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Hospitalization of symptomatic patients with heart failure and moderate to severe functional mitral regurgitation treated with MitraClip
ID Ponikowski, Piotr (Author), ID Lainščak, Mitja (Author), ID Anker, Stefan D. (Author), et al.

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Abstract
Background: For patients with functional mitral regurgitation (FMR) and symptomatic heart failure (HF), randomized trials of mitral transcatheter edge-to-edge repair (M-TEER) have produced conflicting results. Objectives: This study sought to assess the impact of M-TEER on hospitalization rates, and explore the effects of M-TEER on patients who did or did not have a history of recent HF hospitalizations before undergoing M-TEER. Methods: RESHAPE-HF2 (Randomized Investigation of the MitraClip Device in Heart Failure: 2nd Trial in Patients with Clinically Significant Functional Mitral Regurgitation) included patients with symptomatic HF and moderate to severe FMR (mean effective regurgitant orifice area 0.25 cm2; 14% >0.40 cm2, 23% <0.20 cm2) and showed that M-TEER reduced recurrent HF hospitalizations with and without the addition of cardiovascular (CV) death and improved quality of life. We now report the results of prespecified analyses on hospitalization rates and for the subgroup of patients (n = 333) with a HF hospitalization in the 12 months before randomization. Results: At 24 months, the time to first event of CV death or HF hospitalization (HR: 0.65; 95% CI: 0.49-0.85; P = 0.002), the rate of recurrent CV hospitalizations (rate ratio [RR]: 0.75; 95% CI: 0.57-0.99; P = 0.046), the composite rate of recurrent CV hospitalizations and all-cause mortality (RR: 0.74; 95% CI: 0.57-0.95; P = 0.017), and of recurrent CV death and CV hospitalizations (RR: 0.76; 95% CI: 0.58-0.99; P = 0.040), were all lower in the M-TEER group. The RR of recurrent hospitalizations for any cause was 0.82 (95% CI: 0.63-1.07; P = 0.15) for patients in the M-TEER group vs control group patients. Patients randomized to M-TEER lost fewer days due to death or HF hospitalization (13.9% [95% CI: 13.0%-14.8%] vs 17.4% [95% CI: 16.4%-18.4%] of follow-up time; P < 0.0001, and 1,067 vs 1,776 total days lost; P < 0.0001). Patients randomized to M-TEER also had better NYHA functional class at 30 days and at 6, 12, and 24 months of follow-up (P < 0.0001). A history of HF hospitalizations before randomization was associated with worse outcomes and greater benefit with M-TEER on the rate of the composite of recurrent HF hospitalizations and CV death (Pinteraction = 0.03) and of recurrent HF hospitalizations within 24 months (Pinteraction = 0.06). Conclusions: These results indicate that a broader application of M-TEER in addition to optimal guideline-directed medical therapy should be considered among patients with symptomatic HF and moderate to severe FMR, particularly in those with a history of a recent hospitalization for HF.

Language:English
Keywords:M-TEER, MitraClip, clinical trial, heart failure, hospitalization, mitral regurgitation, transcatheter repair
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:MF - Faculty of Medicine
Publication status:Published
Publication version:Version of Record
Year:2024
Number of pages:Str. 2347-2363
Numbering:Vol. 84, iss. 24
PID:20.500.12556/RUL-182422 This link opens in a new window
UDC:616.1
ISSN on article:0735-1097
DOI:10.1016/j.jacc.2024.08.027 This link opens in a new window
COBISS.SI-ID:224962819 This link opens in a new window
Publication date in RUL:11.05.2026
Views:294
Downloads:133
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Record is a part of a journal

Title:Journal of the American college of cardiology
Shortened title:J. Am. Coll. Cardiol.
Publisher:Elsevier
ISSN:0735-1097
COBISS.SI-ID:3605775 This link opens in a new window

Licences

License:CC BY-NC-ND 4.0, Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
Link:http://creativecommons.org/licenses/by-nc-nd/4.0/
Description:The most restrictive Creative Commons license. This only allows people to download and share the work for no commercial gain and for no other purposes.

Secondary language

Language:Slovenian
Keywords:klinični preizkus, srčno popuščanje, hospitalizacija, mitralna regurgitacija, popravilo transkatetra

Projects

Funder:Vifor Pharma

Funder:DFG - Deutsche Forschungsgemeinschaft

Funder:G-BA - Federal Joint Committee

Funder:EC - European Commission

Funder:UMG Göttingen, Clinical Trial Unit
Name:EchoCoreLab IIT

Funder:NIH - National Institutes of Health
Project number:1 UG3 / UH3 HL140144-0

Funder:Bristol Myers Squibb

Funder:CSL-Vifor

Funder:British Heart Foundation

Funder:Pharmacosmos

Funder:Microvision Medical Holding B.V.

Funder:Edwards Lifesciences

Funder:Mars Scientific Advisory Council

Funder:Abiomed Europe GmbH

Funder:B. Braun Melsungen AG

Funder:EC - European Commission
Funding programme:Horizon 2020

Funder:Daiichi-Sankyo Deutschland GmbH

Funder:Abbott

Funder:Novartis

Funder:Abbott Vascular

Funder:Edwards Lifesciences

Funder:Polares Medical

Funder:Boehringer Ingelheim

Funder:Abiomed Inc

Funder:Cytosorb Inc

Funder:Boston Scientific

Funder:BMWK - Germany, Federal Ministry of Economics and climate protection
Name:Project 5G-MedCamp

Funder:Other - Other funder or multiple funders
Name:RESKRIVER

Funder:Other - Other funder or multiple funders
Name:6 G Health

Funder:ARRS - Slovenian Research Agency

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