Canadian Rheumatology Association Recommendations for Pharmacological Management of Rheumatoid Arthritis with Traditional and Biologic Disease-modifying Antirheumatic Drugs

Рекомендации Канадской ревматологической ассоциации по фармакологическому лечению ревматоидного артрита с применением традиционных и биологических базисных противоревматических препаратов
Vivian P. Bykerk, Pooneh Akhavan, Glen Hazlewood, Orit Schieir, Anne Dooley, Boulos Haraoui, Majed Khraishi, Sharon LeClercq, Jean Légaré, DIANE P. MOSHER, James Pencharz, Janet Pope, John Thomson, Carter Thorne, Michel Zummer, Claire Bombardier
2011-09-15

Biologic DMARDsLatent tuberculosis screeningPerioperative careRheumatoid arthritisVaccination practices
OBJECTIVE: The Canadian Rheumatology Association (CRA) has developed recommendations for the pharmacological management of rheumatoid arthritis (RA) with traditional and biologic disease-modifying antirheumatic drugs (DMARD) in 2 parts. Part II, focusing on specific safety aspects of treatment with traditional and biologic DMARD in patients with RA, is reported here. METHODS: Key questions were identified a priori based on results of a national needs-assessment survey. A systematic review of all clinical practice guidelines and consensus statements regarding treatment with traditional and biologic DMARD in patients with RA published between January 2000 and June 2010 was performed in Medline, Embase, and CINAHL databases, and was supplemented with a "grey literature" search including relevant public health guidelines. Systematic reviews of postmarketing surveillance and RA registry studies were performed to update included guideline literature reviews as appropriate. Guideline quality was independently assessed by 2 reviewers. Guideline characteristics, recommendations, and supporting evidence from observational studies and randomized trials were synthesized into evidence tables. The working group voted on recommendations using a modified Delphi technique. RESULTS: Thirteen recommendations addressing perioperative care, screening for latent tuberculosis infection prior to the initiation of biologic DMARD, optimal vaccination practices, and treatment of RA patients with active or a history of malignancy were developed for rheumatologists, other primary prescribers of RA drug therapies, and RA patients. CONCLUSION: These recommendations were developed based on a synthesis of international RA and public health guidelines, supporting evidence, and expert consensus in the context of the Canadian health system. They are intended to help promote best practices and improve healthcare delivery for persons with RA.
1
A modified Delphi process was used to reach expert consensus, with guideline quality independently assessed by two reviewers.
2
Recommendations address perioperative care, latent tuberculosis screening before biologic DMARD initiation, vaccination practices, and treatment in patients with active or previous malignancy.
3
The Canadian Rheumatology Association developed 13 safety-focused recommendations for pharmacological rheumatoid arthritis management with traditional and biologic DMARDs.
4
The recommendations are intended to support rheumatologists, other prescribers, and patients in promoting best practices within the Canadian healthcare system.
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The recommendations were based on systematic reviews of international guidelines, public health guidance, postmarketing surveillance, registry studies, randomized trials, and observational evidence.

Patients with rheumatoid arthritis treated with traditional and biologic disease-modifying antirheumatic drugs

Safety aspects and best-practice management of treatment, including perioperative care, latent tuberculosis screening, vaccination, and management of malignancy

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2011-09-15
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Vivian P. Bykerk
Pooneh Akhavan
Glen Hazlewood
Orit Schieir
Anne Dooley
Boulos Haraoui
Majed Khraishi
Sharon LeClercq
Jean Légaré
DIANE P. MOSHER
James Pencharz
Janet Pope
John Thomson
Carter Thorne
Michel Zummer
Claire Bombardier
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