Literature DB >> 21320113

Socioeconomic status, health care use, and outcomes: persistence of disparities over time.

Charles Begley1, Rituparna Basu, David Lairson, Thomas Reynolds, Stephanie Dubinsky, Michael Newmark, Forbes Barnwell, Allen Hauser, Dale Hesdorffer.   

Abstract

PURPOSE: To determine the persistence of disparities in health care use and outcomes in socioeconomically diverse populations of epilepsy patients.
METHODS: We followed patients for a year at one clinic in Houston and two in New York City that serve predominantly low-income, minority, Medicaid-insured, or uninsured patients, and a fourth clinic in Houston that serves a more balanced racial/ethnic and higher socioeconomic status (SES) population. We interviewed the patients several times regarding health care use, seizures, side effects, and outcomes, and examined differences between the patients at the three low-SES clinics and the patients at the high-SES clinic. KEY
FINDINGS: After controlling for patients' age, gender, race/ethnicity, marital status, seizures, and side effects we found that low SES patients had consistently higher use of the hospital emergency room and more visits to a general practitioner. Hospitalizations were also consistently higher but the differences were not significant in most periods. Neurologist visits were relatively similar. Patients at the low SES sites also had a greater likelihood of having uncontrolled seizures, drug-related side effects, to be stigmatized, and have a lower overall quality of life throughout the study period. SIGNIFICANCE: These findings suggest the persistence of SES-related disparities in health care use and outcomes among patients with epilepsy who are receiving regular care. Wiley Periodicals, Inc.
© 2011 International League Against Epilepsy.

Entities:  

Mesh:

Year:  2011        PMID: 21320113     DOI: 10.1111/j.1528-1167.2010.02968.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  29 in total

1.  Predicting frequent ED use by people with epilepsy with health information exchange data.

Authors:  Zachary M Grinspan; Jason S Shapiro; Erika L Abramson; Giles Hooker; Rainu Kaushal; Lisa M Kern
Journal:  Neurology       Date:  2015-08-26       Impact factor: 9.910

2.  Socioeconomic disparities in SUDEP in the US.

Authors:  Esma Cihan; Dale C Hesdorffer; Michael Brandsoy; Ling Li; David R Fowler; Jason K Graham; Michael Karlovich; Elizabeth J Donner; Orrin Devinsky; Daniel Friedman
Journal:  Neurology       Date:  2020-04-23       Impact factor: 9.910

3.  A 6-month prospective randomized controlled trial of remotely delivered group format epilepsy self-management versus waitlist control for high-risk people with epilepsy.

Authors:  Martha Sajatovic; Kari Colon-Zimmermann; Mustafa Kahriman; Edna Fuentes-Casiano; Hongyan Liu; Curtis Tatsuoka; Kristin A Cassidy; Samden Lhatoo; Douglas Einstadter; Peijun Chen
Journal:  Epilepsia       Date:  2018-08-10       Impact factor: 5.864

4.  One-year follow-up of a remotely delivered epilepsy self-management program in high-risk people with epilepsy.

Authors:  Martha Sajatovic; Kari Colon-Zimmermann; Mustafa Kahriman; Edna Fuentes-Casiano; Christopher Burant; Michelle E Aebi; Kristin A Cassidy; Samden Lhatoo; Douglas Einstadter; Peijun Chen
Journal:  Epilepsy Behav       Date:  2019-05-21       Impact factor: 2.937

5.  Race and health profiles in the United States: an examination of the social gradient through the 2009 CHIS adult survey.

Authors:  A B Nguyen; R Moser; W-Y Chou
Journal:  Public Health       Date:  2014-11-25       Impact factor: 2.427

6.  Electronic medical record analysis of emergency room visits and hospitalizations in individuals with epilepsy and mental illness comorbidity.

Authors:  Martha Sajatovic; Elisabeth Welter; Curtis Tatsuoka; Adam T Perzynski; Douglas Einstadter
Journal:  Epilepsy Behav       Date:  2015-06-25       Impact factor: 2.937

7.  Health literacy and education level correlates of participation and outcome in a remotely delivered epilepsy self-management program.

Authors:  Shwetha Sudhakar; Michelle E Aebi; Christopher J Burant; Betsy Wilson; Jocasta Wenk; Farren B S Briggs; Nataliya Pyatka; Carol Blixen; Martha Sajatovic
Journal:  Epilepsy Behav       Date:  2020-04-02       Impact factor: 2.937

Review 8.  Priorities in pediatric epilepsy research: improving children's futures today.

Authors:  Anne T Berg; Christine B Baca; Tobias Loddenkemper; Barbara G Vickrey; Dennis Dlugos
Journal:  Neurology       Date:  2013-08-21       Impact factor: 9.910

9.  Effects of a remotely delivered group-format epilepsy self-management program on adverse health outcomes in vulnerable people with epilepsy: A causal mediation analysis.

Authors:  Farren B S Briggs; Betsy K Wilson; Nataliya Pyatka; Kari Colón-Zimmermann; Martha M Sajatovic
Journal:  Epilepsy Res       Date:  2020-02-24       Impact factor: 3.045

10.  Improving patient-centered care coordination for children with epilepsy: version 2.0 upgrade required.

Authors:  Marvin A Rossi
Journal:  Epilepsy Curr       Date:  2014-05       Impact factor: 7.500

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.