Literature DB >> 31917096

Seizure Characteristics, Outcome, and Risk of Epilepsy in Pediatric Anti-N-Methyl-d-Aspartate Receptor Encephalitis.

Xin-Ping Qu1, Jorge Vidaurre2, Xiao-Ling Peng3, Li Jiang1, Min Zhong1, Yue Hu4.   

Abstract

BACKGROUND: We identified seizure characteristics, long-term outcome, and predictors of persistent seizures in children with anti-N-methyl-d-aspartate receptor (anti-NMDAR) encephalitis.
METHOD: Data were analyzed from patients with anti-NMDAR encephalitis who presented with seizures at our center between August 2012 and June 2018.
RESULTS: Sixty-two of 86 patients with anti-NMDAR encephalitis experienced seizures. Seizures occurred within two weeks of disease onset in 58 of 62 (93.6%) patients; 36 of 62 (58.1%) had seizures as the initial symptom. Males were more likely to exhibit seizures as the initial symptom (P = 0.039). More than a quarter of patients (17 of 62, 27.4%) manifested two or more seizure types. Focal seizures were the most common (46 of 62, 74.2%). Status epilepticus occurred in 27 of 62 (43.5%) patients, and nonconvulsive status epilepticus, in two of 62 (3.2%) patients. No patient developed refractory status epilepticus. No systemic tumors were found. Electroencephalographic abnormalities included background slowing (77.4%), absence of a posterior dominant rhythm (62.9%), interictal epileptic discharges (50.0%), and extreme delta brush (6.5%). In the acute phase, 45 patients (45 of 62, 72.6%) received antiepileptic drugs. Persistent seizures occurred in only five of 62 (8%) patients. On univariate analysis, status epilepticus and combination antiepileptic drug treatment were associated with persistent seizures, but neither independently predicted persistent seizures.
CONCLUSIONS: Multiple seizure types may develop at any stage of anti-N-methyl-d-aspartate receptor encephalitis. Refractory status epilepticus, systemic tumors, and extreme delta brush in electroencephalography are rare in pediatric patients. Anti-NMDAR encephalitis-associated seizures appear to have good prognosis, without the need for long-term antiepileptic drug treatment.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Anti-NMDAR encephalitis; Autoimmune encephalitis; EEG; Pediatrics; Seizures; Status epilepticus

Mesh:

Year:  2019        PMID: 31917096     DOI: 10.1016/j.pediatrneurol.2019.11.011

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  3 in total

1.  Electroencephalography characteristics to predict one-year outcomes in pediatric anti-NMDA receptor encephalitis.

Authors:  Jenny Lin; Kathryn Elkins; Sonam Bhalla; Satyanarayana Gedela; Ammar Kheder; Guojun Zhang; Leah Loerinc; Laura Blackwell; Robyn Howarth; Grace Gombolay
Journal:  Epilepsy Res       Date:  2021-10-22       Impact factor: 2.991

Review 2.  Diagnostic Value of Structural and Functional Neuroimaging in Autoimmune Epilepsy.

Authors:  Limei Luo; Nian Wei; Jing Wang; Yuemei Luo; Fei Yang; Zucai Xu
Journal:  Contrast Media Mol Imaging       Date:  2020-12-14       Impact factor: 3.161

3.  Serum-Derived Exosomal miR-140-5p as a Promising Biomarker for Differential Diagnosis of Anti-NMDAR Encephalitis With Viral Encephalitis.

Authors:  Xiaofeng Liu; Kengna Fan; Qingwen Lin; Minjie Tang; Qi Wang; Er Huang; Weiqing Zhang; Tianbin Chen; Qishui Ou
Journal:  Front Immunol       Date:  2022-02-22       Impact factor: 7.561

  3 in total

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