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      The independent contribution of Pseudomonas aeruginosa infection to long-term clinical outcomes in bronchiectasis.

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          Abstract

          Pseudomonas aeruginosa is responsible for chronic infection in many bronchiectasis patients but it is not known whether it is associated with worse clinical outcomes independent of the underlying severity of disease.This study analysed data from 2596 bronchiectasis patients included from 10 different bronchiectasis clinical centres across Europe and Israel, with a 5-year follow-up period. Prevalence of P. aeruginosa chronic infection and its independent impact on exacerbations, hospitalisations, quality of life and mortality was assessed.The prevalence of P. aeruginosa chronic infection was 15.0% (n=389). P. aeruginosa was associated with a higher mortality in a univariate analysis (hazard ratio (HR) 2.02; 95% (confidence interval) CI 1.53-2.66; p<0.0001) but an independent impact on mortality was not found in a multivariate analysis (HR 0.98; 95% CI 0.70-1.36; p=0.89). P. aeruginosa was independently associated with increased mortality only in patients with frequent exacerbations (two or more per year) (HR 2.03; 95% CI 1.36-3.03; p=0.001). An independent association with worse quality of life of 7.46 points (95% CI 2.93-12.00; p=0.001) was found in a multivariable linear regression. P. aeruginosa was therefore found to be independently associated with exacerbation frequency, hospital admissions and worse quality of life. Mortality was increased in patients with P. aeruginosa particularly in the presence of frequent exacerbations.

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          Author and article information

          Journal
          Eur. Respir. J.
          The European respiratory journal
          European Respiratory Society (ERS)
          1399-3003
          0903-1936
          February 2018
          : 51
          : 2
          Affiliations
          [1 ] Pulmonology Dept of São João Hospital Center, Porto, Portugal.
          [2 ] Pulmonary Institute and CF Center, Carmel Medical Center, Haifa, Israel.
          [3 ] Dept of Pathophysiology and Transplantation, University of Milan, Milan, Italy.
          [4 ] Internal Medicine Dept, Respiratory Unit and Cystic Fibrosis Adult Center, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
          [5 ] Respiratory Medicine, University Hospital Gasthuisberg, Leuven, Belgium.
          [6 ] Respiratory Disease, AZ Nikolaas, Sint-Niklaas, Belgium.
          [7 ] Royal Infirmary of Edinburgh and University of Edinburgh, Edinburgh, UK.
          [8 ] Scottish Centre for Respiratory Research, University of Dundee, Dundee, UK.
          [9 ] Institute for Pulmonary Diseases of Vojvodina Sremska Kamenica and Faculty of Medicine, University of Novi Sad, Novi Sad, Serbia.
          [10 ] Grifols Inc., Research Triangle, NC, USA.
          [11 ] 5th Dept of Pulmonary Medicine, "Sotiria" Chest Diseases Hospital, Athens, Greece.
          [12 ] Thorax Institute, Institute of Biomedical Research August Pi i Sunyer (IDIBAPS), Ciberes University of Barcelona, Vall d'Hebron Research Institute VHIR, Hospital Vall D'Hebron, Respiratory Disease Dept, Barcelona, Spain.
          [13 ] Adult Bronchiectasis Service and Sir William Leech Centre for Lung Research, Freeman Hospital, Newcastle upon Tyne Hospitals NHS Foundation Trust, Heaton, UK.
          [14 ] Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
          [15 ] Dept of Respiratory Medicine, Galway University Hospitals, Galway, Ireland.
          [16 ] Scottish Centre for Respiratory Research, University of Dundee, Dundee, UK jchalmers@dundee.ac.uk.
          Article
          51/2/1701953
          10.1183/13993003.01953-2017
          29386336
          93829a7c-4feb-4e64-8dab-e44bd8aca1fc
          History

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