...
首页> 外文期刊>Health Communication >Understanding Patterns of Health Communication in Families at Risk for Hereditary Nonpolyposis Colorectal Cancer: Examining the Effect of Conclusive Versus Indeterminate Genetic Test Results
【24h】

Understanding Patterns of Health Communication in Families at Risk for Hereditary Nonpolyposis Colorectal Cancer: Examining the Effect of Conclusive Versus Indeterminate Genetic Test Results

机译:了解遗传性非息肉病性结直肠癌高危家庭的健康交流模式:检验结论性治疗与不确定性遗传测试结果的关系

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

In families meeting criteria for hereditary nonpolyposis colorectal cancer (HNPCC), genetic testing may or may not identify a mutation. Communication about genetic testing and risk in families with identified HNPCC mutations is associated with individual and relational factors. Similar communication patterns would be expected in families with similar clinical and pathological characteristics, but without an identified HNPCC mutation; however, previous studies have not included such families. Social network analysis was used to compare communication networks and associated individual and relational factors in families with and without identified HNPCC mutations. Respondents from families without identified mutations communicated about genetic counseling and testing and risk for HNPCC with a significantly smaller proportion of network members, compared to respondents from mutation-positive families. Members of families without identified mutations were also more likely to share thoughts about risk for HNPCC with network members whose advice they take, compared to members of families with known mutations. These findings extend our knowledge of communication in families at risk of HNPCC to include the many families in which a causative mutation has not yet been identified. Differences in the breadth of communication about genetics and risk for HNPCC, and the possibility that members of families without identified mutations may seek advice from those with whom they communicate about risk, provide new avenues for future research. Understanding existing communication patterns could help improve education and counseling processes, and facilitate the development of interventions designed to assist in family discussions of risk.View full textDownload full textRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/10410236.2011.558338
机译:在满足遗传性非息肉性结直肠癌(HNPCC)标准的家庭中,基因检测可能会或可能不会识别出突变。有关已鉴定出HNPCC突变的家庭的基因检测和风险交流与个人和相关因素有关。具有相似的临床和病理特征,但未发现HNPCC突变的家庭将期待类似的交流方式。但是,以前的研究没有包括这些家庭。社会网络分析用于比较有和没有HNPCC突变的家庭中的通信网络以及相关的个人和相关因素。与来自突变阳性家庭的受访者相比,来自未发现突变的家庭的受访者传达了有关遗传咨询和检测以及HNPCC风险的信息,网络成员的比例要小得多。与具有已知突变的家庭成员相比,未发现突变的家庭成员也更可能与他们接受建议的网络成员分享有关HNPCC风险的想法。这些发现扩展了我们对有HNPCC危险的家庭的交流知识,包括尚未发现致病突变的许多家庭。关于HNPCC遗传学和风险的沟通广度上的差异,以及未发现突变的家庭成员可能会向与其沟通的人寻求有关风险的建议的可能性,为将来的研究提供了新的途径。了解现有的沟通模式可以帮助改善教育和咨询流程,并促进旨在帮助家庭进行风险讨论的干预措施的开发。查看全文下载全文相关的变量add add_id = netvibes,twitter,technorati,可口,linkedin,facebook,stumbleupon,digg,google,更多”,发布:“ ra-4dff56cd6bb1830b”};添加到候选列表链接永久链接http://dx.doi.org/10.1080/10410236.2011.558338

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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