Recommendations on the Selection, Development, and Modification of Performance Outcome Assessments: A Good Practices Report of an ISPOR Task Force

被引:7
|
作者
Edgar, Chris J. [1 ]
Bush, Elizabeth [2 ]
Adams, Heather R. [3 ]
Ballinger, Rachel [4 ]
Byrom, Bill [5 ]
Campbell, Michelle [6 ]
Eremenco, Sonya [7 ]
McDougall, Fiona [8 ]
Papadopoulos, Elektra [9 ]
Slagle, Ashley F. [10 ]
Coons, Stephen Joel [11 ]
机构
[1] Cogstate Ltd, London, England
[2] Janssen Pharmaceut Co Johnson & Johnson, Endpoints & Measurement Strategy, Raritan, NJ USA
[3] Univ Rochester, Rochester, NY USA
[4] ICON, Patient Ctr Outcomes, St Albans, England
[5] Signant Hlth, Sandwich, England
[6] FDA, Off Neurosci, Silver Spring, MD USA
[7] Crit Path Inst, PRO Consortium, Tucson, AZ USA
[8] Genentech Inc, South San Francisco, CA USA
[9] AbbVie, Patient Experience Data & Strategy Immunol & Onco, N Chicago, IL USA
[10] Aspen Consulting LLC, Sci & Regulatory Consulting, Steamboat Springs, CO USA
[11] Crit Path Inst, Tucson, AZ USA
关键词
patient focused drug development; PerfO assessment; performance outcome assessment; task performance; CONTENT VALIDITY;
D O I
10.1016/j.jval.2023.05.003
中图分类号
F [经济];
学科分类号
02 ;
摘要
In evaluating the clinical benefit of new therapeutic interventions, it is critical that the treatment outcomes assessed reflect aspects of health that are clinically important and meaningful to patients. Performance outcome (PerfO) assessments are measurements based on standardized tasks actively undertaken by a patient that reflect physical, cognitive, sensory, and other functional skills that bring meaning to people's lives. PerfO assessments can have substantial value as drug develop-ment tools when the concepts of interest being measured best suit task performance and in cases where patients may be limited in their capacity for self-report. In their development, selection, and modification, including the evaluation and documentation of validity, reliability, usability, and interpretability, the good practice recommendations established for other clinical outcome assessment types should continue to be followed, with concept elicitation as a critical foundation. In addition, the importance of standardization, and the need to ensure feasibility and safety, as well as their utility in patient groups, such as pediatric populations, or those with cognitive and psychiatric challenges, may enhance the need for struc-tured pilot evaluations, additional cognitive interviewing, and evaluation of quantitative data, such as that which would support concept confirmation or provide ecological evidence and other forms of construct evidence within a unitary approach to validity. The opportunity for PerfO assessments to inform key areas of clinical benefit is substantial and establishing good practices in their selection or development, validation, and implementation, as well as how they reflect meaningful aspects of health is critical to ensuring high standards and in furthering patient-focused drug development.
引用
收藏
页码:959 / 967
页数:9
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