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本文引用的文献

1
What to tell cancer patients. A study of medical attitudes.该如何告知癌症患者。一项关于医学态度的研究。
JAMA. 1961 Apr 1;175:1120-8. doi: 10.1001/jama.1961.03040130004002.
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No news is not good news: information preferences of patients with cancer.没有消息并非好消息:癌症患者的信息偏好
Psychooncology. 1995 Oct;4(3):197-202. doi: 10.1002/pon.2960040305.
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Meeting patient expectations in the cancer consultation.在癌症会诊中满足患者期望。
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The dynamics of change: cancer patients' preferences for information, involvement and support.变化的动态:癌症患者对信息、参与和支持的偏好
Ann Oncol. 1997 Sep;8(9):857-63. doi: 10.1023/a:1008284006045.
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Information needs of cancer patients in west Scotland: cross sectional survey of patients' views.苏格兰西部癌症患者的信息需求:患者观点的横断面调查
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Discussing the diagnosis and prognosis with cancer patients.与癌症患者讨论诊断和预后。
Postgrad Med J. 1996 Jan;72(843):25-9. doi: 10.1136/pgmj.72.843.25.
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Communication with cancer patients: does it matter?与癌症患者的沟通:这重要吗?
J Palliat Care. 1995 Winter;11(4):34-8.
8
Characteristics of physicians with participatory decision-making styles.具有参与式决策风格的医生的特征。
Ann Intern Med. 1996 Mar 1;124(5):497-504. doi: 10.7326/0003-4819-124-5-199603010-00007.
9
Disclosing the cancer diagnosis. Procedures that influence patient hopefulness.披露癌症诊断。影响患者希望感的程序。
Cancer. 1993 Dec 1;72(11):3355-65. doi: 10.1002/1097-0142(19931201)72:11<3355::aid-cncr2820721135>3.0.co;2-d.
10
Relationship between preferences for decisional control and illness information among women with breast cancer: a quantitative and qualitative analysis.乳腺癌女性患者的决策控制偏好与疾病信息之间的关系:一项定量与定性分析。
Soc Sci Med. 1994 Jul;39(2):279-89. doi: 10.1016/0277-9536(94)90336-0.

关于参与癌症化疗试验的医患沟通。

Patient-physician communication concerning participation in cancer chemotherapy trials.

作者信息

Sørensen J B, Rossel P, Holm S

机构信息

Department Oncology, National University Hospital, 9 Blegdamsvej, DK-2100 Copenhagen, Denmark.

出版信息

Br J Cancer. 2004 Jan 26;90(2):328-32. doi: 10.1038/sj.bjc.6601524.

DOI:10.1038/sj.bjc.6601524
PMID:14735172
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2409578/
Abstract

Cancer patients demand a high level of involvement in decisions concerning treatment. Many patients are informed about experimental trials, and especially the first consultation may be crucial for the future communication and treatment process. Patients with nonresectable non-small-cell lung cancer or colorectal cancer informed about experimental chemotherapy completed a questionnaire on satisfaction with the communication process, general attitude towards experimental treatments, the substance of information, and personal contact with the physician following their first consultation in a medical oncology unit. Physicians completed a questionnaire on their perception of the patients' satisfaction. Among 68 physician-cancer patient pairs, 29 patients were informed on chemotherapy in randomised trials and 39 in nonrandomised studies. The general attitude towards experimental treatment was positive or very positive in 71% of patients. Information on the treatment was perceived as completely adequate in 93% of patients informed on randomised and in 67% informed on nonrandomised trials. Physicians underestimated the patients' satisfaction with the overall communication process, the personal contact, the patients' perceived sufficiency of the specific treatment information and their ability to decide on study entry. In conclusion, considerable differences were observed between patients informed about experimental chemotherapy in randomised and nonrandomised trials, both with respect to their perception of how adequate the information on the specific treatments were, and whether it was sufficient for decisions on study entry. This study type effect should be accounted for in future evaluations of communication and patient satisfaction. The data also support the fact that cancer patients have a desire for and ability to understand rather detailed and comprehensive treatment information.

摘要

癌症患者要求高度参与有关治疗的决策。许多患者了解试验情况,尤其是首次咨询对于未来的沟通和治疗过程可能至关重要。被告知有实验性化疗的不可切除非小细胞肺癌或结直肠癌患者,在肿瘤内科首次咨询后,完成了一份关于对沟通流程的满意度、对实验性治疗的总体态度、信息内容以及与医生个人接触情况的问卷。医生完成了一份关于他们对患者满意度看法的问卷。在68对医患组合中,29名患者被告知参与随机试验中的化疗,39名患者被告知参与非随机研究中的化疗。71%的患者对实验性治疗的总体态度为积极或非常积极。在被告知参与随机试验的患者中,93%认为治疗信息完全充分;在被告知参与非随机试验的患者中,这一比例为67%。医生低估了患者对整体沟通流程、个人接触、患者认为特定治疗信息是否充分以及他们决定参与研究的能力的满意度。总之,在被告知参与随机和非随机试验的实验性化疗患者之间,在对特定治疗信息充分程度的认知以及该信息是否足以决定参与研究方面,观察到了相当大的差异。在未来对沟通和患者满意度的评估中应考虑这种研究类型效应。这些数据也支持了癌症患者渴望并能够理解相当详细和全面的治疗信息这一事实。