促红细胞生成素对脑外伤患者 SOFA 评分、格拉斯哥昏迷量表和死亡率的影响:随机双盲对照试验

Seyyed Javad Boskabadi, Fatemeh Heydari, Farhad Mohammadnejad, A. Gholipour-Baradari, Mahmood Moosazadeh, Ayat Dashti
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引用次数: 0

摘要

最近的研究表明,红细胞生成素对中枢神经系统具有抗炎作用。我们旨在研究红细胞生成素对创伤性脑损伤患者的 GCS、SOFA 评分和死亡率的影响。 68 名符合纳入标准的患者被随机分配到对照组或干预组。干预组在第一天、第三天和第五天注射促红细胞生成素(4,000 单位)。对照组则在同一天使用生理盐水。主要结果是干预期间 GCS 和 SOFA 评分的变化。次要结果是头两周的通气时间和三个月的死亡率。 随着时间的推移,使用促红细胞生成素会明显影响 SOFA 评分(P=0.008),但两组之间的 GCS 和通气时间没有明显影响。最后,促红细胞生成素对三个月的死亡率没有明显影响(促红细胞生成素组和对照组的死亡率分别为 23.5% 和 38.2%)。不过,干预组的死亡率低于对照组。 我们的研究结果表明,对创伤性脑损伤患者使用促红细胞生成素可改善 SOFA 评分。因此,促红细胞生成素可能对创伤性脑损伤患者的早期发病率和临床改善有益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of erythropoietin on SOFA score, glasgow coma scale and mortality in traumatic brain injury patients: a randomized-double blind controlled trial
Recent studies suggest that erythropoietin has an anti-inflammatory effect on the central nervous system. We aimed to investigate the effect of erythropoietin on GCS, SOFA scores, and the mortality rate of TBI patients. Sixty-eight patients with available inclusion criteria were randomly allocated to the control or intervention groups. In the intervention group, erythropoietin (4,000 units) was administrated on days one, three, and five. In the control group, normal saline on the same days was used. The primary outcomes were the GCS and SOFA score changes during the intervention. The secondary outcomes were the ventilation period during the first two weeks and the three-month mortality rate. Erythropoietin administration significantly affected SOFA score over time (P=0.008), but no significant effect on the GCS, and duration of ventilation between the two groups was observed. Finally, erythropoietin had no significant effect on the three-month mortality (23.5% vs. 38.2% in the erythropoietin and control group respectively). However, the mortality rate in the intervention group was lower than in the control group. Our finding showed that erythropoietin administration in TBI may improve SOFA score. Therefore, erythropoietin may have beneficial effects on early morbidity and clinical improvement in TBI patients.
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