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Six-Month Outcomes in the Long-Term Outcomes After the Multisystem Inflammatory Syndrome in Children Study

24Citations signalées — pas une note de qualité
58Institutions déclarées
2Pays d’affiliation déclarés

Résumé fourni par la source

Importance: Multisystem inflammatory syndrome in children (MIS-C) is a life-threatening complication of COVID-19 infection. Data on midterm outcomes are limited. Objective: To characterize the frequency and time course of cardiac dysfunction (left ventricular ejection fraction [LVEF] <55%), coronary artery aneurysms (z score ≥2.5), and noncardiac involvement through 6 months after MIS-C. Design, Setting, and Participants: This cohort study enrolled participants between March 2020 and January 2022 with a follow-up period of 2 years. Participants were recruited from 32 North American pediatric hospitals, and all participants met the 2020 Centers for Disease Control and Prevention case definition of MIS-C. Exposure: MIS-C after COVID-19 infection. Main Outcomes and Measures: Outcomes included echocardiography core laboratory (ECL) assessments of LVEF and maximum coronary artery z scores (zMax); data collection on cardiac and noncardiac sequelae during hospitalization and at 2 weeks, 6 weeks, and 6 months after discharge; and age-appropriate Patient-Reported Outcomes Measurement Information Systems (PROMIS) Global Health Instruments at follow-up. Descriptive statistics, linear regression models, and Kaplan-Meier analysis were used. Results: Of 1204 participants (median [IQR] age, 9.1 [5.6-12.7] years; 724 male [60.1%]), 325 self-identified with non-Hispanic Black race (27.0%) and 324 with Hispanic ethnicity (26.9%). A total of 548 of 1195 participants (45.9%) required vasoactive support, 17 of 1195 (1.4%) required extracorporeal membrane oxygenation, and 3 (0.3%) died during hospitalization. Of participants with echocardiograms reviewed by the ECL (n = 349 due to budget constraints), 131 of 322 (42.3%) had LVEF less than 55% during hospitalization; of those with follow-up, all but 1 normalized by 6 months. Black race (vs other/unknown race), higher C-reactive protein level, and abnormal troponin level were associated with lowest LVEF (estimate [SE], -3.09 [0.98]; R2 = 0.14; P =.002). Fifteen participants had coronary artery z scores of 2.5 or greater at any time point; 1 participant had a large/giant aneurysm. Of the 13 participants with z scores of 2.5 or greater during hospitalization, 12 (92.3%) had normalized by 6 months. Return to greater than 90% of pre-MIS-C health status (energy, sleep, appetite, cognition, and mood) was reported by 711 of 824 participants (86.3%) at 2 weeks, increasing to 548 of 576 (95.1%) at 6 months. Fatigue was the most common symptom reported at 2 weeks (141 of 889 [15.9%]), falling to 3.4% (22 of 638) by 6 months. PROMIS Global Health parent/guardian proxy median T scores for fatigue, global health, and pain interference improved significantly from 2 weeks to 6 months (fatigue, 56.1 vs 48.9; global health, 48.8 vs 51.3; pain interference, 53.0 vs 43.3; P < .001) and by the 6-week visit were at least equivalent to prepandemic population norms. Conclusions and Relevance: Results of this cohort study suggest that although children and young adults with MIS-C can have severe disease during the acute phase, most recovered quickly and had a reassuring midterm prognosis.

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Contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Six-Month Outcomes in the Long-Term Outcomes After the Multisystem Inflammatory Syndrome in Children Study
Date Crossref
01/03/2025
Éditeur
American Medical Association (AMA)
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude et ne compte pas comme une seconde source scientifique indépendante.

Institutions déclarées

Primary Children's HospitalEmory UniversityUniversity of UtahChildren's Healthcare of AtlantaNational Institutes of HealthNational Heart, Lung, and Blood InstituteBoston Children's HospitalHarvard UniversityUniversity of ArizonaPhoenix Children's HospitalColumbia University Irving Medical CenterTexas Health DallasChildren's Hospital of WisconsinMedical College of WisconsinLouisiana State UniversityChildren's Hospital of New OrleansDuke UniversityDuke Children's Hospital & Health CenterJoe DiMaggio Children's HospitalUniversity of California San DiegoRady Children's Hospital-San DiegoChildren's Hospital of PhiladelphiaUniversity of PennsylvaniaUniversity of Missouri–Kansas CityBaylor College of MedicineTexas Children's HospitalDell Children's Medical Center of Central TexasChildren's of AlabamaUniversity of Alabama at BirminghamLurie Children's HospitalChildren's Hospital ColoradoUniversity of Colorado AnschutzUniversity of Colorado DenverGeorge Washington UniversityCincinnati Children's Hospital Medical CenterUniversity of TorontoHospital for Sick ChildrenMedical University of South CarolinaNorthwell HealthCohen Children's Medical CenterMiami Children's HospitalRiley Hospital for ChildrenIndiana University School of MedicineIndiana University – Purdue University IndianapolisSeattle Children's HospitalUniversity of WashingtonUniversity of MichiganC. S. Mott Children's HospitalCentral Michigan UniversityChildren's Hospital of MichiganUniversity of Mississippi Medical CenterThe University of Texas Southwestern Medical CenterUniversity of North Carolina at Chapel HillUniversity of KentuckyChildren's Hospital Central CaliforniaUniversity of Southern CaliforniaChildren's Hospital of Los AngelesAlfred I. duPont Hospital for Children

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

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