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Treatment of Movement Disorder Emergencies in Autoimmune Encephalitis in the Neurosciences ICU

  • Farwa AliEmail author
  • Eelco F. Wijdicks
Review

Abstract

Immune response against neuronal and glial cell surface and cytosolic antigens is an important cause of encephalitis. It may be triggered by activation of the immune system in response to an infection (para-infectious), cancer (paraneoplastic), or due to a patient’s tendency toward autoimmunity. Antibodies directed toward neuronal cell surface antigens are directly pathogenic, whereas antibodies with intracellular targets may become pathogenic if the antigen is transiently exposed to the cell surface or via activation of cytotoxic T cells. Immune-mediated encephalitis is well recognized and may require intensive care due to status epilepticus, need for invasive ventilation, or dysautonomia. Patients with immune-mediated encephalitis may become critically ill and display clinically complex and challenging to treat movement disorders in over 80% of the cases (Zhang et al. in Neurocrit Care 29(2):264–272, 2018). Treatment options include immunotherapy and symptomatic agents affecting dopamine or acetylcholine neurotransmission. There has been no prior published guidance for management of these movement disorders for the intensivist. Herein, we discuss the immune-mediated encephalitis most likely to cause critical illness, clinical features and mechanisms of movement disorders and propose a management algorithm.

Keywords

Autoimmune Encephalitis Movement disorder Dyskinesia Chorea 

Notes

Author Contributions

FA and EFW involved in: (1) substantial contributions to conception and design, acquisition of data, or analysis and interpretation of data; (2) drafting the article or revising it critically for important intellectual content; (3) final approval of the version to be published.

Source of support

No financial support was used in this project.

Conflict of interest

All authors declare that they have no conflict of interest.

Ethical Approval

IRB approval was not required for this review article and no patient protected health information was accessed.

Supplementary material

Supplementary material 1 (MP4 4643 kb)

12028_2019_875_MOESM2_ESM.pdf (112 kb)
Supplementary material 2 (PDF 111 kb)

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2019

Authors and Affiliations

  1. 1.Department of NeurologyMayo Clinic Rochester MinnesotaRochesterUSA

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