Which Patients May Benefit from Dose Adjustment of Non-Vitamin K Antagonist Oral Anticoagulants?

被引:14
作者
Chin, Paul K. L. [1 ]
机构
[1] Univ Otago, Dept Med, Christchurch, New Zealand
关键词
dabigatran; rivaroxaban; apixaban; edoxaban; dose adjustment; blood coagulation; monitoring; pharmacokinetics; FACTOR-XA INHIBITOR; DIRECT THROMBIN INHIBITOR; NONVALVULAR ATRIAL-FIBRILLATION; ASSAYS LABORATORY RECOMMENDATIONS; DAILY DOSING FREQUENCY; DRUG-DRUG INTERACTION; DABIGATRAN ETEXILATE; VENOUS THROMBOEMBOLISM; COAGULATION ASSAYS; KNEE REPLACEMENT;
D O I
10.1055/s-0035-1546465
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The commercially available non-vitamin K antagonist oral anticoagulants (NOAC) are an emerging therapeutic class, which includes dabigatran, rivaroxaban, apixaban, and edoxaban. Dose adjustment of the NOAC currently takes into account the presence of particular patient characteristics that may alter NOAC concentrations. These characteristics include the presence of renal impairment and concomitant drugs affecting proteins involved with the transport and metabolism of the NOAC. NOAC concentrations reflect anticoagulant activity; some studies have shown some correlation with the risks of adverse events, while others have not, and the association is debated by workers in the field. However, dose adjustment based on characteristics before dosing assumes that the patient has drug oral availability and clearance at the mean of patients with these characteristics. Direct quantification of NOAC concentrations, for example, through the use of calibrated coagulation assays, is likely to add further to individualization of dosing to the particular patient.
引用
收藏
页码:195 / 207
页数:13
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