Extending the usable size range of homografts in the pulmonary circulation: outcome of bicuspid homografts

Ann Thorac Surg. 2002 Mar;73(3):866-9; discussion 869-70. doi: 10.1016/s0003-4975(01)03559-7.

Abstract

Background: Small-sized homografts are often not available, making the use of surgically reduced cryopreserved homograft conduits appealing.

Methods: From January 1993 to January 2000, 21 large homografts were size-reduced by excising one leaflet and were implanted in the pulmonary circulation. Valve function was compared with 21 children-matched for weight, homograft size, and year of operation-who received a standard homograft.

Results: Implanted homograft size and patient weight were equivalent in both the bicuspid and standard groups. Median (range) in-hospital peak instantaneous echocardiographic gradient across the valve was 0 mm Hg (0 to 19) in the bicuspid group versus 0 mm Hg (0 to 17) in the standard group (p = 0.65). Median (range) in-hospital pulmonary insufficiency (scale of 0 to 4) was 2 (0 to 3) in the bicuspid group versus 1.5 (0 to 3) in the standard group (n = 10, p = 0.34). At a follow-up of 54+/-29 months there was no significant difference in conduit reinterventions between the groups.

Conclusions: Surgical creation of a bicuspid valve in the pulmonary circulation results in a functionally equivalent conduit compared with standard homograft as measured by early and midterm valve function.

MeSH terms

  • Cardiac Surgical Procedures*
  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Mitral Valve / transplantation*
  • Transplantation, Homologous