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Drug-drug interactions between direct oral anticoagulants and anticonvulsants and clinical outcomes: A systematic review

BACKGROUND: Direct oral anticoagulants (DOACs) are widely used in patients with atrial fibrillation and venous thromboembolism. However, DOACs have important potential drug-drug interactions (DDIs) with several classes of drugs. In particular, antiepileptic (AE) drugs may induce cytochrome P450 3A4...

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Autores principales: Candeloro, Matteo, Carlin, Stephanie, Shapiro, Michelle J., Douketis, James D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131112/
https://www.ncbi.nlm.nih.gov/pubmed/37122531
http://dx.doi.org/10.1016/j.rpth.2023.100137
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author Candeloro, Matteo
Carlin, Stephanie
Shapiro, Michelle J.
Douketis, James D.
author_facet Candeloro, Matteo
Carlin, Stephanie
Shapiro, Michelle J.
Douketis, James D.
author_sort Candeloro, Matteo
collection PubMed
description BACKGROUND: Direct oral anticoagulants (DOACs) are widely used in patients with atrial fibrillation and venous thromboembolism. However, DOACs have important potential drug-drug interactions (DDIs) with several classes of drugs. In particular, antiepileptic (AE) drugs may induce cytochrome P450 3A4 or P-glycoprotein. Co-administration of DOACs and AE drugs may result in lower DOAC drug levels and reduced DOAC efficacy. However, the clinical significance of such DDIs is uncertain. OBJECTIVES: The aim of this systematic review was to generate an updated review of these DDIs and their clinical relevance, given the rapidly evolving knowledge relating to DOAC and AE DDIs. METHODS: We searched the MEDLINE and Embase databases for studies reporting clinical adverse outcomes (thrombotic events, bleeding events, and all-cause mortality) in patients concomitantly taking DOACs and AE drugs. RESULTS: We retrieved 874 studies of which 15 were deemed eligible for this review, including 4 congress abstracts, 3 case reports, 2 letters to the editor, 5 retrospective cohorts, and 1 prospective cohort study. No randomized clinical trials were found. Most of the included studies reported thrombotic events, 3 studies reported major bleeding, and one study reported all-cause mortality associated with DOAC and AE drug administration. Substantial differences in the study designs did not allow for a meta-analysis to be performed. CONCLUSION: The current literature assessing these adverse clinical outcomes from DOAC and AE drug co-administration is limited. Although the available data point to a possible increased risk of thrombotic events, they are insufficient to draw definitive conclusions. Well-designed clinical studies are of utmost importance.
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spelling pubmed-101311122023-04-27 Drug-drug interactions between direct oral anticoagulants and anticonvulsants and clinical outcomes: A systematic review Candeloro, Matteo Carlin, Stephanie Shapiro, Michelle J. Douketis, James D. Res Pract Thromb Haemost Review BACKGROUND: Direct oral anticoagulants (DOACs) are widely used in patients with atrial fibrillation and venous thromboembolism. However, DOACs have important potential drug-drug interactions (DDIs) with several classes of drugs. In particular, antiepileptic (AE) drugs may induce cytochrome P450 3A4 or P-glycoprotein. Co-administration of DOACs and AE drugs may result in lower DOAC drug levels and reduced DOAC efficacy. However, the clinical significance of such DDIs is uncertain. OBJECTIVES: The aim of this systematic review was to generate an updated review of these DDIs and their clinical relevance, given the rapidly evolving knowledge relating to DOAC and AE DDIs. METHODS: We searched the MEDLINE and Embase databases for studies reporting clinical adverse outcomes (thrombotic events, bleeding events, and all-cause mortality) in patients concomitantly taking DOACs and AE drugs. RESULTS: We retrieved 874 studies of which 15 were deemed eligible for this review, including 4 congress abstracts, 3 case reports, 2 letters to the editor, 5 retrospective cohorts, and 1 prospective cohort study. No randomized clinical trials were found. Most of the included studies reported thrombotic events, 3 studies reported major bleeding, and one study reported all-cause mortality associated with DOAC and AE drug administration. Substantial differences in the study designs did not allow for a meta-analysis to be performed. CONCLUSION: The current literature assessing these adverse clinical outcomes from DOAC and AE drug co-administration is limited. Although the available data point to a possible increased risk of thrombotic events, they are insufficient to draw definitive conclusions. Well-designed clinical studies are of utmost importance. Elsevier 2023-03-28 /pmc/articles/PMC10131112/ /pubmed/37122531 http://dx.doi.org/10.1016/j.rpth.2023.100137 Text en © 2023 The Authors. Published by Elsevier Inc. on behalf of International Society on Thrombosis and Haemostasis. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Candeloro, Matteo
Carlin, Stephanie
Shapiro, Michelle J.
Douketis, James D.
Drug-drug interactions between direct oral anticoagulants and anticonvulsants and clinical outcomes: A systematic review
title Drug-drug interactions between direct oral anticoagulants and anticonvulsants and clinical outcomes: A systematic review
title_full Drug-drug interactions between direct oral anticoagulants and anticonvulsants and clinical outcomes: A systematic review
title_fullStr Drug-drug interactions between direct oral anticoagulants and anticonvulsants and clinical outcomes: A systematic review
title_full_unstemmed Drug-drug interactions between direct oral anticoagulants and anticonvulsants and clinical outcomes: A systematic review
title_short Drug-drug interactions between direct oral anticoagulants and anticonvulsants and clinical outcomes: A systematic review
title_sort drug-drug interactions between direct oral anticoagulants and anticonvulsants and clinical outcomes: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131112/
https://www.ncbi.nlm.nih.gov/pubmed/37122531
http://dx.doi.org/10.1016/j.rpth.2023.100137
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