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Timing of meningococcal vaccination with 4CMenB (Bexsero®) in children with invasive meningococcal group B (MenB) disease in England.
Ladhani, Shamez N; Campbell, Helen; Amin-Chowdhury, Zahin; Lucidarme, Jay; Borrow, Ray; Ramsay, Mary E.
Afiliação
  • Ladhani SN; Immunisation and Countermeasures Division, Public Health England, Colindale, London NW9 5EQ, UK; Paediatric Infectious Diseases Research Group (PIDRG), St. George's University of London, Cranmer Terrace, London SW17 0RE, UK. Electronic address: shamez.ladhani@phe.gov.uk.
  • Campbell H; Immunisation and Countermeasures Division, Public Health England, Colindale, London NW9 5EQ, UK.
  • Amin-Chowdhury Z; Immunisation and Countermeasures Division, Public Health England, Colindale, London NW9 5EQ, UK.
  • Lucidarme J; Meningococcal Reference Unit, Public Health England, Manchester Royal Infirmary, Manchester, UK.
  • Borrow R; Meningococcal Reference Unit, Public Health England, Manchester Royal Infirmary, Manchester, UK.
  • Ramsay ME; Immunisation and Countermeasures Division, Public Health England, Colindale, London NW9 5EQ, UK.
Vaccine ; 40(10): 1493-1498, 2022 03 01.
Article em En | MEDLINE | ID: mdl-35148913
ABSTRACT

BACKGROUND:

Timely vaccination is critical for providing early protection against meningococcal B (MenB) disease because of the high incidence in early childhood. We assessed the timeliness of vaccination in children with confirmed MenB disease after 4CMenB (a recombinant protein-based vaccine) implementation into the national infant immunisation programme in England.

METHODS:

Public Health England (PHE) conducts surveillance of invasive meningococcal disease (IMD) in England. Children born since 01 July 2015 who developed MenB disease between 01 September 2015 and 31 August 2019 (four surveillance years) were included in the analysis.

RESULTS:

There were 276 children with laboratory-confirmed MenB disease, including 36 infants who were too young for vaccination, 59 who were eligible for one 4CMenB dose, 104 for two doses and 77 for 3 doses before they developed MenB disease. Prior to developing MenB disease, there were 59 opportunities for vaccination with two 4CMenB doses in 48/104 (46.5%) eligible infants and 41 opportunities in 28/77 (36.6%) children aged ≥ 1 year who were under-immunised. A schedule with a shorter interval at 8 and 12 weeks of age, compared to the current schedule at 8 and 16 weeks, had the potential to offer an additional 4CMenB dose to 35/58 infants (58.6%) who developed MenB disease between 10 and 18 weeks of age.

CONCLUSIONS:

A high proportion of infants and toddlers with laboratory-confirmed MenB disease had not received their scheduled 4CMenB vaccine prior to developing MenB disease. An infant priming schedule with a shorter interval of 4 weeks has the potential to provide earlier protection against MenB disease.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas Meningocócicas / Neisseria meningitidis Sorogrupo B / Infecções Meningocócicas Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas Meningocócicas / Neisseria meningitidis Sorogrupo B / Infecções Meningocócicas Idioma: En Ano de publicação: 2022 Tipo de documento: Article