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Treatment of Infants and Children With SARS-CoV-2 Monoclonal Antibodies: A European Case Series.
Rau, Cornelius; Auer-Hackenberg, Lorenz; Deubzer, Hedwig E; Schwabel, Elisabeth; Jaros, Maria; Diederichs, Antonia; Lehrnbecher, Thomas; Holm, Mette; von Linstow, Marie-Louise; Martin, Luise; Dinges, Sarah Svenja; Rothensteiner, Maria; Siepermann, Meinolf; Strenger, Volker; von Both, Ulrich; Teig, Norbert; Brinkmann, Folke; Leeb, Franziska; Zeitlinger, Markus; Kobbe, Robin; Götzinger, Florian.
  • Rau C; From the Department of Neonatology and Paediatric Intensive Care, University Children's Hospital, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Auer-Hackenberg L; Department of Paediatrics and Adolescent Medicine, Division of Neonatology, Paracelsus Medical University Salzburg, Salzburg, Austria.
  • Deubzer HE; Department of Paediatric Haematology and Oncology, Charité-Universitätsmedizin Berlin, Berlin, Germany, Berliner Institut für Gesundheitsforschung (BIH), Berlin, Germany.
  • Schwabel E; St. Anna Children's Hospital, Vienna, Austria.
  • Jaros M; St. Anna Children's Hospital, Vienna, Austria.
  • Diederichs A; Division of Paediatric Haematology and Oncology, Hospital for Children and Adolescents, Johann Wolfgang Goethe University, Frankfurt, Germany.
  • Lehrnbecher T; Division of Paediatric Haematology and Oncology, Hospital for Children and Adolescents, Johann Wolfgang Goethe University, Frankfurt, Germany.
  • Holm M; Department of Paediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus N, Denmark.
  • von Linstow ML; Department of Paediatrics and Adolescent Medicine, The Juliane Marie Centre, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Martin L; Department of Paediatric Respiratory Medicine, Immunology and Critical Care Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Dinges SS; Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt - Universität zu Berlin, and Berlin Institute of Health; Medical Directorate, Berlin, Germany.
  • Rothensteiner M; Department of Paediatric Respiratory Medicine, Immunology and Critical Care Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Siepermann M; Department of Paediatrics and Adolescent Medicine, National Reference Centre for Childhood Tuberculosis, Klinik Ottakring, Vienna, Austria.
  • Strenger V; Department of Paediatric Haematology and Oncology, Children's Hospital Amsterdam Street, Cologne, Germany.
  • von Both U; Department of Paediatrics and Adolescent Medicine, Division of Paediatric Pulmonology and Allergology, Medical University Graz, Graz, Austria.
  • Teig N; Department of Paediatrics and Adolescent Medicine, Division of General Paediatrics, Medical University Graz, Graz, Austria.
  • Brinkmann F; Department of Paediatric Infectious Diseases, Hauner Children's Hospital, LMU University Hospital, Ludwig Maximilians University, Munich, Germany.
  • Leeb F; Departments of Neonatology and Paediatric Intensive Care.
  • Zeitlinger M; Paediatric Pulmonology, Ruhr University Bochum, Bochum, Germany.
  • Kobbe R; Departments of Pediatrics and Adolescent Medicine, Division of Pediatric Pulmonology, Allergology and Endocrinology.
  • Götzinger F; Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
Pediatr Infect Dis J ; 42(2): 125-129, 2023 02 01.
Article in English | MEDLINE | ID: covidwho-2190925
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.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Leukopenia Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Topics: Variants Limits: Adult / Child / Child, preschool / Humans / Infant Language: English Journal: Pediatr Infect Dis J Journal subject: Communicable Diseases / Pediatrics Year: 2023 Document Type: Article Affiliation country: Inf.0000000000003773

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Leukopenia Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Topics: Variants Limits: Adult / Child / Child, preschool / Humans / Infant Language: English Journal: Pediatr Infect Dis J Journal subject: Communicable Diseases / Pediatrics Year: 2023 Document Type: Article Affiliation country: Inf.0000000000003773