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Research policy for people with multiple long-term conditions and their carers
People with multiple long-term conditions (MLTC) are a growing population, not only in the United Kingdom but internationally. Health and care systems need to adapt to rise to this challenge. Policymakers need to better understand how medical education and training, and service configuration and del...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201348/ https://www.ncbi.nlm.nih.gov/pubmed/35721799 http://dx.doi.org/10.1177/26335565221104407 |
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author | Owen, Natalie Dew, Leanne Logan, Stuart Denegri, Simon Chappell, Lucy C |
author_facet | Owen, Natalie Dew, Leanne Logan, Stuart Denegri, Simon Chappell, Lucy C |
author_sort | Owen, Natalie |
collection | PubMed |
description | People with multiple long-term conditions (MLTC) are a growing population, not only in the United Kingdom but internationally. Health and care systems need to adapt to rise to this challenge. Policymakers need to better understand how medical education and training, and service configuration and delivery should change to meet the needs of people with MLTC and their carers. A series of workshops with people with MLTC and carers across the life-course identified areas of unmet need including the impact of stigma; poorly coordinated care designed around single conditions; inadequate communication and consultations that focus on clinical outcomes rather than patient-oriented goals and imperfectly integrate mental and physical wellbeing. Research which embeds the patient voice at its centre, from inception to implementation, can provide the evidence to drive the change to patient-centred, coordinated care. This should not only improve the lives of people living with MLTC and their carers but also create a health and care system which is more effective and efficient. The challenge of MLTC needs to be bought to the fore and it will require joint effort by policymakers, practitioners, systems leaders, educators, the third sector and those living with MLTC to design a health and care system from the perspective of patients and carers, and provide practitioners with the skills and tools needed to provide the highest quality care. |
format | Online Article Text |
id | pubmed-9201348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-92013482022-06-17 Research policy for people with multiple long-term conditions and their carers Owen, Natalie Dew, Leanne Logan, Stuart Denegri, Simon Chappell, Lucy C J Multimorb Comorb Policy People with multiple long-term conditions (MLTC) are a growing population, not only in the United Kingdom but internationally. Health and care systems need to adapt to rise to this challenge. Policymakers need to better understand how medical education and training, and service configuration and delivery should change to meet the needs of people with MLTC and their carers. A series of workshops with people with MLTC and carers across the life-course identified areas of unmet need including the impact of stigma; poorly coordinated care designed around single conditions; inadequate communication and consultations that focus on clinical outcomes rather than patient-oriented goals and imperfectly integrate mental and physical wellbeing. Research which embeds the patient voice at its centre, from inception to implementation, can provide the evidence to drive the change to patient-centred, coordinated care. This should not only improve the lives of people living with MLTC and their carers but also create a health and care system which is more effective and efficient. The challenge of MLTC needs to be bought to the fore and it will require joint effort by policymakers, practitioners, systems leaders, educators, the third sector and those living with MLTC to design a health and care system from the perspective of patients and carers, and provide practitioners with the skills and tools needed to provide the highest quality care. SAGE Publications 2022-06-14 /pmc/articles/PMC9201348/ /pubmed/35721799 http://dx.doi.org/10.1177/26335565221104407 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Policy Owen, Natalie Dew, Leanne Logan, Stuart Denegri, Simon Chappell, Lucy C Research policy for people with multiple long-term conditions and their carers |
title | Research policy for people with multiple long-term conditions and their
carers |
title_full | Research policy for people with multiple long-term conditions and their
carers |
title_fullStr | Research policy for people with multiple long-term conditions and their
carers |
title_full_unstemmed | Research policy for people with multiple long-term conditions and their
carers |
title_short | Research policy for people with multiple long-term conditions and their
carers |
title_sort | research policy for people with multiple long-term conditions and their
carers |
topic | Policy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201348/ https://www.ncbi.nlm.nih.gov/pubmed/35721799 http://dx.doi.org/10.1177/26335565221104407 |
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