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Published on: May 26, 2023
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.
Objectives:
The purpose of this multi-institutional study was to review the 15-year outcome of patients who received isolated aortic or mitral valve replacement with the Hancock II bioprosthesis.
Methods:
From 1983 through 2002, 1274 patients underwent 1293 isolated valve replacements, 809 aortic valve replacements and 484 mitral valve replacements, at hospitals in the Venetian area (Padova, Treviso, and Venice). Mean age was 68 +/- 8 years in patients undergoing aortic valve replacement and 66 +/- 9 years in patients undergoing mitral valve replacement; 52% of patients undergoing aortic valve replacement and 63% of patients undergoing mitral valve replacement were in New York Heart Association class III or greater. Coronary artery disease was present in 32% of patients who had undergone aortic valve replacement and 18% of patients who had undergone mitral valve replacement. Follow-up included 8520 patient-years, with a median of 12 years, and was 97% complete.
Results:
Overall 15-year survival was 39.7% +/- 2.4%, similar in both the aortic and mitral positions. Multivariable analysis of late survival showed the incremental risk of male sex, higher New York Heart Association class, coronary artery disease, and mitral position. Freedom from embolism was higher in the aortic position (81% +/- 2.9% in aortic vs 72% +/- 4.7% in mitral valve replacements). Freedom from endocarditis was similar in the aortic and mitral position (95% +/- 1.2% vs 94% +/- 1.7%). Freedom from reoperation (82% +/- 3.7% vs 71% +/- 5.0%) and from valve-related morbidity-mortality (52% +/- 3.6% vs 36% +/- 4.4%) was higher in patients who had undergone AVR. Actual freedom from structural valve deterioration for patients 60 years and older who had undergone aortic valve replacement was 96.5% +/- 1.3% versus 88% +/- 3.2% for patients who had undergone mitral valve replacement and 70% +/- 7.5% versus 77.5% +/- 5.3%, respectively, in younger patients. Multivariable Weibull analysis showed structural valve deterioration related to younger age and preoperative valve incompetence and inversely related to coronary artery disease.
Conclusion:
Optimal 15-year durability can be expected in male patients 60 years and older who have undergone aortic valve replacement and in male patients 65 years and older who have undergone mitral valve replacement, extending safely the age limits for the use of this valve.
