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The Adverse Reactions of Lianhua Qingwen Capsule/Granule Compared With Conventional Drug in Clinical Application: A Meta-Analysis

机译:连华清温胶囊/颗粒与常规药物在临床应用中相比的不良反应:Meta分析

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Objectives: Lianhua Qingwen capsule/granule (LHQW) is an innovative patented traditional Chinese medicine with potential curative effects on respiratory diseases. However, no consensus has been reached on the security of LHQW to date. The current meta-analysis was performed to evaluate the safety profile of LHQW in relation to conventional drugs (PROSPERO CRD-42020224180). Methods: Comprehensive document retrieval was performed from both English and Chinese databases. Results were reported as risk ratio (RR) with 95% confidence interval (CI). Subgroup, sensitivity and meta-regression analyses were conducted to explore the possible sources of heterogeneity across eligible studies. Results: In total, 217 experimental studies were included. For pooled studies, the incidence of adverse reactions was lower in the LHQW group than the conventional drug group (RR = 0.63, 95% CI = 0.58–0.69, p & 0.001). In the evaluation of treating disease, significant reduced incidence of adverse reactions during treatment of influenza A (H1N1) and influenza were detected in the LHQW group. In the evaluation of security indexes, LHQW group has a reduced incidence of respiratory system damage, skin and its appendages injury, nervous system damage and gastrointestinal system damage, along with other adverse reactions. Subgroup analysis additionally revealed a reduced incidence of some adverse reactions in the LHQW group compared to the conventional drug group (Rash of skin and its appendage damage, dizziness or headache owing to nervous system damage, nausea or vomiting from gastrointestinal system damage and resurgence of disease from other adverse reactions). Conclusion: The current study provides potential a reference for the security of LHQW. Further long-term high-quality studies are essential to validate our conclusions. Systematic Review Registration: https://clinicaltrials.gov/ , CRD-42020224180
机译:目的:莲花清温胶囊/颗粒(LHQW)是一种创新的专利中药,具有对呼吸系统疾病的潜在疗效。但是,迄今为止没有达成联系。进行当前的Meta分析以评估与常规药物相关的LHQW的安全性曲线(Prospero CRD-4202024180)。方法:从英文和中文数据库执行全面的文档检索。结果作为风险比(RR)报告为95%置信区间(CI)。进行亚组,敏感性和元回归分析,以探讨符合条件研究的可能的异质性源。结果:总共包括217项实验研究。对于汇集研究,LHQW组的不良反应的发生率低于常规药物基团(RR = 0.63,95%CI = 0.58-0.69,P& 0.001)。在治疗疾病的评估中,在LHQW组中检测到在甲型甲型A(H1N1)和流感期间显着降低的不良反应发生率。在对安全指标的评估中,LHQW集团的发病率降低,皮肤及其阑尾损伤,神经系统损伤和胃肠系统损害以及其他不良反应。亚组分析另外揭示了LHQW组中一些不良反应的发病率降低了与常规药物组(皮疹皮疹,并且由于神经系统损伤,恶心或胃肠系统损伤,恶心或呕吐而胃肠系统损伤和疾病复苏来自其他不良反应)。结论:目前的研究为LHQW的安全提供了潜在的参考。进一步的长期高质量研究对于验证我们的结论至关重要。系统审查注册:https://clinicaltrials.gov/,CRD-42020224180

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