China-Australia International Research Centre for Chinese Medicine, School of Health and Biomedical Sciences, RMIT University, Bundoora, Victoria, Australia.
The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangdong Provincial Academy of Chinese Medical Sciences, and The Second Clinical College, Guangzhou University of Chinese Medicine, Guangzhou, China.
PLoS One. 2023 Oct 5;18(10):e0292138. doi: 10.1371/journal.pone.0292138. eCollection 2023.
This systematic review and meta-analysis aims to: assess the effectiveness and safety of orally administered Chinese herbal medicines (CHMs) as adjuncts to the post-surgical management of chronic rhinosinusitis (CRS); inform clinicians of the current evidence; identify the best available evidence; and suggest directions for further research. Randomised controlled trials (RCTs) were identified from searches of nine databases plus clinical trial registries. Participants were adults and/or children diagnosed with sinusitis or rhinosinusitis, with or without nasal polyps, who had received surgery. Interventions were CHMs used orally following surgery for CRS as additions to conventional post-surgical management. Controls received conventional post-surgical management without CHMs. Studies reported results for Sino-Nasal Outcome Test (SNOT), visual analogue scales (VAS), Lund-Mackay computed tomography score (LM), Lund-Kennedy endoscopic score (LK), mucociliary transport time (MTT), mucociliary transport rate (MTR), mucociliary clearance (MC) or quality of life (QoL). Twenty-one RCTs were included. All used oral CHMs following functional endoscopic sinus surgery (FESS). The pooled results showed no significant difference between groups for SNOT-20 at the end of treatment (EoT) but there was a significant difference at follow up (FU) in favour of additional CHMs. The VAS for total nasal symptoms (VAS-TNS) showed greater improvements in the CHM groups at EoT and FU. Only FU data were reported for LM which showed greater improvement in the CHM groups. LK showed greater improvements at EoT and FU. The measures of mucociliary transport (MTT, MTR, and MC) each showed significantly greater improvement at EoT in the group that received additional CHMs. No study reported QoL. Adverse events were not serious, but reporting was incomplete. The meta-analyses suggested the addition of oral CHMs to conventional management following FESS may improve recovery. However, most studies were not blinded, and substantial heterogeneity was evident in some meta-analyses. Blinded studies are required to further investigate the roles of oral CHMs in post-surgical recovery. Systematic review registration number: The protocol was registered in PROSPERO (CRD42019119586).
评估口服中药(CHM)作为慢性鼻-鼻窦炎(CRS)术后管理辅助手段的有效性和安全性;向临床医生介绍当前的证据;确定最佳可用证据;并提出进一步研究的方向。通过对九个数据库和临床试验注册中心的搜索,确定了随机对照试验(RCT)。参与者为被诊断为鼻窦炎或鼻-鼻窦炎的成年人和/或儿童,有或没有鼻息肉,接受过手术。干预措施是在 CRS 手术后口服 CHM 作为常规术后管理的附加手段。对照组接受常规术后管理而不使用 CHM。研究报告了 Sino-Nasal Outcome Test(SNOT)、视觉模拟量表(VAS)、Lund-Mackay 计算机断层扫描评分(LM)、Lund-Kennedy 内窥镜评分(LK)、黏液纤毛传输时间(MTT)、黏液纤毛传输率(MTR)、黏液清除率(MC)或生活质量(QoL)的结果。纳入了 21 项 RCT。所有研究均在功能性内镜鼻窦手术后(FESS)后使用口服 CHM。汇总结果显示,治疗结束时(EoT)两组之间 SNOT-20 无显著差异,但在随访时(FU)附加 CHM 组有显著改善。CHM 组在 EoT 和 FU 时 VAS 总鼻症状(VAS-TNS)的改善更为显著。仅报告了 LM 的 FU 数据,显示 CHM 组的改善更大。LK 在 EoT 和 FU 时显示出更大的改善。接受额外 CHM 的组在 EoT 时黏液纤毛运输(MTT、MTR 和 MC)的各项指标均有显著改善。没有研究报告 QoL。不良事件不严重,但报告不完整。荟萃分析表明,在 FESS 后常规治疗中加入口服 CHM 可能会促进康复。然而,大多数研究未设盲,一些荟萃分析存在明显的异质性。需要进行设盲研究以进一步探讨口服 CHM 在术后恢复中的作用。系统评价注册号:该方案在 PROSPERO(CRD42019119586)中进行了注册。