| Literature DB >> 24016803 |
Kari Auranen1, Hanna Rinta-Kokko2, David Goldblatt3, Hanna Nohynek2, Katherine L O'Brien4, Catherine Satzke5, Birgit Simell2, Antti Tanskanen2, Helena Käyhty2.
Abstract
Evaluating vaccine efficacy for protection against colonisation (VEcol) with bacterial pathogens is an area of growing interest. In this article, we consider estimation of VEcol for colonisation with Streptococcus pneumoniae (the pneumococcus). Colonisation is a common, recurrent and multi-type endpoint that requires both careful definition of the vaccine efficacy parameter and the corresponding method of estimation. We review recent developments in the area and provide practical guidelines for choosing the estimand and the estimation method in trials with a colonisation endpoint. We concentrate on methods that are based on a cross-sectional study design, in which only one nasopharyngeal sample is obtained per study subject.Entities:
Keywords: NVT; Nasopharyngeal colonisation; OR; PCV; Pneumococcus; Trial endpoint; VE(T); VE(acq); VE(col); VT; Vaccine efficacy; combined vaccine efficacy against acquisition and duration of colonisation; non-vaccine (sero)type(s); odds ratio; pneumococcal conjugate vaccine; vaccine (sero)type(s); vaccine efficacy against acquisition of colonisation; vaccine efficacy against colonisation
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Year: 2013 PMID: 24016803 DOI: 10.1016/j.vaccine.2013.08.061
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641