期刊论文详细信息
Thrombosis Journal
Supporting the use of a coagulometric method for rivaroxaban control: a hypothesis-generating study to define the safety cut-offs
Claudio Daniel Gonzalez2  Raul Altman1 
[1] Centro de Trombosis de Buenos Aires, Buenos Aires, Argentina;Department of Pharmacology, School of Medicine, University of Buenos Aires, Buenos Aires, Argentina
关键词: Safety;    Rivaroxaban;    Reference ranges;    Drug monitoring;    Anticoagulants;   
Others  :  1222781
DOI  :  10.1186/s12959-015-0058-9
 received in 2015-04-02, accepted in 2015-05-29,  发布年份 2015
PDF
【 摘 要 】

Aims

Although quantitative anti-FXa assays can be used to measure rivaroxaban plasma levels, they are not widely performed or available. We aimed to tentatively determine the cut-off for thromboembolism and bleeding prevention based on the clotting effect of non-rivaroxaban conjugate-activated FX plasma levels in patients with rivaroxaban using a coagulometric method.

Methods and results

Rivaroxaban was added in vitro to normal plasma at a range of 0 to 241 μg/L to cover expected peak and trough levels. Rivaroxaban chromogenic (μg/L) and RVV-confirm as a ratio were determined. Patient plasma samples were assayed with the RVV-confirm reagent. The appropriate rivaroxaban plasma concentration to inhibit clotting mechanisms was based on the remaining FXa in plasma, which was expressed as the ratio of patients/normal, R-C. There is a high correlation between R-C in vitro and spiked normal plasma rivaroxaban concentration (R-Square 0.910, linear equation; 0.971 quadratic equation, p < 0.0001 for both) but not with plasma rivaroxaban chromogenic assays. We propose a cut-off R-C value of 1.65 and 4.5 for safety. Based on the proposed therapeutic range, in 158 assays performed in 58 patients, 6.3 % assays were above the level of bleeding tendency at the peak (R-C 5.39 ± 1.01, median 5.13) and 42 % assays were below the prevention cut-off at the trough (R-C 1.31 ± 0.18, median 1.35).

Conclusions

RVVconfirm® is fast and sensitive to measure the effect of rivaroxaban. Clinical studies are needed to establish whether this cut-off is useful for identifying patients at increased risk of hemorrhage or those who exhibit a low level of anticoagulation.

【 授权许可】

   
2015 Altman and Gonzalez.

【 预 览 】
附件列表
Files Size Format View
20150827081613417.pdf 639KB PDF download
Fig. 3. 18KB Image download
Fig. 2. 14KB Image download
Fig. 1. 14KB Image download
【 图 表 】

Fig. 1.

Fig. 2.

Fig. 3.

【 参考文献 】
  • [1]Rodriguez RA, Carrier M, Wells PS. Non-adherence to new oral anticoagulants: a reason for concern during long-term anticoagulation? J Thrombos Haemost. 2013; 11:390-4.
  • [2]Bosworth HB, Bradi B, Granger BB, Mendys P, Brindis R, Burkholder R et al.. Medication adherence: a call for action. Am Heart J. 2011; 162:412-24.
  • [3]Davis NJ, Billett HH, Cohen HW, Arnsten JH. Impact of adherence, knowledge, and quality of life on anticoagulation control. Ann Pharmacother. 2005; 39:632-6.
  • [4]Samama MM, Contant G, Spiro TE, Perzborn E, Le Flem L, Guinet C et al.. Laboratory assessment of rivaroxaban: a review. Thromb J. 2013; 11:11. BioMed Central Full Text
  • [5]Baglin T, Hillarp A, Tripodi A, Elalamy I, Buller H, Ageno W. Measuring oral direct inhibitors of thrombin and factor Xa: a recommendation from the Subcommittee on Control of Anticoagulation of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. J Thromb Haemost. 2013; 11:756-60.
  • [6]Cuker A, Siegal DM, Crowther MA, Garcia DA. Laboratory measurement of the anticoagulant activity of the non-vitamin K oral anticoagulants. J Am Coll Cardiol. 2014; 64:1128-39.
  • [7]Altman R, Gonzalez CD. Simple and rapid assay for effect of the new oral anticoagulant (NOAC) rivaroxaban: preliminary results support further tests with all NOACs. Thromb J. 2014; 12:7. BioMed Central Full Text
  • [8]Exner T, Ellwood L, Rubie J, Barancewicz A. Testing for new oral anticoagulants with LA resistant russells viper venom reagents. an in vitro study. Thromb Haemost. 2013; 109:762-5.
  • [9]Samama MM, Contant G, Spiro TE, Perzborn E, Guinet C, Gourmelin Y et al.. Evaluation of the anti-factor Xa chromogenic assay for the measurement of rivaroxaban plasma concentrations using calibrators and controls. Thromb Haemost. 2012; 107:379-87.
  • [10]Dargaud Y, Hoffman M, Lefrapper L, Lin F-C, Genty A, Chatard B et al.. Bleeding risk in warfarinized patients with a therapeutic international normalized ratio: the effect of low factor IX levels. J Thromb Haemost. 2013; 11:1043-52.
  • [11]Menegatti M, Peyvandi F. Factor X deficiency. Semin Thromb Hemost. 2009; 35:407-15.
  • [12]Brown DL, Kouides PA. Diagnosis and treatment of inherited factor X deficiency. Haemophilia. 2008; 14:1176-82.
  • [13]Shim YJ, Won DI. Pharmacokinetics and prophylactic use of FEIBA® in a child with severe congenital factor X deficiency and recurrent spontaneous intracranial haemorrhage: a case report. Haemophilia. 2013; 19:e364-7.
  • [14]Rauch R, Girisch M, Wiegand G, Schroeder W, Hofbeck M, Welisch E et al.. Factor X deficiency and intracranial bleeding: who is at risk? Haemophilia. 2011; 17:759-63.
  • [15]Furuhata M1, Doki N, Hishima T, Okamoto T, Koyama T, Kaito S. Acquired factor X deficiency associated with atypical AL-amyloidosis. Intern Med. 2014; 53:1841-5.
  • [16]Enjeti AK, Walsh M, Seldon M. Spontaneous major bleeding in acquired factor X deficiency secondary to AL-amyloidosis. Haemophilia. 2005; 11:535-8.
  • [17]Brummel-Ziedins KE, Orfeo T, Gissel M, Mann KG, Rosendaal FR. Factor Xa generation by computational modeling: an additional discriminator to thrombin generation evaluation. PLoS One. 2012; 7: Article ID e29178
  • [18]Mueck W, Schwers S, Stampfuss J. Rivaroxaban and other novel oral anticoagulants: pharmacokinetics in healthy subjects, specific patient populations and relevance of coagulation monitoring. Thromb J. 2013; 11:10. BioMed Central Full Text
  • [19]Buller HR, Lensing AW, Prins MH, Agnelli G, Cohen A, Gallus AS et al.. Einstein-DVT dose-ranging study investigators. a dose-ranging study evaluating once-daily oral administration of the factor Xa inhibitor rivaroxaban in the treatment of patients with acute symptomatic deep vein thrombosis: the einstein-DVT dose-ranging study. Blood. 2008; 112:2242-7.
  • [20]Douros A, Schlemm L, Bolbrinker J, Ebinger M, Kreutz R. Insufficient anticoagulation with dabigatran in a patient with short bowel syndrome. Thromb Haemost. 2014; 112:419-20.
  • [21]Lippi G, Favaloro EJ. Recent guidelines and recommendations for laboratory assessment of the direct oral anticoagulants (DOACs): is there consensus? Clin Chem Lab Med. 2014.
  • [22]Weinz C, Schwarz T, Kubitza D, Mueck W, Lang D. Metabolism and excretion of rivaroxaban, an oral, direct factor Xa inhibitor, in rats, dogs, and humans. Drug Metab Dispos. 2009; 37:1056-64.
  • [23]ten Cate H. New oral anticoagulants: discussion on monitoring and adherence should start now! Thromb J. 2013; 11:8. BioMed Central Full Text
  • [24]Beyer-Westendorf J, Gelbricht V, Thieme C et al.. Rates, management, and outcome of rivaroxaban bleeding in daily care: results from the Dresden NOAC registry. Blood. 2014; 124:955-62.
  文献评价指标  
  下载次数:3次 浏览次数:6次