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用于慢性支气管炎或慢性阻塞性肺疾病的黏液溶解剂。

Mucolytic agents for chronic bronchitis or chronic obstructive pulmonary disease.

作者信息

Poole Phillippa, Black Peter N, Cates Christopher J

机构信息

Department of Medicine, University of Auckland, Auckland, New Zealand.

出版信息

Cochrane Database Syst Rev. 2012 Aug 15(8):CD001287. doi: 10.1002/14651858.CD001287.pub4.

Abstract

BACKGROUND

Individuals with chronic bronchitis or chronic obstructive pulmonary disease (COPD) may suffer recurrent exacerbations with an increase in volume or purulence of sputum, or both. Because of the personal and healthcare costs associated with exacerbations, any therapy that reduces the number of exacerbations is useful. There is a marked difference among countries in terms of prescribing of mucolytics depending on whether or not they are perceived to be effective.

PRIMARY OBJECTIVE

to determine if treatment with mucolytics reduces the frequency of exacerbations, days of disability, or both, in participants with chronic bronchitis or chronic obstructive pulmonary disease, or both.

SECONDARY OBJECTIVES

to determine if mucolytics lead to an improvement in lung function or quality of life and to determine the frequency of adverse effects associated with mucolytics.

SEARCH METHODS

We searched the Cochrane Airways Group Specialised Register and reference lists of articles on ten separate occasions, the most recent being in July 2012.

SELECTION CRITERIA

We included randomised studies that compared oral mucolytic therapy with placebo for at least two months in adults with chronic bronchitis or COPD. We excluded studies of people with asthma and cystic fibrosis.

DATA COLLECTION AND ANALYSIS

The review analysed summary data only, the majority from published studies. For earlier versions, one author extracted data, which was rechecked in subsequent updates. In later versions, we double-checked data extraction. We then entered data into RevMan for analysis.

MAIN RESULTS

Two further trials have been added to the review for the 2012 update. There are now 30 trials in the review, recruiting a total of 7436 participants. Allocation concealment was not clearly described in the early trials, and selection bias may have inflated the results, which reduces our confidence in the findings of these trials.The likelihood of being exacerbation-free during the study period (22 trials in 4886 participants with a mean duration of 10 months) was greater in the mucolytic group for the double-blind trials (Peto odds ratio (OR) 1.84; 95% confidence interval (CI) 1.63 to 2.07). However, the more recent trials show less benefit of treatment than the earlier trials included in this review. The overall number needed to treat with mucolytics to keep an additional participant free from exacerbations over 10 months was seven (NNTB 7; 95% CI 6 to 9). The use of mucolytics was associated with a reduction of 0.04 exacerbations per participant per month (95% CI -0.04 to -0.03) compared with placebo; that is about 0.48 per year, or one exacerbation every two years. There was very high heterogeneity in this outcome (I(2) = 87%) so results need to be interpreted with caution.The number of days of disability per month also fell (mean difference (MD) -0.48; 95% CI -0.65 to -0.30) in 12 trials on 2305 participants. There was no clinically important improvement in lung function or consistent impact on quality of life with mucolytics. Mucolytic treatment was not associated with any significant increase in adverse effects, including mortality (Peto OR 0.75; 95% CI 0.35 to 1.64) in six trials on 1821 participants.

AUTHORS' CONCLUSIONS: In participants with chronic bronchitis or COPD, treatment with a mucolytic may produce a small reduction in acute exacerbations, but may have little or no effect on the overall quality of life. The effects on exacerbations shown in early trials were larger than those found in the more recent studies. This may be because the earlier smaller trials were at higher risk of selection or publication bias, so the benefits of treatment may not be as large as suggested by the previous evidence.

摘要

背景

患有慢性支气管炎或慢性阻塞性肺疾病(COPD)的个体可能会反复出现病情加重,表现为痰液量增加、痰液变脓性或两者皆有。由于病情加重会带来个人和医疗成本,任何能够减少病情加重次数的治疗方法都是有益的。在不同国家,根据对黏液溶解剂有效性的认知,其处方情况存在显著差异。

主要目标

确定黏液溶解剂治疗是否能降低慢性支气管炎或慢性阻塞性肺疾病患者或两者兼具患者的病情加重频率、致残天数或两者皆降低。

次要目标

确定黏液溶解剂是否能改善肺功能或生活质量,并确定与黏液溶解剂相关的不良反应发生频率。

检索方法

我们十次分别检索了Cochrane Airways Group专业注册库及文章参考文献列表,最近一次检索时间为2012年7月。

入选标准

我们纳入了将口服黏液溶解剂疗法与安慰剂进行比较、针对患有慢性支气管炎或COPD的成年人进行至少两个月治疗的随机研究。我们排除了哮喘和囊性纤维化患者的研究。

数据收集与分析

本综述仅分析汇总数据,大部分数据来自已发表的研究。对于早期版本,由一位作者提取数据,并在后续更新中进行复查。在后期版本中,我们对数据提取进行了双重检查。然后我们将数据录入RevMan进行分析。

主要结果

2012年更新的综述中又增加了两项试验。目前该综述中有30项试验,共纳入7436名参与者。早期试验中未明确描述分配隐藏情况,选择偏倚可能夸大了结果,这降低了我们对这些试验结果的信心。在双盲试验中,黏液溶解剂组在研究期间(4886名参与者的22项试验,平均持续时间为10个月)无病情加重的可能性更大(Peto比值比(OR)1.84;95%置信区间(CI)1.63至2.07)。然而,与本综述中纳入的早期试验相比,近期试验显示治疗益处较小。使用黏液溶解剂使额外一名参与者在10个月内避免病情加重所需治疗的总人数为7人(NNTB 7;95% CI 6至9)。与安慰剂相比,使用黏液溶解剂使每位参与者每月的病情加重次数减少0.04次(95% CI -0.04至-0.03);即每年约0.48次,或每两年一次病情加重。该结果存在非常高的异质性(I² = 87%),因此结果需谨慎解读。在2305名参与者的12项试验中,每月的致残天数也有所下降(平均差值(MD)-0.48;95% CI -0.65至-0.30)。黏液溶解剂对肺功能无具有临床意义的改善,对生活质量也无一致影响。黏液溶解剂治疗与不良反应的任何显著增加无关,包括在1821名参与者的6项试验中的死亡率(Peto OR 0.75;95% CI 0.35至1.64)。

作者结论

在患有慢性支气管炎或COPD的参与者中,使用黏液溶解剂治疗可能会使急性病情加重略有减少,但对总体生活质量可能几乎没有影响或无影响。早期试验中显示的对病情加重的影响大于近期研究中的发现。这可能是因为早期规模较小的试验存在更高的选择或发表偏倚风险,因此治疗益处可能不如先前证据所显示的那么大。

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