Effect of neuraminidase inhibitor (oseltamivir) treatment on outcome of hospitalised influenza patients, surveillance data from 11 EU countries, 2010 to 2020
Jazyk angličtina Země Švédsko Médium print
Typ dokumentu časopisecké články
Grantová podpora
001
World Health Organization - International
PubMed
36700868
PubMed Central
PMC9881178
DOI
10.2807/1560-7917.es.2023.28.4.2200340
Knihovny.cz E-zdroje
- Klíčová slova
- EU, Influenza, antiviral treatment, clinic, epidemiology, fatal outcome, hospital, influenza virus, risk factors, surveillance,
- MeSH
- antivirové látky terapeutické užití MeSH
- chřipka lidská * farmakoterapie epidemiologie MeSH
- guanidiny terapeutické užití MeSH
- inhibitory enzymů terapeutické užití MeSH
- lidé MeSH
- mortalita v nemocnicích MeSH
- neuraminidasa MeSH
- oseltamivir * terapeutické užití MeSH
- senioři MeSH
- výsledek terapie MeSH
- zanamivir terapeutické užití MeSH
- Check Tag
- lidé MeSH
- senioři MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antivirové látky MeSH
- guanidiny MeSH
- inhibitory enzymů MeSH
- neuraminidasa MeSH
- oseltamivir * MeSH
- zanamivir MeSH
BackgroundTimely treatment with neuraminidase inhibitors (NAI) can reduce severe outcomes in influenza patients.AimWe assessed the impact of antiviral treatment on in-hospital deaths of laboratory-confirmed influenza patients in 11 European Union countries from 2010/11 to 2019/20.MethodsCase-based surveillance data from hospitalised patients with known age, sex, outcome, ward, vaccination status, timing of antiviral treatment, and hospitalisation were obtained. A mixed effect logistic regression model using country as random intercept was applied to estimate the adjusted odds ratio (aOR) for in-hospital death in patients treated with NAIs vs not treated.ResultsOf 19,937 patients, 31% received NAIs within 48 hours of hospital admission. Older age (60-79 years aOR 3.0, 95% CI: 2.4-3.8; 80 years 8.3 (6.6-10.5)) and intensive care unit admission (3.8, 95% CI: 3.4-4.2) increased risk of dying, while early hospital admission after symptom onset decreased risk (aOR 0.91, 95% CI: 0.90-0.93). NAI treatment initiation within 48 hours and up to 7 days reduced risk of dying (0-48 hours aOR 0.51, 95% CI: 0.45-0.59; 3-4 days 0.59 (0.51-0.67); 5-7 days 0.64 (0.56-0.74)), in particular in patients 40 years and older (e.g. treatment within 48 hours: 40-59 years aOR 0.43, 95% CI: 0.28-0.66; 60-79 years 0.50 (0.39-0.63); ≥80 years 0.51 (0.42-0.63)).ConclusionNAI treatment given within 48 hours and possibly up to 7 days after symptom onset reduced risk of in-hospital death. NAI treatment should be considered in older patients to prevent severe outcomes.
Center for Virology Medical University Vienna Vienna Austria
Department of Infectious Diseases Epidemiology National Institute of Public Health Prague Czechia
European Centre for Disease Prevention and Control Stockholm Sweden
Health Service Executive Health Protection Surveillance Centre Dublin Ireland
Infectious Disease prevention and Control unit Malta
National Centre of Epidemiology CIBERESP Carlos 3 Health Institute Madrid Spain
National Institute for Public Health and the Environment Bilthoven the Netherlands
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