Key result
Severe prosthesis-patient mismatch after mitral valve replacement was associated with significantly lower 60-month survival (55.9%) compared to patients with no mismatch (89.5%, p=0.043).
Why the study?
Does severe prosthesis-patient mismatch after mitral valve replacement increase long-term all-cause mortality in patients receiving mechanical or bioprosthetic valves?
Cohort (n=136)
No
Does severe prosthesis-patient mismatch after mitral valve replacement increase long-term all-cause mortality in patients receiving mechanical or bioprosthetic valves?
Absolute Event Rate: 55.9% vs 89.5%
p-value: p=0.043
Severe prosthesis-patient mismatch after mitral valve replacement, which occurs predominantly with bioprosthetic valves, is associated with significantly reduced 5-year survival, highlighting the importance of preoperative sizing strategies.
May warrant optimized sizing to avoid severe mismatch in mitral replacement; leaves open causal impact on mortality.
BACKGROUND: The aim was to assess the incidence of prosthesis-patient mismatch (PPM) after mitral valve replacement (MVR) in patients receiving Biocor® porcine or mechanical valves, and to evaluate the effect of PPM on long-term survival. METHODS: All patients undergoing MVR between 2009 and 2013 received either mechanical or bioprosthetic valves (Biocor® porcine). PPM was defined as severe when the indexed effective ori-fice area was < 0.9 cm2/m2, moderate between 0.9 cm2/m2 and 1.2 cm2/m2 or absent > 1.2 cm2/m2. The primary endpoint was all-cause long-term mortality. RESULTS: Among a total of 136 MVR, PPM was severe in 27%, moderate in 44% and absent in 29% of patients. Implanted valves were 57% mechanical and 43% bioprosthetic. Only 3% of patients with mechanical valves had severe PPM vs. 59% with bioprostheses (p < 0.0001). Sixty-month survival with severe mismatch was 0.559 (SE 0.149) and with no mismatch 0.895 (SE 0.058) (p = 0.043). Survival of patients suffering from severe mismatch, or moderate mismatch with pulmonary hypertension (PH) was 0.749 (SE 0.101); while for patients with no mismatch or with moderate mismatch without PH, survival was 0.951 (SE 0.028) (p = 0.016). CONCLUSIONS: About one-fourth of patients had severe PPM and almost all of them had received a bioprosthesis. Sixty-month survival was significantly lower in patients with severe mismatch, or moderate mismatch with PH. Specifically, when a bioprothesis is chosen and while further evidence on the impact of PPM on clinical outcomes appears, surgeons are recommended to follow a preoperative strategy to implant a mitral prosthesis of adequate size in order to prevent PPM.
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Borracci et al. (2016) conducted a cohort in Valvular heart disease requiring mitral valve replacement (n=136). Severe prosthesis-patient mismatch vs. No prosthesis-patient mismatch was evaluated on All-cause long-term mortality (assessed via 60-month survival) (p=0.043). Severe prosthesis-patient mismatch after mitral valve replacement was associated with significantly lower 60-month survival (55.9%) compared to patients with no mismatch (89.5%, p=0.043).
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