AI Article Synopsis

  • Inhaled corticosteroids (ICSs) combined with bronchodilators are commonly used for treating COPD but can have negative side effects.
  • A systematic review and meta-analysis of 13 randomized clinical trials was conducted to compare the effects of high versus medium/low doses of ICS on COPD-related outcomes.
  • Results indicated that high-dose ICS did not significantly change the risk of acute exacerbations, mortality, or pneumonia when compared to medium doses, suggesting no advantage to using higher doses in these patients.

Article Abstract

Background: Inhaled corticosteroids (ICSs) combined with bronchodilators have been identified to improve outcomes in COPD but also to be associated with certain adverse effects.

Objective: We performed a systematic review and meta-analysis to compile and summarize data on the efficacy and safety of dosing levels (high versus medium/low) of ICS alongside ancillary bronchodilators following PRISMA guidelines.

Data Sources: Medline and Embase were systematically searched until December 2021. Randomized, clinical trials (RCTs) that met predefined inclusion criteria were included.

Data Extraction: Risk ratios (RRs) with 95% confidence intervals (CI) were extracted. Any acute exacerbation of COPD (AECOPD) risk was chosen as the primary efficacy outcome, mortality rate as the primary safety outcome, moderate/severe AECOPD risk as the secondary efficacy outcome and pneumonia risk as the secondary safety outcome. Subgroup analyses of individual ICS agents, of patients with baseline moderate/severe/very severe COPD and of patients with recent COPD exacerbation history were also performed. A random-effects model was used.

Results: We included 13 RCTs in our study. No data on low doses were included in the analysis. High dose ICS was not associated with a statistically significant difference in any AECOPD risk (RR: 0.98, 95% CI: 0.91-1.05, I: 41.3%), mortality rate (RR: 0.99, 95% CI: 0.75-1.32, I: 0.0%), moderate/severe AECOPD risk (RR: 1.01, 95% CI: 0.96-1.06, I: 0.0%) or pneumonia risk (RR: 1.07, 95% CI: 0.86 -1.33, I: 9.3%) compared to medium dose ICS. The same trend was identified with the several subgroup analyses.

Conclusion: Our study collected RCTs investigating the optimal dosing level of ICS prescribed alongside ancillary bronchodilators to patients with COPD. We identified that the high ICS dose neither reduces AECOPD risk and mortality rates nor increases pneumonia risk relative to the medium dose.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086393PMC
http://dx.doi.org/10.2147/COPD.S401736DOI Listing

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