Abstract

The main challenge of aortic coarctation repair in infants is to obtain durable results without morbidity. We aimed to describe predictors of mortality and of arch aortic re-intervention after aortic coarctation repair. Between January 2000 and March 2014, we retrospectively included consecutive infants with isolated coarctation or coarctation with ventricular septal defect (CoA + VSD) who had surgical repair of the aortic arch before three months of age. Five hundred and thirty patients were included: 308 (58%) patients had isolated coarctation and 222 (42%) had CoA + VSD. Three hundred and eighty-five (72.6%) only had coarctation repair, 51 patients (9.6%) had coarctation repair with closure of VSD, and 94 patients (17.8%) had coarctation repair and pulmonary artery banding. Mean age at operation was 13 ± 1.6 days. Mean weight at repair was 3.2 ± 0.75 kg. Median follow-up was 7.57 [0.25–15.98] years. Sixty-one patients (11.5%) needed reintervention on the aortic arch (surgery or endovascular interventions). Freedom from aortic arch reintervention was 90% at one year, and 88.5% at five years. Rates of aortic arch reintervention were similar in the different surgical strategy groups ( P = 0.80). However, in patients receiving prostaglandin E1 (PGE1), the end-to-end repair was at higher risk of re-coarctation compared to the extended end-to-side repair ( P = 0.0081). The risk factors of aortic arch reintervention were age at repair < 15 days ( P = 0.032), and the need for PGE1 infusion at surgery ( P = 0.0072). Overall mortality was 3.6% (19 patients) without significant difference between surgical strategies ( P = 0.078). In multivariate analysis, the risk factors of death were the presence of VSD ( P = 0.037), and low weight at surgery ( P = 0.001). The use of PGE1 may modify the aortic arch anatomy and mask the boundaries of the resection to be performed. Strategies to improve the surgical strategy preoperatively should be developed.

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