Treatment of Infants and Children With SARS-CoV-2 Monoclonal Antibodies: A European Case Series

  • Cornelius Rau (Geteilte/r Erstautor/in)
  • Lorenz Auer-Hackenberg (Geteilte/r Erstautor/in)
  • Hedwig E Deubzer
  • Elisabeth Schwabel
  • Maria Jaros
  • Antonia Diederichs
  • Thomas Lehrnbecher
  • Mette Holm
  • Marie-Louise von Linstow
  • Luise Martin
  • Sarah Svenja Dinges
  • Maria Rothensteiner
  • Meinolf Siepermann
  • Volker Strenger
  • Ulrich von Both
  • Norbert Teig
  • Folke Brinkmann
  • Franziska Leeb
  • Markus Zeitlinger
  • Robin Kobbe (Geteilte/r Letztautor/in)
  • Florian Götzinger (Geteilte/r Letztautor/in)

Abstract

BACKGROUND: Although severe COVID-19 in children is rare, those with certain pre-existing health conditions are more prone to severe disease. Monoclonal antibodies (mAbs) against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are potent antiviral agents that reduce adverse clinical outcomes in adults, but are commonly not approved for use in pediatric patients.

METHODS: We retrospectively evaluated mAb treatment in children <12 years of age or <40kg with SARS-CoV-2 infection between January 1, 2021, and March 7, 2022, in 12 tertiary care centers in 3 European countries.

RESULTS: We received data from 53 patients from Austria, Denmark and Germany. Median age was 5.4 years [0-13.8, interquartile range (IQR) = 6.2], and median body weight was 20 kg (3-50.1, IQR = 13). The most frequent SARS-CoV-2 variant in this study, if known, was Omicron, followed by Delta and Alpha. Pre-existing conditions included immunodeficiency, malignancy, hematologic disease, cardiac disease, chronic lung disease, chronic liver disease, kidney disease and diabetes. Forty-two patients received sotrovimab (79%), 9 casirivimab/imdevimab (17%) and 2 bamlanivimab (4%). All but 1 patient survived. Median duration of hospital stay was 3 days (0-56, IQR = 6). Seven patients required treatment in an intensive care unit, and 5 required high-flow nasal cannula treatment. Potential side effects included neutropenia (6/53, 11%), lymphopenia (3/53, 6%), nausea or vomiting (2/53, 4%), rise of alanine transaminase (1/53, 2%) and hypotonia (1/53, 2%).

CONCLUSIONS: MAb treatment was well tolerated by children in this cohort.

Bibliografische Daten

OriginalspracheEnglisch
ISSN0891-3668
DOIs
StatusVeröffentlicht - 01.02.2023

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PubMed 36638398