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A qualitative analysis of information sharing for children with medical complexity within and across health care organizations
BACKGROUND: Children with medical complexity (CMC) are characterized by substantial family-identified service needs, chronic and severe conditions, functional limitations, and high health care use. Information exchange is critically important in high quality care of complex patients at high risk for...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085394/ https://www.ncbi.nlm.nih.gov/pubmed/24981205 http://dx.doi.org/10.1186/1472-6963-14-283 |
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author | Quigley, Laura Lacombe-Duncan, Ashley Adams, Sherri Moore Hepburn, Charlotte Cohen, Eyal |
author_facet | Quigley, Laura Lacombe-Duncan, Ashley Adams, Sherri Moore Hepburn, Charlotte Cohen, Eyal |
author_sort | Quigley, Laura |
collection | PubMed |
description | BACKGROUND: Children with medical complexity (CMC) are characterized by substantial family-identified service needs, chronic and severe conditions, functional limitations, and high health care use. Information exchange is critically important in high quality care of complex patients at high risk for poor care coordination. Written care plans for CMC are an excellent test case for how well information sharing is currently occurring. The purpose of this study was to identify the barriers to and facilitators of information sharing for CMC across providers, care settings, and families. METHODS: A qualitative study design with data analysis informed by a grounded theory approach was utilized. Two independent coders conducted secondary analysis of interviews with parents of CMC and health care professionals involved in the care of CMC, collected from two studies of healthcare service delivery for this population. Additional interviews were conducted with privacy officers of associated organizations to supplement these data. Emerging themes related to barriers and facilitators to information sharing were identified by the two coders and the research team, and a theory of facilitators and barriers to information exchange evolved. RESULTS: Barriers to information sharing were related to one of three major themes; 1) the lack of an integrated, accessible, secure platform on which summative health care information is stored, 2) fragmentation of the current health system, and 3) the lack of consistent policies, standards, and organizational priorities across organizations for information sharing. Facilitators of information sharing were related to improving accessibility to a common document, expanding the use of technology, and improving upon a structured communication plan. CONCLUSIONS: Findings informed a model of how various barriers to information sharing interact to prevent optimal information sharing both within and across organizations and how the use of technology to improve communication and access to information can act as a solution. |
format | Online Article Text |
id | pubmed-4085394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40853942014-07-09 A qualitative analysis of information sharing for children with medical complexity within and across health care organizations Quigley, Laura Lacombe-Duncan, Ashley Adams, Sherri Moore Hepburn, Charlotte Cohen, Eyal BMC Health Serv Res Research Article BACKGROUND: Children with medical complexity (CMC) are characterized by substantial family-identified service needs, chronic and severe conditions, functional limitations, and high health care use. Information exchange is critically important in high quality care of complex patients at high risk for poor care coordination. Written care plans for CMC are an excellent test case for how well information sharing is currently occurring. The purpose of this study was to identify the barriers to and facilitators of information sharing for CMC across providers, care settings, and families. METHODS: A qualitative study design with data analysis informed by a grounded theory approach was utilized. Two independent coders conducted secondary analysis of interviews with parents of CMC and health care professionals involved in the care of CMC, collected from two studies of healthcare service delivery for this population. Additional interviews were conducted with privacy officers of associated organizations to supplement these data. Emerging themes related to barriers and facilitators to information sharing were identified by the two coders and the research team, and a theory of facilitators and barriers to information exchange evolved. RESULTS: Barriers to information sharing were related to one of three major themes; 1) the lack of an integrated, accessible, secure platform on which summative health care information is stored, 2) fragmentation of the current health system, and 3) the lack of consistent policies, standards, and organizational priorities across organizations for information sharing. Facilitators of information sharing were related to improving accessibility to a common document, expanding the use of technology, and improving upon a structured communication plan. CONCLUSIONS: Findings informed a model of how various barriers to information sharing interact to prevent optimal information sharing both within and across organizations and how the use of technology to improve communication and access to information can act as a solution. BioMed Central 2014-06-30 /pmc/articles/PMC4085394/ /pubmed/24981205 http://dx.doi.org/10.1186/1472-6963-14-283 Text en Copyright © 2014 Quigley et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Research Article Quigley, Laura Lacombe-Duncan, Ashley Adams, Sherri Moore Hepburn, Charlotte Cohen, Eyal A qualitative analysis of information sharing for children with medical complexity within and across health care organizations |
title | A qualitative analysis of information sharing for children with medical complexity within and across health care organizations |
title_full | A qualitative analysis of information sharing for children with medical complexity within and across health care organizations |
title_fullStr | A qualitative analysis of information sharing for children with medical complexity within and across health care organizations |
title_full_unstemmed | A qualitative analysis of information sharing for children with medical complexity within and across health care organizations |
title_short | A qualitative analysis of information sharing for children with medical complexity within and across health care organizations |
title_sort | qualitative analysis of information sharing for children with medical complexity within and across health care organizations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085394/ https://www.ncbi.nlm.nih.gov/pubmed/24981205 http://dx.doi.org/10.1186/1472-6963-14-283 |
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