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Abstract Number: 1862

The 2012 Canadian Fibromyalgia Guidelines: Clinically Applicable Recommendations for the Management of Fibromyalgia

Mary-Ann Fitzcharles1, Peter A. Ste-Marie2, Don L. Goldenberg3, John X. Pereira4, Susan Abbey5, Manon Choinière2, Gordon Ko5, Dwight Moulin6, Pantelis Panopalis7, Johanne Proulx8 and Yoram Shir9, 1Rheumatology and Pain Management Unit, McGill University Health Centre, Montreal, QC, Canada, 2University of Montreal, Montreal, QC, Canada, 3Rheumatology, Newton-Wellesley Hosp, Newton, MA, 4University of Calgary, Calgary, AB, Canada, 5University of Toronto, Toronto, ON, Canada, 6University of Western Ontario, London, ON, Canada, 7Rheumatology, McGill University Health Centre, Montreal, QC, Canada, 8Patient Representative, Montreal, QC, Canada, 9Alan Edwards Pain Management Unit, McGill University Health Centre, Montreal, QC, Canada

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: Fibromyalgia and practice guidelines

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Session Information

Title: Fibromyalgia and Soft Tissue Disorders

Session Type: Abstract Submissions (ACR)

Background/Purpose: The healthcare community remains challenged regarding the care of fibromyalgia (FM) patients. Previous guidelines have mostly addressed treatment options rather than provide an overall approach to FM care. With new evidence concerning pathogenesis and more diverse treatment strategies, updated direction for global care in FM is needed. These evidence-based guidelines for the diagnosis, management, and patient trajectory of persons with FM were developed taking into account these new advances and new ACR 2010 diagnostic criteria.

Methods: A needs assessment by structured consultation with 139 healthcare professionals from relevant disciplines across Canada generated 18 key questions. Questions drove a literature search to identify evidence, which was graded according to the classification system of the Oxford Centre for Evidence Based Medicine, and supporting recommendations were drafted. Recommendations were edited and appraised by an advisory panel to reflect meaningful clinical practice. The whole document was reviewed by an international expert.

Results:

Sixty recommendations pertaining to the identification, evaluation, and management of persons with FM, incorporating new clinical concepts were drafted. The essence of the recommendations is as follows: FM represents a composite of symptoms, with body pain present as the pivotal symptom. There is a spectrum of severity which associates with functional outcome, with fluctuating symptoms over time. The diagnosis of FM is clinical, not one of exclusion, not needing specialist confirmation, and requires only limited laboratory testing. A physical examination is required to exclude other conditions presenting with body pain, but tender point examination is not required to confirm the diagnosis. There is no confirmatory laboratory test and excessive testing is strongly discouraged. Ideal care for most patients is in the primary care setting. Treatments should be multimodal, incorporating non-pharmacologic and pharmacologic strategies, with focus towards reduction of symptoms and improvement of function. Patients must be active participants in their healthcare and non-pharmacologic strategies are imperative. Patient-tailored management that is symptom-based is recommended.  In the absence of an ideal pharmacologic treatment, an agent impacting multiple symptoms is desirable. Doses of medications lower than those used in clinical trials and combination of medications may facilitate adherence. Emphasis on proper lifestyle practices, periodic assessment of the need for continued medication, and evaluation of efficacy/side effects of ongoing treatments is recommended. New symptoms should be evaluated according to good clinical practice to exclude another illness without summarily attributing symptoms to FM.

Conclusion: These new Canadian guidelines for the care of patients with FM should provide the health community with more confidence in the global care of these patients and thereby improve patient outcome.


Disclosure:

M. A. Fitzcharles,

Pfizer Inc, Lilly, Purdue, Valeant,

5;

P. A. Ste-Marie,
None;

D. L. Goldenberg,

Forest , Lilly, Pfizer Inc,

5,

Pfizer Inc,

2;

J. X. Pereira,

Pfizer Inc,

2;

S. Abbey,

Lilly, Lundbeck, Pfizer Inc,

5;

M. Choinière,

Pfizer Inc, Astra-Zeneca,

2,

Pfizer Inc,

5;

G. Ko,

Allergan, Mayer, Boehringer-Ingelheim, genzyme, Janssen, Lilly, Merck, Pfizer Inc, Purdue, Shire, Valeant,

5;

D. Moulin,

Janssen, Lilly, Paladin, Pfizer Inc, Valeant,

5,

Pfizer Inc,

2;

P. Panopalis,

Abbott, Bristol-Myers Squibb, Pfizer Inc,

5;

J. Proulx,
None;

Y. Shir,

Astra-Zeneca, Janssen, Paladin, Pfize Inc, Purdue,

5.

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