α -硫辛酸对产后大出血急性肺损伤和急性肾损伤的影响

Rania M. Ali, M. Khairy, D. Mansour
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摘要

产后出血(PPH)是孕产妇发病和死亡的主要原因之一。失血性休克复苏患者易发生全身性炎症反应和器官功能障碍。本研究旨在探讨α -硫辛酸(ALA)作为辅助治疗对重度PPH患者急性肺损伤(ALI)和急性肾损伤(AKI)发生的保护作用。患者与方法将40例重度PPH住院患者随机分为两组:ALA组静脉注射ALA 1200 mg,每日1次,连用3天;安慰剂组静脉注射0.9%异音生理盐水500 ml,每日1次,持续60分钟,连用3天。主要研究结果是血清中硫代巴比妥酸反应物质(作为氧化损伤的标志)和白细胞介素-6(作为炎症反应的标志)的水平。次要结局是ALI和AKI的发生率。结果ALA降低了硫代巴比妥酸活性物质和白细胞介素-6的水平(P < 0.001),减轻了氧化损伤和炎症反应。在ICU入院48小时后,5%的ALA组患者发生AKI,而安慰剂组患者为25%。ALA组10%的患者氧合指数(PaO 2 / fio2)低于300,安慰剂组30%的患者低于300。结论ALA可降低PPH患者的氧化应激和炎症反应标志物,对重度PPH患者ALI和AKI的进展具有预防作用。
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 alpha-lipoic acid on acute lung injury and acute kidney injury in major postpartum hemorrhage
Introduction Postpartum hemorrhage (PPH) is a major cause of maternal morbidity and mortality. Resuscitated hemorrhagic shock patients are susceptible to the development of a systemic inflammatory response and organ dysfunction. This study aimed to investigate the effects of alpha-lipoic acid (ALA) as an adjunctive therapy that protects against the occurrence of acute lung injury (ALI) and acute kidney injury (AKI) in patients with major PPH. Patients and methods Forty patients admitted to Ain Shams Obstetric ICU with major PPH were randomly allocated into two equal groups: the ALA group received intravenous 1200 mg ALA once daily for 3 days and the placebo group received 500 ml of 0.9% isotone saline solution over 60 min once daily for 3 days. The primary study outcome was the serum levels of thiobarbituric acid reactive species as a marker of oxidative damage and interleukin-6 as a marker of inflammatory response. The secondary outcomes were the incidence of ALI and AKI. Results ALA attenuated the oxidative damage and the inflammatory response as evidenced by the reduction in both thiobarbituric acid reactive species and interleukin-6 levels, respectively (P < 0.001). AKI developed in 5% of patients in the ALA group versus 25% of patients in the placebo group 48 h after ICU admission. The oxygenation index (PaO 2 /FiO 2 ) reached less than 300 in 10% of patients in the ALA group and in 30% of patients in the placebo group. Conclusion ALA decreases markers of oxidative stress and inflammatory response and also has a preventive effect on the progression of ALI and AKI in patients with major PPH.
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