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Neurological and Psychological Sequelae Associated With Multisystem Inflammatory Syndrome in Children
Caitlin K Rollins1,2, Johanna Calderon1,3,4, David Wypij5,6,7
1Department of Neurology, Boston Children's Hospital, Boston, Massachusetts.
Insights
Children with multisystem inflammatory syndrome (MIS-C) experience lasting neurological and psychological effects, including impaired working memory and reduced quality of life, 6-12 months post-discharge.
Area of Science:
- Pediatric neurology
- Infectious diseases
- Child psychology
Background:
- Multisystem inflammatory syndrome in children (MIS-C) can cause acute neurological issues.
- Long-term neurological, psychological, and cognitive sequelae in MIS-C survivors are not well-documented.
- Direct assessments of cognitive function 6-12 months post-discharge are lacking.
Purpose of the Study:
- To characterize neurological, psychological, and quality of life sequelae in children after MIS-C.
- To compare outcomes in MIS-C patients with sibling or community controls.
Main Methods:
- Cross-sectional cohort study in the US and Canada (November 2020-November 2021).
- Remote neurological examination and neuropsychological assessments (cognition, behavior, quality of life, daily function).
- Generalized estimating equations used for group comparisons.
Main Results:
- MIS-C patients (n=64) showed more frequent neurological abnormalities than controls (n=44) (25% vs 7%).
- MIS-C group had lower working memory scores (executive functioning) and similar performance on most other cognitive measures.
- Parents reported worse psychological outcomes (depression, somatization) and lower quality of life in MIS-C survivors.
Conclusions:
- Children with MIS-C exhibit persistent neurological and psychological deficits 6-12 months post-discharge.
- Findings include abnormal neurologic exams, impaired working memory, increased somatization/depression, and reduced quality of life.
- Enhanced monitoring is recommended for early detection and treatment of these sequelae.
Importance:
Acute neurological involvement occurs in some patients with multisystem inflammatory syndrome in children (MIS-C), but few data report neurological and psychological sequelae, and no investigations include direct assessments of cognitive function 6 to 12 months after discharge.
Objective:
To characterize neurological, psychological, and quality of life sequelae after MIS-C.
Design, Setting, And Participants:
This cross-sectional cohort study was conducted in the US and Canada. Participants included children with MIS-C diagnosed from November 2020 through November 2021, 6 to 12 months after hospital discharge, and their sibling or community controls, when available. Data analysis was performed from August 2022 to May 2023.
Exposure:
Diagnosis of MIS-C.
Main Outcomes And Measures:
A central study site remotely administered a onetime neurological examination and in-depth neuropsychological assessment including measures of cognition, behavior, quality of life, and daily function. Generalized estimating equations, accounting for matching, assessed for group differences.
Results:
Sixty-four patients with MIS-C (mean [SD] age, 11.5 [3.9] years; 20 girls [31%]) and 44 control participants (mean [SD] age, 12.6 [3.7] years; 20 girls [45%]) were enrolled. The MIS-C group exhibited abnormalities on neurological examination more frequently than controls (15 of 61 children [25%] vs 3 of 43 children [7%]; odds ratio, 4.7; 95% CI, 1.3-16.7). Although the 2 groups performed similarly on most cognitive measures, the MIS-C group scored lower on the National Institutes of Health Cognition Toolbox List Sort Working Memory Test, a measure of executive functioning (mean [SD] scores, 96.1 [14.3] vs 103.1 [10.5]). Parents reported worse psychological outcomes in cases compared with controls, particularly higher scores for depression symptoms (mean [SD] scores, 52.6 [13.1] vs 47.8 [9.4]) and somatization (mean [SD] scores, 55.5 [15.5] vs 47.0 [7.6]). Self-reported (mean [SD] scores, 79.6 [13.1] vs 85.5 [12.3]) and parent-reported (mean [SD] scores, 80.3 [15.5] vs 88.6 [13.0]) quality of life scores were also lower in cases than controls.
Conclusions And Relevance:
In this cohort study, compared with contemporaneous sibling or community controls, patients with MIS-C had more abnormal neurologic examinations, worse working memory scores, more somatization and depression symptoms, and lower quality of life 6 to 12 months after hospital discharge. Although these findings need to be confirmed in larger studies, enhanced monitoring may be warranted for early identification and treatment of neurological and psychological symptoms.
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