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. 2025 Aug 23;25(1):628.
doi: 10.1186/s12872-025-04974-4.

Optimizing antithrombotic therapy following mitral valve repair: a comprehensive network meta-analysis

Affiliations

Optimizing antithrombotic therapy following mitral valve repair: a comprehensive network meta-analysis

Mohamed Ibrahim Gbreel et al. BMC Cardiovasc Disord. .

Abstract

Background: Mitral regurgitation (MR) presents either as primary or secondary, with options for surgical or transcatheter repair. Thromboembolic risks following surgery are significant despite the use of antithrombotic medications, and guidelines for postoperative anticoagulation therapy lack consistency. This systematic review aims to compare antithrombotic medications after mitral valve repair (MVR). In this study, we intend to compare antithrombotic medications after MVR.

Materials and methods: The study followed the Cochrane handbook and PRISMA guidelines. We systematically searched databases (PubMed, Scopus, Ovid, Cochrane, Web of Science) until June 2024 for TMVR studies using specific criteria. Quality assessment utilized the Newcastle-Ottawa scale. Data extraction encompassed study characteristics and outcomes. Primary outcomes included thromboembolic events and bleeding within six months. Statistical analysis employed R software to assess heterogeneity and publication bias.

Results: From the 121 articles screened, 12 were included in the study. These cohort studies, involving 20,644 participants, spanned from 2008 to 2022. While most studies were of good to high quality, some exhibited lower quality. Analysis favored oral anticoagulants (OAC) over single antiplatelet therapy (SAPT) for reducing bleeding risk (RR = 0.31, 95% CI: [0.11-0.87], P < 0.05), with moderate heterogeneity. Thromboembolic events did not significantly differ among interventions. Transient ischemic attacks and stroke outcomes were similar between SAPT and vitamin K antagonists (VKA). Six-month mortality rates were comparable between SAPT and VKA, with notable heterogeneity and higher mortality with SAPT in one study. Qualitative synthesis highlighted procedural success rates and bleeding complications across different interventions in transcatheter mitral valve repair studies.

Conclusion: OACs showed a lower risk of bleeding compared to antiplatelet therapies, while VKAs and OAC + SAPT may reduce thromboembolic events. No significant differences were found in stroke, TIA, or short-term mortality. These findings support individualized therapy and highlight the need for further randomized trials.

Keywords: ASA; Anticoagulant; Clopidogrel; Mitral regurgitation; Mitral valve repair; Network meta-analysis.

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Conflict of interest statement

Declarations. Ethics approval and consent to participate: Not applicable. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
PRISMA Flow Diagram, showing the systematic review process, including initial identification, screening, eligibility assessment, and final study inclusion
Fig. 2
Fig. 2
Network Meta-Analysis of Bleeding Events: illustrating the risk ratio comparisons of bleeding events across different antithrombotic treatments after mitral valve repair. A lower risk of bleeding is associated with OAC relative to SAPT
Fig. 3
Fig. 3
Network Meta-Analysis of Bleeding Events: illustrating the risk ratio comparisons of bleeding events across different antithrombotic treatments after mitral valve repair. A lower risk of bleeding is associated with OAC relative to SAPT
Fig. 4
Fig. 4
Comparison of Bleeding Risk Between OAC and DAPT: displaying the relative risk of bleeding in patients treated with OAC compared to DAPT, showing a statistically significant reduction in bleeding risk with OAC
Fig. 5
Fig. 5
Egger’s Test for Publication Bias: presenting the results of Egger’s test, evaluating potential publication bias across studies included in the meta-analysis of bleeding events
Fig. 6
Fig. 6
Thromboembolic Events Across Interventions: compareing thromboembolic event rates among various antithrombotic therapies, showing no significant differences in risk
Fig. 7
Fig. 7
Thromboembolic Events Across Interventions: compareing thromboembolic event rates among various antithrombotic therapies, showing no significant differences in risk
Fig. 8
Fig. 8
Network meta-analysis comparing the relative risk (RR) of different antithrombotic and anticoagulant strategies.
Fig. 9
Fig. 9
Risk of Transient Ischemic Attacks (TIA): showing the comparative risk of TIA between SAPT and VKA, with no significant difference observed
Fig. 10
Fig. 10
Stroke Risk Comparison: providing a visual comparison of stroke risk between SAPT and VKA post-mitral valve repair
Fig. 11
Fig. 11
Six-Month Mortality Risk Analysis: comparing six-month mortality risk across different treatments, with a significant finding upon exclusion of one study to reduce heterogeneity
Fig. 12
Fig. 12
Six-Month Mortality Risk Analysis: comparing six-month mortality risk across different treatments, with a significant finding upon exclusion of one study to reduce heterogeneity

References

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