首页> 美国卫生研究院文献>other >Information Needs of Mothers Regarding Communicating BRCA1/2 Cancer Genetic Test Results to their Children
【2h】

Information Needs of Mothers Regarding Communicating BRCA1/2 Cancer Genetic Test Results to their Children

机译:母亲关于向孩子传达BRCA1 / 2癌症基因检测结果的信息需求

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Mothers who participate in genetic testing for hereditary breast/ovarian cancer risk must decide if, when, and how to ultimately share their BRCA1 and BRCA2 (BRCA1/2) test results with their minor-age children. One of the primary aides for mothers in making this decision is cancer genetic counseling. However, counseling is limited in how well it can educate mothers about such decisions without the availability of resources that are specific to family communication and genetic testing per se. In an effort to fill this gap and identify mothers most likely to benefit from such resources, surveys were conducted with 187 mothers undergoing BRCA1/2 testing who had children 8-21 years-old. Data were collected weeks after genetic testing but prior to mothers' learning of their test results; quantitative assessments of informational resource needs (i.e., speaking with previous BRCA1/2 testing participants who are parents regarding their experiences, reading educational literature about options and what to expect, speaking with a family counselor, attending a family support group, and self-nominated other resources), testing motivations, decision making vigilance, and decisional conflict regarding communicating test results to children were included. Mothers' most-to-least frequently cited information resource needs were: literature (93.4%), family counseling (85.8%), prior participants (79.0%), support groups (53.9%), and other (28.9%; e.g., pediatricians and psychologists). Seventy-eight percent of mothers were interested in accessing 3 or more resources. In multivariate regression analyses, testing motivations (β=0.35, p=.03), decision making vigilance (β=0.16, p=.00) and decisional conflict (β=0.10, p=.00) were associated with mothers' need level; mothers with a greater interest in testing to learn about their children's risks, those with more vigilant decision making styles, and those with higher decisional conflict had the greatest need. In conjunction with enhanced genetic counseling focusing on family disclosure, educational literature and psychosocial support may promote improved outcomes.
机译:参加遗传性乳腺癌/卵巢癌风险基因测试的母亲必须决定是否,何时以及如何与未成年子女最终分享其BRCA1和BRCA2(BRCA1 / 2)测试结果。母亲做出这一决定的主要助手之一是癌症遗传咨询。但是,辅导在没有足够的家庭交流和基因检测本身资源的情况下,可以对母亲进行这样的决定的教育程度受到限制。为了填补这一空白并确定最有可能从此类资源中受益的母亲,我们对187名接受BRCA1 / 2测试的母亲进行了调查,这些母亲的子女年龄在8-21岁之间。基因测试后几周就收集数据,但在母亲了解其测试结果之前;信息资源需求的定量评估(即,与以前的BRCA1 / 2测试参与者交谈,他们是父母,他们的经历,阅读有关选择和期望的教育文献,与家庭顾问交谈,参加家庭支持小组并自我提名)其他资源),测试动机,决策警惕性以及与向孩子传达测试结果有关的决策冲突。母亲最常被引用的信息资源需求是:文学(93.4%),家庭咨询(85.8%),先前参加者(79.0%),支持小组(53.9%)和其他(28.9%;例如,儿科医生和心理学家)。 78%的母亲对访问3种或更多资源感兴趣。在多元回归分析中,测试动机(β= 0.35,p = .03),警惕性决策(β= 0.16,p = .00)和决策冲突(β= 0.10,p = .00)与母亲的需求相关。水平;对测试有更大兴趣以了解孩子的风险的母亲,决策风格更加警惕的母亲以及决策冲突较高的母亲最需要。结合以家庭披露为重点的加强遗传咨询,教育文献和社会心理支持可以促进改善结局。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号