TY - JOUR
T1 - Estimating transmission parameters for respiratory syncytial virus and predicting the impact of maternal and pediatric vaccination
AU - Van Boven, Michiel
AU - Teirlinck, Anne
AU - Meijer, Adam
AU - Hooiveld, Mariëtte
AU - Van Dorp, Christiaan H.
AU - Reeves, Rachel M.
AU - Campbell, Harry
AU - Van Der Hoek, Wim
AU - RESCEU Investigators
A2 - Li, You
A2 - Campbell, Harry
A2 - Nair, Harish
A2 - Van Wijhe, Maarten
A2 - Fischer, Thea Kølsen
A2 - Simonsen, Lone
A2 - Trebbien, Ramona
A2 - Tong, Sabine
A2 - Gallichan, Scott
A2 - Bangert, Mathieu
A2 - Demont, Clarisse
A2 - Lehtonen, Toni
A2 - Heikkinen, Terho
A2 - Van Der Maas, Nicoline
A2 - Fernandez, Liliana Vazquez
A2 - Bøas, Hakon
A2 - Bekkevold, Terese
A2 - Flem, Elmira
A2 - Stona, Luca
A2 - Speltra, Irene
A2 - Giaquinto, Carlo
A2 - Cheret, Arnaud
A2 - Leach, Amanda
A2 - Stoszek, Sonia
A2 - Beutels, Philippe
A2 - Bont, Louis
A2 - Pollard, Andrew
A2 - Openshaw, Peter
A2 - Abram, Michael
A2 - Swanson, Kena
A2 - Rosen, Brian
A2 - Molero, Eva
N1 - This article has been found as a ’Free Version’ from the Publisher on May 20 2021. When access to the article closes, please notify [email protected]
PY - 2021
Y1 - 2021
N2 - Background. Respiratory syncytial virus (RSV) is a leading cause of respiratory tract illness in young children and a major cause of hospital admissions globally. Methods. Here we fit age-structured transmission models with immunity propagation to data from the Netherlands (2012- 2017). Data included nationwide hospitalizations with confirmed RSV, general practitioner (GP) data on attendance for care from acute respiratory infection, and virological testing of acute respiratory infections at the GP. The transmission models, equipped with key parameter estimates, were used to predict the impact of maternal and pediatric vaccination. Results. Estimates of the basic reproduction number were generally high (R0 > 10 in scenarios with high statistical support), while susceptibility was estimated to be low in nonelderly adults (<10% in persons 20-64 years) and was higher in older adults (≥65 years). Scenario analyses predicted that maternal vaccination reduces the incidence of infection in vulnerable infants (<1 year) and shifts the age of first infection from infants to young children. Conclusions. Pediatric vaccination is expected to reduce the incidence of infection in infants and young children (0-5 years), slightly increase incidence in 5 to 9-year-old children, and have minor indirect benefits.
AB - Background. Respiratory syncytial virus (RSV) is a leading cause of respiratory tract illness in young children and a major cause of hospital admissions globally. Methods. Here we fit age-structured transmission models with immunity propagation to data from the Netherlands (2012- 2017). Data included nationwide hospitalizations with confirmed RSV, general practitioner (GP) data on attendance for care from acute respiratory infection, and virological testing of acute respiratory infections at the GP. The transmission models, equipped with key parameter estimates, were used to predict the impact of maternal and pediatric vaccination. Results. Estimates of the basic reproduction number were generally high (R0 > 10 in scenarios with high statistical support), while susceptibility was estimated to be low in nonelderly adults (<10% in persons 20-64 years) and was higher in older adults (≥65 years). Scenario analyses predicted that maternal vaccination reduces the incidence of infection in vulnerable infants (<1 year) and shifts the age of first infection from infants to young children. Conclusions. Pediatric vaccination is expected to reduce the incidence of infection in infants and young children (0-5 years), slightly increase incidence in 5 to 9-year-old children, and have minor indirect benefits.
KW - Evidence synthesis
KW - GP consultations
KW - Hospital data
KW - Respiratory syncytial virus
KW - Transmission model
KW - Vaccination
UR - https://academic.oup.com/jid/article/222/Supplement_7/S688/5895295
U2 - 10.1093/INFDIS/JIAA424
DO - 10.1093/INFDIS/JIAA424
M3 - Journal article
C2 - 32821916
AN - SCOPUS:85092749947
SN - 0022-1899
VL - 222
SP - S688-S694
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
ER -