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North American (Panax quinquefolius) and Asian Ginseng (Panax ginseng) Preparations for Prevention of the Common Cold in Healthy Adults: A Systematic Review

机译:北美(Panax quinquefolius)和亚洲人参(Panax ginseng)预防健康成年人感冒的系统评价

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摘要

Background: Standardized ginseng extract has become the best-selling cold and flu remedy in Canada, yet much controversy regarding the efficacy of ginseng in preventing common colds remains. Objective: To assess the efficacy of ginseng preparations for the prevention of common colds in healthy adults. Methods: Comprehensive bibliographic database, trial registry and grey literature searches were conducted up to December 2007. Randomized controlled trials or controlled clinical trials comparing North American (Panax quinquefolius) or Asian ginseng (Panax ginseng) root extract to placebo or no treatment in healthy adults were included. Two reviewers independently applied the study selection criteria and assessed methodological quality. Results: Five trials involving 747 participants were included. All five trials examined North American ginseng. The methodological quality of the trials varied widely. Ginseng preparations significantly reduced the total number of common colds by 25% compared to placebo (one trial; 95% CI: 5–45). There was a tendency toward a lower incidence of having at least one common cold or other acute respiratory infection (ARI) in the ginseng group compared to the placebo group (five trials; relative risk: 0.70; 95% CI: 0.48–1.02). Compared to placebo, ginseng significantly shortened the duration of colds or ARIs by 6.2 days (two trials; 95% CI: 3.4–9.0). Conclusions: There is insufficient evidence to conclude that ginseng reduces the incidence or severity of common colds. North American ginseng appears to be effective in shortening the duration of colds or ARIs in healthy adults when taken preventatively for durations of 8–16 weeks.
机译:背景:标准化的人参提取物已成为加拿大最畅销的感冒和流感药物,但关于人参在预防普通感冒中的功效方面仍存在许多争议。目的:评估人参制剂预防健康成年人感冒的功效。方法:截止到2007年12月,进行了全面的书目数据库,试验注册和灰色文献检索。在健康成人中,比较了北美(Panax quinquefolius)或亚洲人参(Panax ginseng)根提取物与安慰剂或不进行治疗的随机对照试验或对照临床试验被包括在内。两名评价者独立应用研究选择标准并评估方法学质量。结果:包括747名参与者的五项试验。所有五项试验均检查了北美人参。试验的方法学质量差异很大。与安慰剂相比,人参制剂可将感冒的总人数显着降低25%(一项试验; 95%CI:5-45)。与安慰剂组相比,人参组有至少一种普通感冒或其他急性呼吸道感染(ARI)发生率较低的趋势(五项试验;相对风险:0.70; 95%CI:0.48–1.02)。与安慰剂相比,人参将感冒或ARIs的持续时间显着缩短了6.2天(两项试验; 95%CI:3.4-9.0)。结论:没有足够的证据得出人参降低普通感冒的发病率或严重程度的结论。预防性服用8-16周后,北美人参似乎可以有效缩短健康成年人的感冒或ARIs时间。

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