scholarly journals Sexual Identity Differences in Health Care Access and Satisfaction: Findings from Nationally Representative Data

Author(s):  
Jessica N Fish ◽  
Rodman E Turpin ◽  
Natasha D Williams ◽  
Bradley O Boekeloo

Abstract Identification of barriers to adequate health care for sexual minority populations remains elusive as they are complex and variable across sexual orientation subgroups (e.g., gay, lesbian, bisexual). To address these complexities, we use a U.S. nationally representative sample of health care consumers to assess sexual identity differences in health care access and satisfaction. We conducted a secondary data analysis of 12 waves (2012-2018) of the biannual Consumer Survey of Health Care Access (n=30,548) to assess sexual identity differences in 6 health care access and 3 health care satisfaction indicators. Despite parity in health insurance coverage, sexual minorities – with some variation across sexual minority subgroups and sex – reported more chronic health conditions alongside restricted health care access and unmet health care needs. Gay/lesbian females had the lowest prevalence of health care utilization and higher prevalence rates of delaying needed health care and medical tests relative to heterosexual females. Gay/lesbian females and bisexual males were less likely than their heterosexual counterparts to be able to pay for needed health care services. Sexual minorities also reported less satisfactory experiences with medical providers. Examining barriers to health care among sexual minorities is critical to eliminating health disparities that disproportionately burden this population.

2021 ◽  
pp. 107755872110211
Author(s):  
Erin Brantley ◽  
Leighton Ku

Fluctuating insurance coverage, or churning, is a recognized barrier to health care access. We assessed whether state policies that allow children to remain covered in Medicaid for a 12-month period, regardless of fluctuations in income, are associated with health and health care outcomes, after controlling for individual factors and other Medicaid policies. This cross-sectional study uses a large, nationally representative database of children ages 0 to 17. Continuous eligibility was associated with improved rates of insurance, reductions in gaps in insurance and gaps due to application problems, and lower probability of being in fair or poor health. For children with special health care needs, it was associated with increases in use of medical care and preventive and specialty care access. However, continuous eligibility was not associated with health care utilization outcomes for the full sample. Continuous eligibility may be an effective strategy to reduce gaps in coverage for children and reduce paperwork burden on Medicaid agencies.


2021 ◽  
pp. appi.ps.2021000
Author(s):  
Natasha D. Williams ◽  
Rodman E. Turpin ◽  
Ellesse-Roselee L. Akré ◽  
Bradley O. Boekeloo ◽  
Jessica N. Fish

2012 ◽  
Vol 24 (5) ◽  
pp. 799-811 ◽  
Author(s):  
Giyeon Kim ◽  
Ami N. Bryant ◽  
R. Turner Goins ◽  
Courtney B. Worley ◽  
David A. Chiriboga

Objectives: The present study compared the characteristics of health status and health care access and use among older American Indians and Alaska Natives (AIANs) to those of non-Hispanic Whites (NHWs). Methods: Data were drawn from the 2009 California Health Interview Survey, with a total of 17,156 adults aged 60 and older (198 AIANs and 16,958 NHWs) analyzed. Results: Older AIANs reported poorer physical and mental health than did NHWs. AIANs were less likely than NHWs to see a medical doctor and have a usual source of medical care and were more likely than NHWs to delay getting needed medical care and report difficulty understanding the doctor at their last visit. Discussion: These findings highlight the vulnerability and unmet health care needs of older AIANs. More research on the older AIAN population is clearly needed to document their health care needs in order to better inform efforts to reduce health disparities.


LGBT Health ◽  
2021 ◽  
Vol 8 (3) ◽  
pp. 231-239
Author(s):  
Ellesse-Roselee L. Akré ◽  
Bradley O. Boekeloo ◽  
Typhanye Dyer ◽  
Andrew T. Fenelon ◽  
Luisa Franzini ◽  
...  

2005 ◽  
Vol 9 (S2) ◽  
pp. S109-S116 ◽  
Author(s):  
Moira Inkelas ◽  
Kathryn A. Smith ◽  
Alice A. Kuo ◽  
Linda Rudolph ◽  
Susan Igdaloff

2017 ◽  
Vol 48 (4) ◽  
pp. 286-293 ◽  
Author(s):  
Rajan A. Sonik ◽  
Susan L. Parish ◽  
Ilhom Akobirshoev ◽  
Esther Son ◽  
Eliana Rosenthal

PurposeTo provide estimates for the prevalence of parent-reported speech-language difficulties in U.S. children, and to describe the levels of health care access and material hardship in this population.MethodWe tabulated descriptive and bivariate statistics using cross-sectional data from the 2007 and 2011/2012 iterations of the National Survey of Children's Health, the 2005/2006 and 2009/2010 iterations of the National Survey of Children with Special Health Care Needs, and the 2004 and 2008 panels of the Survey of Income and Program Participation.ResultsPrevalence estimates ranged from 1.8% to 5.0%, with data from two of the three surveys preliminarily indicating increased prevalence in recent years. The largest health care challenge was in accessing care coordination, with 49%–56% of children with parent-reported speech-language difficulties lacking full access. Children with parent-reported speech-language difficulties were more likely than peers without any indications of speech-language difficulties to live in households experiencing each measured material hardship and participating in each measured public benefit program (e.g., 20%–22% experiencing food insecurity, compared to 11%–14% of their peers without any indications of speech-language difficulties).ConclusionsWe found mixed preliminary evidence to suggest that the prevalence of parent-reported speech-language difficulties among children may be rising. These children face heightened levels of material hardship and barriers in accessing health care.


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