Long-term follow-up of patients after coarctation of the aorta repair

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Abstract

Late cardiovascular complications after operative repair of coarctation of the aorta include systemic hypertension, premature coronary artery disease, aortic valve abnormalities, aortic aneurysm, and recoarctation. We report the outcome in 274 subjects ≥50 years after coarctation repair. Operative repair of simple coarctation was performed on 274 patients at the University of Minnesota Hospital between 1948 and 1976. Twenty patients (7%) died in the immediate postoperative period. Of the 254 survivors, 2 were lost to follow-up, 45 (18%) died at a mean age of 34 years, and 207 (81%) were alive ≥50 years after the original operation. Coronary artery disease and perioperative deaths at the time of a second cardiac operation accounted for 17 of the 45 late deaths. Predictors of survival were age at operation and blood pressure at the first postoperative visit. Of the 207 long-term survivors, 92 (48%) participated in a clinical cardiovascular evaluation. Thirty-two of the 92 subjects had systemic hypertension that was predicted by age at operation, blood pressure at the first postoperative visit, and paradoxic hypertension at operative repair. New cardiovascular abnormalities detected at follow-up evaluation included evidence of a previous myocardial infarction, cardiomyopathy, atrial fibrillation, moderate to severe left ventricular outflow tract obstruction, moderate aortic valve regurgitation, recoarctation, and ascending aortic dilation. Thus, long-term survival is significantly affected by age at operation, with the lowest mortality rates observed in patients who underwent surgery between 1 and 5 years of age. More than 1/3 of the survivors developed significant late cardiovascular abnormalities.

Section snippets

Methods

Two hundred seventy-four patients had operative repair of simple coarctation of the aorta at the University of Minnesota between 1948 and 1976. Simple coarctation is defined as an isolated coarctation of the aorta with or without a patent ductus arteriosus or a bicuspid aortic valve and without other cardiac malformations. Twenty patients (7%) died during the immediate postoperative period. Two of the 254 survivors (0.8%) were lost to follow-up. A retrospective analysis including survival

Results

Mean age at follow-up of the 252 long-term survivors (groups I, II, and III) was 40.1 ± 10.3 years (median 38.8, range 23.7 to 62.8). Mean age at diagnosis was 7.8 ± 9.3 years (median 5, range 0 to 41). Mean age at time of operation was 10.3 ± 9.5 years (median 7.3, range 0 to 41.5). Forty-seven patients (23%) were <1 year old at the initial operation, and 31 patients (11%) were >20 years old.

Operative correction was performed by resection and end-to-end anastomosis in 92% of the patients.

Discussion

Several long-term studies following coarctation repair2, 3, 4, 5, 6, 7, 8 have helped identify the most common late cardiovascular complications, but these studies have underestimated the prevalence of silent cardiovascular lesions or concomitant cardiac abnormalities. In addition to evaluating retrospective and questionnaire data, we also evaluated a group of 92 subjects who had undergone coarctation repair >20 years previously.

An undiagnosed cardiovascular abnormality was identified in 35 of

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  • Cited by (0)

    This study was supported by the Viking’s Children Fund and Grant MO1-RR-00400 from the National Center for Research Resources, Minneapolis, Minnesota.

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