Aug 2026· Seizure· Vol 141, pp.
246-253
· 0 citations· 31 references
Medicine
TL;DR
Among patients with acute-phase AE and seizures, the number of ASMs at discharge and the absence of prodromal infection symptom are probable clinical indicators for predicting AEAE, which may facilitate early risk stratification and optimize management strategies for patients with AE-related seizures.
Abstract
Objective
To investigate the clinical features and risk factors for progression from acute-phase autoimmune encephalitis (AE) with epileptic seizures to autoimmune encephalitis-associated epilepsy (AEAE).
Methods
We retrospectively analyzed clinical data from patients with acute-phase autoimmune encephalitis presenting with seizures between January 2016 and July 2024 at two clinical centers. Following a minimum follow-up of one year, patients were categorized into the ASSAE group or the AEAE group. Multivariable logistic regression identified independent predictors. Model performance was assessed by ROC analysis with bootstrap validation (B = 1000) and calibration testing.
Results
32 patients (22.9%) progressed to AEAE. Multivariable logistic regression identified symptom of prodromal infection as a protective factor (OR: 0.336, 95% CI: 0.131-0.862), while the number of ASMs at discharge was identified as a significant clinical indicator of AEAE development (OR: 2.854, 95% CI: 1.551-5.255). The model demonstrated good discrimination (bootstrap AUC: 0.766, 95% CI: 0.684-0.841) and excellent calibration (Hosmer-Lemeshow P = 0.849).
Conclusion
Among patients with acute-phase AE and seizures, the number of ASMs at discharge and the absence of prodromal infection symptom are probable clinical indicators for predicting AEAE. These findings may facilitate early risk stratification and optimize management strategies for patients with AE-related seizures.
BACKGROUND
Early diagnosis of infectious versus autoimmune encephalitis in children is critical for optimizing patient care.
METHODS
We performed a retrospective cohort study of children one to <18 years of age who had magnetic resonance imaging (MRI) reports with key words "encephalitis" or "meningoencephalitis" at...
Amy Bohling, A. Tippett, Morgan Morris et al.· Pediatric Neurology· 0 citations
Objective: To determine the prevalence and predictors of drug-resistant epilepsy among patients with epilepsy.
Methodology: A retrospective observational study was conducted at the Neurology Department of Liaquat National Hospital, Karachi, for the period from November, 2024 to October, 2025. Patients with epilepsy wer...
Saba Zaidi, Umer Barry, Malaika Ali· Pakistan Journal of Medical...· 0 citations
OBJECTIVE
Despite representing the most common and fastest growing form of epilepsy in older adults, the clinical features of late onset epilepsy (LOE) and how it differs from early onset epilepsy (EOE) remain largely underexplored. Therefore, we evaluate the characteristics and risk factors of LOE compared to EOE.
M...
Syeda Amrah Hashmi, Mark Quigg, M. Abbas et al.· Epilepsia· 0 citations
Background: Pediatric encephalitis is associated with significant morbidity. Early recognition of autoimmune encephalitis (AE) is critical for timely immunotherapy and improved outcomes. Objectives: To externally validate a previously published adult encephalitis prediction model in a pediatric cohort and identify pred...
Ruth Vela Sosa, Audrey M. Uong, Alvaro Coronado-Muñoz· Journal of Hospital Medicine· 0 citations
Summary Background Infection-triggered encephalopathy syndromes (ITES) are acute, para-infectious disorders that can cause disability or death. Recognition is increasingly important in viral pandemics, but clinical features and outcomes remain poorly understood. Methods PubMed search (inception to 6 March 2024) identif...
Michael Eyre, V. Han, Terrence Thomas et al.· EClinicalMedicine· 1 citation
Young age at diagnosis of focal epilepsy, diagnosis of cortical dysplasia, MTS, and presence of complex partial seizures are risk factors for drug-resistant epilepsy.
L. Hernández-Ronquillo, P. Lebony-Roy, S. Buckley et al.· 0 citations
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