Wang Xiaohu, Luo Jian, Wang Dan, Liu Bicui, Liu Chuntao
Department of Respiratory and Critical Care Medicine, West China Hospital, Sichuan University, Chengdu, China.
Medicine (Baltimore). 2019 Sep;98(38):e17190. doi: 10.1097/MD.0000000000017190.
Effects of azithromycin on asthma reported in clinical trials are less consistent. We aimed to further clarify the efficacy and safety of azithromycin in treatment of asthma.
The protocol registration number was CRD42017074318 (http://www.crd.york.ac.uk/Prospero). We searched PubMed, EMBASE, Cochrane databases, China National Knowledge Internet (CNKI), and Wanfang databases for the randomized controlled trials (RCTs) with prolonged treatment of azithromycin for more than 3 weeks. Random-effects or fixed-effects model was applied to calculate risk ratio (RR) and mean difference (MD) for dichotomous and continuous data respectively.
A total of eight studies were included for analysis. The pooled result of adjunctive azithromycin therapy in asthma showed a small, but statistically significant increase in forced expiratory volume in one second (FEV1) (MD = 0.06, 95% confidence interval [CI]: 0.01-0.12, P = .02), but no significant differences in exacerbation frequency (MD = -0.42, 95%CI: -1.13 to 0.30, P = .25) and peak expiratory flow (PEF) (MD = 0.20, 95% CI: -0.05 to 0.44, P = .12), fractional exhaled nitric oxide (FeNO) (MD = 4.12, 95% CI: -2.06 to 10.30, P = .19), asthma quality of life questionnaire (AQLQ) (MD: 0.05, 95% CI: -0.17 to 0.28, P = .65), asthma control questionnaire (ACQ) (MD: -0.03, 95% CI: -0.21 to 0.15, P = .75). The subgroup analysis revealed that azithromycin could decrease FeNO among Asian asthma (MD = 15.04, 95% CI: 6.18-23.90, P = .0009).
Add-on therapy of azithromycin in asthma patients could improve the FEV1, but failed to improve asthma exacerbations, PEF, ACQ, AQLQ, and FeNO. Subgroup analysis indicated that azithromycin could improve FeNO in Asian group asthmatics.
临床试验中报道的阿奇霉素对哮喘的影响不太一致。我们旨在进一步阐明阿奇霉素治疗哮喘的疗效和安全性。
方案注册号为CRD42017074318(http://www.crd.york.ac.uk/Prospero)。我们检索了PubMed、EMBASE、Cochrane数据库、中国知网(CNKI)和万方数据库,以查找阿奇霉素治疗时间超过3周的随机对照试验(RCT)。分别应用随机效应或固定效应模型计算二分类和连续数据的风险比(RR)和平均差(MD)。
共纳入8项研究进行分析。哮喘患者辅助使用阿奇霉素治疗的汇总结果显示,一秒用力呼气量(FEV1)有小幅但具有统计学意义的增加(MD = 0.06,95%置信区间[CI]:0.01 - 0.12,P = 0.02),但在发作频率(MD = -0.42,95%CI:-1.13至0.30,P = 0.25)、呼气峰值流速(PEF)(MD = 0.20,95%CI:-0.05至0.44,P = 0.12)、呼出一氧化氮分数(FeNO)(MD = 4.12,95%CI:-2.06至10.30,P = 0.19)、哮喘生活质量问卷(AQLQ)(MD:0.05,95%CI:-0.17至0.28,P = 0.65)、哮喘控制问卷(ACQ)(MD:-0.03,95%CI:-0.21至0.15,P = 0.75)方面无显著差异。亚组分析显示,阿奇霉素可降低亚洲哮喘患者的FeNO(MD = 15.04,95%CI:6.18 - 23.90,P = 0.0009)。
哮喘患者加用阿奇霉素治疗可改善FEV1,但未能改善哮喘发作、PEF、ACQ、AQLQ和FeNO。亚组分析表明,阿奇霉素可改善亚洲组哮喘患者的FeNO。