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Analysis of the 2007–2018 National Health Interview Survey (NHIS): Examining Neurological Complications among Children with Sickle Cell Disease in the United States
This study compared neurological complications among a national sample of United States children with or without sickle cell disease (SCD) and evaluated health status, healthcare and special education utilization patterns, barriers to care, and association of SCD status and demographics/socioeconomi...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298081/ https://www.ncbi.nlm.nih.gov/pubmed/37372724 http://dx.doi.org/10.3390/ijerph20126137 |
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author | Peprah, Emmanuel Gyamfi, Joyce Lee, Justin Tyler Islam, Farha Opeyemi, Jumoke Tampubolon, Siphra Ojo, Temitope Qiao, Wanqiu Mai, Andi Wang, Cong Vieira, Dorice Meda, Shreya Adenikinju, Deborah Osei-Tutu, Nana Ryan, Nessa Ogedegbe, Gbenga |
author_facet | Peprah, Emmanuel Gyamfi, Joyce Lee, Justin Tyler Islam, Farha Opeyemi, Jumoke Tampubolon, Siphra Ojo, Temitope Qiao, Wanqiu Mai, Andi Wang, Cong Vieira, Dorice Meda, Shreya Adenikinju, Deborah Osei-Tutu, Nana Ryan, Nessa Ogedegbe, Gbenga |
author_sort | Peprah, Emmanuel |
collection | PubMed |
description | This study compared neurological complications among a national sample of United States children with or without sickle cell disease (SCD) and evaluated health status, healthcare and special education utilization patterns, barriers to care, and association of SCD status and demographics/socioeconomic status (SES) on comorbidities and healthcare utilization. Data was acquired from the National Health Interview Survey (NHIS) Sample Child Core questionnaire 2007–2018 dataset that included 133,542 children. An affirmation from the guardian of the child determined the presence of SCD. Regression analysis was used to compare the associations between SCD and demographics/SES on neurological conditions at p < 0.05. Furthermore, adjusted odds ratios (AORs) were estimated for having various neurological conditions. Of the 133,481 children included in the NHIS, the mean age was 8.5 years (SD: 0.02) and 215 had SCD. Of the children with SCD, the sample composition included male (n = 110), and Black (n = 82%). The SCD sample had higher odds of having neuro-developmental conditions (p < 0.1). Families of Black children (55% weighted) reported household incomes < 100% of federal poverty level. Black children were more likely to experience longer wait times to see the doctor (AOR, 0.3; CI 0.1–1.1). Compared to children without SCD, those with SCD had a greater chance of seeing a medical specialist within 12 months (AOR 2.3; CI 1.5–3.7). This representative sample of US children with SCD shows higher odds of developing neurological complications, increased healthcare and special education services utilization, with Black children experiencing a disproportionate burden. This creates the urgency to address the health burden for children with SCD by implementing interventions in healthcare and increasing education assistance programs to combat neurocognitive impairments, especially among Black children. |
format | Online Article Text |
id | pubmed-10298081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102980812023-06-28 Analysis of the 2007–2018 National Health Interview Survey (NHIS): Examining Neurological Complications among Children with Sickle Cell Disease in the United States Peprah, Emmanuel Gyamfi, Joyce Lee, Justin Tyler Islam, Farha Opeyemi, Jumoke Tampubolon, Siphra Ojo, Temitope Qiao, Wanqiu Mai, Andi Wang, Cong Vieira, Dorice Meda, Shreya Adenikinju, Deborah Osei-Tutu, Nana Ryan, Nessa Ogedegbe, Gbenga Int J Environ Res Public Health Article This study compared neurological complications among a national sample of United States children with or without sickle cell disease (SCD) and evaluated health status, healthcare and special education utilization patterns, barriers to care, and association of SCD status and demographics/socioeconomic status (SES) on comorbidities and healthcare utilization. Data was acquired from the National Health Interview Survey (NHIS) Sample Child Core questionnaire 2007–2018 dataset that included 133,542 children. An affirmation from the guardian of the child determined the presence of SCD. Regression analysis was used to compare the associations between SCD and demographics/SES on neurological conditions at p < 0.05. Furthermore, adjusted odds ratios (AORs) were estimated for having various neurological conditions. Of the 133,481 children included in the NHIS, the mean age was 8.5 years (SD: 0.02) and 215 had SCD. Of the children with SCD, the sample composition included male (n = 110), and Black (n = 82%). The SCD sample had higher odds of having neuro-developmental conditions (p < 0.1). Families of Black children (55% weighted) reported household incomes < 100% of federal poverty level. Black children were more likely to experience longer wait times to see the doctor (AOR, 0.3; CI 0.1–1.1). Compared to children without SCD, those with SCD had a greater chance of seeing a medical specialist within 12 months (AOR 2.3; CI 1.5–3.7). This representative sample of US children with SCD shows higher odds of developing neurological complications, increased healthcare and special education services utilization, with Black children experiencing a disproportionate burden. This creates the urgency to address the health burden for children with SCD by implementing interventions in healthcare and increasing education assistance programs to combat neurocognitive impairments, especially among Black children. MDPI 2023-06-15 /pmc/articles/PMC10298081/ /pubmed/37372724 http://dx.doi.org/10.3390/ijerph20126137 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Peprah, Emmanuel Gyamfi, Joyce Lee, Justin Tyler Islam, Farha Opeyemi, Jumoke Tampubolon, Siphra Ojo, Temitope Qiao, Wanqiu Mai, Andi Wang, Cong Vieira, Dorice Meda, Shreya Adenikinju, Deborah Osei-Tutu, Nana Ryan, Nessa Ogedegbe, Gbenga Analysis of the 2007–2018 National Health Interview Survey (NHIS): Examining Neurological Complications among Children with Sickle Cell Disease in the United States |
title | Analysis of the 2007–2018 National Health Interview Survey (NHIS): Examining Neurological Complications among Children with Sickle Cell Disease in the United States |
title_full | Analysis of the 2007–2018 National Health Interview Survey (NHIS): Examining Neurological Complications among Children with Sickle Cell Disease in the United States |
title_fullStr | Analysis of the 2007–2018 National Health Interview Survey (NHIS): Examining Neurological Complications among Children with Sickle Cell Disease in the United States |
title_full_unstemmed | Analysis of the 2007–2018 National Health Interview Survey (NHIS): Examining Neurological Complications among Children with Sickle Cell Disease in the United States |
title_short | Analysis of the 2007–2018 National Health Interview Survey (NHIS): Examining Neurological Complications among Children with Sickle Cell Disease in the United States |
title_sort | analysis of the 2007–2018 national health interview survey (nhis): examining neurological complications among children with sickle cell disease in the united states |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298081/ https://www.ncbi.nlm.nih.gov/pubmed/37372724 http://dx.doi.org/10.3390/ijerph20126137 |
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