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Monoclonal Antibody Use for Coronavirus Disease 2019 in Pediatric Patients: A Multicenter Retrospective Study
Gilad Sherman1,2, Gabriella S Lamb1,2, Tanvi S Sharma1,2
1Division of Infectious Diseases, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts, USA.
Insights
Monoclonal antibody treatments for COVID-19 in high-risk pediatric patients showed low rates of adverse events and hospital admissions. This study provides crucial evidence for the safety and efficacy of these therapies in younger populations.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- Pharmacology
Background:
- COVID-19 poses risks to pediatric patients, particularly those with underlying conditions.
- Monoclonal antibodies are authorized for high-risk individuals aged 12 and older.
- Limited data exists on monoclonal antibody use in pediatric populations.
Purpose of the Study:
- To evaluate the safety and effectiveness of monoclonal antibodies in pediatric patients with COVID-19.
- To assess adverse events, hospital admissions, and severe outcomes within 30 days of treatment.
Main Methods:
- A retrospective cohort study was conducted across seven pediatric hospitals.
- Data was collected from 142 pediatric patients treated between December 1, 2020, and July 31, 2021.
- Outcomes included adverse events, 30-day hospital admissions, need for ventilatory support, and mortality.
Main Results:
- Of 142 pediatric patients, 9% experienced adverse events.
- Six percent of patients were admitted for COVID-19 within 30 days of treatment.
- No patients required ventilatory support, and no deaths were reported.
Conclusions:
- Monoclonal antibodies appear to be safe and well-tolerated in high-risk pediatric patients with COVID-19.
- Treatment was associated with low rates of hospitalization and no mortality in this cohort.
- Further research is warranted to confirm these findings in larger pediatric populations.
Abstract:
Monoclonal antibodies for COVID-19 are authorized in high-risk patients aged ≥12 years, but evidence in pediatric patients is limited. In our cohort of 142 patients treated at seven pediatric hospitals between 12/1/20 and 7/31/21, 9% developed adverse events, 6% were admitted for COVID-19 within 30 days, and none received ventilatory support or died.
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