非糖尿病姑息治疗患者低血糖的管理:基于预后的方法

V. Kok, Ping-Hsueh Lee
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引用次数: 5

摘要

在接受姑息治疗的非糖尿病临终患者中,由于潜在的终末期疾病引起的低血糖尚未得到充分的研究。例如,在姑息治疗的不同阶段,我们没有足够的关于患者自发性低血糖发生率的信息。根据姑息治疗病房的病例混合性质,至少2%的姑息治疗患者可能在生命即将结束时出现低血糖,此时剩余的预期寿命以天计。在低血糖发作期间,多达25%-60%的患者既没有自主神经反应,也没有神经性低血糖症状。虽然临床上怀疑低血糖并不难诊断和确认,但在安宁疗护环境中,有些病人的低血糖发作可能会被忽视。目前姑息治疗的趋势侧重于提供基于预后框架的治疗,包括患者和护理人员在考虑预后、专业建议、患者自主权、家庭期望以及当前治疗患者身体症状和存在痛苦的方法后共同决策。本文为专业护理团队对低血糖非糖尿病患者的护理提供了道德和文献支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of Hypoglycemia in Nondiabetic Palliative Care Patients: A Prognosis-Based Approach
Hypoglycemia due to underlying terminal illness in nondiabetic end-of-life patients receiving palliative care has not been fully studied. For example, we do not have adequate information on the frequency of spontaneous hypoglycemia in patients as occurs during the different stages of palliative care. Depending on the case-mix nature of the palliative care ward, at least 2% of palliative care patients may develop hypoglycemia near the end of life when the remaining life expectancy counts down in days. As many as 25%–60% of these patients will neither have autonomic response nor have neuroglycopenic symptoms during a hypoglycemic episode. Although it is not difficult to diagnose and confirm a true hypoglycemia when it is suspected clinically, an episode of hypoglycemic attack may go unnoticed in some patients in a hospice setting. Current trends in palliative care focus on providing treatments based on a prognosis-based framework, involving shared decision-making between the patient and caregivers, after considering the prognosis, professional recommendations, patient's autonomy, family expectations, and the current methods for treating the patient's physical symptoms and existential suffering. This paper provides professional care teams with both moral and literature support for providing care to nondiabetic patients presenting with hypoglycemia.
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来源期刊
自引率
0.00%
发文量
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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