Cryopreserved allograft repair of aortic hypoplasia and interrupted aortic arch.

St Cyr, J A; Campbell, D N; Fullerton, D A; Grosso, M; Bishop, D A; Clarke, D R · Ann Thorac Surg · 1992

case_report · Level V

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Abstract

Mortality for interruption of the aortic arch approaches 100% within the first year of life if untreated. Prostaglandin E1 can stabilize the patient's condition in anticipation of surgical palliation, but total repair is required for long-term survival. Successful complete repair of type B interrupted aortic arch, hypoplasia of the left ventricular outflow tract, and ventricular septal defect was possible using a cryopreserved allograft in a child who previously had undergone unusual palliation.

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