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Comparison of tranexamic acid plasma concentrations when administered via intraosseous and intravenous routes.
Boysen, Søren R; Pang, Jessica M; Mikler, John R; Knight, Cameron G; Semple, Hugh A; Caulkett, Nigel A.
Afiliación
  • Boysen SR; Department of Veterinary Clinical and Diagnostic Sciences, University of Calgary, 3280 Hospital Drive NW, Calgary, Alberta T2N 4Z6, Canada. Electronic address: srboysen@ucalgary.ca.
  • Pang JM; Department of Veterinary Clinical and Diagnostic Sciences, University of Calgary, 3280 Hospital Drive NW, Calgary, Alberta T2N 4Z6, Canada.
  • Mikler JR; Defence Research and Development Canada - Suffield Research Centre, Box 4000, Station Main, Medicine Hat, Alberta T1A 8K6, Canada.
  • Knight CG; Department of Veterinary Clinical and Diagnostic Sciences, University of Calgary, 3280 Hospital Drive NW, Calgary, Alberta T2N 4Z6, Canada.
  • Semple HA; Defence Research and Development Canada - Suffield Research Centre, Box 4000, Station Main, Medicine Hat, Alberta T1A 8K6, Canada.
  • Caulkett NA; Department of Veterinary Clinical and Diagnostic Sciences, University of Calgary, 3280 Hospital Drive NW, Calgary, Alberta T2N 4Z6, Canada.
Am J Emerg Med ; 35(2): 227-233, 2017 Feb.
Article en En | MEDLINE | ID: mdl-27816438
INTRODUCTION: There is a lack of information regarding intraosseous (IO) administration of tranexamic acid (TXA). Our hypothesis was that a single bolus IO injection of TXA will have a similar pharmacokinetic profile to TXA administered at the same dose IV. METHODS: Sixteen male Landrace cross swine (mean body weight 27.6±2.6kg) were divided into an IV group (n=8) and an IO group (n=8). Each animal received 30mg/kg TXA via an IV or IO catheter, respectively. Jugular blood samples were collected for pharmacokinetic analysis over a 3h period. The maximum TXA plasma concentration (Cmax) and corresponding time as well as distribution half-life, elimination half-life, area under the curve, plasma clearance and volume of distribution were calculated. One- and two-way analysis of variance for repeated measures (time, group) with Tukey's and Bonferonni post hoc tests were used to compare TXA plasma concentrations within and between groups, respectively. RESULTS: Plasma concentrations of TXA were significantly higher (p<0.0001) in the IV group during the TXA infusion. Cmax occurred at 4min after initiation of the bolus in the IV group (9.36±3.20ng/µl) and at 5min after initiation of the bolus in the IO group (4.46±0.49ng/µl). Plasma concentrations were very similar from the completion of injection onwards. There were no significant differences between the two administration routes for any other pharmacokinetic variables measured. CONCLUSION: The results of this study support pharmacokinetic bioequivalence of IO and IV administration of TXA.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ácido Tranexámico / Análisis de los Gases de la Sangre / Infusiones Intravenosas / Infusiones Intraóseas Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Am J Emerg Med Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ácido Tranexámico / Análisis de los Gases de la Sangre / Infusiones Intravenosas / Infusiones Intraóseas Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Am J Emerg Med Año: 2017 Tipo del documento: Article