Key result
Transcatheter mitral valve-in-valve replacement was associated with lower in-hospital mortality compared to redo surgical mitral valve replacement (OR 0.64; 95% CI 0.53-0.78; P=0.0023).
Why the study?
Transcatheter mitral valve-in-valve replacement has emerged as an alternative to redo surgical mitral valve replacement in high-risk patients, but outcomes between the two strategies needed comparison.
Does transcatheter mitral valve-in-valve replacement reduce all-cause mortality compared to repeat surgical mitral valve replacement in patients with failed mitral bioprostheses?
Meta-Analysis (n=5,083)
Does transcatheter mitral valve-in-valve replacement reduce all-cause mortality compared to repeat surgical mitral valve replacement in patients with failed mitral bioprostheses?
Odds Ratio: 0.64 (95% CI 0.53–0.78)
p-value: p=.0023
Transcatheter mitral valve-in-valve replacement offers lower in-hospital mortality and major bleeding compared to redo surgical replacement, with similar 1-year mortality outcomes.
Background Transcatheter mitral valve-in-valve (MViV) replacement has emerged as an alternative to redo surgical mitral valve replacement (redo-SMVR) in patients with failed mitral bioprostheses deemed to be at a high surgical risk. The aim of this analysis was to compare the outcomes of MViV replacement with those of redo-SMVR in patients with a failed bioprosthetic mitral valve. Methods We performed a study-level meta-analysis that compared MViV replacement with redo-SMVR in patients with failed mitral bioprostheses. Seven observational studies, with a total of 5083 patients, were included (1138 patients [22.4%] in the MViV replacement arm). The primary focus was all-cause mortality. Additional outcomes included major bleeding, stroke, vascular complications, and mean mitral valve gradient at follow-up. Results The in-hospital mortality was lower in patients who underwent MViV replacement than in those who underwent redo-SMVR (odds ratio [OR], 0.64; 95% CI, 0.53-0.78; P = .0023). The short-term mortality (<1 year) was numerically lower in the MViV replacement group (OR, 0.45; 95% CI, 0.18-1.13; P = .069). At 1 year, the risk of mortality was similar in the 2 groups (OR, 0.99; 95% CI, 0.69-1.40; P = .906), and at midterm follow-up (≥1 year), there was a numerically higher risk of mortality in the MViV replacement group (OR, 1.51; 95% CI, 1.00-2.29; P = .051). The risk of major bleeding was significantly lower in the MViV replacement group (OR, 0.23; 95% CI, 0.10-0.56; P = .01). Additionally, stroke and vascular complications were similar between the 2 groups. Conclusions The in-hospital mortality was lower in the MViV replacement group than in the redo-SMVR group. There were no differences in mortality at short-term (<1 year), 1-year, or midterm (≥1 year) follow-ups.
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Al‐Abcha et al. (2022) conducted a meta-analysis in Failed mitral bioprostheses (n=5,083). Transcatheter mitral valve-in-valve (MViV) replacement vs. Repeat surgical mitral valve replacement (redo-SMVR) was evaluated on In-hospital all-cause mortality (OR 0.64, 95% CI 0.53-0.78, p=.0023). Transcatheter mitral valve-in-valve replacement was associated with lower in-hospital mortality compared to redo surgical mitral valve replacement (OR 0.64; 95% CI 0.53-0.78; P=0.0023).
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