Short to midterm follow-up of multi-system inflammatory syndrome in children with special reference to cardiac involvement.


Journal

Cardiology in the young
ISSN: 1467-1107
Titre abrégé: Cardiol Young
Pays: England
ID NLM: 9200019

Informations de publication

Date de publication:
Mar 2023
Historique:
pubmed: 25 3 2022
medline: 17 3 2023
entrez: 24 3 2022
Statut: ppublish

Résumé

We aim to describe the early and upto 16 months follow-up of post-coronavirus disease (COVID), multi-system inflammatory syndrome in children (MIS-C), with special reference to cardiac involvement. This cohort non-interventional descriptive study included patients <18 years admitted between May, 2020 and April, 2021. Based on underlying similarities, children were classified as post-COVID MIS-C with overlapping Kawasaki Disease, MIS-C with no overlapping Kawasaki Disease, and MIS-C with shock. Post-discharge, patients were followed at 1, 3, 6, 12, and 16 months. Forty-one patients predominantly males (73%), at median age of 7 years (range 0.2-16 years) fulfilled the World Health Organisation criteria for MIS-C. Cardiac involvement was seen in 15 (36.5%); impaired left ventricle (LV) function in 5 (12.2%), coronary artery involvement in 10 (24.4%), pericardial effusion in 6 (14.6%) patients, and no arrhythmias. There were two hospital deaths (4.9%), both in MIS-C shock subgroup (2/10, 20%). At 1 month, there was persistent LV dysfunction in 2/5, coronary artery abnormalities in 7/10, and pericardial effusion resolved completely in all patients. By 6 months, LV function returned to normal in all but coronary abnormalities persisted in two patients. At last follow-up (median 9.8 months, interquartile range 2-16 months), in 36/38 (94.7%) patients, coronary artery dilatation was persistent in 2 (20%) patients. Children with MIS-C have a good early outcome, though MIS-C with shock can be life-threatening subgroup in a resource-constrained country setting. On midterm follow-up, there is normalisation of LV function in all and recovery of coronary abnormalities in 80% of patients.

Identifiants

pubmed: 35321771
pii: S1047951122000828
doi: 10.1017/S1047951122000828
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

371-379

Auteurs

Omeir A Aziz (OA)

Department of Paediatric Cardiology, The Children's Hospital, University of Child Health Sciences, Lahore, Pakistan.

Masood Sadiq (M)

Department of Paediatric Cardiology, The Children's Hospital, University of Child Health Sciences, Lahore, Pakistan.

Ahmad U Qureshi (AU)

Department of Paediatric Cardiology, The Children's Hospital, University of Child Health Sciences, Lahore, Pakistan.

Najam Hyder (N)

Department of Paediatric Cardiology, The Children's Hospital, University of Child Health Sciences, Lahore, Pakistan.

Uzma Kazmi (U)

Department of Paediatric Cardiology, The Children's Hospital, University of Child Health Sciences, Lahore, Pakistan.

Afsheen Batool (A)

Department of Paediatrics, The Children's Hospital, University of Child Health Sciences, Lahore, Pakistan.

Samia Naz (S)

Department of Paediatrics, The Children's Hospital, University of Child Health Sciences, Lahore, Pakistan.

Asma Mushtaq (A)

Department of Paediatrics, The Children's Hospital, University of Child Health Sciences, Lahore, Pakistan.

Attia Bari (A)

Department of Paediatrics, The Children's Hospital, University of Child Health Sciences, Lahore, Pakistan.

Junaid Rashid (J)

Department of Paediatrics, The Children's Hospital, University of Child Health Sciences, Lahore, Pakistan.

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