急性脑损伤患者的限制性输血与自由输血策略:TRAIN 随机临床试验。

Fabio Silvio Taccone, Carla Rynkowski Bittencourt, Kirsten Møller, Piet Lormans, Manuel Quintana-Díaz, Anselmo Caricato, Marco Antonio Cardoso Ferreira, Rafael Badenes, Pedro Kurtz, Christian Baastrup Søndergaard, Kirsten Colpaert, Leticia Petterson, Herve Quintard, Raphael Cinotti, Elisa Gouvêa Bogossian, Cassia Righy, Serena Silva, Erik Roman-Pognuz, Catherine Vandewaeter, Daniel Lemke, Olivier Huet, Ata Mahmoodpoor, Aaron Blandino Ortiz, Mathieu van der Jagt, Russell Chabanne, Walter Videtta, Pierre Bouzat, Jean-Louis Vincent
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引用次数: 0

摘要

重要性:急性脑损伤患者通常需要输血。在这一患者群体中,最佳血红蛋白输血阈值尚不确定:评估两种不同的血红蛋白阈值对急性脑损伤患者输注红细胞的影响:多中心、3 期、平行组、研究者发起、务实、开放标签随机临床试验,在 22 个国家的 72 个重症监护病房进行。符合条件的患者需患有创伤性脑损伤、动脉瘤性蛛网膜下腔出血或脑内出血;伤后头 10 天内血红蛋白值低于 9 g/dL;预计重症监护病房住院时间至少 72 小时。入组时间为 2017 年 9 月 1 日至 2022 年 12 月 31 日。随访的最后一天是 2023 年 6 月 30 日:八百五十名患者被随机分配接受自由输血(由血红蛋白引发的输血):主要结果是随机分配后 180 天内出现不利的神经系统结果,即格拉斯哥结果量表扩展评分在 1 到 5 分之间。预设的严重不良事件有14起,包括随机化后发生脑缺血:在完成试验的 820 名患者中(平均年龄 51 岁;女性 376 人 [45.9%]),806 人有主要结果数据,其中自由策略组 393 人,限制策略组 413 人。自由策略组收到的血液中位数为 2(IQR,1-3)个单位,限制策略组收到的血液中位数为 0(IQR,0-1)个单位,绝对平均差异为 1.0 个单位(95% CI,0.87-1.12 个单位)。随机分组后 180 天,自由策略组中有 246 名患者(62.6%)的神经系统结果不佳,而限制策略组中有 300 名患者(72.6%)的神经系统结果不佳(绝对差异为 -10.0% [95% CI, -16.5% to -3.6%];调整后相对风险为 0.86 [95% CI, 0.79-0.94]; P = .002)。输血阈值对 180 天后神经系统预后的影响在预设亚组中是一致的。在自由策略组中,397 名患者中有 35 人(8.8%)至少发生过一次脑缺血事件,而在限制策略组中,423 名患者中有 57 人(13.5%)发生过脑缺血事件(相对风险为 0.65 [95% CI, 0.44-0.97]):结论和相关性:随机采用自由输血策略的急性颅脑损伤和贫血患者比随机采用限制性输血策略的患者更不可能出现不利的神经系统结果:试验注册:ClinicalTrials.gov Identifier:试验注册:ClinicalTrials.gov Identifier:NCT02968654。
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Restrictive vs Liberal Transfusion Strategy in Patients With Acute Brain Injury: The TRAIN Randomized Clinical Trial.

Importance: Blood transfusions are commonly administered to patients with acute brain injury. The optimal hemoglobin transfusion threshold is uncertain in this patient population.

Objective: To assess the impact on neurological outcome of 2 different hemoglobin thresholds to guide red blood cell transfusions in patients with acute brain injury.

Design, setting, and participants: Multicenter, phase 3, parallel-group, investigator-initiated, pragmatic, open-label randomized clinical trial conducted in 72 intensive care units across 22 countries. Eligible patients had traumatic brain injury, aneurysmal subarachnoid hemorrhage, or intracerebral hemorrhage; hemoglobin values below 9 g/dL within the first 10 days after injury; and an expected intensive care unit stay of at least 72 hours. Enrollment occurred between September 1, 2017, and December 31, 2022. The last day of follow-up was June 30, 2023.

Interventions: Eight hundred fifty patients were randomly assigned to undergo a liberal (transfusion triggered by hemoglobin <9 g/dL; n = 408) or a restrictive (transfusion triggered by hemoglobin <7 g/dL; n = 442) transfusion strategy over a 28-day period.

Main outcomes and measures: The primary outcome was occurrence of an unfavorable neurological outcome, defined as a Glasgow Outcome Scale Extended score between 1 and 5, at 180 days following randomization. There were 14 prespecified serious adverse events, including occurrence of cerebral ischemia after randomization.

Results: Among 820 patients who completed the trial (mean age, 51 years; 376 [45.9%] women), 806 had available data on the primary outcome, 393 in the liberal strategy group and 413 in the restrictive strategy group. The liberal strategy group received a median of 2 (IQR, 1-3) units of blood, and the restrictive strategy group received a median of 0 (IQR, 0-1) units of blood, with an absolute mean difference of 1.0 unit (95% CI, 0.87-1.12 units). At 180 days after randomization, 246 patients (62.6%) in the liberal strategy group had an unfavorable neurological outcome compared with 300 patients (72.6%) in the restrictive strategy group (absolute difference, -10.0% [95% CI, -16.5% to -3.6%]; adjusted relative risk, 0.86 [95% CI, 0.79-0.94]; P = .002). The effect of the transfusion thresholds on neurological outcome at 180 days was consistent across prespecified subgroups. In the liberal strategy group, 35 (8.8%) of 397 patients had at least 1 cerebral ischemic event compared with 57 (13.5%) of 423 in the restrictive strategy group (relative risk, 0.65 [95% CI, 0.44-0.97]).

Conclusions and relevance: Patients with acute brain injury and anemia randomized to a liberal transfusion strategy were less likely to have an unfavorable neurological outcome than those randomized to a restrictive strategy.

Trial registration: ClinicalTrials.gov Identifier: NCT02968654.

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期刊介绍: JAMA, published continuously since 1883, is an international peer-reviewed general medical journal. JAMA is a member of the JAMA Network, a consortium of peer-reviewed, general medical and specialty publications.
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