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Recommendations on the Selection, Development, and Modification of Performance Outcome Assessments: A Good Practices Report of an ISPOR Task Force.
Edgar, Chris J; Bush, Elizabeth Nicki; Adams, Heather R; Ballinger, Rachel; Byrom, Bill; Campbell, Michelle; Eremenco, Sonya; McDougall, Fiona; Papadopoulos, Elektra; Slagle, Ashley F; Coons, Stephen Joel.
Afiliación
  • Edgar CJ; Cogstate Ltd, London, UK. Electronic address: cedgar@cogstate.com.
  • Bush EN; Endpoints and Measurement Strategy, The Janssen Pharmaceutical Companies of Johnson & Johnson, Raritan, NJ, USA.
  • Adams HR; University of Rochester, Rochester, NY, USA.
  • Ballinger R; Patient Centered Outcomes, ICON, St Albans, UK.
  • Byrom B; Signant Health, Sandwich, UK.
  • Campbell M; Office of Neuroscience, Food and Drug Administration, Silver Spring, MD, USA.
  • Eremenco S; PRO Consortium, Critical Path Institute, Tucson, AZ, USA.
  • McDougall F; Genentech, South San Francisco, CA, USA.
  • Papadopoulos E; Patient Experience Data & Strategy in Immunology and Oncology, AbbVie, North Chicago, IL, USA.
  • Slagle AF; Scientific and Regulatory Consulting, Aspen Consulting, LLC, Steamboat Springs, CO, USA.
  • Coons SJ; Critical Path Institute, Tucson, AZ, USA.
Value Health ; 26(7): 959-967, 2023 07.
Article en En | MEDLINE | ID: mdl-37385712
ABSTRACT
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 development 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 structured 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.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Comités Consultivos / Documentación Tipo de estudio: Guideline / Prognostic_studies / Qualitative_research Límite: Child / Humans Idioma: En Revista: Value Health Asunto de la revista: FARMACOLOGIA Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Comités Consultivos / Documentación Tipo de estudio: Guideline / Prognostic_studies / Qualitative_research Límite: Child / Humans Idioma: En Revista: Value Health Asunto de la revista: FARMACOLOGIA Año: 2023 Tipo del documento: Article