Health care access and quality for persons with disability: Patient and provider recommendations. Issue 3 (July 2018)

• Record Type: Journal Article
• Authors: McClintock, Heather F.; Kurichi, Jibby E.; Barg, Frances K.; Krueger, Alice; Colletti, Patrice M.; Wearing, Krizia A.; Bogner, Hillary R.
• Is Part Of: Disability and health journal. Volume 11:Issue 3(2018)
• Page Start: 382
• Page End: 389
• Publication Date: 2018-07
• Subjects: Disability -- Access to care -- Recommendations -- Patient-provider communication -- Online communities; People with disabilities -- Health and hygiene -- Periodicals; Health education -- Periodicals; Disabled Persons -- Periodicals; Health Education -- Periodicals; Electronic journals; 362.4
• DOI: 10.1016/j.dhjo.2017.12.010
• Languages: English
• ISSNs: 1936-6574

Abstract

Abstract: Background: Significant disparities in health care access and quality persist between persons with disabilities (PWD) and persons without disabilities (PWOD). Little research has examined recommendations of patients and providers to improve health care for PWD. Objective: We sought to explore patient and health care provider recommendations to improve health care access and quality for PWD through focus groups in the physical world in a community center and in the virtual world in an online community. Methods: In all, 17 PWD, 4 PWOD, and 6 health care providers participated in 1 of 5 focus groups. Focus groups were conducted in the virtual world in Second Life ® with Virtual Ability, an online community, and in the physical world at Agape Community Center in Milwaukee, WI. Focus group data were analyzed using a grounded theory methodology. Results: Themes that emerged in focus groups among PWD and PWOD as well as health care providers to improve health care access and quality for PWD were: promoting advocacy, increasing awareness and knowledge, improving communication, addressing assumptions, as well as modifying and creating policy. Many participants discussed political empowerment and engagement as central to health care reform. Conclusions: Both PWD and PWOD as well as health care providers identified common themes potentially important for improving health care for PWD. Patient and health care provider recommendations highlight a need for modification of current paradigms, practices, and approaches to improve the quality of health care provision for PWD. Participants emphasized the need for greater advocacy and political engagement.