Comparing the risk of developing uveitis in patients initiating anti-tumor necrosis factor therapy for ankylosing spondylitis: an analysis of a large US claims database

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TitreComparing the risk of developing uveitis in patients initiating anti-tumor necrosis factor therapy for ankylosing spondylitis: an analysis of a large US claims database
Type de publicationJournal Article
Year of Publication2014
AuteursWendling D, Joshi A, Reilly P, Jalundhwala YJ, Mittal M, Bao Y
JournalCURRENT MEDICAL RESEARCH AND OPINION
Volume30
Pagination2515-2521
Date PublishedDEC
Type of ArticleArticle
ISSN0300-7995
Mots-clésankylosing spondylitis, Anti tumor necrosis factor, Extra-articular manifestation, Retrospective study, Uveitis
Résumé

{Objective: To compare the risk of developing uveitis in patients initiating anti-tumor necrosis factor (anti-TNF) agents (adalimumab, etanercept, and infliximab) for ankylosing spondylitis (AS). Methods: Anti-TNF-naive patients with a diagnosis of AS and without a history of uveitis (N = 2115) who subsequently initiated anti-TNF therapy for AS were identified in a large claims database (2005 to 2011). A multivariate Cox proportional-hazards model was used to compare the risk of uveitis in patients who received etanercept or infliximab vs adalimumab. Results: The median number of days to the first occurrence of uveitis after initiation of anti-TNF was 191. Among the three anti-TNF groups, the median time to event of uveitis was longest in patients taking adalimumab (243 days), followed by etanercept (182 days) and infliximab (144 days). The incidence rate for uveitis over 1 year was lowest for patients who received adalimumab (2.4%

DOI10.1185/03007995.2014.969368