Diabetes and Palliative Care: A Framework to Help Clinicians Proactively Plan for Personalized care

T. Dunning, Peter Martin
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引用次数: 2

Abstract

The aim of the chapter is to provide a brief overview of diabetes and the associated morbidities that affect life expectancy to highlight why proactively planning for palliative and end-of-life care is essential to quality personalized diabetes care. Life expectancy may not be significantly reduced if blood glucose, lipids and blood pressure are well controlled; but several diabetes-related complications and long duration of diabetes affect life expectancy. Significantly, complications and related organ and tissue damage can be present 10–15 years before type 2 diabetes is diagnosed. The challenge of prognostication is discussed as recommendations for when to consider changing the focus of care from preventing diabetes complications to palliation and comfort care. Life-limiting illness and palliative and end-of-life care are defined. A framework for integrating diabetes and palliative care is proposed. The framework could help clinicians and people with diabetes prevent/manage complications and plan care to maintain quality of life, dignity and autonomy and ameliorate suffering as their life trajectory changes. The framework aims to facili-tate care transitions and help clinicians proactively initiate management and have timely meaningful conversations about palliative and end-of-life care with older people with diabetes and their families.
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糖尿病和姑息治疗:一个框架,以帮助临床医生积极计划个性化护理
本章的目的是简要概述糖尿病和影响预期寿命的相关疾病,以强调为什么积极规划姑息治疗和临终关怀对于高质量的个性化糖尿病护理至关重要。如果血糖、血脂和血压得到良好控制,预期寿命可能不会显著缩短;但一些与糖尿病相关的并发症和糖尿病持续时间长会影响预期寿命。值得注意的是,并发症和相关的器官和组织损伤可能在2型糖尿病诊断前10-15年出现。预测的挑战被讨论为何时考虑将护理重点从预防糖尿病并发症转变为缓解和舒适护理的建议。定义了限制生命的疾病以及姑息治疗和临终关怀。提出了一个整合糖尿病和姑息治疗的框架。该框架可以帮助临床医生和糖尿病患者预防/管理并发症,并计划护理,以保持生活质量、尊严和自主性,并随着生活轨迹的变化减轻痛苦。该框架旨在促进护理过渡,帮助临床医生主动启动管理,并及时与糖尿病老年人及其家人就姑息治疗和临终关怀进行有意义的对话。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
0.00%
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0
审稿时长
15 weeks
期刊介绍: Palliative Care and Social Practice is an international, peer-reviewed, open access journal that publishes articles on all aspects of palliative care. It welcomes articles from symptom science, clinical practice, and health services research. However, its aim is also to publish cutting-edge research from the realm of social practice - from public health theory and practice, social medicine, and social work, to social sciences related to dying and its care, as well as policy, criticism, and cultural studies. We encourage reports from work with under-represented groups, community development, and studies of civic engagement in end of life issues. Furthermore, we encourage scholarly articles that challenge current thinking about dying, its current care models and practices, and current understandings of grief and bereavement. We want to showcase the next generation of palliative care innovation research and practice - in clinics and in the wider society. Relaunched in July 2019. Partnered with Public Health Palliative Care International (PHPCI) (Title 2008-2018: - Palliative Care: Research and Treatment)
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