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Assessing Systems of Care for US Children with Epilepsy/Seizure Disorder
1Maternal and Child Health Bureau, Health Resources and Services Administration, U.S. Department of Health and Human Services, 5600 Fishers Lane, Rm 18-41, Rockville, MD 20857, USA.
Insights
Children with epilepsy/seizure disorder have lower access to high-quality health services, including medical homes and community care. This highlights a need for improved healthcare systems for these children.
Area of Science:
- Pediatric Health Services Research
- Neurology
- Public Health
Background:
- Examined healthcare quality for US children with special health care needs (CSHCN) with epilepsy/seizure disorder.
- Compared CSHCN with and without epilepsy/seizure disorder regarding access to high-quality health services.
Purpose of the Study:
- To assess the proportion of CSHCN with epilepsy/seizure disorder receiving care within high-quality health service systems.
- To identify disparities in healthcare attainment and unmet needs for CSHCN with epilepsy/seizure disorder.
Main Methods:
- Analyzed data from 40,242 CSHCN using the 2009-2010 National Survey of CSHCN.
- Utilized chi-square and logistic regression to compare attainment rates for 6 federal quality indicators.
- Assessed 14 unmet healthcare needs for CSHCN with and without epilepsy/seizure disorder.
Main Results:
- CSHCN with epilepsy/seizure disorder had lower attainment rates for medical home (32% vs. 43%) and accessible community services (50% vs. 66%).
- Lower adjusted odds for these indicators were observed for CSHCN with epilepsy/seizure disorder.
- Greater unmet needs were reported for specialists, dentistry, prescriptions, therapies, and mental health care.
Conclusions:
- Significant disparities exist in healthcare quality and access for CSHCN with epilepsy/seizure disorder.
- Further efforts are crucial to enhance the attainment of high-quality health care services for this population.
- Addressing unmet needs in specialized care and essential services is paramount.
Abstract:
Background. The proportion of US children with special health care needs (CSHCN) with epilepsy/seizure disorder who receive care in high-quality health service systems was examined. Methodology. We analyzed data for 40,242 CSHCN from the 2009-2010 National Survey of CSHCN and compared CSHCN with epilepsy/seizure disorder to CSHCN without epilepsy/seizure disorder. Measures included attainment rates for 6 federal quality indicators with comparisons conducted using chi square and logistic regression methods. In addition, CSHCN with epilepsy/seizure disorder were compared to CSHCN without epilepsy/seizure disorder on the basis of 14 unmet health care needs. Results. Lower attainment rates for receiving comprehensive care in a medical home and easily accessible community-based services were found for CSHCN with epilepsy/seizure disorder versus CSHCN without epilepsy/seizure disorder (medical home: 32% versus 43%; accessible community-based services: 50% versus 66%, resp.) in unadjusted analyses. Lower adjusted odds for these indicators as well as greater unmet need for specialists, dentistry, prescriptions, therapies, and mental health care were also found for CSHCN with epilepsy/seizure disorder. Conclusions. Further efforts are needed to improve attainment of high-quality health care services for CSHCN with epilepsy/seizure disorders.
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