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Abstract Details

NMDA receptor encephalitis with severe orofacial dyskinesias treated with tramadol and clonazepam
Autoimmune Neurology
P1 - Poster Session 1 (9:00 AM-5:00 PM)
050
N/A

Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is a neuroinflammatory disease mediated by antibodies targeting the GluN1 subunit of the NMDAR. It presents with well-defined neuropsychiatric symptoms, including psychosis, agitation, seizures, and memory disturbances.1 Movement disorders including orofacial dyskinesias are common, but often difficult to manage, with no specific published guidelines.1,2,3

A 23-year-old female was diagnosed with NMDAR encephalitis. She was treated with ovarian teratoma removal, corticosteroids, intravenous immunoglobulin therapy, rituximab, and tocilizumab. She continued to experience severe, self-mutilating orofacial dyskinesias. Tetrabenazine, haloperidol, and diazepam did not yield any sustained improvement. Tramadol was started based on prior case reports suggesting its efficacy as well as clonazepam.3

Tramadol 50 mg po q6h led to immediate improvement in symptoms. Over the next 5 days, tramadol was increased to 150mg NG q6h and further reduced movements. When tramadol was held for one day, the movements significantly worsened and improved when it was restarted. Clonazepam 1mg NG QID also led to further improvement.

Tramadol and clonazepam effectively treated severe orofacial dyskinesias in a patient with NMDAR encephalitis and refractory symptoms despite aggressive management. We propose early use of tramadol and clonazepam be considered for severe orofacial dyskinesias secondary to NMDAR encephalitis.  

 

References:

  1. Dalmau. (2016). NMDA receptor encephalitis and other antibody-mediated disorders of the synapse: The 2016 Cotzias Lecture.Neurology,87(23), 2471–2482.
  2. Huang, Xie, Y., Hu, Z., & Tang, X. (2020). Anti-N-methyl-D-aspartate receptor encephalitis: A review of pathogenic mechanisms, treatment, prognosis.Brain Research,1727, 146549–146549.
  3. Ho KM. Use of tramadol to attenuate severe dyskinesia in anti-N-methyl-D-aspartate receptor encephalitis. Anaesthesia and Intensive Care. 2019;47(6):561-562. 
Authors/Disclosures
Falen Fernandes, MD
PRESENTER
Dr. Fernandes has nothing to disclose.
Fraser M. Clift, MD (Eastern Health) Dr. Clift has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Biogen . Dr. Clift has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for EMD Serono . Dr. Clift has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Novartis. Dr. Clift has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Sanofi . Dr. Clift has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Roche. Dr. Clift has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Alexion. Dr. Clift 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. Dr. Clift has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for EMD Serono. Dr. Clift has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Novartis. Dr. Clift has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Roche. Dr. Clift has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Sanofi.
Laura Chu, MD (BARLO MS Centre) Dr. Chu has nothing to disclose.