Direct Oral Anticoagulants in the Prevention of Venous Thromboembolism: Evidence From Major Clinical Trials

dc.contributor.authorPrandoni, Paolo P.
dc.contributor.authorTemraz, Sally N.
dc.contributor.authorTaher, Ali T.
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision of Hematology Oncology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:42:53Z
dc.date.available2025-01-24T11:42:53Z
dc.date.issued2014
dc.description.abstractHospitalized medical and surgical patients encompass a group of patients in whom venous thromboembolism (VTE) poses a major concern on morbidity and mortality. Recently, direct oral anticoagulants for the prevention of VTE have been developed to overcome the drawbacks of the food/drug interactions and the need for frequent laboratory monitoring and dose adjustments associated with the use of vitamin K antagonists and the inconvenience of the subcutaneous administration of low-molecular-weight heparins and fondaparinux. The novel oral anticoagulants that have been tested in major clinical trials for VTE prevention in medical and surgical patients are the thrombin inhibitor dabigatran and the factor Xa inhibitors apixaban, rivaroxaban, and edoxaban, which will be the focus of this review. While the new drugs proved to be highly effective and safe in the prevention of VTE following major orthopedic surgery, they failed to show a favorable benefit-to-risk profile in hospitalized medical patients receiving extended anticoagulation beyond the hospital stay. © 2014 Elsevier Inc.
dc.identifier.doihttps://doi.org/10.1053/j.seminhematol.2014.03.006
dc.identifier.eid2-s2.0-84901380221
dc.identifier.pmid24861796
dc.identifier.urihttp://hdl.handle.net/10938/30120
dc.language.isoen
dc.publisherW.B. Saunders
dc.relation.ispartofSeminars in Hematology
dc.sourceScopus
dc.subjectAdministration, oral
dc.subjectAnticoagulants
dc.subjectBenzimidazoles
dc.subjectBeta-alanine
dc.subjectClinical trials as topic
dc.subjectHalf-life
dc.subjectHumans
dc.subjectMorpholines
dc.subjectPyrazoles
dc.subjectPyridines
dc.subjectPyridones
dc.subjectThiazoles
dc.subjectThiophenes
dc.subjectVenous thromboembolism
dc.subjectVitamin k
dc.subjectAnticoagulant agent
dc.subjectAntivitamin k
dc.subjectApixaban
dc.subjectDabigatran
dc.subjectDabigatran etexilate
dc.subjectEdoxaban
dc.subjectEnoxaparin
dc.subjectFondaparinux
dc.subjectLow molecular weight heparin
dc.subjectPlacebo
dc.subjectRivaroxaban
dc.subjectThrombin
dc.subjectAnticoagulation
dc.subjectArticle
dc.subjectBleeding
dc.subjectClinical trial (topic)
dc.subjectDrug bioavailability
dc.subjectDrug efficacy
dc.subjectDrug elimination
dc.subjectDrug half life
dc.subjectDrug mechanism
dc.subjectDrug monitoring
dc.subjectDrug protein binding
dc.subjectDrug safety
dc.subjectDrug treatment failure
dc.subjectDrug use
dc.subjectHospitalization
dc.subjectHuman
dc.subjectLaboratory test
dc.subjectMorbidity
dc.subjectMortality
dc.subjectOrthopedic surgery
dc.subjectPriority journal
dc.subjectRisk benefit analysis
dc.subjectTime to maximum plasma concentration
dc.titleDirect Oral Anticoagulants in the Prevention of Venous Thromboembolism: Evidence From Major Clinical Trials
dc.typeArticle

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