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The patient perspective: utilizing focus groups to inform care coordination for high-risk medicaid populations

BACKGROUND: Care coordination programs for high-risk, high-cost patients are a critical component of population health management. These programs aim to improve outcomes and reduce costs and have proliferated over the last decade. Some programs, originally designed for Medicare patients, are now tra...

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Autores principales: Sheff, Alex, Park, Elyse R., Neagle, Mary, Oreskovic, Nicolas M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5526300/
https://www.ncbi.nlm.nih.gov/pubmed/28743288
http://dx.doi.org/10.1186/s13104-017-2638-1
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author Sheff, Alex
Park, Elyse R.
Neagle, Mary
Oreskovic, Nicolas M.
author_facet Sheff, Alex
Park, Elyse R.
Neagle, Mary
Oreskovic, Nicolas M.
author_sort Sheff, Alex
collection PubMed
description BACKGROUND: Care coordination programs for high-risk, high-cost patients are a critical component of population health management. These programs aim to improve outcomes and reduce costs and have proliferated over the last decade. Some programs, originally designed for Medicare patients, are now transitioning to also serve Medicaid populations. However, there are still gaps in the understanding of what barriers to care Medicaid patients experience, and what supports will be most effective for providing them care coordination. METHODS: We conducted two focus groups (n = 13) and thematic analyses to assess the outcomes drivers and programmatic preferences of Medicaid patients enrolled in a high-risk care coordination program at a major academic medical center in Boston, MA. FINDINGS: Two focus groups identified areas where care coordination efforts were having a positive impact, as well as areas of unmet needs among the Medicaid population. Six themes emerged from the focus groups that clustered in three groupings: In the first group (1) enrollment in an existing medical care coordination programs, and (2) provider communication largely presented as positive accounts of assistance, and good relationships with providers, though participants also pointed to areas where these efforts fell short. In the second group (3) trauma histories, (4) mental health challenges, and (5) executive function difficulties all presented challenges faced by high-risk Medicaid patients that would likely require redress through additional programmatic supports. Finally, in the third group, (6) peer-to-peer support tendencies among patients suggested an untapped resource for care coordination programs. CONCLUSIONS: Programs aimed at high-risk Medicaid patients will want to consider programmatic adjustments to attend to patient needs in five areas: (1) provider connection/care coordination, (2) trauma, (3) mental health, (4) executive function/paperwork and coaching support, and (5) peer-to-peer support.
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spelling pubmed-55263002017-08-02 The patient perspective: utilizing focus groups to inform care coordination for high-risk medicaid populations Sheff, Alex Park, Elyse R. Neagle, Mary Oreskovic, Nicolas M. BMC Res Notes Research Article BACKGROUND: Care coordination programs for high-risk, high-cost patients are a critical component of population health management. These programs aim to improve outcomes and reduce costs and have proliferated over the last decade. Some programs, originally designed for Medicare patients, are now transitioning to also serve Medicaid populations. However, there are still gaps in the understanding of what barriers to care Medicaid patients experience, and what supports will be most effective for providing them care coordination. METHODS: We conducted two focus groups (n = 13) and thematic analyses to assess the outcomes drivers and programmatic preferences of Medicaid patients enrolled in a high-risk care coordination program at a major academic medical center in Boston, MA. FINDINGS: Two focus groups identified areas where care coordination efforts were having a positive impact, as well as areas of unmet needs among the Medicaid population. Six themes emerged from the focus groups that clustered in three groupings: In the first group (1) enrollment in an existing medical care coordination programs, and (2) provider communication largely presented as positive accounts of assistance, and good relationships with providers, though participants also pointed to areas where these efforts fell short. In the second group (3) trauma histories, (4) mental health challenges, and (5) executive function difficulties all presented challenges faced by high-risk Medicaid patients that would likely require redress through additional programmatic supports. Finally, in the third group, (6) peer-to-peer support tendencies among patients suggested an untapped resource for care coordination programs. CONCLUSIONS: Programs aimed at high-risk Medicaid patients will want to consider programmatic adjustments to attend to patient needs in five areas: (1) provider connection/care coordination, (2) trauma, (3) mental health, (4) executive function/paperwork and coaching support, and (5) peer-to-peer support. BioMed Central 2017-07-25 /pmc/articles/PMC5526300/ /pubmed/28743288 http://dx.doi.org/10.1186/s13104-017-2638-1 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Sheff, Alex
Park, Elyse R.
Neagle, Mary
Oreskovic, Nicolas M.
The patient perspective: utilizing focus groups to inform care coordination for high-risk medicaid populations
title The patient perspective: utilizing focus groups to inform care coordination for high-risk medicaid populations
title_full The patient perspective: utilizing focus groups to inform care coordination for high-risk medicaid populations
title_fullStr The patient perspective: utilizing focus groups to inform care coordination for high-risk medicaid populations
title_full_unstemmed The patient perspective: utilizing focus groups to inform care coordination for high-risk medicaid populations
title_short The patient perspective: utilizing focus groups to inform care coordination for high-risk medicaid populations
title_sort patient perspective: utilizing focus groups to inform care coordination for high-risk medicaid populations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5526300/
https://www.ncbi.nlm.nih.gov/pubmed/28743288
http://dx.doi.org/10.1186/s13104-017-2638-1
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