Adverse outcomes from initiation of systemic corticosteroids for asthma: long-term observational study

被引:304
作者
Price, David B. [1 ,2 ]
Trudo, Frank [3 ]
Voorham, Jaco [1 ]
Xu, Xiao [4 ]
Kerkhof, Marjan [1 ]
Jie, Joanna Ling Zhi [1 ]
Tran, Trung N. [5 ]
机构
[1] Observat & Pragmat Res Inst, Singapore, Singapore
[2] Univ Aberdeen, Acad Primary Care, Div Appl Hlth Sci, Polwarth Bldg,Foresterhill, Aberdeen AB25 2ZD, Scotland
[3] AstraZeneca, Med Affairs, Wilmington, DE USA
[4] AstraZeneca, Global Payer Evidence & Pricing, Gaithersburg, MD USA
[5] AstraZeneca, Med Evidence & Observat Res, Gaithersburg, MD USA
来源
JOURNAL OF ASTHMA AND ALLERGY | 2018年 / 11卷
关键词
adverse outcomes; asthma; cumulative exposure; oral corticosteroids; systemic corticosteroids; ORAL CORTICOSTEROIDS; COMPLICATIONS; SELECTION; DATABASE; EVENTS; BURDEN; COSTS; RISK; UK;
D O I
10.2147/JAA.S176026
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Purpose: Prior work suggests a threshold of four courses/year of systemic corticosteroid (SCS) therapy is associated with adverse consequences. The objective of this study was to investigate the onset of adverse outcomes beginning at SCS initiation in a broad asthma population. Patients and methods: This historical matched cohort study utilized anonymized, longitudinal medical record data (1984-2017) of patients (>= 18 years) with active asthma. Matched patients with first SCS prescription (SCS arm) and no SCS exposure (non-SCS arm) were followed until first outcome event. Associations between time-varying exposure measures and onset of 17 SCS-associated adverse outcomes were estimated using Cox proportional hazard regression, adjusting for confounders, in separate models. Results: We matched 24,117 pairs of patients with median record availability before SCS initiation of 9.9 and 8.7 years and median follow-up 7.4 and 6.4 years in SCS and non-SCS arms, respectively. Compared with patients in the non-SCS arm, patients prescribed SCS had significantly increased risk of osteoporosis/osteoporotic fracture (adjusted hazard ratio 3.11; 95% CI 1.87-5.19), pneumonia (2.68; 2.30-3.11), cardio-/cerebrovascular diseases (1.53; 1.36-1.72), cataract (1.50; 1.31 1.73), sleep apnea (1.40; 1.04 1.86), renal impairment (1.36; 1.26 1.47), depression/anxiety (1.31; 1.21-1.41), type 2 diabetes (1.26; 1.15-1.37), and weight gain (1.14; 1.10-1.18). A dose-response relationship for cumulative SCS exposure with most adverse outcomes began at cumulative exposures of 1.0-<2.5 g and for some outcomes at cumulative exposures of only 0.5 <1 g (vs >0-<0.5 g reference), equivalent to four lifetime SCS courses. Conclusion: Our findings suggest urgent need for reappraisal of when patients need specialist care and consideration of nonsteroid therapy.
引用
收藏
页码:193 / 204
页数:12
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