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Family, Community, and Health System Considerations for Reducing the Burden of Pediatric Sickle Cell Disease in Uganda Through Newborn Screening
Sickle cell disease (SCD) is associated with high mortality for children under 5 years of age in sub-Saharan Africa. Newborn sickle screening program and enhanced capacity for SCD treatment are under development to reduce disease burden in Uganda and elsewhere in the region. Based on an internationa...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905129/ https://www.ncbi.nlm.nih.gov/pubmed/27336011 http://dx.doi.org/10.1177/2333794X16637767 |
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author | Green, Nancy S. Mathur, Sanyukta Kiguli, Sarah Makani, Julie Fashakin, Victoria LaRussa, Philip Lyimo, Magdalena Abrams, Elaine J. Mulumba, Lukia Mupere, Ezekiel |
author_facet | Green, Nancy S. Mathur, Sanyukta Kiguli, Sarah Makani, Julie Fashakin, Victoria LaRussa, Philip Lyimo, Magdalena Abrams, Elaine J. Mulumba, Lukia Mupere, Ezekiel |
author_sort | Green, Nancy S. |
collection | PubMed |
description | Sickle cell disease (SCD) is associated with high mortality for children under 5 years of age in sub-Saharan Africa. Newborn sickle screening program and enhanced capacity for SCD treatment are under development to reduce disease burden in Uganda and elsewhere in the region. Based on an international stakeholder meeting and a family-directed conference on SCD in Kampala in 2015, and interviews with parents, multinational experts, and other key informants, we describe health care, community, and family perspectives in support of these initiatives. Key stakeholder meetings, discussions, and interviews were held to understand perspectives of public health and multinational leadership, patients and families, as well as national progress, resource needs, medical and social barriers to program success, and resources leveraged from HIV/AIDS. Partnering with program leadership, professionals, patients and families, multinational stakeholders, and leveraging resources from existing programs are needed for building successful programs in Uganda and elsewhere in sub-Saharan Africa. |
format | Online Article Text |
id | pubmed-4905129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-49051292016-06-22 Family, Community, and Health System Considerations for Reducing the Burden of Pediatric Sickle Cell Disease in Uganda Through Newborn Screening Green, Nancy S. Mathur, Sanyukta Kiguli, Sarah Makani, Julie Fashakin, Victoria LaRussa, Philip Lyimo, Magdalena Abrams, Elaine J. Mulumba, Lukia Mupere, Ezekiel Glob Pediatr Health Original Article Sickle cell disease (SCD) is associated with high mortality for children under 5 years of age in sub-Saharan Africa. Newborn sickle screening program and enhanced capacity for SCD treatment are under development to reduce disease burden in Uganda and elsewhere in the region. Based on an international stakeholder meeting and a family-directed conference on SCD in Kampala in 2015, and interviews with parents, multinational experts, and other key informants, we describe health care, community, and family perspectives in support of these initiatives. Key stakeholder meetings, discussions, and interviews were held to understand perspectives of public health and multinational leadership, patients and families, as well as national progress, resource needs, medical and social barriers to program success, and resources leveraged from HIV/AIDS. Partnering with program leadership, professionals, patients and families, multinational stakeholders, and leveraging resources from existing programs are needed for building successful programs in Uganda and elsewhere in sub-Saharan Africa. SAGE Publications 2016-04-07 /pmc/articles/PMC4905129/ /pubmed/27336011 http://dx.doi.org/10.1177/2333794X16637767 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Green, Nancy S. Mathur, Sanyukta Kiguli, Sarah Makani, Julie Fashakin, Victoria LaRussa, Philip Lyimo, Magdalena Abrams, Elaine J. Mulumba, Lukia Mupere, Ezekiel Family, Community, and Health System Considerations for Reducing the Burden of Pediatric Sickle Cell Disease in Uganda Through Newborn Screening |
title | Family, Community, and Health System Considerations for Reducing the Burden of Pediatric Sickle Cell Disease in Uganda Through Newborn Screening |
title_full | Family, Community, and Health System Considerations for Reducing the Burden of Pediatric Sickle Cell Disease in Uganda Through Newborn Screening |
title_fullStr | Family, Community, and Health System Considerations for Reducing the Burden of Pediatric Sickle Cell Disease in Uganda Through Newborn Screening |
title_full_unstemmed | Family, Community, and Health System Considerations for Reducing the Burden of Pediatric Sickle Cell Disease in Uganda Through Newborn Screening |
title_short | Family, Community, and Health System Considerations for Reducing the Burden of Pediatric Sickle Cell Disease in Uganda Through Newborn Screening |
title_sort | family, community, and health system considerations for reducing the burden of pediatric sickle cell disease in uganda through newborn screening |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905129/ https://www.ncbi.nlm.nih.gov/pubmed/27336011 http://dx.doi.org/10.1177/2333794X16637767 |
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