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Establishing a database for sickle cell disease patient mapping and survival tracking: The sickle pan-african research consortium Nigeria example
Background: The Sickle Pan-African Research Consortium (SPARCO) and Sickle Africa Data Coordinating Center (SADaCC) were set up with funding from the US National Institute of Health (NIH) for physicians, scientists, patients, support groups, and statisticians to collaborate to reduce the high diseas...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672677/ https://www.ncbi.nlm.nih.gov/pubmed/36406113 http://dx.doi.org/10.3389/fgene.2022.1041462 |
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author | Nnodu, Obiageli Madu, Anazoeze Chianumba, Reuben Isa, Hezekiah Alkali Olanrewaju, Isaac Osagie, Samuel Oyekanmi, Nash Sangeda, Raphael Zozimus Stewart, Annemie Nembaware, Victoria Morrice, Jack Jonas, Mario Mazandu, Gaston Wonkam, Ambroise Owolabi, Olumide |
author_facet | Nnodu, Obiageli Madu, Anazoeze Chianumba, Reuben Isa, Hezekiah Alkali Olanrewaju, Isaac Osagie, Samuel Oyekanmi, Nash Sangeda, Raphael Zozimus Stewart, Annemie Nembaware, Victoria Morrice, Jack Jonas, Mario Mazandu, Gaston Wonkam, Ambroise Owolabi, Olumide |
author_sort | Nnodu, Obiageli |
collection | PubMed |
description | Background: The Sickle Pan-African Research Consortium (SPARCO) and Sickle Africa Data Coordinating Center (SADaCC) were set up with funding from the US National Institute of Health (NIH) for physicians, scientists, patients, support groups, and statisticians to collaborate to reduce the high disease burden and alleviate the impact of Sickle Cell Disease (SCD) in Africa. For 5 years, SPARCO and SADaCC have been collecting basic clinical and demographic data from Nigeria, Tanzania, and Ghana. The resulting database will support analyses to estimate significant clinical events and provide directions for targeting interventions and assessing their impacts. Method: The Nigerian study sited at Centre of Excellence for Sickle Cell Disease Research and Training (CESRTA), University of Abuja, adopted REDCap for online database management. The case report form (CRF) was adapted from 1,400 data elements adopted by SPARCO sites. It captures 215 data elements of interest across sub-sites, i.e., demographic, social, diagnostic, clinical, laboratory, imaging, and others. These were harmonized using the SADaCC data dictionary. REDCap was installed on University of Abuja cloud server at https://www.redcap.uniabuja.edu.ng. Data collected at the sites are sent to CESRTA for collation, cleaning and uploading to the database. Results: 7,767 people living with sickle cell disease were enrolled at 25 health institutions across the six zones in Nigeria with 5,295 having had at least one follow-up visit with their clinical data updated. They range from 44 to 1,180 from 3 centers from South East, 4 from South, 5 from South West, 8 from North Central, 4 in North West and 3 in the North East. North West has registered 1,383 patients, representing 17.8%; North East, 359 (4.6%); North Central, 2,947 (37.9%); South West, 1,609 (20.7%); South, 442 (5.7%) and South East, 1,027 patients (13.2%). Conclusion: The database is being used to support studies including analysis of clinical phenotypes of SCD in Nigeria, and evaluation of Hydroxyurea use in SCD. Reports undergoing review in journals have relied on the ease of data access in REDCap. The database is regularly updated by batch and individual record uploads while we are utilizing REDCap’s in-built functions to generate simple statistic. |
format | Online Article Text |
id | pubmed-9672677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96726772022-11-19 Establishing a database for sickle cell disease patient mapping and survival tracking: The sickle pan-african research consortium Nigeria example Nnodu, Obiageli Madu, Anazoeze Chianumba, Reuben Isa, Hezekiah Alkali Olanrewaju, Isaac Osagie, Samuel Oyekanmi, Nash Sangeda, Raphael Zozimus Stewart, Annemie Nembaware, Victoria Morrice, Jack Jonas, Mario Mazandu, Gaston Wonkam, Ambroise Owolabi, Olumide Front Genet Genetics Background: The Sickle Pan-African Research Consortium (SPARCO) and Sickle Africa Data Coordinating Center (SADaCC) were set up with funding from the US National Institute of Health (NIH) for physicians, scientists, patients, support groups, and statisticians to collaborate to reduce the high disease burden and alleviate the impact of Sickle Cell Disease (SCD) in Africa. For 5 years, SPARCO and SADaCC have been collecting basic clinical and demographic data from Nigeria, Tanzania, and Ghana. The resulting database will support analyses to estimate significant clinical events and provide directions for targeting interventions and assessing their impacts. Method: The Nigerian study sited at Centre of Excellence for Sickle Cell Disease Research and Training (CESRTA), University of Abuja, adopted REDCap for online database management. The case report form (CRF) was adapted from 1,400 data elements adopted by SPARCO sites. It captures 215 data elements of interest across sub-sites, i.e., demographic, social, diagnostic, clinical, laboratory, imaging, and others. These were harmonized using the SADaCC data dictionary. REDCap was installed on University of Abuja cloud server at https://www.redcap.uniabuja.edu.ng. Data collected at the sites are sent to CESRTA for collation, cleaning and uploading to the database. Results: 7,767 people living with sickle cell disease were enrolled at 25 health institutions across the six zones in Nigeria with 5,295 having had at least one follow-up visit with their clinical data updated. They range from 44 to 1,180 from 3 centers from South East, 4 from South, 5 from South West, 8 from North Central, 4 in North West and 3 in the North East. North West has registered 1,383 patients, representing 17.8%; North East, 359 (4.6%); North Central, 2,947 (37.9%); South West, 1,609 (20.7%); South, 442 (5.7%) and South East, 1,027 patients (13.2%). Conclusion: The database is being used to support studies including analysis of clinical phenotypes of SCD in Nigeria, and evaluation of Hydroxyurea use in SCD. Reports undergoing review in journals have relied on the ease of data access in REDCap. The database is regularly updated by batch and individual record uploads while we are utilizing REDCap’s in-built functions to generate simple statistic. Frontiers Media S.A. 2022-11-04 /pmc/articles/PMC9672677/ /pubmed/36406113 http://dx.doi.org/10.3389/fgene.2022.1041462 Text en Copyright © 2022 Nnodu, Madu, Chianumba, Isa, Olanrewaju, Osagie, Oyekanmi, Sangeda, Stewart, Nembaware, Morrice, Jonas, Mazandu, Wonkam and Owolabi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Nnodu, Obiageli Madu, Anazoeze Chianumba, Reuben Isa, Hezekiah Alkali Olanrewaju, Isaac Osagie, Samuel Oyekanmi, Nash Sangeda, Raphael Zozimus Stewart, Annemie Nembaware, Victoria Morrice, Jack Jonas, Mario Mazandu, Gaston Wonkam, Ambroise Owolabi, Olumide Establishing a database for sickle cell disease patient mapping and survival tracking: The sickle pan-african research consortium Nigeria example |
title | Establishing a database for sickle cell disease patient mapping and survival tracking: The sickle pan-african research consortium Nigeria example |
title_full | Establishing a database for sickle cell disease patient mapping and survival tracking: The sickle pan-african research consortium Nigeria example |
title_fullStr | Establishing a database for sickle cell disease patient mapping and survival tracking: The sickle pan-african research consortium Nigeria example |
title_full_unstemmed | Establishing a database for sickle cell disease patient mapping and survival tracking: The sickle pan-african research consortium Nigeria example |
title_short | Establishing a database for sickle cell disease patient mapping and survival tracking: The sickle pan-african research consortium Nigeria example |
title_sort | establishing a database for sickle cell disease patient mapping and survival tracking: the sickle pan-african research consortium nigeria example |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672677/ https://www.ncbi.nlm.nih.gov/pubmed/36406113 http://dx.doi.org/10.3389/fgene.2022.1041462 |
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