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Imputing HIV treatment start dates from routine laboratory data in South Africa: a validation study

BACKGROUND: Poor clinical record keeping hinders health systems monitoring and patient care in many low resource settings. We develop and validate a novel method to impute dates of antiretroviral treatment (ART) initiation from routine laboratory data in South Africa’s public sector HIV program. Thi...

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Autores principales: Maskew, Mhairi, Bor, Jacob, Hendrickson, Cheryl, MacLeod, William, Bärnighausen, Till, Pillay, Deenan, Sanne, Ian, Carmona, Sergio, Stevens, Wendy, Fox, Matthew P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240407/
https://www.ncbi.nlm.nih.gov/pubmed/28095905
http://dx.doi.org/10.1186/s12913-016-1940-2
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author Maskew, Mhairi
Bor, Jacob
Hendrickson, Cheryl
MacLeod, William
Bärnighausen, Till
Pillay, Deenan
Sanne, Ian
Carmona, Sergio
Stevens, Wendy
Fox, Matthew P
author_facet Maskew, Mhairi
Bor, Jacob
Hendrickson, Cheryl
MacLeod, William
Bärnighausen, Till
Pillay, Deenan
Sanne, Ian
Carmona, Sergio
Stevens, Wendy
Fox, Matthew P
author_sort Maskew, Mhairi
collection PubMed
description BACKGROUND: Poor clinical record keeping hinders health systems monitoring and patient care in many low resource settings. We develop and validate a novel method to impute dates of antiretroviral treatment (ART) initiation from routine laboratory data in South Africa’s public sector HIV program. This method will enable monitoring of the national ART program using real-time laboratory data, avoiding the error potential of chart review. METHODS: We developed an algorithm to impute ART start dates based on the date of a patient’s “ART workup”, i.e. the laboratory tests used to determine treatment readiness in national guidelines, and the time from ART workup to initiation based on clinical protocols (21 days). To validate the algorithm, we analyzed data from two large clinical HIV cohorts: Hlabisa HIV Treatment and Care Programme in rural KwaZulu-Natal; and Right to Care Cohort in urban Gauteng. Both cohorts contain known ART initiation dates and laboratory results imported directly from the National Health Laboratory Service. We assessed median time from ART workup to ART initiation and calculated sensitivity (SE), specificity (SP), positive predictive value (PPV), and negative predictive value (NPV) of our imputed start date vs. the true start date within a 6 month window. Heterogeneity was assessed across individual clinics and over time. RESULTS: We analyzed data from over 80,000 HIV-positive adults. Among patients who had a workup and initiated ART, median time to initiation was 16 days (IQR 7,31) in Hlabisa and 21 (IQR 8,43) in RTC cohort. Among patients with known ART start dates, SE of the imputed start date was 83% in Hlabisa and 88% in RTC, indicating this method accurately predicts ART start dates for about 85% of all ART initiators. In Hlabisa, PPV was 95%, indicating that for patients with a lab workup, true start dates were predicted with high accuracy. SP (100%) and NPV (92%) were also very high. CONCLUSIONS: Routine laboratory data can be used to infer ART initiation dates in South Africa’s public sector. Where care is provided based on protocols, laboratory data can be used to monitor health systems performance and improve accuracy and completeness of clinical records. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12913-016-1940-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-52404072017-01-23 Imputing HIV treatment start dates from routine laboratory data in South Africa: a validation study Maskew, Mhairi Bor, Jacob Hendrickson, Cheryl MacLeod, William Bärnighausen, Till Pillay, Deenan Sanne, Ian Carmona, Sergio Stevens, Wendy Fox, Matthew P BMC Health Serv Res Technical Advance BACKGROUND: Poor clinical record keeping hinders health systems monitoring and patient care in many low resource settings. We develop and validate a novel method to impute dates of antiretroviral treatment (ART) initiation from routine laboratory data in South Africa’s public sector HIV program. This method will enable monitoring of the national ART program using real-time laboratory data, avoiding the error potential of chart review. METHODS: We developed an algorithm to impute ART start dates based on the date of a patient’s “ART workup”, i.e. the laboratory tests used to determine treatment readiness in national guidelines, and the time from ART workup to initiation based on clinical protocols (21 days). To validate the algorithm, we analyzed data from two large clinical HIV cohorts: Hlabisa HIV Treatment and Care Programme in rural KwaZulu-Natal; and Right to Care Cohort in urban Gauteng. Both cohorts contain known ART initiation dates and laboratory results imported directly from the National Health Laboratory Service. We assessed median time from ART workup to ART initiation and calculated sensitivity (SE), specificity (SP), positive predictive value (PPV), and negative predictive value (NPV) of our imputed start date vs. the true start date within a 6 month window. Heterogeneity was assessed across individual clinics and over time. RESULTS: We analyzed data from over 80,000 HIV-positive adults. Among patients who had a workup and initiated ART, median time to initiation was 16 days (IQR 7,31) in Hlabisa and 21 (IQR 8,43) in RTC cohort. Among patients with known ART start dates, SE of the imputed start date was 83% in Hlabisa and 88% in RTC, indicating this method accurately predicts ART start dates for about 85% of all ART initiators. In Hlabisa, PPV was 95%, indicating that for patients with a lab workup, true start dates were predicted with high accuracy. SP (100%) and NPV (92%) were also very high. CONCLUSIONS: Routine laboratory data can be used to infer ART initiation dates in South Africa’s public sector. Where care is provided based on protocols, laboratory data can be used to monitor health systems performance and improve accuracy and completeness of clinical records. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12913-016-1940-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-17 /pmc/articles/PMC5240407/ /pubmed/28095905 http://dx.doi.org/10.1186/s12913-016-1940-2 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Technical Advance
Maskew, Mhairi
Bor, Jacob
Hendrickson, Cheryl
MacLeod, William
Bärnighausen, Till
Pillay, Deenan
Sanne, Ian
Carmona, Sergio
Stevens, Wendy
Fox, Matthew P
Imputing HIV treatment start dates from routine laboratory data in South Africa: a validation study
title Imputing HIV treatment start dates from routine laboratory data in South Africa: a validation study
title_full Imputing HIV treatment start dates from routine laboratory data in South Africa: a validation study
title_fullStr Imputing HIV treatment start dates from routine laboratory data in South Africa: a validation study
title_full_unstemmed Imputing HIV treatment start dates from routine laboratory data in South Africa: a validation study
title_short Imputing HIV treatment start dates from routine laboratory data in South Africa: a validation study
title_sort imputing hiv treatment start dates from routine laboratory data in south africa: a validation study
topic Technical Advance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240407/
https://www.ncbi.nlm.nih.gov/pubmed/28095905
http://dx.doi.org/10.1186/s12913-016-1940-2
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