Literature DB >> 16265711

Progress since OMERACT 6 on including patient perspective in rheumatoid arthritis outcome assessment.

John R Kirwan1, Monica Ahlmén, Maarten de Wit, Turid Heiberg, Maggie Hehir, Sarah Hewlett, Patricia P Katz, Patricia Minnock, Enid M Quest, Pam Richards.   

Abstract

The first OMERACT Patient Perspective Workshop took place at OMERACT 6 in 2002. Through a series of meetings and discussion sessions a research agenda emerged and this report outlines progress made on this agenda. Work on identifying novel outcomes, instruments, and methods has shown similarities across European countries in the importance patients with rheumatoid arthritis (RA) attach to specific outcomes, in particular fatigue. Validation of an appropriate instrument to measure fatigue in patients with RA is currently being investigated. Frequent or repeated real-time assessment of symptoms such as pain and fatigue is becoming possible using electronic systems. An OMERACT Patient Panel has been established, and has produced a glossary for patients involved in supporting clinical research. In some centers, efforts are being made to provide Patient Research Partners with knowledge and skills that will enhance their contribution, and some of these approaches will be incorporated into OMERACT 7. The research agenda that was developed during the first Patient Perspective Workshop has stimulated new work in several areas. In addition, international attention has been drawn to the need to make sure that the patient's perspective is not lost among the technical expertise of rheumatology.

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Mesh:

Year:  2005        PMID: 16265711

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


  14 in total

1.  Managing Hip and Knee Osteoarthritis with Exercise: What is the Best Prescription?

Authors:  Maura Daly Iversen
Journal:  Ther Adv Musculoskelet Dis       Date:  2010-10       Impact factor: 5.346

Review 2.  Incorporating the patient's perspective in outcomes research.

Authors:  Betty Hsiao; Liana Fraenkel
Journal:  Curr Opin Rheumatol       Date:  2017-03       Impact factor: 5.006

Review 3.  Patients' and clinicians' research priorities.

Authors:  Ruth J Stewart; Jenny Caird; Kathryn Oliver; Sandy Oliver
Journal:  Health Expect       Date:  2010-12-22       Impact factor: 3.377

4.  Patient-reported outcome assessment in vasculitis may provide important data and a unique perspective.

Authors:  Karen Herlyn; Bernhard Hellmich; Philip Seo; Peter A Merkel
Journal:  Arthritis Care Res (Hoboken)       Date:  2010-06-15       Impact factor: 4.794

5.  Patient self-assessment of flare in rheumatoid arthritis: criterion and concurrent validity of the Flare instrument.

Authors:  Annette de Thurah; Thomas Maribo; Kristian Stengaard-Pedersen
Journal:  Clin Rheumatol       Date:  2014-12-18       Impact factor: 2.980

Review 6.  Patient-reported outcomes and adult patients' disease experience in the idiopathic inflammatory myopathies. report from the OMERACT 11 Myositis Special Interest Group.

Authors:  Helene Alexanderson; Maria Del Grande; Clifton O Bingham; Ana-Maria Orbai; Catherine Sarver; Katherine Clegg-Smith; Ingrid E Lundberg; Yeong Wook Song; Lisa Christopher-Stine
Journal:  J Rheumatol       Date:  2014-01-15       Impact factor: 4.666

7.  "If i wasn't this robust": patients' expectations and experiences at the Outcome Measures in Rheumatology Conference 2010.

Authors:  Maarten P T de Wit; Marije S Koelewijn-van Loon; Sarah Collins; Tineke A Abma; John Kirwan
Journal:  Patient       Date:  2013       Impact factor: 3.883

8.  Do not forget the professional--the value of the FIRST model for guiding the structural involvement of patients in rheumatology research.

Authors:  Maarten P T de Wit; Janneke E Elberse; Jacqueline E W Broerse; Tineke A Abma
Journal:  Health Expect       Date:  2013-01-31       Impact factor: 3.377

9.  Discriminant validity, responsiveness and reliability of the rheumatoid arthritis-specific Work Productivity Survey (WPS-RA).

Authors:  Jane T Osterhaus; Oana Purcaru; Lance Richard
Journal:  Arthritis Res Ther       Date:  2009-05-20       Impact factor: 5.156

10.  The development and initial validation of a questionnaire to measure help-seeking behaviour in patients with new onset rheumatoid arthritis.

Authors:  Rebecca J Stack; Christian D Mallen; Chris Deighton; Patrick Kiely; Karen L Shaw; Alison Booth; Kanta Kumar; Susan Thomas; Ian Rowan; Rob Horne; Peter Nightingale; Sandy Herron-Marx; Clare Jinks; Karim Raza
Journal:  Health Expect       Date:  2014-06-03       Impact factor: 3.377

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