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一项回顾性队列研究,以确定受伤前抗血小板或抗凝治疗对严重创伤患者死亡率的影响。

Retrospective cohort study to determine the effect of preinjury antiplatelet or anticoagulant therapy on mortality in patients with major trauma.

作者信息

Yamaji Fuminori, Okada Hideshi, Kamidani Ryo, Kawasaki Yuki, Yoshimura Genki, Mizuno Yosuke, Kitagawa Yuichiro, Fukuta Tetsuya, Ishihara Takuma, Suzuki Kodai, Miyake Takahito, Kanda Norihide, Doi Tomoaki, Yoshida Takahiro, Yoshida Shozo, Ogura Shinji

机构信息

Advanced Critical Care Center, Gifu University Hospital, Gifu, Japan.

Abuse Prevention Center, Gifu University Graduate School of Medicine, Gifu, Japan.

出版信息

Front Med (Lausanne). 2023 Jan 9;9:1089219. doi: 10.3389/fmed.2022.1089219. eCollection 2022.

Abstract

OBJECTIVE

This study aimed to compare outcomes among patients who sustained major trauma from injury with and without receiving antiplatelet therapy (APT) or anticoagulant therapy (ACT) to test the hypothesis that APT does not increase the risk of mortality. However, ACT increases the mortality risk in the acute phase of trauma.

METHODS

Patients registered in the Japanese Observational body for Coagulation and Thrombolysis in Early Trauma 2 between April 2017 and March 2018 who had sustained a severe injury in any anatomic region of the body, as determined using an injury severity score (ISS) ≥ 16 were included in this retrospective cohort study. We analyzed the mortality within 24 h from the arrival using a multivariable linear regression analysis adjusted for several confounding variables.

RESULTS

We identified 1,186 eligible participants who met the inclusion criteria for this study: 105 in the APT (cases), 1,081 in the non-antiplatelet therapy (nAPT) group (controls), 65 in the ACT (cases), and 1,121 in the non-anticoagulant therapy (nACT) group (controls). The mortality within 24 h in the ACT group was significantly higher than in the nACT group (odds ratio 4.5; 95%CI: 1.2-16.79; = 0.025); however, there was no significant difference between the two groups with or without the antiplatelet drug (odds ratio 0.32; 95%CI: 0.04-2.79; = 0.3) administration. Other outcomes, like the 28-day mortality, mortality at discharge, and surgery for hemostasis, were not significantly different between regular users and non-users of either antiplatelet or anticoagulant drugs.

CONCLUSION

Regular antiplatelet medications did not increase mortality within 24 h, 28 days, or at discharge in patients with major trauma, suggesting that standard treatment, including surgery, is sufficient.

摘要

目的

本研究旨在比较接受和未接受抗血小板治疗(APT)或抗凝治疗(ACT)的严重创伤患者的预后情况,以验证APT不会增加死亡风险这一假设。然而,ACT会增加创伤急性期的死亡风险。

方法

本回顾性队列研究纳入了2017年4月至2018年3月在日本早期创伤凝血与溶栓观察机构登记的患者,这些患者身体任何解剖区域遭受了严重损伤,损伤严重程度评分(ISS)≥16。我们使用多变量线性回归分析对几个混杂变量进行调整,分析了到达后24小时内的死亡率。

结果

我们确定了1186名符合本研究纳入标准的合格参与者:APT组(病例组)105例,非抗血小板治疗(nAPT)组(对照组)1081例,ACT组(病例组)65例,非抗凝治疗(nACT)组(对照组)1121例。ACT组24小时内的死亡率显著高于nACT组(优势比4.5;95%置信区间:1.2 - 16.79;P = 0.025);然而,使用或未使用抗血小板药物的两组之间无显著差异(优势比0.32;95%置信区间:0.04 - 2.79;P = 0.3)。其他预后指标,如28天死亡率、出院时死亡率和止血手术,在抗血小板或抗凝药物的常规使用者和非使用者之间无显著差异。

结论

常规抗血小板药物不会增加严重创伤患者在24小时、28天或出院时的死亡率,这表明包括手术在内的标准治疗是足够的。

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