桉树脑对急性支气管炎患者的疗效:安慰剂对照双盲试验。

Juergen Fischer, Uwe Dethlefsen
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引用次数: 54

摘要

目的:桉树脑具有黏液溶解、支气管扩张和抗炎作用,可降低COPD患者的加重率,改善哮喘和鼻窦炎患者的症状。基于这些效果,我们假设急性支气管炎患者也可以从桉树脑治疗中获益。方法:作为双盲、安慰剂对照、多中心研究的一部分,随机选择242例确诊的急性支气管炎患者参加。在10天的时间里,所有患者每天服用3 x 200毫克桉树脑或相应的安慰剂。主要结局指标是支气管炎综合评分,该评分总结了急性支气管炎的相关症状。结果:治疗4 d后,桉树脑治疗组的支气管炎积分改善明显高于安慰剂组(p = 0.0383)。4天后咳嗽发作的频率p = 0.0001,特别强调了个体结局指标的统计学显著差异。结论:桉树脑在治疗急性支气管炎中的作用是可以明显测量的,并且可以在仅仅4天的治疗期后被证明。这项研究证实了这样一个事实,即桉树脑在四天后有效地显著减少咳嗽频率。因此,它已被证明具有巨大的社会经济影响。试验注册号:ISRCTN37784439。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of cineole in patients suffering from acute bronchitis: a placebo-controlled double-blind trial.

Objective: Cineole has mucolytic, bronchodilating and anti-inflammatory properties and reduces the exacerbation rate in patients suffering from COPD, as well as ameliorates symptoms in patients suffering from asthma and rhinosinusitis. Based on these effects, we therefore postulated the hypothesis that patients with acute bronchitis would also benefit from therapy with Cineole.

Methods: As part of a double-blind, placebo-controlled, multi-center-study, a total of 242 patients with confirmed acute bronchitis was randomly selected to participate. Over a period of 10 days, all patients were administered 3 x 200 mg of Cineole, or a respective placebo, per day. The primary outcome measure was a Bronchitis Sum Score, which summarises the relevant symptoms of acute bronchitis.

Results: After 4 days of treatment it was notable, that the patient group treated with Cineole, showed significantly more improvements of the bronchitis-sum-score than those of the placebo group (p = 0.0383). The statistical significant difference of the individual outcome measures was especially underlined by the frequency of cough fits by p = 0.0001 after 4 days.

Conclusions: The effects of Cineole in the treatment of acute bronchitis were clearly measurable and could be proven after a treatment period of merely 4 days. This study corroborates the fact that Cineole actively and significantly reduces cough frequency after four days. Therefore it has been shown to have a great socioeconomic impact.

Trial registration isrctn: ISRCTN37784439.

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