TY - JOUR
T1 - Respiratory Syncytial Virus hospitalisation burden in children below 18 years in six European countries (2016-2023) pre- and post-COVID-19 pandemic
AU - Jollivet, Ombeline
AU - Urchueguía-Fornes, Arantxa
AU - Chung-Delgado, Kocfa
AU - Johannesen, Caroline Klint
AU - Lehtonen, Toni
AU - Gideonse, David
AU - Cohen, Rachel A
AU - Kramer, Rolf
AU - Orrico-Sánchez, Alejandro
AU - Fischer, Thea K
AU - Heikkinen, Terho
AU - Van Boven, Michiel
AU - Nair, Harish
AU - Campbell, Harry
AU - Osei-Yeboah, Richard
N1 - Copyright © 2025. Published by Elsevier Ltd.
PY - 2025/6
Y1 - 2025/6
N2 - OBJECTIVES: Respiratory syncytial virus (RSV) is a substantial cause of hospital admission in young children and leads to seasonal pressure on pediatric emergency units in most countries. This study aims to assemble national or large-scale data on RSV hospitalisations from six European countries with a standardised approach to provide recent burden data for all children and assess changes since SARS-CoV-2's emergence.METHODS: We analysed 2016-2023 hospital records from national registries in Denmark, England, Finland, The Netherlands, and Scotland, and from a hospital surveillance network in Spain-Valencia for children below 18 years. We considered separately RSV-coded and RSV laboratory-confirmed cases, comparing them to respiratory tract infections. We studied the temporal evolution of incidence rates and case reporting practices, comparing pre- and post-COVID-19 periods.RESULTS: Post-COVID-19 observed RSV hospital burden was similar to the pre-COVID-19 one for younger children but higher for the 1-2 years, 3-4 years, and 5-17 years age groups. No change in terms of coding-neither diagnosis nor RSV-coding when RSV was laboratory-confirmed-was detected.CONCLUSIONS: Hospital RSV burden in children is significant but currently not fully monitorable. Further efforts to harmonise coding practices both within and across countries would improve the quality of future analyses. Additional data in future seasons should complement current outcomes to inform decisions regarding RSV prevention.
AB - OBJECTIVES: Respiratory syncytial virus (RSV) is a substantial cause of hospital admission in young children and leads to seasonal pressure on pediatric emergency units in most countries. This study aims to assemble national or large-scale data on RSV hospitalisations from six European countries with a standardised approach to provide recent burden data for all children and assess changes since SARS-CoV-2's emergence.METHODS: We analysed 2016-2023 hospital records from national registries in Denmark, England, Finland, The Netherlands, and Scotland, and from a hospital surveillance network in Spain-Valencia for children below 18 years. We considered separately RSV-coded and RSV laboratory-confirmed cases, comparing them to respiratory tract infections. We studied the temporal evolution of incidence rates and case reporting practices, comparing pre- and post-COVID-19 periods.RESULTS: Post-COVID-19 observed RSV hospital burden was similar to the pre-COVID-19 one for younger children but higher for the 1-2 years, 3-4 years, and 5-17 years age groups. No change in terms of coding-neither diagnosis nor RSV-coding when RSV was laboratory-confirmed-was detected.CONCLUSIONS: Hospital RSV burden in children is significant but currently not fully monitorable. Further efforts to harmonise coding practices both within and across countries would improve the quality of future analyses. Additional data in future seasons should complement current outcomes to inform decisions regarding RSV prevention.
UR - http://www.scopus.com/inward/record.url?scp=105003847598&partnerID=8YFLogxK
U2 - 10.1016/j.ijid.2025.107903
DO - 10.1016/j.ijid.2025.107903
M3 - Journal article
C2 - 40204016
SN - 1201-9712
VL - 155
SP - 107903
JO - International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
JF - International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
M1 - 107903
ER -