Literature DB >> 25877496

Recommendations for the Involvement of Patient Research Partners (PRP) in OMERACT Working Groups. A Report from the OMERACT 2014 Working Group on PRP.

Peter P Cheung1, Maarten de Wit2, Clifton O Bingham2, John R Kirwan2, Amye Leong2, Lyn M March2, Pam Montie2, Marieke Scholte-Voshaar2, Laure Gossec2.   

Abstract

OBJECTIVE: Patient participation in research is increasing; however, practical guidelines to enhance this participation are lacking. Specifically within the Outcome Measures in Rheumatology (OMERACT) organization, although patients have participated in OMERACT meetings since 2002, consensus about the procedures for involving patients in working groups has not been formalized. The objective is to develop a set of recommendations regarding patient research partner (PRP) involvement in research working groups.
METHODS: We conducted a systematic literature review on recommendations/guidelines of PRP involvement in research; elaborated a structured consensus process involving multiple participants to develop a set of recommendations; and sought endorsement of recommendations by OMERACT.
RESULTS: In the 18 articles included in the literature review, there was general agreement on the broad concepts for recommendations covering PRP involvement in research although they were heterogeneous in detail. Most considered PRP involvement in all phases of research with early engagement, training, and support important, but details on the content were scarce. This review informed a larger consensus-building process regarding PRP inclusion in OMERACT research. Three overarching principles and 8 recommendations were developed, discussed, and refined at OMERACT 2014. The guiding principles were endorsed during the OMERACT plenary session.
CONCLUSION: These recommendations for PRP involvement in OMERACT research reinforce the importance of patient participation throughout the research process as integral members. Although the applicability of the recommendations in other research contexts should be assessed, the generalizability is expected to be high. Future research should evaluate their implementation and their effect on outcome development.

Entities:  

Keywords:  OMERACT; PATIENT INVOLVEMENT; PATIENT RESEARCH PARTNERS; RECOMMENDATIONS; RHEUMATOLOGY RESEARCH

Mesh:

Year:  2015        PMID: 25877496     DOI: 10.3899/jrheum.141011

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


  18 in total

Review 1.  Framework for Advancing the Reporting of Patient Engagement in Rheumatology Research Projects.

Authors:  Clayon B Hamilton; Jenny C Leese; Alison M Hoens; Linda C Li
Journal:  Curr Rheumatol Rep       Date:  2017-07       Impact factor: 4.592

2.  Using PROMs in Healthcare: Who Should Be in the Driving Seat-Policy Makers, Health Professionals, Methodologists or Patients?

Authors:  Kirstie L Haywood; Roger Wilson; Sophie Staniszewska; Sam Salek
Journal:  Patient       Date:  2016-12       Impact factor: 3.883

3.  OMERACT Endorsement of Patient-reported Outcome Instruments in Antineutrophil Cytoplasmic Antibody-associated Vasculitis.

Authors:  Joanna C Robson; Gunnar Tomasson; Nataliya Milman; Sue Ashdown; Annelies Boonen; George C Casey; Peter F Cronholm; David Cuthbertson; Jill Dawson; Haner Direskeneli; Ebony Easley; Tanaz A Kermani; John T Farrar; Don Gebhart; Georgia Lanier; Raashid A Luqmani; Alfred Mahr; Carol A McAlear; Jacqueline Peck; Beverley Shea; Judy A Shea; Antoine G Sreih; Peter S Tugwell; Peter A Merkel
Journal:  J Rheumatol       Date:  2017-09-01       Impact factor: 4.666

Review 4.  Management of psoriatic arthritis in 2016: a comparison of EULAR and GRAPPA recommendations.

Authors:  Laure Gossec; Laura C Coates; Maarten de Wit; Arthur Kavanaugh; Sofia Ramiro; Philip J Mease; Christopher T Ritchlin; Désirée van der Heijde; Josef S Smolen
Journal:  Nat Rev Rheumatol       Date:  2016-11-10       Impact factor: 20.543

5.  Development of the patient-oriented research curriculum in child health (PORCCH).

Authors:  Colin Macarthur; Catharine M Walsh; Francine Buchanan; Aliza Karoly; Linda Pires; Graham McCreath; Nicola L Jones
Journal:  Res Involv Engagem       Date:  2021-05-10

6.  Impact of red and processed meat and fibre intake on treatment outcomes among patients with chronic inflammatory diseases: protocol for a prospective cohort study of prognostic factors and personalised medicine.

Authors:  Robin Christensen; Berit L Heitmann; Karina Winther Andersen; Ole Haagen Nielsen; Signe Bek Sørensen; Mohamad Jawhara; Anette Bygum; Lone Hvid; Jakob Grauslund; Jimmi Wied; Henning Glerup; Ulrich Fredberg; Jan Alexander Villadsen; Søren Geill Kjær; Jan Fallingborg; Seyed A G R Moghadd; Torben Knudsen; Jacob Brodersen; Jesper Frøjk; Jens Frederik Dahlerup; Anders Bo Bojesen; Grith Lykke Sorensen; Steffen Thiel; Nils J Færgeman; Ivan Brandslund; Tue Bjerg Bennike; Allan Stensballe; Erik Berg Schmidt; Andre Franke; David Ellinghaus; Philip Rosenstiel; Jeroen Raes; Mette Boye; Lars Werner; Charlotte Lindgaard Nielsen; Heidi Lausten Munk; Anders Bathum Nexøe; Torkell Ellingsen; Uffe Holmskov; Jens Kjeldsen; Vibeke Andersen
Journal:  BMJ Open       Date:  2018-02-08       Impact factor: 2.692

7.  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

8.  A Proposal for a Study on Treatment Selection and Lifestyle Recommendations in Chronic Inflammatory Diseases: A Danish Multidisciplinary Collaboration on Prognostic Factors and Personalised Medicine.

Authors:  Vibeke Andersen; Uffe Holmskov; Signe Bek Sørensen; Mohamad Jawhara; Karina W Andersen; Anette Bygum; Lone Hvid; Jakob Grauslund; Jimmi Wied; Henning Glerup; Ulrich Fredberg; Jan Alexander Villadsen; Søren Geill Kjær; Jan Fallingborg; Seyed A G R Moghadd; Torben Knudsen; Jacob Brodersen; Jesper Frøjk; Jens F Dahlerup; Ole Haagen Nielsen; Robin Christensen; Anders Bo Bojesen; Grith Lykke Sorensen; Steffen Thiel; Nils J Færgeman; Ivan Brandslund; Allan Stensballe; Erik Berg Schmidt; Andre Franke; David Ellinghaus; Philip Rosenstiel; Jeroen Raes; Berit Heitmann; Mette Boye; Charlotte Lindgaard Nielsen; Lars Werner; Jens Kjeldsen; Torkell Ellingsen
Journal:  Nutrients       Date:  2017-05-15       Impact factor: 5.717

9.  Patient participation as an integral part of patient-reported outcomes development ensures the representation of the patient voice: a case study from the field of rheumatology.

Authors:  M P T de Wit; T K Kvien; L Gossec
Journal:  RMD Open       Date:  2015-08-05

10.  An empirically based conceptual framework for fostering meaningful patient engagement in research.

Authors:  Clayon B Hamilton; Alison M Hoens; Catherine L Backman; Annette M McKinnon; Shanon McQuitty; Kelly English; Linda C Li
Journal:  Health Expect       Date:  2017-10-06       Impact factor: 3.377

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