The safety of NOACs in atrial fibrillation patient subgroups:A narrative review
Autor: | Gregory Y.H. Lip |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
Stroke/etiology
medicine.medical_specialty Pyridines Pyridones Rivaroxaban/administration & dosage Patient subgroups MEDLINE Administration Oral Hemorrhage 030204 cardiovascular system & hematology Warfarin/adverse effects 03 medical and health sciences 0302 clinical medicine Rivaroxaban Risk Factors Thiazoles/administration & dosage Hemorrhage/chemically induced Atrial Fibrillation medicine Humans Dabigatran/administration & dosage cardiovascular diseases 030212 general & internal medicine Pyridines/administration & dosage Intensive care medicine Stroke Anticoagulants/administration & dosage Pyridones/administration & dosage business.industry Warfarin Age Factors Anticoagulants Atrial fibrillation General Medicine medicine.disease Pyrazoles/administration & dosage Dabigatran Clinical trial Thiazoles Clinical Trials Phase III as Topic Pyrazoles Narrative review business Atrial Fibrillation/complications Major bleeding medicine.drug |
Zdroj: | Lip, G Y H 2019, ' The safety of NOACs in atrial fibrillation patient subgroups : A narrative review ', International Journal of Clinical Practice, vol. 73, no. 2, e13285 . https://doi.org/10.1111/ijcp.13285 INTERNATIONAL JOURNAL OF CLINICAL PRACTICE |
DOI: | 10.1111/ijcp.13285 |
Popis: | AIM: Four non-vitamin K oral anticoagulants (NOACs) have been evaluated in clinical trials for the prevention of stroke in patients with atrial fibrillation (AF). Although each of the NOACs have been shown to be at least non-inferior to warfarin for efficacy and safety outcomes, controversy remains over the relative safety of each NOAC in patient subgroups. This narrative review provides an overview of phase III data on NOAC trials for the prevention of stroke in AF, with a focus on reporting the safety of each agent in key patient subgroups based on age, gender, accumulated risk factors, and primary or secondary prevention of stroke.METHODS: A comprehensive literature search was completed and, where data permit, analyses of phase III trials of the NOACs are presented for each patient subgroup.RESULTS: Analyses of key safety outcomes from NOAC trials were completed using primary trial data, including major bleeding and all-cause mortality. The safety of NOACs was generally consistent and favourable compared to warfarin according to patient age, gender, previous history of stroke, and the presence of risk factors for stroke.CONCLUSIONS: The safety of the NOACs compared to warfarin was generally favourable across different patient subgroups, including those perceived to be at 'high risk' for adverse outcomes. However, certain NOACs may be preferable to warfarin in some subgroups, based on indirect analyses. This article is protected by copyright. All rights reserved. |
Databáze: | OpenAIRE |
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