Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/32870
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dc.contributor.authorOakman, Georgina-
dc.contributor.authorBach, Cindy-Anne-
dc.contributor.authorOng, Cindy-
dc.date2023-
dc.date.accessioned2023-06-07T01:56:42Z-
dc.date.available2023-06-07T01:56:42Z-
dc.date.issued2023-05-15-
dc.identifier.citationInternal Medicine Journal 2023-05-15en_US
dc.identifier.issn1445-5994-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/32870-
dc.description.abstractThe epidemiology of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) varies worldwide. Previous Australian studies described a higher incidence of AAV in rural areas; however, this has not yet been investigated in Victoria. To calculate the incidence of AAV in rural and regional Victoria and characterise the demographics and clinical outcomes of this cohort. We performed a retrospective review of patients with newly diagnosed AAV confirmed on renal biopsy at Bendigo Health between 2013 and 2021. Cases were classified according to the 2022 American College of Rheumatology/European Alliance of Associations for Rheumatology criteria. Local disease incidence was calculated using Estimated Resident Population data for our catchment, the Loddon Mallee region. Twenty-eight cases of new AAV were identified; 17 were classified as microscopic polyangiitis (MPA) and the remainder as granulomatosis with polyangiitis (GPA). The median age at diagnosis was 68 years (interquartile range (IQR): 59-77). The incidence per million person-years was 9.3 for AAV overall (95% CI: 6.2-13.5), 5.7 for MPA (95% CI: 3.3-9.1) and 3.7 for GPA (95% CI: 1.8-6.6). With a median follow-up time of 3.3 years (IQR: 1.9-5.6), one-quarter of patients relapsed (n = 7, 25%), and six required ongoing renal-replacement therapy (21%). The calculated incidence of AAV in rural and regional Victoria is not higher than the reported incidence in most urban Australian cohorts. This study may underestimate the true local disease incidence as only patients with renal vasculitis were included.en_US
dc.language.isoeng-
dc.subjectAustraliaen_US
dc.subjectanti-neutrophil cytoplasmic antibody-associated vasculitisen_US
dc.subjectgranulomatosis with polyangiitisen_US
dc.subjectincidenceen_US
dc.subjectmicroscopic polyangiitisen_US
dc.titleIncidence of anti-neutrophil cytoplasmic antibody-associated renal vasculitis: a retrospective study in rural and regional Victoria, Australia.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleInternal Medicine Journalen_US
dc.identifier.affiliationDepartment of Renal Medicine, Bendigo Health, Victoria, Bendigo, Australia.en_US
dc.identifier.affiliationGeneral Medicineen_US
dc.identifier.doi10.1111/imj.16127en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-1251-782Xen_US
dc.identifier.pubmedid37183767-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.languageiso639-1en-
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