Pharmacodynamics, pharmacokinetics and clinical efficacy of apixaban in the treatment of thrombosis

被引:3
|
作者
Zheng, Shiying Silvia [1 ]
Chong, James J. H. [2 ,3 ,4 ]
Chong, Beng Hock [1 ,5 ,6 ]
机构
[1] St George Hosp, Dept Haematol, Kogarah, NSW, Australia
[2] Univ Sydney, Sch Med, Sydney, NSW 2006, Australia
[3] Westmead Hosp, Westmead Millennium Inst Med Res, Sydney, NSW, Australia
[4] Westmead Hosp, Dept Cardiol, Sydney, NSW, Australia
[5] Sutherland Hosp, Dept Haematol, Sydney, NSW, Australia
[6] Univ New S Wales, St George Clin Sch, Sydney, NSW, Australia
关键词
Anti-factor Xa; apixaban; oral anticoagulant; venous thrombo-embolism; FACTOR XA INHIBITOR; MOLECULAR-WEIGHT HEPARIN; RECURRENT VENOUS THROMBOEMBOLISM; ED AMERICAN-COLLEGE; ANTITHROMBOTIC THERAPY; LABORATORY MEASUREMENT; COAGULATION ACTIVITY; ORAL ANTICOAGULANTS; PULMONARY-EMBOLISM; VEIN THROMBOSIS;
D O I
10.1517/17425255.2016.1164692
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Venous thromboembolism (VTE) is a common disorder. Heparin and vitamin K antagonists have been the standard treatment for VTE for over 50years. The development of apixaban and other direct oral anticoagulants has greatly increased the range of anticoagulants available for the treatment of VTE.Area covered: Studies on the chemistry, pharmacodynamics and pharmacokinetics of apixaban are reviewed. Its clinical efficacy and safety are discussed, with an emphasis on randomized controlled Phase III clinical trials on treatment of thrombosis.Expert opinion: Apixaban is a safe and effective anticoagulant for VTE treatment. It has several attractive features: its oral activity, rapid action, limited drug- interaction profile and limited need for laboratory monitoring. An antidote may become available in the near future. Further studies of certain patient populations such as patients with cancers, elderly (aged 75years and older) and those with severe renal and liver disease, are required as these patients have not yet been studied in sufficient numbers. As clinical trials included only selected patients, data from these studies may not reflect the real-life' patients in clinical practice. There is therefore an unmet need for large post-registration studies of unselected real-life' patients, such as registry studies, to validate the clinical trial findings.
引用
收藏
页码:575 / 580
页数:6
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