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Effect of childhood pneumococcal conjugate vaccination on invasive disease in older adults of 10 European countries: implications for adult vaccination.
Hanquet, Germaine; Krizova, Pavla; Valentiner-Branth, Palle; Ladhani, Shamez N; Nuorti, J Pekka; Lepoutre, Agnes; Mereckiene, Jolita; Knol, Mirjam; Winje, Brita A; Ciruela, Pilar; Ordobas, Maria; Guevara, Marcela; McDonald, Eisin; Morfeldt, Eva; Kozakova, Jana; Slotved, Hans-Christian; Fry, Norman K; Rinta-Kokko, Hanna; Varon, Emmanuelle; Corcoran, Mary; van der Ende, Arie; Vestrheim, Didrik F; Munoz-Almagro, Carmen; Latasa, Pello; Castilla, Jesus; Smith, Andrew; Henriques-Normark, Birgitta; Whittaker, Robert; Pastore Celentano, Lucia; Savulescu, Camelia.
Afiliação
  • Hanquet G; EpiConcept, Paris, France.
  • Krizova P; Antwerp University, Antwerp, Belgium.
  • Valentiner-Branth P; National Institute of Public Health, Prague, Czech Republic.
  • Ladhani SN; Statens Serum Institut, Copenhagen, Denmark.
  • Nuorti JP; Public Health England, London, UK.
  • Lepoutre A; National Institute for Health and Welfare, Helsinki, Finland.
  • Mereckiene J; University of Tampere, Tampere, Finland.
  • Knol M; Santé publique France, Saint-Maurice, France.
  • Winje BA; Health Protection Surveillance Centre, Dublin, Ireland.
  • Ciruela P; National Institute for Public Health and the Environment, Bilthoven, The Netherlands.
  • Ordobas M; Norwegian Institute of Public Health, Oslo, Norway.
  • Guevara M; Public Health Agency of Catalunya, Barcelona, Spain.
  • McDonald E; CIBER Epidemiología y Salud Pública, Madrid, Spain.
  • Morfeldt E; General Directorate of Public Health, Madrid, Spain.
  • Kozakova J; CIBER Epidemiología y Salud Pública, Madrid, Spain.
  • Slotved HC; Instituto de Salud Pública de Navarra - IdiSNA, Pamplona, Spain.
  • Fry NK; Health Protection Scotland, National Services Scotland, Glasgow, UK.
  • Rinta-Kokko H; Public Health Agency of Sweden, Solna, Sweden.
  • Varon E; National Institute of Public Health, Prague, Czech Republic.
  • Corcoran M; Statens Serum Institut, Copenhagen, Denmark.
  • van der Ende A; Public Health England, London, UK.
  • Vestrheim DF; National Institute for Health and Welfare, Helsinki, Finland.
  • Munoz-Almagro C; National Centre for Pneumococci, European Hospital George Pompidou, Paris, France.
  • Latasa P; Irish Pneumococcal Reference Laboratory, Temple Street Children's University Hospital, Dublin, Ireland.
  • Castilla J; Netherlands Reference Laboratory for Bacterial Meningitis, Academic Medical Centre, Amsterdam, The Netherlands.
  • Smith A; Norwegian Institute of Public Health, Oslo, Norway.
  • Henriques-Normark B; CIBER Epidemiología y Salud Pública, Madrid, Spain.
  • Whittaker R; Instituto de Recerca Pediátrica, Hospital Sant Joan de Deu, Universitat Internacional de Catalunya, Barcelona, Spain.
  • Pastore Celentano L; General Directorate of Public Health, Madrid, Spain.
  • Savulescu C; CIBER Epidemiología y Salud Pública, Madrid, Spain.
Thorax ; 74(5): 473-482, 2019 05.
Article em En | MEDLINE | ID: mdl-30355641
BACKGROUND: Pneumococcal conjugate vaccines (PCVs) have the potential to prevent pneumococcal disease through direct and indirect protection. This multicentre European study estimated the indirect effects of 5-year childhood PCV10 and/or PCV13 programmes on invasive pneumococcal disease (IPD) in older adults across 13 sites in 10 European countries, to support decision-making on pneumococcal vaccination policies. METHODS: For each site we calculated IPD incidence rate ratios (IRR) in people aged ≥65 years by serotype for each PCV10/13 year (2011-2015) compared with 2009 (pre-PCV10/13). We calculated pooled IRR and 95% CI using random-effects meta-analysis and PCV10/13 effect as (1 - IRR)*100. RESULTS: After five PCV10/13 years, the incidence of IPD caused by all types, PCV7 and additional PCV13 serotypes declined 9% (95% CI -4% to 19%), 77% (95% CI 67% to 84%) and 38% (95% CI 19% to 53%), respectively, while the incidence of non-PCV13 serotypes increased 63% (95% CI 39% to 91%). The incidence of serotypes included in PCV13 and not in PCV10 decreased 37% (95% CI 22% to 50%) in six PCV13 sites and increased by 50% (95% CI -8% to 146%) in the four sites using PCV10 (alone or with PCV13). In 2015, PCV13 serotypes represented 20-29% and 32-53% of IPD cases in PCV13 and PCV10 sites, respectively. CONCLUSION: Overall IPD incidence in older adults decreased moderately after five childhood PCV10/13 years in 13 European sites. Large declines in PCV10/13 serotype IPD, due to the indirect effect of childhood vaccination, were countered by increases in non-PCV13 IPD, but these declines varied according to the childhood vaccine used. Decision-making on pneumococcal vaccination for older adults must consider the indirect effects of childhood PCV programmes. Sustained monitoring of IPD epidemiology is imperative.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Streptococcus pneumoniae / Vacinação / Vacinas Pneumocócicas Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Streptococcus pneumoniae / Vacinação / Vacinas Pneumocócicas Idioma: En Ano de publicação: 2019 Tipo de documento: Article