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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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.
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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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