The public health value of vaccines beyond efficacy: methods, measures and outcomes

被引:71
作者
Wilder-Smith, A. [1 ,2 ,3 ]
Longini, I. [4 ]
Zuber, P. L. [5 ]
Barnighausen, T. [2 ]
Edmunds, W. J. [3 ]
Dean, N. [4 ]
Spicher, V. Masserey [6 ]
Benissa, M. R. [7 ]
Gessner, B. D. [8 ]
机构
[1] Nanyang Technol Univ, Lee Kong Chian Sch Med, Singapore, Singapore
[2] Heidelberg Univ, Inst Publ Hlth, Heidelberg, Germany
[3] London Sch Hyg & Trop Med, London, England
[4] Univ Florida, Gainesville, FL USA
[5] WHO, Geneva, Switzerland
[6] Fed Off Publ Hlth, Bern, Switzerland
[7] Univ Geneva, Inst Global Hlth, Geneva, Switzerland
[8] AMP, Paris, France
来源
BMC MEDICINE | 2017年 / 15卷
基金
美国国家卫生研究院; 英国惠康基金;
关键词
Vaccine efficacy; Effectiveness; Overall effectiveness; Vaccine-preventable disease incidence; Public health impact; Dynamic modelling; Cluster randomised controlled trial; Pre-licensure; Post-licensure; Quasi-experiments; PNEUMOCOCCAL CONJUGATE VACCINE; PREVENTABLE DISEASE INCIDENCE; ROTAVIRUS VACCINE; DOUBLE-BLIND; POPULATION; PNEUMONIA; INFLUENZA; CHILDREN; PROGRAMS; TRIAL;
D O I
10.1186/s12916-017-0911-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Assessments of vaccine efficacy and safety capture only the minimum information needed for regulatory approval, rather than the full public health value of vaccines. Vaccine efficacy provides a measure of proportionate disease reduction, is usually limited to etiologically confirmed disease, and focuses on the direct protection of the vaccinated individual. Herein, we propose a broader scope of methods, measures and outcomes to evaluate the effectiveness and public health impact to be considered for evidence-informed policymaking in both pre- and post-licensure stages. Discussion: Pre-licensure: Regulatory concerns dictate an individually randomised clinical trial. However, some circumstances (such as the West African Ebola epidemic) may require novel designs that could be considered valid for licensure by regulatory agencies. In addition, protocol-defined analytic plans for these studies should include clinical as well as etiologically confirmed endpoints (e.g. all cause hospitalisations, pneumonias, acute gastroenteritis and others as appropriate to the vaccine target), and should include vaccine-preventable disease incidence and 'number needed to vaccinate' as outcomes. Post-licensure: There is a central role for phase IV cluster randomised clinical trials that allows for estimation of population-level vaccine impact, including indirect, total and overall effects. Dynamic models should be prioritised over static models as the constant force of infection assumed in static models will usually underestimate the effectiveness and cost-effectiveness of the immunisation programme by underestimating indirect effects. The economic impact of vaccinations should incorporate health and non-health benefits of vaccination in both the vaccinated and unvaccinated populations, thus allowing for estimation of the net social value of vaccination. Conclusions: The full benefits of vaccination reach beyond direct prevention of etiologically confirmed disease and often extend across the life course of a vaccinated person, prevent outcomes in the wider community, stabilise health systems, promote health equity, and benefit local and national economies. The degree to which vaccinations provide broad public health benefits is stronger than for other preventive and curative interventions.
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页数:9
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