Pharmacoeconomic implications of thromboprophylaxis with new oral anticoagulants after total hip or knee replacement in the USA

被引:2
作者
Nutescu, Edith A. [1 ,2 ,3 ]
机构
[1] Univ Illinois, Coll Pharm, Ctr Pharmacoecon Res, Chicago, IL 60612 USA
[2] Univ Illinois, Coll Pharm, Dept Pharm Practice, Antithrombosis Ctr, Chicago, IL 60612 USA
[3] Antithrombosis Ctr, Dept Adm, Chicago, IL 60612 USA
关键词
cost; direct thrombin inhibitor; factor Xa inhibitor; pharmacoeconomics; thromboprophylaxis; total hip replacement; total knee replacement; warfarin; DEEP-VEIN THROMBOSIS; VENOUS THROMBOEMBOLISM PROPHYLAXIS; MAJOR ORTHOPEDIC-SURGERY; MOLECULAR-WEIGHT HEPARIN; DABIGATRAN ETEXILATE; COST-EFFECTIVENESS; ECONOMIC BURDEN; DOUBLE-BLIND; ENOXAPARIN; PREVENTION;
D O I
10.1517/14656566.2013.774374
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Adequate thromboprophylaxis after total hip or knee replacement (THR or TKR) is essential to reduce the incidence of venous thromboembolism (VTE) and its associated complications. Although effective, traditional anticoagulants are associated with a considerable economic burden, particularly when used outside the hospital setting. This article explores whether newer oral anticoagulants can reduce costs of VTE prophylaxis and therapy. Areas covered: Cost associated with vitamin K antagonists; indirect costs associated with complicated or inconvenient anticoagulation regimens, non-adherence and associated complications; potential of the newer oral anticoagulants, including direct thrombin inhibitors and direct factor Xa inhibitors, to produce indirect cost savings after THR or TKR through a potential reduction in VTE rates and administration and monitoring costs. Expert opinion: The use of new anticoagulants for VTE prophylaxis after THR or TKR can result in direct and indirect cost savings through improved efficacy by reducing VTE rates and decreased drug administration and monitoring costs compared with traditional anticoagulants. Future research will need to focus on cost analyses driven by clinical outcomes measured on the performance of these agents in actual clinical practice.
引用
收藏
页码:525 / 534
页数:10
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