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    Baseline comorbidities in a population-based cohort of rheumatoid arthritis receiving biological therapy: Data from the Australian Rheumatology Association database

    215822_215822.pdf (1.176Mb)
    Access Status
    Open access
    Authors
    Briggs, Andrew
    March, L.
    Lassere, M.
    Reid, C.
    Henderson, L.
    Murphy, B.
    van den Haak, R.
    Rischin, A.
    Staples, M.
    Buchbinder, R.
    Date
    2009
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Briggs, A. and March, L. and Lassere, M. and Reid, C. and Henderson, L. and Murphy, B. and van den Haak, R. et al. 2009. Baseline comorbidities in a population-based cohort of rheumatoid arthritis receiving biological therapy: Data from the Australian Rheumatology Association database. International Journal of Rheumatology. 2009: Article ID 861481.
    Source Title
    International Journal of Rheumatology
    DOI
    10.1155/2009/861481
    ISSN
    1687-9260
    School
    School of Physiotherapy and Exercise Science
    Remarks

    This article is published under the Open Access publishing model and distributed under the terms of the Creative Commons License http://creativecommons.org/licenses/by/3.0/ Please refer to the licence to obtain terms for any further reuse or distribution of this work

    URI
    http://hdl.handle.net/20.500.11937/39887
    Collection
    • Curtin Research Publications
    Abstract

    Aims. To describe the baseline characteristics of an Australian population-based cohort of rheumatoid arthritis (RA) patients commencing biological therapy. Methods. Descriptive analysis from the Australian Rheumatology Association Database (ARAD). Results. Up to October 2006, there were 681 RA patients taking biologics enrolled in ARAD. Baseline data were available for 624 (72% female, mean (SD) age 57.0 (12.5) years). Of these, 59.5% reported at least one comorbid condition, most commonly hypertension (35.7%) and osteoporosis (30.4%); 61 (9.8%) had a history of malignancy (35 nonmelanoma skin, 5 breast, 4 bowel, 5 cervix, 3 melanoma, 3 prostate and 1 each of lip, lung, myeloma, testis, uterus, vagina). Self-reported infections within the previous 6 months were common (71.5%). Conclusions. History of comorbidities, including recent infections, is common among Australian RA patients commencing biologics, and 10% have a history of malignancy. This may impact future evaluations of health outcomes among this population, including attribution of adverse events of biologic therapy.

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