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2
Key components of shared decision making models: a systematic review.共同决策模型的关键组成部分:一项系统综述。
BMJ Open. 2019 Dec 17;9(12):e031763. doi: 10.1136/bmjopen-2019-031763.
3
Shared Decision Making: Improving Patient Outcomes by Understanding the Benefits of and Barriers to Effective Communication.共同决策:通过了解有效沟通的益处和障碍来改善患者治疗效果
Clin J Oncol Nurs. 2019 Oct 1;23(5):540-542. doi: 10.1188/19.CJON.540-542.
4
Association of Communication Interventions to Discuss Code Status With Patient Decisions for Do-Not-Resuscitate Orders: A Systematic Review and Meta-analysis.探讨患者是否选择不进行心肺复苏的沟通干预与决策的关联:系统评价和荟萃分析。
JAMA Netw Open. 2019 Jun 5;2(6):e195033. doi: 10.1001/jamanetworkopen.2019.5033.
5
Effect of the Serious Illness Care Program in Outpatient Oncology: A Cluster Randomized Clinical Trial.严重疾病照护计划对门诊肿瘤学的影响:一项群组随机临床试验。
JAMA Intern Med. 2019 Jun 1;179(6):751-759. doi: 10.1001/jamainternmed.2019.0077.
6
Evaluating an Intervention to Improve Communication Between Oncology Clinicians and Patients With Life-Limiting Cancer: A Cluster Randomized Clinical Trial of the Serious Illness Care Program.评估一项改善肿瘤临床医生与生命末期癌症患者沟通的干预措施:严重疾病护理计划的一项集群随机临床试验。
JAMA Oncol. 2019 Jun 1;5(6):801-809. doi: 10.1001/jamaoncol.2019.0292.
7
A qualitative systematic review of internal and external influences on shared decision-making in all health care settings.对所有医疗环境中共同决策的内部和外部影响进行的定性系统评价。
JBI Libr Syst Rev. 2012;10(58):4633-4646. doi: 10.11124/jbisrir-2012-432.
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Feeling Heard and Understood: A Patient-Reported Quality Measure for the Inpatient Palliative Care Setting.感到被倾听和理解:一种针对住院姑息治疗环境的患者报告质量指标。
J Pain Symptom Manage. 2016 Feb;51(2):150-4. doi: 10.1016/j.jpainsymman.2015.10.018. Epub 2015 Nov 17.
9
Development of the Serious Illness Care Program: a randomised controlled trial of a palliative care communication intervention.重症护理项目的发展:姑息治疗沟通干预的随机对照试验
BMJ Open. 2015 Oct 6;5(10):e009032. doi: 10.1136/bmjopen-2015-009032.
10
"Doctor, Make My Decisions": Decision Control Preferences, Advance Care Planning, and Satisfaction With Communication Among Diverse Older Adults.“医生,替我做决定”:不同老年人群体的决策控制偏好、预先护理计划与沟通满意度
J Pain Symptom Manage. 2016 Jan;51(1):33-40. doi: 10.1016/j.jpainsymman.2015.07.018. Epub 2015 Sep 3.

患者对病情告知的偏好:一项关于以信息为中心与以患者价值观为中心框架的随机试验。

Patient Preferences for Code Status Discussions: A Randomized Trial of Information- vs. Patient Values-Centered Frameworks.

作者信息

Joshi Christopher, Malik Sehrish, Wang Wei, Ouchi Kei

机构信息

Department of Medicine, Beth Israel Deaconess Medical Center, Boston, USA.

School of Medicine, City University of New York, New York, NY, USA.

出版信息

J Gen Intern Med. 2025 Jun;40(8):1829-1835. doi: 10.1007/s11606-024-09243-2. Epub 2024 Dec 11.

DOI:10.1007/s11606-024-09243-2
PMID:39663339
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12120093/
Abstract

BACKGROUND

Helping patients make decisions about their preferences for cardiopulmonary resuscitation (i.e., code status) is an important way to respect patient autonomy in the hospital. There is a gap in understanding which framework of discussion patients prefer for this decision-making.

OBJECTIVE

To determine which of two frameworks to code status discussions-information-centered or patient values-centered-make patients feel more heard and understood about their preferences regarding cardiopulmonary resuscitation (CPR).

DESIGN

Prospective, randomized study comparing two different frameworks to CPR discussion.

PARTICIPANTS

We enrolled adult patients with one or more serious illnesses who were recently discharged from an urban, tertiary care, academic medical center in Boston, MA.

INTERVENTIONS

Subjects were randomized to receive either the information-centered framework, in which their likelihood of recovery following CPR was shared, or the patient values-centered framework, in which their personal values were elicited and used to make a recommendation.

MAIN MEASURES

Subject-reported heard and understood rating with regard to their preferences for CPR.

KEY RESULTS

Of the 46 subjects enrolled, 25 (54.3%) were male, 42 (91.3%) were White, and 3 (6.5%) were Black. Mean age was 66.4 ± 11.8 years. Subjects reported feeling more "heard and understood" about their preferences for CPR with the patient values-centered framework compared with after the information-centered framework (p = 0.033). When asked, 89% of subjects "definitely" or "probably" wanted to hear their doctor's personalized recommendation about CPR (p < 0.001).

CONCLUSION

Patients, in line with palliative care experts, largely support a patient values-centered framework to CPR, including a recommendation made by the clinician based on the patient's expressed values.

摘要

背景

帮助患者就其心肺复苏偏好(即抢救状态)做出决定是在医院尊重患者自主权的重要方式。在理解患者偏好哪种决策讨论框架方面存在差距。

目的

确定在两种抢救状态讨论框架(以信息为中心或以患者价值观为中心)中,哪一种能让患者在心肺复苏(CPR)偏好方面更感被倾听和理解。

设计

比较两种不同CPR讨论框架的前瞻性随机研究。

参与者

我们招募了患有一种或多种严重疾病且最近从马萨诸塞州波士顿的一家城市三级医疗学术医学中心出院的成年患者。

干预措施

受试者被随机分配接受以信息为中心的框架(其中会告知他们CPR后恢复的可能性)或以患者价值观为中心的框架(其中会引出他们的个人价值观并据此给出建议)。

主要测量指标

受试者报告的关于其CPR偏好的被倾听和理解程度评分。

关键结果

在46名受试者中,25名(54.3%)为男性,42名(91.3%)为白人,3名(6.5%)为黑人。平均年龄为66.4±11.8岁。与以信息为中心的框架相比,受试者报告在以患者价值观为中心的框架下,他们在CPR偏好方面更感“被倾听和理解”(p = 0.033)。当被问及是否想听医生关于CPR的个性化建议时,89%的受试者“肯定”或“可能”想听(p < 0.001)。

结论

与姑息治疗专家一致,患者在很大程度上支持以患者价值观为中心的CPR框架,包括临床医生根据患者表达的价值观给出的建议。