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No Association between Gastrointestinal Rebleeding and DOAC Therapy Resumption: A Systematic Review and Meta-Analysis

Background: There are recommendations for anticoagulation resumption after gastrointestinal bleeding (GIB), although data addressing this topic by direct oral anticoagulants (DOACs)-treated patients is lacking. We aim to determine the safety and efficacy of restarting DOACs after GIB. Methods: Studi...

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Autores principales: Pálinkás, Dániel, Teutsch, Brigitta, Gagyi, Endre Botond, Engh, Marie Anne, Kalló, Patrícia, Veres, Dániel S., Földvári-Nagy, László, Hosszúfalusi, Nóra, Hegyi, Péter, Erőss, Bálint
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953612/
https://www.ncbi.nlm.nih.gov/pubmed/36831090
http://dx.doi.org/10.3390/biomedicines11020554
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author Pálinkás, Dániel
Teutsch, Brigitta
Gagyi, Endre Botond
Engh, Marie Anne
Kalló, Patrícia
Veres, Dániel S.
Földvári-Nagy, László
Hosszúfalusi, Nóra
Hegyi, Péter
Erőss, Bálint
author_facet Pálinkás, Dániel
Teutsch, Brigitta
Gagyi, Endre Botond
Engh, Marie Anne
Kalló, Patrícia
Veres, Dániel S.
Földvári-Nagy, László
Hosszúfalusi, Nóra
Hegyi, Péter
Erőss, Bálint
author_sort Pálinkás, Dániel
collection PubMed
description Background: There are recommendations for anticoagulation resumption after gastrointestinal bleeding (GIB), although data addressing this topic by direct oral anticoagulants (DOACs)-treated patients is lacking. We aim to determine the safety and efficacy of restarting DOACs after GIB. Methods: Studies that reported rebleeding, thromboembolic events, and mortality after restarting or withholding DOACs were selected. The systematic research was conducted in five databases (MEDLINE, EMBASE, CENTRAL, Web of Science, and Scopus). The random effect model was implemented to calculate the pooled odds ratio (OR). The ROBINS-I tool was used for risk of bias assessment, and the certainty of the evidence was evaluated with the GRADE approach. Results: Four retrospective cohort studies (1722 patients) were included in the meta-analysis. We did not find a significant increase in the risk of rebleeding in patients restarting DOACs after index GIB (OR = 1.12; 95% CI: 0.74–1.68). The outcomes of thromboembolic events and mortality data were not suitable for meta-analytic calculations. Single studies did not show statistically significant differences. Data quality assessment showed a serious overall risk of bias and very low quality of evidence (GRADE D). Conclusion: DOAC resumption after a GIB episode may not elevate the risk of rebleeding. However, the need for high-quality randomized clinical trials is crucial.
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spelling pubmed-99536122023-02-25 No Association between Gastrointestinal Rebleeding and DOAC Therapy Resumption: A Systematic Review and Meta-Analysis Pálinkás, Dániel Teutsch, Brigitta Gagyi, Endre Botond Engh, Marie Anne Kalló, Patrícia Veres, Dániel S. Földvári-Nagy, László Hosszúfalusi, Nóra Hegyi, Péter Erőss, Bálint Biomedicines Systematic Review Background: There are recommendations for anticoagulation resumption after gastrointestinal bleeding (GIB), although data addressing this topic by direct oral anticoagulants (DOACs)-treated patients is lacking. We aim to determine the safety and efficacy of restarting DOACs after GIB. Methods: Studies that reported rebleeding, thromboembolic events, and mortality after restarting or withholding DOACs were selected. The systematic research was conducted in five databases (MEDLINE, EMBASE, CENTRAL, Web of Science, and Scopus). The random effect model was implemented to calculate the pooled odds ratio (OR). The ROBINS-I tool was used for risk of bias assessment, and the certainty of the evidence was evaluated with the GRADE approach. Results: Four retrospective cohort studies (1722 patients) were included in the meta-analysis. We did not find a significant increase in the risk of rebleeding in patients restarting DOACs after index GIB (OR = 1.12; 95% CI: 0.74–1.68). The outcomes of thromboembolic events and mortality data were not suitable for meta-analytic calculations. Single studies did not show statistically significant differences. Data quality assessment showed a serious overall risk of bias and very low quality of evidence (GRADE D). Conclusion: DOAC resumption after a GIB episode may not elevate the risk of rebleeding. However, the need for high-quality randomized clinical trials is crucial. MDPI 2023-02-14 /pmc/articles/PMC9953612/ /pubmed/36831090 http://dx.doi.org/10.3390/biomedicines11020554 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Systematic Review
Pálinkás, Dániel
Teutsch, Brigitta
Gagyi, Endre Botond
Engh, Marie Anne
Kalló, Patrícia
Veres, Dániel S.
Földvári-Nagy, László
Hosszúfalusi, Nóra
Hegyi, Péter
Erőss, Bálint
No Association between Gastrointestinal Rebleeding and DOAC Therapy Resumption: A Systematic Review and Meta-Analysis
title No Association between Gastrointestinal Rebleeding and DOAC Therapy Resumption: A Systematic Review and Meta-Analysis
title_full No Association between Gastrointestinal Rebleeding and DOAC Therapy Resumption: A Systematic Review and Meta-Analysis
title_fullStr No Association between Gastrointestinal Rebleeding and DOAC Therapy Resumption: A Systematic Review and Meta-Analysis
title_full_unstemmed No Association between Gastrointestinal Rebleeding and DOAC Therapy Resumption: A Systematic Review and Meta-Analysis
title_short No Association between Gastrointestinal Rebleeding and DOAC Therapy Resumption: A Systematic Review and Meta-Analysis
title_sort no association between gastrointestinal rebleeding and doac therapy resumption: a systematic review and meta-analysis
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953612/
https://www.ncbi.nlm.nih.gov/pubmed/36831090
http://dx.doi.org/10.3390/biomedicines11020554
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