首页> 外文期刊>BMC Women s Health >DNA-testing for BRCA1/2 prior to genetic counselling in patients with breast cancer: design of an intervention study, DNA-direct
【24h】

DNA-testing for BRCA1/2 prior to genetic counselling in patients with breast cancer: design of an intervention study, DNA-direct

机译:乳腺癌患者进行基因咨询之前进行的BRCA1 / 2的DNA检测:DNA直接干预研究的设计

获取原文

摘要

Background Current practice for patients with breast cancer referred for genetic counseling, includes face-to-face consultations with a genetic counselor prior to and following DNA-testing. This is based on guidelines regarding Huntington’s disease in anticipation of high psychosocial impact of DNA-testing for mutations in BRCA1/2 genes. The initial consultation covers generic information regarding hereditary breast cancer and the (im)possibilities of DNA-testing, prior to such testing. Patients with breast cancer may see this information as irrelevant or unnecessary because individual genetic advice depends on DNA-test results. Also, verbal information is not always remembered well by patients. A different format for this information prior to DNA-testing is possible: replacing initial face-to-face genetic counseling (DNA-intake procedure) by telephone, written and digital information sent to patients’ homes (DNA-direct procedure). Methods/design In this intervention study, 150 patients with breast cancer referred to the department of Clinical Genetics of the Radboud University Nijmegen Medical Centre are given the choice between two procedures, DNA-direct (intervention group) or DNA-intake (usual care, control group). During a triage telephone call, patients are excluded if they have problems with Dutch text, family communication, or of psychological or psychiatric nature. Primary outcome measures are satisfaction and psychological distress. Secondary outcome measures are determinants for the participant’s choice of procedure, waiting and processing times, and family characteristics. Data are collected by self-report questionnaires at baseline and following completion of genetic counseling. A minority of participants will receive an invitation for a 30 min semi-structured telephone interview, e.g. confirmed carriers of a BRCA1/2 mutation, and those who report problems with the procedure. Discussion This study compares current practice of an intake consultation (DNA-intake) to a home informational package of telephone, written and digital information (DNA-direct) prior to DNA-testing in patients with breast cancer. The aim is to determine whether DNA-direct is an acceptable procedure for BRCA1/2 testing, in order to provide customized care to patients with breast cancer, cutting down on the period of uncertainty during this diagnostic process. Trial registration The study is registered at the Dutch Trial Registry http://www.trialregister.nl webcite (NTR3018).
机译:背景技术当前被推荐用于遗传咨询的乳腺癌患者的实践包括在DNA测试之前和之后与遗传咨询员进行面对面的咨询。这是基于有关亨廷顿舞蹈病的指导原则,该指导原则预期DNA检测BRCA1 / 2基因突变会产生很大的社会心理影响。最初的咨询涵盖了有关遗传性乳腺癌的常规信息,以及在进行此类测试之前进行DNA测试的可能性。乳腺癌患者可能认为此信息无关紧要或不必要,因为个体遗传建议取决于DNA检测结果。此外,患者并非总是会记住口头信息。在进行DNA测试之前,此信息的格式可能是不同的:通过将电话,书面和数字信息发送到患者家中来代替最初的面对面遗传咨询(DNA摄入程序)(DNA直接程序)。方法/设计在这项干预研究中,向Radboud大学奈梅亨医学中心临床遗传学部门的150名乳腺癌患者提供了两种方法的选择:直接DNA(干预组)或直接DNA摄入(常规护理,控制组)。在分诊电话中,如果患者的荷兰语文字,家庭交流或心理或精神病学方面的问题存在,则将其排除在外。主要结果指标是满意度和心理困扰。次要结局指标是参与者选择手术程序,等待和处理时间以及家庭特征的决定因素。在基线和完成遗传咨询后通过自我报告调查表收集数据。少数参与者将收到30分钟半结构化电话采访的邀请,例如确认携带BRCA1 / 2突变的携带者,以及报告程序问题的携带者。讨论本研究将目前进行的摄入咨询(DNA摄入)与乳腺癌患者进行DNA测试之前的家庭电话,书面和数字信息(DNA直接)信息包进行比较。目的是确定直接DNA是否为BRCA1 / 2测试可接受的程序,以便为乳腺癌患者提供定制化治疗,从而减少诊断过程中的不确定期。试验注册该研究已在荷兰试验注册中心http://www.trialregister.nl网站上注册(NTR3018)。

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