Cargando…

When to Start Antiretroviral Therapy in Children Aged 2–5 Years: A Collaborative Causal Modelling Analysis of Cohort Studies from Southern Africa

BACKGROUND: There is limited evidence on the optimal timing of antiretroviral therapy (ART) initiation in children 2–5 y of age. We conducted a causal modelling analysis using the International Epidemiologic Databases to Evaluate AIDS–Southern Africa (IeDEA-SA) collaborative dataset to determine the...

Descripción completa

Detalles Bibliográficos
Autores principales: Schomaker, Michael, Egger, Matthias, Ndirangu, James, Phiri, Sam, Moultrie, Harry, Technau, Karl, Cox, Vivian, Giddy, Janet, Chimbetete, Cleophas, Wood, Robin, Gsponer, Thomas, Bolton Moore, Carolyn, Rabie, Helena, Eley, Brian, Muhe, Lulu, Penazzato, Martina, Essajee, Shaffiq, Keiser, Olivia, Davies, Mary-Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833834/
https://www.ncbi.nlm.nih.gov/pubmed/24260029
http://dx.doi.org/10.1371/journal.pmed.1001555
_version_ 1782291903589384192
author Schomaker, Michael
Egger, Matthias
Ndirangu, James
Phiri, Sam
Moultrie, Harry
Technau, Karl
Cox, Vivian
Giddy, Janet
Chimbetete, Cleophas
Wood, Robin
Gsponer, Thomas
Bolton Moore, Carolyn
Rabie, Helena
Eley, Brian
Muhe, Lulu
Penazzato, Martina
Essajee, Shaffiq
Keiser, Olivia
Davies, Mary-Ann
author_facet Schomaker, Michael
Egger, Matthias
Ndirangu, James
Phiri, Sam
Moultrie, Harry
Technau, Karl
Cox, Vivian
Giddy, Janet
Chimbetete, Cleophas
Wood, Robin
Gsponer, Thomas
Bolton Moore, Carolyn
Rabie, Helena
Eley, Brian
Muhe, Lulu
Penazzato, Martina
Essajee, Shaffiq
Keiser, Olivia
Davies, Mary-Ann
author_sort Schomaker, Michael
collection PubMed
description BACKGROUND: There is limited evidence on the optimal timing of antiretroviral therapy (ART) initiation in children 2–5 y of age. We conducted a causal modelling analysis using the International Epidemiologic Databases to Evaluate AIDS–Southern Africa (IeDEA-SA) collaborative dataset to determine the difference in mortality when starting ART in children aged 2–5 y immediately (irrespective of CD4 criteria), as recommended in the World Health Organization (WHO) 2013 guidelines, compared to deferring to lower CD4 thresholds, for example, the WHO 2010 recommended threshold of CD4 count <750 cells/mm(3) or CD4 percentage (CD4%) <25%. METHODS AND FINDINGS: ART-naïve children enrolling in HIV care at IeDEA-SA sites who were between 24 and 59 mo of age at first visit and with ≥1 visit prior to ART initiation and ≥1 follow-up visit were included. We estimated mortality for ART initiation at different CD4 thresholds for up to 3 y using g-computation, adjusting for measured time-dependent confounding of CD4 percent, CD4 count, and weight-for-age z-score. Confidence intervals were constructed using bootstrapping. The median (first; third quartile) age at first visit of 2,934 children (51% male) included in the analysis was 3.3 y (2.6; 4.1), with a median (first; third quartile) CD4 count of 592 cells/mm(3) (356; 895) and median (first; third quartile) CD4% of 16% (10%; 23%). The estimated cumulative mortality after 3 y for ART initiation at different CD4 thresholds ranged from 3.4% (95% CI: 2.1–6.5) (no ART) to 2.1% (95% CI: 1.3%–3.5%) (ART irrespective of CD4 value). Estimated mortality was overall higher when initiating ART at lower CD4 values or not at all. There was no mortality difference between starting ART immediately, irrespective of CD4 value, and ART initiation at the WHO 2010 recommended threshold of CD4 count <750 cells/mm(3) or CD4% <25%, with mortality estimates of 2.1% (95% CI: 1.3%–3.5%) and 2.2% (95% CI: 1.4%–3.5%) after 3 y, respectively. The analysis was limited by loss to follow-up and the unavailability of WHO staging data. CONCLUSIONS: The results indicate no mortality difference for up to 3 y between ART initiation irrespective of CD4 value and ART initiation at a threshold of CD4 count <750 cells/mm(3) or CD4% <25%, but there are overall higher point estimates for mortality when ART is initiated at lower CD4 values. Please see later in the article for the Editors' Summary
format Online
Article
Text
id pubmed-3833834
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-38338342013-11-20 When to Start Antiretroviral Therapy in Children Aged 2–5 Years: A Collaborative Causal Modelling Analysis of Cohort Studies from Southern Africa Schomaker, Michael Egger, Matthias Ndirangu, James Phiri, Sam Moultrie, Harry Technau, Karl Cox, Vivian Giddy, Janet Chimbetete, Cleophas Wood, Robin Gsponer, Thomas Bolton Moore, Carolyn Rabie, Helena Eley, Brian Muhe, Lulu Penazzato, Martina Essajee, Shaffiq Keiser, Olivia Davies, Mary-Ann PLoS Med Research Article BACKGROUND: There is limited evidence on the optimal timing of antiretroviral therapy (ART) initiation in children 2–5 y of age. We conducted a causal modelling analysis using the International Epidemiologic Databases to Evaluate AIDS–Southern Africa (IeDEA-SA) collaborative dataset to determine the difference in mortality when starting ART in children aged 2–5 y immediately (irrespective of CD4 criteria), as recommended in the World Health Organization (WHO) 2013 guidelines, compared to deferring to lower CD4 thresholds, for example, the WHO 2010 recommended threshold of CD4 count <750 cells/mm(3) or CD4 percentage (CD4%) <25%. METHODS AND FINDINGS: ART-naïve children enrolling in HIV care at IeDEA-SA sites who were between 24 and 59 mo of age at first visit and with ≥1 visit prior to ART initiation and ≥1 follow-up visit were included. We estimated mortality for ART initiation at different CD4 thresholds for up to 3 y using g-computation, adjusting for measured time-dependent confounding of CD4 percent, CD4 count, and weight-for-age z-score. Confidence intervals were constructed using bootstrapping. The median (first; third quartile) age at first visit of 2,934 children (51% male) included in the analysis was 3.3 y (2.6; 4.1), with a median (first; third quartile) CD4 count of 592 cells/mm(3) (356; 895) and median (first; third quartile) CD4% of 16% (10%; 23%). The estimated cumulative mortality after 3 y for ART initiation at different CD4 thresholds ranged from 3.4% (95% CI: 2.1–6.5) (no ART) to 2.1% (95% CI: 1.3%–3.5%) (ART irrespective of CD4 value). Estimated mortality was overall higher when initiating ART at lower CD4 values or not at all. There was no mortality difference between starting ART immediately, irrespective of CD4 value, and ART initiation at the WHO 2010 recommended threshold of CD4 count <750 cells/mm(3) or CD4% <25%, with mortality estimates of 2.1% (95% CI: 1.3%–3.5%) and 2.2% (95% CI: 1.4%–3.5%) after 3 y, respectively. The analysis was limited by loss to follow-up and the unavailability of WHO staging data. CONCLUSIONS: The results indicate no mortality difference for up to 3 y between ART initiation irrespective of CD4 value and ART initiation at a threshold of CD4 count <750 cells/mm(3) or CD4% <25%, but there are overall higher point estimates for mortality when ART is initiated at lower CD4 values. Please see later in the article for the Editors' Summary Public Library of Science 2013-11-19 /pmc/articles/PMC3833834/ /pubmed/24260029 http://dx.doi.org/10.1371/journal.pmed.1001555 Text en © 2013 Schomaker 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
Schomaker, Michael
Egger, Matthias
Ndirangu, James
Phiri, Sam
Moultrie, Harry
Technau, Karl
Cox, Vivian
Giddy, Janet
Chimbetete, Cleophas
Wood, Robin
Gsponer, Thomas
Bolton Moore, Carolyn
Rabie, Helena
Eley, Brian
Muhe, Lulu
Penazzato, Martina
Essajee, Shaffiq
Keiser, Olivia
Davies, Mary-Ann
When to Start Antiretroviral Therapy in Children Aged 2–5 Years: A Collaborative Causal Modelling Analysis of Cohort Studies from Southern Africa
title When to Start Antiretroviral Therapy in Children Aged 2–5 Years: A Collaborative Causal Modelling Analysis of Cohort Studies from Southern Africa
title_full When to Start Antiretroviral Therapy in Children Aged 2–5 Years: A Collaborative Causal Modelling Analysis of Cohort Studies from Southern Africa
title_fullStr When to Start Antiretroviral Therapy in Children Aged 2–5 Years: A Collaborative Causal Modelling Analysis of Cohort Studies from Southern Africa
title_full_unstemmed When to Start Antiretroviral Therapy in Children Aged 2–5 Years: A Collaborative Causal Modelling Analysis of Cohort Studies from Southern Africa
title_short When to Start Antiretroviral Therapy in Children Aged 2–5 Years: A Collaborative Causal Modelling Analysis of Cohort Studies from Southern Africa
title_sort when to start antiretroviral therapy in children aged 2–5 years: a collaborative causal modelling analysis of cohort studies from southern africa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833834/
https://www.ncbi.nlm.nih.gov/pubmed/24260029
http://dx.doi.org/10.1371/journal.pmed.1001555
work_keys_str_mv AT schomakermichael whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT eggermatthias whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT ndirangujames whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT phirisam whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT moultrieharry whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT technaukarl whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT coxvivian whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT giddyjanet whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT chimbetetecleophas whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT woodrobin whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT gsponerthomas whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT boltonmoorecarolyn whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT rabiehelena whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT eleybrian whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT muhelulu whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT penazzatomartina whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT essajeeshaffiq whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT keiserolivia whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT daviesmaryann whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica
AT whentostartantiretroviraltherapyinchildrenaged25yearsacollaborativecausalmodellinganalysisofcohortstudiesfromsouthernafrica