Abstract |
Anticoagulants are effective at preventing and treating thrombosis, but can cause bleeding. For decades, vitamin K antagonists (VKAs) have been the only available oral anticoagulants. The development of non-VKA oral anticoagulants (NOACs), which inhibit either factor Xa or thrombin stoichiometrically, has provided alternatives to VKAs for several indications. The results of recent large-scale randomised controlled trials comparing NOACs with VKAs for the prevention of stroke in patients with non-valvular atrial fibrillation (AF) have produced some unexpected results. As a group, NOACs showed similar efficacy as warfarin, but a reduced risk of major bleeding. The reduction in bleeding with NOACs was greatest with intracranial hemorrhage. In contrast, the relative risk of gastro-intestinal bleeding was increased with some NOACs. In this review, we explore the potential mechanisms as well as the implications of these organ-specific bleeding patterns.
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Authors | Thomas Vanassche, Jack Hirsh, John W Eikelboom, Jeffrey S Ginsberg |
Journal | Thrombosis and haemostasis
(Thromb Haemost)
Vol. 112
Issue 5
Pg. 918-23
(Nov 2014)
ISSN: 2567-689X [Electronic] Germany |
PMID | 25187203
(Publication Type: Comparative Study, Journal Article, Review)
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Chemical References |
- Anticoagulants
- Blood Coagulation Factors
- Factor Xa Inhibitors
- Vitamin K
- Warfarin
- Thromboplastin
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Topics |
- Anticoagulants
(adverse effects, pharmacokinetics, therapeutic use)
- Atrial Fibrillation
(complications)
- Blood Coagulation Factors
(physiology)
- Endothelium, Vascular
(physiopathology)
- Factor Xa Inhibitors
(adverse effects, pharmacokinetics, therapeutic use)
- Gastrointestinal Hemorrhage
(chemically induced, physiopathology, prevention & control)
- Hemorrhage
(chemically induced)
- Humans
- International Normalized Ratio
- Intestinal Absorption
- Intracranial Hemorrhages
(chemically induced, physiopathology, prevention & control)
- Organ Specificity
- Randomized Controlled Trials as Topic
- Stroke
(prevention & control)
- Thrombophilia
(drug therapy, etiology)
- Thromboplastin
(physiology)
- Vitamin K
(antagonists & inhibitors)
- Warfarin
(adverse effects, therapeutic use)
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