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Treatment failure and hospital readmissions in severe COPD exacerbations treated with azithromycin versus placebo - a post-hoc analysis of the BACE randomized controlled trial.
Vermeersch, Kristina; Belmans, Ann; Bogaerts, Kris; Gyselinck, Iwein; Cardinaels, Nina; Gabrovska, Maria; Aumann, Joseph; Demedts, Ingel K; Corhay, Jean-Louis; Marchand, Eric; Slabbynck, Hans; Haenebalcke, Christel; Vermeersch, Stefanie; Verleden, Geert M; Troosters, Thierry; Ninane, Vincent; Brusselle, Guy G; Janssens, Wim.
Afiliação
  • Vermeersch K; Laboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
  • Belmans A; Department of Respiratory Diseases, University Hospitals Leuven, B-3000, Leuven, Belgium.
  • Bogaerts K; I-BioStat, KU Leuven, B-3000, Leuven, Belgium.
  • Gyselinck I; Universiteit Hasselt, B-3500, Hasselt, Belgium.
  • Cardinaels N; I-BioStat, KU Leuven, B-3000, Leuven, Belgium.
  • Gabrovska M; Universiteit Hasselt, B-3500, Hasselt, Belgium.
  • Aumann J; Laboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
  • Demedts IK; Laboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
  • Corhay JL; Department of Pneumology, Centre Hospitalier Universitaire Saint-Pierre, Université Libre de Bruxelles, B-1000, Brussels, Belgium.
  • Marchand E; Department of Pneumology, Jessa Ziekenhuis, B-3500, Hasselt, Belgium.
  • Slabbynck H; Department of Respiratory Medicine, AZ Delta Roeselare-Menen, B-8800, Roeselare, Belgium.
  • Haenebalcke C; Department of Pneumology, Centre Hospitalier Universitaire, site Sart-Tilman, B-4000, Liège, Belgium.
  • Vermeersch S; Department of Pneumology, CHU-UCL-Namur, site Mont-Godinne, B-5530, Yvoir, Belgium.
  • Verleden GM; Faculty of Medicine, NARILIS, Laboratory of Respiratory Physiology, University of Namur, B-5000, Namur, Belgium.
  • Troosters T; Department of Respiratory Medicine, ZNA Middelheim, B-2020, Antwerpen, Belgium.
  • Ninane V; Department of Pneumology, AZ Sint-Jan, B-8000, Brugge-Oostende, Belgium.
  • Brusselle GG; Department of Respiratory Medicine, Ghent University Hospital, B-9000, Ghent, Belgium.
  • Janssens W; Laboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
Respir Res ; 20(1): 237, 2019 Oct 29.
Article em En | MEDLINE | ID: mdl-31665017
BACKGROUND: In the BACE trial, a 3-month (3 m) intervention with azithromycin, initiated at the onset of an infectious COPD exacerbation requiring hospitalization, decreased the rate of a first treatment failure (TF); the composite of treatment intensification (TI), step-up in hospital care (SH) and mortality. OBJECTIVES: (1) To investigate the intervention's effect on recurrent events, and (2) to identify clinical subgroups most likely to benefit, determined from the incidence rate of TF and hospital readmissions. METHODS: Enrolment criteria included the diagnosis of COPD, a smoking history of ≥10 pack-years and ≥ 1 exacerbation in the previous year. Rate ratio (RR) calculations, subgroup analyses and modelling of continuous variables using splines were based on a Poisson regression model, adjusted for exposure time. RESULTS: Azithromycin significantly reduced TF by 24% within 3 m (RR = 0.76, 95%CI:0.59;0.97, p = 0.031) through a 50% reduction in SH (RR = 0.50, 95%CI:0.30;0.81, p = 0.006), which comprised of a 53% reduction in hospital readmissions (RR = 0.47, 95%CI:0.27;0.80; p = 0.007). A significant interaction between the intervention, CRP and blood eosinophil count at hospital admission was found, with azithromycin significantly reducing hospital readmissions in patients with high CRP (> 50 mg/L, RR = 0.18, 95%CI:0.05;0.60, p = 0.005), or low blood eosinophil count (<300cells/µL, RR = 0.33, 95%CI:0.17;0.64, p = 0.001). No differences were observed in treatment response by age, FEV1, CRP or blood eosinophil count in continuous analyses. CONCLUSIONS: This post-hoc analysis of the BACE trial shows that azithromycin initiated at the onset of an infectious COPD exacerbation requiring hospitalization reduces the incidence rate of TF within 3 m by preventing hospital readmissions. In patients with high CRP or low blood eosinophil count at admission this treatment effect was more pronounced, suggesting a potential role for these biomarkers in guiding azithromycin therapy. TRIAL REGISTRATION: ClinicalTrials.gov number. NCT02135354 .
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Readmissão do Paciente / Índice de Gravidade de Doença / Azitromicina / Progressão da Doença / Doença Pulmonar Obstrutiva Crônica / Antibacterianos Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Respir Res Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Readmissão do Paciente / Índice de Gravidade de Doença / Azitromicina / Progressão da Doença / Doença Pulmonar Obstrutiva Crônica / Antibacterianos Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Respir Res Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Bélgica