Aprotinin improves outcome of single-ventricle palliation

Ann Thorac Surg. 1996 Nov;62(5):1329-35; discussion 1335-6. doi: 10.1016/0003-4975(96)00670-4.

Abstract

Background: Elevation of pulmonary vascular resistance as a consequence of cardiopulmonary bypass may lead to failure of single-ventricle palliation. We reviewed our experience with aprotinin, a nonspecific serine protease inhibitor, to determine whether it could ameliorate the inflammatory effects of cardiopulmonary bypass and improve outcome of single-ventricle palliation.

Methods: Forty-six consecutive patients undergoing single-ventricle palliation using cardiopulmonary bypass were reviewed retrospectively. Aprotinin was used in 8 of 30 bidirectional cavopulmonary shunt and 10 of 16 Fontan procedures.

Results: Aprotinin use was associated with a decrease in the early postoperative transpulmonary gradient among patients undergoing Fontan and bidirectional cavopulmonary shunt procedures. The bidirectional cavopulmonary shunt aprotinin group had a higher oxygen saturation and a decrease in quantity and duration of thoracic drainage. Among patients receiving aprotinin there were no episodes of mediastinitis, thrombus formation, or renal failure.

Conclusions: Aprotinin use in single-ventricle palliation was associated with decreased transpulmonary gradient and increased oxygen saturation consistent with decreased pulmonary vascular resistance. This retrospective study suggests that aprotinin has a favorable impact on the early postoperative course of single-ventricle palliation.

MeSH terms

  • Aprotinin / therapeutic use*
  • Child
  • Child, Preschool
  • Combined Modality Therapy
  • Congenital Abnormalities / drug therapy
  • Congenital Abnormalities / surgery
  • Heart Bypass, Right / adverse effects*
  • Heart Ventricles / abnormalities*
  • Humans
  • Infant
  • Palliative Care*
  • Postoperative Care
  • Pulmonary Circulation
  • Retrospective Studies
  • Serine Proteinase Inhibitors / therapeutic use*
  • Treatment Outcome
  • Vascular Resistance

Substances

  • Serine Proteinase Inhibitors
  • Aprotinin