Direct oral anticoagulants for atrial fibrillation [evidence update]

Boucher M, Spry C
Record ID 32018002256
English
Authors' objectives: Atrial fibrillation (AF) is the most common type of cardiac arrhythmia. Oral anticoagulation is an important intervention to prevent thromboembolic complications of this condition. Drug options include vitamin K antagonists (VKAs), such as warfarin, and direct oral anticoagulants (DOACs), such as apixaban, dabigatran, edoxaban, and rivaroxaban. Updated American (2019), Canadian (2020), and European (2020) guidelines all recommend the use of DOACs over VKAs to prevent stroke and other thromboembolic complications in patients with non-valvular AF. These recommendations are based on evidence of similar or improved efficacy of DOACs in preventing stroke, lowering the risk of intracerebral hemorrhage, and reducing mortality, compared with VKAs. A focused literature search was conducted to retrieve new evidence (systematic reviews, meta-analyses, health technology assessments) published since the North American and European guidelines on AF were updated. No new evidence was retrieved. As such, evidence reviewed by the American, Canadian, and European guidelines is still current.
Details
Project Status: Completed
Year Published: 2021
English language abstract: An English language summary is available
Publication Type: Rapid Review
Country: Canada
MeSH Terms
  • Atrial Fibrillation
  • Anticoagulants
  • Drug Therapy
  • Guidelines as Topic
  • Thromboembolism
Keywords
  • Atrial fibrillation
  • Arrhythmias
  • Anticoagulation
  • Drug therapy
  • Vitamin K antagonists
  • Warfarin
  • Direct oral anticoagulants
  • Apixaban
  • Dabigatran
  • Edoxaban
Contact
Organisation Name: Canadian Agency for Drugs and Technologies in Health
Contact Address: 600-865 Carling Avenue, Ottawa, ON K1S 5S8 Canada. Tel: +1 613 226 2553; Fax: +1 613 226 5392;
Contact Name: requests@cadth.ca
Contact Email: requests@cadth.ca
Copyright: <p>Canadian Agency for Drugs and Technologies in Health (CADTH)</p>
This is a bibliographic record of a published health technology assessment from a member of INAHTA or other HTA producer. No evaluation of the quality of this assessment has been made for the HTA database.