アブストラクト | We examined associations between blood eosinophil counts (BEC) and risk of treatment failure or hospital readmission following acute oral corticosteroid (OCS)-treated COPD exacerbations. We conducted studies from the Optimum Patient Care Research Database (OPCRD) (www.optimumpatientcare.org/opcrd) and Clinical Practice Research Datalink (CPRD) (www.cprd.com/home/), validated databases for medical research, with linked Hospital Episode Statistics (HES) data for approximately 20 000 COPD patients aged >/=40 years. For patients with OCS-treated COPD exacerbations treated in primary care, with BECs recorded on first day of OCS treatment (Cohort 1), we assessed treatment failure (COPD-related hospitalisations and OCS prescriptions beyond index OCS course). For patients hospitalised for COPD exacerbations, with BEC measured over an exacerbation-free period during the year prior to admission (Cohort 2), we assessed readmission rate. Cox proportional hazards regression analysis was adjusted for confounders to estimate the association between BEC and treatment outcomes. Of patients treated with OCS for COPD exacerbations in primary care (Cohort 1), 44% experienced treatment failure following single OCS courses, and 10% (255/2482) were hospitalised for </=6 weeks. Greater BEC was associated with reduced hospital-admission risk (hazard ratio [HR]=0.26; 95% CI: 0.12-0.56, per 100 cells.microL(-1) increase). BEC increases of >/=200 cells.microL(-1) from exacerbation-free periods to exacerbations were associated with least hospitalisation risk (HR=0.32; 95% CI: 0.15-0.71) versus no BEC change. For patients hospitalised for COPD exacerbations (Cohort 2), 4-week hospital readmission was 12% (1189/10 245). BEC increases during an exacerbation-free period within the past year were associated with reduced risk of short-term readmission (HR=0.78; 95% CI: 0.63-0.96). Greater BEC predicted better outcomes for patients with OCS-treated COPD exacerbations, whether community or hospital managed. Eosinopenia predicted worse outcomes. |
投稿者 | Kerkhof, Marjan; Chaudhry, Isha; Pavord, Ian D; Miravitlles, Marc; Kook Rhee, Chin; Halpin, David M G; Usmani, Omar S; Jones, Rupert; Kocks, Janwillem; Alacqua, Marianna; Morris, Tamsin; Kaplan, Alan; Price, David B |
組織名 | Observational and Pragmatic Research Institute, Singapore, Singapore.;Oxford Respiratory NIHR BRC, Nuffield Dept of Medicine, University of Oxford,;Oxford, UK.;Pneumology Dept, Hospital Universitari Vall d'Hebron, Vall d'Hebron Institut de;Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, CIBER de Enfermedades;Respiratorias (CIBERES), Barcelona, Spain.;College of Medicine, Seoul St Mary's Hospital, The Catholic University of Korea,;Seoul, South Korea.;University of Exeter Medical School, College of Medicine and Health, University;of Exeter, Exeter, UK.;Imperial College London, London, UK.;The Peninsula College of Medicine and Dentistry, Plymouth, UK.;AstraZeneca, Cambridge, UK.;AstraZeneca, Luton, UK.;Family Physician Airways Group of Canada, Richmond Hill, ON, Canada.;University of Aberdeen, Aberdeen, UK. |