Author(s):
Rose, Angela ; Kissling, Esther ; Emborg, Hanne-Dorthe ; Larrauri, Amparo ; McMenamin, Jim ; Pozo, Francisco ; Trebbien, Ramona ; Mazagatos, Clara ; Whitaker, Heather ; Machado, Ausenda ; Gómez, Verónica ; Nunes, Baltazar ; Kislaya, Irina ; Pechirra, Pedro ; Conde, Patrícia ; Rodrigues, Ana Paula ; Cristóvão, Paula ; Costa, Inês ; Guiomar, Raquel ; European IVE Group
Date: 2020
Persistent ID: http://hdl.handle.net/10400.18/7331
Origin: Repositório Científico do Instituto Nacional de Saúde
Subject(s): Influenza; Influenza vaccine; Efectiveness; Multicentre Study; Test-negative Design; Efetividade; I-MOVE; EuroEVA; Gripe; Europe; Determinantes da Saúde e da Doença; Observação e Vigilância; Cuidados Saúde Primários; Infecções Respiratórias; Portugal
Description
Background: Influenza A(H1N1)pdm09, A(H3N2) and B viruses were co-circulating in Europe between September 2019 and January 2020. Aim: To provide interim 2019/20 influenza vaccine effectiveness (VE) estimates from six European studies, covering 10 countries and both primary care and hospital settings. Methods: All studies used the test-negative design, although there were some differences in other study characteristics, e.g. patient selection, data sources, case definitions and included age groups. Overall and influenza (sub)type-specific VE was estimated for each study using logistic regression adjusted for potential confounders. Results: There were 31,537 patients recruited across the six studies, of which 5,300 (17%) were cases with 5,310 infections. Most of these (4,466; 84%) were influenza A. The VE point estimates for all ages were 29% to 61% against any influenza in the primary care setting and 35% to 60% in hospitalised older adults (aged 65 years and over). The VE point estimates against A(H1N1)pdm09 (all ages, both settings) was 48% to 75%, and against A(H3N2) ranged from −58% to 57% (primary care) and −16% to 60% (hospital). Against influenza B, VE for all ages was 62% to 83% (primary care only). Conclusions: Influenza vaccination is of continued benefit during the ongoing 2019/20 influenza season. Robust end-of-season VE estimates and genetic virus characterisation results may help understand the variability in influenza (sub) type-specific results across studies.
