Literature DB >> 17552068

Fibromyalgia syndrome.

Philip Mease1, Lesley M Arnold, Robert Bennett, Annelies Boonen, Dan Buskila, Serena Carville, Amy Chappell, Ernest Choy, Daniel Clauw, Dina Dadabhoy, Michael Gendreau, Don Goldenberg, Geoffrey Littlejohn, Susan Martin, Philip Perera, I Jon Russell, Lee Simon, Michael Spaeth, David Williams, Leslie Crofford.   

Abstract

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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Mesh:

Year:  2007        PMID: 17552068

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


  61 in total

1.  Development of responder definitions for fibromyalgia clinical trials.

Authors:  Lesley M Arnold; David A Williams; James I Hudson; Susan A Martin; Daniel J Clauw; Leslie J Crofford; Fujun Wang; Birol Emir; Chinglin Lai; Rong Zablocki; Philip J Mease
Journal:  Arthritis Rheum       Date:  2012-03

Review 2.  Fibromyalgia: mechanisms and potential impact of the ACR 2010 classification criteria.

Authors:  John McBeth; Matthew R Mulvey
Journal:  Nat Rev Rheumatol       Date:  2012-01-24       Impact factor: 20.543

3.  Impact of invalidation and trust in physicians on health outcomes in fibromyalgia patients.

Authors:  Carroline P Lobo; Andrea R Pfalzgraf; Vincent Giannetti; Gibbs Kanyongo
Journal:  Prim Care Companion CNS Disord       Date:  2014-10-09

Review 4.  Fibromyalgia: should the treatment paradigm be monotherapy or combination pharmacotherapy?

Authors:  Philip J Mease; Kristin Seymour
Journal:  Curr Pain Headache Rep       Date:  2008-12

Review 5.  Understanding fibromyalgia: lessons from the broader pain research community.

Authors:  David A Williams; Daniel J Clauw
Journal:  J Pain       Date:  2009-08       Impact factor: 5.820

Review 6.  Chiropractic treatment for fibromyalgia: a systematic review.

Authors:  Edzard Ernst
Journal:  Clin Rheumatol       Date:  2009-06-21       Impact factor: 2.980

7.  The relevance of depressive symptoms and social support to disability in women with multiple sclerosis or fibromyalgia.

Authors:  Lorraine J Phillips; Alexa K Stuifbergen
Journal:  Int J Rehabil Res       Date:  2010-06       Impact factor: 1.479

8.  The Revised Fibromyalgia Impact Questionnaire (FIQR): validation and psychometric properties.

Authors:  Robert M Bennett; Ronald Friend; Kim D Jones; Rachel Ward; Bobby K Han; Rebecca L Ross
Journal:  Arthritis Res Ther       Date:  2009-08-10       Impact factor: 5.156

9.  Validation of the International Classification of Functioning, Disability and Health Core Set for chronic widespread pain from the perspective of fibromyalgia patients.

Authors:  Robin Hieblinger; Michaela Coenen; Gerold Stucki; Andreas Winkelmann; Alarcos Cieza
Journal:  Arthritis Res Ther       Date:  2009-05-14       Impact factor: 5.156

10.  Development and validation of the self-administered Fibromyalgia Assessment Status: a disease-specific composite measure for evaluating treatment effect.

Authors:  Fausto Salaffi; Piercarlo Sarzi-Puttini; Rita Girolimetti; Stefania Gasparini; Fabiola Atzeni; Walter Grassi
Journal:  Arthritis Res Ther       Date:  2009-08-18       Impact factor: 5.156

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