Mucoactive agents in bronchiectasis: a systematic review and meta-analysis.
Eur Respir Rev 2026 Apr; 35(180).

Abstract

BACKGROUND

Mucoactive agents aim to improve mucociliary clearance in bronchiectasis, disrupting the cycle of impaired clearance, infection and inflammation. Registry data show 28% of patients use these agents, but prescribing varies due to limited evidence. We aimed to update evidence on mucoactive agents' effects in adults with bronchiectasis.

METHODS

We conducted a systematic review and meta-analysis, searching Medline, Embase, CENTRAL and trial registries to 1 October 2025. Eligible studies included adults with bronchiectasis, evaluating any mucoactive agent versus placebo or control. Cystic fibrosis and paediatric studies were excluded. The primary outcome was exacerbation frequency; secondary outcomes included lung function, quality of life and adverse events.

FINDINGS

From 1512 records, 24 studies (20 randomised, four observational: n=7051) evaluated eight mucoactive agents (ambroxol, bromhexine, carbocisteine, erdosteine, hypertonic saline, mannitol, N-acetylcysteine, rhDNase). Most trials had high or some risk of bias. Seven randomised studies (n=1259) reported exacerbations; pooled analysis did not demonstrate a statistically significant difference in annualised exacerbation incidence (mean difference -0.40 per patient per year, 95% CI -1.04-0.24; p=0.22; I[2]=91%; very low certainty). Nine studies (n=767) reported percent predicted forced expiratory volume in 1 s (FEV1 % pred), showing a small mean increase of 3.23% (95% CI 0.31-6.15; p=0.03; I[2]=69.9%; very low certainty). Pooled analyses did not demonstrate significant differences for other spirometry measures, quality of life or adverse events.

INTERPRETATION

Pooled evidence did not show a reduction in exacerbations and FEV1 % pred improvements were small. Evidence certainty was low/very low, meaning overall clinical benefit remains uncertain, highlighting the need for targeted trials of specific agents and subgroups.

Authors+Show Affiliations

McCullough B0009-0004-8871-4805Wellcome Trust-Wolfson Northern Ireland Clinical Research Facility, Queen's University Belfast, Belfast, UK.
Busby JCentre for Public Health, Queen's University Belfast, Belfast, UK.
O'Neill BInstitute of Nursing and Health Research, Ulster University, Belfast, UK.
Connolly BWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK. Department of Physiotherapy, The University of Melbourne, Melbourne, Australia.
McLeese RH0000-0003-0647-2503Wellcome Trust-Wolfson Northern Ireland Clinical Research Facility, Queen's University Belfast, Belfast, UK.
Linden DWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
McAuley DF0000-0002-3283-1947Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
Elborn JSWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
De Soyza A0000-0002-8566-0344Population Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle, UK.
Chalmers JDScottish Centre for Respiratory Research, University of Dundee, Ninewells Hospital and Medical School, Dundee, UK.
Clarke MCentre for Public Health, Queen's University Belfast, Belfast, UK.
Bradley JMWellcome Trust-Wolfson Northern Ireland Clinical Research Facility, Queen's University Belfast, Belfast, UK judy.bradley@qub.ac.uk. Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.

Pub Type(s)

Journal Article
Systematic Review
Meta-Analysis
Review

Language

eng

PubMed ID

42342264