The efficacy of mucoactive drugs is not consistently outlined in bronchiectasis recommendations, and the usage of these agents varies by region. Thus, this study was set to evaluate the effectiveness of carbocisteine or hypertonic saline in treating bronchiectasis.
In 20 locations across the United Kingdom, this research recruited people with non-cystic fibrosis bronchiectasis who produced sputum every day and experienced frequent pulmonary exacerbations for a study. Those who were now smokers or had recently had mucoactive therapies were not included. In addition to receiving standard treatment, each subject was randomized to one of three groups of mucoactive drugs: either standard care alone, hypertonic saline (the hypertonic-saline group), hypertonic saline + carbocisteine (the combination group), or carbocisteine (the carbocisteine group).
Each category had 2 groups, and the comparisons were between carbocisteine and no carbocisteine and between hypertonic saline and no hypertonic saline. The number of pulmonary exacerbations within a 52-week period was the main outcome. Time to next pulmonary exacerbation, safety, and ratings on disease-specific health-related quality-of-life measures were important secondary outcomes. Randomization was applied to 288 individuals in total. There were no interactions between treatments.
Over the course of 52 weeks, the mean number of adjudicated fully qualifying pulmonary exacerbations was 0.76 (95% CI], 0.58 to 0.95), with hypertonic saline, compared to 0.98 (95% CI, 0.78 to 1.19), with no hypertonic saline (adjusted between-group difference in the means, −0.25 [95% CI, −0.57 to 0.07; P=0.12]), and 0.86 (95% CI, 0.66 to 1.06) with carbocisteine, compared to 0.90 (95% CI, 0.70 to 1.09), with no carbocisteine (adjusted between-group difference in the means, −0.04 [95% CI, −0.36 to 0.28; P=0.81]). The incidence of adverse events, including major adverse events, and secondary outcomes were comparable among the groups.
Overall, hypertonic saline and carbocisteine did not significantly improve quality of life or decrease pulmonary exacerbations in individuals with non-cystic fibrosis bronchiectasis, according to this investigation. These findings highlight the need for more focused study to identify individuals who may benefit from routine use of mucoactive drugs, as they imply that there is no therapeutic benefit.
Source:
Bradley, J. M., O’Neill, B., McAuley, D. F., Chalmers, J. D., De Soyza, A., Hill, A. T., Carroll, M., Loebinger, M. R., Duckers, J., Clarke, M., McLeese, R. H., Ferguson, K., Jackson, A., Campbell, C., McDowell, C., Agus, A., Norrie, J., Copeland, F., Downey, D. G., … CLEAR Investigator Team. (2025). Hypertonic saline or carbocisteine in bronchiectasis. The New England Journal of Medicine, NEJMoa2510095. https://doi.org/10.1056/NEJMoa2510095
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