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Improving the coverage of the PMTCT programme through a participatory quality improvement intervention in South Africa
BACKGROUND: Despite several years of implementation, prevention of mother-to-child transmission (PMTCT) programmes in many resource poor settings are failing to reach the majority of HIV positive women. We report on a data driven participatory quality improvement intervention implemented in a high H...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777166/ https://www.ncbi.nlm.nih.gov/pubmed/19891775 http://dx.doi.org/10.1186/1471-2458-9-406 |
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author | Doherty, Tanya Chopra, Mickey Nsibande, Duduzile Mngoma, Dudu |
author_facet | Doherty, Tanya Chopra, Mickey Nsibande, Duduzile Mngoma, Dudu |
author_sort | Doherty, Tanya |
collection | PubMed |
description | BACKGROUND: Despite several years of implementation, prevention of mother-to-child transmission (PMTCT) programmes in many resource poor settings are failing to reach the majority of HIV positive women. We report on a data driven participatory quality improvement intervention implemented in a high HIV prevalence district in South Africa. METHODS: A participatory quality improvement intervention was implemented consisting of an initial assessment undertaken by a team of district supervisors, workshops to assess results, identify weaknesses and set improvement targets and continuous monitoring to support changes. RESULTS: The assessment highlighted weaknesses in training and supervision. Routine data revealed poor coverage of all programme indicators except HIV testing. Monthly support to all facilities took place including an orientation to the PMTCT protocol, review of local data and identification of bottlenecks to optimal coverage using a continuous quality improvement approach. One year following the intervention large improvements in programme indicators were observed. Coverage of CD4 testing increased from 40 to 97%, uptake of maternal nevirapine from 57 to 96%, uptake of infant nevirapine from 15 to 68% and six week PCR testing from 24 to 68%. CONCLUSION: It is estimated that these improvements in coverage could avert 580 new infant infections per year in this district. This relatively simple participatory assessment and intervention process has enabled programme managers to use a data driven approach to improve the coverage of this important programme. |
format | Text |
id | pubmed-2777166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27771662009-11-15 Improving the coverage of the PMTCT programme through a participatory quality improvement intervention in South Africa Doherty, Tanya Chopra, Mickey Nsibande, Duduzile Mngoma, Dudu BMC Public Health Research Article BACKGROUND: Despite several years of implementation, prevention of mother-to-child transmission (PMTCT) programmes in many resource poor settings are failing to reach the majority of HIV positive women. We report on a data driven participatory quality improvement intervention implemented in a high HIV prevalence district in South Africa. METHODS: A participatory quality improvement intervention was implemented consisting of an initial assessment undertaken by a team of district supervisors, workshops to assess results, identify weaknesses and set improvement targets and continuous monitoring to support changes. RESULTS: The assessment highlighted weaknesses in training and supervision. Routine data revealed poor coverage of all programme indicators except HIV testing. Monthly support to all facilities took place including an orientation to the PMTCT protocol, review of local data and identification of bottlenecks to optimal coverage using a continuous quality improvement approach. One year following the intervention large improvements in programme indicators were observed. Coverage of CD4 testing increased from 40 to 97%, uptake of maternal nevirapine from 57 to 96%, uptake of infant nevirapine from 15 to 68% and six week PCR testing from 24 to 68%. CONCLUSION: It is estimated that these improvements in coverage could avert 580 new infant infections per year in this district. This relatively simple participatory assessment and intervention process has enabled programme managers to use a data driven approach to improve the coverage of this important programme. BioMed Central 2009-11-05 /pmc/articles/PMC2777166/ /pubmed/19891775 http://dx.doi.org/10.1186/1471-2458-9-406 Text en Copyright © 2009 Doherty 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 Doherty, Tanya Chopra, Mickey Nsibande, Duduzile Mngoma, Dudu Improving the coverage of the PMTCT programme through a participatory quality improvement intervention in South Africa |
title | Improving the coverage of the PMTCT programme through a participatory quality improvement intervention in South Africa |
title_full | Improving the coverage of the PMTCT programme through a participatory quality improvement intervention in South Africa |
title_fullStr | Improving the coverage of the PMTCT programme through a participatory quality improvement intervention in South Africa |
title_full_unstemmed | Improving the coverage of the PMTCT programme through a participatory quality improvement intervention in South Africa |
title_short | Improving the coverage of the PMTCT programme through a participatory quality improvement intervention in South Africa |
title_sort | improving the coverage of the pmtct programme through a participatory quality improvement intervention in south africa |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777166/ https://www.ncbi.nlm.nih.gov/pubmed/19891775 http://dx.doi.org/10.1186/1471-2458-9-406 |
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