for rectal prolapse has high recurrence rates; patients who fail this approach and require subsequent rectopexy have difficult reoperative dissection.Open
StatementTransabdominal approaches for rectal prolapse (rectopexy with or without resection) have approximately 5% recurrence rate, compared to 15-20% recurrence for transanal approaches (transanal pull-through or Altmeier procedure).Open
StatementResection and rectopexy for rectal prolapse may be preferable when constipation control is difficult, but has higher complication rate compared to rectopexy alone.Open
StatementLaparoscopic rectopexy for rectal prolapse can be performed as same-day surgery or with next-day discharge in current practice.Open
StatementVentral mesh rectopexy is a newer procedure popularized by the Cleveland Clinic for rectal prolapse; it involves placing mesh on the anterior rectum surface, elevating the rectum without posterior dissection, and tacking mesh to the sacral promontory.Open
StatementVentral mesh rectopexy is a newer procedure popularized by the Cleveland Clinic for rectal prolapse; it involves placing mesh on the anterior rectum surface, elevating the rectum without posterior dissection, and tacking mesh to the sacral promontory.Open
StatementMesh erosion is a known complication of ventral mesh rectopexy, but the procedure can be effective for refractory rectal prolapse after multiple failed transabdominal repairs.Open
StatementMesh erosion is a known complication of ventral mesh rectopexy, but the procedure can be effective for refractory rectal prolapse after multiple failed transabdominal repairs.Open
StatementVentral mesh rectopexy aims to change the angle between rectum and anal canal; younger patients with rectal prolapse have a straighter rectum-to-anal-canal angle that becomes more acute with age.Open
StatementVentral mesh rectopexy aims to change the angle between rectum and anal canal; younger patients with rectal prolapse have a straighter rectum-to-anal-canal angle that becomes more acute with age.Open
Hirschsprung Disease: Update Course 2015
QuotationI recall having a full day of uh Hirschprung's webcast, and now I get 5 minutes.Open
StatementThe safest approach to Hirschsprung surgery involves some form of biopsy (laparoscopic or full-thickness through umbilicus) prior to definitive pull-through.Open
QuotationI, every time that I do a primary trans anal, I get. I tighten up a little bit to make sure that I'm confident that I can do, and I have an exit strategy in mind if I get in troubleOpen
StatementLeveling colostomy may be the safest approach when institutional pathology expertise in reading Hirschsprung biopsies is limited or unavailable.Open
StatementLeveling colostomy represents a three-stage procedure for Hirschsprung disease management.Open
QuotationBelinda and I talk about this a lot, and it's about a comfort level and how fit, I take, I watch the clock how long I'm doing a trans anal dissection because I do not want to be stretching on those sphincters for 4 hours trying to dig up in a dark hole when I could put a scope in.Open
StatementProlonged transanal dissection (approaching 4 hours) should prompt consideration of converting to laparoscopic approach to avoid excessive sphincter stretching.Open
StatementLaparoscopic mobilization with 3-millimeter ports can be completed in approximately 45 minutes for appropriate cases.Open
StatementStandard rectosigmoid Hirschsprung disease (6-10 centimeters proximal) can be completed transanally in approximately 2 hours when the level is known from a good contrast study.Open
StatementComplications after Hirschsprung surgery are divided into two categories: obstructive symptoms (including enterocolitis, failure to thrive, abdominal distention) and soiling issues.Open
StatementSoiling after Hirschsprung surgery is further classified into true incontinence and pseudo-incontinence.Open
StatementObstructive symptoms after Hirschsprung surgery require differentiation between anatomic problems and pathologic problems.Open
StatementTrue fecal incontinence after Hirschsprung surgery can result from injury to the sphincter or injury to the dentate line.Open
StatementPseudo-incontinence after Hirschsprung surgery may be caused by underlying constipation.Open
StatementWorkup for post-Hirschsprung complications includes water-soluble contrast enema and exam under anesthesia evaluating dentate line position, stricture, stretched sphincter, and anatomic twists.Open
Hirschsprung's Disease
StatementMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementSome infants with Hirschsprung's disease do pass meconium.Open
QuotationMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementSome infants with Hirschsprung's disease do pass meconium.Open
QuotationMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementSuction biopsy technique is typically used for patients less than six months of age.Open
StatementApproximately 10% of newborns with Hirschsprung's disease may lack the typical findings on a contrast enema.Open
StatementA rectosigmoid ratio of less than 1.0 is suggestive of Hirschsprung's disease, meaning the aganglionic bowel is contracted and narrow compared to the dilated ganglionated bowel more proximal.Open
StatementFull thickness biopsy technique should be considered for patients older than six months, or when a suction biopsy is inadequate.Open
QuotationThe three studies that should be considered for evaluating for Hirschsprung's disease include contrast enema, rectal biopsy, and possibly anorectal manometry.Open
StatementThe classic finding on contrast enema is a transition zone in the rectosigmoid, but that transition zone can be located anywhere within the bowel.Open
StatementTo be considered an adequate biopsy, it must be taken from the rectum at least one centimeter above the dentate line and must include both mucosa and submucosal layers.Open
QuotationThe second part of a diagnostic workup for Hirschsprung's disease, and most important, is the rectal biopsy. It is the true definitive diagnosis.Open
QuotationThe three studies that should be considered for evaluating for Hirschsprung's disease include contrast enema, rectal biopsy, and possibly anorectal manometry.Open
StatementFull thickness biopsy technique should be considered for patients older than six months, or when a suction biopsy is inadequate.Open
StatementSuction biopsy technique is typically used for patients less than six months of age.Open
StatementTo be considered an adequate biopsy, it must be taken from the rectum at least one centimeter above the dentate line and must include both mucosa and submucosal layers.Open
StatementTypical features on rectal biopsy include absence of ganglion cells, presence of hypertrophic nerves, abnormal pattern of cholinesterase staining, and an absence of calretinine staining.Open
StatementRectal biopsy is the true definitive diagnosis for Hirschsprung disease.Open
StatementThe classic finding on contrast enema is a transition zone in the rectosigmoid, but that transition zone can be located anywhere within the bowel.Open
StatementA rectosigmoid ratio of less than 1.0 is suggestive of Hirschsprung's disease, meaning the aganglionic bowel is contracted and narrow compared to the dilated ganglionated bowel more proximal.Open
StatementIn total colonic Hirschsprung's disease, a foreshortened or question mark colon can be seen on contrast enema.Open
StatementTypical features on rectal biopsy include absence of ganglion cells, presence of hypertrophic nerves, abnormal pattern of cholinesterase staining, and an absence of calretinine staining.Open
QuotationThe second part of a diagnostic workup for Hirschsprung's disease, and most important, is the rectal biopsy. It is the true definitive diagnosis.Open
StatementRectal biopsy is the true definitive diagnosis for Hirschsprung disease.Open
StatementIn total colonic Hirschsprung's disease, a foreshortened or question mark colon can be seen on contrast enema.Open
StatementApproximately 10% of newborns with Hirschsprung's disease may lack the typical findings on a contrast enema.Open
StatementAny patient with an absent RAIR must undergo a rectal biopsy for confirmation of the diagnosis.Open
StatementThe rectoanal inhibitory reflex may be absent in other conditions as well, and some children have a false positive test.Open
StatementAny patient with an absent RAIR must undergo a rectal biopsy for confirmation of the diagnosis.Open
StatementIn Hirschsprung's disease, anorectal manometry shows a lack of the rectoanal inhibitory reflex (RAIR).Open
StatementIn Hirschsprung's disease, anorectal manometry shows a lack of the rectoanal inhibitory reflex (RAIR).Open
StatementThe rectoanal inhibitory reflex may be absent in other conditions as well, and some children have a false positive test.Open
QuotationThere are three goals to the surgical management of Hirschsprung's disease. First, identify the extent of the aganglionic segment. Second, resect that segment. And third, restore the bowel to its continuity.Open
QuotationThere are three goals to the surgical management of Hirschsprung's disease. First, identify the extent of the aganglionic segment. Second, resect that segment. And third, restore the bowel to its continuity.Open
StatementThe three goals of surgical management are: identify the extent of the aganglionic segment, resect that segment, and restore the bowel to its continuity.Open
StatementThe three goals of surgical management are: identify the extent of the aganglionic segment, resect that segment, and restore the bowel to its continuity.Open
StatementA con of the Suave procedure is that the aganglionic cuff can become stiff enough to cause an obstruction or outlet obstruction.Open
StatementThe Suave procedure theoretically causes less injury to pelvic structures, nerves, urethra and vagina.Open
StatementIn the Suave procedure, the actual anastomosis is performed within a cuff of aganglionic rectum.Open
StatementThe Suave procedure involves performing a mucosectomy from a transanal approach slightly above the dentate line and pulling through the normal bowel.Open
StatementIn the Swenson procedure, it is very important to be cautious about injuring the urethra as it's quite close, especially in boys.Open
StatementIn the Swenson procedure, it is very important to be cautious about injuring the urethra as it's quite close, especially in boys.Open
StatementIn the Swenson procedure, you pull down the aganglionic bowel and perform a full thickness anastomosis one to two centimeters above the dentate line, leaving the most minimal amount of aganglionic bowel possible.Open
StatementIn the Swenson procedure, you pull down the aganglionic bowel and perform a full thickness anastomosis one to two centimeters above the dentate line, leaving the most minimal amount of aganglionic bowel possible.Open
StatementA con of the Suave procedure is that the aganglionic cuff can become stiff enough to cause an obstruction or outlet obstruction.Open
StatementThe Suave procedure theoretically causes less injury to pelvic structures, nerves, urethra and vagina.Open
StatementIn the Suave procedure, the actual anastomosis is performed within a cuff of aganglionic rectum.Open
StatementThe Suave procedure involves performing a mucosectomy from a transanal approach slightly above the dentate line and pulling through the normal bowel.Open
StatementHirschsprung's-associated enterocolitis is likely an inflammatory condition secondary to bacterial overgrowth.Open
StatementFor enterocolitis, antibiotics including metronidazole or broad-spectrum antibiotics are added depending on the severity of presentation.Open
StatementTreatment of enterocolitis includes fluid resuscitation, digital rectal exam, and colonic irrigations.Open
StatementA child with enterocolitis presents with abdominal distension, vomiting, fever, and change in bowel habits that could be either diarrhea or not passing stool at all.Open
StatementHirschsprung's-associated enterocolitis is likely an inflammatory condition secondary to bacterial overgrowth.Open
QuotationHirschsprung's-associated enterocolitis is poorly understood and likely is an inflammatory condition secondary to bacterial overgrowth.Open
QuotationWhen we treat these patients with enterocolitis, it is important to provide fluid resuscitation, digital rectal exam, and colonic irrigations.Open
QuotationWhen we treat these patients with enterocolitis, it is important to provide fluid resuscitation, digital rectal exam, and colonic irrigations.Open
QuotationHirschsprung's-associated enterocolitis is poorly understood and likely is an inflammatory condition secondary to bacterial overgrowth.Open
StatementFor enterocolitis, antibiotics including metronidazole or broad-spectrum antibiotics are added depending on the severity of presentation.Open
StatementTreatment of enterocolitis includes fluid resuscitation, digital rectal exam, and colonic irrigations.Open
StatementA child with enterocolitis presents with abdominal distension, vomiting, fever, and change in bowel habits that could be either diarrhea or not passing stool at all.Open
StatementFor patients with anatomic problems after pull-through, you typically have to revise the pull through.Open
StatementFor patients with anatomic problems after pull-through, you typically have to revise the pull through.Open
StatementFor patients not doing well after pull-through, if there is a stricture at the anastomosis, it needs to be addressed either through dilations or revising the pull through procedure.Open
StatementFor patients without anatomic problems after pull-through, treatment can include bowel management, Botox injection to relieve sphincter tone, or motility studies.Open
StatementFor patients not doing well after pull-through, if there is a stricture at the anastomosis, it needs to be addressed either through dilations or revising the pull through procedure.Open
StatementAnatomic problems after pull-through can include a twist in the pull through, an obstructing cuff, a non-functioning Duhamel pouch, or a transition zone or continued aganglionic segment.Open
StatementFor patients without anatomic problems after pull-through, treatment can include bowel management, Botox injection to relieve sphincter tone, or motility studies.Open
StatementAnatomic problems after pull-through can include a twist in the pull through, an obstructing cuff, a non-functioning Duhamel pouch, or a transition zone or continued aganglionic segment.Open
Colorectal Quiz Episode 3: Hirschsprung Disease
StatementIn Hirschsprung disease, the aganglionic rectum appears narrow due to spasm and inability to relax, while the ganglionated proximal bowel is dilated, creating the recto-sigmoid ratioOpen
StatementQuick diff staining highlights ganglion cells better than standard H&E stainingOpen
StatementThree good biopsy specimens should be obtained for pathologic evaluationOpen
StatementThe crypts are located above the dentate line, so optimal biopsy location is at least 1-2 cm above the dentate lineOpen
The Colorectal Quiz Episode 3.5: Proximal Hirschsprung Disease
QuotationYeah. And I think you could make guesses about this. But like you said, it's hard on a newborn film to really discern small and large bowel. And you can get fooled.Open
StatementIt is hard on a newborn film to really discern small and large bowel, and you can get fooled.Open
StatementA limited upper GI was performed and ruled out malrotation in this child.Open
StatementTo get a perforation, you need distension, and if you have a transition zone at the hepatic flexure, then all the pressure is in the right colon.Open
QuotationSo they were quick to point out that we're lucky this patient didn't show up with a perforation. And usually they perforate in the cecum.Open
StatementPatients with proximal Hirschsprung disease are at risk of perforation, usually in the cecum.Open
StatementA baby that doesn't have a competent ileosecal valve might be saved from perforation because pressure can decompress into the small bowel.Open
StatementYou are obligated at some point, maybe after resuscitation, to get a rectal biopsy in a patient with suspected Hirschsprung disease.Open
QuotationYou're obligated at some point, maybe after resuscitation, to get a rectal biopsy.Open
QuotationTwo different operative approaches for the same disease because one is more proximal and more complicated and the other is more distal.Open
StatementProximal Hirschsprung disease and distal Hirschsprung disease require two different operative approaches.Open
QuotationPreviously, we used to do this transanally, it would take a few hours. Now, the transanal dissection should be usually way under 1 hour, especially in a primary pull-through point.Open
StatementWith proper laparoscopic dissection, the transanal portion of a primary Hirschsprung pull-through should take well under one hour.Open
StatementWith proper laparoscopic dissection, the transanal portion of a primary Hirschsprung pull-through should take well under one hour.Open
QuotationPreviously, we used to do this transanally, it would take a few hours. Now, the transanal dissection should be usually way under 1 hour, especially in a primary pull-through point.Open
StatementFor distal Hirschsprung disease, only distal branches of the IMA need to be taken, but for left colon involvement, the IMA itself may need to be taken to achieve adequate reach.Open
StatementFor distal Hirschsprung disease, only distal branches of the IMA need to be taken, but for left colon involvement, the IMA itself may need to be taken to achieve adequate reach.Open
The Colorectal Quiz Episode 8: Motility Disorders Part 1
QuotationIt's saying that this is not a Monet, that is for certain.Open
StatementContrast studies are not great predictors of how patients will respond to medical or surgical management; normal-looking colons may not respond while abnormal-appearing colons may respond wellOpen
StatementWater-soluble contrast (not barium) is used for contrast enemas because it helps empty the colon and acts as a cleanout for patients starting new medical therapyOpen
StatementIn the past, surgeons did not understand the major role the sphincter played in many patientsOpen
QuotationI think back in the day, Mark, yeah, we, we didn't understand the sphincter and the major role it played.Open
The Colorectal Quiz Episode 10: Total Colonic Hirschsprung Disease Part 1
StatementThe age cutoff for switching from suction rectal biopsy to full-thickness biopsy is around 6 monthsOpen
QuotationMy cutoff is around 6 months when I switch from suction rectal biopsy to full thickness biopsy.Open
StatementIf the patient is doing well and can be managed with irrigations, it is preferable to have final pathology diagnosis of Hirschsprung disease from rectal biopsy before entering the abdomenOpen
QuotationIf the patient is doing well and able to be managed with irrigations, would love to have my final diagnosis of Hirschprung's disease through the rectal biopsy before entering the abdomen.Open
StatementStandard biopsy locations during operative mapping include rectosigmoid, proximal sigmoid around the left colon, splenic flexure/transverse colon, and right colon or hepatic flexure areaOpen
The Colorectal Quiz Episode 20: Hirschsprung Disease Obstruction Part 2
StatementBotox is being studied to prevent enterocolitis with the theory of chemo-denervating nerves in the area instead of permanent stretch or anatomic destruction from surgeryOpen
QuotationIs now, let's say 3 centimeters, or 4, or 5. Well, is that the problem that this kid did well until that cuff got to a length, that's a ganglionic, and now it's causing obstructive problems.Open
StatementInitial treatment for obstructed Hirschsprung's patient must include rectal irrigation, done earlyOpen
StatementEvery institution should have a protocol for obstructed Hirschsprung's patients to ensure quick and efficient responseOpen
StatementSystematic workup for obstructed Hirschsprung's includes: resuscitation, imaging studies, and comprehensive rectal exam under anesthesiaOpen
The Colorectal Quiz Episode 21: The History of Hirschsprung Disease
StatementDoctor Martin developed the Martin procedure, an extended Duhamel procedure that leaves a longer aganglionic segment of rectum for long-segment Hirschsprung disease.Open
StatementIn 1977, Doctor Martin was the first to apply the endorectal pull-through technique used in Hirschsprung disease to the surgical treatment of ulcerative colitis, performing total proctocolectomy with ileoanal anastomosis.Open
StatementDoctor Martin's ulcerative colitis technique predated the J-pouch, which later modified his approach.Open
The Colorectal Quiz Episode 22: Hirschsprung Disease - the Soiling Patient Part 1
StatementPathology can change over time; cases exist where ganglion cells were present at pull-through but absent with hypertrophic nerves 7 years later when problems developed.Open
StatementSphincters should be assessed with the patient awake; examination under anesthesia makes it harder to assess sphincter function.Open
StatementDuring normal bowel movements, sphincters relax and the anus opens with some mucosal descent, but as soon as sphincters tighten, the mucosa retracts back in; prolapse at rest indicates damaged muscles and/or mucosa brought too low at anastomosis.Open
The Colorectal Quiz Episode 23: Hirschsprung Disease - The Soiling Patient...
QuotationCan I scare you for a moment? Can we talk scientifically for one minute? I know this is crazy.Open
StatementThe dentate (or pectinate) line is the transition from squamous epithelium to columnar epithelium, located about 2/3 of the way up the anal canal.Open
StatementBlood supply changes occur at the dentate line (splanchnic versus systemic), and there is also innervation in that area.Open
QuotationI talk about that dentate line in the area where the nerves are located that tell you gas, liquid, solid. How hard do I need to squeeze, how long do I have to squeeze for, how tight do I have to squeeze?Open
StatementThe nerves located at the dentate line region tell you gas, liquid, solid; how hard, how long, and how tight to squeeze.Open
StatementPreserving the dentate line region is key because injury to that region affects a patient's ability to be continent.Open
StatementIn children with anorectal malformation, Hirschsprung disease, spinal conditions, or combinations thereof, the ability to sense stool in the rectum or neorectum region is critical to success; the right consistency and bulk of stool is very important.Open
StatementIf clinicians make stool too soft or too loose with medications, they put a child on the edge of having control or not and throw them over that edge, preventing success.Open
QuotationAnd if we make it too soft or too loose, we're putting a child or a person who is on the teeter of having control or not, and you throw them over that edge, and, and you just won't be successful.Open
QuotationI mean, it makes sense that they should if the muscle is intact, right, because this is no different than an anorectal malformation, anastomosis. That's right. But it's, it's, it's rectum or colon mucosa to skin.Open
StatementA Hirschsprung patient with missing dentate line and intact muscle should be able to achieve continence, similar to an anorectal malformation anastomosis (rectum or colon mucosa to skin).Open
StatementPatients with no dentate line and patulous sphincters who are soiling develop severe skin irritation from sitting in pull-ups or diapers.Open
QuotationThat is a patient with no dentate line and pattula sphincters, and you clearly see with the skin changes around that, that this patient has really struggled and has been soiling and, and, and sitting in, in pull-ups or a diaper, really causing severe skin irritation.Open
StatementFor hypermotile patients (stooling 7-8 times a day), the approach is to constipate them first, then figure out how to empty them in a time-controlled fashion.Open
QuotationThis, this is, these are the harder patients to take care of, and the trick that I use is you have to constipate them. And then if they're able to empty with continence on their own, then great. If they're not, then you have to mechanically help them empty.Open
QuotationBut it, it's, it's like, it sounds counterintuitive, but at least the way I treat these patients, I constipate them, and then I empty them.Open
StatementWhether hypermotile patients can empty on their own versus needing mechanical emptying to maintain social continence depends on their sphincter function.Open
QuotationBut that's how I sort of explain it to the families. It sounds weird, but we're gonna constipate you, and then we have to figure out how to empty you in a time-controlled fashion.Open
StatementSome Hirschsprung patients who have a good operation have super strong sphincters that just need a little relaxation to allow passage of stool until they learn proper sphincter coordination for evacuation.Open
StatementBotox helps train sphincters in Hirschsprung patients; anorectal manometry can provide objective data showing resting pressures are usually on the higher end of normal, and some patients need extra relaxation to allow them to go.Open
StatementNutrition in Hirschsprung patients is very important; some patients are very sensitive to certain foods, particularly lactose.Open
StatementPaying attention to diet (whether breastfed infants or older children) is important because lactose is particularly problematic in some Hirschsprung patients.Open
QuotationNone. We have to get it right the first time.Open
QuotationAnd if you don't get it right, you gotta use these techniques and this algorithm to figure out what's wrong, cause we could get every patient doing well. They might need help, and they might need mechanical evacuations, Botox, etc. but we could, we all should be able to get these patients on the right track.Open
StatementEvery Hirschsprung patient should be able to do well; they might need help and might need mechanical evacuations or Botox, but all should be able to get on the right track.Open
Colorectal Quiz Episode 37: The Yancey-Soave story of the original surgical descriptions for Hirschsprung disease
StatementDr. Newman brought Dr. Yancey's story to the attention of the Hirschsprung interest group at APSA.Open
StatementA fellow at Children's National wrote an operative note describing a patient as status post a 'Yancey-Suave procedure,' indicating the terminology has become part of standard practice.Open
QuotationI was reading the operative note from one of my fellows who provided the history of the patient. I had to do a reoperation on the patient. And the history read that this five-year-old child is status post a Yancey Suave procedure in such and such date and had an asthmatic stricture.Open
Colorectal Quiz: Episode 46
StatementIn anorectal malformation patients with perforation, the sigmoid colon typically perforates with a linear, longitudinal tear along the taenia.Open
QuotationYou need to break the cycle of the physiologic obstruction. They are obstructed both at the sphincter level and in the aganglionic segment. And you have to break that cycle by getting a tube across it and then a lumen of that tube then to allow for egress of that stool because it's the stasis that's the problem. It's the stasis, the bacterial overgrowth. That overgrowth leads to translocation and that's where the sepsis comes in.Open
StatementThe pathophysiology of Hirschsprung enterocolitis involves physiologic obstruction at both the sphincter level and in the aganglionic segment, leading to stasis, bacterial overgrowth, translocation, and sepsis.Open
StatementCold saline used for irrigations in small children can significantly change the child's body temperature, so warm saline should be used.Open
StatementSawtoothing in the rectum on contrast enema represents hyperperistalsis and is very classic for Hirschsprung disease, particularly when associated with enterocolitis.Open
QuotationIf it was a reliable family and irrigations were going well, I probably would have sent them home for a couple, a month or two, and then brought them back for their definitive operation.Open
StatementIf a patient has recovered from enterocolitis and irrigations are going well with reliable family, it is reasonable to send them home for 1-2 months before definitive operation rather than operating at 2 weeks.Open
StatementLiterature from the PCPLC and Michael Rollins shows that delayed definitive surgery for Hirschsprung disease (around 3 months out) has similar outcomes, so it is okay to wait as long as patient receives good irrigations and is growing and healthy.Open
QuotationI agree with Mark. I would wait minimum four weeks from getting healthy after treating enterocolitis, maybe even longer before doing this. And I think there's good literature out there from the PCPLC and Michael Rollins on outcomes of Hirschsprung's disease and delayed treatment and delayed mepeter, wrong term. But just doing the definitive surgery, they looked at about three months out and had similar outcomes.Open
StatementIf mapping the colon without frozen section available, the entire colon should be mapped (left colon, transverse colon, and hepatic flexure/right colon) to avoid missing ganglionic segments.Open
QuotationI'm a fan of doing ileostomies in these cases where we need to divert and we have time and we're in a place where we're able to keep the patients hydrated well.Open
StatementIn settings where patients can be kept well hydrated with easy healthcare access, ileostomy is preferred over colostomy for diversion because colostomy mesentery becomes shortened and inflamed after division, making subsequent pull-through technically difficult with inadequate reach.Open
StatementWhen performing ileostomy for Hirschsprung diversion, frozen section should be done on the ileostomy to ensure it will function.Open
StatementCincinnati group is conducting a non-randomized study of Botox injection at the anal sphincter at time of ileostomy closure, with retrospective baseline comparison and prospective data collection currently in mid-30s patients; some patients in the protocol have still developed enterocolitis, so it is not 100% effective.Open
StatementFamilies should be sent home with equipment to irrigate and taught how to irrigate before the pull-through so they can practice, ensuring they know the technique before discharge and avoiding catheter passage through fresh anastomosis post-op day 5.Open
QuotationWe send the families home with the equipment to irrigate. That's a must, right? And also we teach how to irrigate before we do our pull through so that they are, and make the parents practice whether the child has enterocolitis or not pre-op so that they know how to do it.Open
Colorectal Quiz: Episode 40
StatementOptions for vaginal reconstruction when native vagina cannot reach include: dilating the existing introitus, opening the area and laying in a buccal graft, or waiting for tissue engineering options expected within 20 years or less.Open
QuotationI think it's going to be, there are people right now taking a few vaginal cells and growing them and hopeful, just like you said, Mark, we're going to have some great tissue engineering that will assist us and make this a easier and better procedure for our patients.Open
StatementIf a neovagina bridge is functioning well without problems, there may be no reason to remove it later.Open
The Colorectal Quiz Episode 21: The History of Hirschsprung Disease
QuotationHe united us. Yeah. In a way. And he doesn't even know it.Open
StatementDr. Martin developed the Martin procedure, an expansion of the Duhamel for long-segment Hirschsprung disease, leaving a longer aganglionated segment of rectum and pulling through ganglionated bowel.Open
StatementDr. Martin was the first surgeon-in-chief and pediatric surgeon at Cincinnati Children's Hospital.Open
QuotationI think that's the who's who of Hirschsprung's right there.Open
QuotationI have a feeling we're going to have way more discussions about Hirschsprung disease because just because, because I think it's a fascinating disease that there are so many intricacies. You just mentioned dentorocolitis. We could talk forever about that.Open
The Colorectal Quiz Episode 4
Quotationthey must see submucosa. And if you send them a biopsy without submucosa, our pathologist will say, hey, where's the submucosa? Because you want to make sure, again, that you don't find ganglion cells in the seromuscular layer and hypertrophic nerves in the submucosal layer.Open
StatementFrozen section biopsy must include submucosa to avoid missing hypertrophic nerves in submucosal layer while finding ganglion cells in seromuscular layerOpen
StatementMesenteric dissection should stay close to bowel wall, not deep in mesentery, to reduce bleedingOpen
QuotationYou need to be very careful of preserving that arcade along the left colon and sigmoid colon so you could get enough distance to reach the pelvis.Open
StatementMust preserve arcade along left colon and sigmoid to get enough length to reach pelvisOpen
StatementResection margin should be approximately five centimeters above biopsy site where bowel looks goodOpen
Jason's statements about Hirschsprung Disease: Diagnosis to Long-Term Management16 statements
QuotationI think I agree, Mark. If you see free air, I don't think irrigation is the thing to do. You're going to stir up the pot, but, uh, an irrigation typically is going to be the lifesaver for these children, these types, these types of situations.Open
StatementIrrigation technique requires instilling small aliquots of saline (20-40 mL at a time) and then evacuating it rather than just infusing into the colon lumen.Open
QuotationA few key tips to irrigation for those listening to me, an irrigation is instilling a, a small aloquat of saline, usually warm saline. Somewhere between 20 and 40 mLs um at a time. And it's infusing, instilling it in and getting it removed, whether that be by withdrawing from, with a catheter, so that you evacuate that saline and not just infuse it into the lumen of the colon, I think is important.Open
StatementExperts recommend waiting minimum 4 weeks after treating enterocolitis before performing definitive pull-through surgery, as long as the patient is receiving good irrigations and growing and healthy otherwise.Open
QuotationI would wait minimum 4 weeks from getting healthy. Um, after treating enterocolitis, maybe even longer, uh, before doing this. And I think there's good literature out there from the PCPLC and Michael Rawlins on outcomes of Hirschprung's disease and delayed treatment, and delayed might be the wrong term, but just doing the definitive surgery, they looked at about 3 months out and had similar outcomes.Open
StatementLiterature from the PCPLC and Michael Rawlins shows that delayed definitive surgery for Hirschsprung disease (around 3 months out) has similar outcomes to earlier surgery.Open
StatementWhen mapping the colon without frozen section available, biopsies should be taken from left colon, transverse colon, and hepatic flexure/distal ascending colon, as cecal pull-throughs do not succeed very well.Open
QuotationDo not biopsy the appendix. That's not helpful. Save the appendix for maybe future use.Open
StatementModern telemedicine technology allows pathologists to evaluate H&E stained slides for ganglion cells via Zoom using a camera and microscope, enabling better surgical planning in resource-limited settings and potentially saving 80% of colons in rectosigmoid Hirschsprung disease.Open
StatementApproximately 80% of Hirschsprung disease cases are rectosigmoid in extent.Open
QuotationMy new motto is let's try to save colons.Open
StatementIleostomy is preferred over colostomy for diversion in Hirschsprung disease because colonic diversion can shorten the mesentery through division and inflammation, making subsequent pull-through technically more difficult with inadequate reach.Open
QuotationI'm a fan of doing ileostomies in these cases where, where we need to divert. And we have time and we're in a, a place where we're able to keep the patients hydrated well.Open
QuotationI do a lot of pull-throughs of patients that have a diverting colostomy. And I find it sometimes hard to get it to reach. I think the mesentery is shortened a little bit, um, cause it's divided and then it gets inflamed.Open
StatementBotox injection at the anal sphincter at time of ileostomy closure is being studied prospectively but is not 100% effective, as some patients in the protocol still developed enterocolitis.Open
StatementFamilies should be sent home with irrigation equipment and taught irrigation technique before pull-through surgery, with parents practicing the technique, to avoid having catheters go through the anastomosis post-operatively when issues arise.Open
Jason's statements about Hirschsprung Disease: Diagnosis to Long-Term Management16 statements
QuotationI think I agree, Mark. If you see free air, I don't think irrigation is the thing to do. You're going to stir up the pot, but, uh, an irrigation typically is going to be the lifesaver for these children, these types, these types of situations.Open
StatementIrrigation technique requires instilling small aliquots of saline (20-40 mL at a time) and then evacuating it rather than just infusing into the colon lumen.Open
QuotationA few key tips to irrigation for those listening to me, an irrigation is instilling a, a small aloquat of saline, usually warm saline. Somewhere between 20 and 40 mLs um at a time. And it's infusing, instilling it in and getting it removed, whether that be by withdrawing from, with a catheter, so that you evacuate that saline and not just infuse it into the lumen of the colon, I think is important.Open
StatementExperts recommend waiting minimum 4 weeks after treating enterocolitis before performing definitive pull-through surgery, as long as the patient is receiving good irrigations and growing and healthy otherwise.Open
QuotationI would wait minimum 4 weeks from getting healthy. Um, after treating enterocolitis, maybe even longer, uh, before doing this. And I think there's good literature out there from the PCPLC and Michael Rawlins on outcomes of Hirschprung's disease and delayed treatment, and delayed might be the wrong term, but just doing the definitive surgery, they looked at about 3 months out and had similar outcomes.Open
StatementLiterature from the PCPLC and Michael Rawlins shows that delayed definitive surgery for Hirschsprung disease (around 3 months out) has similar outcomes to earlier surgery.Open
StatementWhen mapping the colon without frozen section available, biopsies should be taken from left colon, transverse colon, and hepatic flexure/distal ascending colon, as cecal pull-throughs do not succeed very well.Open
QuotationDo not biopsy the appendix. That's not helpful. Save the appendix for maybe future use.Open
StatementModern telemedicine technology allows pathologists to evaluate H&E stained slides for ganglion cells via Zoom using a camera and microscope, enabling better surgical planning in resource-limited settings and potentially saving 80% of colons in rectosigmoid Hirschsprung disease.Open
StatementApproximately 80% of Hirschsprung disease cases are rectosigmoid in extent.Open
QuotationMy new motto is let's try to save colons.Open
StatementIleostomy is preferred over colostomy for diversion in Hirschsprung disease because colonic diversion can shorten the mesentery through division and inflammation, making subsequent pull-through technically more difficult with inadequate reach.Open
QuotationI'm a fan of doing ileostomies in these cases where, where we need to divert. And we have time and we're in a, a place where we're able to keep the patients hydrated well.Open
QuotationI do a lot of pull-throughs of patients that have a diverting colostomy. And I find it sometimes hard to get it to reach. I think the mesentery is shortened a little bit, um, cause it's divided and then it gets inflamed.Open
StatementBotox injection at the anal sphincter at time of ileostomy closure is being studied prospectively but is not 100% effective, as some patients in the protocol still developed enterocolitis.Open
StatementFamilies should be sent home with irrigation equipment and taught irrigation technique before pull-through surgery, with parents practicing the technique, to avoid having catheters go through the anastomosis post-operatively when issues arise.Open
Jason's statements about Hirschsprung's-associated Enterocolitis13 statements
Colorectal Quiz Episode 19: Hirschsprung Disease - The Obstructed Patient Part 1
StatementWhen performing initial rectal exam on a distended child with suspected enterocolitis, step to the side because there may be an explosive release of stool and gas.Open
QuotationI think one key thing to talk about with all our listeners is when you do that exam, make sure you step to the side. A little bit funny, but a little bit, you don't wanna be in the way of what could be coming out.Open
QuotationIf you have a patient that comes in with a diagnosis of Hirschprung's in the past and comes with, comes in sick, you have to assume it's Hirschprung's associated enterocolitis.Open
StatementFor a patient with prior Hirschsprung diagnosis presenting sick, assume Hirschsprung-associated enterocolitis; treatment with rectal irrigations, IV fluids, and antibiotics will not cause harm even if the diagnosis is different (e.g., Crohn's disease, E. coli enterocolitis).Open
StatementFamilies should not undergo Hirschsprung pull-through surgery until they can demonstrate ability to perform rectal irrigations, and they should be discharged with supplies to perform irrigations at home.Open
StatementIn a logical workup, obtain the contrast study before going to the OR for rectal exam under anesthesia, as it may reveal findings that guide the surgical approach.Open
QuotationI think we all agree we get the contrast study before going to the operating room for a rectal examOpen
StatementA lateral view on contrast enema is important because it provides significant information about the presacral space and distal rectum anatomy.Open
The Colorectal Quiz Episode 20: Hirschsprung Disease Obstruction Part 2
StatementBotox is being studied to prevent enterocolitis with the theory of chemo-denervating nerves in the area instead of permanent stretch or anatomic destruction from surgeryOpen
QuotationIs now, let's say 3 centimeters, or 4, or 5. Well, is that the problem that this kid did well until that cuff got to a length, that's a ganglionic, and now it's causing obstructive problems.Open
StatementInitial treatment for obstructed Hirschsprung's patient must include rectal irrigation, done earlyOpen
StatementEvery institution should have a protocol for obstructed Hirschsprung's patients to ensure quick and efficient responseOpen
StatementSystematic workup for obstructed Hirschsprung's includes: resuscitation, imaging studies, and comprehensive rectal exam under anesthesiaOpen
Jason's statements about Inflammatory Bowel Disease16 statements
StatementIf terminal ileum cannot be intubated, gastroenterologists may treat presumptively and re-scope after a few months of treatment when inflammation has decreased.Open
StatementThe highest risk factors for lymphoma with biologic therapy are male gender, teenage age, and combination therapy with methotrexate.Open
StatementMale gender over the age of 10, and presence of a fistula are risk factors with much higher incidence of Crohn's disease being diagnosed in patients presenting with perianal lesions to the emergency room.Open
StatementIn pediatric patients, unlike adult patients, the first presenting factor for Crohn's disease can often be perianal disease.Open
QuotationI don't like to make holes when there aren't holes there.Open
StatementThe mucosa heals first compared to skin in perianal disease, so leaving a mucosal opening without a seton risks recurrent abscess when biologics heal the mucosa.Open
QuotationThe thing that's going to heal first is the mucosa.Open
StatementMaking a large cruciate incision and packing a perianal abscess in a child with undiagnosed Crohn's disease may result in non-healing and potentially require colostomy or ileostomy.Open
QuotationYou may have bought that kid a colostomy or ileostomy.Open
StatementHydrogen peroxide is preferred over methylene blue for identifying fistula tracts because it is neater; 3% hydrogen peroxide in a syringe with 16-20 gauge angiocath is used with a speculum in the anus.Open
StatementWhen a fistula opening cannot be found despite hydrogen peroxide testing, a seton should not be placed at that time to avoid creating a hole where there isn't one.Open
StatementSource control of infection must be achieved before starting immunosuppressive therapy including steroids and biologics.Open
StatementIf an abscess is not adequately drained, reimaging should be performed before giving biologics or steroids.Open
StatementBefore removing a seton, the bottom must look better, drainage must be better, the patient must be symptom-free, and they must have reached steady state of biologic (loading dose plus at least 3 more doses, typically 2-3 months from start).Open
StatementInflammatory markers including fecal calprotectin, ESR, and CRP should be checked before removing a seton to ensure systemic disease is under control.Open
StatementThe initial Remicade paper from 1998 or 1999 in the New England Journal of Medicine was on perianal disease and demonstrated improved healing time and improved length of time between recurrence when combination of seton and infliximab is used versus either separately.Open
Jason's statements about Intestinal Rehab66 statements
Gastroschisis and sutureless abdominal wall closure
StatementMany patients who underwent sutureless repair were done in more recent cohorts and tended towards less interventions.Open
QuotationI think it was probably what we were expecting, I think, for a couple of reasons. One, due to the heterogeneity of this disease, you know, especially with gastroschisis, a lot of the patients that were able to undergo, you know, especially a primary repair, they probably had more favorable bowel. And then those patients, you know, theoretically would have less hospital stay and theoretically feed faster and things like that.Open
StatementDue to the heterogeneity of gastroschisis, patients able to undergo primary repair probably had more favorable bowel and theoretically would have less hospital stay and feed faster.Open
QuotationMoreover, too, if you think about just the way that we close a sutured repair, you mobilize flaps from the skin and flaps from the fascia. So there's always, you know, redness around the incision, bruising around the incision. And so, you know, even that tissue manipulation is going to put you at higher risk for a potential infection or calling it erythema infection.Open
StatementThe finding of increased antibiotics needed after sutured repair was expected due to tissue manipulation.Open
StatementIn sutured repair, mobilizing flaps from the skin and fascia causes redness and bruising around the incision, which puts patients at higher risk for potential infection.Open
StatementThe consortium is working on operationalizing protocolization of gastroschisis closure across member institutions for a more prospective study with long-term follow-up.Open
StatementThe next phase of the study is examining the same patients over several years of follow-up to assess growth and umbilical hernia repair rates.Open
The Colorectal Quiz Episode 8: Motility Disorders Part 1
QuotationIt's saying that this is not a Monet, that is for certain.Open
StatementContrast studies are not great predictors of how patients will respond to medical or surgical management; normal-looking colons may not respond while abnormal-appearing colons may respond wellOpen
StatementWater-soluble contrast (not barium) is used for contrast enemas because it helps empty the colon and acts as a cleanout for patients starting new medical therapyOpen
StatementIn the past, surgeons did not understand the major role the sphincter played in many patientsOpen
QuotationI think back in the day, Mark, yeah, we, we didn't understand the sphincter and the major role it played.Open
QuotationBut I think our management style now here at Cincinnati Children's has been to try to maximize medical therapy, understand the anatomic and functional issues, and then if we can't overcome those issues with medical management, resort to surgical intervention and potential resection.Open
StatementThe management approach at Cincinnati Children's is to maximize medical therapy and understand anatomic and functional issues before resorting to surgical intervention and potential resection.Open
QuotationI want to stress that we shouldn't resort to resection right away just because we have one abnormal finding.Open
StatementResection should not be performed immediately based on one abnormal finding; multiple factors must be considered.Open
StatementThe first step in evaluating a patient with suspected motility disorder is to ensure normal anatomy, which can be assessed with contrast studies.Open
QuotationOne, you have to ensure normal anatomy.Open
Neonatal Gastric Volvulus with Dr. Jason Frischer
QuotationI've seen it associated with congenital diaphragmatic hernias a few times, and I think that's when we have a high suspicion for it.Open
Quotation60% happen in the first year of life in the pediatric population, and so about 21% in the first month and over a third in the first year of life.Open
Statement60% of gastric volvulus cases in the pediatric population happen in the first year of life, with about 21% in the first month.Open
QuotationIf the child's like 4 months old, is it more likely, are you're more likely to have an acute problem or a chronic problem? So they're acute.Open
StatementIn a 4-month-old child with gastric volvulus, acute presentation is more likely than chronic.Open
QuotationThat's the big one, I think, right there. I think a little bit of bloody aspirate from the. Logo can't advance it. Funny looking stomach bubble on the X-ray.Open
StatementA little bit of bloody aspirate from the NG tube and a funny looking stomach bubble on X-ray are key findings in gastric volvulus.Open
QuotationThose are more to do with the laxity of the gastric ligaments, and the stomach has ligamentous attachments basically surrounding the entire stomach from gastrophrenic, gastrosplenic, gastrocolic. And of course. Gastropatic ligament.Open
StatementChronic gastric volvulus is more related to laxity of the gastric ligaments including gastrophrenic, gastrosplenic, gastrocolic, and gastrohepatic ligaments.Open
QuotationThe first one, the first and most common is organoaxial volvulus.Open
StatementOrganoaxial volvulus is the first and most common type of gastric volvulus.Open
StatementIn organoaxial volvulus, the stomach spins around an axis drawn between the GE junction and the pylorus, with the greater curvature flipping up and over to become more superior than the lesser curvature.Open
QuotationThey describe a line that's drawn on this diagram between the GE junction and the pylorus, and it's spinning around that axis. The greater curvature then sort of flips up and over and becomes more superior than the lesser curvature.Open
StatementIn mesenteroaxial volvulus, rotation occurs around a line through the middle of the stomach from lesser to greater curvature, with the stomach flipping behind and back over.Open
QuotationThen, and flip the stomach up and over that way, so it's going sort of behind. The stomach and back over it.Open
QuotationWhen the pylorus is at, right next to the GE junction or near the GE junction, and above the body of the stomach.Open
StatementIn gastric volvulus, when filled with contrast, the pylorus appears right next to or near the GE junction and above the body of the stomach.Open
StatementIn mesenteroaxial volvulus, the duodenum may fill above or superior to the GE junction because the pylorus has flipped up and over or behind and over the top of the stomach.Open
QuotationMesentero axial favulus. Again, this is the sort of pylorus flipping up and over or behind and over the top of the stomach, and then therefore, your pylorus is located all the way up here.Open
StatementWhen managing gastric volvulus found during CDH repair, viability of the stomach must always be checked, especially if chronically volvulized or volvulized for a couple of days, by looking at the serosa and blood flow.Open
QuotationAlso, you always want to check the viability of the stomach. So, right, if this is chronically volvulized or been volvulized for a couple of days, uh, at least looking at the cirrhosa and looking at the blood flow.Open
Update Course 2022 - UPDATES IN GASTROSCHISIS FEEDING PROTOCOLS - Jason Fraser, Beth Rymeski, and Steven Lee
StatementJason Fraser's institution starts feeding immediately after dressing placement as long as the baby is not sick, not having horrible output, and not vomiting.Open
Quotationwe start feeding essentially you have to put the dressing on uh as long as the baby's not sick not having horrible output not puking or anything like thatOpen
Quotationwe don't innovate our babies at all so we put the dressing plastic dressing on and as long as the kid's not you know has voluminous output we'll try to start start feedings on itOpen
StatementFraser's institution does not intubate gastroschisis babies for reduction.Open
StatementAwake reduction can be successful if performed slowly, with stomach emptying, colon decompression, oral sucrose, and gradual abdominal wall stretching.Open
Quotationif you try to just keep pushing and pushing pushing the baby kind of can squirm and stuff but if you go slow if you empty out the stomach if you kind of squish out the colon a little bit and you go slow you give the baby some sweeties the nurses are there to kind of relax the baby you have a couple people that that are there doing it you go slow you slowly kind of push things in you stretch out the belly a little bitOpen
StatementCincinnati Children's feeding protocol is based on patient tolerance and data from resource-limited settings where TPN is unavailable and feeding is mandatory.Open
Quotationit's really just based upon patient tolerance and it's kind of based upon some of the data that's out there from the rest of the world where they don't have tpn and so they just you have to feed the kid if the kid does okay then they keep goingOpen
StatementThe multi-institutional study showed inconclusive results due to significant variation in feeding protocols across institutions.Open
Quotationa lot of the inconclusivity from the the study showed that you know most likely due to the fact that there was lots of different feeding protocols that were used uh across our member institutionsOpen
StatementThe reduction in surgical site infections with protocol feeding was likely due to decreased care variability rather than the feeding protocol itself.Open
Quotationthe ssi thing was probably just because patients that were fed via protocol were cared for via protocol and so that they actually had less variability and less uh less changes uh in the way that these these patients are not you know look forOpen
Quotationour length of stay for gastroschisis and cincinnati was astronomically higher than like any other nick micu in the cooperative network that we worked with so we sat down we're like what is going on here so our average length of stay was 49 daysOpen
StatementCincinnati Children's average gastroschisis length of stay was 49 days before protocol implementation, which was astronomically higher than comparable NICUs in their cooperative network.Open
Quotationwe instituted this uh a feeding protocol we spent a lot of time trying to get people to follow it and and making some adjustments and over two years we dropped the length of stay by 10 days and the mix of patients is not differentOpen
StatementAfter implementing a feeding protocol, Cincinnati Children's reduced gastroschisis length of stay by 10 days over two years.Open
StatementCincinnati Children's has seen a decrease in time from first feed to full feeds but has not yet reduced the time from admission to first feed (except in 2020).Open
StatementCincinnati Children's gastroschisis protocol includes prenatal care coordination with obstetricians and neonatologists, with surgery continuing to follow patients throughout hospitalization.Open
Quotationthe most important thing that kind of keeps showing up is the fact that we really need to define what your own institution has for tolerance and to kind of stay on the protocol and then really just look at the infant condition as you continue to go is the most important thingOpen
StatementThe most important aspects of gastroschisis feeding are defining institutional tolerance criteria, adhering to protocol, and continuously evaluating the infant's condition.Open
Quotationyes you can have a protocol yes you know you need to follow it but the most really you really need to continually evaluate the patient as they continue to go to make sure that you know yes your protocol is working but also to the patient does okay throughoutOpen
StatementFor significant feeding intolerance, Cincinnati Children's protocol calls for stopping feeds for six hours, though this is not clearly evidence-based.Open
StatementCincinnati Children's current average gastroschisis length of stay is 30 to 34 days.Open
StatementOne recent Cincinnati Children's gastroschisis patient who was primarily reduced on day of life zero was discharged at approximately two weeks and remained well at two-week follow-up, though this is an outlier on the faster end.Open
StatementCincinnati Children's has not seen any aspirations with their early aggressive feeding approach, though they acknowledge they are still early in implementation and continue to monitor data.Open
StatementAt Cincinnati Children's, approximately two-thirds of gastroschisis cases cannot be reduced immediately and are placed in a silo for gradual reduction followed by sutureless closure, with feeds started after closure.Open
QuotationYeah. And I think you could make guesses about this. But like you said, it's hard on a newborn film to really discern small and large bowel. And you can get fooled.Open
StatementIt is hard on a newborn film to really discern small and large bowel, and you can get fooled.Open
StatementA limited upper GI was performed and ruled out malrotation in this child.Open
QuotationSo they were quick to point out that we're lucky this patient didn't show up with a perforation. And usually they perforate in the cecum.Open
StatementPatients with proximal Hirschsprung disease are at risk of perforation, usually in the cecum.Open
StatementTo get a perforation, you need distension, and if you have a transition zone at the hepatic flexure, then all the pressure is in the right colon.Open
StatementA baby that doesn't have a competent ileosecal valve might be saved from perforation because pressure can decompress into the small bowel.Open
QuotationYou're obligated at some point, maybe after resuscitation, to get a rectal biopsy.Open
StatementYou are obligated at some point, maybe after resuscitation, to get a rectal biopsy in a patient with suspected Hirschsprung disease.Open
QuotationTwo different operative approaches for the same disease because one is more proximal and more complicated and the other is more distal.Open
StatementProximal Hirschsprung disease and distal Hirschsprung disease require two different operative approaches.Open
Jason's statements about Motility / Pseudo-obstruction11 statements
The Colorectal Quiz Episode 8: Motility Disorders Part 1
QuotationIt's saying that this is not a Monet, that is for certain.Open
StatementContrast studies are not great predictors of how patients will respond to medical or surgical management; normal-looking colons may not respond while abnormal-appearing colons may respond wellOpen
StatementWater-soluble contrast (not barium) is used for contrast enemas because it helps empty the colon and acts as a cleanout for patients starting new medical therapyOpen
StatementIn the past, surgeons did not understand the major role the sphincter played in many patientsOpen
QuotationI think back in the day, Mark, yeah, we, we didn't understand the sphincter and the major role it played.Open
QuotationBut I think our management style now here at Cincinnati Children's has been to try to maximize medical therapy, understand the anatomic and functional issues, and then if we can't overcome those issues with medical management, resort to surgical intervention and potential resection.Open
StatementThe management approach at Cincinnati Children's is to maximize medical therapy and understand anatomic and functional issues before resorting to surgical intervention and potential resection.Open
StatementResection should not be performed immediately based on one abnormal finding; multiple factors must be considered.Open
QuotationI want to stress that we shouldn't resort to resection right away just because we have one abnormal finding.Open
QuotationOne, you have to ensure normal anatomy.Open
StatementThe first step in evaluating a patient with suspected motility disorder is to ensure normal anatomy, which can be assessed with contrast studies.Open
Jason's statements about Myelomeningocele9 statements
Colorectal Quiz Episode 15: Bowel Management in Spinal Patients - Need for a UrologistPart 1
StatementSenna-induced perineal rash is thought to be a chemical burn rather than a true allergy, presenting with blistering.Open
Quotationit's almost like a chemical burn. The cause they're blistered usually.Open
StatementSenna rash is treated with silver sulfadiazine and resolves with time; some patients tolerate senna upon reintroduction.Open
QuotationWe treat it with silver sulfadiazine, and they've all gotten better with time.Open
StatementTiming senna doses in the early morning so that bowel movements occur during the day (when diapers are changed promptly) reduces the risk of senna rash.Open
Quotationwhat we've done is we timed the dose of Senna in these patients, usually in the early morning, so that they're pooping during the day. And their diapers changed rather quickly versus potentially being in a diaper over a long period of time at night.Open
StatementBisacodyl can be administered as an enema or suppository in infants.Open
QuotationIf there's one take-home message from this podcast, you just said itOpen
Quotationthat care coordination, collaboration with the urologist might be the most beneficial thing we could do for our patients.Open
StatementTwo major surgical decision points in cloacal exstrophy are: (1) whether the omphalocele is large or small enough to close the abdominal wall, and (2) the staging of the exstrophy procedure—whether to just bring bladder plates together in a multi-stage approach or to close the bladder and bring the symphysis pubis together.Open
QuotationThe overriding principle in this patient population is the overriding principle of bowel preservation, right? The small intestine can be shortened in some of these patients. Some of these patients have nutritional concerns, not immediately, but long term. In general, I think the theme should be preserve all bowel.Open
StatementThe overriding principle in cloacal exstrophy management is bowel preservation, as small intestine can be shortened and some patients have long-term nutritional concerns.Open
StatementOne reason for not performing early pull-through in cloacal exstrophy is concern about rash and managing a perineal stoma.Open
Jason's statements about Perineal Fistula18 statements
StatementPerineal groove with mucosal lining will keratinize and look like normal perineal body over timeOpen
QuotationMy conversation with the family often involves that this will keratinize and look like a normal peroneal body over time.Open
StatementSurgical intervention for perineal groove is indicated only if secreting mucus, causing irritation, or developing ulcersOpen
StatementVestibular fistula is very common in females and needs formal repair with hole transposed to center of sphincterOpen
StatementPatients diagnosed with vestibular fistula at 6-12 months who have dilated rectosigmoid need diversion as first step, then repairOpen
StatementFor vestibular fistula diagnosed in newborn period, options are primary repair if baby is well, or allow stooling through fistula for couple months then elective repair without stomaOpen
StatementPurpose of diversion in ARM repair is to avoid perineal body dehiscenceOpen
StatementTo evaluate for vestibular fistula, pull labia towards examiner with both hands to visualize vaginal opening and urethraOpen
Colorectal Quiz Episode 28: Female ARM Management - Perineal Fistula
Quotationwhen you do find neurologic anomalies. That leads to more likely gynecological anomalies as well, especially on the same side.Open
StatementWhen neurologic anomalies are found in anorectal malformation patients, gynecological anomalies are more likely, especially on the same side.Open
Colorectal Quiz Episode 29: Female ARM-Post Op Management
StatementDr. Fisher's protocol for perineal body primary repair (no stoma) is 5-7 days NPO on D10 via midline catheter (not PICC line) until the repair is confirmed healed.Open
QuotationJust because it's published doesn't mean it works.Open
QuotationMy only concern is what's the continence rate of your patients?Open
QuotationI guess my question is somewhere around 20% required a redo either local or total operation. Most just like local, but what did a functional out in the end of the game, all the parents want is their kid pooping in the potty. And we don't know that answer.Open
QuotationThat's a very valid point. So what you're saying, wait, wait, Mark agreed with me.Open
QuotationAnd when I was working with Mark here, I know, especially in the older patients that we were doing redos on, used to teach me to make the anoplasty maybe a little larger.Open
Colorectal Quiz Episode 29: Female ARM
StatementDr. Frisher uses a midline catheter (not PICC line) with D10 until the repair is confirmed healed, typically five to seven days NPO.Open
StatementApproximately 20% of patients in the dilation study required a redo operation, either local or total, with most being local procedures.Open
Jason's statements about Rectal Prolapse12 statements
StatementFor anorectoplasty, if you don't get it perfect, you might not have the best outcomes, which separates it from other surgical procedures.Open
QuotationHow many patients, Jason, have you seen on laxatives that comes with an anus in the wrong place? How many patients have you seen having had a cecostomy with perfect anatomy? That's the real frustrating one. Right? A lot.Open
StatementThe family doesn't really care how technically elegant is your analplasty. What they care about is whether that analplasty that you make is going to work and is the child going to be clean and in normal underwear.Open
QuotationI can tell you, the family doesn't really care how technically elegant is your analplasty. What they care about is whether that analplasty that you make is going to work. And is the child going to be clean and in normal underwear and just like all the other kids?Open
StatementThe higher the malformation, the worse the prognosis.Open
StatementA sacrum ratio of 0.7 or greater usually means normal or close to normal sphincters and good muscle tone, indicating that spine innervation of that area is probably good.Open
StatementPatients can come with associated spinal anomaly, most commonly tethered cord, but the worst is a myelomeningocele, and those patients have much more trouble with continence.Open
StatementIt's amazingly common to have a mislocated anus, either because the surgeon misses where the center is during laparoscopic pull-through or opens the PSARP incision first.Open
StatementA key pitfall is opening the PSARP incision first; instead, mark the sphincters first, then open the PSARP so you don't get confused when placing the anoplasty in the correct location.Open
QuotationA key pitfall is not do that. Mark the sphincters first, then open the PSARP because then you don't get confused at the end when you're trying to place the anoplasty in the correct location.Open
StatementIn higher malformations such as a bladder neck fistula in a boy, the sphincter complex isn't always where you think it's going to be and is sometimes more anterior than anticipated.Open
StatementAn alternative approach for borderline cases is to let the child take their car out for a ride first and see how it works—if it drives well, stay with that anatomy; if not, then consider the redo.Open
Jason's statements about Spina Bifida22 statements
Colorectal Quiz Episode 15: Bowel Management in Spinal Patients - Need for a UrologistPart 1
StatementSenna-induced perineal rash is thought to be a chemical burn rather than a true allergy, presenting with blistering.Open
Quotationit's almost like a chemical burn. The cause they're blistered usually.Open
QuotationWe treat it with silver sulfadiazine, and they've all gotten better with time.Open
StatementSenna rash is treated with silver sulfadiazine and resolves with time; some patients tolerate senna upon reintroduction.Open
StatementTiming senna doses in the early morning so that bowel movements occur during the day (when diapers are changed promptly) reduces the risk of senna rash.Open
Quotationwhat we've done is we timed the dose of Senna in these patients, usually in the early morning, so that they're pooping during the day. And their diapers changed rather quickly versus potentially being in a diaper over a long period of time at night.Open
StatementBisacodyl can be administered as an enema or suppository in infants.Open
QuotationIf there's one take-home message from this podcast, you just said itOpen
Quotationthat care coordination, collaboration with the urologist might be the most beneficial thing we could do for our patients.Open
Colorectal Quiz Episode 16: Bowel Management in Spinal Patients - Need for a Urologist Part 2
QuotationWhen you get that really short stumpy appendix, whether it be from splitting it, and the urologist, if I have a 7 centimeter appendix, the urologist takes 6.25 centimeters and I get 0.75.Open
StatementWhen a 7 cm appendix is shared between urology and colorectal surgery, the urologist typically takes 6.25 cm leaving only 0.75 cm for colorectal useOpen
StatementThe colorectal team benefits from using the appendix portion closer to the cecum which has a stronger blood supplyOpen
StatementA short appendiceal stump can be extended by suturing or using a laparoscopic non-cutting linear stapler along the cecal wall to add 2-3 cm of lengthOpen
StatementOne of the problems with Malone appendicostomy is leakageOpen
StatementThe longer the Malone channel, the less likely it is to leakOpen
QuotationThe longer the channel, the less likely that Malone's going to leak.Open
StatementExtending the Malone channel by 2-3 cm using suturing or stapling can be extremely helpful in preventing leakageOpen
StatementRectal irrigation using pressurized water systems made for patients with hand difficulties is an alternative to Malone and Mitrofanoff proceduresOpen
StatementColoplast makes a rectal irrigation device for self-administration of enemasOpen
StatementAt Cincinnati Children's, 99% of Malones are placed in the umbilicus and almost all Mitrofanoffs are in the right lower quadrant with a tunnel channel through the rectus to prevent leakageOpen
StatementThe primary determinant of orifice location is where the appendix reaches and its blood supplyOpen
StatementLaxity of the pelvic floor and anal canal is a huge issue in spinal patients, especially when doing retrograde enemasOpen
Jason's statements about Total Colonic Aganglionosis5 statements
The Colorectal Quiz Episode 10: Total Colonic Hirschsprung Disease Part 1
QuotationMy cutoff is around 6 months when I switch from suction rectal biopsy to full thickness biopsy.Open
StatementThe age cutoff for switching from suction rectal biopsy to full-thickness biopsy is around 6 monthsOpen
QuotationIf the patient is doing well and able to be managed with irrigations, would love to have my final diagnosis of Hirschprung's disease through the rectal biopsy before entering the abdomen.Open
StatementIf the patient is doing well and can be managed with irrigations, it is preferable to have final pathology diagnosis of Hirschsprung disease from rectal biopsy before entering the abdomenOpen
StatementStandard biopsy locations during operative mapping include rectosigmoid, proximal sigmoid around the left colon, splenic flexure/transverse colon, and right colon or hepatic flexure areaOpen
StatementMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementSome infants with Hirschsprung's disease do pass meconium.Open
QuotationMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementSome infants with Hirschsprung's disease do pass meconium.Open
QuotationMore than 95% of neonates pass meconium within the first 48 hours of life, and failure to pass meconium is typical of Hirschsprung's disease.Open
StatementIn total colonic Hirschsprung's disease, a foreshortened or question mark colon can be seen on contrast enema.Open
StatementThe classic finding on contrast enema is a transition zone in the rectosigmoid, but that transition zone can be located anywhere within the bowel.Open
StatementA rectosigmoid ratio of less than 1.0 is suggestive of Hirschsprung's disease, meaning the aganglionic bowel is contracted and narrow compared to the dilated ganglionated bowel more proximal.Open
StatementApproximately 10% of newborns with Hirschsprung's disease may lack the typical findings on a contrast enema.Open
StatementRectal biopsy is the true definitive diagnosis for Hirschsprung disease.Open
StatementTypical features on rectal biopsy include absence of ganglion cells, presence of hypertrophic nerves, abnormal pattern of cholinesterase staining, and an absence of calretinine staining.Open
StatementTo be considered an adequate biopsy, it must be taken from the rectum at least one centimeter above the dentate line and must include both mucosa and submucosal layers.Open
StatementSuction biopsy technique is typically used for patients less than six months of age.Open
StatementFull thickness biopsy technique should be considered for patients older than six months, or when a suction biopsy is inadequate.Open
QuotationThe three studies that should be considered for evaluating for Hirschsprung's disease include contrast enema, rectal biopsy, and possibly anorectal manometry.Open
QuotationThe second part of a diagnostic workup for Hirschsprung's disease, and most important, is the rectal biopsy. It is the true definitive diagnosis.Open
StatementThe classic finding on contrast enema is a transition zone in the rectosigmoid, but that transition zone can be located anywhere within the bowel.Open
StatementA rectosigmoid ratio of less than 1.0 is suggestive of Hirschsprung's disease, meaning the aganglionic bowel is contracted and narrow compared to the dilated ganglionated bowel more proximal.Open
StatementIn total colonic Hirschsprung's disease, a foreshortened or question mark colon can be seen on contrast enema.Open
StatementApproximately 10% of newborns with Hirschsprung's disease may lack the typical findings on a contrast enema.Open
StatementRectal biopsy is the true definitive diagnosis for Hirschsprung disease.Open
StatementTypical features on rectal biopsy include absence of ganglion cells, presence of hypertrophic nerves, abnormal pattern of cholinesterase staining, and an absence of calretinine staining.Open
StatementTo be considered an adequate biopsy, it must be taken from the rectum at least one centimeter above the dentate line and must include both mucosa and submucosal layers.Open
StatementSuction biopsy technique is typically used for patients less than six months of age.Open
StatementFull thickness biopsy technique should be considered for patients older than six months, or when a suction biopsy is inadequate.Open
QuotationThe three studies that should be considered for evaluating for Hirschsprung's disease include contrast enema, rectal biopsy, and possibly anorectal manometry.Open
QuotationThe second part of a diagnostic workup for Hirschsprung's disease, and most important, is the rectal biopsy. It is the true definitive diagnosis.Open
StatementIn Hirschsprung's disease, anorectal manometry shows a lack of the rectoanal inhibitory reflex (RAIR).Open
StatementThe rectoanal inhibitory reflex may be absent in other conditions as well, and some children have a false positive test.Open
StatementAny patient with an absent RAIR must undergo a rectal biopsy for confirmation of the diagnosis.Open
StatementThe rectoanal inhibitory reflex may be absent in other conditions as well, and some children have a false positive test.Open
StatementIn Hirschsprung's disease, anorectal manometry shows a lack of the rectoanal inhibitory reflex (RAIR).Open
StatementAny patient with an absent RAIR must undergo a rectal biopsy for confirmation of the diagnosis.Open
StatementThe three goals of surgical management are: identify the extent of the aganglionic segment, resect that segment, and restore the bowel to its continuity.Open
QuotationThere are three goals to the surgical management of Hirschsprung's disease. First, identify the extent of the aganglionic segment. Second, resect that segment. And third, restore the bowel to its continuity.Open
QuotationThere are three goals to the surgical management of Hirschsprung's disease. First, identify the extent of the aganglionic segment. Second, resect that segment. And third, restore the bowel to its continuity.Open
StatementThe three goals of surgical management are: identify the extent of the aganglionic segment, resect that segment, and restore the bowel to its continuity.Open
StatementThe Suave procedure theoretically causes less injury to pelvic structures, nerves, urethra and vagina.Open
StatementIn the Swenson procedure, you pull down the aganglionic bowel and perform a full thickness anastomosis one to two centimeters above the dentate line, leaving the most minimal amount of aganglionic bowel possible.Open
StatementIn the Swenson procedure, it is very important to be cautious about injuring the urethra as it's quite close, especially in boys.Open
StatementThe Suave procedure involves performing a mucosectomy from a transanal approach slightly above the dentate line and pulling through the normal bowel.Open
StatementIn the Suave procedure, the actual anastomosis is performed within a cuff of aganglionic rectum.Open
StatementThe Suave procedure theoretically causes less injury to pelvic structures, nerves, urethra and vagina.Open
StatementA con of the Suave procedure is that the aganglionic cuff can become stiff enough to cause an obstruction or outlet obstruction.Open
StatementIn the Swenson procedure, you pull down the aganglionic bowel and perform a full thickness anastomosis one to two centimeters above the dentate line, leaving the most minimal amount of aganglionic bowel possible.Open
StatementIn the Swenson procedure, it is very important to be cautious about injuring the urethra as it's quite close, especially in boys.Open
StatementThe Suave procedure involves performing a mucosectomy from a transanal approach slightly above the dentate line and pulling through the normal bowel.Open
StatementIn the Suave procedure, the actual anastomosis is performed within a cuff of aganglionic rectum.Open
StatementA con of the Suave procedure is that the aganglionic cuff can become stiff enough to cause an obstruction or outlet obstruction.Open
StatementA child with enterocolitis presents with abdominal distension, vomiting, fever, and change in bowel habits that could be either diarrhea or not passing stool at all.Open
StatementTreatment of enterocolitis includes fluid resuscitation, digital rectal exam, and colonic irrigations.Open
QuotationWhen we treat these patients with enterocolitis, it is important to provide fluid resuscitation, digital rectal exam, and colonic irrigations.Open
StatementFor enterocolitis, antibiotics including metronidazole or broad-spectrum antibiotics are added depending on the severity of presentation.Open
QuotationHirschsprung's-associated enterocolitis is poorly understood and likely is an inflammatory condition secondary to bacterial overgrowth.Open
StatementHirschsprung's-associated enterocolitis is likely an inflammatory condition secondary to bacterial overgrowth.Open
QuotationWhen we treat these patients with enterocolitis, it is important to provide fluid resuscitation, digital rectal exam, and colonic irrigations.Open
QuotationHirschsprung's-associated enterocolitis is poorly understood and likely is an inflammatory condition secondary to bacterial overgrowth.Open
StatementHirschsprung's-associated enterocolitis is likely an inflammatory condition secondary to bacterial overgrowth.Open
StatementA child with enterocolitis presents with abdominal distension, vomiting, fever, and change in bowel habits that could be either diarrhea or not passing stool at all.Open
StatementTreatment of enterocolitis includes fluid resuscitation, digital rectal exam, and colonic irrigations.Open
StatementFor enterocolitis, antibiotics including metronidazole or broad-spectrum antibiotics are added depending on the severity of presentation.Open
StatementFor patients with anatomic problems after pull-through, you typically have to revise the pull through.Open
StatementAnatomic problems after pull-through can include a twist in the pull through, an obstructing cuff, a non-functioning Duhamel pouch, or a transition zone or continued aganglionic segment.Open
StatementFor patients not doing well after pull-through, if there is a stricture at the anastomosis, it needs to be addressed either through dilations or revising the pull through procedure.Open
StatementFor patients not doing well after pull-through, if there is a stricture at the anastomosis, it needs to be addressed either through dilations or revising the pull through procedure.Open
StatementAnatomic problems after pull-through can include a twist in the pull through, an obstructing cuff, a non-functioning Duhamel pouch, or a transition zone or continued aganglionic segment.Open
StatementFor patients without anatomic problems after pull-through, treatment can include bowel management, Botox injection to relieve sphincter tone, or motility studies.Open
StatementFor patients without anatomic problems after pull-through, treatment can include bowel management, Botox injection to relieve sphincter tone, or motility studies.Open
StatementFor patients with anatomic problems after pull-through, you typically have to revise the pull through.Open
The Colorectal Quiz Episode 1: ARM - Low Bulbar Fistula
StatementCross-table lateral radiograph is obtained at approximately 24 hours of life to visualize the rectal gas column positionOpen
StatementCross-table lateral is performed with the baby prone and a bump under the buttocks to position the buttock as the highest point where air will riseOpen
StatementA marker should be placed at the expected anal location on cross-table lateral to enable distance measurementsOpen
StatementWell-formed buttocks and visible sphincter mechanism location on physical exam contribute to good prognosisOpen
QuotationWe both agree that probably in real life, we would have done a primary posterior sagittal approach on this patient, and we would have found the rectum, and we could have made that rectum reach the perineum and done our anoplasty. How do we handle this? Because I didn't know that there was a fistula there. This is troublesome.Open
StatementLow bulbar fistulas are located very close to the rectum, requiring careful plane dissectionOpen
StatementBulbar fistula nomenclature refers to anatomic location at the elbow of the urethraOpen
Hirschsprung Disease in Brief
StatementHirschsprung disease is a congenital anomaly of the GI tract that results in a functional bowel obstruction.Open
StatementMore than 95% of neonates pass meconium within the first 48 hours of life.Open
StatementFailure to pass meconium within the first 48 hours of life is typical of Hirschsprung's disease.Open
QuotationMore than 95% of neonates pass meconium within the first 48 hours of life. And failure to pass meconium is typical of Hirschsprung's disease.Open
StatementThe RET gene is a predisposing genetic condition associated with Hirschsprung disease.Open
StatementAbout 10% of children with Hirschsprung disease will have a positive family history.Open
StatementHirschsprung disease is associated with Wordenberg syndrome and congenital central hyperventilation (Andine's curse).Open
Summaries Jason gave as host
· 41 summaries
Recaps of other experts' statements, not Jason's own clinical position.
Summaries Jason gave as host · Abdominal Wall Defects2 summaries
Gastroschisis and sutureless abdominal wall closure
Host summaryJason Frischer summarizes what Dr. Jason Fraser said: Initial small studies showed that some sutureless patients had a high umbilical hernia repair rate, or at least a high umbilical hernia rate.Open
Update Course 2022 - UPDATES IN GASTROSCHISIS FEEDING PROTOCOLS - Jason Fraser, Beth Rymeski, and Steven Lee
Host summaryJason Frischer summarizing the discussion: Some institutions ignore bilious emesis or bilious NG residuals completely during gastroschisis feeding advancement.Open
Summaries Jason gave as host · Anorectal Malformation4 summaries
Host summaryJason Frischer summarizes what Dr. Marc Levitt said: A lot of surgeons agree that oftentimes your first shot might be your only shot to give this patient a good outcome and the right anatomy.Open
Colorectal Quiz Episode 29: Female ARM-Post Op Management
Host summaryJason Frischer summarizing the discussion: In the dilation trial, 4 patients required redo operations for stricture: 2 in the dilation arm (who didn't actually dilate) and 2 in the non-dilation arm. Additional patients required Heineke-Mikulicz procedures (3 in one group, 47 total procedures mentioned).Open
Colorectal Quiz: Episode 40
Host summaryJason Frischer summarizing the discussion: Fred Reichman used to say, you are judged by what you are willing to stop for. And as surgeons, you have to be willing to say, hold on, I'm not exactly sure what I'm dealing with here. I'm going to stop. I'm going to get more information. I'm going to go get some help. I'm not going to plow through.Open
Host summaryJason Frischer summarizing the discussion: Fred Reichman used to say 'you are judged by what you are willing to stop for'—surgeons must be willing to stop when uncertain, get more information or help, rather than plowing through.Open
Host summaryJason Frischer summarizing the discussion: Fred Reichman used to say, you are judged by what you are willing to stop for. And as surgeons, you have to be willing to say, hold on, I'm not exactly sure what I'm dealing with here. I'm going to stop. I'm going to get more information. I'm going to go get some help. I'm not going to plow through.Open
Host summaryJason Frischer summarizing the discussion: Fred Reichman used to say 'you are judged by what you are willing to stop for'—surgeons must be willing to stop when uncertain, get more information or help, rather than plowing through.Open
Summaries Jason gave as host · Colorectal / ARM & Hirschsprung9 summaries
Host summaryJason Frischer summarizing the discussion: Transabdominal approaches for rectal prolapse (rectopexy with or without resection) have approximately 5% recurrence rate, compared to 15-20% recurrence for transanal approaches (transanal pull-through or Altmeier procedure).Open
Host summaryJason Frischer summarizing the discussion: Resection and rectopexy for rectal prolapse may be preferable when constipation control is difficult, but has higher complication rate compared to rectopexy alone.Open
Host summaryJason Frischer summarizing the discussion: Laparoscopic rectopexy for rectal prolapse can be performed as same-day surgery or with next-day discharge in current practice.Open
Hirschsprung Disease: Update Course 2015
Host summaryJason Frischer summarizing the discussion: Jack Langer published an algorithm for working up patients with problems after Hirschsprung disease.Open
Colorectal Quiz Episode 16: Bowel Management in Spinal Patients - Need for a Urologist Part 2
Host summaryJason Frischer summarizing the discussion: Fecal impaction can push on the bladder and change the angle of the ureter entering the bladder, causing refluxOpen
Host summaryJason Frischer summarizing the discussion: The last steps of combined procedures should be maturing the Mitrofanoff, maturing the Malone, then closing the abdomenOpen
Colorectal Quiz Episode 29: Female ARM-Post Op Management
Host summaryJason Frischer summarizing the discussion: In the dilation trial, 4 patients required redo operations for stricture: 2 in the dilation arm (who didn't actually dilate) and 2 in the non-dilation arm. Additional patients required Heineke-Mikulicz procedures (3 in one group, 47 total procedures mentioned).Open
Colorectal Quiz: Episode 40
Host summaryJason Frischer summarizing the discussion: Fred Reichman used to say 'you are judged by what you are willing to stop for'—surgeons must be willing to stop when uncertain, get more information or help, rather than plowing through.Open
Host summaryJason Frischer summarizing the discussion: Fred Reichman used to say, you are judged by what you are willing to stop for. And as surgeons, you have to be willing to say, hold on, I'm not exactly sure what I'm dealing with here. I'm going to stop. I'm going to get more information. I'm going to go get some help. I'm not going to plow through.Open
Summaries Jason gave as host · Congenital Lung Lesions (CPAM)1 summary
Host summaryJason Frischer summarizing the discussion: In asymptomatic newborns with prenatally diagnosed lung lesions, most US practitioners obtain chest X-ray initially in NICUOpen
Summaries Jason gave as host · Congenital Pulmonary Airway Malformation1 summary
Host summaryJason Frischer summarizing the discussion: In asymptomatic newborns with prenatally diagnosed lung lesions, most US practitioners obtain chest X-ray initially in NICUOpen
Summaries Jason gave as host · Constipation2 summaries
Colorectal Quiz Episode 16: Bowel Management in Spinal Patients - Need for a Urologist Part 2
Host summaryJason Frischer summarizing the discussion: Fecal impaction can push on the bladder and change the angle of the ureter entering the bladder, causing refluxOpen
Host summaryJason Frischer summarizing the discussion: The last steps of combined procedures should be maturing the Mitrofanoff, maturing the Malone, then closing the abdomenOpen
Summaries Jason gave as host · Enterocolitis4 summaries
Host summaryJason Frischer summarizing the discussion: Transabdominal approaches for rectal prolapse (rectopexy with or without resection) have approximately 5% recurrence rate, compared to 15-20% recurrence for transanal approaches (transanal pull-through or Altmeier procedure).Open
Host summaryJason Frischer summarizing the discussion: Resection and rectopexy for rectal prolapse may be preferable when constipation control is difficult, but has higher complication rate compared to rectopexy alone.Open
Host summaryJason Frischer summarizing the discussion: Laparoscopic rectopexy for rectal prolapse can be performed as same-day surgery or with next-day discharge in current practice.Open
Hirschsprung Disease: Update Course 2015
Host summaryJason Frischer summarizing the discussion: Jack Langer published an algorithm for working up patients with problems after Hirschsprung disease.Open
Summaries Jason gave as host · Etiologies (Gastroschisis/NEC/Atresia/Volvulus)2 summaries
Gastroschisis and sutureless abdominal wall closure
Host summaryJason Frischer summarizes what Dr. Jason Fraser said: Initial small studies showed that some sutureless patients had a high umbilical hernia repair rate, or at least a high umbilical hernia rate.Open
Update Course 2022 - UPDATES IN GASTROSCHISIS FEEDING PROTOCOLS - Jason Fraser, Beth Rymeski, and Steven Lee
Host summaryJason Frischer summarizing the discussion: Some institutions ignore bilious emesis or bilious NG residuals completely during gastroschisis feeding advancement.Open
Summaries Jason gave as host · Gastroschisis2 summaries
Gastroschisis and sutureless abdominal wall closure
Host summaryJason Frischer summarizes what Dr. Jason Fraser said: Initial small studies showed that some sutureless patients had a high umbilical hernia repair rate, or at least a high umbilical hernia rate.Open
Update Course 2022 - UPDATES IN GASTROSCHISIS FEEDING PROTOCOLS - Jason Fraser, Beth Rymeski, and Steven Lee
Host summaryJason Frischer summarizing the discussion: Some institutions ignore bilious emesis or bilious NG residuals completely during gastroschisis feeding advancement.Open
Summaries Jason gave as host · Hirschsprung disease6 summaries
Host summaryJason Frischer summarizing the discussion: Transabdominal approaches for rectal prolapse (rectopexy with or without resection) have approximately 5% recurrence rate, compared to 15-20% recurrence for transanal approaches (transanal pull-through or Altmeier procedure).Open
Host summaryJason Frischer summarizing the discussion: Resection and rectopexy for rectal prolapse may be preferable when constipation control is difficult, but has higher complication rate compared to rectopexy alone.Open
Host summaryJason Frischer summarizing the discussion: Laparoscopic rectopexy for rectal prolapse can be performed as same-day surgery or with next-day discharge in current practice.Open
Hirschsprung Disease: Update Course 2015
Host summaryJason Frischer summarizing the discussion: Jack Langer published an algorithm for working up patients with problems after Hirschsprung disease.Open
Colorectal Quiz: Episode 40
Host summaryJason Frischer summarizing the discussion: Fred Reichman used to say 'you are judged by what you are willing to stop for'—surgeons must be willing to stop when uncertain, get more information or help, rather than plowing through.Open
Host summaryJason Frischer summarizing the discussion: Fred Reichman used to say, you are judged by what you are willing to stop for. And as surgeons, you have to be willing to say, hold on, I'm not exactly sure what I'm dealing with here. I'm going to stop. I'm going to get more information. I'm going to go get some help. I'm not going to plow through.Open
Summaries Jason gave as host · Intestinal Rehab2 summaries
Gastroschisis and sutureless abdominal wall closure
Host summaryJason Frischer summarizes what Dr. Jason Fraser said: Initial small studies showed that some sutureless patients had a high umbilical hernia repair rate, or at least a high umbilical hernia rate.Open
Update Course 2022 - UPDATES IN GASTROSCHISIS FEEDING PROTOCOLS - Jason Fraser, Beth Rymeski, and Steven Lee
Host summaryJason Frischer summarizing the discussion: Some institutions ignore bilious emesis or bilious NG residuals completely during gastroschisis feeding advancement.Open
Summaries Jason gave as host · Perineal Fistula1 summary
Colorectal Quiz Episode 29: Female ARM-Post Op Management
Host summaryJason Frischer summarizing the discussion: In the dilation trial, 4 patients required redo operations for stricture: 2 in the dilation arm (who didn't actually dilate) and 2 in the non-dilation arm. Additional patients required Heineke-Mikulicz procedures (3 in one group, 47 total procedures mentioned).Open
Summaries Jason gave as host · Rectal Prolapse1 summary
Host summaryJason Frischer summarizes what Dr. Marc Levitt said: A lot of surgeons agree that oftentimes your first shot might be your only shot to give this patient a good outcome and the right anatomy.Open
Summaries Jason gave as host · Spina Bifida2 summaries
Colorectal Quiz Episode 16: Bowel Management in Spinal Patients - Need for a Urologist Part 2
Host summaryJason Frischer summarizing the discussion: Fecal impaction can push on the bladder and change the angle of the ureter entering the bladder, causing refluxOpen
Host summaryJason Frischer summarizing the discussion: The last steps of combined procedures should be maturing the Mitrofanoff, maturing the Malone, then closing the abdomenOpen