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Computed CD4 percentage as a low-cost method for determining pediatric antiretroviral treatment eligibility
BACKGROUND: The performance of the WHO recommendations for pediatric antiretroviral treatment (ART) in resource poor settings is insufficiently documented in routine care. METHODS: We compared clinical and immunological criteria in 366 children aged 0 to 12 years in Kinshasa and evaluated a simple c...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292192/ https://www.ncbi.nlm.nih.gov/pubmed/18325119 http://dx.doi.org/10.1186/1471-2334-8-31 |
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author | Callens, Steven FJ Kitetele, Faustin Lusiama, Jean Shabani, Nicole Edidi, Samuel Colebunders, Robert Behets, Frieda Van Rie, Annelies |
author_facet | Callens, Steven FJ Kitetele, Faustin Lusiama, Jean Shabani, Nicole Edidi, Samuel Colebunders, Robert Behets, Frieda Van Rie, Annelies |
author_sort | Callens, Steven FJ |
collection | PubMed |
description | BACKGROUND: The performance of the WHO recommendations for pediatric antiretroviral treatment (ART) in resource poor settings is insufficiently documented in routine care. METHODS: We compared clinical and immunological criteria in 366 children aged 0 to 12 years in Kinshasa and evaluated a simple computation to estimate CD4 percent, based on CD4 count, total white blood cell count and percentage lymphocytes. Kappa (κ) statistic was used to evaluate eligibility criteria and linear regression to determine trends of CD4 percent, count and total lymphocyte count (TLC). RESULTS: Agreement between clinical and immunological eligibility criteria was poor (κ = 0.26). One third of children clinically eligible for ART were ineligible using immunological criteria; one third of children immunologically eligible were ineligible using clinical criteria. Among children presenting in WHO stage I or II, 54 (32%) were eligible according to immunological criteria. Agreement with CD4 percent was poor for TLC (κ = 0.04), fair for total CD4 count (κ = 0.39) and substantial for CD4 percent computational estimate (κ = 0.71). Among 5 to 12 years old children, total CD4 count was higher in younger age groups (-32 cells/mm(3 )per year older), CD4 percent was similar across age groups. CONCLUSION: Age-specific thresholds for CD4 percent optimally determine pediatric ART eligibility. The use of CD4 percent computational estimate may increase ART access in settings with limited access to CD4 percent assays. |
format | Text |
id | pubmed-2292192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22921922008-04-11 Computed CD4 percentage as a low-cost method for determining pediatric antiretroviral treatment eligibility Callens, Steven FJ Kitetele, Faustin Lusiama, Jean Shabani, Nicole Edidi, Samuel Colebunders, Robert Behets, Frieda Van Rie, Annelies BMC Infect Dis Research Article BACKGROUND: The performance of the WHO recommendations for pediatric antiretroviral treatment (ART) in resource poor settings is insufficiently documented in routine care. METHODS: We compared clinical and immunological criteria in 366 children aged 0 to 12 years in Kinshasa and evaluated a simple computation to estimate CD4 percent, based on CD4 count, total white blood cell count and percentage lymphocytes. Kappa (κ) statistic was used to evaluate eligibility criteria and linear regression to determine trends of CD4 percent, count and total lymphocyte count (TLC). RESULTS: Agreement between clinical and immunological eligibility criteria was poor (κ = 0.26). One third of children clinically eligible for ART were ineligible using immunological criteria; one third of children immunologically eligible were ineligible using clinical criteria. Among children presenting in WHO stage I or II, 54 (32%) were eligible according to immunological criteria. Agreement with CD4 percent was poor for TLC (κ = 0.04), fair for total CD4 count (κ = 0.39) and substantial for CD4 percent computational estimate (κ = 0.71). Among 5 to 12 years old children, total CD4 count was higher in younger age groups (-32 cells/mm(3 )per year older), CD4 percent was similar across age groups. CONCLUSION: Age-specific thresholds for CD4 percent optimally determine pediatric ART eligibility. The use of CD4 percent computational estimate may increase ART access in settings with limited access to CD4 percent assays. BioMed Central 2008-03-06 /pmc/articles/PMC2292192/ /pubmed/18325119 http://dx.doi.org/10.1186/1471-2334-8-31 Text en Copyright © 2008 Callens et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Callens, Steven FJ Kitetele, Faustin Lusiama, Jean Shabani, Nicole Edidi, Samuel Colebunders, Robert Behets, Frieda Van Rie, Annelies Computed CD4 percentage as a low-cost method for determining pediatric antiretroviral treatment eligibility |
title | Computed CD4 percentage as a low-cost method for determining pediatric antiretroviral treatment eligibility |
title_full | Computed CD4 percentage as a low-cost method for determining pediatric antiretroviral treatment eligibility |
title_fullStr | Computed CD4 percentage as a low-cost method for determining pediatric antiretroviral treatment eligibility |
title_full_unstemmed | Computed CD4 percentage as a low-cost method for determining pediatric antiretroviral treatment eligibility |
title_short | Computed CD4 percentage as a low-cost method for determining pediatric antiretroviral treatment eligibility |
title_sort | computed cd4 percentage as a low-cost method for determining pediatric antiretroviral treatment eligibility |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292192/ https://www.ncbi.nlm.nih.gov/pubmed/18325119 http://dx.doi.org/10.1186/1471-2334-8-31 |
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