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Abstract Details

Specific Psychiatric Features Identify Anti-NMDAR Encephalitis Before Neurological Deterioration
Autoimmune Neurology
P10 - Poster Session 10 (5:30 PM-6:30 PM)
15-010

Evaluate the psychiatric presentation of anti-NMDAR encephalitis to identify features that help differentiate from a primary psychiatric disorder.

Anti-NMDAR encephalitis results from antibodies binding the glycine subunit of the NMDA receptor, with consequent capping and internalisation of the receptor causing neuronal dysfunction. Presentation with psychiatric disturbance is common but identification of cases prior to neurological deterioration is difficult. Early treatment is associated with better outcomes, however, diagnosis requires CSF analysis which is not routinely performed.

Retrospective review of all positive serum and CSF anti-NMDAR encephalitis cases in QLD, Australia between 2010 – 2018 and all published cases from inception of PubMed and Embase until Jan 2018. Comparison analysis with control cases of first episode psychosis with an anti-NMDAR antibody negative result.

There were 706 cases identified in literature and 24 cases locally. These were typically young (mean 22.6 years), female (F:M ratio 3.5:1) and presented with significant behavioural disturbance. Psychosis was present in 45.8%. The most common psychiatric symptoms were severe agitation and aggression, abnormal speech and catatonia. In addition, prodromal cognitive deficits and antipsychotic sensitivity were seen before neurological deterioration in cases but not in the 103 control cases.

Several features including prodromal cognitive deficits, speech disturbance, antipsychotic sensitivity and catatonia are seen early in the course of anti-NMDAR encephalitis. These key features would not be typical of primary psychiatric disease and clinicians should have a low index of suspicion to proceed to lumbar puncture.

Authors/Disclosures
Cullen M. O'Gorman, MBBS (Queensland Health)
PRESENTER
Dr. O'Gorman has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Biogen Australia Pty. An immediate family member of Dr. O'Gorman has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Lundbeck Australia. An immediate family member of Dr. O'Gorman has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Otsuka.
No disclosure on file
Andrew Swayne, MBBS (Princess Alexandra Hsopital) No disclosure on file
No disclosure on file
Stefan Blum, PhD, FRACP (Princess Alexandra Hospital) The institution of Dr. Blum has received research support from Merck. The institution of Dr. Blum has received research support from MSRA. The institution of Dr. Blum has received research support from PA Research Foundation.