dc.contributor.author | Pérez-Breva, Lina | |
dc.contributor.author | Villanueva, Rafael J | |
dc.contributor.author | Villanueva-Oller, Javier | |
dc.contributor.author | Acedo, Luis | |
dc.contributor.author | Santonja, Francisco | |
dc.contributor.author | Moraño, José A | |
dc.contributor.author | Abad, Raquel | |
dc.contributor.author | Vazquez-Moreno, Julio Alberto | |
dc.contributor.author | Díez-Domingo, Javier | |
dc.date.accessioned | 2019-02-07T10:29:00Z | |
dc.date.available | 2019-02-07T10:29:00Z | |
dc.date.issued | 2014-05-21 | |
dc.identifier.citation | BMC Infect Dis. 2014 May 21;14:280. | es_ES |
dc.identifier.issn | 1471-2334 | es_ES |
dc.identifier.uri | http://hdl.handle.net/20.500.12105/7135 | |
dc.description.abstract | BACKGROUND: Meningococcal C (MenC) conjugate vaccines have controlled invasive diseases associated with this serogroup in countries where they are included in National Immunization Programs and also in an extensive catch-up program involving subjects up to 20 years of age. Catch-up was important, not only because it prevented disease in adolescents and young adults at risk, but also because it decreased transmission of the bacteria, since it was in this age group where the organism was circulating. Our objective is to develop a new vaccination schedule to achieve maximum seroprotection in these groups. METHODS: A recent study has provided detailed age-structured information on the seroprotection levels against MenC in Valencia (Spain), where vaccination is routinely scheduled at 2 months and 6 months, with a booster dose at 18 months of age. A complementary catch-up campaign was also carried out in n for children from 12 months to 19 years of age. Statistical analyses of these data have provided an accurate picture on the evolution of seroprotection in the last few years. RESULTS: An agent-based model has been developed to study the future evolution of the seroprotection histogram. We have shown that the optimum strategy for achieving high protection levels in all infants, toddlers and adolescents is a change to a 2 months, 12 months and 12 years of age vaccination pattern. If the new schedule were implemented in January 2014, high-risk subjects between 15-19 years of age would have very low seroprotection for the next 6 years, thereby threatening the program. CONCLUSIONS: High protection levels and a low incidence of meningococcal C disease can be achieved in the future by means of a cost-free change in vaccination program. However, we recommend a new catch-up program simultaneous to the change in regular vaccination program. | es_ES |
dc.description.sponsorship | This paper has been supported by grant FIS PI-10/01433 from the Instituto de Salud Carlos III, and grant PAID-06-11 ref: 2087 from the Universitat Politècnica de València. An agreement between CSISP-FISABIO and Baxter Laboratories for epidemiological studies of meningococcal C disease is also acknowledged. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | BioMed Central (BMC) | es_ES |
dc.type.hasVersion | VoR | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.subject | Meningococcal C conjugate vaccines | es_ES |
dc.subject | Seroprotection study | es_ES |
dc.subject | Agent-based modelling | es_ES |
dc.subject | Vaccination programs | es_ES |
dc.subject.mesh | Adolescent | es_ES |
dc.subject.mesh | Adult | es_ES |
dc.subject.mesh | Child | es_ES |
dc.subject.mesh | Child, Preschool | es_ES |
dc.subject.mesh | Female | es_ES |
dc.subject.mesh | Humans | es_ES |
dc.subject.mesh | Male | es_ES |
dc.subject.mesh | Meningococcal Infections | es_ES |
dc.subject.mesh | Meningococcal Vaccines | es_ES |
dc.subject.mesh | Middle Aged | es_ES |
dc.subject.mesh | Spain | es_ES |
dc.subject.mesh | Vaccination | es_ES |
dc.subject.mesh | Young Adult | es_ES |
dc.subject.mesh | Immunization Programs | es_ES |
dc.title | Optimizing strategies for meningococcal C disease vaccination in Valencia (Spain) | es_ES |
dc.type | journal article | es_ES |
dc.rights.license | Atribución 4.0 Internacional | * |
dc.identifier.pubmedID | 24886054 | es_ES |
dc.format.volume | 14 | es_ES |
dc.format.number | 1 | es_ES |
dc.format.page | 280 | es_ES |
dc.identifier.doi | 10.1186/1471-2334-14-280 | es_ES |
dc.contributor.funder | Instituto de Salud Carlos III | |
dc.contributor.funder | University of Valencia (España) | |
dc.description.peerreviewed | Sí | es_ES |
dc.identifier.e-issn | 1471-2334 | es_ES |
dc.relation.publisherversion | https://doi.org/10.1186/1471-2334-14-280 | es_ES |
dc.identifier.journal | BMC infectious diseases | es_ES |
dc.repisalud.centro | ISCIII::Centro Nacional de Microbiología | es_ES |
dc.repisalud.institucion | ISCIII | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/ES/PI-10/01433 | es_ES |
dc.rights.accessRights | open access | es_ES |