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Azithromycin during Acute COPD Exacerbations Requiring Hospitalization (BACE): a Multicentre, Randomized, Double-blind, Placebo-controlled Trial.

Authors :
UCL - (MGD) Service de pneumologie
UCL - SSS/IREC/PNEU - Pôle de Pneumologie, ORL et Dermatologie
Vermeersch, Kristina
Gabrovska, Maria
Aumann, Joseph
Demedts, Ingel K
Corhay, Jean-Louis
Marchand, Eric
Slabbynck, Hans
Haenebalcke, Christel
Haerens, Michiel
Hanon, Shane
Jordens, Paul
Peché, Rudi
Fremault, Antoine
Lauwerier, Tine
Delporte, Anja
Vandenberk, Bert
Willems, Rik
Everaerts, Stephanie
Belmans, Ann
Bogaerts, Kris
Verleden, Geert M
Troosters, Thierry
Ninane, Vincent
Brusselle, Guy G
Janssens, Wim
BACE trial investigators
UCL - (MGD) Service de pneumologie
UCL - SSS/IREC/PNEU - Pôle de Pneumologie, ORL et Dermatologie
Vermeersch, Kristina
Gabrovska, Maria
Aumann, Joseph
Demedts, Ingel K
Corhay, Jean-Louis
Marchand, Eric
Slabbynck, Hans
Haenebalcke, Christel
Haerens, Michiel
Hanon, Shane
Jordens, Paul
Peché, Rudi
Fremault, Antoine
Lauwerier, Tine
Delporte, Anja
Vandenberk, Bert
Willems, Rik
Everaerts, Stephanie
Belmans, Ann
Bogaerts, Kris
Verleden, Geert M
Troosters, Thierry
Ninane, Vincent
Brusselle, Guy G
Janssens, Wim
BACE trial investigators
Source :
American journal of respiratory and critical care medicine, Vol. 200, no. 7, p. 857-868 (2019)
Publication Year :
2019

Abstract

RATIONALE: Azithromycin prevents acute exacerbations of chronic obstructive pulmonary disease (AECOPDs); however, its value in the treatment of an AECOPD requiring hospitalization remains to be defined. OBJECTIVES: We investigated whether a 3-month intervention with low-dose azithromycin could decrease treatment failure (TF) when initiated at hospital admission and added to standard care. METHODS: In an investigator-initiated, multicenter, randomized, double-blind, placebo-controlled trial, patients who had been hospitalized for an AECOPD and had a smoking history of ≥10 pack-years and one or more exacerbations in the previous year were randomized (1:1) within 48 hours of hospital admission to azithromycin or placebo. The study drug (500 mg/d for 3 d) was administered on top of a standardized acute treatment of systemic corticosteroids and antibiotics, and subsequently continued for 3 months (250 mg/2 d). The patients were followed for 6 months thereafter. Time-to-first-event analyses evaluated the TF rate within 3 months as a novel primary endpoint in the intention-to-treat population, with TF defined as the composite of treatment intensification with systemic corticosteroids and/or antibiotics, a step-up in hospital care or readmission for respiratory reasons, or all-cause mortality. MEASUREMENTS AND MAIN RESULTS: A total of 301 patients were randomized to azithromycin (n = 147) or placebo (n = 154). The TF rate within 3 months was 49% in the azithromycin group and 60% in the placebo group (hazard ratio, 0.73; 95% confidence interval, 0.53-1.01; P = 0.0526). Treatment intensification, step-up in hospital care, and mortality rates within 3 months were 47% versus 60% (P = 0.0272), 13% versus 28% (P = 0.0024), and 2% versus 4% (P = 0.5075) in the azithromycin and placebo groups, respectively. Clinical benefits were lost 6 months after withdrawal. CONCLUSIONS: Three months of azithromycin for an infectious AECOPD requiring hospitalization may significantly reduce TF d

Details

Database :
OAIster
Journal :
American journal of respiratory and critical care medicine, Vol. 200, no. 7, p. 857-868 (2019)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1104520634
Document Type :
Electronic Resource