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Acceptability of Health Information Exchange and Patient Portal Use in Depression Care Among Underrepresented Patients
BACKGROUND: Depression is often untreated or undertreated, particularly among underrepresented groups, such as racial and ethnic minorities, and individuals of lower socioeconomic status. Electronic health information exchange (HIE) is a recommended practice to improve care coordination and encourag...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8821856/ https://www.ncbi.nlm.nih.gov/pubmed/35132548 http://dx.doi.org/10.1007/s11606-022-07427-2 |
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author | Matthews, Elizabeth B. Savoy, Margot Paranjape, Anuradha Washington, Diana Hackney, Treanna Galis, Danielle Zisman-Ilani, Yaara |
author_facet | Matthews, Elizabeth B. Savoy, Margot Paranjape, Anuradha Washington, Diana Hackney, Treanna Galis, Danielle Zisman-Ilani, Yaara |
author_sort | Matthews, Elizabeth B. |
collection | PubMed |
description | BACKGROUND: Depression is often untreated or undertreated, particularly among underrepresented groups, such as racial and ethnic minorities, and individuals of lower socioeconomic status. Electronic health information exchange (HIE) is a recommended practice to improve care coordination and encourage patient engagement in services, but it remains underutilized in depression care. Understanding factors affecting acceptance and adoption of this technology among underrepresented patient populations is needed to increase dissemination of HIE within mental health treatment. OBJECTIVE: The present study aims to identify patient barriers and facilitators towards the acceptance of HIE within the context of depression treatment and to examine how HIE impacts depression-related care coordination and patient activation. DESIGN: Semi-structured qualitative interviews were conducted with 27 patients. PARTICIPANTS: Respondents were English-speaking adults (> 18) receiving depression treatment within a large, safety-net primary care clinic. APPROACH: A grounded theory approach was used to code and analyze data for emergent themes. Thematic analysis was guided by the Unified Theory of Acceptance and Use of Technology, a leading informatics theory used to predict end-user adoption of technology. KEY RESULTS: Respondents reported that HIE made depression care more convenient, transparent, and trustworthy. Though respondents desired greater access to their health records, stigma surrounding depression inhibited acceptance of electronic communication and information sharing. Confusing electronic interface also diminished perceived benefits of HIE. CONCLUSION(S): Respondents desire greater transparency in their depression care. While HIE was perceived to improve the overall quality of depression care, stigma associated with mental illness undermined more robust adoption of this technology among underserved populations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11606-022-07427-2. |
format | Online Article Text |
id | pubmed-8821856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-88218562022-02-08 Acceptability of Health Information Exchange and Patient Portal Use in Depression Care Among Underrepresented Patients Matthews, Elizabeth B. Savoy, Margot Paranjape, Anuradha Washington, Diana Hackney, Treanna Galis, Danielle Zisman-Ilani, Yaara J Gen Intern Med Original Research: Qualitative Research BACKGROUND: Depression is often untreated or undertreated, particularly among underrepresented groups, such as racial and ethnic minorities, and individuals of lower socioeconomic status. Electronic health information exchange (HIE) is a recommended practice to improve care coordination and encourage patient engagement in services, but it remains underutilized in depression care. Understanding factors affecting acceptance and adoption of this technology among underrepresented patient populations is needed to increase dissemination of HIE within mental health treatment. OBJECTIVE: The present study aims to identify patient barriers and facilitators towards the acceptance of HIE within the context of depression treatment and to examine how HIE impacts depression-related care coordination and patient activation. DESIGN: Semi-structured qualitative interviews were conducted with 27 patients. PARTICIPANTS: Respondents were English-speaking adults (> 18) receiving depression treatment within a large, safety-net primary care clinic. APPROACH: A grounded theory approach was used to code and analyze data for emergent themes. Thematic analysis was guided by the Unified Theory of Acceptance and Use of Technology, a leading informatics theory used to predict end-user adoption of technology. KEY RESULTS: Respondents reported that HIE made depression care more convenient, transparent, and trustworthy. Though respondents desired greater access to their health records, stigma surrounding depression inhibited acceptance of electronic communication and information sharing. Confusing electronic interface also diminished perceived benefits of HIE. CONCLUSION(S): Respondents desire greater transparency in their depression care. While HIE was perceived to improve the overall quality of depression care, stigma associated with mental illness undermined more robust adoption of this technology among underserved populations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11606-022-07427-2. Springer International Publishing 2022-02-07 2022-11 /pmc/articles/PMC8821856/ /pubmed/35132548 http://dx.doi.org/10.1007/s11606-022-07427-2 Text en © The Author(s) under exclusive licence to Society of General Internal Medicine 2022 |
spellingShingle | Original Research: Qualitative Research Matthews, Elizabeth B. Savoy, Margot Paranjape, Anuradha Washington, Diana Hackney, Treanna Galis, Danielle Zisman-Ilani, Yaara Acceptability of Health Information Exchange and Patient Portal Use in Depression Care Among Underrepresented Patients |
title | Acceptability of Health Information Exchange and Patient Portal Use in Depression Care Among Underrepresented Patients |
title_full | Acceptability of Health Information Exchange and Patient Portal Use in Depression Care Among Underrepresented Patients |
title_fullStr | Acceptability of Health Information Exchange and Patient Portal Use in Depression Care Among Underrepresented Patients |
title_full_unstemmed | Acceptability of Health Information Exchange and Patient Portal Use in Depression Care Among Underrepresented Patients |
title_short | Acceptability of Health Information Exchange and Patient Portal Use in Depression Care Among Underrepresented Patients |
title_sort | acceptability of health information exchange and patient portal use in depression care among underrepresented patients |
topic | Original Research: Qualitative Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8821856/ https://www.ncbi.nlm.nih.gov/pubmed/35132548 http://dx.doi.org/10.1007/s11606-022-07427-2 |
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