Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/39185
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dc.contributor.authorMarijam, Alen-
dc.contributor.authorSchuerman, Lode-
dc.contributor.authorIzurieta, Patricia-
dc.contributor.authorPereira, Priya-
dc.contributor.authorVan Oorschot, Desiree-
dc.contributor.authorMehta, Shailesh-
dc.contributor.authorOta, Martin O. C.-
dc.contributor.authorSTANDAERT, Baudouin-
dc.date.accessioned2023-01-09T10:23:57Z-
dc.date.available2023-01-09T10:23:57Z-
dc.date.issued2022-
dc.date.submitted2023-01-05T12:16:11Z-
dc.identifier.citationHuman Vaccines & Immunotherapeutics, 18 (7)-
dc.identifier.urihttp://hdl.handle.net/1942/39185-
dc.description.abstractPlain Language SummaryWhat is the context?The WHO added the pneumococcal conjugate vaccine and the rotavirus vaccine in the recommended vaccination schedule of all countries in 2007 and 2009, respectively.Previous studies estimated the public health benefit of these vaccines by approximating the number of children who received them.What is new?We used an alternative approach to estimate the benefit based on actual number of doses of the vaccines, human rotavirus vaccine (HRV; Rotarix) and pneumococcal polysaccharide protein D-conjugate vaccine (PHiD-CV; Synflorix) delivered to each country considered.The study analyzed data from children under 5 years of age in 60 Gavi-supported countries by identifying the number of vaccine doses delivered, estimating the number of children fully covered, applying the country-specific disease epidemiology, estimating the number of severe disease cases and deaths avoided.From 2009 to 2019, approximately 143 million children were vaccinated with HRV avoiding an estimated 18.7 million severe rotavirus disease cases and 153,000 deaths.From 2011 to 2019, about 146 million children were vaccinated with pneumococcal vaccine avoiding an estimated 5.0 million severe pneumococcal disease cases and 587,000 deaths.What is the impact?The benefit of HRV and PHiD-CV in Gavi-supported countries is often estimated based on assumptions of vaccine coverage rates.A modeling approach based on doses delivered by the vaccine manufacturer can provide an additional view on the potential vaccine benefits and improve planning, contribution, and sustainability of the immunization programs at a country level.In 2019, HRV and PHiD-CV together averted nine cases of severe disease each minute and one child death every 4 minutes. Vaccine impact models against rotavirus disease (RD) and pneumococcal disease (PD) in low- and middle-income countries assume vaccine coverage based on other vaccines. We propose to assess the impact on severe disease cases and deaths avoided based on vaccine doses delivered by one manufacturer to Gavi-supported countries. From the number of human rotavirus vaccine (HRV) and pneumococcal polysaccharide protein D-conjugate vaccine (PHiD-CV) doses delivered, we estimated the averted burden of disease 1) in a specific year and 2) for all children vaccinated during the study period followed-up until 5 years (y) of age. Uncertainty of the estimated impact was assessed in a probabilistic sensitivity analysis using Monte-Carlo simulations to provide 95% confidence intervals. From 2009 to 2019, approximately 143 million children received HRV in 57 Gavi-supported countries, avoiding an estimated 18.7 million severe RD cases and 153,000, deaths. From 2011 to 2019, approximately 146 million children received PHiD-CV in 36 countries, avoiding an estimated 5.0 million severe PD cases and 587,000 deaths. The number of severe cases and deaths averted for all children vaccinated during the study period until 5 years of age were about 23.2 million and 190,000, respectively, for HRV, and 6.6 million and 749,000, respectively, for PHiD-CV. Models based on doses delivered help to assess the impact of vaccination, plan vaccination programs and understand public health benefits. In 2019, HRV and PHiD-CV doses delivered over a 5-y period may have, on average, averted nine severe disease cases every minute and one child death every 4 min.-
dc.description.sponsorshipGlaxoSmithKline Biologicals SA funded this study and was involved in all stages of study conduct, including analysis of the data. GlaxoSmithKline Biologicals SA also paid all costs associated with the development and publication of this manuscript. The authors would like to thank Tathyana Giannotti Cousseau for her input regarding the initiation, collection of the actual sales volume per year and assessment of various methodologies adopted by Supranational agencies like Gavi and John Hopkins for “Lives Saved” model. The authors would also like to thank Business & Decision Life Sciences platform for editorial assistance and manuscript coordination, on behalf of GSK, and TVF communications platform for the design support for the digital illustration, on behalf of GSK. Mary Greenacre (An Sgriobhadair Ltd) provided writing support for this literature review.-
dc.language.isoen-
dc.publisherTAYLOR & FRANCIS INC-
dc.rights2022 GlaxoSmithKline Biologicals S.A. Published with license by Taylor & Francis Group, LLC. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.-
dc.subject.otherRotavirus-
dc.subject.otherpneumococcal disease-
dc.subject.otherrotavirus vaccine-
dc.subject.otherpneumococcal vaccine-
dc.subject.otherGavi-
dc.subject.otherdoses delivered-
dc.titleEstimated public health impact of human rotavirus vaccine (HRV) and pneumococcal polysaccharide protein D-conjugate vaccine (PHiD-CV) on child morbidity and mortality in Gavi-supported countries-
dc.typeJournal Contribution-
dc.identifier.issue7-
dc.identifier.volume18-
local.bibliographicCitation.jcatA1-
dc.description.notesMarijam, A (corresponding author), GSK, Vaccines, Upper Providence, PA USA.; Marijam, A (corresponding author), GSK, Upper Providence, PA 19063 USA.-
dc.description.notesalen.x.marijam@gsk.com-
local.publisher.place530 WALNUT STREET, STE 850, PHILADELPHIA, PA 19106 USA-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.bibliographicCitation.statusEarly view-
dc.identifier.doi10.1080/21645515.2022.2135916-
dc.identifier.pmid36507685-
dc.identifier.isi000898210500001-
dc.contributor.orcidMarijam, Alen/0000-0003-1046-9702-
local.provider.typewosris-
local.description.affiliation[Marijam, Alen] GSK, Vaccines, Upper Providence, PA USA.-
local.description.affiliation[Schuerman, Lode; Izurieta, Patricia; Pereira, Priya; Van Oorschot, Desiree; Mehta, Shailesh; Ota, Martin O. C.; Standaert, Baudouin] GSK, Vaccines, Wavre, Belgium.-
local.description.affiliation[Marijam, Alen] GSK, Upper Providence, PA 19063 USA.-
local.description.affiliation[Standaert, Baudouin] Univ Hasselt, Hasselt, Belgium.-
local.uhasselt.internationalyes-
item.accessRightsOpen Access-
item.fullcitationMarijam, Alen; Schuerman, Lode; Izurieta, Patricia; Pereira, Priya; Van Oorschot, Desiree; Mehta, Shailesh; Ota, Martin O. C. & STANDAERT, Baudouin (2022) Estimated public health impact of human rotavirus vaccine (HRV) and pneumococcal polysaccharide protein D-conjugate vaccine (PHiD-CV) on child morbidity and mortality in Gavi-supported countries. In: Human Vaccines & Immunotherapeutics, 18 (7).-
item.fulltextWith Fulltext-
item.validationecoom 2023-
item.contributorMarijam, Alen-
item.contributorSchuerman, Lode-
item.contributorIzurieta, Patricia-
item.contributorPereira, Priya-
item.contributorVan Oorschot, Desiree-
item.contributorMehta, Shailesh-
item.contributorOta, Martin O. C.-
item.contributorSTANDAERT, Baudouin-
crisitem.journal.issn2164-5515-
crisitem.journal.eissn2164-554X-
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