Intravenous Lipid Emulsion Does Not Reverse Dabigatran-induced Anticoagulation in a Rat Model

被引:9
作者
Blum, Jared [1 ]
Carreiro, Stephanie [1 ]
Hack, Jason B. [1 ,2 ]
机构
[1] Brown Univ, Dept Emergency Med, Warren Alpert Med Sch, Providence, RI 02912 USA
[2] Brown Univ, Div Med Toxicol, Warren Alpert Med Sch, Providence, RI 02912 USA
关键词
DIRECT THROMBIN INHIBITOR; LOCAL-ANESTHETIC TOXICITY; ATRIAL-FIBRILLATION; COAGULATION ASSAYS; RESCUE THERAPY; ETEXILATE; RESUSCITATION; LAMOTRIGINE; OVERDOSE;
D O I
10.1111/acem.12225
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
ObjectivesThe anticoagulant dabigatran has no reversal agent and may cause life-threatening bleeding in patients with trauma or closed-space hemorrhage. Intravenous lipid emulsion (ILE) is thought to create a lipid compartment in serum that sequesters lipophilic drugs. Dabigatran is lipophilic, and its anticoagulant effects are concentration dependent. The study objective was to determine if ILE therapy reverses dabigatran's anticoagulant effects. MethodsTwenty rats were selected at random, 10 in the ILE group and 10 in a normal saline (NS) control group. Animals had a baseline tail bleeding time (T0), followed by oral dabigatran administration (15mg/kg). At 45minutes (T45), a second tail bleed time measurement was performed, followed by a 7-minute infusion of 15mL/kg ILE or NS. A final 60-minute (T60) bleed time measurement was obtained. An ILE-only group of five animals had bleeding times assessed prior to (T0) and 15minutes after (T15) ILE therapy. A mixed-effect repeated-measures analysis of variance modeling the effect of time, group, and the interaction of group and time on bleed times was conducted. ResultsThere was a significant within-subject change in bleeding time across the assessment points (F(2,36)=33; p<0.001), but there were no effect of group (F(1,18)=1.42, p=0.25) or an interaction between group and assessment point on mean bleeding time (F(2,36)=0.59, p=56). Between T0 and T45, average bleeding times increased from 109.5seconds (95% confidence interval [CI]=94 to 125seconds) to 231.8seconds (95% CI=193 to 271seconds; p<0.0001) for both the ILE group and the NS control group. Between T45 and T60, bleeding times in the ILE group decreased by 31.5seconds (95% CI=-77 to 14seconds) and by 6seconds (95% CI=-67 to 55seconds) in the NS group (p=0.46). In the five ILE-only animals, the average bleeding time at T0 was 114seconds (95% CI=62 to 166seconds), which increased significantly at T15 to 237seconds (95% CI=161 to 313seconds; p=0.02). ConclusionsThe anticoagulant effects of dabigatran are not reversed with ILE therapy. Although ILE itself significantly prolonged bleeding times, when administered to dabigatran-anticoagulated rats, bleeding times did not change significantly. There may be a complex interaction of ILE with dabigatran that this study was not able to elucidate.
引用
收藏
页码:1022 / 1025
页数:4
相关论文
共 26 条
[1]  
[Anonymous], FDA APPR PRAD PREV S
[2]   Advances in Anticoagulation: Focus on Dabigatran, an Oral Direct Thrombin Inhibitor [J].
Augoustides, John G. T. .
JOURNAL OF CARDIOTHORACIC AND VASCULAR ANESTHESIA, 2011, 25 (06) :1208-1212
[3]   Reversal of New Oral Anticoagulants [J].
Battinelli, Elisabeth M. .
CIRCULATION, 2011, 124 (14) :1508-1510
[4]   LIPID EMULSION AS RESCUE THERAPY IN LAMOTRIGINE OVERDOSE [J].
Castanares-Zapatero, Diego ;
Wittebole, Xavier ;
Huberlant, Vincent ;
Morunglav, Mihaiela ;
Hantson, Philippe .
JOURNAL OF EMERGENCY MEDICINE, 2012, 42 (01) :48-51
[5]   The role of fat emulsion therapy in a rodent model of propranolol toxicity: a preliminary study. [J].
Cave G. ;
Harvey M.G. ;
Castle C.D. .
Journal of Medical Toxicology, 2006, 2 (1) :4-7
[6]   Intravenous Lipid Emulsion as Antidote Beyond Local Anesthetic Toxicity: A Systematic Review [J].
Cave, Grant ;
Harvey, Martyn .
ACADEMIC EMERGENCY MEDICINE, 2009, 16 (09) :815-824
[7]   Dabigatran versus Warfarin in Patients with Atrial Fibrillation. [J].
Connolly, Stuart J. ;
Ezekowitz, Michael D. ;
Yusuf, Salim ;
Eikelboom, John ;
Oldgren, Jonas ;
Parekh, Amit ;
Pogue, Janice ;
Reilly, Paul A. ;
Themeles, Ellison ;
Varrone, Jeanne ;
Wang, Susan ;
Alings, Marco ;
Xavier, Denis ;
Zhu, Jun ;
Diaz, Rafael ;
Lewis, Basil S. ;
Darius, Harald ;
Diener, Hans-Christoph ;
Joyner, Campbell D. ;
Wallentin, Lars .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 361 (12) :1139-1151
[8]   Impact of dabigatran on a large panel of routine or specific coagulation assays Laboratory recommendations for monitoring of dabigatran etexilate [J].
Douxfils, Jonathan ;
Mullier, Francois ;
Robert, Severine ;
Chatelain, Christian ;
Chatelain, Bernard ;
Dogne, Jean-Michel .
THROMBOSIS AND HAEMOSTASIS, 2012, 107 (05) :985-997
[9]   Reversal of Rivaroxaban and Dabigatran by Prothrombin Complex Concentrate A Randomized, Placebo-Controlled, Crossover Study in Healthy Subjects [J].
Eerenberg, Elise S. ;
Kamphuisen, Pieter W. ;
Sijpkens, Meertien K. ;
Meijers, Joost C. ;
Buller, Harry R. ;
Levi, Marcel .
CIRCULATION, 2011, 124 (14) :1573-1579
[10]   Partition constant and volume of distribution as predictors of clinical efficacy of lipid rescue for toxicological emergencies [J].
French, Deborah ;
Smollin, Craig ;
Ruan, Weiming ;
Wong, Alicia ;
Drasner, Kenneth ;
Wu, Alan H. B. .
CLINICAL TOXICOLOGY, 2011, 49 (09) :801-809