Treatment and care received by children hospitalized with COVID-19 in a large hospital network in the United States, February 2020 to September 2021

PLoS One. 2023 Jul 11;18(7):e0288284. doi: 10.1371/journal.pone.0288284. eCollection 2023.

Abstract

We described care received by hospitalized children with COVID-19 or multi-system inflammatory syndrome (MIS-C) prior to the 2021 COVID-19 Omicron variant surge in the US. We identified hospitalized children <18 years of age with a COVID-19 or MIS-C diagnosis (COVID-19 not required), separately, from February 2020-September 2021 (n = 126 hospitals). We described high-risk conditions, inpatient treatments, and complications among these groups. Among 383,083 pediatric hospitalizations, 2,186 had COVID-19 and 395 had MIS-C diagnosis. Less than 1% had both COVID-19 and MIS-C diagnosis (n = 154). Over half were >6 years old (54% COVID-19, 70% MIS-C). High-risk conditions included asthma (14% COVID-19, 11% MIS-C), and obesity (9% COVID-19, 10% MIS-C). Pulmonary complications in children with COVID-19 included viral pneumonia (24%) and acute respiratory failure (11%). In reference to children with COVID-19, those with MIS-C had more hematological disorders (62% vs 34%), sepsis (16% vs 6%), pericarditis (13% vs 2%), myocarditis (8% vs 1%). Few were ventilated or died, but some required oxygen support (38% COVID-19, 45% MIS-C) or intensive care (42% COVID-19, 69% MIS-C). Treatments included: methylprednisolone (34% COVID-19, 75% MIS-C), dexamethasone (25% COVID-19, 15% MIS-C), remdesivir (13% COVID-19, 5% MIS-C). Antibiotics (50% COVID-19, 68% MIS-C) and low-molecular weight heparin (17% COVID-19, 34% MIS-C) were frequently administered. Markers of illness severity among hospitalized children with COVID-19 prior to the 2021 Omicron surge are consistent with previous studies. We report important trends on treatments in hospitalized children with COVID-19 to improve the understanding of real-world treatment patterns in this population.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • COVID-19* / complications
  • COVID-19* / epidemiology
  • COVID-19* / therapy
  • Child
  • Hospitals
  • Humans
  • SARS-CoV-2
  • Systemic Inflammatory Response Syndrome
  • United States / epidemiology

Supplementary concepts

  • pediatric multisystem inflammatory disease, COVID-19 related
  • SARS-CoV-2 variants

Grants and funding

This study was a Sentinel System study. The Sentinel System is funded by the U.S. Food and Drug Administration (FDA) through the Department of Health and Human Services contract number 75F40119D10037. CCF, AC, MS, ER, KH, CH, RP, NMC are employees of Harvard Pilgrim Health Care Institute, a non-profit organization that conducts work for government and private organizations, including pharmaceutical companies. JP, REP, KES, LEM are employees of HCA Healthcare. The funder had no role in data collection and analysis. Employees of the funding organization, the US FDA (NP, PB, SKD), contributed as coauthors to the design and conduct of the study; interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication. The FDA had the opportunity to review the final manuscript but did not have the right to either prevent publication or direct it to a specific journal.