2011
DOI: 10.3899/jrheum.110207
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Canadian Rheumatology Association Recommendations for Pharmacological Management of Rheumatoid Arthritis with Traditional and Biologic Disease-modifying Antirheumatic Drugs

Abstract: These recommendations were developed based on a synthesis of international guidelines, supporting evidence, and expert consensus considering the Canadian healthcare context with the intention of promoting best practices and improving healthcare delivery for persons with RA.

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Cited by 262 publications
(291 citation statements)
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References 75 publications
(214 reference statements)
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“…Guidelines, quality standards, and quality indicators recommend that RA patients be seen at least yearly in followup to evaluate their disease status, screen for comorbidities, and review medications 5, 7, 28, 29. There has unfortunately been little published evaluation on RA patients who may have gaps in care or get lost to followup and on the consequences of lack of rheumatologist care.…”
Section: Discussionmentioning
confidence: 99%
“…Guidelines, quality standards, and quality indicators recommend that RA patients be seen at least yearly in followup to evaluate their disease status, screen for comorbidities, and review medications 5, 7, 28, 29. There has unfortunately been little published evaluation on RA patients who may have gaps in care or get lost to followup and on the consequences of lack of rheumatologist care.…”
Section: Discussionmentioning
confidence: 99%
“…Evidence reports for each of the 5 candidate items were conducted and reviewed by the CRA Choosing Wisely Methodology subcommittee, key opinion leaders, CRA Board of Directors, and 3 patient members of the Canadian Arthritis Patient Alliance. We used a modified system developed by the Scottish Intercollegiate Guideline Network to grade evidence 9 . A Supplementary Table (Online Supplementary Data 1, available online at jrheum.org) shows the custom system for assigning levels of evidence and strength of recommendations.…”
Section: Methodsmentioning
confidence: 99%
“…Develop trial designs that better reflect the patients who will receive the products (reflected in current guidelines 5,6 ), and good clinical practice (GCP). Regulators play a significant role in shaping industry drug development programs; they must consider and encourage alternative study designs, outcomes, and endpoints through education from regional experts.…”
Section: Rheumatologymentioning
confidence: 99%