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Incidence rate estimation, periodic testing and the limitations of the mid-point imputation approach

BACKGROUND: It is common to use the mid-point between the latest-negative and earliest-positive test dates as the date of the infection event. However, the accuracy of the mid-point method has yet to be systematically quantified for incidence studies once participants start to miss their scheduled t...

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Autores principales: Vandormael, Alain, Dobra, Adrian, Bärnighausen, Till, de Oliveira, Tulio, Tanser, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5837439/
https://www.ncbi.nlm.nih.gov/pubmed/29024978
http://dx.doi.org/10.1093/ije/dyx134
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author Vandormael, Alain
Dobra, Adrian
Bärnighausen, Till
de Oliveira, Tulio
Tanser, Frank
author_facet Vandormael, Alain
Dobra, Adrian
Bärnighausen, Till
de Oliveira, Tulio
Tanser, Frank
author_sort Vandormael, Alain
collection PubMed
description BACKGROUND: It is common to use the mid-point between the latest-negative and earliest-positive test dates as the date of the infection event. However, the accuracy of the mid-point method has yet to be systematically quantified for incidence studies once participants start to miss their scheduled test dates. METHODS: We used a simulation-based approach to generate an infectious disease epidemic for an incidence cohort with a high (80–100%), moderate (60–79.9%), low (40–59.9%) and poor (30–39.9%) testing rate. Next, we imputed a mid-point and random-point value between the participant’s latest-negative and earliest-positive test dates. We then compared the incidence rate derived from these imputed values with the true incidence rate generated from the simulation model. RESULTS: The mid-point incidence rate estimates erroneously declined towards the end of the observation period once the testing rate dropped below 80%. This decline was in error of approximately 9%, 27% and 41% for a moderate, low and poor testing rate, respectively. The random-point method did not introduce any systematic bias in the incidence rate estimate, even for testing rates as low as 30%. CONCLUSIONS: The mid-point assumption of the infection date is unjustified and should not be used to calculate the incidence rate once participants start to miss the scheduled test dates. Under these conditions, we show an artefactual decline in the incidence rate towards the end of the observation period. Alternatively, the single random-point method is straightforward to implement and produces estimates very close to the true incidence rate.
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spelling pubmed-58374392018-03-09 Incidence rate estimation, periodic testing and the limitations of the mid-point imputation approach Vandormael, Alain Dobra, Adrian Bärnighausen, Till de Oliveira, Tulio Tanser, Frank Int J Epidemiol Methods BACKGROUND: It is common to use the mid-point between the latest-negative and earliest-positive test dates as the date of the infection event. However, the accuracy of the mid-point method has yet to be systematically quantified for incidence studies once participants start to miss their scheduled test dates. METHODS: We used a simulation-based approach to generate an infectious disease epidemic for an incidence cohort with a high (80–100%), moderate (60–79.9%), low (40–59.9%) and poor (30–39.9%) testing rate. Next, we imputed a mid-point and random-point value between the participant’s latest-negative and earliest-positive test dates. We then compared the incidence rate derived from these imputed values with the true incidence rate generated from the simulation model. RESULTS: The mid-point incidence rate estimates erroneously declined towards the end of the observation period once the testing rate dropped below 80%. This decline was in error of approximately 9%, 27% and 41% for a moderate, low and poor testing rate, respectively. The random-point method did not introduce any systematic bias in the incidence rate estimate, even for testing rates as low as 30%. CONCLUSIONS: The mid-point assumption of the infection date is unjustified and should not be used to calculate the incidence rate once participants start to miss the scheduled test dates. Under these conditions, we show an artefactual decline in the incidence rate towards the end of the observation period. Alternatively, the single random-point method is straightforward to implement and produces estimates very close to the true incidence rate. Oxford University Press 2018-02 2017-08-09 /pmc/articles/PMC5837439/ /pubmed/29024978 http://dx.doi.org/10.1093/ije/dyx134 Text en © The Author 2017. Published by Oxford University Press on behalf of the International Epidemiological Association http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Methods
Vandormael, Alain
Dobra, Adrian
Bärnighausen, Till
de Oliveira, Tulio
Tanser, Frank
Incidence rate estimation, periodic testing and the limitations of the mid-point imputation approach
title Incidence rate estimation, periodic testing and the limitations of the mid-point imputation approach
title_full Incidence rate estimation, periodic testing and the limitations of the mid-point imputation approach
title_fullStr Incidence rate estimation, periodic testing and the limitations of the mid-point imputation approach
title_full_unstemmed Incidence rate estimation, periodic testing and the limitations of the mid-point imputation approach
title_short Incidence rate estimation, periodic testing and the limitations of the mid-point imputation approach
title_sort incidence rate estimation, periodic testing and the limitations of the mid-point imputation approach
topic Methods
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5837439/
https://www.ncbi.nlm.nih.gov/pubmed/29024978
http://dx.doi.org/10.1093/ije/dyx134
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