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本文引用的文献

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Guidelines for the psychosocial and bereavement support of family caregivers of palliative care patients.姑息治疗患者家属的心理社会和丧亲支持指南。
J Palliat Med. 2012 Jun;15(6):696-702. doi: 10.1089/jpm.2011.0466. Epub 2012 Mar 2.
2
Bereaved family members' assessments of the quality of end-of-life care: what is important?
J Palliat Care. 2011 Winter;27(4):261-9.
3
Does palliative care improve outcomes for patients with incurable illness? A review of the evidence.姑息治疗能否改善不治之症患者的预后?证据综述。
J Support Oncol. 2011 May-Jun;9(3):87-94. doi: 10.1016/j.suponc.2011.03.003.
4
Palliative care consultation teams cut hospital costs for Medicaid beneficiaries.姑息治疗咨询团队为医疗补助受益人的医院费用。
Health Aff (Millwood). 2011 Mar;30(3):454-63. doi: 10.1377/hlthaff.2010.0929.
5
Psychological and social profile of family caregivers on commencement of palliative care.开始姑息治疗时的家庭照护者的心理和社会特征。
J Pain Symptom Manage. 2011 Mar;41(3):522-34. doi: 10.1016/j.jpainsymman.2010.05.006. Epub 2010 Dec 3.
6
What is the evidence that palliative care teams improve outcomes for cancer patients and their families?姑息治疗团队改善癌症患者及其家属结局的证据是什么?
Cancer J. 2010 Sep-Oct;16(5):423-35. doi: 10.1097/PPO.0b013e3181f684e5.
7
Early palliative care for patients with metastatic non-small-cell lung cancer.转移性非小细胞肺癌患者的早期姑息治疗。
N Engl J Med. 2010 Aug 19;363(8):733-42. doi: 10.1056/NEJMoa1000678.
8
Potential for response bias in family surveys about end-of-life care in the ICU.关于重症监护病房临终关怀的家庭调查中存在回应偏差的可能性。
Chest. 2009 Dec;136(6):1496-1502. doi: 10.1378/chest.09-0589. Epub 2009 Jul 17.
9
Educating nursing home staff about the progression of dementia and the comfort care option: impact on family satisfaction with end-of-life care.向养老院工作人员传授痴呆症的发展过程及舒适护理选择:对家属临终关怀满意度的影响。
J Am Med Dir Assoc. 2009 Jan;10(1):50-5. doi: 10.1016/j.jamda.2008.07.008. Epub 2008 Dec 10.
10
Cost savings associated with US hospital palliative care consultation programs.美国医院姑息治疗咨询项目相关的成本节约
Arch Intern Med. 2008 Sep 8;168(16):1783-90. doi: 10.1001/archinte.168.16.1783.

家庭成员对不同护理地点临终关怀的看法。

Family members' perceptions of end-of-life care across diverse locations of care.

机构信息

Division of Palliative Care, Department of Family and Community Medicine, Providence Health Care, University of British Columbia.

出版信息

BMC Palliat Care. 2013 Jul 20;12(1):25. doi: 10.1186/1472-684X-12-25.

DOI:10.1186/1472-684X-12-25
PMID:23870101
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3750390/
Abstract

BACKGROUND

The goal of the study was to assess perceived level of satisfaction with end-of-life care, focusing on the last 48 hours of life.

METHODS

A previously validated instrument was used in a telephone survey with bereaved family members (n=90) of patients who died within an organization in British Columbia.

RESULTS

Bereaved family members had many unmet needs for information about the patient's changing condition, the process of dying, how symptoms would be managed and what to do at the time of death. In addition, many bereaved relatives felt that the patient or resident had an unmet need for emotional support and that their own emotional needs were not addressed adequately. The last place of care had the most significant effect on all of these variables, with acute care and residential care having the most unmet needs. Hospice had the fewest unmet needs, followed by the palliative and the intensive care units.

CONCLUSIONS

We discuss these findings in relation to overall satisfaction with care, focus on individual, ethno-cultural and diversity issues, information and decision-making, symptom management and attending to the family. We conclude by offering possible practices address the end-of-life needs of patients and family members.

摘要

背景

本研究旨在评估临终关怀的满意度,重点关注生命的最后 48 小时。

方法

采用经先前验证的工具,对不列颠哥伦比亚省一家机构内死亡患者的家属(n=90)进行电话调查。

结果

在患者病情变化、死亡过程、如何处理症状以及死亡时该做什么等方面,患者家属有许多未满足的信息需求。此外,许多失去亲人的亲属感到患者或居民在情感支持方面存在未满足的需求,而他们自己的情感需求也没有得到充分满足。临终关怀的地点对所有这些变量都有最显著的影响,急性护理和住院护理的未满足需求最多。临终关怀中心的未满足需求最少,其次是姑息治疗和重症监护病房。

结论

我们根据总体护理满意度讨论了这些发现,重点关注个人、种族文化和多样性问题、信息和决策、症状管理以及家属的照顾。最后,我们提出了一些可能的做法,以满足患者和家属的临终需求。