Effectiveness of antitussives, anticholinergics, and honey versus usual care in adults with uncomplicated acute bronchitis: a multiarm randomized clinical trial.


Journal

Family practice
ISSN: 1460-2229
Titre abrégé: Fam Pract
Pays: England
ID NLM: 8500875

Informations de publication

Date de publication:
28 03 2023
Historique:
medline: 30 3 2023
pubmed: 15 10 2022
entrez: 14 10 2022
Statut: ppublish

Résumé

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. Cough is the most frequent symptom reported by patients with lower respiratory tract infections. Despite being a defense mechanism, cough is unpleasant and negatively affects sleep and overall well-being. Accordingly, many patients with acute cough seek medical help to mitigate symptoms and reduce their duration despite the typically self-limiting nature of the condition. In this randomized clinical trial, we explored the benefit of 3 common symptomatic treatments recommended in some guidelines for relieving this symptom during the course of uncomplicated acute bronchitis, a cough suppressant, an inhaler, and honey intake. Although the total number of patients initially expected could not be achieved due to the disruption caused by the COVID-19 pandemic, the results of our study demonstrate a lack of efficacy of these products as the number of days of severe-to-moderate cough was similar in the 3 arms and comparable to the group of patients allocated to usual care.

Sections du résumé

BACKGROUND
Despite the frequent use of symptomatic therapies in cough, evidence of their benefits is lacking.
OBJECTIVE
We compared the effectiveness of 3 symptomatic therapies and usual care in acute bronchitis.
METHODS
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.
RESULTS
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.
CONCLUSION
The symptomatic treatment evaluated has shown to be ineffective against cough.
Cough is the most frequent symptom reported by patients with lower respiratory tract infections. Despite being a defense mechanism, cough is unpleasant and negatively affects sleep and overall well-being. Accordingly, many patients with acute cough seek medical help to mitigate symptoms and reduce their duration despite the typically self-limiting nature of the condition. In this randomized clinical trial, we explored the benefit of 3 common symptomatic treatments recommended in some guidelines for relieving this symptom during the course of uncomplicated acute bronchitis, a cough suppressant, an inhaler, and honey intake. Although the total number of patients initially expected could not be achieved due to the disruption caused by the COVID-19 pandemic, the results of our study demonstrate a lack of efficacy of these products as the number of days of severe-to-moderate cough was similar in the 3 arms and comparable to the group of patients allocated to usual care.

Autres résumés

Type: plain-language-summary (eng)
Cough is the most frequent symptom reported by patients with lower respiratory tract infections. Despite being a defense mechanism, cough is unpleasant and negatively affects sleep and overall well-being. Accordingly, many patients with acute cough seek medical help to mitigate symptoms and reduce their duration despite the typically self-limiting nature of the condition. In this randomized clinical trial, we explored the benefit of 3 common symptomatic treatments recommended in some guidelines for relieving this symptom during the course of uncomplicated acute bronchitis, a cough suppressant, an inhaler, and honey intake. Although the total number of patients initially expected could not be achieved due to the disruption caused by the COVID-19 pandemic, the results of our study demonstrate a lack of efficacy of these products as the number of days of severe-to-moderate cough was similar in the 3 arms and comparable to the group of patients allocated to usual care.

Identifiants

pubmed: 36239199
pii: 6760956
doi: 10.1093/fampra/cmac112
pmc: PMC9619792
doi:

Substances chimiques

Antitussive Agents 0
Dextromethorphan 7355X3ROTS
Cholinergic Antagonists 0
Ipratropium GR88G0I6UL

Banques de données

ClinicalTrials.gov
['NCT03738917']
EudraCT
['2018-002563-25']

Types de publication

Randomized Controlled Trial Multicenter Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

407-413

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Carl Llor (C)

Department of Public Health, General Practice. University of Southern Denmark, Odense, Denmark.
Primary Care Research Institute Jordi Gol (IDIAPJGol), Barcelona, Spain.
CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, Madrid, Spain.
Via Roma Health Centre, Institut Català de la Salut, Barcelona, Spain.

Ana Moragas (A)

Primary Care Research Institute Jordi Gol (IDIAPJGol), Barcelona, Spain.
CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, Madrid, Spain.
Jaume I Health Centre, Institut Català de la Salut, Tarragona, Spain.
University Rovira i Virgili, Reus, Spain.

Dan Ouchi (D)

Primary Care Research Institute Jordi Gol (IDIAPJGol), Barcelona, Spain.
Plataforma SCReN, UICEC IDIAPJGol, Barcelona, Spain.

Ramon Monfà (R)

Primary Care Research Institute Jordi Gol (IDIAPJGol), Barcelona, Spain.
Plataforma SCReN, UICEC IDIAPJGol, Barcelona, Spain.

Ana Garcia-Sangenís (A)

Primary Care Research Institute Jordi Gol (IDIAPJGol), Barcelona, Spain.
CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, Madrid, Spain.
Plataforma SCReN, UICEC IDIAPJGol, Barcelona, Spain.

Ainhoa Gómez-Lumbreras (A)

Primary Care Research Institute Jordi Gol (IDIAPJGol), Barcelona, Spain.
Plataforma SCReN, UICEC IDIAPJGol, Barcelona, Spain.

Helena Pera (H)

Primary Care Research Institute Jordi Gol (IDIAPJGol), Barcelona, Spain.
Plataforma SCReN, UICEC IDIAPJGol, Barcelona, Spain.

Jesus Pujol (J)

Balaguer Health Centre, Institut Català de la Salut, Balaguer, Spain.

Rosa Morros (R)

Primary Care Research Institute Jordi Gol (IDIAPJGol), Barcelona, Spain.
CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, Madrid, Spain.
Plataforma SCReN, UICEC IDIAPJGol, Barcelona, Spain.
Universitat Autònoma de Barcelona, Bellaterra, Spain.

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Classifications MeSH