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PLoS One. 2018 Jul 25;13(7):e0201143. doi: 10.1371/journal.pone.0201143. eCollection 2018.

Association between blood eosinophil count and risk of readmission for patients with asthma: Historical cohort study.

Author information

1
Observational & Pragmatic Research Institute Pte Ltd, Singapore, Singapore.
2
AstraZeneca, Gaithersburg, MD, United States of America.
3
University of Groningen, University Medical Center Groningen, Groningen, Netherlands.
4
Ghent University Hospital, Ghent, Belgium.
5
The Peninsula College of Medicine and Dentistry, Plymouth, United Kingdom.
6
Royal Brompton and Harefield NHS Foundation Trust, London, United Kingdom.
7
AstraZeneca, Madrid, Spain.
8
Respiratory Medicine Unit and Oxford Respiratory NIHR BRC, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
9
Academic Primary Care, University of Aberdeen, Aberdeen, United Kingdom.

Abstract

BACKGROUND:

Recent studies have demonstrated an association between high blood eosinophil counts and greater risk of asthma exacerbations. We sought to determine whether patients hospitalized for an asthma exacerbation were at greater risk of readmission if they had a high blood eosinophil count documented before the first hospitalization.

METHODS:

This historical cohort study drew on 2 years of medical record data (Clinical Practice Research Datalink with Hospital Episode Statistics linkage) of patients (aged ≥5 years) admitted to hospital in England for asthma, with recorded blood eosinophil count within 1 baseline year before admission. We analyzed the association between high blood eosinophil count (≥0.35x109 cells/L) and readmission risk during 1 year of follow-up after hospital discharge, with adjustment for predefined, relevant confounders using forward selection.

RESULTS:

We identified 2,613 eligible patients with asthma-related admission, of median age 51 years (interquartile range, 36-69) and 76% women (1,997/2,613). Overall, 835/2,613 (32.0%) had a preadmission high blood eosinophil count. During the follow-up year, 130/2,613 patients (5.0%) were readmitted for asthma, including 55/835 (6.6%) with vs. 75/1,778 (4.2%) without high blood eosinophil count at baseline (adjusted hazard ratio [HR] 1.49; 95% CI 1.04-2.13, p = 0.029). The association was strongest in never-smokers (n = 1,296; HR 2.16, 95% CI 1.27-3.68, p = 0.005) and absent in current smokers (n = 547; HR 1.00, 95% CI 0.49-2.04, p = 0.997).

CONCLUSIONS:

A high blood eosinophil count in the year before an asthma-related hospitalization is associated with increased risk of readmission within the following year. These findings suggest that patients with asthma and preadmission high blood eosinophil count require careful follow-up, with treatment optimization, after discharge.

Conflict of interest statement

I have read the journal's policy and the authors of this manuscript have the following competing interests: All authors, including those employed by AstraZeneca, participated in the data interpretation, decision to publish, and preparation of the manuscript. All authors had full access to study results and had final responsibility for the decision to submit for publication. MK is an employee of the Observational and Pragmatic Research Institute Pte LTD, which conducted this study and which has conducted paid research in respiratory disease on behalf of the following other organizations in the past 5 years: Aerocrine; AKL Ltd.; Almirall; AstraZeneca; British Lung Foundation; Boehringer Ingelheim; Chiesi; GlaxoSmithKline; Mylan; Mundipharma; Napp; Novartis; Orion; Respiratory Effectiveness Group; Takeda; Teva; and Zentiva, a Sanofi company. JN is an employee, and TNT, GG, and SR are employees and shareholders of AstraZeneca, which supplied the funding for this study. MvdB has, within the last 5 years, received research grants paid to the University of Groningen from AstraZeneca, GlaxoSmithKline, Teva, and Chiesi. GB has, within the last 5 years, received honoraria for lectures from AstraZeneca, Boehringer-Ingelheim, Chiesi, GlaxoSmithKline, Novartis, Pfizer, and Teva; he is a member of advisory boards for AstraZeneca, Boehringer-Ingelheim, GlaxoSmithKline, Novartis, Sanofi/Regeneron, and Teva. RJ reports grants, personal fees and non-financial support from Astra Zeneca, personal fees from Boehringer Ingelheim, personal fees from Chiesi, personal fees and non-financial support from GSK, grants and personal fees from Novartis, non-financial support from Nutricia, personal fees from Pfizer, outside the submitted work.JWHK reports grants and personal fees from AstraZeneca, grants and personal fees from Boehringer Ingelheim, grants from Chiesi, grants and personal fees from GSK, grants and personal fees from Novartis, grants from Mundi Pharma, grants from TEVA, outside the submitted work. AMG has attended advisory boards for Glaxo SmithKline, Novartis, AstraZeneca, Boehringer Ingelheim andTeva. He has received speaker fees from Novartis, AstraZeneca, Vectura, Boehringer Ingelheim and Teva. He has participated in research with Hoffman La Roche, GlaxoSmithKline and Boehringer Ingelheim. He has attended international conferences sponsored by AstraZeneca and Boehringer Ingelheim. He has consultancy agreements with AstraZeneca and Vectura. IDP has received speaker’s honoraria for speaking at sponsored meetings from AstraZeneca, Boehringer Inglehiem, Aerocrine, Almirall, Novartis, and GSK and a payment for organising an educational event for SPRs from AZ. He has received honoraria for attending advisory panels with Almirall, Genentech, Regeneron, AstraZeneca, Boehringer Ingelheim, GSK, MSD, Schering-Plough, Novartis, Dey, Napp and Respivert. He has received sponsorship to attend international scientific meetings from Boehringer Ingelheim, GSK, AstraZeneca and Napp. DBP has board membership with Aerocrine, Amgen, AstraZeneca, Boehringer Ingelheim, Chiesi, Mylan, Mundipharma, Napp, Novartis, and Teva Pharmaceuticals; consultancy agreements with Almirall, Amgen, AstraZeneca, Boehringer Ingelheim, Chiesi, GlaxoSmithKline, Mylan, Mundipharma, Napp, Novartis, Pfizer, Teva Pharmaceuticals, and Theravance; grants and unrestricted funding for investigator-initiated studies (conducted through Observational and Pragmatic Research Institute Pte Ltd) from Aerocrine, AKL Research and Development Ltd, AstraZeneca, Boehringer Ingelheim, British Lung Foundation, Chiesi, Mylan, Mundipharma, Napp, Novartis, Pfizer, Respiratory Effectiveness Group, Teva Pharmaceuticals, Theravance, UK National Health Service, Zentiva; payment for lectures/speaking engagements from Almirall, AstraZeneca, Boehringer Ingelheim, Chiesi, Cipla, GlaxoSmithKline, Kyorin, Mylan, Merck, Mundipharma, Novartis, Pfizer, Skyepharma, and Teva Pharmaceuticals; payment for manuscript preparation from Mundipharma and Teva Pharmaceuticals; payment for the development of educational materials from Mundipharma and Novartis; payment for travel/accommodation/meeting expenses from Aerocrine, AstraZeneca, Boehringer Ingelheim, Mundipharma, Napp, Novartis, and Teva Pharmaceuticals; funding for patient enrolment or completion of research from Chiesi, Novartis, Teva Pharmaceuticals, and Zentiva; stock/stock options from AKL Research and Development Ltd which produces phytopharmaceuticals; owns 74% of the social enterprise Optimum Patient Care Ltd (Australia and UK) and 74% of Observational and Pragmatic Research Institute Pte Ltd (Singapore); and is peer reviewer for grant committees of the Efficacy and Mechanism Evaluation programme, and Health Technology Assessment. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

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