首页> 外文期刊>JAMA: the Journal of the American Medical Association >Diaspirin cross-linked hemoglobin (DCLHb) in the treatment of severe traumatic hemorrhagic shock: a randomized controlled efficacy trial.
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Diaspirin cross-linked hemoglobin (DCLHb) in the treatment of severe traumatic hemorrhagic shock: a randomized controlled efficacy trial.

机译:Diaspirin交联血红蛋白(DCLHb)在治疗严重创伤性出血性休克中的作用:一项随机对照疗效试验。

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CONTEXT: Severe, uncompensated, traumatic hemorrhagic shock causes significant morbidity and mortality, but resuscitation with an oxygen-carrying fluid might improve patient outcomes. OBJECTIVE: To determine if the infusion of up to 1000 mL of diaspirin cross-linked hemoglobin (DCLHb) during the initial hospital resuscitation could reduce 28-day mortality in traumatic hemorrhagic shock patients. DESIGN AND SETTING: Multicenter, randomized, controlled, single-blinded efficacy trial conducted between February 1997 and January 1998 at 18 US trauma centers selected for their high volume of critically injured trauma patients, but 1 did not enroll patients. PATIENTS: A total of 112 patients with traumatic hemorrhagic shock and unstable vital signs or a critical base deficit, who had a mean (SD) patient age of 39 (20) years. Of the infused patients, 79% were male and 56% were white. An exception to informed consent was used when necessary. INTERVENTION: All patients were to be infused with 500 mL of DCLHb or saline solution. Critically ill patients who still met entry criteria could have received up to an additional 500 mL during the 1-hour infusion period. MAIN OUTCOME MEASURES: Twenty-eight day mortality, 28-day morbidity, 48-hour mortality, and 24-hour lactate levels. RESULTS: Of the 112 patients, 98 (88%) were infused with DCLHb or saline solution. At 28 days, 24 (46%) of the 52 patients infused with DCLHb died, and 8 (17%) of the 46 patients infused with the saline solution died (P = .003). At 48 hours, 20 (38%) of the 52 patients infused with DCLHb died and 7 (15%) of the 46 patients infused with the saline solution died (P = .01). The 28-day morbidity rate, as measured by the multiple organ dysfunction score, was 72% higher in the DCLHb group (P = .03). There was no difference in adverse event rates or the 24-hour lactate levels. CONCLUSIONS: Mortality was higher for patients treated with DCLHb. Although further analysis should investigate whether the mortality difference was solely due to a direct treatment effect or to other factors, DCLHb does not appear to be an effective resuscitation fluid.
机译:背景:严重的,无偿的,创伤性的失血性休克会导致明显的发病率和死亡率,但是用载氧液体进行复苏可能会改善患者的预后。目的:确定在最初的医院复苏过程中最多注入1000 mL的diaspirin交联血红蛋白(DCLHb)是否可以降低创伤性失血性休克患者的28天死亡率。设计与地点:1997年2月至1998年1月间在美国18个创伤中心进行了多中心,随机,对照,单盲疗效试验,这些中心因大量重伤创伤患者而被选择,但其中1个没有入组。患者:共有112例创伤性失血性休克,生命体征不稳定或基础严重不足的患者,平均(SD)患者年龄为39(20)岁。在输液患者中,男性占79%,白人占56%。必要时使用知情同意的例外。干预:所有患者均应注入500 mL DCLHb或盐溶液。仍然符合入院标准的重症患者在1小时的输液期间可能会再接受多达500 mL的药物。主要观察指标:二十八天死亡率,二十八天发病率,四十八小时死亡率和二十四小时乳酸水平。结果:112例患者中,有98例(88%)被注入DCLHb或盐溶液。在第28天,输注DCLHb的52例患者中有24例(46%)死亡,而输注盐溶液的46例患者中有8例(17%)死亡(P = .003)。在48小时时,输注DCLHb的52例患者中有20例(38%)死亡,输注盐溶液的46例患者中有7例(15%)死亡(P = .01)。 DCLHb组的28天发病率(通过多器官功能障碍评分来衡量)高72%(P = .03)。不良事件发生率或24小时乳酸水平无差异。结论:DCLHb治疗的患者死亡率较高。尽管应进行进一步的分析调查死亡率差异是否仅是由于直接治疗效果还是其他因素引起的,但DCLHb似乎不是有效的复苏液。

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