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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...

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Autores principales: Green, Nancy S., Mathur, Sanyukta, Kiguli, Sarah, Makani, Julie, Fashakin, Victoria, LaRussa, Philip, Lyimo, Magdalena, Abrams, Elaine J., Mulumba, Lukia, Mupere, Ezekiel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
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.
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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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