Pediatric Hypoplastic Left Heart Syndrome

Updated: Dec 15, 2020
Author: Syamasundar Rao Patnana, MD; Chief Editor: Stuart Berger, MD 



The term hypoplastic left heart syndrome (HLHS), initially proposed by Noonan and Nadas,[1] describes a spectrum of cardiac abnormalities characterized by marked hypoplasia of the left ventricle and ascending aorta. This is the same disorder characterized as hypoplasia of the aortic tract complex by Lev.[2] The aortic and mitral valves are atretic, hypoplastic, or stenotic. A patent foramen ovale or an atrial septal defect is usually present. The ventricular septum is usually intact. A large patent ductus arteriosus supplies blood to the systemic circulation. Systemic arterial desaturation may be present because of complete mixing of pulmonary and systemic venous blood in the right atrium. Coarctation of the aorta is also commonly present. See the images below.

This echocardiographic still frame shows a long-ax This echocardiographic still frame shows a long-axis view of the aortic arch in a patient with hypoplastic left heart syndrome (HLHS). The ascending aorta is markedly hypoplastic, serving only to deliver blood in a retrograde fashion to the coronary arteries. An echo-bright coarctation shelf is seen at the insertion of the ductus arteriosus.
This echocardiographic still frame shows a 4-chamb This echocardiographic still frame shows a 4-chamber view of the heart in a patient with hypoplastic left heart syndrome (HLHS). A large right ventricle (RV) and hypoplastic left ventricle (star) are seen. Right atrium = RA. Left atrium = LA.

Hypoplastic left heart syndrome is a uniformly lethal cardiac abnormality if not surgically addressed. Since the description of surgical palliation by Norwood in the early 1980s[3, 4] and the description of allograft cardiac transplantation by Bailey in the mid 1980s,[5] the interest in this lesion has remarkably increased. Currently, the Norwood surgical approach consists of a series of 3 operations: the Norwood procedure (stage I), the hemi-Fontan or bidirectional Glenn procedure (stage II), and the Fontan procedure (stage III). Orthotopic heart transplantation provides an alternative therapy, with results similar to those of the staged surgical palliation. Currently, the survival rate of infants treated with these surgical approaches is similar to that of infants with other complex forms of congenital heart disease in which a 2-ventricle repair is not possible.

Pathologic anatomy

Hypoplasia of the left heart structures is noted, with enlargement and hypertrophy of the right heart. Similar to other congenital heart defects, hypoplastic left heart syndrome also has a spectrum of severity.[6] In the most severe form, aortic and mitral valve are atretic, with a diminutive ascending aorta and markedly hypoplastic left ventricle. The left atrium is usually smaller than normal, although it may be normal in size or enlarged. It receives all pulmonary veins. Pulmonary vein stenosis is a rare but important abnormality.

The mitral valve may be atretic, hypoplastic or severely stenotic. The atretic mitral valve consists of fibromuscular tissue instead of a membrane. When the valve is stenotic, the entire mitral valve apparatus, including the valve annulus, valve leaflets, papillary muscles, and chordae tendineae, is small and hypoplastic.

The left ventricle is usually a thick-walled, slitlike cavity, especially when mitral atresia is present. When the mitral valve is perforate, the left ventricular cavity is small. Endocardial fibroelastosis is usually present. The aortic valve is either severely stenotic or atretic. The ascending aorta is often severely hypoplastic, measuring 2-3 mm in diameter, serving as a conduit to supply blood to both coronary arteries in a retrograde fashion. However, it may approach normal dimensions.[7, 8]

Coarctation of the aorta may be present in a significant number of patients with hypoplastic left heart syndrome,[3, 9, 10, 11] but interrupted aortic arch is rare. The right heart (ie, right atrium, right ventricle, pulmonary arteries) is markedly enlarged.

A patent foramen ovale is common; herniation of the valve of the septum into the right atrium may be noted. Rarely, the patent foramen ovale is completely closed. A true atrial septal defect is rarely present. Ventricular septal defect is not considered to be an integral part of hypoplastic left heart syndrome, although it may be present in the syndrome of mitral atresia with normal aortic root.

The most common presentation is visceroatrial situs solitus with D-ventricular loop and atrioventricular and ventriculoarterial concordance, as well as levocardia. Rarely, dextrocardia and heterotaxy may be present.

Severely hypoplastic left ventricle can be present in hearts with double-outlet right ventricle and common atrioventricular canal; in some studies, these variants constitute as many as 25% of hypoplastic left heart syndrome cases.[12]


Prenatal circulation

The oxygenated blood from the placenta is returned to the inferior vena cava and is not shunted preferentially across the patent foramen ovale into the left atrium; instead, it mixes with the superior vena caval blood in the right atrium. The pulmonary veins drain into the left atrium, and the pulmonary venous blood gets shunted across the atrial septum into the right atrium because of mitral valve obstruction. The vena caval and pulmonary venous blood along with the coronary sinus flow enters the right ventricle and the pulmonary artery.[13, 14]

Because of widely patent ductus arteriosus and high pulmonary vascular resistance in the fetus, a small portion of the blood from the right heart enters the lungs. Most of the blood is directed into the aorta via the ductus. Once in the aorta, the blood gets distributed into the brachiocephalic vessels, ascending aorta, and descending aorta. The quantitative distribution into these different vascular beds depends on their relative vascular resistances. The ascending aortic blood flows in a reverse direction and supplies the coronary arteries.

The fetal hypoplastic left heart syndrome circulation differs from the normal fetus in the following manner:

  • Larger quantity of flow across the ductus with a higher PO2: Whether these factors influence the development of ductal musculature, which may, in turn, influence postnatal ductal closure, is unclear.

  • Lower PO2 and questionably lower blood flow to the brain: The weight of the brain is generally normal, although no detailed studies on the cellular development of brain have been performed. However, whether the reported association between brain anomalies and hypoplastic left heart syndrome is related to abnormal flow and PO2 to the brain remains unknown.

  • Higher PO2 to the lungs: The low PO2 in the pulmonary artery blood in the normal fetus is believed to be responsible for development of muscular pulmonary arterioles. Higher-than-normal PO2 in hypoplastic left heart syndrome may lead to lack of normal medial muscular hypertrophy, which may result in rapid decline of pulmonary vascular resistance after birth.

  • Retrograde coronary blood flow via a long channel with lower PO2: This abnormality is not believed to interfere with supply of normal quantities of oxygen and nutrients to the myocardium. However, whether myocardial reserve is adversely affected is unclear.

Postnatal circulation

The newborn infant with hypoplastic left heart syndrome has a complex cardiovascular physiology. Fully saturated pulmonary venous blood returning to the left atrium cannot flow into the left ventricle because of atresia, hypoplasia, or stenosis of the mitral valve. Therefore, pulmonary venous blood must cross the atrial septum. In most babies, a patent foramen ovale is present and is small and partially obstructive.[15] This blood mixes with desaturated systemic venous blood in the right atrium. The right ventricle then must pump this mixed blood to both the pulmonary and the systemic circulations that are connected in parallel, rather than in series, by the ductus arteriosus. Blood exiting the right ventricle may flow (1) to the lungs via the branch pulmonary arteries or (2) to the body via the ductus arteriosus. The amount of blood that flows into each circulation is based on the resistance in each circuit.[6, 13]

Blood flow is inversely proportional to resistance (Ohm law); that is, when resistance in blood vessels decreases, blood flow through these vessels increases. Following birth, pulmonary vascular resistance decreases, which allows a higher percentage of the fixed right ventricular output to go to the lungs instead of the body. Although increased pulmonary blood flow results in higher oxygen saturation, systemic blood flow is decreased. Perfusion becomes poor, and metabolic acidosis and oliguria may develop. Coronary artery and cerebral perfusion also depend on blood flow through the ductus arteriosus and then retrograde flow via the aortic arch and ascending aorta. Therefore, increased pulmonary blood flow results in decreased flow to the coronary arteries and brain, with a risk of myocardial or cerebral ischemia.

Alternatively, if pulmonary vascular resistance is significantly higher than systemic vascular resistance, systemic blood flow is increased at the expense of pulmonary blood flow. This may result in hypoxemia. A delicate balance between pulmonary and systemic vascular resistances should be maintained to ensure adequate oxygenation and tissue perfusion.

Most patients with hypoplastic left heart syndrome also have coarctation of the aorta. This can be significant enough to interfere with retrograde flow to the proximal aorta.

In summary, the postnatal circulation in hypoplastic left heart syndrome depends on 3 major factors:

  1. Adequacy of interatrial communication

  2. Patency of the ductus arteriosus

  3. level of pulmonary vascular resistance


The exact cause of hypoplastic left heart syndrome is unknown. Although familial cases with autosomal recessive inheritance have been reported,[6]  hypoplastic left heart syndrome is generally postulated to follow multifactorial mode of inheritance.[16]

Most likely, the primary abnormality occurs during aortic and mitral valve development. During cardiac development, adequate flow of blood through a structure is largely responsible for the growth of that structure. With little or no blood flow because of aortic and mitral valve atresia, growth of the left ventricle does not occur.

Similarly, growth of the ascending aorta does not occur because of lack of left ventricular output. The ascending aorta is perfused in retrograde manner from the ductus arteriosus functioning only as a common coronary artery.

Premature closure or absence of the foramen ovale represents another theoretical cause of hypoplastic left heart syndrome because it eliminates fetal blood flow from the inferior vena cava to the left atrium.[17]  Fetal pulmonary blood flow is not sufficient for normal development of the left atrium, left ventricle, and ascending aorta.

Another postulated cause is misalignment of the atrial septum to the left.[18]

More recent studies suggest that hypoplastic left heart syndrome is genetically heterogeneous and hypoplastic left heart syndrome and bicuspid aortic valve are genetically related.[19, 20]


United States statistics

The prevalence of hypoplastic left heart syndrome is 2.60 per 10,000 live births with approximately 1025 cases annually.[21] It accounts for 2-3% of all congenital heart defects.[22, 23] Hypoplastic left heart syndrome accounts for 7-9% of all congenital heart disease diagnosed in the first year of life.[12] Before surgical treatment was available, hypoplastic left heart syndrome was responsible for 25% of cardiac deaths in the neonatal period.[12] The rate of occurrence is increased in patients with Turner syndrome, Noonan syndrome, Smith-Lemli-Opitz syndrome, or Holt-Oram syndrome. Certain chromosomal duplications, translocations, and deletions are also associated with hypoplastic left heart syndrome.

The international frequency is similar to that in the United States.

Sex- and age-related demographics

Hypoplastic left heart syndrome is more common in males than in females, with a 55-70% male predominance.

Hypoplastic left heart syndrome typically presents within the first 24-48 hours of life. Presentation occurs as soon as the ductus arteriosus constricts, thereby decreasing systemic blood flow, producing shock, and, without intervention, causing death. Infants with pulmonary venous obstruction (absent or restrictive patent foramen ovale) may present sooner. Very rarely, an infant with persistence of high pulmonary vascular resistance and the ductus arteriosus may present later because of balanced pulmonary and systemic blood flow.


Overall survival to the time of hospital discharge after the Norwood procedure is nearly 75%.[24] Success rates are higher in uncomplicated cases and lower in cases in which important preoperative risk factors are present, such as age greater than 1 month, significant preoperative tricuspid insufficiency, pulmonary venous hypertension, associated major chromosomal or noncardiac abnormalities, and prematurity.

Note the following:

  • High Aristotle scores (>20) are associated with high hospital mortality and low survival at follow-up.[25]

  • Low cerebral near-infrared spectroscopy oxygen saturations during the first 48 hours after Norwood procedure are strongly associated with adverse outcomes.[26]

  • Survival after the bidirectional Glenn/hemi-Fontan and Fontan operations is nearly 90-95%.

  • The actuarial survival rate after staged reconstruction is 70% at 5 years.

  • Institutional success rates vary.

  • Neurodevelopmental prognosis is not known; however, abnormalities are reported.

  • Approximately 20% of infants listed for cardiac transplantation die while waiting for a donor heart. After successful transplantation, the survival rate at 5 years is approximately 80%.

  • When the preoperative mortality is considered, the overall survival rate after cardiac transplantation is approximately 70%, or similar to the results for staged reconstruction.


Hypoplastic left heart syndrome has the greatest mortality rate among all coronary heart conditions.[27] Without surgery, hypoplastic left heart syndrome is uniformly fatal,[27] usually within the first 2 weeks of life. Survival for a longer period occurs rarely and only with persistence of the ductus arteriosus and balanced systemic and pulmonary circulations.

Following the Norwood procedure (stage I), overall success (survival to hospital discharge) is approximately 75%. Success rates are higher (85%) in patients with low preoperative risk and lower (45%) in patients with important risk factors. The risk factors for poor result are multiple and vary from study to study and include prematurity and major noncardiac malformations. Other identified risk factors include surgery in older infants (>1 mo), significant tricuspid regurgitation, and pulmonary venous hypertension. High Aristotle scores are also associated with poor prognosis.

A study of data from the Society of Thoracic Surgeons Congenital Heart Surgery Database assessed the mortality rates and postoperative complications after the Norwood procedure in 2,557 patients. The overall mortality rate was noted as 22%, with 75% having at least one complication. Increases in mortality rate correlated with increases in the number of complications, with renal and cardiovascular complications carrying the greatest risk of mortality. Factors associated with complications included weight less than 2.5 kg, single right versus single left ventricle, preoperative shock, genetic abnormality, and preoperative mechanical ventilatory or circulatory support.[28]

Some centers have reported stage I survival rates in excess of 90%. This appears to be related, in part, to institutional surgical volume. The overall success following the bidirectional Glenn or hemi-Fontan procedure (stage II) approaches 95%. Success after completing the Fontan procedure (stage III) approaches 90%. Orthotopic heart transplantation results in early and long-term success similar to that of staged reconstruction. Among low-risk patients who undergo staged reconstruction or transplantation, actuarial survival at 5 years is approximately 70%.

Substantial morbidity is associated with multiple cardiac catheterizations, cardiac interventions, and cardiac surgery in patients undergoing Norwood palliation. Similarly the need for multiple cardiac biopsies and hospitalizations related to immunologic management and infections exist in patients who had cardiac transplantation.

Most studies report neurodevelopmental disabilities in a significant number of patients who survive either staged surgical reconstruction or cardiac transplantation.


Preoperative complications include acidosis, congestive heart failure (CHF), renal failure, liver failure, necrotizing enterocolitis, sepsis, and death.

Postoperative complications include acidosis, CHF, thrombosis, renal failure, liver failure, necrotizing enterocolitis, sepsis, pericardial or pleural effusion, phrenic or recurrent laryngeal nerve damage, stroke, coarctation of the aorta, and death. Early graft rejection and opportunist infection may occur after cardiac transplantation.

Approximately 20% of infants undergoing staged surgeries for single‐ventricle congenital heart disease experience a thrombotic event between the stage I procedure and stage II discharge (the rate of thrombotic events in infants with hypoplastic left heart syndrome is considerably lower than in infants with non-HLHS).[29] Thrombosis is associated with longer cardiopulmonary bypass time, longer stage I intensive care unit and hospital lengths of stay, and lower stage I hospitalization discharge oxygen saturation.[29]

Major complications following the Norwood procedure include aortic arch obstruction at the site of surgical anastomosis and progressive cyanosis caused by limited blood flow through the shunt. An inadequate atrial communication contributes to progressive cyanosis. A study of data from the Society of Thoracic Surgeons Congenital Heart Surgery Database assessed the mortality rates and postoperative complications after the Norwood procedure in 2,557 patients. Factors associated with complications included weight less than 2.5 kg, single right versus single left ventricle, preoperative shock, genetic abnormality, and preoperative mechanical ventilatory or circulatory support.[28]

Major complications following the bidirectional Glenn/hemi-Fontan procedure include transient superior vena cava syndrome and persistent pleural or pericardial effusion. The development of systemic venous to pulmonary venous collateral vessels is possible.

Major complications following the Fontan procedure include persistent pleural or pericardial effusion. Neurodevelopmental abnormalities are reported and may be inherent in some patients with hypoplastic left heart syndrome.

Arrhythmias, obstructed venous pathways, and protein-losing enteropathy are some of the other complications observed following the Fontan operation.

Patient Education


At the outset, appropriately warn the parents and other caregivers that hypoplastic left heart syndrome is a complex heart defect that requires multiple hospitalizations, surgeries, catheter interventions and long-term follow-up.


Educate parents regarding the doses and side effects of their child's cardiac medications.

Discuss interactions with other medications with the family and the infant's general pediatrician.


Many infants require nasogastric or G-tube tube feeding after discharge from the hospital. Parents must become comfortable with placement of the nasogastric feeding tube and/or care for the G-tube, as the case may be.

Frequently, increased-calorie formula is required for adequate growth. Provide the formula recipe or a source for purchasing it to the caregiver.

Follow-up care

Stress the importance of follow-up care. If necessary, provide cab or bus vouchers to ensure compliance.

If noncompliance becomes a critical issue, physicians are required to report to the appropriate family services agency.




The clinical features of hypoplastic left heart syndrome (HLHS) largely depend on the patency of the ductus arteriosus, the level of pulmonary vascular resistance, and the size of the interatrial communication.

Although hypoplastic left heart syndrome can easily be detected on fetal echocardiography,[30] many infants are not identified prenatally because routine obstetric ultrasonography examination may not concentrate on cardiac anatomy. An increase in use of routine prenatal ultrasonography and examination by obstetricians of the 4-chamber anatomy of the heart to ensure its normalcy is likely to identify hypoplastic left heart syndrome more frequently than in the past.

Pregnancies are typically uncomplicated. The fetus grows and develops normally because the fetal circulation is not significantly altered.[6, 13] Most neonates are born at term and initially appear normal.

Occasionally, respiratory symptoms and profound cyanosis are apparent at birth (2-5% of cases). In these infants, significant obstruction to pulmonary venous return (a congenitally small or absent patent foramen ovale) is usually present.

As the ductus arteriosus begins to close normally over the first 24-48 hours of life, symptoms of cyanosis, tachypnea, respiratory distress, pallor, lethargy, metabolic acidosis, and oliguria develop. Without intervention to reopen the ductus arteriosus, death rapidly ensues. Similar symptomatology may be expected if a precipitous drop in pulmonary vascular resistance occurs.

Physical Examination

Before the initiation of prostaglandin E1 infusion to reestablish patency of the ductus arteriosus, infants may exhibit signs of cardiogenic shock, including the following:

  • Hypothermia

  • Tachycardia

  • Respiratory distress

  • Central cyanosis and pallor

  • Poor peripheral perfusion with weak pulses in all extremities and in the neck

  • Hepatosplenomegaly

After reestablishment of systemic blood flow via the ductus arteriosus, signs of shock resolve, leaving the stable infant with tachycardia, tachypnea, and mild central cyanosis. If a coarctation of the aorta is present, arterial pulses in the legs may be more prominent than those in the arms, particularly the right arm.

Cardiac examination findings may include the following:

  • A prominent right ventricular impulse may be noted.

  • A normal first heart sound may be observed.

  • A loud single second heart sound may be present.

Usually no murmur is noted; however, the following murmurs may be heard:

  • Nonspecific, soft, systolic ejection murmur at the left sternal border (not always present)

  • High-pitched holosystolic murmur at the lower left sternal border, indicating tricuspid regurgitation (not always present)[3]

  • Diastolic flow rumble over the precordium, indicating increased right ventricular diastolic filling (not always present)



Diagnostic Considerations

Important considerations

It is important that clinicians do not misdiagnose and/or they not fail to recognize the infant with hypoplastic left heart syndrome and the obstruction to pulmonary venous return.

Special concerns

The newborn with hypoplastic left heart syndrome dies rapidly if untreated. Surgical techniques, both reconstruction and heart transplantation, offer an opportunity to preserve the newborn's life. Survival rates given above represent the best results and reflect only survival, not quality of life. Mortality rates in many centers exceed those mentioned. Incidence of neurodevelopmental abnormalities in hypoplastic left heart syndrome appears to exceed that of other single-ventricle conditions.

Hypoplastic left heart syndrome affects family structure. For example, reproductive studies indicate that the incidence of subsequent pregnancy is significantly lower in mothers of a living patient with hypoplastic left heart syndrome than in mothers after death of an infant with hypoplastic left heart syndrome. For these reasons, most pediatric cardiologists continue to offer no treatment as an acceptable option to parents of a newborn with hypoplastic left heart syndrome. It is incumbent on physicians caring for a newborn with hypoplastic left heart syndrome to clearly communicate all of this information to the parents. An ethically appropriate consent for surgery requires this. Allowing an affected infant to die without surgical intervention is a difficult decision but is still chosen by some families and should not be discouraged.

Ethical issues related to transplantation compared with multistage reconstructive surgery were recently reviewed.[31] Although the decision regarding this choice must be made in the best interest of the infant with hypoplastic left heart syndrome, considerations such as interests of the family members and society-at-large may have to be taken into account.

Other problems to be considered

Also consider the following conditions in patients with suspected hypoplastic left heart syndrome:

  • Associated cardiac abnormalities, including anomalous pulmonary venous connection, coarctation of the aorta, complete atrioventricular canal, coronary artery abnormalities (especially in patients with aortic atresia and mitral stenosis), persistent left superior vena cava, and endocardial fibroelastosis (especially in patients with aortic atresia and mitral stenosis)

  • Associated noncardiac abnormalities: Genetic disorders

  • Significant noncardiac abnormalities, including CNS malformation, diaphragmatic hernia, and necrotizing enterocolitis

Differential Diagnoses



Laboratory Studies

Laboratory studies indicated in workup of hypoplastic left heart syndrome (HLHS) are summarized below.

Complete blood cell count

Measure hemoglobin levels, because severe neonatal anemia can cause high-output congestive heart failure (CHF) and cardiogenic shock. The hemoglobin level is usually normal in hypoplastic left heart syndrome.

Obtain a total white blood cell (WBC) count with differential. Sepsis can cause symptoms of shock. The WBC count is typically normal.

Electrolyte levels

Electrolyte abnormalities may be present in infants with poor oral intake secondary to CHF. Use carbon dioxide and bicarbonate to assess acid-base status.

Electrolyte levels are usually normal. The carbon dioxide level may be low if a metabolic acidosis is present. The carbon dioxide level may be high if respiratory failure sets in.

BUN/creatinine levels

Infants with critical illness and significantly reduced systemic perfusion may show evidence of renal failure. The creatinine level may be transiently elevated.

Liver function tests

Infants with critical illness and significantly reduced systemic perfusion and CHF may show evidence of hepatocellular damage.

Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels may be transiently elevated.

Arterial blood gas and lactic acid measurements

Assessing acid-base status is paramount, especially to rule out metabolic acidosis. Most infants have some evidence of metabolic acidosis, which should be immediately corrected. This is usually secondary to decreased systemic perfusion. Appropriate intervention to augment systemic flow should be promptly undertaken. Elevated levels of serum lactic acid generally precede a fall in pH, as acidosis develops.

Assessment of PaO2 and PaCO2 is important for respiratory management and manipulation of pulmonary vascular resistance by mechanical ventilation and the addition of supplemental inhaled nitrogen. The PaO2 is optimally 30-45 mm Hg, and the PaCO2 is ideally 45-50 mm Hg.

Karyotype analysis

Chromosomal analysis is indicated for infants with dysmorphic features. Nearly 25% of infants have chromosomal abnormalities.

Other studies


Electrocardiography typically reveals sinus tachycardia, right-axis deviation, right atrial enlargement, and right ventricular hypertrophy with a qR configuration in the right precordial leads.

A paucity of left ventricular forces is noted in the left precordial leads.

ST-T wave changes suggestive of myocardial ischemia may be present in some patients.

Imaging Studies

Chest radiography

Cardiomegaly and increased pulmonary vascular markings are typically present.

Marked pulmonary edema may be noted in infants with obstructed pulmonary venous return, usually due to markedly restrictive patent foramen ovale.

Although the radiography findings are not specific for the condition, the presence of a large heart with increased pulmonary vascular markings in a mildly cyanotic neonate should always prompt inclusion of hypoplastic left heart syndrome in the differential diagnosis.


Echocardiography is the test of choice for diagnosing hypoplastic left heart syndrome. Two-dimensional imaging clearly shows the hypoplastic left ventricle and ascending aorta. The right atrium, tricuspid valve, right ventricle, and main pulmonary artery are larger than usual. See the images below.

This echocardiographic still frame shows a long-ax This echocardiographic still frame shows a long-axis view of the aortic arch in a patient with hypoplastic left heart syndrome (HLHS). The ascending aorta is markedly hypoplastic, serving only to deliver blood in a retrograde fashion to the coronary arteries. An echo-bright coarctation shelf is seen at the insertion of the ductus arteriosus.
This echocardiographic still frame shows a 4-chamb This echocardiographic still frame shows a 4-chamber view of the heart in a patient with hypoplastic left heart syndrome (HLHS). A large right ventricle (RV) and hypoplastic left ventricle (star) are seen. Right atrium = RA. Left atrium = LA.

Other structural abnormalities should be excluded.

Doppler and color Doppler imaging are also important.[4]

Evaluate tricuspid regurgitation, which is a preoperative risk factor for the Norwood procedure, and blood flow across the atrial septum. High-velocity Doppler jet across the atrial septum indicates restrictive interatrial communication. Observe retrograde blood flow from the ductus arteriosus into the transverse aortic arch and ascending aorta.

Evaluate the aortic arch and thoracic aorta for evidence of coarctation.

Two-dimensional and Doppler echocardiographic features are sufficiently characteristic of hypoplastic left heart syndrome such that cardiac catheterization and angiography are no longer necessary for diagnosis of this anomaly.

Variability of the chamber and vessel size is seen in hypoplastic left heart syndrome.

Ultrasonography of the head and abdomen

Ultrasonography of the head was thought to be necessary only if the infant has had a significantly long period in shock with potentially poor cerebral perfusion. However, at most institutions, routine head ultrasonography to exclude central nervous system abnormality and abdominal ultrasonography to evaluate kidneys are performed prior to the Norwood procedure or cardiac transplantation.

A significant prevalence of abnormalities is observed using ultrasonography of the head[32] and abdomen.


Cardiac catheterization (pre–Norwood procedure)

Routine diagnostic catheterization is not necessary because 2-dimensional and Doppler echocardiography can provide the necessary anatomic and hemodynamic data. However, a focused catheterization may become necessary to resolve any echocardiographic discrepancies that may be deemed important in surgical management.

If catheterization is performed, the features reflect the pathophysiology described above.

Oxygen saturation data indicate moderate-to-severe systemic venous desaturation, with a step-up at the level of right atrium secondary to left to right shunt across the atrial septum. The oxygen saturations in the right ventricle, pulmonary artery and aorta are similar reflecting common mixing in the right atrium. Mild systemic arterial desaturation is usually present unless severe pulmonary edema is noted.

The right atrial pressure is mildly elevated, and the left atrial pressure is moderate to severely elevated, unless a large atrial septal defect is present. The right ventricular and pulmonary arterial systolic pressures are at systemic level. If the ductus arteriosus is constricted, these pressures are higher than those in the aorta.

Angiography, although not necessary in all cases, reveals hypoplasia of the mitral valve, left ventricle and aorta. The ascending aorta is perfused in a retrograde fashion and serves as a common coronary artery, supplying both the right and left coronary arteries.

Perform interventional catheterization with blade/balloon atrial septostomy or static dilatation of the atrial septum to relieve pulmonary venous hypertension if blood flow from left atrium to right atrium is severely restricted at the atrial septum.[33, 34] Because of marked hypoplasia of the left atrium, conventional Rashkind balloon or Park blade atrial septostomy may not be possible. In such situations, static dilatation of the atrial septum may be performed.[34, 35] If the atrial septum is extremely thick with a markedly restrictive atrial septum, stent implantation to keep the atrial septum open may become necessary.[34]

When hybrid procedures are contemplated, stenting of the ductus, atrial septum, or both may become necessary.

Cardiac catheterization (pre–bidirectional Glenn [stage II] procedure)

Perform routine catheterization before the operation to obtain hemodynamic data and several important angiograms.

Calculate pulmonary vascular resistance to ensure the patient's suitability for the stage II procedure.

Perform angiography in the right ventricle to show ventricular function and tricuspid regurgitation.

Perform angiography in the transverse aortic arch near the shunt to show pulmonary artery size and distribution and to rule out recurrent aortic coarctation or significant aortopulmonary collateral vessels.

If collateral vessels are found, they may be occluded with coils at the same catheterization.

Pre-Fontan (stage III) procedure

Routine catheterization before completing the operation is generally recommended.

Measure pulmonary artery pressure and calculate pulmonary vascular resistance and perform right ventricular angiography.

Delineate pulmonary artery anatomy by performing angiography at the superior vena cava–pulmonary artery anastomosis via an internal jugular approach.

Recurrent coarctation of the aorta and significant collateral vessels are excluded again.

Descending aortography and selective right and left subclavian artery angiography to identify any collateral vessels to lungs is recommended.

Postcatheterization complications include hemorrhage, vascular disruption after balloon dilation, pain, nausea and vomiting, and arterial or venous obstruction from thrombosis or spasm but are rare.

Catheter intervention

In the neonate, obstruction at the level of the patent foramen ovale (atrial septum) may be treated with conventional Rashkind balloon atrial septostomy. However, because the left atrium is small, Rashkind septostomy[33] may not be feasible. In addition, the septum may be too thick to be torn by balloon septostomy; therefore, Park blade septostomy may be necessary and should precede the Rashkind procedure.[36, 37] However, hypoplastic left atrium may preclude blade septostomy. Static dilatation of the atrial septum with a balloon angioplasty catheter may be used and may not only relieve the obstruction but also keep some restriction, such that no rapid fall in the pulmonary vascular resistance occurs. Static balloon dilatation is preferred by the senior author.[34, 35]

In some patients, the atrial septum may be intact or have a tight patent foramen ovale that may not even allow passage of a catheter. In such situations, puncture of the atrial septum by a Brockenbrough technique or radiofrequency perforation of the atrial septum followed by static balloon atrial septal dilatation or, preferably, stent implantation may become necessary.[34, 38]

If progressive cyanosis develops after a previous Blalock-Taussig shunt, and if the hypoxemia is due to a stenotic shunt, balloon dilatation may be used to improve oxygen saturation.[39] However, if the patient is of sufficient size and age to undergo a bidirectional Glenn procedure, this procedure should be performed instead of balloon angioplasty of a narrowed Blalock-Taussig shunt.

If severe aortic coarctation is present, particularly after Norwood procedure, balloon angioplasty may be useful in relieving aortic obstruction and may help achieve reduce right ventricular afterload.[40]

If significant branch pulmonary artery stenosis is present before a bidirectional Glenn or Fontan conversion or after a Fontan procedure, balloon angioplasty or placement of intravascular stents is recommended.[41, 42]

Development of aortopulmonary collateral vessels has been increasingly observed in recent studies. Before the final Fontan conversion, occlusion of these vessels in the catheterization laboratory, usually by means of coil embolization,[43, 44] is recommended to reduce left ventricular volume overloading and, probably, the duration of chest tube drainage following surgery.

Following completion of Fontan procedure, some patients may develop recurrent pleural effusion, liver dysfunction, plastic bronchitis or protein-losing enteropathy.[45] In these patients, following exclusion of obstructive lesion in the Fontan circuit, puncture of the atrial septum by a Brockenbrough technique followed by static balloon atrial septal dilatation or stent implantation may be beneficial.

Patients who have undergone a fenestrated Fontan operation or have a residual atrial defect, despite correction, may have significant right-to-left shunting causing severe hypoxemia. These residual atrial defects may be closed using transcatheter techniques.[46, 47]



Approach Considerations

No consensus has been reached in the approach to the treatment of neonates with hypoplastic left heart syndrome (HLHS). Supportive care, multistage surgical intervention (ie, Norwood, Glenn, and Fontan procedures) and cardiac transplantation are available options. A thorough explanation of each of these options, including their advantages and disadvantages, should be provided to the parents.

Occasionally, some anatomic features favor one choice over the others. In the presence of severe tricuspid or pulmonary valve anomalies, the multistage surgical approach is not likely to be beneficial; cardiac transplantation is the only surgical choice. In most cases, the choice of treatment is based on the parents' preference. While such a decision is being made, the infant should be stabilized.

If supportive care is chosen by the parents, they need strong emotional support because the condition is fatal without active treatment.

Medical Care

Prenatal diagnosis of hypoplastic left heart syndrome (HLHS) by fetal echocardiography is possible. When the HLHS is identified, it is advisable to have the baby deliver at an institution where tertiary care, including neonatal cardiac surgery, is performed routinely. There was some suggestion in the past that elective cesarean delivery may provide better outcomes. A recent study examining this issue found that there was no hemodynamic advantage for elective cesarean delivery section over vaginal delivery.[48]

Successful preoperative management depends on providing adequate systemic blood flow while limiting pulmonary overcirculation.

Note the following:

  • Initial preoperative management and postoperative care of hypoplastic left heart syndrome (HLHS) take place in the neonatal, pediatric, or cardiac ICUs.

  • When postoperative patients are clinically stable, transfer them to the general cardiac unit for adjusting oral medications, addressing feeding issues, and completing discharge teaching.

  • Involve a pediatric cardiologist during any noncardiac hospital admission of a patient who is status post (S/P) Norwood procedure. This is because of the complex cardiovascular physiology in infants after this surgery.

  • Hospitalization and inpatient care may be required for cardiac catheterizations, catheter interventions, and surgical procedures and for treatment of intercurrent infections as well as for management of postsurgical complications, including those after Fontan operation.

Open the ductus arteriosus

Blood flow to the systemic circulation (coronary arteries, brain, liver, kidneys) depends on flow through the ductus arteriosus. If a diagnosis of hypoplastic left heart syndrome is suspected, start prostaglandin E1 infusion immediately to establish ductal patency and ensure adequate systemic perfusion.

If the diagnosis is made prenatally or when the infant is relatively asymptomatic, a smaller dose of prostaglandin E1 may be sufficient to keep the ductus arteriosus patent while limiting its side effects.

A larger dose of prostaglandin E1 is often required to reopen the ductus arteriosus if an infant has cardiovascular collapse and shock due to ductal closure.

Ideally, prostaglandin E1 is administered centrally via an umbilical venous catheter.

Correct metabolic acidosis

Metabolic acidosis indicates inadequate cardiac output to meet the metabolic demands of the body. Acidosis adversely affects the myocardium.

Correction of metabolic acidosis with sodium bicarbonate infusion is essential in early management. This therapy is futile if the ductus arteriosus remains constricted.

Manipulate pulmonary vascular resistance

The pulmonary vascular resistance of a newborn is slightly less than the systemic vascular resistance and begins to fall soon after birth. In the patient with hypoplastic left heart syndrome, decreased pulmonary vascular resistance causes increased pulmonary blood flow and an undesirable obligatory decrease in systemic blood flow. Increased alveolar oxygen decreases pulmonary vascular resistance, leading to increased pulmonary blood flow. Therefore, oxygen should not be administered unless pulmonary parenchymal disease or pulmonary edema, causing severe hypoxemia, is present. The oxygen should be discontinued once these abnormalities resolve.

Consequently, most infants should remain in room air with acceptable oxygen saturation (pulse oximeter) in the low 70s. An exceptional circumstance is the infant with severe hypoxemia caused by pulmonary venous hypertension.

Achieving a slightly higher PaCO2, in the range of 45-50 mm Hg, can increase pulmonary vascular resistance. This can be accomplished by intubation, sedation, mechanical hypoventilation, or the addition of nitrogen or carbon dioxide (FIO2 of 15-19%) to the infant's inspired gas via the endotracheal tube or hood.

Intubation is not preferred. However, intubation and ventilation along with measures to balance pulmonary and systemic flows may improve tricuspid regurgitation.[49]

Serial blood gas analysis is necessary. Initially, an umbilical arterial catheter is useful to obtain frequent blood samples.

Although administration of subambient inspired oxygen to balance systemic and pulmonary blood flows is an attractive concept and should be applied during stabilization of the neonate, it should not be pursued for long periods because severe pulmonary hypertension may complicate the postoperative course. However, this does not seem to adversely affect the pulmonary vasculature on long-term follow-up.[50]



Inotropic support is indicated only in severely ill neonates with concurrent sepsis or profound cardiogenic shock and acidosis. The administration of inotropes can adversely affect the balance between pulmonary and systemic vascular resistance.

If needed, wean from inotropic support as soon as the infant is clinically stable.


Consider diuretics to manage pulmonary overcirculation before surgery. Agents commonly used include furosemide and spironolactone.


Antibiotics are indicated if the infant is at risk for antepartum infection.

Discontinue antibiotics after obtaining negative blood cultures.


Consult a pediatric cardiologist, pediatric cardiovascular surgeon, genetic specialist if a chromosomal abnormality is suspected, and an interventional pediatric cardiologist.


Transfer the infant to a hospital with appropriate ICUs. Pediatric cardiology and cardiovascular surgery services must be immediately available.

Carefully monitor the infant for apnea during transfer while on prostaglandin E1 therapy. If prostaglandin E1 has been started, consider elective endotracheal intubation before transfer.

Surgical Care

Sinha and associates,[15] Caylor and colleagues,[51] and Dotty and associates[52] proposed various palliative operations; however, survival was not feasible until Norwood and associates[3, 4] demonstrated that a multistage operative approach could be used to treat hypoplastic left heart syndrome.

After Fontan and Kreutzer's initial description of the physiologically corrective operation for tricuspid atresia,[53, 54] corrective surgery was widely adapted to treat this entity. The concept was extended to treat other cardiac defects with a functionally single ventricle, including hypoplastic left heart syndrome.

The originally described Fontan operation consisted of the following[53] :

  • Superior vena cava–to–right pulmonary artery end-to-end anastomosis (Glenn procedure)

  • Anastomosis of the proximal end of the divided right pulmonary artery to the right atrium directly or by means of an aortic homograft

  • Closure of the atrial septal defect

  • Insertion of a pulmonary valve homograft into the inferior vena caval orifice

  • Ligation of the main pulmonary artery, thus completely bypassing the right ventricle

Kreutzer performed anastomosis of the right atrial appendage and pulmonary artery directly or via a pulmonary homograft and closed the atrial septal defect.[54] A Glenn procedure was not performed, and a prosthetic valve was not inserted into the inferior vena cava. Fontan's concept was to use the right atrium as a pumping chamber[53] ; therefore, he inserted prosthetic valves into the inferior vena cava and right atrial–pulmonary artery junction. Kreutzer’s view was that the right atrium may not function as a pump and that the left ventricle functions as a suction pump in the system.[54]

Numerous modifications to the aforementioned procedures were undertaken by these and other workers in the field (see Tricuspid Atresia). Currently, staged total cavopulmonary connection is the procedure of choice.[55]

The goal of surgical reconstruction of hypoplastic left heart syndrome is to eventually separate the pulmonary and systemic circulations by achieving a Fontan circulation. The right ventricle remains the systemic ventricle while blood passively flows to the lungs. This ultimate reconstruction is accomplished in the following 3 stages:

Norwood procedure (stage I)

This procedure is usually performed during the first weeks of life, after the infant has been stabilized in the neonatal intensive care unit (ICU). The goals of the procedure are (1) to establish reliable systemic circulation without the ductus arteriosus and (2) to provide enough pulmonary blood flow for adequate oxygenation, while simultaneously protecting the pulmonary vascular bed in preparation for stages II and III.

The Norwood procedure includes (1) performing an atrial septectomy to provide unrestricted blood flow across the atrial septum, (2) ligating the ductus arteriosus, (3) creating an anastomosis between the main pulmonary artery and the aorta to provide systemic blood flow, (4) eliminating coarctation of the aorta, and (5) placing an aorta–to–pulmonary artery shunt (usually a modified Blalock-Taussig shunt) to provide pulmonary circulation.

Connecting a Gore-Tex graft from the right ventricular outflow tract to the pulmonary artery (ie, Sano operation) was advocated instead of conventional modified Blalock-Taussig (BT) shunt;[56, 57] some surgeons showed better results with the Sano procedure than with the conventional Norwood approach.[58] However, prospective randomized studies from a single institution,[59] as well as multiple institutions,[60] compared the techniques and have not found significant advantage of Sano over Blalock-Taussig shunt or vice versa.

Upon hospital discharge, most infants remain on digoxin to augment cardiac function, on diuretics to help manage right ventricular volume overload, and on aspirin to prevent thrombosis of the shunt. If tricuspid regurgitation is present, use afterload reduction with captopril.[3] Oxygen saturation is typically 70-80% in room air.[5]

A retrospective study (2005-2013) reported that mitral stenosis and aortic atresia was a risk factor for perioperative myocardial ischemia and mortality in patients who underwent a modified Norwood procedure.[61] Compared to patients with other hypoplastic left heart syndrome anatomic subgroups, operative mortality was higher in the mitral stenosis/aortic atresia group (29% vs 7%) and accounted for 50% of the total operative mortality, despite the mitral stenosis/aortic atresia patients comprising only 19% of the total study population.[61]

Bidirectional Glenn procedure (stage II)

This procedure is performed approximately 6 months after the Norwood procedure. Before surgery, perform a cardiac catheterization to assess right ventricular function, pulmonary artery anatomy, and pulmonary vascular resistance. If results are favorable, schedule elective surgery.

The bidirectional Glenn procedure includes creating an anastomosis between the superior vena cava and the right pulmonary artery, end-to-side so that venous return from the upper body can flow directly into both lungs. In the hemi-Fontan, the superior vena cava–right atrial junction is closed with a patch that is removed during the next stage. Blood from the inferior vena cava continues to drain into the right atrium. The aorta–to–pulmonary artery shunt that was placed at stage I is ligated.

When both right and left superior vena cavae are present, bilateral bidirectional Glenn shunts should be performed, especially if the bridging innominate vein is absent or small.

At the time of bidirectional Glenn, repair of pulmonary artery narrowing, if present, should be undertaken. Issues related to tricuspid valve regurgitation, restrictive atrial septum and any other abnormalities should also be addressed.

At discharge, infants usually remain on digoxin, diuretics, aspirin, and captopril for the reasons mentioned above.

Fontan procedure (stage III)

The Fontan procedure is performed approximately 12 months after the bidirectional Glenn procedure. Again, catheterization is necessary to ensure that the child is a candidate for surgery.

Completion of the Fontan procedure includes directing blood flow from the inferior vena cava to the pulmonary arteries either via a lateral tunnel procedure or via an extracardiac conduit. Extracardiac conduit diversion of inferior vena caval blood into the right pulmonary artery is currently preferred by most surgeons. To address the growth issue related to extracardiac Fontan, some surgeons use autologous pericardial roll grafts. At the conclusion of the procedure, systemic venous blood returns to the lungs passively without passing through a ventricle.

Choussat et al's criteria have been modified by many cardiologists and surgeons.[62] Patients violating these criteria are at a higher risk for poor prognosis following Fontan operation than patients within the limits set by Choussat. In this high-risk group, the concept of leaving a small atrial septal defect open to facilitate decompression of the right atrium has been advanced. Laks et al advocated closure of the atrial defect by constricting the preplaced suture in the postoperative period,[63] whereas Bridges et al used a transcatheter closure technique.[64] Although the fenestrated Fontan was initially conceived for high-risk patients, it has since been used in patients with modest or even low risk. Rare reports of cerebrovascular or other systemic arterial embolic events following the fenestrated Fontan procedure tend to contraindicate its use in non–high-risk patients. Some studies suggest routine fenestration is unnecessary[65]

At discharge, most children remain on digoxin, diuretics, aspirin, and captopril if necessary. In an uncomplicated case, most of these medications can be weaned over 6 months following the Fontan operation. Some cardiologists advocate using aspirin indefinitely. Routine use of more aggressive anticoagulation with Coumadin is debated. When warfarin and aspirin regimens were compared, no difference in thrombotic complications between the groups was detected.[66] Similar early uncontrolled studies indicated similar finding; thus, most pediatric cardiologists use aspirin for prevention of thrombotic events in children. Use of more potent drugs such clopidogrel (Plavix) may be reasonable in adolescents and adults.

Ruotsalainen et al investigated the impact of initial shunt type, comparing outcomes of a Blalock-Taussig (BT) shunt with a right ventricle to pulmonary artery conduit (RV-PA), on myocardial function at different stages of surgical palliation in a population-based cohort of 63 Finnish children with hypoplastic left heart syndrome. Investigators studied patients retrospectively by echocardiography prior to stages I, II, and III palliation and 0.5-3 years after stage III. Patients with a BT shunt had better systolic performance after stage III compared to patients with an RV-PA conduit.[67]

Heart transplantation is another surgical option.[5, 6] The infant must remain on prostaglandin E1 infusion to keep the ductus arteriosus patent while waiting for a donor heart to become available. Approximately 20% of infants listed for heart transplantation die while waiting for a suitable donor organ. After successful cardiac transplantation, infants require multiple medications for modulation of the immune system and prevention of graft rejection. Perform frequent outpatient surveillance to identify rejection early and prevent lasting damage to the transplanted heart. Periodic endomyocardial biopsy usually is performed for more precise monitoring.

Emerging therapies

Catheter-assisted Fontan

Following Norwood procedure, 2-stage cavopulmonary connection is currently recommended for achieving Fontan circulation. Konert et al proposed a staged surgical-catheter approach;[68] they initially perform a modified hemi-Fontan procedure that is later completed by transcatheter methodology. This reduces the total number of operations required.

The modified hemi-Fontan procedure involves the usual bidirectional Glenn procedure. The lower end of the divided superior vena cava is anastomosed to the undersurface of the right pulmonary artery. The superior vena cava is then banded around a 16-gauge catheter with 6-0 Prolene slightly above the cavoatrial junction. A lateral tunnel with a Gore-Tex baffle is created, diverting the inferior vena caval blood toward the superior vena cava. The Gore-Tex baffle is then fenestrated with three to five 5-mm holes. Thus, the first stage achieves a physiologic bidirectional Glenn procedure.

At the time of the second stage (the transcatheter stage), the superior vena caval constriction is balloon dilated, and fenestrations are closed with devices or by placement of covered stent. These procedures have been performed in a limited number of patients, and preliminary data suggest that the usual post-Fontan operation complications, such as pleural effusion and ascites, have not occurred with this approach. Additional experience is reported;[69, 70] however, scrutiny of results of larger experience and longer-term follow-up and ready availability of covered stents are necessary for routine application of this innovative approach. To the authors knowledge, this approach is not well documented in patients with hypoplastic left heart syndrome.

Sano’s modification of the Norwood procedure

Because of high mortality that Sano and his associates observed with the conventional Norwood procedure, they performed right ventricular outflow–to–pulmonary artery Gore-Tex graft anastomosis to provide for the pulmonary blood flow instead of conventional modified aortopulmonary shunt.[56, 57] Significant improvement was demonstrated in both immediate and late mortality with this modification.[58]

A multi-institutional study comparing the results of these 2 types of stage I palliation of hypoplastic left heart syndrome suggested no significant difference between the groups.[60]

Other hybrid approaches

Again, because of high mortality following stage I Norwood reconstruction, several groups have performed bilateral banding of the branch pulmonary arteries via median sternotomy and implant stent in the ductus arteriosus.[71, 72] Maintaining ductal patency with long-term prostaglandin infusion instead of ductal stenting is advocated by some. At the time of the second stage, aortic arch reconstruction, atrial septectomy, and bidirectional Glenn shunt are performed. This is followed by Fontan conversion. Although reduction of early mortality is theoretically feasible, larger experience with this approach than is currently available is necessary prior to general adaptation of this method of management of hypoplastic left heart syndrome.

Bugnitz et al evaluated right ventricular functional changes in 20 neonates with hypoplastic left heart syndrome who underwent the hybrid procedure under steady-state conditions. Systolic and diastolic functions significantly decreased after the hybrid procedure, even though patients avoided cardiopulmonary bypass. Results were comparable with prior reports in patients with hypoplastic left heart syndrome who underwent the Norwood procedure.[73]

Prevention by fetal intervention

Fetal echocardiography studies have shown development of hypoplastic left heart syndrome in fetuses initially found to have severe/critical aortic stenosis or absent of markedly restrictive patent foramen ovale. Some data suggest that fetal intervention to relieve aortic valve stenosis (by balloon aortic valvuloplasty) or creation of atrial septal defects (by percutaneous septostomy), both under the guidance of ultrasonography), may promote normal development of the left ventricle or confer benefit following birth.[74, 75] Further research into this type of approach is needed.


Adequate nutrition is important before and after surgery. Many infants require nasogastric feeding with increased-calorie breast milk or formula after the Norwood procedure.[76] Routine insertion of gastrostomy tube in the immediate postoperative period is used in some institutions to provide adequate caloric intake. However, normal oral feeding is reestablished with time. Adequate oral iron intake prevents development of iron deficiency anemia.

After completion of the Fontan operation, specific dietary restrictions are not necessary unless protein-losing enteropathy develops.[45] In such cases, a medium-chain triglyceride diet may be helpful.


Specific activity restrictions are not imposed on children after completion of the Fontan operation. In general, encourage children to participate in activities that they are able to tolerate. Children who underwent a Fontan procedure may not be able to tolerate highly competitive sports.

Studies have shown that these children may have impaired exercise performance when compared to age-matched peers. Perform an exercise stress test when the child is old enough.

Neurodevelopmental abnormalities occur often in patients with hypoplastic left heart syndrome.

Long-Term Monitoring

Note the following:

  • Schedule outpatient follow-up care 2 weeks after discharge in the typical postoperative patient.

  • Schedule those who are S/P cardiac transplantation earlier for necessary laboratory studies.

  • Earlier follow-up care is also necessary if a pericardial effusion is discovered on the discharge echocardiogram.

  • Periodic follow-up visits after stage I, II, and III operations are mandatory. Individualize outpatient follow-up care based on the needs of each patient.

  • Substantial (5-15%) interstage mortality (between stages I and II) is observed.[77] Restrictive atrial communication, obstruction of aortic arch (coarctation), obstructed Blalock-Taussig shunt or Sano shunt, pulmonary artery distortion, and tricuspid valve insufficiency are associated with interstage mortality. In addition, childhood GI or respiratory diseases may produce hypovolemia and/or acute hypoxemia, leading to interstage death.[77] Careful observation, follow-up and home surveillance with optimal nutrition with good growth may decrease interstage mortality.[78, 79] Interstage mortality between stage II (bidirectional Glenn) and stage III (Fontan) is lower that after stage I (Norwood)[80] ; however, follow-up is necessary.



Medication Summary

Before the Norwood procedure or cardiac transplantation in patients with hypoplastic left heart syndrome (HLHS), treat infants with prostaglandin E1 infusion, diuretics, inotropes, and afterload reduction. Drug management after cardiac transplantation is not discussed in this article.

Inpatient medications include the following:

  • Prostaglandin E1

  • Dopamine/dobutamine/milrinone

  • Furosemide (Lasix/Aldactone)

  • Captopril/enalapril

  • Digoxin

  • Potassium chloride

Outpatient medications include the following:

  • Furosemide (Lasix/Aldactone)

  • Captopril/enalapril

  • Digoxin

  • Potassium chloride


Class Summary

Prostaglandin E1 promotes dilatation of the ductus arteriosus in infants with ductal-dependent cardiac abnormalities.

Alprostadil (Prostaglandin E1, Prostin)

Causes relaxation of smooth muscle, primarily within the ductus arteriosus. Used in infants with ductal-dependent congenital heart disease due to restricted systemic blood flow. The drug is also useful in neonates with ductal dependent pulmonary circulation.

Diuretic agents

Class Summary

These agents decrease preload by increasing free-water excretion. Decreasing preload may improve systolic ventricular function.

Furosemide (Lasix)

Loop diuretic that blocks sodium reabsorption in the ascending limb of loop of Henle.

Spironolactone (Aldactone)

This drug is a potassium-sparing loop diuretic.

Cardiac glycosides

Class Summary

These medications improve ventricular systolic function by increasing the calcium supply available for myocyte contraction.

Digoxin (Lanoxin)

This form inhibits the sodium-potassium ATPase pump in cardiac myocytes.

Inotropic agents

Class Summary

These agents stimulate alpha-adrenergic and beta-adrenergic and beta-dopaminergic receptors in the heart and vascular bed.

Dopamine (Intropin)

At lower doses, stimulation of beta1-adrenergic and beta1-dopaminergic receptors results in positive inotropism and renal vasodilatation; at higher doses, stimulation of alpha-adrenergic receptors results in peripheral and renal vasoconstriction.

Dobutamine (Dobutrex)

This drug primarily stimulates the beta1-adrenergic receptor and has less alpha-adrenergic stimulation, leading primarily to increased myocardial contractility.

Afterload-reducing agents

Class Summary

Afterload reduction improves myocardial performance and theoretically reduces atrioventricular and semilunar valve insufficiency.

Captopril (Capoten)

ACE inhibitor, which decreases the production of angiotensin II, a potent vasoconstrictor, resulting in peripheral vasodilatation and afterload reduction, improving myocardial performance and theoretically reducing AV and semilunar valve insufficiency.

Administer a test dose of 0.1 mg PO to assess initial response

Antiplatelet agents

Class Summary

These agents are used in the treatment or prevention of thrombo-occlusive disease mediated by the action of platelets. They inhibit platelet function by blocking cyclooxygenase and subsequent aggregation.

Aspirin (Anacin, Ascriptin, Bayer Aspirin)

Inhibits the enzyme cyclooxygenase that reduces production of thromboxane A2, which is a potent vasoconstrictor and platelet-aggregating agent.

Antiplatelet effects of aspirin last the entire life of the platelet (6-10 d) and are not reversible.