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系统评价临床试验评估常春藤叶(常春藤)治疗急性上呼吸道感染的疗效。

Systematic review of clinical trials assessing the effectiveness of ivy leaf (hedera helix) for acute upper respiratory tract infections.

机构信息

Department of General Practice/Family Medicine, University Medicine Goettingen, Humboldtallee 38, 37073 Goettingen, Germany.

出版信息

Evid Based Complement Alternat Med. 2011;2011:382789. doi: 10.1155/2011/382789. Epub 2010 Oct 3.

DOI:10.1155/2011/382789
PMID:20976077
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2957147/
Abstract

Introduction. Among nonantibiotic cough remedies, herbal preparations containing extracts from leaves of ivy (Hedera helix) enjoy great popularity. Objective. A systematic review to assess the effectiveness and tolerability of ivy for acute upper respiratory tract infections (URTIs). Methods. We searched for randomized controlled trials (RCTs), nonrandomized controlled clinical trials and observational studies evaluating the efficacy of ivy preparations for acute URTIs. Study quality was assessed by the Jadad score or the EPHPP tool. Results. 10 eligible studies were identified reporting on 17463 subjects. Studies were heterogeneous in design and conduct; 2 were RCTs. Three studies evaluated a combination of ivy and thyme, 7 studies investigated monopreparations of ivy. Only one RCT (n = 360) investigating an ivy/thyme combination used a placebo control and showed statistically significant superiority in reducing the frequency and duration of cough. All other studies lack a placebo control and show serious methodological flaws. They all conclude that ivy extracts are effective for reducing symptoms of URTI. Conclusion. Although all studies report that ivy extracts are effective to reduce symptoms of URTI, there is no convincing evidence due to serious methodological flaws and lack of placebo controls. The combination of ivy and thyme might be more effective but needs confirmation.

摘要

简介。在非抗生素咳嗽治疗药物中,含有常春藤(Hedera helix)叶提取物的草药制剂广受欢迎。目的。系统评价评估常春藤治疗急性上呼吸道感染(URTIs)的疗效和耐受性。方法。我们搜索了评估常春藤制剂治疗急性 URTIs 疗效的随机对照试验(RCTs)、非随机对照临床试验和观察性研究。研究质量通过 Jadad 评分或 EPHPP 工具进行评估。结果。确定了 10 项符合条件的研究,共报告了 17463 名受试者。研究在设计和实施方面存在异质性;其中 2 项为 RCT。3 项研究评估了常春藤和百里香的联合用药,7 项研究调查了常春藤的单一制剂。只有一项 RCT(n = 360)研究了常春藤/百里香的联合用药,使用了安慰剂对照,并显示在减少咳嗽频率和持续时间方面具有统计学意义的优势。所有其他研究都缺乏安慰剂对照,并存在严重的方法学缺陷。它们都得出结论,常春藤提取物对减轻 URTI 症状有效。结论。尽管所有研究都报告常春藤提取物对减轻 URTI 症状有效,但由于严重的方法学缺陷和缺乏安慰剂对照,没有令人信服的证据。常春藤和百里香的组合可能更有效,但需要进一步证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba2b/2957147/661a33514cb9/ECAM2011-382789.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba2b/2957147/661a33514cb9/ECAM2011-382789.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba2b/2957147/661a33514cb9/ECAM2011-382789.001.jpg

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