Fifteen-year results with the Hancock II valve: a multicenter experience

Giulio Rizzoli1, Salvatore Mirone, Paolo Ius

  • 1Cardiac Surgery Unit, Ca Foncello Hospital of Treviso, Treviso, Italy. giulio.rizzoli@unipd.it

Insights

The Hancock II bioprosthesis shows good 15-year durability, especially in older male patients undergoing aortic or mitral valve replacement. This valve extends safe age limits for cardiac surgery.

Area of Science:

  • Cardiovascular Surgery
  • Bioprosthetic Valves
  • Cardiac Valve Replacement

Background:

  • The Hancock II bioprosthesis is a widely used option for aortic and mitral valve replacement.
  • Long-term outcomes data are crucial for guiding clinical decision-making in valve surgery.

Purpose of the Study:

  • To evaluate the 15-year clinical outcomes and durability of the Hancock II bioprosthesis in isolated aortic valve replacement (AVR) and mitral valve replacement (MVR).

Main Methods:

  • A multi-institutional review of 1293 isolated AVR/MVR procedures performed between 1983 and 2002.
  • Analysis included 8520 patient-years of follow-up, with a median of 12 years and 97% completeness.
  • Multivariable analyses were used to identify predictors of survival and valve-related events.

Main Results:

  • Overall 15-year survival was 39.7%. Male sex, higher NYHA class, coronary artery disease, and mitral position were associated with increased mortality risk.
  • Freedom from embolism was higher for AVR (81%) than MVR (72%). Freedom from endocarditis was similar for both positions (approx. 95%).
  • Freedom from reoperation and valve-related morbidity-mortality was better for AVR than MVR. Structural valve deterioration was lower in older patients (≥60 years) and inversely related to coronary artery disease.

Conclusions:

  • The Hancock II bioprosthesis demonstrates optimal 15-year durability in male patients aged 60+ for AVR and 65+ for MVR.
  • These findings support extending the safe age limits for using this bioprosthesis.
  • Patient age, sex, and comorbidities influence long-term outcomes of Hancock II valve replacement.
Abstract