Post-MIS-C cardiovascular outcomes: a systematic review
- Giancarlo Alvarado-Gamarrai, k(Author),
- Katherine Alcala-Marcosg(Author),
- Carlos R. Celisi(Author),
- Pía Balmaceda-Nietof(Author),
- Luigi Ciezai(Author),
- Cristian Morán-Mariñosb(Author)
- ,
- bUniversidad San Ignacio de Loyola,
- cHospital Daniel Alcides Carrión,
- dVanderbilt University Medical Centre,
- eUniversidad Peruana Cayetano Heredia,
- fUniversity of Utah School of Medicine
Publication Information
Output type
Original language
EnglishArticle number
140Journal (Volume, Issue Number)
European Journal of Pediatrics (Volume 185, Issue 3)Publication milestones
- Published- 03/2026
Publication status
ISSN
0340-6199External Publication IDs
- Scopus: 105030547491
- PubMed: 41721085
Abstract
Limited knowledge and variability in findings exist regarding the resolution of cardiovascular outcomes following Multisystem Inflammatory Syndrome in Children (MIS-C). We conducted a systematic review to estimate the frequency of cardiovascular outcomes following MIS-C. A systematic search was conducted in Pubmed/Medline, Scopus, Embase, SciELO, LILACS, Cochrane Library, Web of Science, and medRxiv were searched up to February 2024. We included studies reporting cardiovascular events that began in acute MIS-C and persisted after discharge. Screening and data extraction were performed by independent reviewers. We performed a random-effects meta-analysis and assessed the certainty of the evidence using the GRADE approach. Eighty-four studies (n = 4,778) were included; seven had a comparator group. The frequency of cardiovascular outcomes—including coronary abnormalities (Z-score ≥ 2), left ventricle ejection fraction < 55%, diastolic dysfunction, myocarditis, and pericardial effusion—decreased over time, with most resolving by 6 to 9 months. However, cardiac magnetic resonance imaging studies identified myocardial edema and/or fibrosis persisting up to 12 months, and two studies reported coronary abnormalities at 18- to 24-month follow-up. Evidence certainty was very low. Compared to children with COVID-19 or healthy controls, MIS-C showed more cardiovascular events and greater subclinical myocardial dysfunction, as assessed by strain analysis, during a 6-month follow-up. Compared with other etiologies of myocarditis, MIS-C myocarditis was associated with better cardiovascular outcomes but shorter exercise duration and lower aerobic capacity on stress testing. Conclusions: Cardiovascular outcomes following MIS-C improved over time, but certain subclinical cardiac abnormalities persisted up to 12 to 24 months. These findings may support long-term follow-up after MIS-C. Trial registration: Protocol registration number: PROSPERO, CRD42022336784.
