Evidence map›Paper›PMID 40455448›Full record

ArticleJAMA network open2025

Neurologic and Psychological Outcomes 2 Years After Multisystem Inflammatory Syndrome in Children.

Caitlin K Rollins, David Wypij, Laura D Zambrano, Johanna Calderon, Alex M Taylor, Jennifer Worhach, Susan Rodriguez, Paul A Licht, Moshe Maiman, Nicholas Hart and 14 more

Abstract read
In one paragraph

Article in JAMA network open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Post-MIS-C cardiovascular outcomes: a systematic review.European journal of pediatrics · 2026
    Pooled it
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Caitlin K RollinsDepartment of Neurology, Boston Children's Hospital, Boston, Massachusetts.
David WypijDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
Laura D ZambranoCoronavirus and Other Respiratory Viruses Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Johanna CalderonNational Institute of Health and Medical Research INSERM U1046, PhyMedExp, Montpellier, France.
Alex M TaylorDepartment of Psychiatry and Behavioral Sciences, Boston Children's Hospital, Boston, Massachusetts.
Jennifer WorhachDepartment of Neurology, Boston Children's Hospital, Boston, Massachusetts.
Susan RodriguezDepartment of Neurology, Boston Children's Hospital, Boston, Massachusetts.
Paul A LichtDepartment of Cardiology, Boston Children's Hospital, Boston, Massachusetts.
Moshe MaimanDepartment of Psychiatry and Behavioral Sciences, Boston Children's Hospital, Boston, Massachusetts.
Nicholas HartDepartment of Neurology, Boston Children's Hospital, Boston, Massachusetts.
Mary Beth F SonDepartment of Pediatrics, Harvard Medical School, Boston, Massachusetts.
Joe KossowskyDepartment of Pediatrics, Harvard Medical School, Boston, Massachusetts.
Matthew L FriedmanDivision of Pediatric Critical Care Medicine, Department of Pediatrics, Indiana University School of Medicine and Riley Hospital for Children, Indianapolis.
Charlotte V HobbsDivision of Infectious Diseases, Department of Pediatrics, University of Mississippi Medical Center, Jackson.
Michele KongDivision of Pediatric Critical Care Medicine, Department of Pediatrics, University of Alabama at Birmingham.
Aline B MadduxDepartment of Pediatrics, Section of Critical Care Medicine, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora.
Jennifer L McGuireDivision of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Mary Allen StaatDivision of Infectious Diseases, Department of Pediatrics, University of Cincinnati, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Lael M YonkerDepartment of Pediatrics, Harvard Medical School, Boston, Massachusetts.
Maitreyi MazumdarDepartment of Neurology, Boston Children's Hospital, Boston, Massachusetts.
Jane W NewburgerDepartment of Cardiology, Boston Children's Hospital, Boston, Massachusetts.
Adrienne G RandolphDepartment of Pediatrics, Harvard Medical School, Boston, Massachusetts.
Angela P CampbellCoronavirus and Other Respiratory Viruses Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Overcoming COVID-19 Investigators

Funding

Genetic Analysis and Manipulation Core (GAEC)P50HD105351 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI Hisashi Umemori · 2021 to 2026
$9.4M
Defining neutrophil pathobiology in pediatric Long COVIDR01HL173059 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI Lael Yonker · 2024 to 2026
$2.4M
Fetal Brain MRI as a Predictor of Late Neurodevelopmental Outcome in Congenital Heart DiseaseR01NS121334 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI Caitlin Rollins · 2022 to 2026
$2.2M
NHLBI NIH HHS R01 HL173059NICHD NIH HHS P50 HD105351NINDS NIH HHS R01 NS121334
6 · The paper itself

Abstract

Importance: Neurologic and psychological sequelae are observed 1 year after hospitalization for multisystem inflammatory syndrome in children (MIS-C), but whether these concerns persist is not known. Objective: To examine the trajectory of neurologic, psychological, and quality-of-life sequelae up to 2 years after MIS-C. Design, Setting, and Participants: This longitudinal cohort study assessed children diagnosed with MIS-C from August 1, 2020, to August 31, 2021, and matched sibling and community controls, when available. The study was conducted 6 to 12 months and 18 to 24 months after discharge from a US or Canadian hospital. Data analysis was performed from May 2024 to January 2025. Exposure: Hospitalization for MIS-C. Main Outcomes and Measures: A central study site remotely administered a structured interview, surveys, neuropsychological assessment, and neurologic examination. Group differences were assessed using generalized estimating equations, accounting for matching. Variables extracted from hospital records included intensive care unit admission and echocardiographic left ventricular ejection fraction (LVEF). Results: Overall, 95 participants were included in the study; 93 of 108 participants (86%) returned from the year 1 study and 2 participants were added in year 2 (median [IQR] age, 12.6 [11.0-15.7] years; 38 [40%] female and 57 [60%] male). Fifty-nine patients with MIS-C (mean [SD] age, 13.2 [4.0] years; 39 [66%] male) and 36 controls (mean [SD] age, 13.5 [3.5] years; 18 [50%] male) enrolled. In year 2, the MIS-C group was similar to controls on all outcome measures, except they had more somatization symptoms (Behavior Assessment Scale for Children, Third Edition mean [SD] somatization score, 52.1 [13.0] vs 46.5 [8.5]; mean difference, 5.2; 95% CI, 1.3-9.1). Within the MIS-C group, scores generally improved between initial and follow-up evaluations, a finding that was not observed in controls. Eight of 13 children with MIS-C (62%) who had abnormal neurologic examination findings in year 1 had normal examination findings by year 2. Among patients with MIS-C, measures of higher illness severity during hospitalization were associated with worse executive function in year 2 (National Institutes of Health [NIH] List Sort Working Memory Test score, -7.3 points per intensive care unit admission vs not [95% CI, -14.3 to -0.3 points] and -5.8 points per LVEF category change [95% CI, -9.1 to -2.6 points]; verbal fluency switching score, -0.8 points per LVEF category change [95% CI, -1.5 to -0.1 points]). Conclusions and Relevance: In this longitudinal, matched cohort study of children with MIS-C and controls followed up sequentially up to 2 years after hospital discharge, children with MIS-C had more somatic symptoms than control children. Overall, however, patients with MIS-C had improved neurologic and psychological outcomes between the testing intervals, performing similarly to controls on most measures by year 2 follow-up. These findings suggest that these concerns may improve over time.

Indexed as

COVID-19Nervous System DiseasesQuality of LifeSystemic Inflammatory Response SyndromeAdolescentCanadaChildChild, PreschoolFemaleHospitalizationHumansLongitudinal StudiesMaleSARS-CoV-2

Identifiers

PMID40455448
PMCPMC12131094

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.