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

Abstract 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 confir...

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Main Authors: A. Wilder-Smith, I. Longini, P. L. Zuber, T. Bärnighausen, W. J. Edmunds, N. Dean, V. Masserey Spicher, M. R. Benissa, B. D. Gessner
Format: Article
Language:English
Published: BMC 2017-07-01
Series:BMC Medicine
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12916-017-0911-8
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spelling doaj-b740c0fe479c43d18fefc51bb630b2ad2020-11-24T21:39:05ZengBMCBMC Medicine1741-70152017-07-011511910.1186/s12916-017-0911-8The public health value of vaccines beyond efficacy: methods, measures and outcomesA. Wilder-Smith0I. Longini1P. L. Zuber2T. Bärnighausen3W. J. Edmunds4N. Dean5V. Masserey Spicher6M. R. Benissa7B. D. Gessner8Lee Kong Chian School of Medicine, Nanyang Technological UniversityUniversity of FloridaWorld Health OrganizationInstitute of Public Health, University of HeidelbergLondon School of Hygiene and Tropical MedicineUniversity of FloridaFederal Office of Public HealthInstitute of Global Health, University of GenevaAgence de Médecine Preventive (AMP)Abstract 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.http://link.springer.com/article/10.1186/s12916-017-0911-8Vaccine efficacyEffectivenessOverall effectivenessVaccine-preventable disease incidencePublic health impactDynamic modelling
collection DOAJ
language English
format Article
sources DOAJ
author A. Wilder-Smith
I. Longini
P. L. Zuber
T. Bärnighausen
W. J. Edmunds
N. Dean
V. Masserey Spicher
M. R. Benissa
B. D. Gessner
spellingShingle A. Wilder-Smith
I. Longini
P. L. Zuber
T. Bärnighausen
W. J. Edmunds
N. Dean
V. Masserey Spicher
M. R. Benissa
B. D. Gessner
The public health value of vaccines beyond efficacy: methods, measures and outcomes
BMC Medicine
Vaccine efficacy
Effectiveness
Overall effectiveness
Vaccine-preventable disease incidence
Public health impact
Dynamic modelling
author_facet A. Wilder-Smith
I. Longini
P. L. Zuber
T. Bärnighausen
W. J. Edmunds
N. Dean
V. Masserey Spicher
M. R. Benissa
B. D. Gessner
author_sort A. Wilder-Smith
title The public health value of vaccines beyond efficacy: methods, measures and outcomes
title_short The public health value of vaccines beyond efficacy: methods, measures and outcomes
title_full The public health value of vaccines beyond efficacy: methods, measures and outcomes
title_fullStr The public health value of vaccines beyond efficacy: methods, measures and outcomes
title_full_unstemmed The public health value of vaccines beyond efficacy: methods, measures and outcomes
title_sort public health value of vaccines beyond efficacy: methods, measures and outcomes
publisher BMC
series BMC Medicine
issn 1741-7015
publishDate 2017-07-01
description Abstract 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.
topic Vaccine efficacy
Effectiveness
Overall effectiveness
Vaccine-preventable disease incidence
Public health impact
Dynamic modelling
url http://link.springer.com/article/10.1186/s12916-017-0911-8
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