Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30612
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dc.contributor.authorGriffith, Sarah-
dc.contributor.authorWesselingh, Robb-
dc.contributor.authorBroadley, James-
dc.contributor.authorO'Shea, Marie F-
dc.contributor.authorKyndt, Chris-
dc.contributor.authorMeade, Catherine-
dc.contributor.authorLong, Brian-
dc.contributor.authorSeneviratne, Udaya-
dc.contributor.authorReidy, Natalie-
dc.contributor.authorBourke, Robert-
dc.contributor.authorBuzzard, Katherine-
dc.contributor.authorD'Souza, Wendyl-
dc.contributor.authorMacdonell, Richard A L-
dc.contributor.authorBrodtmann, Amy-
dc.contributor.authorButzkueven, Helmut-
dc.contributor.authorO'Brien, Terence J-
dc.contributor.authorAlpitsis, Rubina-
dc.contributor.authorMalpas, Charles B-
dc.contributor.authorMonif, Mastura-
dc.date2022-
dc.date.accessioned2022-07-27T23:26:54Z-
dc.date.available2022-07-27T23:26:54Z-
dc.date.issued2022-08-
dc.identifier.citationEuropean Journal of Neurology 2022; 29(8): 2355-2366en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/30612-
dc.description.abstractDespite the rapid increase in research examining outcomes in autoimmune encephalitis (AE) patients, there are few cohort studies examining cognitive outcomes in this population. The current study aimed to characterise psychometric outcomes in this population, and explore variables that may predict psychometric outcomes. This retrospective observational study collected psychometric data from 59 patients across six secondary and tertiary referral centres in metropolitan hospitals in Victoria, Australia between January 2008 and July 2019. Frequency and pattern analysis were employed to define and characterize psychometric outcomes. Univariable logistic regression was performed to examine predictors of intact and pathological psychometric outcomes. Deficits in psychometric markers of executive dysfunction were the most common finding in this cohort, followed by deficits on tasks sensitive to memory. A total of 54.2% of patients were classified as having psychometric impairments across at least two cognitive domains. Twenty-nine patterns were observed, suggesting outcomes in AE are complex. None of the demographic data, clinical features or auxiliary examination variables were predictors of psychometric outcome. Cognitive outcomes in AE are complex. Further detailed and standardized cognitive testing, in combination with magnetic resonance imaging volumetrics and serum/cerebrospinal fluid biomarkers, is required to provide rigorous assessments of disease outcomes.en
dc.language.isoeng-
dc.subjectautoimmune diseasesen
dc.subjectautoimmune encephalitisen
dc.subjectcognitive outcomesen
dc.subjectneuropsychologyen
dc.titlePsychometric deficits in autoimmune encephalitis: A retrospective study from the Australian Autoimmune Encephalitis Consortium.en
dc.typeJournal Articleen
dc.identifier.journaltitleEuropean journal of neurologyen
dc.identifier.affiliationDepartment of Neurosciences, Central Clinical School, Faculty of Medicine, Nursing and Health Sciences, Monash University, Alfred Centre, Melbourne, Vic., Australia..en
dc.identifier.affiliationDepartment of Neurology, Alfred Health, Alfred Centre, Melbourne, Vic., Australia..en
dc.identifier.affiliationClinical Neuropsychologyen
dc.identifier.affiliationMelbourne School of Psychological Sciences, The University of Melbourne, Melbourne, Vic., Australia..en
dc.identifier.affiliationDepartment of Neurosciences, Eastern Health Clinical School, Box Hill Hospital, Monash University, Melbourne, Vic., Australia..en
dc.identifier.affiliationDepartment of Neurosciences, St Vincent's Hospital, Fitzroy, Vic., Australia..en
dc.identifier.affiliationNeuropsychology Unit, Monash Medical Centre, Monash Health, Clayton, Vic., Australia..en
dc.identifier.affiliationDepartment of Neurosciences, Monash Health, Clayton, Vic., Australia..en
dc.identifier.affiliationDepartment of Neurology, Melbourne Health, Parkville, Vic., Australia..en
dc.identifier.affiliationDepartment of Medicine, St Vincent's Hospital, The University of Melbourne, Fitzroy, Vic., Australia..en
dc.identifier.affiliationNeurologyen
dc.identifier.affiliationDepartment of Medicine, Royal Melbourne Hospital, The University of Melbourne, Melbourne, Vic., Australia..en
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35460305/en
dc.identifier.doi10.1111/ene.15367en
dc.type.contentTexten
dc.identifier.orcidhttps://orcid.org/0000-0002-7087-8703en
dc.identifier.orcidhttps://orcid.org/0000-0003-0182-9702en
dc.identifier.orcidhttps://orcid.org/0000-0001-6604-3968en
dc.identifier.orcidhttps://orcid.org/0000-0001-9466-2862en
dc.identifier.pubmedid35460305-
local.name.researcherBrodtmann, Amy
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptClinical Neuropsychology-
crisitem.author.deptNeurology-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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