Single Ventricle / HLHS
Also covered as: cloaca · anorectal malformation · tethered cord · pulmonary hypoplasia · scoliosis · hypoplastic left heart syndrome · urogenital sinus · pulmonary hypertension
Educational content from recorded physician discussions — not medical advice. Always talk to your child's care team about your child's situation.
Content of this collection
Fundamentals
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How Does the Blood Go Round in Single Ventricles and Fontans? New Horizons in...
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Physicians from theCincinnati Children’s Heart Institutediscuss the long-term care of single ventricle patients from infancy to adulthood, including new insights on Fontan management and quality of life.During this session, Dr. Andrew Redin
video24:58 · Jan 2019
Diagnosis & Workup
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Case Review Dynamic Assessment of the Fontan Part II: New Horizons in Medical...
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Physicians from theCincinnati Children’s Heart Institutediscuss the long-term care of single ventricle patients from infancy to adulthood, including new insights on Fontan management and quality of life.During this session, Dr. Veldtman foc
video14:38 · Jan 2019
Case Review Dynamic Assessment of the Fontan Part I: New Horizons in Medical...
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Physicians from theCincinnati Children’s Heart Institutediscuss the long-term care of single ventricle patients from infancy to adulthood, including new insights on Fontan management and quality of life.During this session, Dr. Bryan Goldst
video22:46 · Jan 2019
Advanced Imaging of the Fontan, What is Driving Fontan Failure: New Horizons...
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Physicians from theCincinnati Children’s Heart Institutediscuss the long-term care of single ventricle patients from infancy to adulthood, including new insights on Fontan management and quality of life.During this session, Dr. Andrew Crean
video24:44 · Jan 2019
Medical Management
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How do we manage thrombogenicity and thrombosis in the Fontan? New Horizons...
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Physicians from theCincinnati Children’s Heart Institutediscuss the long-term care of single ventricle patients from infancy to adulthood, including new insights on Fontan management and quality of life.During this session, Dr. Joseph Palum
video16:51 · Jan 2019
The Role of Trans-Catheter Arrhythmia Management - Patient Based Decision...
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Physicians from theCincinnati Children’s Heart Institutediscuss the long-term care of single ventricle patients from infancy to adulthood, including new insights on Fontan management and quality of life.During this session, Dr. Richard Czos
video20:55 · Jan 2019
Surgical Management
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Update on Surgical Practice and Current State on Fontan Conversion Surgery:...
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Physicians from theCincinnati Children’s Heart Institutediscuss the long-term care of single ventricle patients from infancy to adulthood, including new insights on Fontan management and quality of life.During this session,Dr. James Tweddel
video25:00 · Jan 2019
Transplantation and Ventricular Assist Devices: New Horizons in Medical and...
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Physicians from theCincinnati Children’s Heart Institutediscuss the long-term care of single ventricle patients from infancy to adulthood, including new insights on Fontan management and quality of life.During this session, Dr. Angela Lorts
video23:13 · Jan 2019
Trans-Catheter Interventions: New Horizons in Medical and Surgical Fontan...
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Physicians from theCincinnati Children’s Heart Institutediscuss the long-term care of single ventricle patients from infancy to adulthood, including new insights on Fontan management and quality of life.During this session, Dr. Bryan Goldst
video17:26 · Jan 2019
Ovarian Torsion with Dr. Jennifer Dietrich
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Dr Jennifer E. Dietrich, discusses ovarian torsion with Dr Todd A. Ponsky Edited by Nicholas E. Bruns, MD Ian C. Glenn, MD
podcast47:22 · Jan 2019
Cloaca Management with Dr. Marc Levitt & Dr. Aaron Garrison
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Marc Levitt, MD discusses Cloaca with Todd Ponsky, MD and Aaron Garrison, MDEdited by Ian C Glenn, MD and Sophia Abdulhai, MDDr. Levitt is surgical director of the Center for Colorectal and Pelvic Reconstruction as well as program director
podcast43:47 · Jan 2019
Neonatal Lung Lesions with Dr. Steven Rothenberg
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Dr. Steven Rothenberg discusses Newborn Lung Lesions with Dr Todd Ponsky. Edited by Ian C. Glenn, MD Nicholas E. Bruns, MD
podcast66:58 · Jan 2019
Chest Wall Deformities with Dr. Robert Kelly
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Dr. Robert Kelly discuses chest wall deformities with Dr. Todd Ponsky. Edited by Ian C Glenn, MD and Nicholas Bruns, MD
podcast46:50 · Jan 2019
Neonatal Lung Lesions with Dr. Steven Rothenberg
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Dr. Steven Rothenberg discusses Newborn Lung Lesions with Dr Todd Ponsky. Edited by Ian C. Glenn, MD & Nicholas E. Bruns, MDPrenatal evaluationPatients with prenatal diagnosis of cystic lung lesions are referred for prenatal evaluation and
podcast66:58 · Dec 2020
Ovarian Torsion with Dr. Jennifer Dietrich
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Dr Jennifer E. Dietrich, discusses ovarian torsion with Dr Todd A. Ponsky Edited by Nicholas E. Bruns, MD & Ian C. Glenn, MDEvaluation of the adolescent female with pelvic painObtain sexual history and urine b-hCGMenstrual history (hemorrha
podcast47:22 · Dec 2020
Chest Wall Deformities with Dr. Robert Kelly
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Dr. Robert Kelly discuses chest wall deformities with Dr. Todd Ponsky. Edited by Ian C Glenn, MD and Nicholas Bruns, MDPectus excavatumHistoryApproximately 2/3 of patients presenting with symptoms, which include dyspnea on exertion, easy fa
podcast46:50 · Dec 2020
Cloaca Management with Dr. Marc Levitt & Dr. Aaron Garrison
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Marc Levitt, MD discusses Cloaca with Todd Ponsky, MD and Aaron Garrison, MDEdited by Ian C Glenn, MD and Sophia Abdulhai, MDDr. Levitt is surgical director of the Center for Colorectal and Pelvic Reconstruction as well as program director
podcast43:47 · Dec 2020
Complications
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Complications of Anorectal Malformations with Dr. Marc Levitt
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Dr Marc Levitt discusses ARM Complications with Dr Todd Ponsky Edited by Nicholas Bruns, MD and Ian C. Glenn, MD In this episode, Dr. Marc Levitt from Nationwide Children’s Hospital discusses complications of anorectal malformations. This e
podcast48:09 · Jan 2019
Management of Retained Central Venous Catheters
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Ian Glenn and Todd Ponsky discuss the management of retained central venous canulas.
video3:41 · Apr 2019
Complications of Anorectal Malformations with Dr. Marc Levitt
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Dr Marc Levitt discusses ARM Complications with Dr Todd Ponsky
Edited by Nicholas Bruns, MD and Ian C. Glenn, MD
In this episode, Dr. Marc Levitt from Nationwide Children’s Hospital discusses complications of anorectal malformations. This e
podcast48:09 · Dec 2020
Evidence & Research
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Posterior Tracheopexy For Severe Tracheomalacia
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Dr. Ian Glenn and Dr. Todd Ponsky give a two minute review of "posterior tracheopexy for severe tracheomalacia," and article published in the Journal of Pediatric Surgery. Dr. Hester Shieh and colleagues performed posterior tracheopexy on p
video2:17 · Sep 2018
Posterior Tracheopexy For Severe Tracheomalacia
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Dr. Ian Glenn and Dr. Todd Ponskygive a two minute review of "posterior tracheopexy for severe tracheomalacia," and article published in the Journal of Pediatric Surgery.Dr. Hester Shieh and colleagues performed posterior tracheopexy on pat
video2:18 · Sep 2018
Esophagogastric Dissociation for GERD in Severe Neurodisability
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Dr. Ian Glenn and Dr. Todd Ponsky discuss an article comparing esophagogatric dissociation and laparoscopic Nissen fundoplication in patients with severe gastroesophageal reflux disease (GERD) and severe neurodisability
video2:49 · Oct 2018
Esophagogastric Dissociation for GERD in Severe Neurodisability
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Dr. Ian Glenn and Dr. Todd Ponsky discuss an article comparing esophagogatric dissociation and laparoscopic Nissen fundoplication in patients with severe gastroesophageal reflux disease (GERD) and severe neurodisability
video2:49 · Jan 2019
Do we need Bowel Prep
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Ian Glenn gives a review of the literature to answer the question of whether or not we need bowel prep in children.
video1:15 · Apr 2019
Outcomes of Fontan Patients Undergoing Combined Heart - Liver Transplantation in Pediatric Hospitals Across the U.S.
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Grant Chappell, Amir Mehdizadeh-Shrifi, Darren Turner, Alexander Bondoc, Suzanne Evans, Alexander G Miethke, Gregory Tiao, Meghan M Chlebowski, Alexander R Opotowsky, David Lehenbauer, Marco Ricci, Awais Ashfaq, David L S MoralesBackground:
video0:59 · Dec 2025
Pancreas, Muscle, and Subcutaneous Fat Atrophy in Patients Undergoing Radiation for Neuroblastoma
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Pradipta Debnath, Marissa Ray, Luke Pater, Alexandra O Glenn, Stephen Hartman, Elanchezhian Somasundaram, Todd Jenkins, Juan P Gurria, Katherine Somers, Andrew T Trout, Meera KotagalBackground/objectives: Radiation therapy (RT) is part of s
video1:10 · Apr 2026
Case-Based Learning
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Intussusception - Soft Tissue Abscess - Pilonidal Cyst - Bleeding Meckel's...
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Dr. Nicholas Bruns gives a presentation on intussusception, soft tissue abscess, pilonidal cyst, bleeding Meckel's Diverticulum. His presentation generates discussion onreduced ileocolic intussusception and an appendectomy, age cutoff for a
video19:53 · Nov 2018
Pregnancy in a Fontan Patient: New Horizons in Medical and Surgical Fontan...
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Physicians from theCincinnati Children’s Heart Institutediscuss the long-term care of single ventricle patients from infancy to adulthood, including new insights on Fontan management and quality of life.During this session, Drs Anisa Chaudr
video18:27 · Jan 2019
Pilonidal Cyst Case Presentation: Update Course 2015
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During the 3rd Annual Stay Current in Pediatric Surgery Update Course in 2015, Dr. Ian Glenn leads this case based discussionon pilonidal cysts. Topics discussed include definitive treatment for pilonidal cyst disease, factors altering mana
video5:08 · Jan 2019
In-Depth Reviews
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Congenital Diaphragmatic Hernia with Dr. Charlie Stolar
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Dr Charlie Stolar discusses key points of CDH with Dr. Todd Ponsky. EDITED BY NICHOLAS BRUNS, MD and IAN GLENN, MD.
podcast82:05 · Jan 2019
Abdominal Wall Defects with Dr. Jacob Langer
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Dr Jacob Langer discusses abdominal wall defects with Dr. Todd Ponsky.Edited by Ian C. Glenn, MD and Sophia Abdulhai, MDAn interactive discussion about gastroschisis and omphalocele between Todd Ponsky, MD and Jacob "Jack" Langer, MD. Dr. L
podcast52:45 · Jan 2019
Congenital Diaphragmatic Hernia with Dr. Charlie Stolar
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Dr Charlie Stolar discusses key points of CDH with Dr. Todd Ponsky. EDITED BY NICHOLAS BRUNS, MD and IAN GLENN, MD.In this episode, Dr. Charles Stolar from Columbia University College of Physicians and Surgeons and California Pediatric Sur
podcast82:05 · Dec 2020
Abdominal Wall Defects with Dr. Jacob Langer
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Dr Jacob Langer discusses abdominal wall defects with Dr. Todd Ponsky.Edited by Ian C. Glenn, MD and Sophia Abdulhai, MDAn interactive discussion about gastroschisis and omphalocele between Todd Ponsky, MD and Jacob "Jack" Langer, MD. Dr. L
podcast52:45 · Dec 2020
Long-Term Care
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Psychosocial Outcomes: New Horizons in Medical and Surgical Fontan Management...
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Physicians from theCincinnati Children’s Heart Institutediscuss the long-term care of single ventricle patients from infancy to adulthood, including new insights on Fontan management and quality of life.During this session,Dr. Stacey Morris
video22:39 · Jan 2019
Summaries and takeaways+ Show
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Key points, with the moment each was said+ Show
Featured picks for families are being prepared — the summaries above are written for you.
Takeaways+ Show
Single ventricle physiology culminating in Fontan palliation creates a unique circulation characterized by chronic venous hypertension, absent subpulmonary ventricle, and profoundly altered hemodynamics . The Fontan circuit represents severe chronic right heart failure with sequelae including hepatic congestion, lymphatic dysfunction, restrictive lung disease, and progressive single ventricle dysfunction . Pulmonary vascular resistance in Fontan patients is typically both fixed and elevated, limiting cardiac output augmentation during exercise [e895-c5, e895-c12]. Diastolic dysfunction is nearly universal, with approximately 75% demonstrating abnormalities of early relaxation or elevated filling pressure on echo, and 35% showing occult diastolic dysfunction unmasked by volume challenge [e895-c14, e895-c19]. The circulation is profoundly prothrombotic—comparable to paroxysmal nocturnal hemoglobinuria—with cumulative thrombotic event risk reaching 22% and rising inexorably over time [e886-c5, e886-c6, e886-c7]. Arrhythmias, particularly macro-reentrant atrial tachycardia, were ubiquitous in early atriopulmonary Fontans and remain a significant predictor of adverse outcomes even in modern cohorts [e890-c1, e890-c14]. Fontan-associated liver disease progresses silently, with subclinical hepatocellular damage occurring when hepatic venous pressures exceed 25 mmHg . Protein-losing enteropathy and plastic bronchitis—manifestations of lymphatic pathology—carry 50% five-year freedom from death or transplant but resolve post-transplant in survivors [e891-c4, e891-c6, e891-c14, e891-c15]. Transplant outcomes have improved, with survival approaching 80% at one year and 75% at five years, though Fontan patients face higher waitlist mortality and early graft failure risk than dilated cardiomyopathy patients [e891-c8, e891-c11]. Mechanical support with continuous-flow VADs works well in appropriately selected patients ≥25 kg, offering bridge to transplant when medical management fails [e891-c19, e891-c21]. The key to optimizing long-term outcomes lies in dynamic assessment—exercise testing with hemodynamic monitoring reveals occult abnormalities invisible at rest—and aggressive management of modifiable risk factors including arrhythmia, thrombosis, and diastolic dysfunction [e894-c12, e894-c24].
- Fontan circulation is profoundly prothrombotic with 22% cumulative thrombotic risk; warfarin with excellent time-in-range (>80%) is superior to aspirin, achieving near-zero event rates.
- Diastolic dysfunction is the primary hemodynamic limitation: 75% show abnormal relaxation on echo, 35% have occult dysfunction on volume challenge, worsening with ventricular morphology and Fontan duration.
- Atrial arrhythmias predict sudden death and worse outcomes; catheter ablation achieves 40-50% freedom from recurrence versus near-zero for antiarrhythmics alone, with earlier intervention yielding simpler circuits.
- Protein-losing enteropathy and plastic bronchitis reflect lymphatic pathology with 50% five-year survival but resolve post-transplant; innominate vein decompression may offer palliation in select cases.
- Dynamic exercise assessment is essential even in well-functioning Fontans to detect occult obstruction, diastolic dysfunction, or elevated PVR invisible at rest; static hemodynamics underestimate disease burden.
For patients & families
Single ventricle heart defects and hypoplastic left heart syndrome (HLHS) are conditions where a baby is born with only one working pumping chamber instead of two. Doctors describe this as a problem affecting both lungs from birth, not just the heart. The condition creates challenges with blood flow and oxygen delivery that require careful medical management. When babies with these conditions are born, the medical team focuses on supporting breathing and circulation without rushing to surgery. Most babies (80-85%) survive to become teenagers with proper care. The treatment journey typically involves multiple surgeries over the first few years of life, ultimately creating what doctors call a "Fontan circulation" — a special arrangement where blood flows passively to the lungs without a pumping chamber. As children with single ventricle conditions grow, they face ongoing health considerations. The altered blood flow can affect the liver, intestines, and other organs over time. Families work closely with heart specialists, surgeons, and other doctors who monitor growth, nutrition, development, and organ function. Many children do well in school and activities, though some may need extra support for learning or attention challenges. Regular follow-up appointments continue throughout life to watch for complications and adjust care as needed.
Single ventricle heart defects and hypoplastic left heart syndrome (HLHS) are conditions where a baby is born with only one working pumping chamber instead of two. Doctors describe this as a problem affecting both lungs from birth, not just the heart. The condition creates challenges with blood flow and oxygen delivery that require careful medical management. When babies with these conditions are born, the medical team focuses on supporting breathing and circulation without rushing to surgery. Most babies (80-85%) survive to become teenagers with proper care. The treatment journey typically involves multiple surgeries over the first few years of life, ultimately creating what doctors call a "Fontan circulation" — a special arrangement where blood flows passively to the lungs without a pumping chamber. As children with single ventricle conditions grow, they face ongoing health considerations. The altered blood flow can affect the liver, intestines, and other organs over time. Families work closely with heart specialists, surgeons, and other doctors who monitor growth, nutrition, development, and organ function. Many children do well in school and activities, though some may need extra support for learning or attention challenges. Regular follow-up appointments continue throughout life to watch for complications and adjust care as needed.
The doctors in this collection+ Show
All expert statements+ Show
Every expert statement below comes from the recorded discussions, with its speaker and moment.
Congenital Diaphragmatic Hernia with Dr. Charlie Stolar
CDH occurs in approximately 1 out of every 3,000-4,000 pregnancies
epidemiologicalCharlie Stolar2:45 ↗
CDH diagnosis is typically made at the 20-week anatomy scan when ultrasonographers see the stomach in the same cross-sectional plane as the heart
clinicalCharlie Stolar3:37 ↗
CDH represents a growth arrest of both lungs, with the ipsilateral side more severely affected than the contralateral side
clinicalCharlie Stolar4:14 ↗
At birth, CDH lungs are affected by a mix of pulmonary hypoplasia and altered pulmonary vascular resistance with altered transitional circulation
clinicalCharlie Stolar4:23 ↗
CDH is a field defect; the most common neonatal comorbidity is foregut motility difficulty
clinicalCharlie Stolar4:39 ↗
CDH is a medical physiologic emergency but not a surgical emergency
clinicalCharlie Stolar5:00 ↗
The diagnosis of CDH alone is not an indication for cesarean section; elective spontaneous vaginal delivery is recommended assuming no obstetric issues
guidelineCharlie Stolar5:24 ↗
Antenatal interventions for CDH are no better than investigational and experimental at best
opinionCharlie Stolar6:35 ↗
Babies with CDH should be born at a full-service children's facility with ECMO capability; maybe 10-15% will benefit from ECMO
guidelineCharlie Stolar7:23 ↗
In single-center experiences, presence of liver in the chest or stomach in the chest is of no prognostic value
clinicalCharlie Stolar8:31 ↗
Lung-to-head ratio is of limited prognostic value except when very low (less than 0.8), where prognosis is concerning
clinicalCharlie Stolar8:42 ↗
Associated congenital heart disease and central nervous system abnormalities augur for poor prognosis
clinicalCharlie Stolar9:07 ↗
If shown 100 children with CDH, 80-85% will survive to become teenagers
epidemiologicalCharlie Stolar10:13 ↗
Antenatal steroids have tremendous value for preterm labor under 35 weeks but most CDH babies are near-term (37-39 weeks) where steroid role is arguable
clinicalCharlie Stolar10:37 ↗
Exit to ECMO for CDH is nonsense; it moves the goalposts on almost certainly non-viable babies
opinionCharlie Stolar12:06 ↗
We are born with about 1/2 to 2/3 of our full complement of alveoli and can grow the balance sometime after birth
clinicalCharlie Stolar13:00 ↗
Initial evaluation of newborn with CDH includes looking for morphology, associated anomalies, respiratory distress, pre- and post-ductal oxygen gradients, and early cardiac echo for right heart function
clinicalCharlie Stolar14:45 ↗
Not every baby with CDH needs or is a candidate for ECMO; approximately 5% have insufficient lung to support life based on inability to saturate preductal blood
clinicalCharlie Stolar15:55 ↗
ECMO is a drug delivery system for oxygen; indication is when end organs aren't getting enough oxygen despite best care
clinicalCharlie Stolar17:06 ↗
The best way to assess end-organ function is urine output
clinicalCharlie Stolar17:44 ↗
ECMO indication is typically oxygenation index in excess of 40 for 4 hours or more
guidelineCharlie Stolar18:21 ↗
All therapy is guided by preductal oximetry, not postductal; if preductal saturation is 90% (PaO2 ~65 torr), the brain is doing fine with fetal hemoglobin
clinicalCharlie Stolar19:06 ↗
When managing dropping preductal saturation, first ensure adequate hemoglobin and circulating volume, then increase FiO2 or ventilator pressure, but avoid trying to control PCO2 as this will destroy the lungs
clinicalCharlie Stolar20:25 ↗
Neonatal ventilators would be thrown out as lethal devices if someone tried to invent them today
opinionCharlie Stolar21:38 ↗
CDH babies are not paralyzed during ventilation; minimal sedation is used and babies should be awake and breathing spontaneously
clinicalCharlie Stolar21:56 ↗
Initial conventional ventilator settings (IMV rate ~40, peak pressure 25-28, PEEP ~5) are not tolerated by most CDH babies
clinicalCharlie Stolar22:15 ↗
Unconventional ventilation mode for CDH uses high rate (100 breaths/min), low peak pressure (turned down to zero due to stacking), and high gas flow rate with permissive hypercapnia
clinicalCharlie Stolar22:53 ↗
High-frequency oscillatory ventilation (HFOV) as rescue therapy rarely spares CDH babies from ECMO; when they get out the oscillator, it's time to prime an ECMO circuit
clinicalCharlie Stolar24:30 ↗
Nitric oxide is a waste of money for CDH; it's terrific for premature babies with immature lung disease but of no value in CDH
opinionCharlie Stolar25:45 ↗
The best drug for CDH is oxygen
opinionCharlie Stolar26:07 ↗
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