Sample size calculation for estimating key epidemiological parameters using serological data and mathematical modelling
Abstract Background Our work was motivated by the need to, given serum availability and/or financial resources, decide on which samples to test in a serum bank for different pathogens. Simulation-based sample size calculations were performed to determine the age-based sampling structures and optimal...
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doaj-c65a485261884085af98794f2d0104262020-11-25T01:31:23ZengBMCBMC Medical Research Methodology1471-22882019-03-0119111210.1186/s12874-019-0692-1Sample size calculation for estimating key epidemiological parameters using serological data and mathematical modellingStéphanie Blaizot0Sereina A. Herzog1Steven Abrams2Heidi Theeten3Amber Litzroth4Niel Hens5Centre for Health Economics Research and Modelling Infectious Diseases (CHERMID), Vaccine and Infectious Disease Institute (VAXINFECTIO), University of AntwerpCentre for Health Economics Research and Modelling Infectious Diseases (CHERMID), Vaccine and Infectious Disease Institute (VAXINFECTIO), University of AntwerpInteruniversity Institute for Biostatistics and statistical Bioinformatics, UHASSELT, Hasselt UniversityCentre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute (VAXINFECTIO), University of AntwerpService of Epidemiology of infectious diseases, Scientific Directorate Epidemiology and Public Health, SciensanoCentre for Health Economics Research and Modelling Infectious Diseases (CHERMID), Vaccine and Infectious Disease Institute (VAXINFECTIO), University of AntwerpAbstract Background Our work was motivated by the need to, given serum availability and/or financial resources, decide on which samples to test in a serum bank for different pathogens. Simulation-based sample size calculations were performed to determine the age-based sampling structures and optimal allocation of a given number of samples for testing across various age groups best suited to estimate key epidemiological parameters (e.g., seroprevalence or force of infection) with acceptable precision levels in a cross-sectional seroprevalence survey. Methods Statistical and mathematical models and three age-based sampling structures (survey-based structure, population-based structure, uniform structure) were used. Our calculations are based on Belgian serological survey data collected in 2001–2003 where testing was done, amongst others, for the presence of Immunoglobulin G antibodies against measles, mumps, and rubella, for which a national mass immunisation programme was introduced in 1985 in Belgium, and against varicella-zoster virus and parvovirus B19 for which the endemic equilibrium assumption is tenable in Belgium. Results The optimal age-based sampling structure to use in the sampling of a serological survey as well as the optimal allocation distribution varied depending on the epidemiological parameter of interest for a given infection and between infections. Conclusions When estimating epidemiological parameters with acceptable levels of precision within the context of a single cross-sectional serological survey, attention should be given to the age-based sampling structure. Simulation-based sample size calculations in combination with mathematical modelling can be utilised for choosing the optimal allocation of a given number of samples over various age groups.http://link.springer.com/article/10.1186/s12874-019-0692-1Infectious diseasesMathematical modelsStudy designSample sizeAllocationPrecision |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Stéphanie Blaizot Sereina A. Herzog Steven Abrams Heidi Theeten Amber Litzroth Niel Hens |
spellingShingle |
Stéphanie Blaizot Sereina A. Herzog Steven Abrams Heidi Theeten Amber Litzroth Niel Hens Sample size calculation for estimating key epidemiological parameters using serological data and mathematical modelling BMC Medical Research Methodology Infectious diseases Mathematical models Study design Sample size Allocation Precision |
author_facet |
Stéphanie Blaizot Sereina A. Herzog Steven Abrams Heidi Theeten Amber Litzroth Niel Hens |
author_sort |
Stéphanie Blaizot |
title |
Sample size calculation for estimating key epidemiological parameters using serological data and mathematical modelling |
title_short |
Sample size calculation for estimating key epidemiological parameters using serological data and mathematical modelling |
title_full |
Sample size calculation for estimating key epidemiological parameters using serological data and mathematical modelling |
title_fullStr |
Sample size calculation for estimating key epidemiological parameters using serological data and mathematical modelling |
title_full_unstemmed |
Sample size calculation for estimating key epidemiological parameters using serological data and mathematical modelling |
title_sort |
sample size calculation for estimating key epidemiological parameters using serological data and mathematical modelling |
publisher |
BMC |
series |
BMC Medical Research Methodology |
issn |
1471-2288 |
publishDate |
2019-03-01 |
description |
Abstract Background Our work was motivated by the need to, given serum availability and/or financial resources, decide on which samples to test in a serum bank for different pathogens. Simulation-based sample size calculations were performed to determine the age-based sampling structures and optimal allocation of a given number of samples for testing across various age groups best suited to estimate key epidemiological parameters (e.g., seroprevalence or force of infection) with acceptable precision levels in a cross-sectional seroprevalence survey. Methods Statistical and mathematical models and three age-based sampling structures (survey-based structure, population-based structure, uniform structure) were used. Our calculations are based on Belgian serological survey data collected in 2001–2003 where testing was done, amongst others, for the presence of Immunoglobulin G antibodies against measles, mumps, and rubella, for which a national mass immunisation programme was introduced in 1985 in Belgium, and against varicella-zoster virus and parvovirus B19 for which the endemic equilibrium assumption is tenable in Belgium. Results The optimal age-based sampling structure to use in the sampling of a serological survey as well as the optimal allocation distribution varied depending on the epidemiological parameter of interest for a given infection and between infections. Conclusions When estimating epidemiological parameters with acceptable levels of precision within the context of a single cross-sectional serological survey, attention should be given to the age-based sampling structure. Simulation-based sample size calculations in combination with mathematical modelling can be utilised for choosing the optimal allocation of a given number of samples over various age groups. |
topic |
Infectious diseases Mathematical models Study design Sample size Allocation Precision |
url |
http://link.springer.com/article/10.1186/s12874-019-0692-1 |
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