Lee Boram, Kwon Chan-Young, Park Man Young
KM Science Research Division, Korea Institute of Oriental Medicine, Daejeon, South Korea.
Department of Oriental Neuropsychiatry, Dong-eui University College of Korean Medicine, Busan, South Korea.
Front Pharmacol. 2022 Jul 18;13:908941. doi: 10.3389/fphar.2022.908941. eCollection 2022.
Chronic rhinosinusitis (CRS) is a disease with a high prevalence and a high socioeconomic burden. This study aimed to conduct a comprehensive systematic review to update the evidence on the use of herbal medicine (HM) for CRS treatment. A total of 14 electronic databases for randomized controlled trials (RCTs) evaluating the effects of HM on the treatment of CRS were searched for articles published before July 2021. The primary outcome was CRS severity post-treatment, measured with the Visual Analogue Scale (VAS) and Total Effective Rate (TER). The risk of bias of the included studies and the quality of evidence of the main findings were assessed using the Cochrane Collaboration's risk of bias tool and the Grading of Recommendations, Assessment, Development, and Evaluations tool. A total of 80 RCTs were included. Compared to placebo, HM significantly improved CRS severity as measured by TER and VAS. When HM was compared with conventional treatment (CT) as monotherapy or adjuvant therapy, CRS severity measured by TER and VAS, quality of life, Lund-Kennedy endoscopy score, Lund-Mackay computed tomography score, and nasal mucociliary function were significantly improved in the HM group. No serious adverse events associated with HM were reported. The risk of bias was generally unclear, and the quality of evidence ranged from moderate to low. This review found some limited clinical evidence that HM or HM combined with CT may be more effective and safer than CT alone in treating CRS. However, the methodological quality of the included studies was generally low, and the quality of the evidence needs to be improved.
慢性鼻-鼻窦炎(CRS)是一种高患病率且社会经济负担重的疾病。本研究旨在进行一项全面的系统评价,以更新关于使用草药(HM)治疗CRS的证据。检索了14个电子数据库,查找2021年7月之前发表的评估HM对CRS治疗效果的随机对照试验(RCT)文章。主要结局是治疗后CRS的严重程度,采用视觉模拟量表(VAS)和总有效率(TER)进行测量。使用Cochrane协作网的偏倚风险工具和推荐分级、评估、制定与评价工具对纳入研究的偏倚风险和主要研究结果的证据质量进行评估。共纳入80项RCT。与安慰剂相比,HM通过TER和VAS测量显著改善了CRS严重程度。当将HM与传统治疗(CT)作为单一疗法或辅助疗法进行比较时,HM组通过TER和VAS测量的CRS严重程度、生活质量、Lund-Kennedy内镜评分、Lund-Mackay计算机断层扫描评分以及鼻黏膜纤毛功能均得到显著改善。未报告与HM相关的严重不良事件。偏倚风险总体尚不清楚,证据质量从中等到低不等。本评价发现一些有限的临床证据表明,HM或HM联合CT在治疗CRS方面可能比单独使用CT更有效、更安全。然而,纳入研究的方法学质量总体较低,证据质量有待提高。