Cochrane re-arranged: Support for policies to vaccinate elderly people against influenza

被引:136
作者
Beyer, Walter E. P. [1 ]
McElhaney, Janet [2 ]
Smith, Derek J. [1 ,3 ,4 ]
Monto, Arnold S. [5 ]
Nguyen-Van-Tam, Jonathan S. [6 ]
Osterhaus, Albert D. M. E. [1 ]
机构
[1] Erasmus MC, Dept Virosci, NL-3000 CA Rotterdam, Netherlands
[2] Univ Connecticut, Ctr Hlth, Dept Immunol, Farmington, CT 06030 USA
[3] Univ Cambridge, Dept Zool, Cambridge CB2 3EJ, England
[4] World Hlth Org, Collaborating Ctr Modeling Evolut & Control Emerg, Cambridge CB2 3EJ, England
[5] Univ Michigan, Sch Publ Hlth, Ann Arbor, MI 48109 USA
[6] Univ Nottingham, Hlth Protect & Influenza Res Grp, Div Epidemiol & Publ Hlth, Nottingham NG5 1PB, England
关键词
Efficacy; Effectiveness; Safety; Influenza; Vaccination; Elderly;
D O I
10.1016/j.vaccine.2013.09.063
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The 2010 Cochrane review on efficacy, effectiveness and safety of influenza vaccination in the elderly by Jefferson et al. covering dozens of clinical studies over a period of four decades, confirmed vaccine safety, but found no convincing evidence for vaccine effectiveness (VE) against disease thus challenging the ongoing efforts to vaccinate the elderly. However, the Cochrane review analyzed and presented the data in a way that may itself have hampered the desired separation of real vaccine benefits from inevitable 'background noise'. The data are arranged in more than one hundred stand-alone meta-analyses, according to various vaccine types, study designs, populations, and outcome case definitions, and then further subdivided according to virus circulation and antigenic match. In this way, general vaccine effects could not be separated from an abundance of environmental and operational, non vaccine-related variation. Furthermore, expected impacts of changing virus circulation and antigenic drift on VE could not be demonstrated. We re-arranged the very same data according to a biological and conceptual framework based on the basic sequence of events throughout the 'patient journey' (exposure, infection, clinical outcome, observation) and using broad outcome definitions and simple frequency distributions of VE values. This approach produced meaningful predictions for VE against influenza-related fatal and non-fatal complications (average similar to 30% with large dispersion), typical influenza-like illness (similar to 40%), disease with confirmed virus infection (similar to 50%), and biological vaccine efficacy against infection (similar to 60%), under conditions of virus circulation. We could also demonstrate a VE average around zero in the absence of virus circulation, and decreasing VE values with decreasing virus circulation and increasing antigenic drift. We regard these findings as substantial evidence for the ability of influenza vaccine to reduce the risk of influenza infection and influenza-related disease and death in the elderly. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6030 / 6033
页数:4
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