Literature DB >> 21807790

Patient perspective workshop: moving towards OMERACT guidelines for choosing or developing instruments to measure patient-reported outcomes.

John R Kirwan1, James F Fries, Sarah E Hewlett, Richard H Osborne, Stanton Newman, Sabina Ciciriello, Mart A van de Laar, Emma Dures, Patricia Minnock, Turid Heiberg, Tessa C Sanderson, Caroline A Flurey, Amy L Leong, Pamela Montie, Pam Richards.   

Abstract

The workshop Choosing or Developing Instruments held at the Outcome Measures in Rheumatology (OMERACT) 10 meeting was designed to help participants think about the underlying methods of instrument development. Conference pre-reading material and 3 brief introductory presentations elaborated the issues, and participants broke into discussion groups before reconvening to share insights, engage in a more general discussion of the issues, and vote on recommendations. Tradeoffs between using current imperfect measures and the long and complex process of developing new instruments were considered, together with the need for rigor in patient-reported outcome (PRO) instrument development. The main considerations for PRO instrument development were listed and a research agenda for action produced. As part of the agenda for action, it is recommended that researchers and patient partners work together to tackle these issues, and that OMERACT bring forward proposals for acceptable instrument development protocols that would meet an enhanced "Truth" statement in the OMERACT Filter.

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Year:  2011        PMID: 21807790     DOI: 10.3899/jrheum.110391

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


  9 in total

1.  Responsiveness and Minimally Important Differences for 4 Patient-Reported Outcomes Measurement Information System Short Forms: Physical Function, Pain Interference, Depression, and Anxiety in Knee Osteoarthritis.

Authors:  Augustine C Lee; Jeffrey B Driban; Lori Lyn Price; William F Harvey; Angie Mae Rodday; Chenchen Wang
Journal:  J Pain       Date:  2017-05-10       Impact factor: 5.820

2.  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

3.  Advancing the Development of Patient-reported Outcomes for Adult Myositis at OMERACT 2016: An International Delphi Study.

Authors:  Jin Kyun Park; Christopher A Mecoli; Helene Alexanderson; Malin Regardt; Lisa Christopher-Stine; María Casal-Domínguez; Ingrid de Groot; Catherine Sarver; Ingrid E Lundberg; Clifton O Bingham; Yeong Wook Song
Journal:  J Rheumatol       Date:  2017-08-01       Impact factor: 4.666

4.  "An impediment to living life": why and how should we measure stiffness in polymyalgia rheumatica?

Authors:  Sarah Louise Mackie; Rodney Hughes; Margaret Walsh; John Day; Marion Newton; Colin Pease; John Kirwan; Marianne Morris
Journal:  PLoS One       Date:  2015-05-08       Impact factor: 3.240

5.  A brief patient-reported outcome instrument for primary care: German translation and validation of the Measure Yourself Medical Outcome Profile (MYMOP).

Authors:  Katja Hermann; Katharina Kraus; Kathrin Herrmann; Stefanie Joos
Journal:  Health Qual Life Outcomes       Date:  2014-07-19       Impact factor: 3.186

6.  Successful Stepwise Development of Patient Research Partnership: 14 Years' Experience of Actions and Consequences in Outcome Measures in Rheumatology (OMERACT).

Authors:  Maarten de Wit; John R Kirwan; Peter Tugwell; Dorcas Beaton; Maarten Boers; Peter Brooks; Sarah Collins; Philip G Conaghan; Maria-Antonietta D'Agostino; Cathie Hofstetter; Rod Hughes; Amye Leong; Ann Lyddiatt; Lyn March; James May; Pamela Montie; Pamela Richards; Lee S Simon; Jasvinder A Singh; Vibeke Strand; Marieke Voshaar; Clifton O Bingham; Laure Gossec
Journal:  Patient       Date:  2017-04       Impact factor: 3.883

Review 7.  Patient involvement in outcome measures for psoriatic arthritis.

Authors:  William Tillett; Ade Adebajo; Mel Brooke; Willemina Campbell; Laura C Coates; Oliver FitzGerald; Laure Gossec; Philip Helliwell; Sarah Hewlett; Jana James; Patricia Minnock; Aisling Reast; Dennis O'Sullivan; Maarten de Wit; Neil McHugh
Journal:  Curr Rheumatol Rep       Date:  2014-05       Impact factor: 4.592

8.  Development of a new occupational balance-questionnaire: incorporating the perspectives of patients and healthy people in the design of a self-reported occupational balance outcome instrument.

Authors:  Mona Dür; Günter Steiner; Veronika Fialka-Moser; Alexandra Kautzky-Willer; Clemens Dejaco; Birgit Prodinger; Michaela Alexandra Stoffer; Alexa Binder; Josef Smolen; Tanja Alexandra Stamm
Journal:  Health Qual Life Outcomes       Date:  2014-04-05       Impact factor: 3.186

9.  Linking the effect of psoriatic arthritis-related foot involvement to the Leeds Foot Impact Scale using the International Classification for Functioning, Disability and Health: a study to assess content validity.

Authors:  Kate Carter; Caterina Tannous; Steven Walmsley; Keith Rome; Deborah E Turner
Journal:  J Foot Ankle Res       Date:  2020-08-24       Impact factor: 2.303

  9 in total

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