Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/110827
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Type: Journal article
Title: A systematic review of the epidemiology, disease characteristics and management of systemic sclerosis in Australian adults
Author: Morrisroe, K.
Stevens, W.
Proudman, S.
Nikpour, M.
Citation: International Journal of Rheumatic Diseases, 2017; 20(11):1728-1750
Publisher: Wiley
Issue Date: 2017
ISSN: 1756-1841
1756-185X
Statement of
Responsibility: 
Kathleen Morrisroe, Wendy Stevens, Susanna Proudman and Mandana Nikpour
Abstract: Objective: Australia has one of the highest prevalence rates of systemic sclerosis (SSc) worldwide. In order to highlight management deficiencies and key areas for further research, it is essential to understand its local epi- demiological patterns, natural history, prognosis and mortality trends over time. Methods: To identify Australian SSc-specific information through a systematic review focusing on areas of epi- demiology, disease characteristics, treatment, functional ability, disease burden and health-related quality of life (HRQoL). Results: MEDLINE, EMBASE and the Cochrane Library were searched on 14 September, 2016. All original full text articles on SSc in Australia were included. Of the 54 articles included in this review, the majority of studies recruited from South Australia, Victoria and New South Wales. The prevalence of SSc in Australia is increasing and is similar among the general population and the Aboriginal population. Despite improvements in care over the last three decades, morbidity and mortality remain high, with an overall standardized mortality ratio of 3.4 and a 10- year survival of 84% in a newly diagnosed patient. Cardiorespiratory manifestations are the leading cause of SSc- related death. Malignancy is the leading cause of non-SSc-related death. The role of autoantibodies in predicting disease subtype, visceral involvement and their use as a prognostic marker is becoming increasingly recognized. Conclusion: Information on SSc in Australia, particularly unmet healthcare needs, HRQoL and economic bur- den, is limited. As a heterogenous condition, SSc requires a multi-disciplinary approach to care. Research aimed at quantifying HRQoL and burden of disease in Australia is essential for advocacy and resource allocation.
Keywords: Australia; epidemiology; scleroderma; systemic sclerosis
Rights: © 2017 Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltd
RMID: 0030077102
DOI: 10.1111/1756-185X.13203
Grant ID: http://purl.org/au-research/grants/nhmrc/1113954
http://purl.org/au-research/grants/nhmrc/1126370
Appears in Collections:Medicine publications

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