首页> 外文期刊>Genetics in medicine >Association between screening family medical history in general medical care and lower burden of cancer worry among women with a close family history of breast cancer.
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Association between screening family medical history in general medical care and lower burden of cancer worry among women with a close family history of breast cancer.

机译:乳腺癌家族史密切的女性中,筛查一般医疗中的家庭病史与降低癌症负担之间的关联。

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PURPOSE: Soliciting family medical history (FMH) is the initial step in the process of screening for heritable cancer risk in medical care. We investigate whether recent solicitation of FMH in general medical care is associated with cancer worry among a sample of women having a first-degree relative with a breast cancer diagnosis. METHODS: Surveys were mailed to women registered with the Cancer Genetics Network having a first-degree relative with a breast cancer diagnosis and a regular source of medical care. The independent measure consisted of two items for solicitation of FMH based on validated measures of clinical interactions with one's physician; the dependent measure was a novel measure of cancer worry based on validated patient-centered measure of distress; and the secondary measures were 6-point scales for perceived likelihood of developing breast cancer and perceived severity of breast cancer as a health outcome. RESULTS: A total of 353 women responded and met eligibility criteria (76.4% minimum response rate). One fifth reported no cancer worry during the past 4 weeks. After adjustment for age, education, pedigree features, and clustering within families, recent FMH solicitation was associated with lower odds of cancer worry (odds ratio = 0.58; 95% confidence interval = 0.51-0.70). FMH solicitation was associated with lower perceptions of the severity of developing breast cancer but not with the perception of cancer likelihood. CONCLUSIONS: Our data do not support the hypothesis that FMH solicitation in general medical practice causes cancer worry. In fact, we observed a protective association possibly explained by influences on perceptions of breast cancer severity. Prospective research among less select populations is necessary.
机译:目的:提高家族病史(FMH)是筛查医疗中遗传性癌症风险的第一步。我们调查在具有一级亲属乳腺癌诊断的女性样本中,最近在一般医疗服务中招募FMH是否与癌症担忧有关。方法:将调查问卷邮寄给在癌症遗传学网络注册的女性,这些女性具有乳腺癌诊断的一级亲戚和定期的医疗护理。这项独立措施包括两项基于对与医生的临床相互作用的有效措施而招募FMH的项目;依赖措施是一种基于经过验证的以患者为中心的遇险度量的新的癌症担忧度量。二级指标是6点量表,用于感知患乳腺癌的可能性和感知为健康后果的乳腺癌严重程度。结果:共有353名妇女做出了回应,并符合入选标准(最低回应率76.4%)。五分之一的人表示在过去的4周中没有癌症担忧。在对年龄,教育程度,血统特征和家庭聚类进行调整后,最近的FMH征招与患癌症忧虑的几率降低有关(赔率= 0.58; 95%置信区间= 0.51-0.70)。 FMH征集与对发生乳腺癌的严重程度的较低认知有关,但与癌症可能性的认知无关。结论:我们的数据不支持以下假设:在一般医学实践中,FMH招募会引起癌症担忧。实际上,我们观察到一种保护性关联,可能是由于对乳腺癌严重程度的感知产生了影响。在选择较少的人群中进行前瞻性研究是必要的。

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