Literature DB >> 21464643

Dabigatran etexilate: the first oral anticoagulant available in the United States since warfarin.

Arlene Tran1, Angela Cheng-Lai.   

Abstract

For more than 5 decades, warfarin has been the mainstay of therapy when oral anticoagulation is required. It has been shown to be effective in the prevention as well as treatment of various thromboembolic disorders. However, drawbacks of warfarin, such as time-consuming requirements for frequent international normalized ratio monitoring, as well as drug and food interactions, have encouraged the development of alternative oral agents. One such agent, dabigatran, has risen up to the challenge. Due to its predictable anticoagulation response, dabigatran does not require routine anticoagulation monitoring. Another advantage dabigatran has over warfarin is its more favorable drug and food interaction profiles. Dabigatran was shown to be noninferior to warfarin in studies evaluating the prevention of stroke and systemic embolism in patients with atrial fibrillation, thus leading to the US Food and Drug Administration approval for this indication. Dabigatran has also demonstrated efficacy in the prevention of venous thromboembolism in patients undergoing total hip or knee replacement surgery as well as the prevention of recurrent venous thromboembolism, although these are not current Food and Drug Administration-approved indications. The safety profile appears to be similar to warfarin with regards to overall bleeding risk, though the risk for gastrointestinal bleeds was higher in patients on dabigatran 150 mg twice daily. Disadvantages of dabigatran may include a higher frequency of dyspepsia compared with warfarin, lack of dosing information in severe renal impairment, possible missed opportunities for periodic health examinations and interventions due to elimination of regular physician's visit for international normalized ratio monitoring, and drug costs. This article provides an overview of the clinical studies, pharmacokinetic profile, adverse effects, drug interactions as well as advantages and disadvantages associated with dabigatran.
© 2011 Lippincott Williams & Wilkins

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21464643     DOI: 10.1097/CRD.0b013e3182137758

Source DB:  PubMed          Journal:  Cardiol Rev        ISSN: 1061-5377            Impact factor:   2.644


  6 in total

Review 1.  Evidence behind quality of care measures for venous thromboembolism and atrial fibrillation.

Authors:  G Eymin; A K Jaffer
Journal:  J Thromb Thrombolysis       Date:  2014       Impact factor: 2.300

Review 2.  Injury in the aged: Geriatric trauma care at the crossroads.

Authors:  Rosemary A Kozar; Saman Arbabi; Deborah M Stein; Steven R Shackford; Robert D Barraco; Walter L Biffl; Karen J Brasel; Zara Cooper; Samir M Fakhry; David Livingston; Frederick Moore; Fred Luchette
Journal:  J Trauma Acute Care Surg       Date:  2015-06       Impact factor: 3.313

3.  Review of the randomized evaluation of long-term anticoagulation therapy (RE-LY) trial: warfarin versus dabigatran.

Authors:  Christopher Ingelmo; Oussama Wazni
Journal:  Curr Cardiol Rep       Date:  2011-10       Impact factor: 2.931

Review 4.  Anticoagulation during pregnancy in patients with a prosthetic heart valve.

Authors:  Jose M Castellano; Rajeev L Narayan; Prashant Vaishnava; Valentin Fuster
Journal:  Nat Rev Cardiol       Date:  2012-05-15       Impact factor: 32.419

5.  Management of venous thromboembolism in patients with advanced gastrointestinal cancers: what is the role of novel oral anticoagulants?

Authors:  Ludmila Katherine Martin; Tanios Bekaii-Saab
Journal:  Thrombosis       Date:  2012-09-11

6.  Distribution characteristics and factors influencing oral warfarin adherence in patients after heart valve replacement.

Authors:  Xiaowu Wang; Bo Xu; Hongliang Liang; Shuyun Jiang; Hongmei Tan; Xinrong Wang; Xia Wang; Shiqiang Yu; Jincheng Liu
Journal:  Patient Prefer Adherence       Date:  2018-09-03       Impact factor: 2.711

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.