Loading...
Observational studies suggest that patients with asthma or chronic obstructive pulmonary disease (COPD) are underrepresented among COVID-19 hospitalizations. These observations raise the question of whether inhaled corticosteroids (ICS) might mitigate COVID-19 symptoms, since many patients with asthma or COPD routinely use ICS. In one small trial, patients with mild COVID-19 infections who did not use ICS before SARS-CoV-2 exposure had fewer hospitalizations when they received inhaled budesonide (Lancet Respir Med 2021; 9:763). Researchers now report results from a much larger, randomized, non–placebo-controlled intervention.
This trial involved 1856 older high-risk patients (age, ≥65 [or ≥50 with comorbidities such as cancer, diabetes, cardiovascular or lung disease, or obesity]) with symptomatic COVID-19 for as long as 14 days (average, 6 days) who did not require hospitalization. Patients received usual care plus budesonide (800 µg, inhaled twice daily for 14 days) or usual care alone. Median time to self-reported recovery was 2.9 days shorter in the budesonide group, with a nonsignificant trend toward fewer hospitalizations and deaths.
Yu L-M et al. Inhaled budesonide for COVID-19 in people at high risk of complications in the community in the UK (PRINCIPLE): A randomised, controlled, open-label, adaptive platform trial. Lancet 2021 Aug 10; [e-pub]. (https://doi.org/10.1016/S0140-6736(21)01744-X)
Comment
This study was limited by lack of a placebo control, poor follow-up, and failure to find a significant difference in the most important endpoint of fewer hospitalizations and deaths. However, it suggests that older patients and those with comorbidities might benefit from ICS if they have mild COVID-19. Monoclonal antibody treatment (given within 3 to 7 days of symptoms) is preferable, because of its proven ability to prevent COVID-19–related hospitalizations and mortality, but ICS is a simple and inexpensive option with little apparent downside, and offering it to select higher-risk patients (similar to those in this trial) would be reasonable.