Key result
MVP cuts early mortality ~37% and improves long-term survival versus MVR in RHD.
Why the study?
Clinical outcomes of rheumatic mitral valve repair remain controversial, particularly regarding reoperation rates.
Does mitral valve repair improve clinical outcomes and reduce reoperation rates compared to mitral valve replacement in patients with rheumatic heart disease?
Meta-Analysis (n=12,405)
Does mitral valve repair improve clinical outcomes and reduce reoperation rates compared to mitral valve replacement in patients with rheumatic heart disease?
Odds Ratio: 0.63 (95% CI 0.5–0.78)
p-value: p=<0.001
In patients with rheumatic heart disease, mitral valve repair offers superior survival and fewer complications compared to replacement, and the historically higher reoperation rates associated with repair have equalized since 2010.
Supports MVP selection in rheumatic disease when durable; extends meta-analyses but leaves RCTs needed for reoperation guidance.
Background: The clinical outcomes of rheumatic mitral valve repair (MVP) remain controversial, particularly regarding reoperation rates. Therefore, we conducted a meta-analysis to comprehensively and systematically evaluate clinical outcomes, with a focus on reoperation rates. Methods: PubMed, EMBASE, Web of Science, and the Cochrane Library were searched for articles and abstracts published from 1 January 1990 to 21 September 2023, to compare the clinical outcomes of MVP versus mitral valve replacement (MVR) in patients with rheumatic heart disease (RHD). Results: After screening the titles and abstracts of 2703 articles, a total of 165 articles were reviewed. A total of 20 articles met the inclusion criteria, comprising 4492 MVP and 7913 MVR cases. MVP was associated with lower early mortality (odds ratio (OR): 0.63, 95% confidence interval (CI): 0.50–0.78; p < 0.001) and long-term mortality (OR: 0.57, 95% CI: 0.42–0.77; p < 0.001), as well as reduced rates of thromboembolism (OR: 0.58, 95% CI: 0.46–0.74; p < 0.001), bleeding (OR: 0.70, 95% CI: 0.55–0.89; p = 0.004), and heart failure (OR: 0.28, 95% CI: 0.12–0.67; p = 0.004). There were no significant differences between groups in the incidence of infective endocarditis (p = 0.786), stroke (p = 0.503), or atrial fibrillation (p = 0.180). To analyze reoperation rates more objectively, studies were stratified by surgical era into three subgroups. The risk of reoperation after MVP was high before 2000 (OR: 3.67, 95% CI: 1.98–6.78; p < 0.001). However, from 2000 to 2010, the risk of reoperation decreased but remained high overall, whereas after 2010, the reoperation rate was similar to that observed with MVR. Conclusion: In patients with RHD, MVP is associated with lower early and long-term mortality, as well as reduced thromboembolism, bleeding, and heart failure compared with MVR. Although MVP historically carried a higher reoperation rate than MVR, this rate has gradually declined in recent years, and since 2010, reoperation rates have not differed significantly between MVP and MVR.
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Yuan et al. (2026) conducted a meta-analysis in Rheumatic heart disease (n=12,405). Mitral valve repair vs. Mitral valve replacement was evaluated on Early mortality (OR 0.63, 95% CI 0.50-0.78, p=<0.001). Mitral valve repair significantly reduced early mortality (OR 0.63) and long-term mortality (OR 0.57) compared to mitral valve replacement in patients with rheumatic heart disease.
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