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Assays for the Specific Growth Rate and Cell-binding Ability of Rotavirus
Published on: January 28, 2019
First year experience of rotavirus immunisation programme in Finland
Tuija Leino1, Jukka Ollgren, Heini Salo
1Department of Vaccination and Immune Protection, National Institute for Health and Welfare (THL), Mannerheimintie 166, Helsinki, Finland. tuija.leino@thl.fi
Vaccine
|November 6, 2012
Summary
Rotavirus (RV) immunisation significantly reduced hospital-treated acute gastroenteritis (AGE) and severe RV disease in Finland. The vaccine program demonstrated a high overall impact, controlling severe RVGE in young children.
Area of Science:
- Public Health
- Vaccinology
- Epidemiology
Background:
- Rotavirus (RV) immunisation programs aim to reduce the burden of acute gastroenteritis (AGE) and severe RV disease.
- Vaccine-probe studies estimate unspecific disease burden reduction attributable to the targeted agent.
Purpose of the Study:
- To estimate the impact of the rotavirus (RV) immunisation program on total hospital-treated AGE and severe RV disease burden in Finland.
- To assess the vaccine's effectiveness in the first year post-introduction.
Main Methods:
- Utilized the National Hospital Discharge Register data coded with ICD-10 codes (A00-A09, R11, K52).
- Compared incidences of hospitalised and outpatient cases of AGE and RVGE before (1999-2005) and after (2010) the immunisation program.
- Focused on children under 5 years of age.
Main Results:
- Significant reductions observed in hospital inpatient RV-associated gastroenteritis (RVGE) by 80.3% and total inpatient AGE by 53.9% in toddlers (<1 year).
- Hospital outpatient cases showed reductions of 78.8% in RVGE and 12.5% in total AGE.
- Overall vaccine impact against confirmed RVGE in eligible cohorts was 97%.
Conclusions:
- The RV immunisation program effectively controlled severe, hospital-treated RVGE in its first year.
- Total disease burden is a more reliable endpoint than diagnosed cases, as diagnostic practices evolve post-vaccination.
- The study's follow-up period was limited to the first post-introduction year.
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