Literature DB >> 24128775

Including health equity considerations in development of instruments for rheumatology research: an introduction to a novel OMERACT paradigm.

Jennifer O'Neill1, Tamara Rader, Francis Guillemin, Annelies Boonen, Robin Christensen, Anne Lyddiatt, Jordi Pardo Pardo, Vivian Welch, Jasvinder A Singh, Peter Tugwell.   

Abstract

The Outcome Measures in Rheumatology (OMERACT) Equity Special Interest Group (SIG) was established in 2008 to create a preliminary core set of outcome measures for clinical trials that can assess equity gaps in healthcare and the effectiveness of interventions to close or narrow gaps between advantaged and disadvantaged populations with musculoskeletal (MSK) conditions. At the OMERACT 11 meeting in 2012, the Equity SIG workshop focused on health assessment scales and their applicability for disadvantaged patients with MSK conditions. The intent was to determine whether the items and domains in 2 common questionnaires, the Health Assessment Questionnaire and the Medical Outcome Study Short Form-36 Survey, are appropriate for the activities and life experiences of certain disadvantaged populations, and whether completion of any of the scales would present a challenge to disadvantaged persons. To generate discussion, we considered the reading level of items in these questionnaires and whether they would be accessible to people with different levels of literacy. The group concluded that the choice of measurement instrument may contribute to "outcome measure-generated inequalities" because disadvantaged groups might have difficulty understanding some of the questions. The future work of the Equity SIG will explore the appropriateness of different measurement scales as they relate to inequities in arthritis as well as the risk of exacerbating disadvantages for patients with low literacy.

Entities:  

Keywords:  HEALTH EQUITY; MUSCULOSKELETAL CONDITIONS; RHEUMATOLOGY

Mesh:

Year:  2013        PMID: 24128775     DOI: 10.3899/jrheum.130812

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   4.666


  3 in total

1.  Health Equity Considerations for Developing and Reporting Patient-reported Outcomes in Clinical Trials: A Report from the OMERACT Equity Special Interest Group.

Authors:  Jennifer Petkovic; Jennifer L Barton; Caroline Flurey; Niti Goel; Christie M Bartels; Cheryl Barnabe; Maarten P T de Wit; Anne Lyddiatt; Diane Lacaille; Vivian Welch; Annelies Boonen; Beverley Shea; Robin Christensen; Lara J Maxwell; Willemina Campbell; Janet Jull; Karine Toupin-April; Jasvinder A Singh; Charles H Goldsmith; Antoine G Sreih; Christoph Pohl; Catherine Hofstetter; Dorcas E Beaton; Rachelle Buchbinder; Francis Guillemin; Peter S Tugwell
Journal:  J Rheumatol       Date:  2017-02-15       Impact factor: 4.666

2.  Poverty, Depression, or Lost in Translation? Ethnic and Language Variation in Patient-Reported Outcomes in Rheumatoid Arthritis.

Authors:  Patricia P Katz; Jennifer Barton; Laura Trupin; Gabriela Schmajuk; Jinoos Yazdany; Pedro J Ruiz; Edward Yelin
Journal:  Arthritis Care Res (Hoboken)       Date:  2016-05       Impact factor: 4.794

3.  Socioeconomic inequities in perceived health among patients with musculoskeletal disorders compared with other chronic disorders: results from a cross-sectional Dutch study.

Authors:  P Putrik; S Ramiro; A M Chorus; A P Keszei; A Boonen
Journal:  RMD Open       Date:  2015-05-21
  3 in total

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