Intracardiac shunts are abnormal pathways for blood flow in the heart that form either in addition to or in place of normal pathways for blood flow. They are the most common congenital heart defects. Approximately 0.8% to 1.2% of live births worldwide have some type of congenital heart anomaly. Management of a shunt depends on the disease type and ranges from simple clinical observation, medical therapy, lifestyle modification to surgical intervention. This activity reviews the evaluation and treatment of intracardiac shunts and highlights the role of the interprofessional team in evaluating and treating patients with this condition.
Review the etiology of intracardiac shunts.
Explain the evaluation process for finding intracardiac shunts.
Review the management options available for intracardiac shunts
Summarize the importance of collaboration and communication amongst the interprofessional team members to ensure the appropriate selection of candidates for surgical intervention
Intracardiac shunts are abnormal pathways for blood flow in the heart that form either in addition to or in place of normal pathways for blood flow. They are congenital heart defects resulting from abnormal embryologic development. The resultant blood flow is pathological and often causes significant changes in normal physiology. Intracardiac shunts are a spectrum of disorders that could range in presentation from being asymptomatic to fatal. The two big categories of intracardiac shunts are cyanotic and acyanotic. Cyanotic shunts impair oxygenation of blood by the pulmonary system and result in cyanosis. Acyanotic shunts do not impair blood flow to the lungs, and the process of oxygenation is intact. Following are different types of acyanotic and cyanotic shunts.
Cyanotic shunts: Tetralogy of Fallot, truncus arteriosus, total anomalous pulmonary venous return (TAPVR), pulmonary atresia with ventricular septal defect, tricuspid atresia, hypoplastic left heart syndrome, transposition of great arteries, double-outlet right ventricle
The prevalence of different types of these shunts is shown in the pie chart.
The etiology of Intracardiac shunt formation is multifactorial and is a combination of genetic and external factors. Genetic factors include chromosomal deletions, trisomies, and single-gene mutations. For example, 40 to 50% of those born with trisomy 21 or Down syndrome have ASD, VSD, TOF, or TGA. Maternal factors that increase the risk for intracardiac shunt formation are pregestational diabetes, marijuana use, rubella, ibuprofen, influenza, febrile illness, and vitamin A exposure.
Intracardiac shunts are the most common congenital heart defects. One in eight newly born infants worldwide has some type of congenital heart anomaly. The prevalence of congenital heart defects varies with geography. Asia has the highest prevalence, with 9.3 cases reported for every 1,000 live births, and the least prevalence was noticed in Africa, with 1.3 cases reported for every 1,000 live births. North America has 6.9 cases per 1,000 live births. The difference in prevalence could also be attributed to the better availability of diagnostic modalities in certain parts of the world than others. In the US, the prevalence of congenital heart defects is slightly higher in whites and Hispanics than in the black population. Overall, female predominance was seen in the US, with 8.03 females affected compared to 7.67 males for every 1,000 live births. Due to the invention of better medical and surgical therapies, the survival of patients with congenital heart diseases is increasing, which also increases their prevalence in the adult population.
Intracardiac shunts are anatomic defects that occur from derangements in the embryologic development of the heart, mainly in the first trimester of pregnancy. Fetal heart development occurs from the mesoderm. It is a complex process where a single heart tube is initially formed, which later develops into four chambers with separate inflow and outflow tracts by processes like cell migration and looping of the structures. Incomplete separation of right and left-sided structures leads to defects like ASD, VSD, and PDA. Since left-sided cardiac pressures are higher, defects in atrial or ventricular septums or patency of ductus arteriosus lead to blood shunting into the right side where pressures are lower. Since all deoxygenated blood from systemic circulation makes its way to the lungs, oxygenation is not a problem. Shunting only sends additional blood into the lungs; this blood is already oxygenated. Therefore, these lesions are called acyanotic shunts.
Small defects can close by themselves with time; however, larger defects can require surgical intervention at times. Left to right shunts are often asymptomatic in childhood; however, symptoms can appear by adolescent and adult age. Presentation often includes shortness of breath, exercise intolerance, and easy fatigability. In these defects, the right side of the heart receives more blood, which causes pulmonary hypertension over time in some patients. A rare complication of these shunts is Eisenmenger syndrome, in which shunt reversal occurs due to severe pulmonary hypertension to the point that right-sided pressures exceed left-sided pressures. This syndrome causes cyanosis and carries a high mortality.
The other group of intracardiac shunts is called cyanotic shunts. In these disorders, there are anatomic defects that impede the flow of deoxygenated blood to the lungs. Oxygenation is impaired in these disorders, and partial pressure of oxygen in arterial circulation is low. Tissues do not get enough oxygen supply, and characteristic bluish discoloration of the skin called cyanosis is seen. Cyanotic lesions are associated with significant morbidity and mortality and typically present early after the birth; however, small lesions could be minimally acyanotic or even completely asymptomatic at first. Symptoms include cyanosis, clubbing of fingers and toenails, dyspnea, poor weight gain, hemoptysis, and recurrent infections.  A classic phenomenon historically seen in patients with cyanotic spells was squatting, which increases systemic vascular resistance, thereby increasing pulmonary flow. This improves oxygen and relieves symptoms. Squatting is not seen as common now due to early diagnosis and improved therapeutic interventions.
History and Physical
Congenital disorders are present at the time of birth, and history is often not practicable. However, history is important as a child grows up and can talk. When possible, patients should be asked for clinical symptoms, including dyspnea, exercise capacity, recurrent infections, skin discoloration, hemoptysis, presyncope or syncope, and pedal edema. Physical examination is critical and often is the only indication of the disease. It should include thorough inspection, palpation, and auscultation. Inspection should particularly be done for cyanosis, nail clubbing, growth stunting, jugular venous distension, pedal edema, and breathing difficulty. Palpation should be done to notice any thrill, heave, or displacement of the apex beat.
Characteristic murmurs are present in different types of shunts at different locations, which aid in diagnosis. Typical murmurs heard are fixed widely split S2 with ejection systolic murmur at the pulmonary area in ASD, holosystolic murmur at the left lower sternal border in VSD, and continuous machinery murmur in PDA. The murmur in TOF would be due to the pulmonic stenosis and not due to the concomitantly present VSD, and systolic ejection sound will be heard at the left upper sternal border. Murmurs can often be unclear, and a formal echocardiogram should be obtained to evaluate a pathological murmur.
After the initial history and physical examination, further workup should be done as warranted. The extent of evaluation for intracardiac shunts depends on a case-by-case basis and could include blood testing, EKG, echocardiogram, chest x-ray, CT scan, and cardiac catheterization. EKG could indicate signs of pulmonary hypertension from right ventricular hypertrophy (RVH), right axis deviation, and right atrial enlargement. RVH shows tall R wave in V1, dominant S wave in leads V5 and V6 and can also produce p pulmonale and right ventricular strain pattern on EKG that could be evidenced by ST depressions and T wave inversions in the right precordial (V1-V4) and inferior (II, III, aVF) leads.
A chest X-ray could show characteristic heart shapes in different defects. TOF could make the heart boot-shaped on CXR, TAPVR could show a snowman-shaped heart, and TGA could give an "egg-on-string" appearance to the heart. Blood work could show reactive polycythemia in cyanotic defects indicating the severity of hypoxemia. Cardiac catheterization is not typically needed for diagnostic purposes; however, it should be done once the surgical intervention is planned. It gives accurate pressures in heart chambers. Induction of oxygen or nitric oxide could be done in the pulmonary system to see vascular reactivity, which could help decide if the patient is a candidate for surgical intervention or pulmonary vasodilator therapy.
Treatment / Management
Management of a shunt depends on the disease type and ranges from simple clinical observation, medical therapy, lifestyle modification to surgical intervention. Small noncyanotic shunts can often be clinically observed. Large left to right shunts do need closure to avoid the development of complications. Cyanotic shunts are associated with higher morbidity and mortality and often require surgical intervention for correction. For example, TOF needs surgical intervention, which is often done in stages. In the first phase, a connection is created between the subclavian artery and the pulmonary artery called the Blalock-Tussing shunt.
Some surgeons choose not to perform this procedure anymore and directly proceed to the next steps. In the second phase, the superior vena cava is connected to the right pulmonary artery via Glenn shunt. In the third phase, the inferior vena cava is connected to the pulmonary artery in a Fontan procedure. In cyanotic conditions, vessel thrombosis could occur due to increased hematocrit from reactive polycythemia. Phlebotomy is done on a case by case bases to correct the hematocrit. For female patients desiring to get pregnant, a discussion should be held with an obstetrician prior to conception to discuss the plans. Some disorders are associated with high obstetric mortality, and pregnancy is not advised.
Careful evaluation should be done as clinical features overlap between different types of intracardiac shunts and can also mimic extracardiac disease processes. Cyanotic intracardiac shunts could mimic pulmonary, neurologic, and infectious diseases. Transient tachypnea of newborn, bronchopulmonary dysplasia, pulmonary hypoplasia, laryngotracheomalacia, vocal cord paralysis, neonatal myasthenia gravis, spinal muscular atrophy, infantile botulism, and pneumonia should be considered in the differential diagnosis.
Prognosis depends on the particular type of shunt. Noncyanotic shunts carry remarkably better prognosis over cyanotic shunts. Small lesions can often close spontaneously or could remain asymptomatic for life. Large lesions need closure to avoid complications. Once severe pulmonary hypertension has developed, the prognosis worsens, and heart-lung transplantation is often warranted, which is not widely available. Severe cyanotic lesions present soon after the birth, and often there is no chance of survival without timely surgical intervention.
Complications of intracardiac shunts include failure to thrive, recurrent infections, pulmonary hypertension, right heart failure, Eisenmenger syndrome, infective endocarditis, dysrhythmias, and death. However, not all shunts result in complications, and most are benign.
Deterrence and Patient Education
Intracardiac shunts are caused by a combination of modifiable and nonmodifiable factors. Prior to conception, family physicians and obstetricians should counsel the mothers about safe prenatal approaches to minimize the incidence of such diseases. These approaches include but are not limited to better control of diabetes, avoiding teratogenic substances like retinoids and ibuprofen, and steering clear of recreational drugs. As kids grow into adolescence and start understanding things, they should be educated about their conditions compassionately and realistically.
Enhancing Healthcare Team Outcomes
Managing intracardiac shunts requires an interprofessional team approach; while pediatricians and cardiologists are mostly at the frontlines for the diagnosis and treatment plans, it is important to consult with multiple disciplines including cardiothoracic surgeons, physical therapists, bedside nursing staff, and psychologists to improve overall outcomes, patient safety, and enhance team performance. Diagnostic studies are required for both diagnosis and operative planning. This requires EKG, echocardiogram, chest X-ray, CT scan, and cardiac catheterization, comprising a coordinated effort between multiple teams. This ultimately results in more accurate diagnoses, better surgical outcomes, and more patient and family satisfaction.
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Birth prevalence of CHDs. Please insert this in introduction part of the article.
Contributed by Rai Dilawar Shahjehan, MD, MBBS
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