Experience with 813 aortic or mitral valve replacements with the Carpentier-Edwards bioprosthesis: Five year results

European Heart Journal
|October 1, 1984
PubMed

Insights

The Carpentier-Edwards bioprosthesis demonstrated favorable outcomes in 813 patients undergoing aortic (AVR) and mitral valve replacement (MVR). Low rates of thromboembolism and tissue failure suggest bioprosthetic valves are a viable option for long-term cardiac health.

Area of Science:

  • Cardiovascular Surgery
  • Biomedical Engineering
  • Prosthetic Heart Valves

Background:

  • Bioprosthetic heart valves are crucial for treating valvular heart disease.
  • The Carpentier-Edwards bioprosthesis has been widely used, necessitating long-term outcome evaluation.
  • Understanding complication rates and survival is vital for patient selection and management.

Purpose of the Study:

  • To assess the long-term efficacy and safety of the Carpentier-Edwards bioprosthesis.
  • To evaluate operative mortality, late survival, and complication rates (thromboembolism, bleeding, valve failure) after aortic valve replacement (AVR) and mitral valve replacement (MVR).

Main Methods:

  • Retrospective analysis of 813 patients who received Carpentier-Edwards bioprosthetic valves between 1976 and 1983.
  • Classification of late mortality and complications using Stanford Group criteria.
  • Actuarial survival analysis and calculation of complication rates per patient-year (pt yr).

Main Results:

  • Operative mortality: 5.49% for AVR, 4.59% for MVR.
  • 5-year actuarial survival: 87.9% +/- 2.7% for AVR, 91.1% +/- 1.4% for MVR.
  • Low rates of thromboembolism (0.48% pt yr AVR, 0.90% pt yr MVR) and valve failure (2.04% pt yr AVR, 1.55% pt yr MVR) were observed.
  • Reoperation rates for tissue failure were low (0.24% pt yr AVR, 0.32% pt yr MVR).

Conclusions:

  • The Carpentier-Edwards bioprosthesis offers a favorable balance of low thromboembolic events and acceptable valve failure rates at 5 years.
  • The benefits of reduced thromboembolism outweigh the specific risks associated with bioprosthetic valves in this cohort.
  • These findings support the continued use of bioprosthetic valves in selected patients requiring aortic and mitral valve replacement.

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