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Informing patients about cancer in Nepal: what do people prefer?

机译:向患者介绍尼泊尔的癌症:人们喜欢什么?

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INTRODUCTION: Traditionally, doctors in Nepal do not discuss a diagnosis of malignancy with their patient. Instead, discussion is more likely to take place with family members, who then filter the information that the patient receives. This study aims to quantify the amount of actual disclosure of a cancer diagnosis that takes place, through a survey of patients admitted for hospice care, and to compare this with preferences regarding cancer disclosure from a survey of the general population. OBJECTIVES: (a) To determine what proportion of patients, referred for hospice care with advanced cancer, who were aware of their disease and prognosis. (b) To determine the attitude among the public toward disclosure of information of a diagnosis of malignancy, if they or a close relative were to develop the disease. (c) To observe if educational attainment impacts on issues related to disclosure of a cancer diagnosis. METHOD: (a) Prospective survey of patients with cancer admitted to 'Hospice Nepal' over a one-year period, recording details of how much patients knew of their diagnosis. (b) Survey of the general population in and around the Kathmandu valley, with a questionnaire asking the following two questions: If you were diagnosed with cancer would you like to be informed of your cancer? If a close relative was diagnosed with cancer would you like them to be informed of their cancer? RESULTS: A survey of the 96 patients admitted to 'Hospice Nepal' over the one-year study period showed that 19 (20%) of the patients had knowledge of both their disease and the stage of the disease; 16 (17%) knew that they had cancer but did not know about their disease progression or prognosis; 61 (63%) were unaware of the nature, seriousness or prognosis of their disease. A survey of the general population in Kathmandu showed 204 (80%) of the 256 respondents wanted to be informed if they were diagnosed with cancer, even if it was incurable; 44 (17%) wanted to be informed of such a diagnosis only if it was curable; and 8 (3%) did not want to be informed of such a diagnosis at all. CONCLUSION: In Nepal, there is a clear disparity between what patients would like to be told should they develop cancer, and what patients with cancer know about their disease. In the Asian context, it is not unusual to be advised that western practices of disclosure are inappropriate, yet this study, conducted in a very non-western culture, shows that the patient's wish to know about their illness is a desire which can transcend cultural and ethnic differences.
机译:简介:传统上,尼泊尔的医生不会与患者讨论恶性肿瘤的诊断。取而代之的是与家人进行讨论,然后由家人过滤患者收到的信息。本研究旨在通过对入院接受临终关怀的患者进行调查来量化发生的癌症诊断的实际披露量,并将其与一般人群调查中有关癌症披露的偏好进行比较。目的:(a)确定知道自己的疾病和预后的接受晚期癌症临终关怀治疗的患者比例。 (b)确定公众或恶性亲戚是否患上该病的公众对诊断恶性肿瘤信息披露的态度。 (c)观察学历是否影响与癌症诊断披露有关的问题。方法:(a)对接受“尼泊尔临终关怀”治疗的癌症患者进行为期一年的前瞻性调查,记录患者对诊断的了解程度。 (b)对加德满都河谷及其周围地区的总人口进行调查,并通过问卷调查提出以下两个问题:如果您被诊断出患有癌症,您想知道自己的癌症吗?如果近亲被诊断出患有癌症,您是否希望他们被告知癌症?结果:在为期一年的研究期间对“临终关怀医院”收治的96例患者进行的一项调查显示,其中19例(20%)患者既了解自己的疾病,也了解疾病的阶段。 16(17%)知道自己患有癌症,但不知道自己的疾病进展或预后; 61名(63%)不了解其疾病的性质,严重性或预后。一项对加德满都总人口的调查显示,在256名受访者中,有204名(80%)希望被告知是否被诊断出患有癌症,即使无法治愈。 44(17%)人希望仅在可治愈的情况下才能获知这种诊断; 8(3%)人根本不想被告知这种诊断。结论:在尼泊尔,患者想告诉他们应该患什么癌症以及哪些癌症患者知道自己的疾病之间存在明显的差距。在亚洲,通常不建议西方人进行披露是不寻常的,但是这项研究是在非常非西方的文化中进行的,表明患者希望了解自己的疾病是一种超越文化的渴望。和种族差异。

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