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Changes in Invasive Pneumococcal Disease Caused by Streptococcus pneumoniae Serotype 1 Following Introduction of PCV10 and PCV13: Findings from the PSERENADE Project.
Bennett, Julia C; Hetrich, Marissa K; Garcia Quesada, Maria; Sinkevitch, Jenna N; Deloria Knoll, Maria; Feikin, Daniel R; Zeger, Scott L; Kagucia, Eunice W; Cohen, Adam L; Ampofo, Krow; Brandileone, Maria-Cristina C; Bruden, Dana; Camilli, Romina; Castilla, Jesús; Chan, Guanhao; Cook, Heather; Cornick, Jennifer E; Dagan, Ron; Dalby, Tine; Danis, Kostas; de Miguel, Sara; De Wals, Philippe; Desmet, Stefanie; Georgakopoulou, Theano; Gilkison, Charlotte; Grgic-Vitek, Marta; Hammitt, Laura L; Hilty, Markus; Ho, Pak-Leung; Jayasinghe, Sanjay; Kellner, James D; Kleynhans, Jackie; Knol, Mirjam J; Kozakova, Jana; Kristinsson, Karl G; Ladhani, Shamez N; MacDonald, Laura; Mackenzie, Grant A; Mad'arová, Lucia; McGeer, Allison; Mereckiene, Jolita; Morfeldt, Eva; Mungun, Tuya; Muñoz-Almagro, Carmen; Nuorti, J Pekka; Paragi, Metka; Pilishvili, Tamara; Puentes, Rodrigo; Saha, Samir K; Sahu Khan, Aalisha.
Affiliation
  • Bennett JC; Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
  • Hetrich MK; Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
  • Garcia Quesada M; Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
  • Sinkevitch JN; Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
  • Deloria Knoll M; Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
  • Feikin DR; Independent Consultant, 1296 Coppet, Switzerland.
  • Zeger SL; Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
  • Kagucia EW; KEMRI-Wellcome Trust Research Programme, Epidemiology and Demography Department, Centre for Geographic Medicine-Coast, P.O. Box 230-80108, Kilifi, Kenya.
  • Cohen AL; World Health Organization, 1202 Geneva, Switzerland.
  • Ampofo K; Division of Pediatric Infectious Diseases, Department of Pediatrics, University of Utah Health Sciences Center, Salt Lake City, UT 84132, USA.
  • Brandileone MC; National Laboratory for Meningitis and Pneumococcal Infections, Center of Bacteriology, Institute Adolfo Lutz (IAL), São Paulo 01246-902, Brazil.
  • Bruden D; Arctic Investigations Program, Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Anchorage, AK 99508, USA.
  • Camilli R; Department of Infectious Diseases, Italian National Institute of Health (Istituto Superiore di Sanità, ISS), 00161 Rome, Italy.
  • Castilla J; CIBER Epidemiología y Salud Pública (CIBERESP), 28029 Madrid, Spain.
  • Chan G; Instituto de Salud Pública de Navarra-IdiSNA, 31003 Pamplona, Navarra, Spain.
  • Cook H; Singapore Ministry of Health, Communicable Diseases Division, Singapore 308442, Singapore.
  • Cornick JE; Centre for Disease Control, Department of Health and Community Services, Darwin, NT 8000, Australia.
  • Dagan R; Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool CH64 7TE, UK.
  • Dalby T; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, P.O. Box 30096, Chichiri, Blantyre 3, Malawi.
  • Danis K; Faculty of Health Sciences, Ben-Gurion University of the Negev, 8410501 Beer-Sheva, Israel.
  • de Miguel S; Bacteria, Parasites and Fungi, Statens Serum Institut, DK-2300 Copenhagen, Denmark.
  • De Wals P; Santé Publique France, the French National Public Health Agency, Saint Maurice CEDEX, 94415 Paris, France.
  • Desmet S; Epidemiology Department, Dirección General de Salud Pública, 28009 Madrid, Spain.
  • Georgakopoulou T; Department of Social and Preventive Medicine, Laval University, Québec, QC G1V 0A6, Canada.
  • Gilkison C; Department of Microbiology, Immunology and Transplantation, KU Leuven, BE-3000 Leuven, Belgium.
  • Grgic-Vitek M; National Reference Centre for Streptococcus Pneumoniae, University Hospitals Leuven, 3000 Leuven, Belgium.
  • Hammitt LL; National Public Health Organisation, 15123 Athens, Greece.
  • Hilty M; Epidemiology Team, Institute of Environmental Science and Research, Porirua, 5240 Wellington, New Zealand.
  • Ho PL; Communicable Diseases Centre, National Institute of Public Health, 1000 Ljubljana, Slovenia.
  • Jayasinghe S; Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
  • Kellner JD; KEMRI-Wellcome Trust Research Programme, Epidemiology and Demography Department, Centre for Geographic Medicine-Coast, P.O. Box 230-80108, Kilifi, Kenya.
  • Kleynhans J; Swiss National Reference Centre for Invasive Pneumococci, Institute for Infectious Diseases, University of Bern, 3012 Bern, Switzerland.
  • Knol MJ; Department of Microbiology and Carol Yu Centre for Infection, The University of Hong Kong, Hong Kong, China.
  • Kozakova J; National Centre for Immunisation Research and Surveillance and Discipline of Child and Adolescent Health, Children's Hospital Westmead Clinical School, Faculty of Medicine and Health, University of Sydney, Westmead, NSW 2145, Australia.
  • Kristinsson KG; Department of Pediatrics, University of Calgary, and Alberta Health Services, Calgary, AB T3B 6A8, Canada.
  • Ladhani SN; Centre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases of the National Health Laboratory Service, 2192 Johannesburg, South Africa.
  • MacDonald L; School of Public Health, Faculty of Health Sciences, University of the Witwatersrand, 2000 Johannesburg, South Africa.
  • Mackenzie GA; National Institute for Public Health and the Environment, 3721 MA Bilthoven, The Netherlands.
  • Mad'arová L; National Institute of Public Health (NIPH), 100 42, Praha Czech Republic.
  • McGeer A; Department of Clinical Microbiology, Landspitali-The National University Hospital, Hringbraut, 101 Reykjavik, Iceland.
  • Mereckiene J; Immunisation and Countermeasures Division, Public Health England, London NW9 5EQ, UK.
  • Morfeldt E; Public Health Scotland, Glasgow G2 6QE, UK.
  • Mungun T; Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, Keppel St, London, WC1E 7HT, UK.
  • Muñoz-Almagro C; Medical Research Council Unit the Gambia atLondon School of Hygiene & Tropical Medicine, P.O. Box 273, Banjul, The Gambia.
  • Nuorti JP; New Vaccines Group, Murdoch Children's Research Institute, Parkville, Melbourne, 3052, Victoria, Australia.
  • Paragi M; National Reference Centre for Pneumococcal and Haemophilus Diseases, Regional Authority of Public Health, 975 56 Banská Bystrica, Slovakia.
  • Pilishvili T; Toronto Invasive Bacterial Diseases Network, Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON M5S 1A8, Canada.
  • Puentes R; HSE Health Protection Surveillance Centre, Mountjoy, Dublin D01 A4A3, Ireland.
  • Saha SK; Department of Microbiology, Public Health Agency of Sweden, 171 82 Solna, Sweden.
  • Sahu Khan A; National Center of Communicable Diseases (NCCD), Ministry of Health, Bayanzurkh District, Ulaanbaatar 13336, Mongolia.
Microorganisms ; 9(4)2021 03 27.
Article in En | MEDLINE | ID: mdl-33801760
ABSTRACT
Streptococcus pneumoniae serotype 1 (ST1) was an important cause of invasive pneumococcal disease (IPD) globally before the introduction of pneumococcal conjugate vaccines (PCVs) containing ST1 antigen. The Pneumococcal Serotype Replacement and Distribution Estimation (PSERENADE) project gathered ST1 IPD surveillance data from sites globally and aimed to estimate PCV10/13 impact on ST1 IPD incidence. We estimated ST1 IPD incidence rate ratios (IRRs) comparing the pre-PCV10/13 period to each post-PCV10/13 year by site using a Bayesian multi-level, mixed-effects Poisson regression and all-site IRRs using a linear mixed-effects regression (N = 45 sites). Following PCV10/13 introduction, the incidence rate (IR) of ST1 IPD declined among all ages. After six years of PCV10/13 use, the all-site IRR was 0.05 (95% credibility interval 0.04-0.06) for all ages, 0.05 (0.04-0.05) for <5 years of age, 0.08 (0.06-0.09) for 5-17 years, 0.06 (0.05-0.08) for 18-49 years, 0.06 (0.05-0.07) for 50-64 years, and 0.05 (0.04-0.06) for ≥65 years. PCV10/13 use in infant immunization programs was followed by a 95% reduction in ST1 IPD in all ages after approximately 6 years. Limited data availability from the highest ST1 disease burden countries using a 3+0 schedule constrains generalizability and data from these settings are needed.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Microorganisms Year: 2021 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Microorganisms Year: 2021 Document type: Article Affiliation country: Estados Unidos
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