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Conditional probability and ratio‐based approaches for mapping the coverage of multi‐dose vaccines

Many vaccines are often administered in multiple doses to boost their effectiveness. In the case of childhood vaccines, the coverage maps of the doses and the differences between these often constitute an evidence base to guide investments in improving access to vaccination services and health syste...

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Autores principales: Utazi, Chigozie Edson, Aheto, Justice Moses K., Chan, Ho Man Theophilus, Tatem, Andrew J., Sahu, Sujit K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826002/
https://www.ncbi.nlm.nih.gov/pubmed/36129171
http://dx.doi.org/10.1002/sim.9586
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author Utazi, Chigozie Edson
Aheto, Justice Moses K.
Chan, Ho Man Theophilus
Tatem, Andrew J.
Sahu, Sujit K.
author_facet Utazi, Chigozie Edson
Aheto, Justice Moses K.
Chan, Ho Man Theophilus
Tatem, Andrew J.
Sahu, Sujit K.
author_sort Utazi, Chigozie Edson
collection PubMed
description Many vaccines are often administered in multiple doses to boost their effectiveness. In the case of childhood vaccines, the coverage maps of the doses and the differences between these often constitute an evidence base to guide investments in improving access to vaccination services and health system performance in low and middle‐income countries. A major problem often encountered when mapping the coverage of multi‐dose vaccines is the need to ensure that the coverage maps decrease monotonically with successive doses. That is, for doses [Formula: see text] and [Formula: see text] , [Formula: see text] , where [Formula: see text] is the coverage of dose [Formula: see text] at spatial location [Formula: see text]. Here, we explore conditional probability (CP) and ratio‐based (RB) approaches for mapping [Formula: see text] , embedded within a binomial geostatistical modeling framework, to address this problem. The fully Bayesian model is implemented using the INLA and SPDE approaches. Using a simulation study, we find that both approaches perform comparably for out‐of‐sample estimation under varying point‐level sample size distributions. We apply the methodology to map the coverage of the three doses of diphtheria‐tetanus‐pertussis vaccine using data from the 2018 Nigeria Demographic and Health Survey. The coverage maps produced using both approaches are almost indistinguishable, although the CP approach yielded more precise estimates on average in this application. We also provide estimates of zero‐dose children and the dropout rates between the doses. The methodology is straightforward to implement and can be applied to other vaccines and geographical contexts.
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spelling pubmed-98260022023-01-09 Conditional probability and ratio‐based approaches for mapping the coverage of multi‐dose vaccines Utazi, Chigozie Edson Aheto, Justice Moses K. Chan, Ho Man Theophilus Tatem, Andrew J. Sahu, Sujit K. Stat Med Research Articles Many vaccines are often administered in multiple doses to boost their effectiveness. In the case of childhood vaccines, the coverage maps of the doses and the differences between these often constitute an evidence base to guide investments in improving access to vaccination services and health system performance in low and middle‐income countries. A major problem often encountered when mapping the coverage of multi‐dose vaccines is the need to ensure that the coverage maps decrease monotonically with successive doses. That is, for doses [Formula: see text] and [Formula: see text] , [Formula: see text] , where [Formula: see text] is the coverage of dose [Formula: see text] at spatial location [Formula: see text]. Here, we explore conditional probability (CP) and ratio‐based (RB) approaches for mapping [Formula: see text] , embedded within a binomial geostatistical modeling framework, to address this problem. The fully Bayesian model is implemented using the INLA and SPDE approaches. Using a simulation study, we find that both approaches perform comparably for out‐of‐sample estimation under varying point‐level sample size distributions. We apply the methodology to map the coverage of the three doses of diphtheria‐tetanus‐pertussis vaccine using data from the 2018 Nigeria Demographic and Health Survey. The coverage maps produced using both approaches are almost indistinguishable, although the CP approach yielded more precise estimates on average in this application. We also provide estimates of zero‐dose children and the dropout rates between the doses. The methodology is straightforward to implement and can be applied to other vaccines and geographical contexts. John Wiley & Sons, Inc. 2022-09-21 2022-12-20 /pmc/articles/PMC9826002/ /pubmed/36129171 http://dx.doi.org/10.1002/sim.9586 Text en © 2022 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Utazi, Chigozie Edson
Aheto, Justice Moses K.
Chan, Ho Man Theophilus
Tatem, Andrew J.
Sahu, Sujit K.
Conditional probability and ratio‐based approaches for mapping the coverage of multi‐dose vaccines
title Conditional probability and ratio‐based approaches for mapping the coverage of multi‐dose vaccines
title_full Conditional probability and ratio‐based approaches for mapping the coverage of multi‐dose vaccines
title_fullStr Conditional probability and ratio‐based approaches for mapping the coverage of multi‐dose vaccines
title_full_unstemmed Conditional probability and ratio‐based approaches for mapping the coverage of multi‐dose vaccines
title_short Conditional probability and ratio‐based approaches for mapping the coverage of multi‐dose vaccines
title_sort conditional probability and ratio‐based approaches for mapping the coverage of multi‐dose vaccines
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826002/
https://www.ncbi.nlm.nih.gov/pubmed/36129171
http://dx.doi.org/10.1002/sim.9586
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