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[Management of bleeding associated with direct oral anticoagulants: update on reversal strategies]. / Manejo de hemorragia asociada a anticoagulantes orales directos: estado actual de las estrategias de reversión.
Enríquez, Andrés; Baranchuk, Adrian; Corbalán, Ramón.
Afiliação
  • Enríquez A; Departamento de Cardiología, Hospital Guillermo Grant Benavente, Concepción, Chile.
  • Baranchuk A; Division of Cardiology, Queen's University, Kingston, Ontario, Canada.
  • Corbalán R; División de Enfermedades Cardiovasculares, Hospital Clínico, Pontificia Universidad Católica de Chile, Santiago, Chile.
Rev Med Chil ; 147(1): 73-82, 2019.
Article em Es | MEDLINE | ID: mdl-30848768
ABSTRACT
Direct oral anticoagulants (DOACs), including the direct thrombin inhibitor dabigatran and the direct factor Xa inhibitors rivaroxaban, apixaban and edoxaban have at least comparable efficacy as vitamin K antagonists along with a better safety profile, reflected by a lower incidence of intracranial hemorrhage. Specific reversal agents have been developed in recent years. Namely, idarucizumab, a specific antidote for dabigatran, is currently approved in most countries. Andexanet, which reverses factor Xa inhibitors, has been recently approved by the FDA, and ciraparantag, a universal antidote targeted to reverse all DOACs, is still under investigation. In this review we provide an update on the pharmacology of DOACs, the risk of hemorrhagic complications associated with their use, the measurement of their anticoagulant effect and the reversal strategies in case of DOAC-associated bleeding.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Coagulação Sanguínea / Antitrombinas / Anticorpos Monoclonais Humanizados / Hemorragia Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: Es Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Coagulação Sanguínea / Antitrombinas / Anticorpos Monoclonais Humanizados / Hemorragia Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: Es Ano de publicação: 2019 Tipo de documento: Article