TY - JOUR
T1 - Comorbidities and the risk of mortality in patients with bronchiectasis
T2 - an international multicentre cohort study
AU - McDonnell, Melissa J.
AU - Aliberti, Stefano
AU - Goeminne, Pieter C.
AU - Restrepo, Marcos I.
AU - Finch, Simon
AU - Pesci, Alberto
AU - Dupont, Lieven J.
AU - Fardon, Thomas C.
AU - Wilson, Robert
AU - Loebinger, Michael R.
AU - Skrbic, Dusan
AU - Obradovic, Dusanka
AU - De Soyza, Anthony
AU - Ward, Chris
AU - Laffey, John G.
AU - Rutherford, Robert M.
AU - Chalmers, James D.
N1 - Funding Information:
MJM acknowledges fellowship support from the European Respiratory Society/European Lung Foundation and Health Research Board, Ireland. JDC acknowledges fellowship support from the Medical Research Council and the Wellcome Trust. This study was supported by the European Bronchiectasis Network (EMBARC; CRC-2013-06)—a European Respiratory Society Clinical Research Collaboration, which has received funding from the European Respiratory Society and Bayer HealthCare. The funding agencies had no role in the preparation, review, or approval of the manuscript.
Funding Information:
MJM reports grants from European Respiratory Society, grants from Health Research Board, Ireland; and personal fees from Bayer Healthcare, outside of the submitted work. SA reports personal fees from AstraZeneca, Basilea, Zambon, and Griffols; and grants and personal fees from Bayer Healthcare, Aradigm Corporation, European Respiratory Society, outside of the submitted work. PCG reports personal fees and non-financial support from Novartis and Bayer Healthcare; and non-financial support from Chiesi, outside of the submitted work. MIR's time is partially protected by Award Number K23HL096054 from the National Heart, Lung, and Blood Institute. ADS has received medical education grant support for a UK bronchiectasis network from GlaxoSmithKline, Gilead Chiesi, and Forest labs. ADS's employing institution receives fees for his work as Coordinating investigator in a phase 3 trial in Bronchiectasis sponsored by Bayer. JDC reports grants and personal fees from Bayer Healthcare, AstraZeneca, and Pfizer; personal fees from Griffols; and grants from Basilea and Novartis, outside of the submitted work. SF, AP, LJD, TCF, RW, MRL, DS, DO, CW, JGL, and RMR declare no competing interests.
Publisher Copyright:
© 2016 Elsevier Ltd
PY - 2016/12/1
Y1 - 2016/12/1
N2 - Background Patients with bronchiectasis often have concurrent comorbidities, but the nature, prevalence, and impact of these comorbidities on disease severity and outcome are poorly understood. We aimed to investigate comorbidities in patients with bronchiectasis and establish their prognostic value on disease severity and mortality rate. Methods An international multicentre cohort analysis of outpatients with bronchiectasis from four European centres followed up for 5 years was done for score derivation. Eligible patients were those with bronchiectasis confirmed by high-resolution CT and a compatible clinical history. Comorbidity diagnoses were based on standardised definitions and were obtained from full review of paper and electronic medical records, prescriptions, and investigator definitions. Weibull parametric survival analysis was used to model the prediction of the 5 year mortality rate to construct the Bronchiectasis Aetiology Comorbidity Index (BACI). We tested the BACI as a predictor of outcomes and explored whether the BACI added further prognostic information when used alongside the Bronchiectasis Severity Index (BSI). The BACI was validated in two independent international cohorts from the UK and Serbia. Findings Between June 1, 2006, and Nov 22, 2013, 1340 patients with bronchiectasis were screened and 986 patients were analysed. Patients had a median of four comorbidities (IQR 2–6; range 0–20). 13 comorbidities independently predicting mortality rate were integrated into the BACI. The overall hazard ratio for death conferred by a one-point increase in the BACI was 1·18 (95% CI 1·14–1·23; p<0·0001). The BACI predicted 5 year mortality rate, hospital admissions, exacerbations, and health-related quality of life across all BSI risk strata (p<0·0001 for mortality and hospital admissions, p=0·03 for exacerbations, p=0·0008 for quality of life). When used in conjunction with the BSI, the combined model was superior to either model alone (p=0·01 for combined vs BACI; p=0·008 for combined vs BSI). Interpretation Multimorbidity is frequent in bronchiectasis and can negatively affect survival. The BACI complements the BSI in the assessment and prediction of mortality and disease outcomes in patients with bronchiectasis. Funding European Bronchiectasis Network (EMBARC).
AB - Background Patients with bronchiectasis often have concurrent comorbidities, but the nature, prevalence, and impact of these comorbidities on disease severity and outcome are poorly understood. We aimed to investigate comorbidities in patients with bronchiectasis and establish their prognostic value on disease severity and mortality rate. Methods An international multicentre cohort analysis of outpatients with bronchiectasis from four European centres followed up for 5 years was done for score derivation. Eligible patients were those with bronchiectasis confirmed by high-resolution CT and a compatible clinical history. Comorbidity diagnoses were based on standardised definitions and were obtained from full review of paper and electronic medical records, prescriptions, and investigator definitions. Weibull parametric survival analysis was used to model the prediction of the 5 year mortality rate to construct the Bronchiectasis Aetiology Comorbidity Index (BACI). We tested the BACI as a predictor of outcomes and explored whether the BACI added further prognostic information when used alongside the Bronchiectasis Severity Index (BSI). The BACI was validated in two independent international cohorts from the UK and Serbia. Findings Between June 1, 2006, and Nov 22, 2013, 1340 patients with bronchiectasis were screened and 986 patients were analysed. Patients had a median of four comorbidities (IQR 2–6; range 0–20). 13 comorbidities independently predicting mortality rate were integrated into the BACI. The overall hazard ratio for death conferred by a one-point increase in the BACI was 1·18 (95% CI 1·14–1·23; p<0·0001). The BACI predicted 5 year mortality rate, hospital admissions, exacerbations, and health-related quality of life across all BSI risk strata (p<0·0001 for mortality and hospital admissions, p=0·03 for exacerbations, p=0·0008 for quality of life). When used in conjunction with the BSI, the combined model was superior to either model alone (p=0·01 for combined vs BACI; p=0·008 for combined vs BSI). Interpretation Multimorbidity is frequent in bronchiectasis and can negatively affect survival. The BACI complements the BSI in the assessment and prediction of mortality and disease outcomes in patients with bronchiectasis. Funding European Bronchiectasis Network (EMBARC).
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U2 - 10.1016/S2213-2600(16)30320-4
DO - 10.1016/S2213-2600(16)30320-4
M3 - Article
C2 - 27864036
AN - SCOPUS:84997051957
VL - 4
SP - 969
EP - 979
JO - The Lancet Respiratory Medicine
JF - The Lancet Respiratory Medicine
SN - 2213-2600
IS - 12
ER -