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人尿激肽原酶治疗急性缺血性脑卒中的疗效及安全性的Meta 分析。

Efficacy and safety of human urinary kallidinogenase for acute ischemic stroke: a meta-analysis.

机构信息

Department of Neurology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.

Hebei Key Laboratory of Vascular Homeostasis and Hebei Collaborative Innovation Center for Cardio-cerebrovascular Disease, Shijiazhuang, Hebei, China.

出版信息

J Int Med Res. 2020 Sep;48(9):300060520943452. doi: 10.1177/0300060520943452.

Abstract

OBJECTIVE

Human urinary kallidinogenase (HUK) is a glycoprotein extracted from human urine that is used to treat stroke by triggering positive regulation of the kallikrein-kinin system. Our aim was to evaluate the efficacy and safety of HUK treatment for acute ischemic stroke.

METHODS

We searched the online databases PubMed, Embase, Cochrane Library, Google Scholar, and China National Knowledge Infrastructure (CNKI) for papers published between January 2015 and December 2019. The quality of each trial was assessed using the Cochrane Reviewers' Handbook. Randomized controlled trials of HUK in patients with acute ischemic stroke were included.

RESULTS

Sixteen trials with 1326 participants were included. The HUK injection groups had more neurological improvement than the control groups in National Institutes of Health Stroke Scale scores (mean difference, -1.65; 95% confidence interval [CI], -2.12 to -1.71) and clinical efficacy (1.30; 95% CI, 1.21 to 1.41). Subgroup analysis indicated that age may influence heterogeneity. Eleven trials reported adverse effects and there were no significant differences between the control and HUK groups (risk difference, 0.01; 95% CI, -0.02 to 0.04).

CONCLUSIONS

HUK ameliorates neurological symptoms in stroke patients with few adverse effects. Further high-quality, large-scale randomized trials are needed to confirm these results.

摘要

目的

人尿激肽原酶(HUK)是从人尿中提取的糖蛋白,通过触发激肽释放酶-激肽系统的正调节,用于治疗中风。我们旨在评估 HUK 治疗急性缺血性中风的疗效和安全性。

方法

我们在 PubMed、Embase、Cochrane 图书馆、Google Scholar 和中国知网(CNKI)在线数据库中检索了 2015 年 1 月至 2019 年 12 月期间发表的论文。使用 Cochrane 评论员手册评估每个试验的质量。纳入 HUK 治疗急性缺血性中风患者的随机对照试验。

结果

纳入了 16 项试验,共 1326 名参与者。与对照组相比,HUK 注射组 NIHSS 评分(平均差值,-1.65;95%置信区间[CI],-2.12 至-1.71)和临床疗效(1.30;95%CI,1.21 至 1.41)的神经改善更多。亚组分析表明年龄可能影响异质性。11 项试验报告了不良反应,对照组和 HUK 组之间无显著差异(风险差,0.01;95%CI,-0.02 至 0.04)。

结论

HUK 可改善中风患者的神经症状,且不良反应较少。需要进一步开展高质量、大规模的随机试验来证实这些结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7662/7780570/321ca72c0206/10.1177_0300060520943452-fig1.jpg

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