The St. Jude valve prosthesis: analysis of the clinical results in 815 implants and the need for systemic anticoagulation

J Am Coll Cardiol. 1989 Jan;13(1):57-62. doi: 10.1016/0735-1097(89)90549-4.

Abstract

Between July 1979 and December 1984, 785 patients received 815 St. Jude Medical valve prostheses. Valve-related mortality in the follow-up period was due to thromboembolism in seven cases, anticoagulant-related hemorrhage in three and perivalvular leak in two. Freedom from valve-related death or reoperation at 3 years was 96.4% for aortic valve replacement and 98.3% for mitral valve replacement. The overall rate of thromboembolism was 2.6%/patient-year with warfarin, 9.2%/patient-year with antiplatelet medication and 15.6%/patient-year in patients with no anticoagulant therapy. One episode of thrombotic obstruction of a mitral valve, in a patient receiving no anticoagulant therapy, resulted in an occurrence rate of such obstruction of 0.22%/patient-year. Valve replacement with the St. Jude valve produced excellent clinical results, but long-term anticoagulation with warfarin was required to minimize thromboembolic complications. The use of antiplatelet agents alone provided inadequate protection.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Anticoagulants / adverse effects
  • Anticoagulants / therapeutic use*
  • Evaluation Studies as Topic
  • Female
  • Heart Valve Prosthesis* / adverse effects
  • Heart Valve Prosthesis* / mortality
  • Hemorrhage / chemically induced
  • Humans
  • Male
  • Middle Aged
  • Reoperation
  • Thromboembolism / etiology
  • Thromboembolism / prevention & control
  • Warfarin / therapeutic use

Substances

  • Anticoagulants
  • Warfarin