Clinical features and outcomes in children with seronegative autoimmune encephalitis

Author:

Madani Jihan1,Yea Carmen2,Mahjoub Areej1,Brna Paula3,Jones Kevin4,Longoni Giulia1,Nouri Maryam Nabavi5,Rizk Tamer6,Stewart Wendy A.6,Wilbur Colin7ORCID,Yeh E. Ann12ORCID

Affiliation:

1. Division of Neurology, Department of Pediatrics The Hospital for Sick Children, University of Toronto Toronto Ontario Canada

2. Neurosciences and Mental Health Program SickKids Research Institute, The Hospital for Sick Children Toronto Ontario Canada

3. Division of Neurology Dalhousie University IWK Health Center Halifax Nova Scotia Canada

4. Division of Neurology McMaster University Hamilton Ontario Canada

5. Division of Pediatric Neurology, Department of Pediatrics Children's Hospital, London Health Science Center London Ontario Canada

6. Pediatric Neurology, Department of Pediatrics Saint John Regional Hospital St. John New Brunswick Canada

7. Division of Neurology, Department of Pediatrics University of Alberta Alberta Canada

Abstract

AbstractAimTo characterize the presenting features and outcomes in children with seronegative autoimmune encephalitis, and to evaluate whether scores at nadir for the Modified Rankin Scale (mRS) and Clinical Assessment Scale for Autoimmune Encephalitis (CASE) or its paediatric‐specific modification (ped‐CASE) are predictive of outcomes.MethodThis observational study included children younger than 18 years of age with seronegative autoimmune encephalitis. Demographics and clinical data were collected. The mRS and CASE/ped‐CASE scores were used to evaluate disease severity. Descriptive statistics and logistic regression were used for data analysis and to evaluate associations between scale scores and outcomes.ResultsSixty‐three children were included (39 [62%] females, median age 7 years, interquartile range [IQR] 4 years 1 months–11 years 6 months), with follow‐up available for 56 out of 63 patients (median follow‐up 12.2 months, IQR 13.4–17.8). The most frequent presenting neurological manifestation was encephalopathy (81%). Median CASE/ped‐CASE and mRS scores at nadir were 12.0 (IQR 7.0–17.0) and 1.0 (IQR 0–2.0) respectively. Thirty‐three patients (59%) had persistent neurological deficits at follow‐up. Both scoring systems suggested good functional recovery (mRS score ≤2, 95%; CASE/ped‐CASE score <5, 91%). CASE/ped‐CASE score was more likely than mRS to distinguish children with worse outcomes.InterpretationChildren with seronegative autoimmune encephalitis are likely to have neurological deficits at follow‐up. CASE/ped‐CASE is more likely to distinguish children with worse outcomes than MRS.What this paper adds Encephalopathy was the most common reason for presentation in children with seronegative autoimmune encephalitis. Children with seronegative autoimmune encephalitis are likely to have neurological deficits at follow‐up. The Clinical Assessment Scale for Autoimmune Encephalitis or its paeditric version at nadir was better at distinguishing children with poor outcomes than the Modified Rankin Scale.

Funder

Biogen

Publisher

Wiley

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