Prehospital Lyophilized Plasma Transfusion for Trauma-Induced Coagulopathy in Patients at Risk for Hemorrhagic Shock

医学 凝血病 随机对照试验 输血 损伤严重程度评分 入射(几何) 新鲜冰冻血浆 麻醉 休克(循环) 外科 急诊医学 内科学 毒物控制 伤害预防 血小板 物理 光学
作者
Daniel Jost,Sabine Lemoine,F. Lemoine,Clément Derkenne,Sébastien Beaume,Vincent Lanoë,Olga Maurin,Emilie Louis-Delaurière,Maëlle Delacôte,Pascal Dang-Minh,Marilyn Franchin-Frattini,René Bihannic,Dominique Savary,Albrice Levrat,Clémence Baudouin,Julie Trichereau,Marina Salomé,Benoît Frattini,Vivien Hong Tuan Ha,Romain Jouffroy
出处
期刊:JAMA network open [American Medical Association]
卷期号:5 (7): e2223619-e2223619 被引量:52
标识
DOI:10.1001/jamanetworkopen.2022.23619
摘要

Importance

Blood transfusion is a mainstay of therapy for trauma-induced coagulopathy, but the optimal modalities for plasma transfusion in the prehospital setting remain to be defined.

Objective

To determine whether lyophilized plasma transfusion can reduce the incidence of trauma-induced coagulopathy compared with standard care consisting of normal saline infusion.

Design, Setting, and Participants

This randomized clinical trial was performed at multiple centers in France involving prehospital medical teams. Participants included 150 adults with trauma who were at risk for hemorrhagic shock and associated coagulopathy between April 1, 2016, and September 30, 2019, with a 28-day follow-up. Data were analyzed from November 1, 2019, to July 1, 2020.

Intervention

Patients were randomized in a 1:1 ratio to receive either plasma or standard care with normal saline infusion (control).

Main Outcomes and Measures

The primary outcome was the international normalized ratio (INR) on arrival at the hospital. Secondary outcomes included the need for massive transfusion and 30-day survival. As a safety outcome, prespecified adverse events included thrombosis, transfusion-related acute lung injury, and transfusion-associated circulatory overload.

Results

Among 150 randomized patients, 134 were included in the analysis (median age, 34 [IQR, 26-49] years; 110 men [82.1%]), with 68 in the plasma group and 66 in the control group. Median INR values were 1.21 (IQR, 1.12-1.49) in the plasma group and 1.20 (IQR, 1.10-1.39) in the control group (median difference, −0.01 [IQR, −0.09 to 0.08];P = .88). The groups did not differ significantly in the need for massive transfusion (7 [10.3%] vs 4 [6.1%]; relative risk, 1.78 [95% CI, 0.42-8.68];P = .37) or 30-day survival (hazard ratio for death, 1.07 [95% CI, 0.44-2.61];P = .89). In the full intention-to-treat population (n = 150), the groups did not differ in the rates of any of the prespecified adverse events.

Conclusions and Relevance

In this randomized clinical trial including severely injured patients at risk for hemorrhagic shock and associated coagulopathy, prehospital transfusion of lyophilized plasma was not associated with significant differences in INR values vs standard care with normal saline infusion. Nevertheless, these findings show that lyophilized plasma transfusion is a feasible and safe procedure for this patient population.

Trial Registration

ClinicalTrials.gov Identifier:NCT02736812
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