Cécile Chauvel

and 11 more

Background: Respiratory Syncytial Virus (RSV) is a major health concern, particularly for infants. In France, Nirsevimab, a long-acting monoclonal antibody to prevent RSV-associated lower respiratory tract infections (LRTI) was available from September 2023. We described RSV-associated LRTI hospitalisations during the 2023-2024 season among infants younger than six months born at the Hospices Civils de Lyon (HCL), and evaluated the effectiveness of Nirsevimab against RSV-LRTI hospitalisation. Methods: This observational study included infants born and hospitalised at the HCL during the 2023-2024 season, along with pre-COVID-19 and 2022-2023 seasons. Information on Nirsevimab immunisation status, clinical and perinatal variables were collected through routine care. Infants’ characteristics and incidence risk of hospitalisation per 100 births during 2023-2024 were compared with the historical periods overall and by delay between birth and the onset of the RSV season. Nirsevimab effectiveness was computed by the screening method. Results: During the 2023-2024 season, 83 infants younger than six months were hospitalised with an RSV-associated LRTI. Compared with the historical periods these infants were older. Incidence risk for infants born during the period when immunisation was available were lower than the previous seasons; incidence risk ratios were 0.45 (95% confidence interval (CI): [0.33;0.62]) in 2023-2024 compared with pre-COVID-19 period and 0.53 (95%CI: [0.36;0.77]) compared with 2022-2023 season. Nirsevimab effectiveness was 78.3% (95%CI: [55.9 ;89.5]) with a coverage of 79.3% in the HCL maternities. Conclusions: This study revealed a change in the epidemiology of RSV-associated LRTI hospitalisations in 2023-2024. High coverage and effectiveness were estimated in real-world setting.

Bronke Boudewijns

and 24 more

Background: This study aimed to establish a Severity Scale for influenza and other acute respiratory infections (ARI), requiring hospitalization, for surveillance and research purposes (the SevScale). Such a scale could aid the interpretation of data gathered from disparate settings. This could facilitate pooled analyses linking viral genetic sequencing data to clinical severity, bringing insights to inform influenza surveillance and the vaccine strain selection process. Methods: We used a subset of data from the Global Influenza Hospital Surveillance Network database, including data from different geographical areas and income levels. To quantify the underlying concept of severity, an item response model was developed using sixteen indicators of severity related to the hospital stay. Each patient in the dataset was assigned a Severity Score and a Severity Category (low, medium, or high severity). Finally, we compared the model scores across different subgroups. Results: Data from 9 countries were included, covering between 4 and 11 seasons from 2012 to 2022, with a total of 96,190 ARI hospitalizations. Not for all severity indicators data was available for all included seasons. Subgroups with a high percentage of patients in the High Severity Category included influenza A(H1N1)pdm09, age ≥50, lower-middle income countries, and admission since the start of the COVID-19 pandemic. Conclusions: The initial model successfully highlighted severity disparities across patient subgroups. Repeating this exercise with new, more complete data would allow recalibration and validation of the current model. The SevScale proved to be a promising method to define severity for influenza vaccine strain selection, surveillance and research.