Preventive Strategies against Bleeding due to Nonvitamin K Antagonist Oral Anticoagulants
Dabigatran etexilate (DE), rivaroxaban, and apixaban are nonvitamin K antagonist oral anticoagulants (NOACs) that have been compared in clinical trials with existing anticoagulants (warfarin and enoxaparin) in several indications for the prevention and treatment of thrombotic events. All NOACs prese...
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doaj-657ec868d2b8479a87ac14dc858290882020-11-25T00:31:21ZengHindawi LimitedBioMed Research International2314-61332314-61412014-01-01201410.1155/2014/616405616405Preventive Strategies against Bleeding due to Nonvitamin K Antagonist Oral AnticoagulantsLessire Sarah0Dincq Anne-Sophie1Douxfils Jonathan2Devalet Bérangère3Nicolas Jean-Baptiste4Spinewine Anne5Larock Anne-Sophie6Dogné Jean-Michel7Gourdin Maximilien8Mullier François9Department of Anesthesiology, CHU Dinant-Godinne UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), NAmur Research Institute of Life Sciences (NARILIS), 5530 Yvoir, BelgiumDepartment of Anesthesiology, CHU Dinant-Godinne UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), NAmur Research Institute of Life Sciences (NARILIS), 5530 Yvoir, BelgiumDepartment of Pharmacy, Namur Thrombosis and Hemostasis Center (NTHC), NAmur Research Institute of Life Sciences (NARILIS), University of Namur, 5000 Namur, BelgiumDepartment of Pharmacy, Namur Thrombosis and Hemostasis Center (NTHC), NAmur Research Institute of Life Sciences (NARILIS), University of Namur, 5000 Namur, BelgiumDepartment of Internal Medicine, CHU Dinant-Godinne UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), NAmur Research Institute of Life Sciences (NARILIS), 5530 Yvoir, BelgiumDepartment of Pharmacy, CHU Dinant-Godinne UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), NAmur Research Institute of Life Sciences (NARILIS), 5530 Yvoir, BelgiumDepartment of Pharmacy, CHU Dinant-Godinne UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), NAmur Research Institute of Life Sciences (NARILIS), 5530 Yvoir, BelgiumDepartment of Pharmacy, Namur Thrombosis and Hemostasis Center (NTHC), NAmur Research Institute of Life Sciences (NARILIS), University of Namur, 5000 Namur, BelgiumDepartment of Anesthesiology, CHU Dinant-Godinne UCL Namur, Namur Thrombosis and Hemostasis Center (NTHC), NAmur Research Institute of Life Sciences (NARILIS), 5530 Yvoir, BelgiumDepartment of Pharmacy, Namur Thrombosis and Hemostasis Center (NTHC), NAmur Research Institute of Life Sciences (NARILIS), University of Namur, 5000 Namur, BelgiumDabigatran etexilate (DE), rivaroxaban, and apixaban are nonvitamin K antagonist oral anticoagulants (NOACs) that have been compared in clinical trials with existing anticoagulants (warfarin and enoxaparin) in several indications for the prevention and treatment of thrombotic events. All NOACs presented bleeding events despite a careful selection and control of patients. Compared with warfarin, NOACs had a decreased risk of intracranial hemorrhage, and apixaban and DE (110 mg BID) had a decreased risk of major bleeding from any site. Rivaroxaban and DE showed an increased risk of major gastrointestinal bleeding compared with warfarin. Developing strategies to minimize the risk of bleeding is essential, as major bleedings are reported in clinical practice and specific antidotes are currently not available. In this paper, the following preventive approaches are reviewed: improvement of appropriate prescription, identification of modifiable bleeding risk factors, tailoring NOAC’s dose, dealing with a missed dose as well as adhesion to switching, bridging and anesthetic procedures.http://dx.doi.org/10.1155/2014/616405 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lessire Sarah Dincq Anne-Sophie Douxfils Jonathan Devalet Bérangère Nicolas Jean-Baptiste Spinewine Anne Larock Anne-Sophie Dogné Jean-Michel Gourdin Maximilien Mullier François |
spellingShingle |
Lessire Sarah Dincq Anne-Sophie Douxfils Jonathan Devalet Bérangère Nicolas Jean-Baptiste Spinewine Anne Larock Anne-Sophie Dogné Jean-Michel Gourdin Maximilien Mullier François Preventive Strategies against Bleeding due to Nonvitamin K Antagonist Oral Anticoagulants BioMed Research International |
author_facet |
Lessire Sarah Dincq Anne-Sophie Douxfils Jonathan Devalet Bérangère Nicolas Jean-Baptiste Spinewine Anne Larock Anne-Sophie Dogné Jean-Michel Gourdin Maximilien Mullier François |
author_sort |
Lessire Sarah |
title |
Preventive Strategies against Bleeding due to Nonvitamin K Antagonist Oral Anticoagulants |
title_short |
Preventive Strategies against Bleeding due to Nonvitamin K Antagonist Oral Anticoagulants |
title_full |
Preventive Strategies against Bleeding due to Nonvitamin K Antagonist Oral Anticoagulants |
title_fullStr |
Preventive Strategies against Bleeding due to Nonvitamin K Antagonist Oral Anticoagulants |
title_full_unstemmed |
Preventive Strategies against Bleeding due to Nonvitamin K Antagonist Oral Anticoagulants |
title_sort |
preventive strategies against bleeding due to nonvitamin k antagonist oral anticoagulants |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2014-01-01 |
description |
Dabigatran etexilate (DE), rivaroxaban, and apixaban are nonvitamin K antagonist oral anticoagulants (NOACs) that have been compared in clinical trials with existing anticoagulants (warfarin and enoxaparin) in several indications for the prevention and treatment of thrombotic events. All NOACs presented bleeding events despite a careful selection and control of patients. Compared with warfarin, NOACs had a decreased risk of intracranial hemorrhage, and apixaban and DE (110 mg BID) had a decreased risk of major bleeding from any site. Rivaroxaban and DE showed an increased risk of major gastrointestinal bleeding compared with warfarin. Developing strategies to minimize the risk of bleeding is essential, as major bleedings are reported in clinical practice and specific antidotes are currently not available. In this paper, the following preventive approaches are reviewed: improvement of appropriate prescription, identification of modifiable bleeding risk factors, tailoring NOAC’s dose, dealing with a missed dose as well as adhesion to switching, bridging and anesthetic procedures. |
url |
http://dx.doi.org/10.1155/2014/616405 |
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