Emery J
School of Primary, Aboriginal and Rural Health Care, The University of Western Australia, Perth, Australia.
Ann Hum Biol. 2005 Mar-Apr;32(2):218-27. doi: 10.1080/03014460500074921.
The development and evaluation of computer decision support for the assessment of cancer genetic risk in primary care is reported with two series of studies described: the RAGs (Risk Assessment in Genetics) studies and the GRAIDS (Genetic Risk Assessment in an Intranet and Decision Support) Trial. In the GRAIDS Trial, 45 general practices in Eastern England have been recruited and randomised. Comparison practices attend an educational session and receive clinical guidelines about familial breast and colorectal cancer. In the intervention practices a lead clinician is trained in cancer genetics and use of the GRAIDS software. The GRAIDS software is a simple pedigree-drawing program that implements clinical guidelines for familial breast and colorectal cancer and presents individualised information about breast cancer risk in a range of formats. Outcome measures of the trial include: frequency of software use, practitioners' attitudes towards the software, total number of referrals to secondary care about familial cancer and the proportion that meet regional referral criteria, and a patient-centred measure of informed decision making. The family history will become an increasingly important tool in primary care to assess genetic risk. This research evaluates an approach to support high-quality advice about cancer genetics in primary care which could be applied more broadly as our understanding of complex disease genetics increases.
本文报告了针对基层医疗中癌症遗传风险评估的计算机决策支持系统的开发与评估,介绍了两个系列的研究:RAGs(遗传学风险评估)研究和GRAIDS(内联网中的遗传风险评估与决策支持)试验。在GRAIDS试验中,英格兰东部的45家全科诊所被招募并随机分组。对照诊所参加一次教育课程并接收有关家族性乳腺癌和结直肠癌的临床指南。在干预诊所,一名牵头临床医生接受癌症遗传学及GRAIDS软件使用方面的培训。GRAIDS软件是一个简单的系谱绘制程序,它实施家族性乳腺癌和结直肠癌的临床指南,并以多种格式呈现关于乳腺癌风险的个性化信息。该试验的结果指标包括:软件使用频率、从业者对软件的态度、转诊至二级医疗的家族性癌症患者总数以及符合区域转诊标准的比例,还有一项以患者为中心的知情决策衡量指标。家族病史将成为基层医疗中评估遗传风险日益重要的工具。这项研究评估了一种在基层医疗中支持高质量癌症遗传学建议的方法,随着我们对复杂疾病遗传学理解的增加,该方法可更广泛地应用。