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Effectiveness of Immunization Products Against Medically Attended Respiratory Syncytial Virus Infection: Generic Protocol for a Test-Negative Case-Control Study.
van Roekel, Caren; Poukka, Eero; Turunen, Topi; Nohynek, Hanna; Presser, Lance; Meijer, Adam; Heikkinen, Terho; Kramer, Rolf; Begier, Elizabeth; Teirlinck, Anne C; Knol, Mirjam J.
Afiliação
  • van Roekel C; Centre for Infectious Disease Control, National Institute for Public Health and Environment, Bilthoven, the Netherlands.
  • Poukka E; Infectious Disease Control and Vaccinations Unit, Department of Health Security, Finnish Institute for Health and Welfare, Helsinki, Finland.
  • Turunen T; Infectious Disease Control and Vaccinations Unit, Department of Health Security, Finnish Institute for Health and Welfare, Helsinki, Finland.
  • Nohynek H; Infectious Disease Control and Vaccinations Unit, Department of Health Security, Finnish Institute for Health and Welfare, Helsinki, Finland.
  • Presser L; Centre for Infectious Disease Control, National Institute for Public Health and Environment, Bilthoven, the Netherlands.
  • Meijer A; Centre for Infectious Disease Control, National Institute for Public Health and Environment, Bilthoven, the Netherlands.
  • Heikkinen T; Department of Pediatrics, University of Turku and Turku University Hospital, Turku, Finland.
  • Kramer R; Sanofi Pasteur, SA, Lyon, France.
  • Begier E; Pfizer, Ltd, NewYork City, New York, USA.
  • Teirlinck AC; Centre for Infectious Disease Control, National Institute for Public Health and Environment, Bilthoven, the Netherlands.
  • Knol MJ; Centre for Infectious Disease Control, National Institute for Public Health and Environment, Bilthoven, the Netherlands.
J Infect Dis ; 229(Supplement_1): S92-S99, 2024 Mar 01.
Article em En | MEDLINE | ID: mdl-37935046
ABSTRACT
Monitoring the real-life effectiveness of respiratory syncytial virus (RSV) products is of major public health importance. This generic protocol for a test-negative design study aims to address currently envisioned approaches for RSV prevention (monoclonal antibodies and vaccines) to study effectiveness of these products among target groups children, older adults, and pregnant women. The generic protocol approach was chosen to allow for flexibility in adapting the protocol to a specific setting. This protocol includes severe acute respiratory infection (SARI) and acute respiratory infection (ARI), both due to RSV, as end points. These end points can be applied to studies in hospitals, primarily targeting patients with more severe disease, but also to studies in general practitioner clinics targeting ARI.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Aged / Child / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Aged / Child / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2024 Tipo de documento: Article