Rivaroxaban reversal with prothrombin complex concentrate or tranexamic acid in healthy volunteers

被引:41
作者
Levy, J. H. [1 ]
Moore, K. T. [2 ]
Neal, M. D. [3 ]
Schneider, D. [4 ,5 ,6 ]
Marcsis, V. S. [2 ]
Ariyawansa, J. [2 ]
Weitz, J. I. [5 ,6 ]
机构
[1] Duke Univ, Med Ctr, Dept Anesthesiol & Crit Care, Durham, NC USA
[2] Janssen Sci Affairs, Janssen Pharmaceut, Titusville, NJ USA
[3] Univ Pittsburgh, Dept Surg, Pittsburgh, PA USA
[4] Univ Vermont, Dept Med, Cardiovasc Res Inst, Burlington, VT USA
[5] McMaster Univ, Hamilton, ON, Canada
[6] Thrombosis & Atherosclerosis Res Inst, Hamilton, ON, Canada
关键词
anticoagulants; antidotes; hemorrhage; prothrombin complex concentrate; rivaroxaban; tranexamic acid; SEVERE HEMOPHILIA-A; FACTOR-VIII PRODUCTS; INHIBITOR DEVELOPMENT; PLASMA; CHILDREN;
D O I
10.1111/jth.13894
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Oral activated factor X inhibitors such as rivaroxaban are widely used, but specific reversal agents are lacking. Although four-factor prothrombin complex concentrate (4F-PCC) and tranexamic acid (TXA) are sometimes used to manage serious bleeding, their efficacy is unknown. Prior studies in healthy subjects taking rivaroxaban revealed that 4F-PCC partially reverses the prolonged prothrombin time (PT), and fully restores the endogenous thrombin potential (ETP). The effect of TXA has not been evaluated. Methods: In this double-blind, parallel-group study, 147 healthy volunteers given rivaroxaban 20 mg twice daily for 3 days were randomized after their morning dose on day 4 to receive intravenous 4F-PCC (50 IU kg(-1)), TXA (1.0 g), or saline. Standardized punch biopsies were performed at baseline and after 4F-PCC, TXA or saline administration. Reversal was assessed by measuring bleeding duration and bleeding volume at biopsy sites, and by determining the PT and ETP. Results: As compared with saline, 4F-PCC partially reversed the PT and completely reversed the ETP, whereas TXA had no effect. Neither 4F-PCC nor TXA reduced bleeding duration or volume. All treatments were well tolerated, with no recorded adverse events. Conclusions: Although 4F-PCC reduced the PT and increased the ETP in volunteers given supratherapeutic doses of rivaroxaban, neither 4F-PCC nor TXA influenced punch biopsy bleeding.
引用
收藏
页码:54 / 64
页数:11
相关论文
共 23 条
[1]   Interval estimation for a binomial proportion - Comment - Rejoinder [J].
Brown, LD ;
Cai, TT ;
DasGupta, A ;
Agresti, A ;
Coull, BA ;
Casella, G ;
Corcoran, C ;
Mehta, C ;
Ghosh, M ;
Santner, TJ ;
Brown, LD ;
Cai, TT ;
DasGupta, A .
STATISTICAL SCIENCE, 2001, 16 (02) :101-133
[2]   Recombinant factor VIII products and inhibitor development in previously untreated boys with severe hemophilia A [J].
Calvez, Thierry ;
Chambost, Herve ;
Claeyssens-Donadel, Segolene ;
d'Oiron, Roseline ;
Goulet, Veronique ;
Guillet, Benoit ;
Heritier, Virginie ;
Milien, Vanessa ;
Rothschild, Chantal ;
Roussel-Robert, Valerie ;
Vinciguerra, Christine ;
Goudemand, Jenny .
BLOOD, 2014, 124 (23) :3398-3408
[3]   Factor VIII brand and the incidence of factor VIII inhibitors in previously untreated UK children with severe hemophilia A, 2000-2011 [J].
Collins, Peter W. ;
Palmer, Benedict P. ;
Chalmers, Elizabeth A. ;
Hart, Daniel P. ;
Liesner, Ri ;
Rangarajan, Savita ;
Talks, Katherine ;
Williams, Michael ;
Hay, Charles R. M. .
BLOOD, 2014, 124 (23) :3389-3397
[4]   Inhibitor development in haemophilia according to concentrate Four-year results from the European HAemophilia Safety Surveillance (EUHASS) project [J].
Fischer, Kathelijn ;
Lassila, Riita ;
Peyvandi, Flora ;
Calizzani, Gabriele ;
Gatt, Alex ;
Lambert, Thierry ;
Windyga, Jerzy ;
Iorio, Alfonso ;
Gilman, Estelle ;
Makris, Michael .
THROMBOSIS AND HAEMOSTASIS, 2015, 113 (05) :968-975
[5]   Systematic Review of the Role of FVIII Concentrates in Inhibitor Development in Previously Untreated Patients with Severe Hemophilia A: A 2013 Update [J].
Franchini, Massimo ;
Coppola, Antonio ;
Rocino, Angiola ;
Santagostino, Elena ;
Tagliaferri, Annarita ;
Zanon, Ezio ;
Morfini, Massimo .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2013, 39 (07) :752-766
[6]  
Fuchs B, 2009, J THROMB HAEMOST, V7, P838
[7]   Influence of the type of F8 gene mutation on inhibitor development in a single centre cohort of severe haemophilia A patients [J].
Gouw, S. C. ;
Van der Bom, J. G. ;
Van den Berg, H. M. ;
Zewald, R. A. ;
Van Amstel, J. K. Ploos ;
Mauser-Bunschoten, E. P. .
HAEMOPHILIA, 2011, 17 (02) :275-281
[8]   Intensity of factor VIII treatment and inhibitor development in children with severe hemophilia A: the RODIN study [J].
Gouw, Samantha C. ;
van den Berg, H. Marijke ;
Fischer, Kathelijn ;
Auerswald, Guenter ;
Carcao, Manuel ;
Chalmers, Elizabeth ;
Chambost, Herve ;
Kurnik, Karin ;
Liesner, Ri ;
Petrini, Pia ;
Platokouki, Helen ;
Altisent, Carmen ;
Oldenburg, Johannes ;
Nolan, Beatrice ;
Perez Garrido, Rosario ;
Mancuso, M. Elisa ;
Rafowicz, Anne ;
Williams, Mike ;
Clausen, Niels ;
Middelburg, Rutger A. ;
Ljung, Rolf ;
van der Bom, Johanna G. .
BLOOD, 2013, 121 (20) :4046-4055
[9]   Factor VIII Products and Inhibitor Development in Severe Hemophilia A [J].
Gouw, Samantha C. ;
van der Bom, Johanna G. ;
Ljung, Rolf ;
Escuriola, Carmen ;
Cid, Ana R. ;
Claeyssens-Donadel, Segolene ;
van Geet, Christel ;
Kenet, Gili ;
Makipernaa, Anne ;
Molinari, Angelo Claudio ;
Muntean, Wolfgang ;
Kobelt, Rainer ;
Rivard, George ;
Santagostino, Elena ;
Thomas, Angela ;
van den Berg, H. Marijke .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 368 (03) :231-239
[10]  
HIRONAKA T, 1992, J BIOL CHEM, V267, P8012