Surgical management of aortopulmonary window associated with interrupted aortic arch: A Congenital Heart Surgeons Society study

Igor Konstantinov, T. Karamiou, W.G. Williams, J.M. Quaegebeur, P.J. Del Nido, T.L. Spray, C.A. Caldarone, E.H. Blackstone, B.W. Mccrindle

    Research output: Contribution to journalArticlepeer-review

    67 Citations (Scopus)

    Abstract

    ObjectiveThe objective was to determine outcomes and risk factors of surgical management of patients with aortopulmonary window associated with interrupted aortic arch.MethodsFrom 1987 to 1997, 472 neonates with interrupted aortic arch were enrolled prospectively from 33 institutions. Associated aortopulmonary window was present in 20 patients. Competing risk methodology determined the prevalence of reintervention for postrepair pulmonary artery and aortic arch obstruction.ResultsInterrupted aortic arch was type A in 17 patients and type B in 3 patients. Aortopulmonary window morphology was type I (n = 10), type II (n = 5), and type III (n = 5). Associated cardiovascular anomalies were common, including atrial septal defect (n = 13) and systemic venous anomalies (n = 3). Overall survival after initial admission was 91%, 86%, and 84% at 1, 5, and 10 years, respectively. Fifteen patients underwent single-stage repair, and 4 patients underwent staged repair. There was an increased prevalence of patch augmentation of the interrupted aortic arch anastomosis in lower-weight infants (2.3 kg vs 3.1 kg, P = .07). Competing risk analysis estimated that 5 years after repair, 51% had initial arch reintervention, 6% had initial pulmonary artery reintervention, and 43% were alive without reintervention. Reintervention for arch obstruction was more likely for those with interrupted aortic arch type B (P = .08) and for those with higher weight at initial repair (P = .003).ConclusionsComplete correction of aortopulmonary window in the setting of interrupted aortic arch can be performed with low mortality in the neonatal period. Reinterventions for aortic arch obstruction are the most frequent complication after repair, but pulmonary artery stenosis also occurs. Use of patch augmentation may reduce the need for subsequent arch reintervention.
    Original languageEnglish
    Pages (from-to)1136-1141
    JournalThe Journal of Thoracic and Cardiovascular Surgery
    Volume131
    Issue number5
    DOIs
    Publication statusPublished - 2006

    Fingerprint

    Dive into the research topics of 'Surgical management of aortopulmonary window associated with interrupted aortic arch: A Congenital Heart Surgeons Society study'. Together they form a unique fingerprint.

    Cite this