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Ulinastatin for acute lung injury and acute respiratory distress syndrome: A systematic review and meta-analysis

机译:乌司他丁治疗急性肺损伤和急性呼吸窘迫综合征的系统评价和荟萃分析

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摘要

AIM: To investigate the efficacy and safety of ulinastatin for patients with acute lung injury (ALI) and those with acute respiratory distress syndrome (ARDS).METHODS: A systematic review of randomized controlled trials (RCTs) of ulinastatin for ALI/ARDS was conducted. Oxygenation index, mortality rate [intensive care unit (ICU) mortality rate, 28-d mortality rate] and length of ICU stay were compared between ulinastatin group and conventional therapy group. Meta-analysis was performed by using Rev Man 5.1.RESULTS: Twenty-nine RCTs with 1726 participants were totally included, the basic conditions of which were similar. No studies discussed adverse effect. Oxygenation index was reported in twenty-six studies (1552 patients). Ulinastatin had a significant effect in improving oxygenation [standard mean difference (SMD) = 1.85, 95%CI: 1.42-2.29, P < 0.00001, I2 = 92%]. ICU mortality and 28-d mortality were respectively reported in eighteen studies (987 patients) and three studies (196 patients). We found that ulinastatin significantly decreased the ICU mortality [I2 = 0%, RR = 0.48, 95%CI: 0.38-0.59, number needed to treat (NNT) = 5.06, P < 0.00001], while the 28-d mortality was not significantly affected (I2 = 0%, RR = 0.78, 95%CI: 0.51-1.19, NNT = 12.66, P = 0.24). The length of ICU stay (six studies, 364 patients) in the ulinastatin group was significantly lower than that in the control group (SMD = -0.97, 95%CI: -1.20--0.75, P < 0.00001, I2 = 86%).CONCLUSION: Ulinastatin seems to be effective for ALI and ARDS though most trials included were of poor quality and no information on safety was provided.
机译:目的:探讨乌司他丁对急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)患者的疗效和安全性。方法:对乌司他丁对ALI / ARDS的随机对照试验(RCT)进行了系统评价。比较了乌司他丁组和常规治疗组的氧合指数,死亡率[重症监护病房(ICU)死亡率,28 d死亡率]和ICU住院时间。结果采用Rev Man 5.1进行荟萃分析。结果:共纳入29个RCT,共有1726名参与者,其基本条件相似。没有研究讨论不良反应。在26项研究中(1552例患者)报道了氧合指数。乌司他丁具有改善氧合的显著作用[标准平均差异(SMD)= 1.85,95%CI:1.42-2.29,P <0.00001,I 2 = 92%]。在18项研究(987例患者)和3项研究(196例患者)中分别报告了ICU死亡率和28天死亡率。我们发现,乌司他丁可显着降低ICU死亡率[I 2 = 0%,RR = 0.48,95%CI:0.38-0.59,需要治疗的人数(NNT)= 5.06,P <0.00001],而28天死亡率并未受到显着影响(I 2 = 0%,RR = 0.78,95%CI:0.51-1.19,NNT = 12.66,P = 0.24)。乌司他丁组的ICU住院时间(六项研究,364例患者)显着低于对照组(SMD = -0.97,95%CI:-1.20--0.75,P <0.00001,I 2 = 86%)。结论:尽管包括的大多数试验质量较差且未提供安全性信息,但乌司他丁似乎对ALI和ARDS有效。

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