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dc.contributor.authorZochling J.en
dc.contributor.authorScott J.en
dc.contributor.authorBird P.en
dc.contributor.authorBurnet S.en
dc.contributor.authorDe Jager J.en
dc.contributor.authorGriffiths H.en
dc.contributor.authorTymms K.en
dc.contributor.authorNicholls D.en
dc.contributor.authorRoberts L.en
dc.contributor.authorArnold M.en
dc.contributor.authorLittlejohn G.en
dc.date.accessioned2021-05-14T14:24:36Zen
dc.date.available2021-05-14T14:24:36Zen
dc.date.copyright2014en
dc.date.created20140212en
dc.date.issued2014-02-12en
dc.identifier.citationArthritis Care and Research. 66 (2) (pp 190-196), 2014. Date of Publication: February 2014.en
dc.identifier.issn2151-464Xen
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/42004en
dc.description.abstractObjective To evaluate barriers that prevent rheumatoid arthritis (RA) patients from achieving Disease Activity Score in 28 joints using the erythrocyte sedimentation rate (DAS28-ESR) scores within the current recommended levels for low disease activity (LDA) or clinical remission (DAS28-ESR score <3.2). Methods Using an electronic medical record program, clinical data for RA patients treated in Optimising Patient Outcomes in Australian Rheumatology clinics, with a recorded DAS28-ESR score, were collected at one point in time. The data included demographics, medications, disease measures, and the rheumatologist's opinion of the main barriers preventing improvement to the recommended DAS28 score. Results Of the 4,037 patients with a recorded DAS28-ESR score, 304 patients (7.5%) had high disease activity (HDA) and 1,211 patients (30%) had moderate disease activity (MDA). For 584 HDA or MDA patients, the barriers to disease control (BTCs) were recorded by the rheumatologist when there was no adjustment to disease-modifying antirheumatic drug (DMARD) therapy. The recorded BTCs were irreversible joint damage (19.7%), patient-driven preference (14.7%), noninflammatory musculoskeletal pain (9.2%), insufficient time to assess the effect of recently initiated DMARDs (9.2%), safety concerns (7.5%), comorbidities (6.5%), resistant disease (6.3%), and other less common reasons. These patients received DMARDs (97.4%), including biologic agents (34.1%), methotrexate (74.8%), and oral corticosteroids (41.8%). Conclusion This study identified clinical situations in which rheumatologists elected to continue RA patients with MDA or HDA on DMARD therapy without adjustment to achieve clinical remission or an LDA target of a DAS28-ESR score <3.2. Copyright © 2014 by the American College of Rheumatology.en
dc.languageEnglishen
dc.languageenen
dc.publisherJohn Wiley and Sons Inc. (P.O.Box 18667, Newark NJ 07191-8667, United States)en
dc.titleBarriers to optimal disease control for rheumatoid arthritis patients with moderate and high disease activity.en
dc.typeArticleen
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1002/acr.22108en
dc.publisher.placeUnited Statesen
dc.identifier.pubmedid23983001 [http://www.ncbi.nlm.nih.gov/pubmed/?term=23983001]en
dc.identifier.source372243913en
dc.identifier.institution(Tymms) Canberra Rheumatology, 9/40 Marcus Clarke Street, Canberra City, ACT 2601, Australia (Zochling) Menzies Research Institute Tasmania, Hobart, TAS, Australia (Scott) Roche Products, Dee Why, NSW, Australia (Bird) Combined Rheumatology Practice, Sydney, NSW, Australia (Burnet) Queen Elizabeth Hospital, Adelaide, SA, Australia (De Jager) Olser House, Southport, QLD, Australia (Griffiths) Barwon Rheumatology Service, Geelong, VIC, Australia (Nicholls) Coast Joint Care, Maroochydore, QLD, Australia (Roberts) Townsville Hospital, Douglas, QLD, Australia (Arnold) Orthopaedic and Arthritis Specialist Centre, Chatswood, NSW, Australia (Littlejohn) Monash Medical Centre, Clayton, VIC, Australiaen
dc.description.addressK. Tymms, Canberra Rheumatology, 9/40 Marcus Clarke Street, Canberra City, ACT 2601, Australia. E-mail: ktymms@canberrarheumatology.com.auen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2014 Elsevier B.V., All rights reserved.en
dc.identifier.authoremailTymms K.; ktymms@canberrarheumatology.com.auen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeArticle-
crisitem.author.deptRheumatology-
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