Measurement properties of the minimal disease activity criteria for psoriatic arthritis

被引:15
|
作者
Coates, Laura C. [1 ]
Strand, Vibeke [2 ]
Wilson, Hilary [3 ]
Revicki, Dennis [4 ]
Stolshek, Brad [5 ]
Samad, Ahmed [6 ]
Chung, James B. [7 ]
Gladman, Dafna [8 ]
Mease, Philip J. [9 ,10 ]
机构
[1] Univ Oxford, Nuffield Dept Orthopaed Rheumatol & Musculoskelet, Oxford, England
[2] Stanford Univ, Immunol Rheumatol, Stanford, CA 94305 USA
[3] Boehringer Ingelheim GmbH & Co KG, Ridgefield, CT 06877 USA
[4] Evidera Inc, Bethesda, MD USA
[5] Amgen Inc, Thousand Oaks, CA USA
[6] Pharmaceut Prod Dev, San Diego, CA USA
[7] Amgen Inc, Thousand Oaks, CA USA
[8] Krembil Res Inst, Med Rheumatol, Toronto, ON, Canada
[9] Swedish Med Ctr, Sch Med, Seattle, WA USA
[10] Univ Washington, Seattle, WA 98195 USA
来源
RMD OPEN | 2019年 / 5卷 / 02期
关键词
INADEQUATE RESPONSE; CLINICAL-PRACTICE; OUTCOME MEASURE; ACTIVITY STATES; DOUBLE-BLIND; RECOMMENDATIONS; REMISSION; PLACEBO; EPIDEMIOLOGY; TOFACITINIB;
D O I
10.1136/rmdopen-2019-001002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective To comprehensively assess evidence on the measurement properties of the minimal disease activity (MDA) criteria, a composite measure of the state of disease activity in psoriatic arthritis (PsA). Methods A targeted literature review was conducted to identify studies that informed the validity and/or ability of the MDA to detect change among patients known to have experienced a change in clinical status. The search was conducted using MEDLINE and Embase databases (published as of October 2017). Pertinent articles provided by investigators and identified from select conference proceedings were also evaluated. Results A total of 20 publications met the inclusion criteria. The MDA criteria were consistently associated with other indicators of disease activity/severity. The ability of the MDA criteria to detect change was supported in randomised controlled trials (n=10), with a greater percentage of patients randomised to active treatments achieving MDA relative to patients in comparator arms. Long-term observational studies (n=2) provided additional support for the ability of the MDA to detect within-subject change in the real-world settings. Conclusion Evidence supports the MDA as a valid measure of disease activity in PsA that can detect between-group and within-subject change. The MDA is a comprehensive measure and clinically meaningful endpoint to assess the impact of interventions on PsA disease activity.
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页数:11
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