TB Research

Antibiotic in non-purulent hospitalised-treated exacerbations of COPD: a randomised double-blind placebo-controlled trial

Néstor Soler, Arturo Humberto Huerta Garcia, Adrián Ceccato, Rebeca Domingo, Olivia Vilaró, Albert Gabarrús, Jesús Aibar, Antoní Torres

Abstract

Prescription of antibiotics is wide and generalised in COPD exacerbated patients requiring hospitalisation. Previous data showed that sputum purulence-guided antibiotic treatment strategy might be useful in severe exacerbations. The aim of this study was to investigate the non-inferiority of placebo compared to antibiotic treatment in non-purulent severe exacerbations of COPD. <b>Methods:</b> In this RCT, we recruited a cohort of patients with non-purulent severe exacerbation of COPD. We randomly assigned them to a 5-day course of oral moxifloxacin (400 mg daily) or placebo. The primary outcome was the rate of treatment failure on day 3. <b>Findings:</b> We randomly allocated 73 (25%) patients from the total cohort of 287 evaluated patients with non-purulent exacerbations, and 72 were included in the ITT analysis (35 in the placebo arm and 37 in the moxifloxacin arm). For the primary outcome, 4 patients (11%) in the placebo group and 3 patients (8%) in the moxifloxacin group presented treatment failure (difference 3%, p =0.71; 2-sided 95% CI -0.10-0.17) not reaching the pre-specified non-inferiority failure limit of 15%. We did not observe significant differences between groups in length of stay (LOS) median 6 days (IQR 4-7) in placebo group vs 5 days (IQR 4-7) in moxifloxacin group. <b>Interpretation:</b> In patients with COPD requiring hospitalisation for non-purulent exacerbation, treatment without antibiotic was not inferior to antibiotics in treatment failure or LOS.

MeSH terms

  • Medicine
  • Moxifloxacin
  • Placebo
  • Exacerbation
  • COPD
  • Internal medicine
  • Antibiotics
  • Cohort
  • Randomized controlled trial
  • Sputum
  • Surgery