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Efficacy and safety of low-dose acetylsalicylic acid for the prevention of thromboembolic events in individuals positive for antiphospholipid antibodies: A systematic review and meta-analysis.
- Source :
-
Thrombosis research [Thromb Res] 2024 Nov 26; Vol. 245, pp. 109225. Date of Electronic Publication: 2024 Nov 26. - Publication Year :
- 2024
- Publisher :
- Ahead of Print
-
Abstract
- Background: Anti-Phospholipid Antibodies (aPL) are autoantibodies predisposing to an increased risk of thrombotic events. The net clinical benefit of antithrombotic prophylaxis in aPL carriers is still unclear. We performed a systematic review to assess the efficacy and safety of antiplatelet drugs for the primary prevention of thrombotic events in aPL carriers.<br />Methods: Studies were identified by electronic search of MEDLINE and EMBASE database until May 2023. The differences in the outcomes among groups were estimated as pooled odds ratio (OR) and corresponding 95 % confidence interval (CI). Statistical heterogeneity was evaluated using the I2 statistic.<br />Results: 1056 participants were included in 10 studies, 2 RCTs and 8 cohorts. Low-dose acetylsalicylic acid (LDA) was the antiplatelet drug in treated patients. Thrombotic events were significantly reduced in the LDA group compared to the control group [OR 0.46 (95 % CI 0.30-0.71), I2 27%, fixed-effects model]. Arterial thrombotic events were significantly reduced in the LDA group compared to the control group [OR 0.47 (95 % CI 0.26-0.86), I2 0%, fixed-effects model]. Venous thrombotic events were significantly reduced in the LDA group compared to the control group [OR 0.44 (95 % CI 0.21-0.89, I2 1%, fixed-effects model]. No major bleedings occurred in the five studies reporting them.<br />Conclusions: aPL carriers receiving long-term LDA had a significant reduction of thrombotic events, without a significant increase of the risk of major bleeding. It remains unclear if LDA has the same benefit/risk profile in all aPL profile, i.e. single, double, or triple positivity.<br />Competing Interests: Declaration of competing interest Alessandro Squizzato reports a relationship with Daiichi Sankyo, Bayer, Pfizer, Bristol-Myers Squibb, Boehringer-Ingelheim, Sanofi, Werfen, Alexion, Roche, and Viatris that includes: speaking and lecture fees. Vittorio Pengo reports a relationship with Werfen that includes: speaking and lecture fees. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Ltd. All rights reserved.)
Details
- Language :
- English
- ISSN :
- 1879-2472
- Volume :
- 245
- Database :
- MEDLINE
- Journal :
- Thrombosis research
- Publication Type :
- Academic Journal
- Accession number :
- 39603009
- Full Text :
- https://doi.org/10.1016/j.thromres.2024.109225