High-Dose Diazepam Controls Severe Dyskinesia in Anti-NMDA Receptor Encephalitis.


Journal

Neurology. Clinical practice
ISSN: 2163-0402
Titre abrégé: Neurol Clin Pract
Pays: United States
ID NLM: 101577149

Informations de publication

Date de publication:
Aug 2021
Historique:
received: 21 03 2020
accepted: 21 09 2020
entrez: 6 9 2021
pubmed: 7 9 2021
medline: 7 9 2021
Statut: ppublish

Résumé

Because there is no standard treatment to control dyskinesia in anti-NMDA receptor (NMDAR) encephalitis, we analyzed the therapeutic efficacy of high-dose diazepam in dyskinesia associated with NMDAR encephalitis. We reviewed patients with NMDAR encephalitis with dyskinesia who were admitted to Seoul National University Hospital between November 2012 and July 2018. High-dose diazepam was administered orally or via a nasogastric tube 3-6 times a day. We assessed the treatment effect by comparing dyskinesia severity between the first day of the highest dose of diazepam and one week after the treatment. Among 68 patients with NMDAR encephalitis during the study period, 33 patients were treated with enteral diazepam (ranging from 6 to 180 mg) to control dyskinesia, along with immunotherapy. The severity of dyskinesia improved from average grade 2.4 ± 0.6 to 1.1 ± 0.7 after 1 week of the highest dose of diazepam (mean severity change -1.4 ± 0.6, 95% confidence interval -1.2 to -1.6; Dyskinesia in NMDAR encephalitis improved after treatment with enteral diazepam without significant side effects. This study suggests that enteral diazepam could be a treatment option for control dyskinesia in NMDAR encephalitis. This study provides Class IV evidence that for patients with dyskinesias associated with NMDAR encephalitis, enteral diazepam is effective and safe in dyskinesia control.

Identifiants

pubmed: 34484945
doi: 10.1212/CPJ.0000000000001001
pii: NEURCLINPRACT2020052787
pmc: PMC8382394
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e480-e487

Informations de copyright

© 2021 American Academy of Neurology.

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Auteurs

Hye-Rim Shin (HR)

Department of Neurology (YJ, Y-WS, KC, SKL, S-TL), Seoul National University Hospital; Department of Neurology (H-RS), Dankook University Hospital, Cheonan; and Department of Neurosurgery (Y-WS), Seoul National University Hospital, South Korea.

Yoonhyuk Jang (Y)

Department of Neurology (YJ, Y-WS, KC, SKL, S-TL), Seoul National University Hospital; Department of Neurology (H-RS), Dankook University Hospital, Cheonan; and Department of Neurosurgery (Y-WS), Seoul National University Hospital, South Korea.

Yong-Won Shin (YW)

Department of Neurology (YJ, Y-WS, KC, SKL, S-TL), Seoul National University Hospital; Department of Neurology (H-RS), Dankook University Hospital, Cheonan; and Department of Neurosurgery (Y-WS), Seoul National University Hospital, South Korea.

Kon Chu (K)

Department of Neurology (YJ, Y-WS, KC, SKL, S-TL), Seoul National University Hospital; Department of Neurology (H-RS), Dankook University Hospital, Cheonan; and Department of Neurosurgery (Y-WS), Seoul National University Hospital, South Korea.

Sang Kun Lee (SK)

Department of Neurology (YJ, Y-WS, KC, SKL, S-TL), Seoul National University Hospital; Department of Neurology (H-RS), Dankook University Hospital, Cheonan; and Department of Neurosurgery (Y-WS), Seoul National University Hospital, South Korea.

Soon-Tae Lee (ST)

Department of Neurology (YJ, Y-WS, KC, SKL, S-TL), Seoul National University Hospital; Department of Neurology (H-RS), Dankook University Hospital, Cheonan; and Department of Neurosurgery (Y-WS), Seoul National University Hospital, South Korea.

Classifications MeSH