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BED Estimates of HIV Incidence: Resolving the Differences, Making Things Simpler

OBJECTIVE: Develop a simple method for optimal estimation of HIV incidence using the BED capture enzyme immunoassay. DESIGN: Use existing BED data to estimate mean recency duration, false recency rates and HIV incidence with reference to a fixed time period, T. METHODS: Compare BED and cohort estima...

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Detalles Bibliográficos
Autores principales: Hargrove, John, van Schalkwyk, Cari, Eastwood, Hayden
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250478/
https://www.ncbi.nlm.nih.gov/pubmed/22235334
http://dx.doi.org/10.1371/journal.pone.0029736
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author Hargrove, John
van Schalkwyk, Cari
Eastwood, Hayden
author_facet Hargrove, John
van Schalkwyk, Cari
Eastwood, Hayden
author_sort Hargrove, John
collection PubMed
description OBJECTIVE: Develop a simple method for optimal estimation of HIV incidence using the BED capture enzyme immunoassay. DESIGN: Use existing BED data to estimate mean recency duration, false recency rates and HIV incidence with reference to a fixed time period, T. METHODS: Compare BED and cohort estimates of incidence referring to identical time frames. Generalize this approach to suggest a method for estimating HIV incidence from any cross-sectional survey. RESULTS: Follow-up and BED analyses of the same, initially HIV negative, cases followed over the same set time period T, produce estimates of the same HIV incidence, permitting the estimation of the BED mean recency period for cases who have been HIV positive for less than T. Follow-up of HIV positive cases over T, similarly, provides estimates of the false-recent rate appropriate for T. Knowledge of these two parameters for a given population allows the estimation of HIV incidence during T by applying the BED method to samples from cross-sectional surveys. An algorithm is derived for providing these estimates, adjusted for the false-recent rate. The resulting estimator is identical to one derived independently using a more formal mathematical analysis. Adjustments improve the accuracy of HIV incidence estimates. Negative incidence estimates result from the use of inappropriate estimates of the false-recent rate and/or from sampling error, not from any error in the adjustment procedure. CONCLUSIONS: Referring all estimates of mean recency periods, false-recent rates and incidence estimates to a fixed period T simplifies estimation procedures and allows the development of a consistent method for producing adjusted estimates of HIV incidence of improved accuracy. Unadjusted BED estimates of incidence, based on life-time recency periods, would be both extremely difficult to produce and of doubtful value.
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spelling pubmed-32504782012-01-10 BED Estimates of HIV Incidence: Resolving the Differences, Making Things Simpler Hargrove, John van Schalkwyk, Cari Eastwood, Hayden PLoS One Research Article OBJECTIVE: Develop a simple method for optimal estimation of HIV incidence using the BED capture enzyme immunoassay. DESIGN: Use existing BED data to estimate mean recency duration, false recency rates and HIV incidence with reference to a fixed time period, T. METHODS: Compare BED and cohort estimates of incidence referring to identical time frames. Generalize this approach to suggest a method for estimating HIV incidence from any cross-sectional survey. RESULTS: Follow-up and BED analyses of the same, initially HIV negative, cases followed over the same set time period T, produce estimates of the same HIV incidence, permitting the estimation of the BED mean recency period for cases who have been HIV positive for less than T. Follow-up of HIV positive cases over T, similarly, provides estimates of the false-recent rate appropriate for T. Knowledge of these two parameters for a given population allows the estimation of HIV incidence during T by applying the BED method to samples from cross-sectional surveys. An algorithm is derived for providing these estimates, adjusted for the false-recent rate. The resulting estimator is identical to one derived independently using a more formal mathematical analysis. Adjustments improve the accuracy of HIV incidence estimates. Negative incidence estimates result from the use of inappropriate estimates of the false-recent rate and/or from sampling error, not from any error in the adjustment procedure. CONCLUSIONS: Referring all estimates of mean recency periods, false-recent rates and incidence estimates to a fixed period T simplifies estimation procedures and allows the development of a consistent method for producing adjusted estimates of HIV incidence of improved accuracy. Unadjusted BED estimates of incidence, based on life-time recency periods, would be both extremely difficult to produce and of doubtful value. Public Library of Science 2012-01-03 /pmc/articles/PMC3250478/ /pubmed/22235334 http://dx.doi.org/10.1371/journal.pone.0029736 Text en Hargrove et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hargrove, John
van Schalkwyk, Cari
Eastwood, Hayden
BED Estimates of HIV Incidence: Resolving the Differences, Making Things Simpler
title BED Estimates of HIV Incidence: Resolving the Differences, Making Things Simpler
title_full BED Estimates of HIV Incidence: Resolving the Differences, Making Things Simpler
title_fullStr BED Estimates of HIV Incidence: Resolving the Differences, Making Things Simpler
title_full_unstemmed BED Estimates of HIV Incidence: Resolving the Differences, Making Things Simpler
title_short BED Estimates of HIV Incidence: Resolving the Differences, Making Things Simpler
title_sort bed estimates of hiv incidence: resolving the differences, making things simpler
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250478/
https://www.ncbi.nlm.nih.gov/pubmed/22235334
http://dx.doi.org/10.1371/journal.pone.0029736
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