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本文引用的文献

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I don't want to be the one saying 'we should just let him die': intrapersonal tensions experienced by surrogate decision makers in the ICU.我不想成为那个说“我们应该让他死”的人:重症监护病房中代理人决策者所经历的内心紧张。
J Gen Intern Med. 2012 Dec;27(12):1657-65. doi: 10.1007/s11606-012-2129-y. Epub 2012 Jul 28.
2
Association between physicians' beliefs and the option of comfort care for critically ill patients.医生信念与危重症患者接受舒适护理选择的关联。
Intensive Care Med. 2012 Oct;38(10):1607-15. doi: 10.1007/s00134-012-2671-4. Epub 2012 Aug 11.
3
Time-limited trials near the end of life.生命末期的限时试验。
JAMA. 2011 Oct 5;306(13):1483-4. doi: 10.1001/jama.2011.1413.
4
Systematic review: the effect on surrogates of making treatment decisions for others.系统评价:为他人做出治疗决策对代理人的影响。
Ann Intern Med. 2011 Mar 1;154(5):336-46. doi: 10.7326/0003-4819-154-5-201103010-00008.
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Effectiveness trial of an intensive communication structure for families of long-stay ICU patients.长期住 ICU 患者家庭强化沟通结构的有效性试验。
Chest. 2010 Dec;138(6):1340-8. doi: 10.1378/chest.10-0292. Epub 2010 Jun 24.
6
Expanding the paradigm of the physician's role in surrogate decision-making: an empirically derived framework.扩展医师在代理决策中的角色范式:一个经验衍生的框架。
Crit Care Med. 2010 Mar;38(3):743-50. doi: 10.1097/CCM.0b013e3181c58842.
7
Hope, truth, and preparing for death: perspectives of surrogate decision makers.希望、真相与面对死亡:替代决策者的观点
Ann Intern Med. 2008 Dec 16;149(12):861-8. doi: 10.7326/0003-4819-149-12-200812160-00005.
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Surrogate decision making: reconciling ethical theory and clinical practice.替代决策:协调伦理理论与临床实践
Ann Intern Med. 2008 Jul 1;149(1):48-53. doi: 10.7326/0003-4819-149-1-200807010-00010.
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Recommendations for end-of-life care in the intensive care unit: a consensus statement by the American College [corrected] of Critical Care Medicine.重症监护病房临终关怀建议:美国危重病医学会共识声明[已修正]
Crit Care Med. 2008 Mar;36(3):953-63. doi: 10.1097/CCM.0B013E3181659096.
10
The pressure to withhold or withdraw life-sustaining therapy from critically ill patients in the United States.在美国,对重症患者停止或撤销维持生命治疗的压力。
Am J Respir Crit Care Med. 2007 Jun 1;175(11):1104-8. doi: 10.1164/rccm.200609-1397CP. Epub 2007 Mar 22.

讨论重症监护中的治疗试验。

Discussion of treatment trials in intensive care.

机构信息

Division of General Internal Medicine, Section of Palliative Care and Medical Ethics, University of Pittsburgh, Pittsburgh, PA.

出版信息

J Crit Care. 2013 Oct;28(5):862-9. doi: 10.1016/j.jcrc.2013.04.015. Epub 2013 Jun 13.

DOI:10.1016/j.jcrc.2013.04.015
PMID:23768446
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3770796/
Abstract

PURPOSE

This study aimed to characterize whether and how the option of a treatment trial is discussed with surrogates in intensive care units.

MATERIALS AND METHODS

We audio-recorded 72 family conferences for 72 patients at high risk for death or severe functional impairment in 5 intensive care units in San Francisco, California. We analyzed transcripts to develop a coding framework for whether and how trials were discussed.

RESULTS

Trials were offered in 15% of conferences. We identified 2 types: (1) time-limited trials, defined as continuing all intensive, life-sustaining treatments, with a plan to reassess after a defined time period based on prespecified clinical milestones, and (2) symptom-limited trials, defined as using basic medical care aimed at survival (rather than purely comfort-focused treatment) once ventilatory support is withdrawn, with a plan to reassess based on patient symptoms. Clinicians frequently did not inform surrogates about key elements of the trial such as criteria by which the effectiveness of the trial would be evaluated and possible next steps based on trial results.

CONCLUSIONS

In this cohort of critically ill patients, trials were infrequently and incompletely discussed. Additional work is needed to improve communication about treatment trials and evaluate their impact on patient and family outcomes.

摘要

目的

本研究旨在描述在重症监护病房中,治疗试验的选择是否以及如何与代理人进行讨论。

材料与方法

我们在加利福尼亚州旧金山的 5 家重症监护病房对 72 名处于死亡或严重功能障碍高风险的患者进行了 72 次家庭会议的音频记录。我们分析了转录本,以制定一个用于讨论试验的编码框架,包括是否以及如何讨论试验。

结果

在 15%的会议中提出了试验。我们确定了两种类型:(1)限时试验,定义为继续所有强化、维持生命的治疗,根据预先规定的临床里程碑,在规定的时间后重新评估;(2)症状限制试验,定义为一旦停止通气支持,使用旨在生存的基本医疗护理(而不是纯粹以舒适为中心的治疗),并根据患者症状重新评估。临床医生经常没有告知代理人有关试验的关键要素,例如评估试验效果的标准以及基于试验结果的可能下一步措施。

结论

在本队列的危重患者中,试验很少且不完整地进行讨论。需要进一步努力改善关于治疗试验的沟通,并评估其对患者和家属结局的影响。