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Charting a new course for the delivery of high-quality cancer care.为提供高质量癌症护理规划新路径。
J Clin Oncol. 2013 Dec 20;31(36):4485-7. doi: 10.1200/JCO.2013.53.7993. Epub 2013 Nov 18.
2
Marital status and survival in patients with cancer.婚姻状况与癌症患者的生存。
J Clin Oncol. 2013 Nov 1;31(31):3869-76. doi: 10.1200/JCO.2013.49.6489. Epub 2013 Sep 23.
3
Representativeness of participants in the cancer care outcomes research and surveillance consortium relative to the surveillance, epidemiology, and end results program.癌症护理结果研究和监测联盟参与者与监测、流行病学和最终结果计划的代表性。
Med Care. 2013 Feb;51(2):e9-15. doi: 10.1097/MLR.0b013e318222a711.
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Family presence in routine medical visits: a meta-analytical review.家庭在常规医疗就诊中的参与:一项荟萃分析综述。
Soc Sci Med. 2011 Mar;72(6):823-31. doi: 10.1016/j.socscimed.2011.01.015. Epub 2011 Feb 24.
5
Caregivers' participation in the oncology clinic visit mediates the relationship between their information competence and their need fulfillment and clinic visit satisfaction.照护者参与肿瘤临床就诊能够调节其信息能力与其需求满足度和临床就诊满意度之间的关系。
Patient Educ Couns. 2010 Dec;81 Suppl:S94-9. doi: 10.1016/j.pec.2010.08.022. Epub 2010 Sep 28.
6
Cancer patients' roles in treatment decisions: do characteristics of the decision influence roles?癌症患者在治疗决策中的角色:决策特征是否影响角色?
J Clin Oncol. 2010 Oct 1;28(28):4364-70. doi: 10.1200/JCO.2009.26.8870. Epub 2010 Aug 16.
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Race and shared decision-making: perspectives of African-Americans with diabetes.种族与共同决策:糖尿病的非裔美国人的观点。
Soc Sci Med. 2010 Jul;71(1):1-9. doi: 10.1016/j.socscimed.2010.03.014. Epub 2010 Mar 24.
8
Family caregivers, patients and physicians: ethical guidance to optimize relationships.家庭成员照护者、患者和医生:优化关系的伦理指导。
J Gen Intern Med. 2010 Mar;25(3):255-60. doi: 10.1007/s11606-009-1206-3.
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Decision involvement and receipt of mastectomy among racially and ethnically diverse breast cancer patients.不同种族和族裔乳腺癌患者的决策参与情况及乳房切除术接受情况
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10
Multiple imputation in a large-scale complex survey: a practical guide.大规模复杂调查中的多重插补:实用指南。
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家庭在癌症治疗决策中的作用。

The role of families in decisions regarding cancer treatments.

作者信息

Hobbs Gabriela S, Landrum Mary Beth, Arora Neeraj K, Ganz Patricia A, van Ryn Michelle, Weeks Jane C, Mack Jennifer W, Keating Nancy L

机构信息

Department of Medical Oncology, Harvard Medical School, Massachusetts General Hospital, Boston, Massachusetts.

出版信息

Cancer. 2015 Apr 1;121(7):1079-87. doi: 10.1002/cncr.29064. Epub 2015 Feb 23.

DOI:10.1002/cncr.29064
PMID:25708952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4368490/
Abstract

BACKGROUND

Shared decision-making is an important component of patient-centered care and is associated with improved outcomes. To the authors' knowledge, little is known concerning the extent and predictors of the involvement of a patient's family in decisions regarding cancer treatments.

METHODS

The Cancer Care Outcomes Research and Surveillance (CanCORS) Consortium is a large, multiregional, prospective cohort study of the cancer care and outcomes of patients with lung and colorectal cancer. Participants reported the roles of their families in decision-making regarding treatment. Multinomial logistic regression was used to assess patient factors associated with family roles in decisions.

RESULTS

Among 5284 patients, 80 (1.5%) reported family-controlled decisions, with the highest adjusted rates (12.8%) noted among non-English-speaking Asians. Among the 5204 remaining patients, 49.4% reported equally sharing decisions with family, 22.1% reported some family input, and 28.5% reported little family input. In adjusted analyses, patients who were married, female, older, and insured more often reported equally shared decisions with family (all P <.001). Adjusted family involvement varied by race/ethnicity and language, with Chinese-speaking Asian (59.8%) and Spanish-speaking Hispanic (54.8%) patients equally sharing decisions with family more often than white individuals (47.6%). Veterans Affairs patients were least likely to report sharing decisions with family, even after adjustment for marital status and social support (P <.001).

CONCLUSIONS

The majority of patients with newly diagnosed lung or colorectal cancer involve family members in treatment decisions. Non-English-speaking Asians and Hispanics rely significantly on family. Further studies are needed to determine the impact of family involvement in treatment decisions on outcomes; until then, physicians should consider eliciting patients' preferences for family involvement.

摘要

背景

共同决策是患者为中心的医疗的重要组成部分,且与改善治疗结果相关。据作者所知,关于患者家属参与癌症治疗决策的程度和预测因素知之甚少。

方法

癌症护理结果研究与监测(CanCORS)联盟是一项针对肺癌和结直肠癌患者的癌症护理及结果的大型多地区前瞻性队列研究。参与者报告了其家属在治疗决策中的作用。采用多项逻辑回归来评估与决策中家属角色相关的患者因素。

结果

在5284名患者中,80名(1.5%)报告由家属控制决策,其中非英语亚裔的调整后比例最高(12.8%)。在其余5204名患者中,49.4%报告与家属平等分担决策,22.1%报告家属有一定参与,28.5%报告家属参与很少。在调整分析中,已婚、女性、年龄较大且有保险的患者更常报告与家属平等分担决策(所有P <.001)。家属参与程度经调整后因种族/族裔和语言而异,说中文的亚裔(59.8%)和说西班牙语的西班牙裔(54.8%)患者比白人(47.6%)更常与家属平等分担决策。退伍军人事务部的患者即使在调整婚姻状况和社会支持后,报告与家属分担决策的可能性也最小(P <.001)。

结论

大多数新诊断的肺癌或结直肠癌患者会让家庭成员参与治疗决策。非英语亚裔和西班牙裔显著依赖家属。需要进一步研究以确定家属参与治疗决策对治疗结果的影响;在此之前,医生应考虑了解患者对家属参与的偏好。