Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/37166
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dc.contributor.authorSTANDAERT, Baudouin-
dc.contributor.authorStrens, Danielle-
dc.contributor.authorRAES, Marc-
dc.contributor.authorBenninghoff, Bernd-
dc.date.accessioned2022-04-04T14:09:37Z-
dc.date.available2022-04-04T14:09:37Z-
dc.date.issued2022-
dc.date.submitted2022-03-31T11:29:24Z-
dc.identifier.citationVACCINE, 40 (13) , p. 1948 -1957-
dc.identifier.urihttp://hdl.handle.net/1942/37166-
dc.description.abstractBackground: Observational data on the reduction in hospitalisations after rotavirus vaccine introduction in Belgium suggest that vaccine impact plateaued at an unexpectedly high residual hospitalisation rate. The objective of this analysis was to identify factors that influence real-world vaccine impact. Methods: Data were collected on hospitalisations in children aged < 5 years with rotavirus disease from 11 hospitals since 2005 (the RotaBIS study). The universal rotavirus vaccination campaign started late in 2006. A mathematical model simulated rotavirus hospitalisations in different age groups using vaccine efficacy and herd effect, influenced by vaccine coverage, vaccine waning, and secondary infection sources. The model used optimisation analysis to fit the simulated curve to the observed data, applying Solver add-in software. It also simulated an 'ideal' vaccine introduction maximising hospitalisation reduction (maximum coverage, maximum herd effect, no waning), and compared this with the best-fit simulated curve. Modifying model input values identified factors with the largest impact on hospitalisations. Results: Compared with the 'ideal' simulation, observed data showed a slower decline in hospitalisations and levelled off after three years at a higher residual hospitalisation rate. The slower initial decline was explained by the herd effect in unvaccinated children. The higher residual hospitalisation rate was explained by starting the vaccine programme in November, near the rotavirus seasonal peak. This resulted in low accumulated vaccine coverage during the first rotavirus disease peak season, with the consequential appearance of secondary infection sources. This in turn reduced the herd effect, resulting in a diminished net impact. Conclusions: Our results indicate that countries wishing to maximise the impact of rotavirus vaccination should start vaccinating well ahead of the rotavirus seasonal disease peak. This maximises herd effect during the first year leading to rapid and high reduction in hospitalisations. Secondary infection sources explain the observed data in Belgium better than vaccine waning. (c) 2022 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/).-
dc.description.sponsorshipBS was an employee of GSK until retirement in September 2020. The current research was conducted after he left GSK. He recently joined the Faculty of Medicine and Life Sciences, Research Group Care and Ethics, at the University of Hasselt, Hasselt, Belgium, as guest professor. DS is a consultant and has not been paid for her contribution to this work. MR is a paediatric professor and clinician. He has not been paid for his contribution to this work. BB is an employee of GSK and holds shares of the GSK group of companies. The authors would like to thank Carole Nadin (Fleetwith Ltd, on behalf of HEBO) for editorial assistance.-
dc.language.isoen-
dc.publisherELSEVIER SCI LTD-
dc.rights2022 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).-
dc.subject.otherRotavirus vaccination-
dc.subject.otherImplementation-
dc.subject.otherOptimisation-
dc.subject.otherSecondary sources of infection-
dc.subject.otherVaccine waning-
dc.titleExplaining the formation of a plateau in rotavirus vaccine impact on rotavirus hospitalisations in Belgium-
dc.typeJournal Contribution-
dc.identifier.epage1957-
dc.identifier.issue13-
dc.identifier.spage1948-
dc.identifier.volume40-
local.format.pages10-
local.bibliographicCitation.jcatA1-
dc.description.notesStandaert, B (corresponding author), HEBO Bv, Della Faillelaan 75, B-2020 Antwerp, Belgium.-
dc.description.notesbaudouin.standaert@skynet.be; dstrens@realidad.be; fa303885@skynet.be;-
dc.description.notesbernd.benninghoff@gmx.de-
local.publisher.placeTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLAND-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1016/j.vaccine.2022.02.053-
dc.identifier.isiWOS:000767174300006-
local.provider.typewosris-
local.description.affiliation[Standaert, Baudouin] HEBO Bv, Della Faillelaan 75, B-2020 Antwerp, Belgium.-
local.description.affiliation[Standaert, Baudouin] Univ Hasselt, Hasselt, Belgium.-
local.description.affiliation[Strens, Danielle] Realidad Bvba, Grimbergen, Belgium.-
local.description.affiliation[Raes, Marc] Jesse Hosp, Hasselt, Belgium.-
local.description.affiliation[Benninghoff, Bernd] GSK, Wavre, Belgium.-
local.uhasselt.internationalyes-
item.validationecoom 2023-
item.accessRightsOpen Access-
item.fullcitationSTANDAERT, Baudouin; Strens, Danielle; RAES, Marc & Benninghoff, Bernd (2022) Explaining the formation of a plateau in rotavirus vaccine impact on rotavirus hospitalisations in Belgium. In: VACCINE, 40 (13) , p. 1948 -1957.-
item.fulltextWith Fulltext-
item.contributorSTANDAERT, Baudouin-
item.contributorStrens, Danielle-
item.contributorRAES, Marc-
item.contributorBenninghoff, Bernd-
crisitem.journal.issn0264-410X-
crisitem.journal.eissn1873-2518-
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