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Approach to the Management of Pediatric-Onset Anti-N-Methyl-<scp>d</scp>-Aspartate (Anti-NMDA) Receptor Encephalitis
- Source :
- Journal of Child Neurology. 31:1150-1155
- Publication Year :
- 2016
- Publisher :
- SAGE Publications, 2016.
-
Abstract
- Anti- N-methyl-d-aspartate (anti-NMDA) receptor encephalitis is a treatable cause of autoimmune encephalitis. It remains unclear if the natural history of this disease is altered by choice of acute therapy or the employment of chronic immunotherapy. Chart review was undertaken for pediatric patients diagnosed with anti-NMDA receptor encephalitis. Data obtained included patient demographics, disease manifestations, treatment course, and clinical outcomes. Ten patients with anti-NMDA receptor encephalitis were identified. All patients were treated with immunotherapy in the acute period, and all patients experienced good recovery. Neurologic relapse did not occur in any patient. All patients received varied forms of chronic immunosuppression to prevent relapses. Complications of chronic immunotherapy occurred in 50% of patients. The benefits of chronic immunotherapy and the duration of use should be carefully weighed against the risks. Complications from immunotherapy are not uncommon and can be serious. Clinical trials assessing the benefit of long-term immunotherapy in this population are needed.
- Subjects :
- Anti-NMDA receptor encephalitis
Autoimmune encephalitis
medicine.medical_specialty
education.field_of_study
business.industry
medicine.medical_treatment
Population
Immunosuppression
Immunotherapy
Disease
medicine.disease
Clinical trial
03 medical and health sciences
0302 clinical medicine
030225 pediatrics
Internal medicine
Pediatrics, Perinatology and Child Health
Immunology
Medicine
Neurology (clinical)
business
education
030217 neurology & neurosurgery
Encephalitis
Subjects
Details
- ISSN :
- 17088283 and 08830738
- Volume :
- 31
- Database :
- OpenAIRE
- Journal :
- Journal of Child Neurology
- Accession number :
- edsair.doi...........0c4d75d25d442109b138b0a6cfeb2bc9
- Full Text :
- https://doi.org/10.1177/0883073816643406