Evidence map›Paper›PMID 40886242›Full record

ArticleQuality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation2025

The relationship between patient-reported quality of life and clinician-rated outcome scores in patients with autoimmune encephalitis: a study of the Australian Autoimmune Encephalitis Consortium.

Christina Kazzi, Nabil Seery, Sarah Griffith, Robb Wesselingh, Tiffany Rushen, Tracie H Tan, Katherine Y Ko, Liora Ter Horst, Genevieve Skinner, Laurie McLaughlin and 20 more

Abstract read
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Article in Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

30 authors.

Christina KazziDepartment of Neuroscience, School of Translational Medicine, Monash University, Level 6, Alfred Centre, 99 Commercial Rd, Melbourne, VIC, 3004, Australia.ORCID http://orcid.org/0000-0001-6737-5489
Nabil SeeryDepartment of Neuroscience, School of Translational Medicine, Monash University, Level 6, Alfred Centre, 99 Commercial Rd, Melbourne, VIC, 3004, Australia.
Sarah GriffithDepartment of Neuroscience, School of Translational Medicine, Monash University, Level 6, Alfred Centre, 99 Commercial Rd, Melbourne, VIC, 3004, Australia.
Robb WesselinghDepartment of Neuroscience, School of Translational Medicine, Monash University, Level 6, Alfred Centre, 99 Commercial Rd, Melbourne, VIC, 3004, Australia.
Tiffany RushenDepartment of Neuroscience, School of Translational Medicine, Monash University, Level 6, Alfred Centre, 99 Commercial Rd, Melbourne, VIC, 3004, Australia.
Tracie H TanDepartment of Neuroscience, School of Translational Medicine, Monash University, Level 6, Alfred Centre, 99 Commercial Rd, Melbourne, VIC, 3004, Australia.
Katherine Y KoDepartment of Neuroscience, School of Translational Medicine, Monash University, Level 6, Alfred Centre, 99 Commercial Rd, Melbourne, VIC, 3004, Australia.
Liora Ter HorstDepartment of Neurology, Princess Alexandra Hospital, Woolloongabba, QLD, Australia.
Genevieve SkinnerDepartment of Neurology, Princess Alexandra Hospital, Woolloongabba, QLD, Australia.
Laurie McLaughlinDepartment of Neurology, Princess Alexandra Hospital, Woolloongabba, QLD, Australia.
Hannah FordDepartment of Neuroscience, Monash Medical Centre, Clayton, VIC, Australia.
Catherine MeadeNeuropsychology Unit, Department of Clinical Neurosciences, St Vincent's Hospital, Melbourne, VIC, Australia.
Marie O'SheaMelbourne School of Psychological Sciences, University of Melbourne, Parkville, VIC, Australia.
Katherine BuzzardDepartment of Neurosciences, Eastern Health, Melbourne, VIC, Australia.
Mirasol ForcadelaDepartment of Neurology, Austin Health, Melbourne, VIC, Australia.
Andrew DuncanDepartment of Medicine (St Vincent's Hospital), University of Melbourne, Melbourne, VIC, Australia.
Anneke van der WaltDepartment of Neuroscience, School of Translational Medicine, Monash University, Level 6, Alfred Centre, 99 Commercial Rd, Melbourne, VIC, 3004, Australia.
Wendyl D'SouzaDepartment of Medicine (St Vincent's Hospital), University of Melbourne, Melbourne, VIC, Australia.
Udaya SenvieratneDepartment of Neuroscience, Monash Medical Centre, Clayton, VIC, Australia.
Richard MacdonellDepartment of Neurology, Austin Health, Melbourne, VIC, Australia.
Sudarshini RamanathanDepartment of Neurology, Concord Clinical School, Concord Hospital, Concord, NSW, Australia.
Stefan BlumDepartment of Neurology, Princess Alexandra Hospital, Woolloongabba, QLD, Australia.
Stephen W ReddelDepartment of Neurology, Concord Clinical School, Concord Hospital, Concord, NSW, Australia.
Todd A HardyDepartment of Neurology, Concord Clinical School, Concord Hospital, Concord, NSW, Australia.
Helmut ButzkuevenDepartment of Neuroscience, School of Translational Medicine, Monash University, Level 6, Alfred Centre, 99 Commercial Rd, Melbourne, VIC, 3004, Australia.
Terence J O'BrienDepartment of Neuroscience, School of Translational Medicine, Monash University, Level 6, Alfred Centre, 99 Commercial Rd, Melbourne, VIC, 3004, Australia.
Rubina AlpitsisDepartment of Neuroscience, School of Translational Medicine, Monash University, Level 6, Alfred Centre, 99 Commercial Rd, Melbourne, VIC, 3004, Australia.
Charles B MalpasDepartment of Neuroscience, School of Translational Medicine, Monash University, Level 6, Alfred Centre, 99 Commercial Rd, Melbourne, VIC, 3004, Australia.
Mastura MonifDepartment of Neuroscience, School of Translational Medicine, Monash University, Level 6, Alfred Centre, 99 Commercial Rd, Melbourne, VIC, 3004, Australia. mastura.monif@monash.edu.ORCID http://orcid.org/0000-0001-6404-9768
Australian Autoimmune Encephalitis Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with Autoimmune Encephalitis (AE) commonly report poor quality of life. There is a lack of evidence on whether clinician-rated outcome measures adequately capture patient-reported experiences. This study aimed to characterise long-term quality of life in AE patients and examine its relationship with clinician-rated disability (modified Rankin Score, mRS) and symptom severity (Clinical Assessment Scale in Autoimmune Encephalitis, CASE).

methodsPatients with AE were recruited through the Australian Autoimmune Encephalitis Consortium Project. Patients with completed NeuroQoL instruments, as well as CASE and/or mRS scores within 6 months of the NeuroQoL were included.

resultsFifty-four patients with AE (50% female, median age at symptom onset = 49.70 years) completed the NeuroQoL instruments at a median of 50 months (IQR: 18.25-87.50 months) post-disease onset. The median CASE score was 2 (IQR: 0.0-3.0). The median mRS was 1.5 (IQR: 1.0-2.0). In the total AE sample, CASE scores were positively associated with all NeuroQoL domains (r = .42-.53), except Fatigue (r = .28). Total NeuroQoL, Cognitive Function, Satisfaction in Social Roles and Activities, and Stigma T-scores were significantly higher in seropositive AE patients with an mRS > 2 (d = 0.94-1.66). The mRS significantly predicted most NeuroQoL domains in the total AE sample, and the CASE score explained little or no additional variance over and above mRS scores. Similarly, the CASE score was significantly associated with most NeuroQoL domains, with no additional variance explained by mRS scores. DISCUSSION: The relationships between clinician-rated outcomes and domains of quality of life varied from weak to moderate. This highlights the importance of integrating clinical measures and patient-reported outcomes when assessing outcomes post-AE.

Indexed as

EncephalitisHashimoto DiseasePatient Reported Outcome MeasuresQuality of LifeAdultAgedAustraliaFemaleHumansMaleMiddle AgedSeverity of Illness IndexSurveys and QuestionnairesAutoimmune encephalitisClinical outcome scoresPatient-reported outcomesQuality of life

Identifiers

PMID40886242
PMCPMC12689736

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.