Key result
Valve-in-valve transcatheter mitral valve replacement was associated with significantly lower in-hospital all-cause mortality (2.6% vs 7.3%) compared to redo surgical mitral valve replacement.
Why the study?
Does valve-in-valve transcatheter mitral valve replacement reduce mortality and readmissions compared to redo surgical mitral valve replacement in patients with failed mitral bioprostheses?
Cohort (n=3,691)
Yes
Does valve-in-valve transcatheter mitral valve replacement reduce mortality and readmissions compared to redo surgical mitral valve replacement in patients with failed mitral bioprostheses?
ViV-TMVR is associated with lower in-hospital mortality, shorter length of stay, and reduced costs compared to redo-SMVR, with similar medium-term readmission and mortality rates.
Answers are grounded in this paper and cite their sources.
Supports ViV-TMVR in high-risk patients with failed mitral bioprostheses; leaves open causality pending randomized trials.
BACKGROUND: Data on the safety of valve-in-valve transcatheter mitral valve replacement (ViV-TMVR) compared with redo surgical mitral valve replacement (SMVR) in patients with a history of bioprosthetic mitral valve (MV) remain limited. AIMS: We aimed to evaluate the in-hospital, 30-day and 6-month readmission outcomes of ViV-TMVR compared with redo-SMVR in a real-world cohort. METHODS: The Nationwide Readmission Database was utilised, analysing data from 2015 to 2019. To determine the adjusted odds ratio (aOR), we used the propensity-matched analysis for major outcomes at index hospitalisation, 30 days, and 6 months during the episode of readmission. RESULTS: A total of 3,691 patients were included, of these, 24.2% underwent ViV-TMVR and 75.8% underwent redo-SMVR. Patients undergoing ViV-TMVR were older with higher rates of comorbidities. The mean length of stay (15 days vs 4 days) and cost of hospitalisation ($76,558 vs $46,743) were significantly higher for redo-SMVR. The rate of in-hospital all-cause mortality was also significantly lower in ViV-TMVR (2.6% vs 7.3%). By contrast, 30-day all-cause mortality during the episode of readmission (aOR 1.01, 95% confidence interval [CI]: 0.40-2.55) and all-cause readmission rates (aOR 0.82, 95% CI: 0.66-1.02) were similar between both groups. The incidence of all-cause readmissions at 6 months (aOR 0.83, 95% CI: 0.65-1.05) and all-cause mortality during the episode of readmission at 6 months (aOR 1.84, 95% CI: 0.54-6.36) were also comparable. The utilisation of the ViV-TMVR procedure increased significantly during our study duration, from 5.2% to 36.8%, (ptrend<0.01). CONCLUSIONS: ViV-TMVR is associated with lower odds of in-hospital mortality, complications, and resource utilisation. The all-cause readmissions and 30-day and 6-month mortality during the episode of readmissions were comparable between both groups.
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Zahid et al. (2022) conducted a cohort in failed mitral bioprostheses (n=3,691). Valve-in-valve transcatheter mitral valve replacement (ViV-TMVR) vs. Redo surgical mitral valve replacement (redo-SMVR) was evaluated on In-hospital all-cause mortality. Valve-in-valve transcatheter mitral valve replacement was associated with significantly lower in-hospital all-cause mortality (2.6% vs 7.3%) compared to redo surgical mitral valve replacement.
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