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Anti-NMDAR encephalitis in Southeast Asia - A single-centre, longitudinal study
You-Jiang Tan1, Isabel E Siow2, Chiew Sern Ong1
1Department of Neurology, National Neuroscience Institute (Singapore General Hospital), Singapore; Duke-NUS Medical School, Singapore.
Anti-NMDA receptor encephalitis (ANMDARE) in Southeast Asian patients often presents with delirium and seizures. Early diagnosis and treatment are crucial for favorable outcomes, especially in females with neoplasms.
Area of Science:
- Neurology
- Immunology
Background:
- Anti-NMDA receptor encephalitis (ANMDARE) is a severe autoimmune neurological disorder.
- Understanding its clinical spectrum in diverse populations like Southeast Asians is crucial for timely diagnosis and management.
Purpose of the Study:
- To delineate the clinical features and treatment outcomes of ANMDARE in Southeast Asian (SEA) patients.
- To identify potential demographic or clinical differences within this population.
Main Methods:
- Retrospective analysis of 20 SEA patients diagnosed with ANMDARE.
- Data collected included clinical presentations, demographics, associated neoplasms, and 1-year outcomes.
Main Results:
- Delirium and seizures were the most common presenting symptoms.
- Females had a higher incidence of movement disorders and underlying neoplasms (teratomas, neuroendocrine tumors).
- While dysautonomia prolonged ICU stays, 1-year outcomes were favorable for most patients (mRS 0-2).
Conclusions:
- SEA patients with ANMDARE commonly present with delirium and seizures.
- Recognizing gender-specific differences in clinical characteristics and associated neoplasms can aid early diagnosis and treatment.
- Prompt management strategies are essential for improving outcomes in SEA patients with ANMDARE.
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