Utility of Fluorescence In Situ Hybridization as a Fetal Surgery Eligibility Criterion for....
Many centers require genetic testing to rule out chromosome abnormalities before fetal surgery, even when ultrasounds and blood tests already look reassuring
Host summaryLizzy Lee summarizing a resource — not the host's own clinical position0:09
A study reviewed nearly 1000 pregnancies evaluated for fetal surgery
Host summaryLizzy Lee summarizing a resource — not the host's own clinical position0:23
When imaging and cell-free DNA screening showed low risk for aneuploidy, the FISH test matched those results 100% of the time
Host summaryLizzy Lee summarizing a resource — not the host's own clinical position0:23
For low-risk pregnancies, FISH did not provide any new information that changed surgery candidacy
Host summaryLizzy Lee summarizing a resource — not the host's own clinical position0:36
In carefully selected low-risk cases, non-invasive screening may be enough, potentially avoiding the FISH procedure
Host summaryLizzy Lee summarizing a resource — not the host's own clinical position0:42
Neonatal Lung Lesions with Dr. Steven Rothenberg
Serial prenatal ultrasounds are the best way to follow cystic lung lesions; they are noninvasive, quick, and performed every couple of weeks.
Fetal MRI for lung lesions provides little additional benefit and does not change the management plan.
Expert opinionSteven Rothenberg4:11
Anywhere from 6 to 40% of prenatally detected lung lesions will regress over time, and in some cases appear to completely disappear.
Fetal intervention (open surgery) for lung lesions is extremely rare; CHOP performs less than one open fetal surgery every couple of years.
Fetal thoracentesis or thoracoamniotic shunt is done only if the fetus shows significant distress or evidence of hydrops, which significantly increases mortality.
Steroids are given if larger cysts cause mediastinal shift, or to mature the lung if early delivery is anticipated.
A cyst volume ratio (CVR) greater than 2 has an extremely bad prognosis and is more likely to require fetal intervention.
Congenital lung lesions (CAMs, sequestrations, bronchogenic cysts) represent a spectrum; hybrid lesions are common on pathology.
Sequestrations are classified by the presence of a systemic artery (usually from the aorta); intralobar sequestrations share pleura with the lobe, extralobar have their own pleural lining.
If a baby is born doing well with no respiratory distress and a normal or mildly abnormal chest X-ray, the family can go home; CT scan is obtained at 4–6 weeks.
A chest X-ray or ultrasound is not adequate to prove a prenatally detected lung lesion has completely resolved; CT scan is required.
Some children with normal postnatal chest X-ray or ultrasound later present with pneumonia (9 months to 6–7 years) and are found to have an infected CPAM.
Depending on the series, 20–40% of untreated congenital lung lesions will develop a significant infection at some point.
The incidence of malignancy in untreated congenital lung lesions is over 1% in Rothenberg's series, which he considers significant.
Rothenberg prefers to operate by 3 months of age to avoid infection, because surgery is technically easier with smaller vessels and fresh anatomy, and to allow compensatory lung growth.
Expert opinionSteven Rothenberg17:49
In Rothenberg's series, hospital stay, chest tube duration, recovery, and operative time were shorter in patients under 5 kg compared to those under 10 kg.
Most infants undergoing early lobectomy are discharged within 48 hours; by one month post-op, chest X-ray shows no evidence of surgery.
Even in asymptomatic children, waiting until around one year of age often reveals significantly enlarged lymph nodes and inflammation in the fissure, suggesting low-grade infection.
The key to success in small infants is proper setup and port placement; with the right approach, there is plenty of room to work.
Blood is typed and crossed for all lobectomies; it is one of the few pediatric cases where this is routine, because bleeding can be significant.
Most asymptomatic children on room air tolerate single-lung ventilation without problem.
Single-lung ventilation is achieved by main-stem intubation of the contralateral bronchus; bronchial blockers are difficult to place and add time, so are avoided.
After lung collapse, infants initially desaturate (low 90s to high 80s) due to shunting; saturations improve once shunting to the collapsed lung stops.
Anesthesiologists should use lower peak ventilatory pressures and increase rate (not pressure) to improve ventilation, avoiding high-pressure bagging that re-inflates the operative lung.
End-tidal CO₂ in the mid-40s is tolerable and does not cause significant acidosis during thoracoscopic lobectomy.