Comorbidity in severe asthma requiring systemic corticosteroid therapy: Cross-sectional data from the Optimum Patient Care Research Database and the British Thoracic Difficult Asthma Registry

Joan Sweeney, Chris C Patterson, Andrew Menzies-Gow, Rob M Niven, Adel H Mansur, Christine Bucknall, Rekha Chaudhuri, David Price, Chris E. Brightling, Liam G. Heaney

Research output: Contribution to journalArticlepeer-review

262 Citations (Scopus)

Abstract

Objective: To determine the prevalence of systemic corticosteroid-induced morbidity in severe asthma.
Design: Cross-sectional observational study.Setting The primary care Optimum Patient Care Research Database and the British Thoracic Society Difficult Asthma Registry.
Participants: Optimum Patient Care Research Database (7195 subjects in three age- and gender-matched groups)—severe asthma (Global Initiative for Asthma (GINA) treatment step 5 with four or more prescriptions/year of oral corticosteroids, n=808), mild/moderate asthma (GINA treatment step 2/3, n=3975) and non-asthma controls (n=2412). 770 subjects with severe asthma from the British Thoracic Society Difficult Asthma Registry (442 receiving daily oral corticosteroids to maintain disease control).
Main outcome measures: Prevalence rates of morbidities associated with systemic steroid exposure were evaluated and reported separately for each group.
Results: 748/808 (93%) subjects with severe asthma had one or more condition linked to systemic corticosteroid exposure (mild/moderate asthma 3109/3975 (78%), non-asthma controls 1548/2412 (64%); p<0.001 for severe asthma versus non-asthma controls). Compared with mild/moderate asthma, morbidity rates for severe asthma were significantly higher for conditions associated with systemic steroid exposure (type II diabetes 10% vs 7%, OR=1.46 (95% CI 1.11 to 1.91), p<0.01; osteoporosis 16% vs 4%, OR=5.23, (95% CI 3.97 to 6.89), p<0.001; dyspeptic disorders (including gastric/duodenal ulceration) 65% vs 34%, OR=3.99, (95% CI 3.37 to 4.72), p<0.001; cataracts 9% vs 5%, OR=1.89, (95% CI 1.39 to 2.56), p<0.001). In the British Thoracic Society Difficult Asthma Registry similar prevalence rates were found, although, additionally, high rates of osteopenia (35%) and obstructive sleep apnoea (11%) were identified.

Conclusions: Oral corticosteroid-related adverse events are common in severe asthma. New treatments which reduce exposure to oral corticosteroids may reduce the prevalence of these conditions and this should be considered in cost-effectiveness analyses of these new treatments.
Original languageEnglish
Pages (from-to)339-346
Number of pages8
JournalThorax
Volume71
Issue number4
Early online date27 Jan 2016
DOIs
Publication statusPublished - Mar 2016

Keywords

  • Administration, Oral
  • Adult
  • Aged
  • Asthma/diagnosis
  • Body Mass Index
  • Cataract/chemically induced
  • Cross-Sectional Studies
  • Diabetes Mellitus, Type 2/chemically induced
  • Duodenal Ulcer/chemically induced
  • Female
  • Glucocorticoids/administration & dosage
  • Humans
  • Male
  • Middle Aged
  • Obesity/chemically induced
  • Osteoporosis/chemically induced
  • Prevalence
  • Quality of Life
  • Registries
  • Risk Factors
  • Severity of Illness Index
  • Sex Distribution
  • Sleep Apnea, Obstructive/chemically induced
  • Stomach Ulcer/chemically induced
  • United Kingdom/epidemiology

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