Drug-drug interactions affecting drug levels of direct oral anticoagulants in the real world: A systematic review

Background: Direct oral anticoagulants (DOACs) have emerged as safe and effective alternatives to Vitamin-K antagonists for treatment and prevention of arterial and venous thrombosis. Due to their novelty, pharmacokinetic DOAC drug-drug interactions (DDIs) that result in clinical adverse events have...

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Autores:
Tipo de recurso:
Article of investigation
Fecha de publicación:
2020
Institución:
Universidad de Bogotá Jorge Tadeo Lozano
Repositorio:
Expeditio: repositorio UTadeo
Idioma:
eng
OAI Identifier:
oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/12503
Acceso en línea:
https://doi.org/10.1016/j.thromres.2020.08.016
http://hdl.handle.net/20.500.12010/12503
Palabra clave:
Direct oral anticoagulant
Drug interaction
Bleeding
Thrombosis
Thromboembolism
Adverse event
Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
Rights
License
Acceso restringido
id UTADEO2_58f37d80c901800b7f0da0f7b36f0aef
oai_identifier_str oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/12503
network_acronym_str UTADEO2
network_name_str Expeditio: repositorio UTadeo
repository_id_str
dc.title.spa.fl_str_mv Drug-drug interactions affecting drug levels of direct oral anticoagulants in the real world: A systematic review
title Drug-drug interactions affecting drug levels of direct oral anticoagulants in the real world: A systematic review
spellingShingle Drug-drug interactions affecting drug levels of direct oral anticoagulants in the real world: A systematic review
Direct oral anticoagulant
Drug interaction
Bleeding
Thrombosis
Thromboembolism
Adverse event
Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
title_short Drug-drug interactions affecting drug levels of direct oral anticoagulants in the real world: A systematic review
title_full Drug-drug interactions affecting drug levels of direct oral anticoagulants in the real world: A systematic review
title_fullStr Drug-drug interactions affecting drug levels of direct oral anticoagulants in the real world: A systematic review
title_full_unstemmed Drug-drug interactions affecting drug levels of direct oral anticoagulants in the real world: A systematic review
title_sort Drug-drug interactions affecting drug levels of direct oral anticoagulants in the real world: A systematic review
dc.subject.spa.fl_str_mv Direct oral anticoagulant
Drug interaction
Bleeding
Thrombosis
Thromboembolism
Adverse event
topic Direct oral anticoagulant
Drug interaction
Bleeding
Thrombosis
Thromboembolism
Adverse event
Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
dc.subject.lemb.spa.fl_str_mv Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
description Background: Direct oral anticoagulants (DOACs) have emerged as safe and effective alternatives to Vitamin-K antagonists for treatment and prevention of arterial and venous thrombosis. Due to their novelty, pharmacokinetic DOAC drug-drug interactions (DDIs) that result in clinical adverse events have not been well-documented. Objective: This study aims to systematically review reported pharmacokinetic DDIs resulting in clinical adverse events through documented observational evidence to better inform clinicians in clinical practice. Methods: A comprehensive literature review of EMBASE, MEDLINE, and Ovid HealthStar was conducted through March 10th, 2020. Two independent reviewers screened and extracted data from eligible articles according to pre-established inclusion and exclusion criteria. Articles reporting bleeding or thrombotic outcomes in noncontrolled (observational) settings resulting from suggested pharmacokinetic DOAC DDIs were included. Results: A total of 5,567 citations were reviewed, of which 24 were included following data extraction. The majority were case reports (n=21) documenting a single adverse event resulting from a suspected DOAC DDI, while the remaining papers were a case series (n=1) and cohort studies (n=2). The most commonly reported interacting drugs were amiodarone and ritonavir (bleeding), and phenobarbital, phenytoin, and carbamazepine (thrombosis). Bleeding events more often resulted from a combined mechanism (P-glycoprotein AND CYP3A4 inhibition), whereas thrombotic events resulted from either combined OR single P-glycoprotein/CYP3A4 induction.Conclusion: Current literature evaluating the real-world risk of DOAC DDIs is limited to few case reports and retrospective observational analyses. Clinicians are encouraged to continue to report suspected drug interactions resulting in adverse events.
publishDate 2020
dc.date.accessioned.none.fl_str_mv 2020-08-31T20:52:00Z
dc.date.available.none.fl_str_mv 2020-08-31T20:52:00Z
dc.date.created.none.fl_str_mv 2020
dc.type.local.spa.fl_str_mv Artículo
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dc.identifier.issn.spa.fl_str_mv 0049-3848
dc.identifier.other.spa.fl_str_mv https://doi.org/10.1016/j.thromres.2020.08.016
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12010/12503
dc.identifier.doi.spa.fl_str_mv https://doi.org/10.1016/j.thromres.2020.08.016
identifier_str_mv 0049-3848
url https://doi.org/10.1016/j.thromres.2020.08.016
http://hdl.handle.net/20.500.12010/12503
dc.language.iso.spa.fl_str_mv eng
language eng
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dc.rights.local.spa.fl_str_mv Acceso restringido
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dc.format.extent.spa.fl_str_mv 28 páginas
dc.format.mimetype.spa.fl_str_mv image/jepg
dc.publisher.spa.fl_str_mv Thrombosis Research
dc.source.spa.fl_str_mv reponame:Expeditio Repositorio Institucional UJTL
instname:Universidad de Bogotá Jorge Tadeo Lozano
instname_str Universidad de Bogotá Jorge Tadeo Lozano
institution Universidad de Bogotá Jorge Tadeo Lozano
reponame_str Expeditio Repositorio Institucional UJTL
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spelling 2020-08-31T20:52:00Z2020-08-31T20:52:00Z20200049-3848https://doi.org/10.1016/j.thromres.2020.08.016http://hdl.handle.net/20.500.12010/12503https://doi.org/10.1016/j.thromres.2020.08.016Background: Direct oral anticoagulants (DOACs) have emerged as safe and effective alternatives to Vitamin-K antagonists for treatment and prevention of arterial and venous thrombosis. Due to their novelty, pharmacokinetic DOAC drug-drug interactions (DDIs) that result in clinical adverse events have not been well-documented. Objective: This study aims to systematically review reported pharmacokinetic DDIs resulting in clinical adverse events through documented observational evidence to better inform clinicians in clinical practice. Methods: A comprehensive literature review of EMBASE, MEDLINE, and Ovid HealthStar was conducted through March 10th, 2020. Two independent reviewers screened and extracted data from eligible articles according to pre-established inclusion and exclusion criteria. Articles reporting bleeding or thrombotic outcomes in noncontrolled (observational) settings resulting from suggested pharmacokinetic DOAC DDIs were included. Results: A total of 5,567 citations were reviewed, of which 24 were included following data extraction. The majority were case reports (n=21) documenting a single adverse event resulting from a suspected DOAC DDI, while the remaining papers were a case series (n=1) and cohort studies (n=2). The most commonly reported interacting drugs were amiodarone and ritonavir (bleeding), and phenobarbital, phenytoin, and carbamazepine (thrombosis). Bleeding events more often resulted from a combined mechanism (P-glycoprotein AND CYP3A4 inhibition), whereas thrombotic events resulted from either combined OR single P-glycoprotein/CYP3A4 induction.Conclusion: Current literature evaluating the real-world risk of DOAC DDIs is limited to few case reports and retrospective observational analyses. Clinicians are encouraged to continue to report suspected drug interactions resulting in adverse events.28 páginasimage/jepgengThrombosis Researchreponame:Expeditio Repositorio Institucional UJTLinstname:Universidad de Bogotá Jorge Tadeo LozanoDirect oral anticoagulantDrug interactionBleedingThrombosisThromboembolismAdverse eventSíndrome respiratorio agudo graveCOVID-19SARS-CoV-2CoronavirusDrug-drug interactions affecting drug levels of direct oral anticoagulants in the real world: A systematic reviewArtículohttp://purl.org/coar/resource_type/c_2df8fbb1Acceso restringidohttp://purl.org/coar/access_right/c_f1cfLi, AllenLi, Ming K.Crowther, MarkVazquez, Sara R.ORIGINALCaptura.PNGCaptura.PNGVer portadaimage/png80914https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/12503/1/Captura.PNGb3e89cf5b46f4c0133077ee28e68b76bMD51open accessDrug-drug-interactions-affecting-drug-levels-of-direct-oral-_2020_Thrombosis.pdfDrug-drug-interactions-affecting-drug-levels-of-direct-oral-_2020_Thrombosis.pdfArtículo reservadoapplication/pdf702225https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/12503/3/Drug-drug-interactions-affecting-drug-levels-of-direct-oral-_2020_Thrombosis.pdff8cb1edf337a30c8a150b902e28e61abMD53embargoed access|||2200-08-31LICENSElicense.txtlicense.txttext/plain; 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