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Encyclopedia of Health and Medicine

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congenital heart disease 39<br />

term treatment is HEART TRANSPLANTATION. The most<br />

frequently occurring <strong>of</strong> these grave malformations<br />

are<br />

• Tetralogy <strong>of</strong> Fallot, which is a complex <strong>of</strong> four<br />

structural anomalies: VSD, pulmonary artery<br />

<strong>and</strong> valve malformation, aortic displacement<br />

(the aorta arises between the ventricles rather<br />

than solely from the left ventricle), <strong>and</strong> hypertrophic<br />

left ventricle (thickening <strong>of</strong> the left ventricle’s<br />

wall).<br />

• Transposition <strong>of</strong> the great arteries (TGA), in<br />

which the aorta <strong>and</strong> the pulmonary artery are<br />

switched. The aorta arises from the right ventricle<br />

instead <strong>of</strong> the left, carrying the deoxygenated<br />

blood from the right ventricle out to<br />

the body. The pulmonary artery arises from the<br />

left ventricle instead <strong>of</strong> the right, taking oxygenated<br />

blood back to the lungs from the left<br />

ventricle.<br />

• Hypoplastic (or hypotrophic) left heart syndrome<br />

(HLHS), in which the left ventricle or<br />

the entire left heart fails to develop, resulting in<br />

essentially a two-chamber heart. The aorta is<br />

usually small or deformed. Blood in the heart is<br />

a mix <strong>of</strong> oxygenated <strong>and</strong> deoxygenated, <strong>and</strong><br />

the right ventricle pumps to both the lungs <strong>and</strong><br />

the body.<br />

• Persistent truncus arteriosus, which is a combination<br />

<strong>of</strong> VSD <strong>and</strong> deformities <strong>of</strong> the PULMONARY<br />

ARTERIES <strong>and</strong> aorta that disrupts the heart’s ability<br />

to pump oxygenated blood to the body.<br />

• Anomalous pulmonary venous return, in<br />

which the PULMONARY VEINS attach to the right<br />

atrium instead <strong>of</strong> the left atrium, returning<br />

oxygenated blood to the same chamber that<br />

pumps deoxygenated blood to the lungs. This<br />

malformation typically occurs in combination<br />

with ASD, so the flow <strong>of</strong> blood between the<br />

atria moves some oxygenated blood into the<br />

left atrium <strong>and</strong> subsequently the left ventricle.<br />

Often, ULTRASOUND during PREGNANCY reveals<br />

these significant heart deformities, allowing the<br />

neonatal team to be prepared for them at the<br />

infant’s birth. In many situations initial treatment<br />

includes administering PROSTAGLANDINS to maintain<br />

a patent ductus arteriosus, which allows some<br />

oxygenated blood into the body’s circulation.<br />

Congenital heart disease in adults Some forms<br />

<strong>of</strong> congenital heart disease first manifest in adulthood,<br />

such as hypertrophic cardiomyopathy <strong>and</strong><br />

LQTS. Other forms <strong>of</strong> heart disease in adults may<br />

have congenital origins, such as the ARRHYTHMIA<br />

disorder WOLFF-PARKINSON-WHITE SYNDROME <strong>and</strong><br />

some VALVULAR HEART DISEASE. Cardiologists believe<br />

that most situations <strong>of</strong> SUDDEN CARDIAC DEATH<br />

reflect undetected congenital heart anomalies,<br />

either structural or functional (arrhythmias). With<br />

congenital heart disease, whether undetected or<br />

previously treated, comes increased risk for ENDO-<br />

CARDITIS (especially with valve malformations),<br />

arrhythmias, <strong>and</strong> clot formation leading to HEART<br />

ATTACK, STROKE, or PULMONARY EMBOLISM.<br />

A growing number <strong>of</strong> adults had corrective surgery<br />

for congenital heart disease as infants or children.<br />

Cardiologists do not yet know the long-term<br />

effects <strong>of</strong> these operations or what precautions are<br />

necessary to protect cardiovascular health later in<br />

life. The generation born in the 1970s was the first<br />

to have these options available. As this generation<br />

comes into middle age, cardiologists will learn<br />

much about how repaired hearts accommodate the<br />

routine cardiovascular stresses <strong>of</strong> life <strong>and</strong> whether<br />

they are more susceptible to acquired forms <strong>of</strong><br />

heart disease such as CORONARY ARTERY DISEASE (CAD)<br />

<strong>and</strong> HEART FAILURE. At present, the longest survival<br />

<strong>of</strong> infant heart transplantation is 15 years <strong>and</strong> <strong>of</strong><br />

adolescent heart transplantation is 16 years.<br />

Rejection <strong>of</strong> the donor heart remains a significant<br />

concern, <strong>and</strong> most cardiologists expect retransplantation<br />

will become necessary for most people who<br />

receive heart transplants in infancy or childhood.<br />

Symptoms <strong>and</strong> Diagnostic Path<br />

The most common symptoms <strong>of</strong> congenital heart<br />

disease, notably malformations <strong>of</strong> the heart, in<br />

newborns is cyanosis <strong>and</strong> difficulty BREATHING.<br />

Congenital heart disease not immediately apparent<br />

at birth may manifest later in childhood with<br />

symptoms such as fainting with physical exertion,<br />

shortness <strong>of</strong> breath with mild activity, slowed<br />

growth, rapid heartbeat <strong>and</strong> respirations, <strong>and</strong> frequent<br />

upper respiratory infections. Young children<br />

experiencing shortness <strong>of</strong> breath <strong>of</strong>ten squat,<br />

which makes it easier for them to breathe.

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