Development and validation of the crohn’s disease patient-reported outcomes signs and symptoms (CD-PRO/SS) diary

被引:35
|
作者
Higgins P.D.R. [1 ,6 ]
Harding G. [2 ]
Leidy N.K. [2 ]
Debusk K. [3 ]
Patrick D.L. [4 ]
Viswanathan H.N. [5 ,7 ]
Fitzgerald K. [3 ]
Donelson S.M. [3 ]
Cyrille M. [5 ]
Ortmeier B.G. [5 ]
Wilson H. [2 ]
Revicki D.A. [2 ]
Globe G. [5 ]
机构
[1] University of Michigan, Ann Arbor, MI
[2] Evidera, Bethesda, MD
[3] Genentech Inc, South San Francisco, CA
[4] University of Washington, Seattle, WA
[5] Amgen Inc, Thousand Oaks, CA
[6] University of Michigan, SPC 5682, 1650 West Medical Center Drive, Ann Arbor, 48109, MI
[7] Allergan Inc, Irvine, CA
关键词
Clinical trial endpoints; Crohn’s disease; Patient-reported outcome; Reliability; Signs and symptoms; Validity;
D O I
10.1186/s41687-018-0044-7
中图分类号
学科分类号
摘要
Background: The clinical course of Crohn’s disease (CD) and the effect of its treatment are monitored through patient-reported signs and symptoms (S&S), and endoscopic evidence of inflammation. The Crohn’s Disease Patient-reported Outcomes Signs and Symptoms (CD-PRO/SS) measure was developed to standardize the quantification of gastrointestinal S&S of CD through direct report from patient ratings. Methods: The CD-PRO/SS was developed based on data from concept elicitation (focus groups, interviews; n = 29), then refined through cognitive interviews of CD patients (n = 20). Measurement properties, including item-level statistics, scaling structure, reliability, and validity, were examined using secondary analyses of baseline and two-week clinical trial data of adults with moderate-to-severe CD (n = 238). Results: Findings from qualitative interviews identified nine S&S items covering bowel and abdominal symptoms. The final CD-PRO/SS daily diary includes two scales: Bowel S&S (three items) and Abdominal Symptoms (three items), each scored separately. Each scale showed evidence of adequate reliability (α = 0.74 and 0.67, respectively); reproducibility (intraclass correlation coefficient > 0.80), and validity, with the last including moderate correlations with the Inflammatory Bowel Disease Questionnaire bowel symptom score and select items (ranging from r = 0.43– 0.54). Scores distinguished patients categorized by patient global ratings of disease severity (p < 0.0001). Conclusions: Results suggest the CD-PRO/SS is a reliable and valid measure of gastrointestinal symptom severity in CD patients. Additional longitudinal data are needed to evaluate the ability of the CD-PRO/SS scores to detect responsiveness and inform the selection of responder definitions. © The Author(s). 2018 Open Access.
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