Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33082
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dc.contributor.authorOwen, Claire E-
dc.contributor.authorYates, Max-
dc.contributor.authorLiew, David F L-
dc.contributor.authorPoon, Aurora M T-
dc.contributor.authorKeen, Helen I-
dc.contributor.authorHill, Catherine L-
dc.contributor.authorMackie, Sarah L-
dc.date2023-
dc.date.accessioned2023-06-16T06:48:43Z-
dc.date.available2023-06-16T06:48:43Z-
dc.date.issued2023-03-
dc.identifier.citationBest Practice & Research. Clinical Rheumatology 2023-03; 37(1)en_US
dc.identifier.issn1532-1770-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33082-
dc.description.abstractImaging is increasingly being used to guide clinical decision-making in patients with giant cell arteritis (GCA). While ultrasound has been rapidly adopted in fast-track clinics worldwide as an alternative to temporal artery biopsy for the diagnosis of cranial disease, whole-body PET/CT is emerging as a potential gold standard test for establishing large vessel involvement. However, many unanswered questions remain about the optimal approach to imaging in GCA. For example, it is uncertain how best to monitor disease activity, given there is frequent discordance between imaging findings and conventional disease activity measures, and imaging changes typically fail to resolve completely with treatment. This chapter addresses the current body of evidence for the use of imaging modalities in GCA across the spectrum of diagnosis, monitoring disease activity, and long-term surveillance for structural changes of aortic dilatation and aneurysm formation and provides suggestions for future research directions.en_US
dc.language.isoeng-
dc.subjectAngiographyen_US
dc.subjectComputed tomographyen_US
dc.subjectDiagnosisen_US
dc.subjectGiant cell arteritisen_US
dc.subjectImagingen_US
dc.subjectMagnetic resonance imagingen_US
dc.subjectMonitoringen_US
dc.subjectPositron emission tomographyen_US
dc.subjectUltrasounden_US
dc.titleImaging of giant cell arteritis - recent advances.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleBest Practice & Research. Clinical Rheumatologyen_US
dc.identifier.affiliationRheumatologyen_US
dc.identifier.affiliationDepartment of Rheumatology, Norfolk and Norwich University Hospital, Norwich, United Kingdomen_US
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Parkville, Victoria, Australia.en_US
dc.identifier.affiliationMolecular Imaging and Therapyen_US
dc.identifier.affiliationDepartment of Rheumatology, Fiona Stanley Hospital, Murdoch, Western Australia, Australiaen_US
dc.identifier.affiliationRheumatology Unit, Royal Adelaide Hospital, Adelaide, South Australia, Australiaen_US
dc.identifier.affiliationLeeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdomen_US
dc.identifier.affiliationMedical School, University of Western Australia, Perth, Western Australia, Australia.en_US
dc.identifier.affiliationNorwich Medical School, University of East Anglia, Norwich, United Kingdom.en_US
dc.identifier.affiliationDiscipline of Medicine, The University of Adelaide, Adelaide, South Australia, Australia.en_US
dc.identifier.affiliationNIHR-Leeds Biomedical Research Centre, Leeds Teaching Hospitals NHS Trust, United Kingdom.en_US
dc.identifier.doi10.1016/j.berh.2023.101827en_US
dc.type.contentTexten_US
dc.identifier.pubmedid37277245-
dc.description.startpage101827-
local.name.researcherLiew, David F L-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptRheumatology-
crisitem.author.deptRheumatology-
crisitem.author.deptClinical Pharmacology and Therapeutics-
crisitem.author.deptMolecular Imaging and Therapy-
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