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

被引:261
作者
Sweeney, Joan [1 ]
Patterson, Chris C. [2 ]
Menzies-Gow, Andrew [3 ]
Niven, Rob M. [4 ,5 ]
Mansur, Adel H. [6 ]
Bucknall, Christine [7 ]
Chaudhuri, Rekha [8 ,9 ]
Price, David [10 ]
Brightling, Chris E. [11 ]
Heaney, Liam G. [1 ]
机构
[1] Queens Univ Belfast, Ctr Infect & Immun, Belfast BT9 7BL, Antrim, North Ireland
[2] Queens Univ Belfast, Ctr Publ Hlth, Belfast BT9 7BL, Antrim, North Ireland
[3] Royal Brompton Hosp, London SW3 6LY, England
[4] Univ Manchester, MAHSC, Manchester, Lancs, England
[5] UHSM, Manchester, Lancs, England
[6] Birmingham Heartlands Hosp, Severe & Brittle Asthma Unit, Birmingham B9 5ST, W Midlands, England
[7] Royal Infirm, Dept Resp Med, Glasgow G31 2ER, Lanark, Scotland
[8] Univ Glasgow, Dept Resp Med, Div Immunol Infect & Inflammat, Glasgow, Lanark, Scotland
[9] Gartnavel Gen, Glasgow, Lanark, Scotland
[10] Univ Aberdeen, Acad Primary Care, Aberdeen, Scotland
[11] Univ Leicester, Inst Lung Hlth, Dept Infect Inflammat & Immun, Leicester, Leics, England
关键词
TERM STEROID-THERAPY; QUALITY-OF-LIFE; ADVERSE EVENTS; ECONOMIC-IMPLICATIONS; CUMULATIVE BURDEN; DISEASE; ADULTS; RISK; COMPLICATIONS; FREQUENCY;
D O I
10.1136/thoraxjnl-2015-207630
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
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 nonasthma 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.
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收藏
页码:339 / 346
页数:8
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