2019年冠状病毒病患者使用雪碧注射液的有效性和安全性:系统回顾和Meta分析。

Sun Wu, Zhao Yuwei, Liao Liang, Zhao Zhonghui, Chen Shiqi, Yan Xiaoling, Wang Xueyao, Chao Guojun, Zhou Jian
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引用次数: 0

摘要

目的评估雪碧注射液(XBJ)对冠状病毒病2019(COVID-19)患者的有效性和安全性:检索截至 2021 年 12 月 11 日的多个生物学数据库和网站上的相关研究,无语言和出版时间限制。使用Review Manager V.5.3和Stata 14软件进行数据分析:结果:最终纳入了 7 项研究。Meta分析显示,与单纯常规治疗相比,XBJ联合常规治疗可降低28天死亡率(=0.3,95%:0.12,0.74)、Creactive蛋白(=-12.8,95%:-23.13,3.46)、红细胞沉降率(=-9.32,95%:-14.66,-3.98)和白细胞介素-6(S = -0.6,95%:-1.04,-0.17)水平,并增加外周血中的白细胞(=0.73,95%:0.42,1.04)和淋巴细胞计数(=0.18,95%:0.07,0.29);此外,它没有明显的副作用(=1.11,95%:0.65,1.9)。没有证据表明XBJ联合疗法可以提高COVID19患者的核酸转换率和计算机断层扫描改善率:初步证据表明,XBJ联合常规治疗似乎比常规治疗对COVID19患者更有效。受纳入论文数量和质量的限制,这一发现仍需更多研究的进一步验证。
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Effectiveness and safety of Xuebijing injection for patients with coronavirus disease 2019: a systematic review and Metaanalysis.

Objective: To evaluate the effectiveness and safety of Xuebijing injection (XBJ) on coronavirus disease 2019 (COVID-19) in patients.

Methods: Related studies on multiple biological databases and websites were searched up to December 11, 2021 without language and publication time restrictions. Review Manager V.5.3 and Stata 14 software were used for data analysis.

Results: Seven studies were finally included. The Metaanalysis showed that compared with the routine treatment alone, XBJ combined with the routine treatment can reduce the 28day mortality ( = 0.3, 95% : 0.12, 0.74), Creactive protein ( = -12.8, 95% : -23.13, 3.46), erythrocyte sedimentation rate ( = -9.32, 95% : -14.66, -3.98) and interleukin-6 (S = -0.6, 95% : -1.04, -0.17) levels and increase the leukocyte ( = 0.73, 95% : 0.42, 1.04) and lymphocyte count ( = 0.18, 95% : 0.07, 0.29) in peripheral blood; additionally, it has no obvious side effects ( = 1.11, 95% : 0.65, 1.9). There was no evidence that the XBJ combined therapy can improve the nucleic acid conversion rate and computed tomography improvement rate of COVID19 patients.

Conclusions: Preliminary evidence suggests that XBJ combined with routine treatment seems to be more effective than routine treatment for patients with COVID19. Limited by the number and quality of included papers, this finding still needs further validation by more studies.

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