The new oral anti-coagulants and the phase 3 clinical trials - a systematic review of the literature
Affiliation
Dow Medical College, Dow University of Health Sciences, Baba-e-Urdu Road, Karachi, PakistanDepartment of Medicine, Indiana University, Indianapolis, Indiana, USA
Department of Medicine, University of Arizona, Arizona, USA
Quaid-e-Azam Medical College, Bahawalpur, Pakistan
Issue Date
2013Keywords
Vitamin K antagonistsOral anticoagulants
Apixaban
Rivaroxaban
Dabigatran
Orthopedic surgery
Knee replacement
Hip replacement
Acute coronary syndrome
Atrial fibrillation
Venous thromboembolism
Critically ill patients
Systematic review
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BioMed CentralCitation
Tahir et al. Thrombosis Journal 2013, 11:18 http://www.thrombosisjournal.com/content/11/1/18Journal
Thrombosis JournalRights
© 2013 Tahir et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0).Collection Information
This item is part of the UA Faculty Publications collection. For more information this item or other items in the UA Campus Repository, contact the University of Arizona Libraries at repository@u.library.arizona.edu.Abstract
BACKGROUND:Anticoagulation with vitamin K antagonists such as warfarin has historically been used for the long term management of patients with thromboembolic disease. However, these agents have a slow onset of action which requires bridging therapy with heparin and its analogues, which are available only in parenteral route. To overcome these limitations, new oral anticoagulants such as factor Xa inhibitors and direct thrombin inhibitors have been developed. The aim of this article is to systematically review the phase 3 clinical trials of new oral anticoagulants in common medical conditions.METHODS:We searched PubMed (Medline) from January 2007 to February 2013 using "Oral anticoagulants", "New oral anticoagulants", "Randomized controlled trial", "Novel anticoagulants", "Apixaban", "Rivaroxaban", "Edoxaban", "Dabigatran etexilate", "Dabigatran" and a combination of the above terms. The available evidence from the phase 3 RCTs was summarized on the basis of individual drug and the medical conditions categorized into "atrial fibrillation", "acute coronary syndrome", "orthopedic surgery", "venous thromboembolism" and "medically ill patients".RESULTS:Apixaban, rivaroxaban and dabigatran have been found to be either non-inferior or superior to enoxaparin in prophylaxis of venous thromboembolism in knee and hip replacement with similar bleeding risk, superior to warfarin for stroke prevention in atrial fibrillation with significant reduction in the risk of major bleeding, non-inferior to aspirin for reducing cardiovascular death and stroke in acute coronary syndrome with significant increase in the risk of major bleed. Rivaroxaban and dabigatran are also superior to the conventional agents in the management of symptomatic venous thromboembolism. However, compared to enoxaparin, apixaban and rivaroxaban use lead to significantly increased bleeding risk in medically ill patients. Additional studies evaluating the specific reversal agents of these new drugs for the management of life-threatening bleeding or other adverse effects are necessary.CONCLUSION:Considering their pharmacological properties, their efficacy and bleeding complications, the new oral agents offer a net favourable clinical profile in orthopedic surgery, atrial fibrillation, acute coronary syndrome and increase the risk of bleeding in critically ill patients. Further studies are necessary to determine the long term safety and to identify the specific reversal agents of these new drugs.EISSN
1477-9560Version
Final published versionAdditional Links
http://www.thrombosisjournal.com/content/11/1/18ae974a485f413a2113503eed53cd6c53
10.1186/1477-9560-11-18
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Except where otherwise noted, this item's license is described as © 2013 Tahir et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0).

