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鼻渊通窍颗粒治疗慢性鼻窦炎有效性和安全性的系统评价与Meta分析

[Systematic review and Meta-analysis of efficacy and safety of Biyuan Tongqiao Granules in treatment of chronic sinusitis].

作者信息

Tan Chang, Zhang Li-Dan, Zhi Ying-Jie, Xie Yan-Ming

机构信息

Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences Beijing 100700, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2022 Aug;47(16):4489-4504. doi: 10.19540/j.cnki.cjcmm.20220512.503.

Abstract

The present study conducted a systematic review and Meta-analysis on the efficacy and safety of Biyuan Tongqiao Granules in the treatment of chronic sinusitis. CNKI, Wanfang, VIP, SinoMed, PubMed, Cochrane Library, EMbase, and Web of Science were searched for randomized controlled trials(RCTs) of Biyuan Tongqiao Granules in the treatment of chronic sinusitis. The quality of the included RCTs was assessed according to the Cochrane risk-of-bias assessment tool and the final included trials underwent Meta-analysis with RevMan 5.4.1. Fifty-four RCTs were included, with a total sample size of 7 278 cases. The results of Meta-analysis showed that the clinical efficacy of Biyuan Tongqiao Granules alone or in combination in the experimental group in the treatment of chronic sinusitis was superior to that in the control group with conventional western medicine, Chinese medicinal preparations, or surgery only(RR=1.19, 95%CI[1.15, 1.24], P<0.000 01). The combined use of Biyuan Tongqiao Granules on the basis of the control group was superior to the control group in improving the main symptoms and signs of chronic sinusitis [RR_(nasal congestion)=1.33, 95%CI[1.21, 1.45], P<0.000 01, RR_(runny nose)=1.28, 95%CI[1.18, 1.40], P<0.000 01, RR_(turbinate congestion or swelling)=1.28, 95%CI[1.16, 1.41], P<0.000 01]. Biyuan Tongqiao Granules alone or in combination could effectively reduce the Snot-20 score, which was superior to the control group(MD=-2.94, 95%CI[-3.60,-2.28], P<0.000 01). Biyuan Tongqiao Granules alone and in combination could effectively reduce the VAS score, which was superior to the control group(MD_(total score)=-4.44, 95%CI[-6.05,-2.82], P<0.000 01; MD_(nasal congestion VAS score)=-0.99, 95%CI[-1.38,-0.60], P<0.000 01; MD_(runny nose VAS score)=-1.19, 95%CI[-1.62,-0.76], P<0.000 01; MD_(dysosmia VAS score)=-0.96, 95%CI[-1.26,-0.65], P<0.000 01; MD_(head and face pain VAS score)=-0.73, 95%CI[-0.98,-0.47], P<0.000 01). The combined use of Biyuan Tongqiao Granules could effectively reduce the sinus CT score and the Lund-Mackey score of the endoscopic mucosal morphology(MD_(sinus CT score)=-3.68, 95%CI[-5.47,-1.88], P<0.000 1, MD_(endoscopic mucosal morphology score)=-3.06, 95%CI[-5.53,-0.59], P=0.02). Compared with the control group with conventional western medicine, Chinese medicinal preparations, or surgery only, combined use of Biyuan Tongqiao Granules did not increase the occurrence of adverse reactions(RR=0.68, 95%CI[0.26, 1.77], P=0.43). As demonstrated by the existing evidence, Biyuan Tongqiao Granules can improve the clinical efficacy of chronic sinusitis, relieve the clinical symptoms and signs, and reduce the Snot-20 score, VAS score, and Lund-Mackey score, without inducing serious adverse reactions, indicating that Biyuan Tongqiao Granules alone or in combination are more effective and safe in the treatment of chronic sinusitis than conventional western medicine, Chinese medicinal preparations, or surgical treatment. Since the quality of the included trials was generally low, large-scale, high-quality, rigorous, multi-center, and blinded-designed RCTs that meet international standards should be adopted in the future to increase the strength and level of evidence.

摘要

本研究对鼻渊通窍颗粒治疗慢性鼻窦炎的疗效和安全性进行了系统评价和Meta分析。检索了中国知网、万方、维普、中国生物医学文献数据库、PubMed、Cochrane图书馆、EMbase和Web of Science,查找鼻渊通窍颗粒治疗慢性鼻窦炎的随机对照试验(RCT)。根据Cochrane偏倚风险评估工具对纳入的RCT质量进行评估,最终纳入的试验采用RevMan 5.4.1进行Meta分析。共纳入54项RCT,总样本量为7278例。Meta分析结果显示,试验组单独使用或联合使用鼻渊通窍颗粒治疗慢性鼻窦炎的临床疗效优于对照组(采用单纯西医常规治疗、中药制剂或手术治疗)(RR = 1.19,95%CI[1.15, 1.24],P < 0.000 01)。在对照组基础上加用鼻渊通窍颗粒在改善慢性鼻窦炎主要症状和体征方面优于对照组[RR(鼻塞)= 1.33,95%CI[1.21, 1.45],P < 0.000 01,RR(流涕)= 1.28,95%CI[1.18, 1.40],P < 0.000 01,RR(鼻甲充血或肿胀)= 1.28,95%CI[1.16, 1.41],P < 0.000 01]。单独或联合使用鼻渊通窍颗粒可有效降低Snot-20评分,优于对照组(MD = -2.94,95%CI[-3.60, -2.28],P < 0.000 01)。单独或联合使用鼻渊通窍颗粒可有效降低VAS评分,优于对照组(MD(总分)= -4.44,95%CI[-6.05, -2.82],P < 0.000 01;MD(鼻塞VAS评分)= -0.99,95%CI[-1.38, -0.60],P < 0.000 01;MD(流涕VAS评分)= -1.19,95%CI[-1.62, -0.76],P < 0.000 01;MD(嗅觉障碍VAS评分)= -0.96,95%CI[-1.26, -0.65],P < 0.000 01;MD(头面部疼痛VAS评分)= -0.73,95%CI[-0.98, -0.47],P < 0.000 01)。联合使用鼻渊通窍颗粒可有效降低鼻窦CT评分及内镜下黏膜形态的Lund-Mackey评分(MD(鼻窦CT评分)= -3.68,95%CI[-5.47, -1.88],P < 0.000 1,MD(内镜下黏膜形态评分)= -3.06,95%CI[-5.53, -0.59],P = 0.02)。与单纯西医常规治疗、中药制剂或手术治疗的对照组相比,联合使用鼻渊通窍颗粒未增加不良反应的发生(RR = 0.68,95%CI[0.26, 1.77],P = 0.43)。现有证据表明,鼻渊通窍颗粒可提高慢性鼻窦炎的临床疗效,缓解临床症状和体征,降低Snot-20评分、VAS评分及Lund-Mackey评分,且不引起严重不良反应,表明单独或联合使用鼻渊通窍颗粒治疗慢性鼻窦炎比单纯西医常规治疗、中药制剂或手术治疗更有效、更安全。由于纳入试验的质量普遍较低,未来应采用符合国际标准的大规模、高质量、严谨的多中心双盲设计RCT,以提高证据的强度和水平。

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