Vaccination against COVID-19 is the most effective tool to protect both the individual and the community from this potentially life-threatening infectious disease. Data from phase-3 trials showed that two doses of the BNT162b2 vaccine were safe, immunogenic, and effective against COVID-19 in children aged 5-11 years. However, no surveys in real-life settings have been carried out in this age range. Here, we conducted a cross-sectional study to evaluate the short-term adverse reactions (ARs) and the rate of protection against infection of the BNT162b2 vaccine in children aged 5-11 years by the compilation of two surveillance questionnaires conceived using Google Forms. Five-hundred and ninety one children were included in the analysis. ARs were reported by 68.9% of the children, being mainly local. The incidence of systemic ARs, especially fever, was higher after the second dose. The incidence of infection after completing the immunization accounted for 13.6% of the children. COVID-19 symptoms reported were mild, with the exception of one case of pneumonia. Only 40% of infected participants needed to take medication to relieve symptoms, mostly paracetamol and NSAIDs, and none reported persistent symptoms. The Pfizer-BioNTech vaccine in children aged 5-11 years is safe and well tolerated. The mild clinical course of COVID-19 in immunized children confirmed the favorable risk-benefit ratio, encouraging parents to immunize their children.

Short-Term Side Effects and SARS-CoV-2 Infection after COVID-19 Pfizer–BioNTech Vaccine in Children Aged 5–11 Years: An Italian Real-World Study / Capponi, Martina; Pulvirenti, Federica; Cinicola, BIANCA LAURA; Brindisi, Giulia; Conti, MARIA GIULIA; Colaiocco, Giovanni; DE CASTRO, Giovanna; Guido, Cristiana Alessia; Duse, Marzia; Midulla, Fabio; Zicari, Anna Maria; Spalice, Alberto. - In: VACCINES. - ISSN 2076-393X. - 10:7(2022), p. 1056. [10.3390/vaccines10071056]

Short-Term Side Effects and SARS-CoV-2 Infection after COVID-19 Pfizer–BioNTech Vaccine in Children Aged 5–11 Years: An Italian Real-World Study

Martina Capponi;Federica Pulvirenti;Bianca Laura Cinicola;Giulia Brindisi;Maria Giulia Conti;Giovanni Colaiocco;Giovanna de Castro;Cristiana Alessia Guido;Marzia Duse;Fabio Midulla;Anna Maria Zicari;Alberto Spalice
2022

Abstract

Vaccination against COVID-19 is the most effective tool to protect both the individual and the community from this potentially life-threatening infectious disease. Data from phase-3 trials showed that two doses of the BNT162b2 vaccine were safe, immunogenic, and effective against COVID-19 in children aged 5-11 years. However, no surveys in real-life settings have been carried out in this age range. Here, we conducted a cross-sectional study to evaluate the short-term adverse reactions (ARs) and the rate of protection against infection of the BNT162b2 vaccine in children aged 5-11 years by the compilation of two surveillance questionnaires conceived using Google Forms. Five-hundred and ninety one children were included in the analysis. ARs were reported by 68.9% of the children, being mainly local. The incidence of systemic ARs, especially fever, was higher after the second dose. The incidence of infection after completing the immunization accounted for 13.6% of the children. COVID-19 symptoms reported were mild, with the exception of one case of pneumonia. Only 40% of infected participants needed to take medication to relieve symptoms, mostly paracetamol and NSAIDs, and none reported persistent symptoms. The Pfizer-BioNTech vaccine in children aged 5-11 years is safe and well tolerated. The mild clinical course of COVID-19 in immunized children confirmed the favorable risk-benefit ratio, encouraging parents to immunize their children.
2022
COVID-19; SARS-CoV-2; children; immunization; safety; side effects; vaccine
01 Pubblicazione su rivista::01a Articolo in rivista
Short-Term Side Effects and SARS-CoV-2 Infection after COVID-19 Pfizer–BioNTech Vaccine in Children Aged 5–11 Years: An Italian Real-World Study / Capponi, Martina; Pulvirenti, Federica; Cinicola, BIANCA LAURA; Brindisi, Giulia; Conti, MARIA GIULIA; Colaiocco, Giovanni; DE CASTRO, Giovanna; Guido, Cristiana Alessia; Duse, Marzia; Midulla, Fabio; Zicari, Anna Maria; Spalice, Alberto. - In: VACCINES. - ISSN 2076-393X. - 10:7(2022), p. 1056. [10.3390/vaccines10071056]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1652359
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