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莱斯特郡亚裔和英国白人癌症患者及其家属的信息需求:一项横断面调查。

Information needs of Asian and White British cancer patients and their families in Leicestershire: a cross-sectional survey.

作者信息

Muthu Kumar D, Symonds R P, Sundar S, Ibrahim K, Savelyich B S P, Miller E

机构信息

Department of Oncology, Leicester Royal Infirmary, University of Leicester, Leicester, LE1 5WW, UK.

出版信息

Br J Cancer. 2004 Apr 19;90(8):1474-8. doi: 10.1038/sj.bjc.6601774.

DOI:10.1038/sj.bjc.6601774
PMID:15083171
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2409694/
Abstract

The aim of this questionnaire survey was to find the information needs of British Asian cancer patients. An additional objective was to find the extent of family involvement when the patient was given the cancer diagnosis and the patients' views about information disclosure. We interviewed 82 Asian patients and 220 random white control patients. More white British patients gave positive answers to the statement 'I want as much information as possible' than Asian patients (93.1 vs 77.5%, P<or=0.001). However, 92.6% of Asian patients wanted to know if they had cancer. Many more Asians (66.2 vs 5.1%, P<0.001) indicated the general practitioner (GP) as the preferred source of information. This may be because 56% of English-speaking Asian patients would prefer to discuss their illness in their mother tongue. In Leicester, many Asian patients have Asian GPs. The vast majority of both Asian and British patients agreed that family or friends should be present when patients are given the cancer diagnosis. However, Asians were more likely to be alone (24 vs 15%, P=0.008) when told they have had cancer. The majority of patients (both white British and Asian) want to control the disclosure of information to relatives and friends and would like to be present at doctor/family meetings.

摘要

本次问卷调查的目的是了解英国亚裔癌症患者的信息需求。另一个目标是了解患者被诊断出癌症时家庭参与的程度以及患者对信息披露的看法。我们采访了82名亚裔患者和220名随机选取的白人对照患者。对于“我希望获得尽可能多的信息”这一表述,给出肯定回答的英国白人患者比亚裔患者更多(93.1%对77.5%,P≤0.001)。然而,92.6%的亚裔患者想知道自己是否患癌。更多的亚裔患者(66.2%对5.1%,P<0.001)表示全科医生(GP)是首选的信息来源。这可能是因为56%会说英语的亚裔患者更愿意用母语讨论自己的病情。在莱斯特,许多亚裔患者有亚裔全科医生。绝大多数亚裔和英国患者都认为在患者被诊断出癌症时家人或朋友应该在场。然而,在得知自己患癌时,亚裔患者更有可能独自面对(24%对15%,P = 0.008)。大多数患者(包括英国白人和亚裔)希望控制向亲戚和朋友披露信息的情况,并且希望出席医生/家庭会议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b00/2409694/3ced605eba81/90-6601774f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b00/2409694/3ced605eba81/90-6601774f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b00/2409694/3ced605eba81/90-6601774f1.jpg

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本文引用的文献

1
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2
Recent changes in lung cancer incidence for south Asians: a population based register study.南亚人肺癌发病率的近期变化:一项基于人群登记的研究
BMJ. 2003 Jan 11;326(7380):81-2. doi: 10.1136/bmj.326.7380.81.
3
Poor cancer-screening uptake among ethnic minorities.少数族裔人群对癌症筛查的接受程度较低。
告知还是不告知:探究患者及家庭照顾者对癌症相关诊断和预后信息披露的偏好与态度。
J Glob Oncol. 2019 Nov;5:1-12. doi: 10.1200/JGO.19.00132.
4
Does the cancer patient want to know? Results from a study in an Indian tertiary cancer center.癌症患者想知道吗?来自印度一家三级癌症中心的研究结果。
South Asian J Cancer. 2013 Apr;2(2):57-61. doi: 10.4103/2278-330X.110487.
5
Recruitment of ethnic minorities into cancer clinical trials: experience from the front lines.少数民族参与癌症临床试验的招募:来自前线的经验。
Br J Cancer. 2012 Sep 25;107(7):1017-21. doi: 10.1038/bjc.2012.240. Epub 2012 May 31.
6
Challenges of mediated communication, disclosure and patient autonomy in cross-cultural cancer care.跨文化癌症护理中中介沟通、披露和患者自主性的挑战。
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7
The experience of symptoms and information needs of cancer patients undergoing radiotherapy.接受放射治疗的癌症患者的症状体验和信息需求。
J Cancer Educ. 2012 Mar;27(1):46-53. doi: 10.1007/s13187-011-0254-7.
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