P19 Predictors of COPD Mortality, 2 year Follow-up Data from the ARCADE study. (12th November 2015)

• Record Type: Journal Article
• Authors: Gale, NS; Albarrati, A; Munnery, MM; Tal-Singer, R; Cockcroft, JR; Shale, DJ
• Is Part Of: Thorax. Volume 70(2015)Supplement 3
• Page Start: A84
• Page End: A84
• Publication Date: 2015-11-12
• Subjects: Chest -- Diseases -- Periodicals; Thorax; Chest -- Diseases; Periodicals; Periodicals; 617.54
• DOI: 10.1136/thoraxjnl-2015-207770.156
• Languages: English
• ISSNs: 0040-6376

Abstract

Abstract : Background: COPD is a systemic disease with associated comorbidities including cardiovascular disease which have significant impact on morbidity and mortality. 1 However, the progression of the disease is not well understood as there are few longitudinal studies of sufficient duration which include outcome data. The aim of this analysis was to evaluate predictors of mortality from the Assessment of Risk in Chronic Airways Disease Evaluation Study (ARCADE), Clinical Trials registration: NCT01656421 . 2 Methods: The ARCADE study is a longitudinal observational study of cardiovascular risk and other comorbidities in patients with COPD. Patients were assessed at recruitment and after 2 years including the following outcomes: Spirometry, BMI, St Georges Respiratory Questionnaire (SGRQ), mMRC breathlessness, number of exacerbations and 6 min walk distance (6MWD). A sample of blood was analysed for the inflammatory mediator fibrinogen. Results: At baseline 524 patients with COPD, confirmed with spirometry, were recruited to the study. Thus far, at the 2 year follow up there have been 47 deaths. According to hospital records, causes of death were: respiratory n = 22 (including acute exacerbations/respiratory infections (n = 12) and pneumonia (n = 10)), cardiovascular n = 9, cancer n = 10, septicaemia n = 3 and unknown n = 4. At baseline the subjects who did not survive were similar to survivors in age, gender and BMI, but had greater airflow limitation, worse SGRQ, more breathlessness, more exacerbations and lower 6MWD, fibrinogen was also higher (Table 1 ). Using logistic regression of the objective markers which differed between the groups; FEV1% predicted, number of exacerbations, 6MWD and fibrinogen were entered into the model. Of these Fibrinogen (p = 0.013) and 6MWD (p = 0.024) were significant predictors of mortality (X2 (4) = 18.678, p = 0.001). Conclusions: The follow up mortality rate was 9%, with the majority of deaths due to respiratory causes, followed by cancer and cardiovascular events. The non-survivors had poorer objective and patient reported outcomes. Further follow-up of this cohort will provide greater power to predict outcomes. Thanks to all our volunteers and GlaxoSmithKline who funded the study. References: 1 Mannino DM, Thorn D, Swensen A, Holguin F. Prevalence and outcomes of diabetes, hypertension and cardiovascular disease in COPD. Eur Respir J . 2008;32 :962–69 2 Gale NS, Albarrati AM, Munnery MM, et al . Assessment of Risk in Chronic Airways Disease Evaluation (ARCADE): Protocol and preliminary data. Chron Respir Dis . 2014;11 (4):199–207