Cryopreserved allograft repair of aortic hypoplasia and interrupted aortic arch

Ann Thorac Surg. 1992 Jun;53(6):1110-3. doi: 10.1016/0003-4975(92)90402-p.

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.

Publication types

  • Case Reports

MeSH terms

  • Aorta, Thoracic / abnormalities*
  • Aorta, Thoracic / surgery
  • Aortic Valve / transplantation*
  • Cryopreservation*
  • Heart Defects, Congenital / surgery
  • Humans
  • Infant, Newborn
  • Male
  • Methods
  • Palliative Care
  • Reoperation