Abstract

BackgroundEvidence on prehospital administration of the antifibrinolytic tranexamic acid (TXA) in civilian trauma populations is scarce. The aim was to study whether prehospital TXA use in trauma patients was associated with improved outcomes.MethodsThe prehospital database of the ADAC (General German Automobile Club) Air Rescue Service was linked with the TraumaRegister of the German Trauma Society to reidentify patients documented in both registries. Primarily admitted trauma patients (2012 until 2014) who were treated with TXA during the prehospital phase were matched with patients who had not received prehospital TXA, applying propensity score-based matching.ResultsThe matching yielded two identical cohorts (n = 258 in each group), since there were no significant differences in demographics or injury characteristics (mean Injury Severity Score 24 ± 14 [TXA] vs. 24 ± 16 [control]; p = 0.46). The majority had sustained blunt injury (90.3 % vs. 93.0 %; p = 0.34). There were no differences with respect to prehospital therapy, including rates of intubation, chest tube insertion or both administration of i.v. fluids and catecholamines. During ER treatment, the TXA cohort received fewer numbers of red blood cells and plasma units, but without reaching statistical significance. Incidences of organ failure, sepsis or thromboembolism showed no significant differences as well, although data were incomplete for these parameters. Early mortality was significantly lower in the TXA group (e.g., 24-h mortality 5.8 % [TXA] vs. 12.4 % [control]; p = 0.01), and mean time to death was 8.8 ± 13.4 days vs. 3.6 ± 4.9 days, respectively (p = 0.001). Overall hospital mortality was similar in both groups (14.7 % vs. 16.3 %; p = 0.72). The most pronounced mortality difference was observed in patients with a high propensity score, reflecting severe injury load.ConclusionsThis is the first civilian study, to our knowledge, in which the effect of prehospital TXA use in trauma patients has been examined. TXA was associated with prolonged time to death and significantly improved early survival. Until further evidence emerges, the results of this study support the use of TXA during prehospital treatment of severely injured patients.

Highlights

  • Evidence on prehospital administration of the antifibrinolytic tranexamic acid (TXA) in civilian trauma populations is scarce

  • Since no other drug is approved for coagulation support during prehospital treatment, the aim of the present study was to assess whether prehospital intravenous (i.v.) administration of TXA in trauma patients is associated with improved outcomes

  • Mortality was significantly lower in the TXA group (e.g., 24-h mortality 5.8 % [TXA] vs. 12.4 % [control]; p = 0.01), and mean time to death was 8.8 ± 13.4 days (TXA) vs. 3.6 ± 4.9 days (p = 0.001)

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Summary

Introduction

Evidence on prehospital administration of the antifibrinolytic tranexamic acid (TXA) in civilian trauma populations is scarce. The aim was to study whether prehospital TXA use in trauma patients was associated with improved outcomes. Wafaisade et al Critical Care (2016) 20:143 in-hospital TXA administration in trauma, but the results have been discussed controversially due to several weaknesses of the trial, such as that the majority of patients were enrolled in developing countries [8, 9]. Evidence on prehospital TXA use in trauma, especially from European countries, is scarce. Since no other drug is approved for coagulation support during prehospital treatment, the aim of the present study was to assess whether prehospital intravenous (i.v.) administration of TXA in trauma patients is associated with improved outcomes. The TR-DGU documents the prothrombin time as prothrombin time index (expressed as a percentage of normal; commonly referred to as Quick’s test), where a value of 1.3 [3, 18]

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