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Development of models of care coordination for rare conditions: a qualitative study
INTRODUCTION: Improving care coordination for people with rare conditions may help to reduce burden on patients and carers and improve the care that patients receive. We recently developed a taxonomy of different ways of coordinating care for rare conditions. It is not yet known which models of care...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843018/ https://www.ncbi.nlm.nih.gov/pubmed/35164822 http://dx.doi.org/10.1186/s13023-022-02190-3 |
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author | Walton, Holly Simpson, Amy Ramsay, Angus I. G. Hunter, Amy Jones, Jennifer Ng, Pei Li Leeson-Beevers, Kerry Bloom, Lara Kai, Joe Kokocinska, Maria Sutcliffe, Alastair G. Morris, Stephen Fulop, Naomi J. |
author_facet | Walton, Holly Simpson, Amy Ramsay, Angus I. G. Hunter, Amy Jones, Jennifer Ng, Pei Li Leeson-Beevers, Kerry Bloom, Lara Kai, Joe Kokocinska, Maria Sutcliffe, Alastair G. Morris, Stephen Fulop, Naomi J. |
author_sort | Walton, Holly |
collection | PubMed |
description | INTRODUCTION: Improving care coordination for people with rare conditions may help to reduce burden on patients and carers and improve the care that patients receive. We recently developed a taxonomy of different ways of coordinating care for rare conditions. It is not yet known which models of care coordination are appropriate in different situations. This study aimed to: (1) explore what types of care coordination may be appropriate in different situations, and (2) use these findings to develop hypothetical models of care coordination for rare conditions. METHODS: To explore appropriateness of different types of care coordination, we conducted interviews (n = 30), four focus groups (n = 22) and two workshops (n = 27) with patients, carers, healthcare professionals, commissioners, and charity representatives. Participants were asked about preferences, benefits and challenges, and the factors influencing coordination. Thematic analysis was used to develop hypothetical models of care coordination. Models were refined following feedback from workshop participants. RESULTS: Stakeholders prefer models of care that: are nationally centralised or a hybrid of national and local care, involve professionals collaborating to deliver care, have clear roles and responsibilities outlined (including administrative, coordinator, clinical and charity roles), provide access to records and offer flexible appointments (in terms of timing and mode). Many factors influenced coordination, including those relating to the patient (e.g., condition complexity, patient’s location and ability to coordinate their own care), the healthcare professional (e.g., knowledge and time), the healthcare environment (e.g., resources) and societal factors (e.g., availability of funding). We developed and refined ten illustrative hypothetical models of care coordination for rare conditions. CONCLUSION: Findings underline that different models of care coordination may be appropriate in different situations. It is possible to develop models of care coordination which are tailored to the individual in context. Findings may be used to facilitate planning around which models of care coordination may be appropriate in different services or circumstances. Findings may also be used by key stakeholders (e.g. patient organisations, clinicians and service planners) as a decision-making tool. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02190-3. |
format | Online Article Text |
id | pubmed-8843018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88430182022-02-16 Development of models of care coordination for rare conditions: a qualitative study Walton, Holly Simpson, Amy Ramsay, Angus I. G. Hunter, Amy Jones, Jennifer Ng, Pei Li Leeson-Beevers, Kerry Bloom, Lara Kai, Joe Kokocinska, Maria Sutcliffe, Alastair G. Morris, Stephen Fulop, Naomi J. Orphanet J Rare Dis Research INTRODUCTION: Improving care coordination for people with rare conditions may help to reduce burden on patients and carers and improve the care that patients receive. We recently developed a taxonomy of different ways of coordinating care for rare conditions. It is not yet known which models of care coordination are appropriate in different situations. This study aimed to: (1) explore what types of care coordination may be appropriate in different situations, and (2) use these findings to develop hypothetical models of care coordination for rare conditions. METHODS: To explore appropriateness of different types of care coordination, we conducted interviews (n = 30), four focus groups (n = 22) and two workshops (n = 27) with patients, carers, healthcare professionals, commissioners, and charity representatives. Participants were asked about preferences, benefits and challenges, and the factors influencing coordination. Thematic analysis was used to develop hypothetical models of care coordination. Models were refined following feedback from workshop participants. RESULTS: Stakeholders prefer models of care that: are nationally centralised or a hybrid of national and local care, involve professionals collaborating to deliver care, have clear roles and responsibilities outlined (including administrative, coordinator, clinical and charity roles), provide access to records and offer flexible appointments (in terms of timing and mode). Many factors influenced coordination, including those relating to the patient (e.g., condition complexity, patient’s location and ability to coordinate their own care), the healthcare professional (e.g., knowledge and time), the healthcare environment (e.g., resources) and societal factors (e.g., availability of funding). We developed and refined ten illustrative hypothetical models of care coordination for rare conditions. CONCLUSION: Findings underline that different models of care coordination may be appropriate in different situations. It is possible to develop models of care coordination which are tailored to the individual in context. Findings may be used to facilitate planning around which models of care coordination may be appropriate in different services or circumstances. Findings may also be used by key stakeholders (e.g. patient organisations, clinicians and service planners) as a decision-making tool. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02190-3. BioMed Central 2022-02-14 /pmc/articles/PMC8843018/ /pubmed/35164822 http://dx.doi.org/10.1186/s13023-022-02190-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Walton, Holly Simpson, Amy Ramsay, Angus I. G. Hunter, Amy Jones, Jennifer Ng, Pei Li Leeson-Beevers, Kerry Bloom, Lara Kai, Joe Kokocinska, Maria Sutcliffe, Alastair G. Morris, Stephen Fulop, Naomi J. Development of models of care coordination for rare conditions: a qualitative study |
title | Development of models of care coordination for rare conditions: a qualitative study |
title_full | Development of models of care coordination for rare conditions: a qualitative study |
title_fullStr | Development of models of care coordination for rare conditions: a qualitative study |
title_full_unstemmed | Development of models of care coordination for rare conditions: a qualitative study |
title_short | Development of models of care coordination for rare conditions: a qualitative study |
title_sort | development of models of care coordination for rare conditions: a qualitative study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843018/ https://www.ncbi.nlm.nih.gov/pubmed/35164822 http://dx.doi.org/10.1186/s13023-022-02190-3 |
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