Pham Thai Son, Tam Tran, Mohammed Abdellatif, Nguyen Ngoc Tuong Vi, Nguyen Hoang Phuong Anh, Nguyen Le Trung Hieu, Soe Mar, Nguyen Tien Huy
Our results suggest that the NEOS score could be a useful prognostic tool for identifying poor outcomes in children with antibody-negative AE, but may lack discriminatory value in anti-NMDAR cases. Further multicenter prospective studies are needed to validate these findings and optimize prognostic tools for pediatric autoimmune encephalitis.
BACKGROUND: Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis and antibody-negative autoimmune encephalitis (AE) are important contributors to pediatric neurological morbidities; however, long-term outcomes and prognostic scores in these entities remain poorly defined, particularly in resource-limited areas.
OBJECTIVE: To evaluate the predictive value of prognosis of the anti-NMDAR Encephalitis One-Year Functional Status (NEOS) score in children with antibody-negative and anti-NMDAR AE in Vietnam.
METHODS: We performed a retrospective and prospective cohort study of children with AE, evaluated at Children's Hospital 2 (CH2), Vietnam between January 2019 and June 2022, with follow-up completed in August 2023. Outcomes were evaluated at discharge and at final follow-up by the modified Rankin Scale (mRS). The NEOS score, estimated at initial hospitalization, was used to predict poor outcomes (mRS ≥ 2).
RESULTS: This study included 82 pediatric patients with AE (<16 years old, 40 with anti-NMDAR encephalitis and 42 with antibody-negative AE), with median ages of 6.7 years (IQR: 4.2-12.2) and 7.4 years (IQR: 4.6-9.6), respectively. NEOS scores and complete outcome data were available for 78 patients (39 per group). At final follow-up, 79.5% of anti-NMDAR patients and 75.0% of antibody-negative AE patients achieved good functional outcomes (mRS 0-1), showing no significant between-group difference (p = 0.634). In antibody-negative AE, the NEOS score demonstrated predictive value for poor outcomes (mRS ≥ 2) with an AUC of 0.785 (p = 0.010), achieving 90% specificity and 55.6% sensitivity at a cut-off > 2, while showing no predictive ability in anti-NMDAR encephalitis (AUC = 0.520, p = 0.862). Both patient groups showed significant functional improvement, with median mRS scores decreasing from 2.0 (IQR: 1-4) at discharge to 0.0 (IQR: 0-1) at follow-up (p < 0.001). Follow-up assessments were conducted at a median of 19.5 months (IQR: 13.9-26.1) for anti-NMDAR patients and 23.7 months (IQR: 18.5-28.2) for antibody-negative AE patients.
CONCLUSIONS: Our results suggest that the NEOS score could be a useful prognostic tool for identifying poor outcomes in children with antibody-negative AE, but may lack discriminatory value in anti-NMDAR cases. Further multicenter prospective studies are needed to validate these findings and optimize prognostic tools for pediatric autoimmune encephalitis.