Dose tailoring of dabigatran etexilate: obvious or excessive?

被引:21
作者
Douxfils, Jonathan [1 ]
Mullier, Francois [1 ,2 ]
Dogne, Jean-Michel [1 ]
机构
[1] Univ Namur, NTHC, Namur Res Inst LIfe Sci NARILIS, Fac Med,Dept Pharm, B-5000 Namur, Belgium
[2] Catholic Univ Louvain, NTHC, Namur Res Inst LIfe Sci NARILIS, Hematol Lab,CHU Dinant Godinne UcL Namur,CHU Dina, B-5530 Yvoir, Belgium
关键词
anticoagulant drugs; benefit-risk assessment; dabigatran etexilate; drug monitoring; NONVALVULAR ATRIAL-FIBRILLATION; LABORATORY MONITORING; ORAL ANTITHROMBOTICS; THROMBIN TIME; REGISTRY; RISK; NEED;
D O I
10.1517/14740338.2015.1049995
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Dabigatran etexilate is used for preventing blood clots and tends to replace older anticoagulants in many of their indications. However, the 'one dose fits all' policy is subject to criticism. Recent findings assert the anxiety of the scientific community concerning the pharmacokinetic properties of dabigatran etexilate, that is, an important, interindividual variability including an important genetic variant with a significant dependence of the renal function as route of elimination. Areas covered: This meta-opinion provides an overview of the current knowledge and evidence on the dose tailoring of dabigatran etexilate. It also discusses the remaining challenges to benefit from this perspective strategy to enhance the benefit-risk balance of dabigatran etexilate. Data were searched in the published literature and on regulatory agencies' websites. Additionally, unpublished data were searched and discussed. Expert opinion: Causality between dabigatran exposure and bleeding risk is now established and recommendations on how to best estimate the drug exposure are published. Additionally, simulating studies revealed that a dose adaptation based on dabigatran plasma concentration estimations could improve the benefit-risk profile of the drug. This accumulating evidence suggests that some patients under dabigatran etexilate may benefit from a tailoring of the dose beyond the ones already proposed by the manufacturer.
引用
收藏
页码:1283 / 1289
页数:7
相关论文
共 34 条
  • [1] Effects on routine coagulation screens and assessment of anticoagulant intensity in patients taking oral dabigatran or rivaroxaban: Guidance from the British Committee for Standards in Haematology
    Baglin, Trevor
    Keeling, David
    Kitchen, Steve
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2012, 159 (04) : 427 - 429
  • [2] New oral antithrombotics: a need for laboratory monitoring. Against
    Bounameaux, H.
    Reber, G.
    [J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2010, 8 (04) : 627 - 630
  • [3] Real-world variability in dabigatran levels in patients with atrial fibrillation
    Chan, N. C.
    Coppens, M.
    Hirsh, J.
    Ginsberg, J. S.
    Weitz, J. I.
    Vanassche, T.
    Douketis, J. D.
    Schulman, S.
    Eikelboom, J. W.
    [J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2015, 13 (03) : 353 - 359
  • [4] Douxfils J, 2014, BIOMED RES INT
  • [5] Douxfils J, 2015, J THROMB HAEMOST, DOI [10.1111/jth.12880, DOI 10.1111/JTH.12880.[EPUB]
  • [6] Estimation of dabigatran plasma concentrations in the perioperative setting An ex vivo study using dedicated coagulation assays
    Douxfils, Jonathan
    Lessire, Sarah
    Dincq, Anne-Sophie
    Hjemdahl, Paul
    Ronquist-Nii, Yuko
    Pohanka, Anton
    Gourdin, Maximilien
    Chatelain, Bernard
    Dogne, Jean-Michel
    Mullier, Francois
    [J]. THROMBOSIS AND HAEMOSTASIS, 2015, 113 (04) : 862 - 869
  • [7] Comparison of calibrated dilute thrombin time and aPTT tests with LC-MS/MS for the therapeutic monitoring of patients treated with dabigatran etexilate
    Douxfils, Jonathan
    Dogne, Jean-Michel
    Mullier, Francois
    Chatelain, Bernard
    Ronquist-Nii, Yuko
    Malmstrom, Rickard E.
    Hjemdahl, Paul
    [J]. THROMBOSIS AND HAEMOSTASIS, 2013, 110 (03) : 543 - 549
  • [8] European Medicines Agency, 2011, EMEAHC000829X13G EUR
  • [9] European Medicines Agency, 2015, PRAD SUMM PROD CHAR
  • [10] FDA, 2010, US Food and Drug Administration. Pradaxa: Clinical pharmacology and biopharmaceutics review(s)