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Successful paediatric HIV treatment in rural primary care in Africa
OBJECTIVE: Clinical outcomes of HIV-infected children on antiretroviral treatment (ART) in a decentralised, nurse/counsellor-led programme. DESIGN: Clinical cohort. SETTING: KwaZulu-Natal, South Africa. PATIENTS: HIV-infected children aged ≤15 years on ART, June 2004–2008. MAIN OUTCOME MEASURES: Sur...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Group
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181433/ https://www.ncbi.nlm.nih.gov/pubmed/19880392 http://dx.doi.org/10.1136/adc.2009.169367 |
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author | Janssen, N Ndirangu, J Newell, M-L Bland, RM |
author_facet | Janssen, N Ndirangu, J Newell, M-L Bland, RM |
author_sort | Janssen, N |
collection | PubMed |
description | OBJECTIVE: Clinical outcomes of HIV-infected children on antiretroviral treatment (ART) in a decentralised, nurse/counsellor-led programme. DESIGN: Clinical cohort. SETTING: KwaZulu-Natal, South Africa. PATIENTS: HIV-infected children aged ≤15 years on ART, June 2004–2008. MAIN OUTCOME MEASURES: Survival according to baseline characteristics including age, WHO clinical stage, haemoglobin and CD4%, was assessed in Kaplan–Meier analyses. Hazard ratios for mortality were estimated using Cox proportional hazards regression and changes in laboratory parameters and weight-for-age z scores after 6–12 months' treatment were calculated. RESULTS: 477 HIV-infected children began ART at a median age of 74 months (range 4–180), median CD4 count (CD4%) of 433 cells/mm(3) (17%) and median HIV viral load of log 4.2 copies/ml; 105 (22%) were on treatment for tuberculosis and 317 (76.6%) were WHO stage 3/4. There were significant increases after ART initiation in CD4% (17% vs 22%; p<0.001), haemoglobin (9.9 vs 11.7 g/l; p≤0.001) and albumin (30 vs 36 g/l; p≤0.001). 32 (6.7%) children died over 732 child-years of follow-up (43.7 deaths/1000 child-years; 95% CI 32.7 to 58.2), 17 (53.1%) within 90 days of treatment initiation; median age of death was 84 (IQR 10–181) months. Children with baseline haemoglobin ≤8 g/l were more likely to die (adjusted HR 4.5; 95% CI 1.6 to 12.3), as were those aged <18 months compared with >60 months (adjusted HR 3.2; 95% CI 1.2 to 9.1). CONCLUSIONS: Good clinical outcomes in HIV-infected children on ART are possible in a rural, decentralised service. Few young children are on ART, highlighting the urgent need to identify HIV-exposed infants. |
format | Online Article Text |
id | pubmed-3181433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BMJ Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-31814332011-10-04 Successful paediatric HIV treatment in rural primary care in Africa Janssen, N Ndirangu, J Newell, M-L Bland, RM Arch Dis Child Original Articles OBJECTIVE: Clinical outcomes of HIV-infected children on antiretroviral treatment (ART) in a decentralised, nurse/counsellor-led programme. DESIGN: Clinical cohort. SETTING: KwaZulu-Natal, South Africa. PATIENTS: HIV-infected children aged ≤15 years on ART, June 2004–2008. MAIN OUTCOME MEASURES: Survival according to baseline characteristics including age, WHO clinical stage, haemoglobin and CD4%, was assessed in Kaplan–Meier analyses. Hazard ratios for mortality were estimated using Cox proportional hazards regression and changes in laboratory parameters and weight-for-age z scores after 6–12 months' treatment were calculated. RESULTS: 477 HIV-infected children began ART at a median age of 74 months (range 4–180), median CD4 count (CD4%) of 433 cells/mm(3) (17%) and median HIV viral load of log 4.2 copies/ml; 105 (22%) were on treatment for tuberculosis and 317 (76.6%) were WHO stage 3/4. There were significant increases after ART initiation in CD4% (17% vs 22%; p<0.001), haemoglobin (9.9 vs 11.7 g/l; p≤0.001) and albumin (30 vs 36 g/l; p≤0.001). 32 (6.7%) children died over 732 child-years of follow-up (43.7 deaths/1000 child-years; 95% CI 32.7 to 58.2), 17 (53.1%) within 90 days of treatment initiation; median age of death was 84 (IQR 10–181) months. Children with baseline haemoglobin ≤8 g/l were more likely to die (adjusted HR 4.5; 95% CI 1.6 to 12.3), as were those aged <18 months compared with >60 months (adjusted HR 3.2; 95% CI 1.2 to 9.1). CONCLUSIONS: Good clinical outcomes in HIV-infected children on ART are possible in a rural, decentralised service. Few young children are on ART, highlighting the urgent need to identify HIV-exposed infants. BMJ Group 2009-10-29 /pmc/articles/PMC3181433/ /pubmed/19880392 http://dx.doi.org/10.1136/adc.2009.169367 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode. |
spellingShingle | Original Articles Janssen, N Ndirangu, J Newell, M-L Bland, RM Successful paediatric HIV treatment in rural primary care in Africa |
title | Successful paediatric HIV treatment in rural primary care in Africa |
title_full | Successful paediatric HIV treatment in rural primary care in Africa |
title_fullStr | Successful paediatric HIV treatment in rural primary care in Africa |
title_full_unstemmed | Successful paediatric HIV treatment in rural primary care in Africa |
title_short | Successful paediatric HIV treatment in rural primary care in Africa |
title_sort | successful paediatric hiv treatment in rural primary care in africa |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181433/ https://www.ncbi.nlm.nih.gov/pubmed/19880392 http://dx.doi.org/10.1136/adc.2009.169367 |
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