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A Paper-Based Test for Screening Newborns for Sickle Cell Disease
The high cost, complexity and reliance on electricity, specialized equipment and supplies associated with conventional diagnostic methods limit the scope and sustainability of newborn screening for sickle cell disease (SCD) in sub-Saharan Africa and other resource-limited areas worldwide. Here we de...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5377336/ https://www.ncbi.nlm.nih.gov/pubmed/28367971 http://dx.doi.org/10.1038/srep45488 |
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author | Piety, Nathaniel Z. George, Alex Serrano, Sonia Lanzi, Maria R. Patel, Palka R. Noli, Maria P. Kahan, Silvina Nirenberg, Damian Camanda, João F. Airewele, Gladstone Shevkoplyas, Sergey S. |
author_facet | Piety, Nathaniel Z. George, Alex Serrano, Sonia Lanzi, Maria R. Patel, Palka R. Noli, Maria P. Kahan, Silvina Nirenberg, Damian Camanda, João F. Airewele, Gladstone Shevkoplyas, Sergey S. |
author_sort | Piety, Nathaniel Z. |
collection | PubMed |
description | The high cost, complexity and reliance on electricity, specialized equipment and supplies associated with conventional diagnostic methods limit the scope and sustainability of newborn screening for sickle cell disease (SCD) in sub-Saharan Africa and other resource-limited areas worldwide. Here we describe the development of a simple, low-cost, rapid, equipment- and electricity-free paper-based test capable of detecting sickle hemoglobin (HbS) in newborn blood samples with a limit of detection of 2% HbS. We validated this newborn paper-based test in a cohort of 159 newborns at an obstetric hospital in Cabinda, Angola. Newborn screening results using the paper-based test were compared to conventional isoelectric focusing (IEF). The test detected the presence of HbS with 81.8% sensitivity and 83.3% specificity, and identified SCD newborns with 100.0% sensitivity and 70.7% specificity. The use of the paper-based test in a two-stage newborn screening process could have excluded about 70% of all newborns from expensive confirmatory testing by IEF, without missing any of the SCD newborns in the studied cohort. This study demonstrates the potential utility of the newborn paper-based test for reducing the overall cost of screening newborns for SCD and thus increasing the practicality of universal newborn SCD screening programs in resource-limited settings. |
format | Online Article Text |
id | pubmed-5377336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53773362017-04-10 A Paper-Based Test for Screening Newborns for Sickle Cell Disease Piety, Nathaniel Z. George, Alex Serrano, Sonia Lanzi, Maria R. Patel, Palka R. Noli, Maria P. Kahan, Silvina Nirenberg, Damian Camanda, João F. Airewele, Gladstone Shevkoplyas, Sergey S. Sci Rep Article The high cost, complexity and reliance on electricity, specialized equipment and supplies associated with conventional diagnostic methods limit the scope and sustainability of newborn screening for sickle cell disease (SCD) in sub-Saharan Africa and other resource-limited areas worldwide. Here we describe the development of a simple, low-cost, rapid, equipment- and electricity-free paper-based test capable of detecting sickle hemoglobin (HbS) in newborn blood samples with a limit of detection of 2% HbS. We validated this newborn paper-based test in a cohort of 159 newborns at an obstetric hospital in Cabinda, Angola. Newborn screening results using the paper-based test were compared to conventional isoelectric focusing (IEF). The test detected the presence of HbS with 81.8% sensitivity and 83.3% specificity, and identified SCD newborns with 100.0% sensitivity and 70.7% specificity. The use of the paper-based test in a two-stage newborn screening process could have excluded about 70% of all newborns from expensive confirmatory testing by IEF, without missing any of the SCD newborns in the studied cohort. This study demonstrates the potential utility of the newborn paper-based test for reducing the overall cost of screening newborns for SCD and thus increasing the practicality of universal newborn SCD screening programs in resource-limited settings. Nature Publishing Group 2017-04-03 /pmc/articles/PMC5377336/ /pubmed/28367971 http://dx.doi.org/10.1038/srep45488 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Piety, Nathaniel Z. George, Alex Serrano, Sonia Lanzi, Maria R. Patel, Palka R. Noli, Maria P. Kahan, Silvina Nirenberg, Damian Camanda, João F. Airewele, Gladstone Shevkoplyas, Sergey S. A Paper-Based Test for Screening Newborns for Sickle Cell Disease |
title | A Paper-Based Test for Screening Newborns for Sickle Cell Disease |
title_full | A Paper-Based Test for Screening Newborns for Sickle Cell Disease |
title_fullStr | A Paper-Based Test for Screening Newborns for Sickle Cell Disease |
title_full_unstemmed | A Paper-Based Test for Screening Newborns for Sickle Cell Disease |
title_short | A Paper-Based Test for Screening Newborns for Sickle Cell Disease |
title_sort | paper-based test for screening newborns for sickle cell disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5377336/ https://www.ncbi.nlm.nih.gov/pubmed/28367971 http://dx.doi.org/10.1038/srep45488 |
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