4.4 Review

Corticosteroid-related adverse events in patients with giant cell arteritis: A claims-based analysis

Journal

SEMINARS IN ARTHRITIS AND RHEUMATISM
Volume 46, Issue 2, Pages 246-252

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.semarthrit.2016.05.009

Keywords

Adverse events; Corticosteroids; Epidemiology; Giant cell arteritis; Health care insurance claims

Categories

Funding

  1. Genentech Inc., a member of the Roche Group
  2. F. Hoffmann-La Roche Ltd.

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Objective: Corticosteroids (CS) are standard treatment for giant cell arteritis (GCA), but concerns persist over toxicities associated with long-term use. In this retrospective study of medical claims data, we estimated risks for adverse events (AEs) in CS-treated GCA patients. Methods: Cox regression analyses with CS use as a time-dependent variable were conducted on data from the 2003 to 2012 Truven Health Analytics MarketScan Database. Patients 50 years of age and older who had >= 2 claims of newly diagnosed GCA, >= 1 filled oral CS prescription, and no AEs before GCA diagnosis were included. The primary outcome was presence of a new CS-related AE. Results: In total, 2497 patients were included. Their mean age was 71.0 years, and 71% were women. Follow-up was 9680 patient-years (PY). CS treatment continued for a mean (SD) of 1.196 (729.2) days; mean (SD) prescribed cumulative CS dose was 6983.3 mg (6519.9). The overall AE rate was 0.43 events/PY; the most frequent AEs were cataract and bone disease. For each 1000-mg increase in CS exposure, the hazard ratio (HR) increased by 3% (HR = 1.03; 95% CI: 1.02-1.05; P < 0.001). Additionally, statistically significant individual associations between increased CS exposure and AE risk were observed for bone related AEs (P < 0.001), cataract (P < 0.001), glaucoma (P = 0.005), pneumonia (P = 0.003), and diabetes mellitus (P < 0.001 in a subset of patients with no previous history of diabetes). Conclusion: CS exposure significantly increased risk for potentially serious AEs, emphasizing a need for new treatment options for GCA patients. (C) 2016 Elsevier Inc. All rights reserved.

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