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Using a patient‐centered approach to benefit–harm assessment in treatment decision‐making: a case study in uveitis
Author(s) -
Yu Tsung,
Holbrook Janet T.,
Thorne Jennifer E.,
Puhan Milo A.
Publication year - 2016
Publication title -
pharmacoepidemiology and drug safety
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.023
H-Index - 96
eISSN - 1099-1557
pISSN - 1053-8569
DOI - 10.1002/pds.3959
Subject(s) - medicine , intensive care medicine , harm , medical prescription , clinical trial , quality of life (healthcare) , nursing , political science , law , pharmacology
Background Synthesizing evidence from comparative effectiveness trials can be difficult because multiple outcomes of different importance are to be considered. The goal of this study was to demonstrate an approach to conducting quantitative benefit–harm assessment that considers patient preferences. Methods We conducted a benefit–harm assessment using data from the Multicenter Uveitis Steroid Treatment Trial that compared corticosteroid implant versus systemic corticosteroids and immunosuppression in non‐infectious intermediate, posterior, and panuveitis. We focused on clinical outcomes considered important to patients, including visual acuity, development of cataracts/glaucoma, need for eye surgery, prescription‐requiring hypertension, hyperlipidemia, and infections. Patient preferences elicited in a recent survey were then incorporated into our assessment of the benefit–harm balance. Results Benefit–harm metrics were calculated for each time point that summarized the numbers of outcomes, caused or prevented by implant therapy versus systemic therapy if 1000 patients were treated. The benefit–harm metric was −129 (95% confidence interval: −242 to −14), −317 (−436 to −196), −390 (−514 to −264), and −526 (−687 to −368) at 6, 12, 18, and 24 months follow up, respectively, suggesting that systemic therapy may have a better benefit–harm balance. However, measures of quality of life for patients treated with implant therapy were found to be better than patients treated with systemic therapy over the same time period. Conclusions Results of benefit–harm assessment were different from the prospectively collected quality of life data during trial follow up. Future studies should explore the reasons for such discrepancies and the strength and weakness of each method to assess treatment benefits and harms. Copyright © 2016 John Wiley & Sons, Ltd.

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