Recognition and treatment of anti-n-methyl-d-aspartate receptor encephalitis

Sue Hong*, Marisa Klein-Gitelman, Mark S. Wainwright

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Anti-N-methyl-d-aspartate receptor encephalitis should be considered for pediatric patients who present with seizures, dysautonomia, dyskinesias, and psychiatric disturbances. Life-threatening complications from this disorder, including seizures, hypoventilation, bradycardia, and ictal asystole, should be anticipated, and the patient should be closely monitored and supported. Morbidity and mortality can be mitigated with early detection and initiation of immunotherapy and resection of a teratoma, if found. In young patients treated soon after symptom onset, the prognosis is favorable with most patients having no or mild residual neurologic deficit. Early recognition of the protean signs of this disorder in the emergency department is essential to help establish immunomodulation therapy in a timely fashion.

Original languageEnglish (US)
Pages (from-to)3-10
Number of pages8
JournalClinical Pediatric Emergency Medicine
Volume16
Issue number1
DOIs
StatePublished - Mar 1 2015

Funding

Supported by The Ruth D. & Ken M. Davee Pediatric Neurocritical Care Program.

Keywords

  • Anti-NMDA receptor encephalitis
  • Dysautonomia
  • Dyskinesias
  • Seizures

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Emergency Medicine

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