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Targeted Retreatment of Incompletely Recovered Chronic Obstructive Pulmonary Disease Exacerbations with Ciprofloxacin. A Double-Blind, Randomized, Placebo-controlled, Multicenter, Phase III Clinical Trial

Ritchie, AI; Brill, SE; Vlies, BH; Finney, LJ; Allinson, JP; Alves-Moreira, L; Wiseman, DJ; Walker, PP; Baker, E; Elkin, SL; et al. Ritchie, AI; Brill, SE; Vlies, BH; Finney, LJ; Allinson, JP; Alves-Moreira, L; Wiseman, DJ; Walker, PP; Baker, E; Elkin, SL; Mallia, P; Law, M; Donaldson, GC; Calverley, PMA; Wedzicha, JA (2020) Targeted Retreatment of Incompletely Recovered Chronic Obstructive Pulmonary Disease Exacerbations with Ciprofloxacin. A Double-Blind, Randomized, Placebo-controlled, Multicenter, Phase III Clinical Trial. Am J Respir Crit Care Med, 202 (4). pp. 549-557. ISSN 1535-4970 https://doi.org/10.1164/rccm.201910-2058OC
SGUL Authors: Baker, Emma Harriet

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Abstract

RATIONALE: COPD exacerbations are prone to non-recovery but there are no data about the effectiveness of retreatment on these prolonged events. We examined whether further therapy with ciprofloxacin for incompletely resolved COPD exacerbations prolonged the time until the next event. METHODS: This multi-centre randomised double-blind placebo-controlled trial studied retreatment with oral ciprofloxacin 500mg or matched placebo twice daily for 7 days in patients with GOLD stage II - IV COPD with persistent symptoms and/or serum C-reactive protein (CRP) ≥8mg/L initiated 14 (+/- 3) days after an index COPD exacerbation. The primary outcome was the time to the next exacerbation within a 90-day period. RESULTS: Of 826 patients screened at 4 centres, 144 eligible participants with incomplete recovery were randomised to receive ciprofloxacin (n=72) or placebo (n=72). 57% of patients in the ciprofloxacin group had experienced 1 or more exacerbations, compared to 53% in the placebo group. The median time to the next exacerbation was 32.5 days (IQR 13-50) in the placebo arm and 34 days (IQR 17-62) in the ciprofloxacin arm, which was not significantly different (adjusted hazard ratio = 1.07, 95% CI 0.68-1.68; p=0.76). No significant differences were seen in quality of life scores or lung function between treatment groups. CONCLUSION: In patients with persistent symptoms and/or raised CRP 14 days following a COPD exacerbation, an additional course of ciprofloxacin resulted in no additional benefit compared to placebo. This suggests that non-recovered exacerbations are not driven by ongoing bacterial infection and may potentially be targeted with anti-inflammatory therapy.

Item Type: Article
Additional Information: Originally Published in: Andrew I Ritchie , Simon E Brill , Ben H. Vlies , Lydia J Finney , James P Allinson , Luana Alves-Moreira , Dexter J. Wiseman , Paul P Walker , Emma Baker , Sarah L Elkin , Patrick Mallia , Martin Law , Gavin C. Donaldson , Peter M.A. Calverley , and Jadwiga A Wedzicha. Targeted Retreatment of Incompletely Recovered COPD Exacerbations With Ciprofloxacin: A Double-blind, Randomised, Placebo-controlled, Multicentre Phase III Trial. American Journal of Respiratory and Critical Care Medicine 2020. 2020;2020:549-557. DOI: 10.1164/rccm.201910-2058OC Copyright © 2020 by the American Thoracic Society The final publication is available at https://doi.org/10.1164/rccm.201910-2058OC.
Keywords: Chronic Obstructive Pulmonary Disease, ciprofloxacin, exacerbations, incomplete recovery, retreatment, 11 Medical and Health Sciences, Respiratory System
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Am J Respir Crit Care Med
ISSN: 1535-4970
Language: eng
Dates:
DateEvent
15 August 2020Published
8 April 2020Published Online
23 March 2020Accepted
Publisher License: Publisher's own licence
Projects:
Project IDFunderFunder ID
RP-PG-0109-10056National Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
PubMed ID: 32267724
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/111853
Publisher's version: https://doi.org/10.1164/rccm.201910-2058OC

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