Pediatric cardiology
Management of symptomatic infants with anomalous origin of the left coronary artery from the pulmonary artery

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Abstract

There is disagreement concerning the optimal management of infants with congestive heart failure due to anomalous origin of the left coronary artery from the pulmonary artery. This report describes treatment in 23 such patients who had congestive heart failure before age 6 months. Eight patients had an operation in the 1st year of life and only two (25 percent) of these patients survived. Fifteen patients received initial medical treatment, and operation was delayed until an average age of 7.5 years; 13 (87 percent) of these patients survived. The two patients who survived early operation are still alive at an average age of 2.5 years. The 13 survivors in the medical group are still alive at an average age of 14.5 years. The age at onset and the severity of congestive heart failure were similar in the two groups. The frequency of the electrocardiographic pattern of myocardial infarction was similar in both groups. The radiographic cardiothoracic ratio was 0.74 in the surgical and 0.66 in the medical group. In 10 patients the left ventricular ejection fraction was less than 20 percent in the 1st year of life. In 7 of these 10 patients operation was performed before age 1 year and 2 (28 percent) survived; of the 3 patients treated medically, 1 (33 percent) survived.

The outcome of surgical or medical treatment of the infant with anomalous origin of the left coronary artery from the pulmonary artery may be biased by patient selection. In the infants with depressed left ventricular function, the results of surgical and medical treatment are equally disappointing. Because coronary arterial surgery in the 1st year of life in infants with severely depressed myocardial function has an extremely high mortality rate (75 percent) and because many symptomatic infants with anomalous origin of the left coronary artery from the pulmonary artery can be treated medically and survive, we recommend delay of operative intervention until at least age 18 months.

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This study was supported in part by Grant HL-07190 from the National Institutes of Health, U.S. Public Health Service, Washington, D.C., and by U.S. Public Health Grant RR-00188 from the General Clinical Research Branch, National Institutes of Health, Bethesda, Maryland.

Recipient of Young Investigator's Award HL62230-9-01 from the National Heart, Lung, and Blood Institute, Bethesda, Maryland.

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