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少数民族妇女乳腺癌风险基因检测障碍:一项探索性研究。

Barriers to genetic testing for breast cancer risk among ethnic minority women: an exploratory study.

机构信息

Fielding School of Public Health, and Jonsson Comprehensive Cancer Center, University of California, Los Angeles, CA 90095-6900, USA. USA.

出版信息

Ethn Dis. 2012 Summer;22(3):267-73.

Abstract

BACKGROUND/AIMS: To assess awareness of genetic testing for breast cancer risk and identify influences on the decision-making process regarding counseling and testing among an ethnically-diverse sample of women.

METHODS

Semi-structured interviews were conducted with 33 women who were breast or ovarian cancer survivors or first degree relatives of survivors. Interviews were audiotaped, translated, and transcribed. Analysis of transcripts identified relevant themes and quotes were extracted for illustration.

RESULTS

Low levels of awareness were observed in minority women, including those with a significant family history of cancer. A number of potential influences on the decision-making process emerged including beliefs about risk factors for cancer and opinions about the options following testing. Distinct issues were identified within ethnic groups that may function as barriers such as concern about the misuse of genetic information (African Americans), unfamiliarity with Western preventive medicine (Asians), and women prioritizing family obligations over personal health needs (Latinas).

CONCLUSIONS

Results suggest there may be a need for interventions to raise awareness about genetic counseling and testing among minorities. Our findings contribute to the literature by using in-depth interviews to uncover potential barriers and facilitators to counseling and testing and by including Asians and Latinas, groups under-represented in previous research.

摘要

背景/目的:评估在一个种族多样化的女性样本中,对乳腺癌风险的遗传检测的认知,并确定影响咨询和检测决策过程的因素。

方法

对 33 名乳腺癌或卵巢癌幸存者或幸存者的一级亲属进行了半结构式访谈。访谈进行了录音、翻译和转录。对转录本进行分析,确定了相关主题,并提取了说明性的引语。

结果

在少数族裔女性中观察到低水平的认知,包括那些有显著家族癌症史的女性。有许多潜在的影响决策过程的因素出现,包括对癌症危险因素的信念和对检测后的选择的看法。在不同的族裔群体中确定了一些可能作为障碍的特定问题,例如担心遗传信息的滥用(非裔美国人)、对西方预防医学的不熟悉(亚洲人),以及女性将家庭义务置于个人健康需求之上(拉丁裔)。

结论

结果表明,可能需要干预措施来提高少数民族对遗传咨询和检测的认识。我们的研究结果通过使用深入访谈来揭示咨询和检测的潜在障碍和促进因素,并包括亚洲人和拉丁裔,这些群体在以前的研究中代表性不足,为文献做出了贡献。

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