Murdoch Childrens Research Institute, Melbourne, Victoria, Australia.
BMJ Open. 2013 Sep 10;3(9):e003660. doi: 10.1136/bmjopen-2013-003660.
Fragile X syndrome (FXS) is the leading cause of inherited intellectual and developmental disability. Policy development relating to carrier screening programmes for FXS requires input from large studies examining not only test uptake but also psychosocial aspects. This study will compare carrier screening in pregnant and non-pregnant populations, examining informed decision-making, psychosocial issues and health economics.
Pregnant and non-pregnant women are being recruited from general practices and obstetric services. Women receive study information either in person or through clinic mail outs. Women are provided pretest counselling by a genetic counsellor and make a decision about testing in their own time. Data are being collected from two questionnaires: one completed at the time of making the decision about testing and the second 1 month later. Additional data are gathered through qualitative interviews conducted at several time points with a subset of participating women, including all women with a positive test result, and with staff from recruiting clinics. A minimum sample size of 500 women/group has been calculated to give us 88% power to detect a 10% difference in test uptake and 87% power to detect a 10% difference in informed choice between the pregnant and non-pregnant groups. Questionnaire data will be analysed using descriptive statistics and multivariate logistic regression models. Interview data will be thematically analysed. Willingness-to-pay and cost effectiveness analyses will also be performed. Recruitment started in July 2009 and data collection will be completed by December 2013.
Ethics approval has been granted by the Universities of Melbourne and Western Australia and by recruiting clinics, where required. Results will be reported in peer-reviewed publications, conference presentations and through a website http://www.fragilexscreening.net.au. The results of this study will make a significant contribution to discussions about the wider introduction of population carrier screening for FXS.
脆性 X 综合征(FXS)是遗传性智力和发育障碍的主要原因。与 FXS 携带者筛查计划相关的政策制定需要来自大型研究的投入,这些研究不仅要检查检测率,还要检查社会心理方面。本研究将比较孕妇和非孕妇人群中的携带者筛查,检查知情决策、社会心理问题和健康经济学。
正在从普通诊所和产科服务中招募孕妇和非孕妇。女性通过个人或诊所邮件获得研究信息。女性接受遗传咨询师的预测试咨询,并在自己的时间内决定是否进行检测。数据来自两份问卷:一份在做出检测决定时填写,另一份在一个月后填写。通过对部分参与女性(包括所有检测结果阳性的女性)和招募诊所的工作人员进行定性访谈,收集了额外的数据。在几个时间点进行。已计算出最小样本量为 500 名女性/组,以便我们有 88%的能力检测到孕妇和非孕妇组之间检测率的 10%差异,有 87%的能力检测到知情选择的 10%差异。将使用描述性统计和多变量逻辑回归模型分析问卷数据。将对访谈数据进行主题分析。还将进行意愿支付和成本效益分析。招募工作于 2009 年 7 月开始,数据收集将于 2013 年 12 月完成。
墨尔本大学、西澳大利亚大学和招募诊所(如有要求)已批准伦理。结果将在同行评议的出版物、会议演讲和网站 http://www.fragilexscreening.net.au 上报告。本研究的结果将对关于更广泛引入 FXS 人群携带者筛查的讨论做出重要贡献。