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      Effect of childhood pneumococcal conjugate vaccination on invasive disease in older adults of 10 European countries: implications for adult vaccination

      research-article
      1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 13 , 15 , 16 , 17 , 3 , 4 , 5 , 6 , 18 , 19 , 20 , 11 , 13 , 21 , 14 , 13 , 15 , 22 , 17 , 23 , 24 , 25 , 25 , 1
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      Thorax
      BMJ Publishing Group
      bacterial infection, clinical epidemiology

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          Abstract

          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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          Most cited references31

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          Effect of use of 13-valent pneumococcal conjugate vaccine in children on invasive pneumococcal disease in children and adults in the USA: analysis of multisite, population-based surveillance.

          In 2000, seven-valent pneumococcal conjugate vaccine (PCV7) was introduced in the USA and resulted in dramatic reductions in invasive pneumococcal disease (IPD) and moderate increases in non-PCV7 type IPD. In 2010, PCV13 replaced PCV7 in the US immunisation schedule. We aimed to assess the effect of use of PCV13 in children on IPD in children and adults in the USA.
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            Herd immunity and serotype replacement 4 years after seven-valent pneumococcal conjugate vaccination in England and Wales: an observational cohort study.

            The seven-valent pneumococcal conjugate vaccine (PCV7) has reduced vaccine-type (VT) invasive pneumococcal disease but increases in non-vaccine-type (NVT) disease have varied between countries. We assess the effect of the PCV7 vaccination on VT and NVT disease in England and Wales. The study cohort was the population of England and Wales from July, 2000, to June, 2010. We calculated incidence rate ratios (IRRs) to compare incidences of VT and NVT disease before (2000-06) and after (2009-10) the introduction of PCV7. We used data from the national surveillance database. Cases included in our analysis were restricted to those confirmed by culture linked with isolates referred for serotyping at the national reference centre by laboratories in England and Wales. We adjusted for potential bias from missing data (serotype and age of patient) and changes in case ascertainment rates during the study period. 5809 cases of invasive pneumococcal disease were reported in 2009-10, giving an incidence of 10·6 per 100,000 population in 2009-10, which, when compared with the adjusted average annual incidence of 16·1 in 2000-06, gives an overall reduction of 34% (95% CI 28-39). VT disease decreased in all age groups, with reductions of 98% in individuals younger than 2 years and 81% in those aged 65 years or older. NVT disease increased by 68% in individuals younger than 2 years and 48% in those aged 65 years or older, giving an overall reduction in invasive pneumococcal disease of 56% in those younger than 2 years and 19% in those aged 65 years or older. After vaccine introduction, more NVT serotypes increased in frequency than decreased, which is consistent with vaccine-induced replacement. Key serotypes showing replacement were 7F, 19A, and 22F. Increases in NVT invasive pneumococcal disease were not associated with antimicrobial resistance. Despite much serotype replacement, a substantial reduction in invasive pneumococcal disease in young children can be achieved with PCV7 vaccination, with some indirect benefit in older age groups. Further reductions should be achievable by use of higher valency vaccines. Robust surveillance data are needed to properly assess the epidemiological effect of multivalent pneumococcal disease vaccines. Health Protection Agency. Copyright © 2011 Elsevier Ltd. All rights reserved.
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              Rapid increase in non-vaccine serotypes causing invasive pneumococcal disease in England and Wales, 2000–17: a prospective national observational cohort study

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                Author and article information

                Journal
                Thorax
                Thorax
                thoraxjnl
                thorax
                Thorax
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                0040-6376
                1468-3296
                May 2019
                24 October 2018
                : 74
                : 5
                : 473-482
                Affiliations
                [1 ] EpiConcept , Paris, France
                [2 ] Antwerp University , Antwerp, Belgium
                [3 ] National Institute of Public Health , Prague, Czech Republic
                [4 ] Statens Serum Institut , Copenhagen, Denmark
                [5 ] Public Health England , London, UK
                [6 ] National Institute for Health and Welfare , Helsinki, Finland
                [7 ] University of Tampere , Tampere, Finland
                [8 ] Santé publique France , Saint-Maurice, France
                [9 ] Health Protection Surveillance Centre , Dublin, Ireland
                [10 ] National Institute for Public Health and the Environment , Bilthoven, The Netherlands
                [11 ] Norwegian Institute of Public Health , Oslo, Norway
                [12 ] Public Health Agency of Catalunya , Barcelona, Spain
                [13 ] CIBER Epidemiología y Salud Pública , Madrid, Spain
                [14 ] General Directorate of Public Health , Madrid, Spain
                [15 ] Instituto de Salud Pública de Navarra – IdiSNA , Pamplona, Spain
                [16 ] Health Protection Scotland, National Services Scotland , Glasgow, UK
                [17 ] Public Health Agency of Sweden , Solna, Sweden
                [18 ] departmentNational Centre for Pneumococci , European Hospital George Pompidou , Paris, France
                [19 ] departmentIrish Pneumococcal Reference Laboratory , Temple Street Children’s University Hospital , Dublin, Ireland
                [20 ] departmentNetherlands Reference Laboratory for Bacterial Meningitis , Academic Medical Centre , Amsterdam, The Netherlands
                [21 ] departmentInstituto de Recerca Pediátrica, Hospital Sant Joan de Deu , Universitat Internacional de Catalunya , Barcelona, Spain
                [22 ] Scottish Haemophilus, Legionella, Meningococcus and Pneumococcus Reference Laboratory , Glasgow, UK
                [23 ] departmentDepartment of Microbiology, Tumor and Cell Biology , Karolinska Institutet , Stockholm, Sweden
                [24 ] departmentDepartment of Clinical Microbiology , Karolinska University Hospital , Stockholm, Sweden
                [25 ] European Centre for Disease Prevention and Control , Stockholm, Sweden
                Author notes
                [Correspondence to ] Dr Germaine Hanquet, Epidemiology Department, EpiConcept, Paris 75012, France; ghanquet@ 123456skynet.be
                Article
                thoraxjnl-2018-211767
                10.1136/thoraxjnl-2018-211767
                6484683
                30355641
                d853eaae-9d50-4d4d-abea-11142e9bf045
                © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 14 March 2018
                : 31 July 2018
                : 20 August 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100000805, European Centre for Disease Prevention and Control;
                Funded by: FundRef http://dx.doi.org/10.13039/100010677, H2020 Health;
                Categories
                Respiratory Epidemiology
                1506
                2313
                Original article
                Custom metadata
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                Surgery
                bacterial infection,clinical epidemiology
                Surgery
                bacterial infection, clinical epidemiology

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