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Using emergency department syndromic surveillance to investigate the impact of a national vaccination program: A retrospective observational study.
Hughes, Helen E; Elliot, Alex J; Hughes, Thomas C; Hungerford, Daniel; Morbey, Roger A; Smith, Gillian E; Vivancos, Roberto; O'Brien, Sarah J.
Afiliação
  • Hughes HE; Real-time Syndromic Surveillance Team, Field Service, National Infection Service, Public Health England, Birmingham, United Kingdom.
  • Elliot AJ; Farr Institute at HeRC, University of Liverpool, Liverpool, United Kingdom.
  • Hughes TC; Real-time Syndromic Surveillance Team, Field Service, National Infection Service, Public Health England, Birmingham, United Kingdom.
  • Hungerford D; John Radcliffe Hospital, Oxford, United Kingdom.
  • Morbey RA; The Centre for Global Vaccine Research, Institute of Infection and Global Health, University of Liverpool, Liverpool, United Kingdom.
  • Smith GE; Field Epidemiology North West, Field Service, National Infection Service, Public Health England, Liverpool, United Kingdom.
  • Vivancos R; Real-time Syndromic Surveillance Team, Field Service, National Infection Service, Public Health England, Birmingham, United Kingdom.
  • O'Brien SJ; Real-time Syndromic Surveillance Team, Field Service, National Infection Service, Public Health England, Birmingham, United Kingdom.
PLoS One ; 15(10): e0240021, 2020.
Article em En | MEDLINE | ID: mdl-33031389
BACKGROUND: Rotavirus infection is a common cause of gastroenteritis in children worldwide, with a high mortality burden in developing countries, particularly during the first two years of life. Rotavirus vaccination was introduced into the United Kingdom childhood vaccination schedule in July 2013, with high coverage (>90%) achieved by June 2016. We used an emergency department (ED) syndromic surveillance system to assess the impact of the rotavirus vaccination programme, specifically through the demonstration of any immediate and continuing impact on ED gastroenteritis visits in England. METHODS: This retrospective, observational study used syndromic surveillance data collected from 3 EDs in the two years before (July 2011-June 2013) and 3 years post (July 2013-June 2016) introduction of rotavirus vaccination. The weekly levels of ED visits for gastroenteritis (by age group and in total) during the period before rotavirus vaccination was first described alongside the findings of laboratory surveillance of rotavirus during the same period. An interrupted time-series analysis was then performed to demonstrate the impact of rotavirus vaccination introduction on gastroenteritis ED visit levels. RESULTS: During the two years before vaccine introduction ED visits for gastroenteritis in total and for the 0-4 years age group were seen to rise and fall in line with the seasonal rotavirus increases reported by laboratory surveillance. ED gastroenteritis visits by young children were lower in the three years following introduction of rotavirus vaccination (reduced from 8% of visits to 6% of visits). These attendance levels in young children (0-4years) remained higher than in older age groups, however the previously large seasonal increases in children were greatly reduced, from peaks of 16% to 3-10% of ED visits per week. CONCLUSIONS: ED syndromic surveillance demonstrated a reduction in gastroenteritis visits following rotavirus vaccine introduction. This work establishes ED syndromic surveillance as a platform for rapid impact assessment of future vaccine programmes.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Programas de Imunização / Serviço Hospitalar de Emergência Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Programas de Imunização / Serviço Hospitalar de Emergência Idioma: En Ano de publicação: 2020 Tipo de documento: Article