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亚洲癌症遗传检测高危个体决策的影响因素。

Factors shaping at-risk individuals' decisions to undergo genetic testing for cancer in Asia.

机构信息

Sociology, School of Social Sciences, Nanyang Technology University, Singapore.

Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore.

出版信息

Health Soc Care Community. 2020 Sep;28(5):1569-1577. doi: 10.1111/hsc.12981. Epub 2020 Mar 20.

Abstract

This study aims to enrich our understanding of factors influencing medically indicated at-risk individuals' decisions to take genetic tests (or not) in the context of cancer treatment and prevention. While previous studies have explored this topic in communities in Europe and the United States, we know relatively little about the situation in Asia. In this study, we conducted in-depth interviews with 24 women who underwent genetic testing for hereditary breast and ovarian cancer syndromes in Singapore. Grounded theory with thematic analysis was applied. Six encouraging and three discouraging factors are identified in the analysis. The six encouraging factors are: desire to create awareness for self and family; perceived benefits for self and family; strong family history of cancer; presence of family support; medical professional recommendation and adequate amount of time to consider undertaking the test. The three discouraging factors are: high costs of tests; perceived lack of ability to cope with test results; and insufficient information about genetic testing. Taken together, the findings in this study add to the current literature by providing empirical evidence regarding the importance of holding family included pre-test counselling and providing adequate time for patients to decide to undergo genetic testing for hereditary cancer syndromes.

摘要

本研究旨在丰富我们对影响医学上有风险的个体在癌症治疗和预防背景下决定进行基因检测(或不进行)的因素的理解。虽然之前的研究已经在欧洲和美国的社区中探讨了这个主题,但我们对亚洲的情况知之甚少。在这项研究中,我们对 24 名在新加坡接受遗传性乳腺癌和卵巢癌综合征基因检测的女性进行了深入访谈。采用扎根理论和主题分析。在分析中确定了六个鼓励因素和三个阻碍因素。六个鼓励因素是:提高自我和家庭意识的愿望;对自我和家庭的潜在益处;强烈的癌症家族史;有家庭支持;医疗专业人员的建议和足够的时间考虑进行测试。三个阻碍因素是:测试费用高;认为自己无法应对测试结果;以及关于基因检测的信息不足。总的来说,这项研究的结果通过提供关于进行遗传性癌症综合征基因检测时进行家庭纳入的预测试咨询和为患者提供足够的时间做出决定的重要性的实证证据,为当前文献做出了贡献。

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