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Multisystem Inflammatory Syndrome in Children: Follow-Up of a Cohort from North India.
Awasthi, Puspraj; Kumar, Vijay; Naganur, Sanjeev; Nallasamy, Karthi; Angurana, Suresh Kumar; Bansal, Arun; Manoj, Rohit Kumar; Jayashree, Muralidharan.
  • Awasthi P; Division of Pediatric Critical Care, Department of Pediatrics, Advanced Pediatrics Centre, Chandigarh, India.
  • Kumar V; Division of Pediatric Critical Care, Department of Pediatrics, Advanced Pediatrics Centre, Chandigarh, India.
  • Naganur S; Department of Cardiology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
  • Nallasamy K; Division of Pediatric Critical Care, Department of Pediatrics, Advanced Pediatrics Centre, Chandigarh, India.
  • Angurana SK; Division of Pediatric Critical Care, Department of Pediatrics, Advanced Pediatrics Centre, Chandigarh, India.
  • Bansal A; Division of Pediatric Critical Care, Department of Pediatrics, Advanced Pediatrics Centre, Chandigarh, India.
  • Manoj RK; Department of Cardiology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
  • Jayashree M; Division of Pediatric Critical Care, Department of Pediatrics, Advanced Pediatrics Centre, Chandigarh, India.
Am J Trop Med Hyg ; 2022 Feb 16.
Article in English | MEDLINE | ID: covidwho-1689935
ABSTRACT
Multisystem inflammatory syndrome in children (MIC-S) is a hyperinflammatory manifestation of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection. Information on the long-term outcome of MIS-C is limited. This study was conducted to describe the long-term outcome of MIS-C from a tertiary care center in North India. Children admitted with MIS-C from September 2020 to January 2021 were followed up after discharge until June 2021. The details during the acute phase (clinical features, investigations, treatment, and outcome) and follow-up (symptoms, echocardiographic findings, ongoing treatment, and outcome) were collected retrospectively. During the acute phase, 40 children presented at median (interquartile range [IQR]) age of 7 (5-10) years with fever, mucocutaneous, gastrointestinal, and respiratory symptoms. The majority (66.7%) of the children had positive SARS-CoV-2 serology and elevated inflammatory markers (C-reactive protein, procalcitonin, ferritin, D-dimer, and fibrinogen), lymphopenia, and thrombocytopenia. Eighty percent had shock, 72.5% had myocardial dysfunction (left ventricular ejection fraction <55%), and 22.5% had coronary artery dilatation or aneurysm. Treatment included pediatric intensive care unit admission (85%), intravenous immunoglobulin (100%), steroids (85%), aspirin (80%), vasoactive drugs (72.5%), and invasive mechanical ventilation (22.5%). Two (5%) children died because of refractory shock. Thirty-four children were followed up with until a median (IQR) of 5 (3-6) months. During the follow-up, a majority were asymptomatic, myocardial function returned to normal in all, and only one had coronary artery aneurysm. Prednisolone and aspirin were given for a median (IQR) of 3 (2-4) weeks and 4 (4-6) weeks after discharge, respectively. There was one readmission and no death during the follow-up. To conclude, the long-term outcome of MIS-C is generally favorable with resolution of cardiovascular manifestations (myocardial dysfunction and coronary artery changes) in the majority of children during follow-up.

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid Language: English Year: 2022 Document Type: Article Affiliation country: Ajtmh.21-0801

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid Language: English Year: 2022 Document Type: Article Affiliation country: Ajtmh.21-0801