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Psoriatic arthritis treatment regimens, therapy duration and reasons for cessation in the biologics era: A multi-centre Australian study

dc.contributor.authorTymms, Kathleen
dc.contributor.authorKelly, Ayano
dc.contributor.authorBIRD, Paul
dc.contributor.authorGriffiths, Hedley
dc.contributor.authorde Jager, Julien
dc.contributor.authorLittlejohn, Geoffrey
dc.contributor.authorLouw, Sandra
dc.contributor.authorRoberts, Lynden
dc.contributor.authorYoussef, Peter
dc.contributor.authorZochling, J.
dc.contributor.authorNichols, Dave
dc.date.accessioned2020-04-27T05:50:26Z
dc.date.issued2018
dc.date.updated2019-11-25T07:57:59Z
dc.description.abstractAim: To describe the treatment regimens, duration of therapy and reasons for disease-modifying antirheumatic drug (DMARD) cessation in a large psoriatic arthritis (PsA) cohort. Methods: A retrospective non-interventional multi-centre study using Audit4 electronic medical records, with de-identified, routinely collected clinical data from rheumatology practices in the OPAL consortium (Optimising Patient outcomes in Australian rheumatoLogy) during November 2015. Baseline characteristics, type and duration of conventional and biologic DMARDs (cDMARD and bDMARD, respectively), disease activity (Disease Activity Score of 28 joints C-reactive protein [DAS28-CRP]), and reasons for treatment cessation were recorded. Results: A total of 3422 rheumatologist-diagnosed PsA patients were included: 60% female, mean age 54 years and disease duration 10 years. Of patients with treatment recorded (n = 2948), 46% were on cDMARD monotherapy, 19% bDMARD monotherapy, 13% combination bDMARD and cDMARDs, 11% combination cDMARDs and 10% no DMARDs. Of those with DAS28-CRP results (n = 494), the highest mean DAS28-CRP was 3.32 on combination cDMARDs, and the lowest was 2.19 on bDMARD monotherapy. Median duration on cDMARD monotherapy was 33.5 months (n = 2232), on bDMARD monotherapy 110.1 months (n = 751), on combination bDMARD and cDMARDs 68.5 months (n = 559). The most common reasons for cessation of cDMARD monotherapy was adverse reactions (41%), for bDMARD monotherapy lack of efficacy (26%), and for combination bDMARD and cDMARDs treatment completed or no longer required (37%). Conclusion: Most PsA patients were prescribed DMARD therapies with a large proportion receiving cDMARDs. Patients on combination cDMARD therapies had the highest DAS28-CRP results. Adverse reactions were the most common reason for cessation of cDMARD monotherapy, whereas for bDMARD monotherapy it was lack of efficacy.en_AU
dc.description.sponsorshipThe project has received funding and support from Celgene Pty. Ltd. as a quality use of medicines initiative.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1756-1841en_AU
dc.identifier.urihttp://hdl.handle.net/1885/203417
dc.language.isoen_AUen_AU
dc.publisherBlackwell Publishing Inc.en_AU
dc.rights© 2017 Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltden_AU
dc.sourceInternational Journal of Rheumatic Diseasesen_AU
dc.subjectclinical aspects, drug treatment, epidemiology, psoriatic arthritisen_AU
dc.titlePsoriatic arthritis treatment regimens, therapy duration and reasons for cessation in the biologics era: A multi-centre Australian studyen_AU
dc.typeJournal articleen_AU
local.bibliographicCitation.issue2en_AU
local.bibliographicCitation.lastpage516en_AU
local.bibliographicCitation.startpage510en_AU
local.contributor.affiliationTymms, Kathleen, College of Health and Medicine, ANUen_AU
local.contributor.affiliationKelly, Ayano, College of Health and Medicine, ANUen_AU
local.contributor.affiliationBIRD, Paul, Combined Rheumatology Practiceen_AU
local.contributor.affiliationGriffiths, Hedley, Barwon Rheumatology Serviceen_AU
local.contributor.affiliationde Jager, Julien, Gold Coast Rheumatologyen_AU
local.contributor.affiliationLittlejohn, Geoffrey, Monash Universityen_AU
local.contributor.affiliationLouw, Sandra, McCloud Consulting Groupen_AU
local.contributor.affiliationRoberts, Lynden, Southern Rheumatologyen_AU
local.contributor.affiliationYoussef, Peter, Royal Prince Alfred Hospitalen_AU
local.contributor.affiliationZochling, J., Department of Rheumatologyen_AU
local.contributor.affiliationNichols, Dave, Coast Joint Careen_AU
local.contributor.authoruidTymms, Kathleen, u5095765en_AU
local.contributor.authoruidKelly, Ayano, u5924485en_AU
local.description.embargo2037-12-31
local.description.notesImported from ARIESen_AU
local.identifier.absfor110799 - Immunology not elsewhere classifieden_AU
local.identifier.absseo920199 - Clinical Health (Organs, Diseases and Abnormal Conditions) not elsewhere classifieden_AU
local.identifier.ariespublicationu5234101xPUB78en_AU
local.identifier.citationvolume21en_AU
local.identifier.doi10.1111/1756-185X.13127en_AU
local.publisher.urlhttps://www.wiley.com/en-gben_AU
local.type.statusPublished Versionen_AU

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