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Fibromyalgia syndrome
The fibromyalgia syndrome (FM) workshop at OMERACT 8 continued the work initiated in the first FM workshop at OMERACT 7 in 2004. The principal objectives were to work toward consensus on core domains for assessment in FM studies, evaluate the performance quality of outcome measures used in a review...
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Published in: | Journal of rheumatology 2007-06, Vol.34 (6), p.1415-1425 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | The fibromyalgia syndrome (FM) workshop at OMERACT 8 continued the work initiated in the first FM workshop at OMERACT 7 in
2004. The principal objectives were to work toward consensus on core domains for assessment in FM studies, evaluate the performance
quality of outcome measures used in a review of recent trials in FM, and discuss the research agenda of the FM working group.
An initiative to include the patient perspective on identification and prioritization of domains, consisting of focus groups
and a patient Delphi exercise, was completed prior to OMERACT 8. Patient-identified domains were, for the most part, similar
to those identified by clinician-investigators in terms of symptoms and relative importance. However, patients identified
certain domains, such as stiffness, that were not included by physicians, and emphasized the importance of domains such as
dyscognition and impaired motivation. Many of the principal domains agreed upon by the clinician-investigators, patients,
and OMERACT participants, including pain, fatigue, sleep, mood, and global measures, have been used in clinical trials and
performed well when viewed through the OMERACT filter. The research agenda items reviewed and approved for continued study
included development of objective "biomarkers" in FM, development of a responder index for FM, and coordination with the WHO's
International Classification of Functioning Disability and Health (ICF) Research Branch and the US National Institutes of
Health's Patient Reported Outcome Measures Information System network (PROMIS) to develop improved measures of function, quality
of life, and participation. The OMERACT process has provided a framework for identification of key domains to be assessed
and a path toward validation and standardization of outcome measures for clinical trials in FM. |
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ISSN: | 0315-162X 1499-2752 |