Department of Public Health, General Practice. University of Southern Denmark, Odense, Denmark.
Primary Care Research Institute Jordi Gol (IDIAPJGol), Barcelona, Spain.
Fam Pract. 2023 Mar 28;40(2):407-413. doi: 10.1093/fampra/cmac112.
Despite the frequent use of symptomatic therapies in cough, evidence of their benefits is lacking.
We compared the effectiveness of 3 symptomatic therapies and usual care in acute bronchitis.
Multicenter, pragmatic, multiarm parallel group, open randomized trial in primary care (ClinicalTrials.gov, Identifier: NCT03738917) was conducted in Catalonia. Patients ≥18 with uncomplicated acute bronchitis, with cough<3 weeks as the main symptom, scoring ≥4 in either daytime or nocturnal cough (7-point Likert scale), were randomized to usual care, dextromethorphan 15 mg t.i.d., ipratropium bromide inhaler 20 µg 2 puffs t.i.d, or 30 mg of honey t.i.d., all taken for up to 14 days. The main outcome measure was the number of days with moderate-to-severe cough. A symptom diary was given. A second visit was scheduled at days 2-3 for assessing evolution, with 2 more visits at days 15 and 29 for clinical assessment, evaluation of adverse effects, re-attendance, and complications.
We failed to achieve the sample size scheduled due to the COVID-19 pandemic. We finally recruited 194 patients. The median number of days with moderate-to-severe cough (score ≥ 3) in the usual care arm was 5 (interquartile range [IQR], 4, 8.75), 5 in the ipratropium bromide arm (IQR, 3, 8), 5 in the dextromethorphan arm (IQR, 4, 9.75), and 6 in the honey arm (IQR, 3.5, 7). The same results were obtained in the Kaplan-Meier survival analysis for the median survival time of each arm with the usual care as the reference group.
The symptomatic treatment evaluated has shown to be ineffective against cough.
尽管在咳嗽中经常使用对症治疗,但缺乏其疗效的证据。
我们比较了 3 种对症治疗方法和常规护理在急性支气管炎中的疗效。
在加泰罗尼亚进行了一项多中心、实用、多臂平行组、开放性随机试验(ClinicalTrials.gov,标识符:NCT03738917),纳入了≥18 岁的患有单纯性急性支气管炎、以咳嗽(7 分李克特量表)<3 周为主要症状、白天或夜间咳嗽评分≥4 的患者,将其随机分配至常规护理、右美沙芬 15mg tid、异丙托溴铵气雾剂 20µg 2 喷 tid 或 30mg 蜂蜜 tid,所有药物均使用 14 天。主要结局测量是中度至重度咳嗽的天数。患者填写症状日记。第 2-3 天安排了第二次就诊以评估病情,第 15 天和第 29 天进行了 2 次临床评估、不良反应评估、再就诊和并发症评估。
由于 COVID-19 大流行,我们未能达到预定的样本量。最终我们共招募了 194 名患者。在常规护理组,中度至重度咳嗽(评分≥3)的中位天数为 5(四分位距 [IQR],4,8.75),在异丙托溴铵组为 5(IQR,3,8),在右美沙芬组为 5(IQR,4,9.75),在蜂蜜组为 6(IQR,3.5,7)。以常规护理作为参考组,对每个组的中位生存时间进行 Kaplan-Meier 生存分析,结果相同。
评估的对症治疗对咳嗽无效。