首页> 外文期刊>Genetic testing and molecular biomarkers >Providing Appropriate Genetic Information to Healthy Carriers of Hemoglobinopathy Can Be a Welcome and Safe Initiative: The Latium Example
【24h】

Providing Appropriate Genetic Information to Healthy Carriers of Hemoglobinopathy Can Be a Welcome and Safe Initiative: The Latium Example

机译:向血红蛋白病的健康携带者提供适当的遗传信息可能是一个受欢迎且安全的举措:La的例子

获取原文
获取原文并翻译 | 示例
           

摘要

Aims: To register the opinions and feelings of (presumed) unaware healthy hemoglobinopathy carriers, receiving information on their carrier status. Methods: We collected 259 interviews from the parents of secondary school students, after their children had been provisionally diagnosed as hemoglobinopathy carriers during the routine school screening campaign imbedded in the public health care program of the Latium region (Central Italy). After screening of the children, all parents received a standard reassuring letter informing them about the presumed healthy carrier status of their children and were invited for a confirmation of the trait and for an additional explanation if needed. Results: We have analyzed 219 interviews (84.5%) from indigenous subjects and 40 from allochthonous people (15.5%) being either recent immigrants or mixed couples. The average age of the parents was 45.5 years. Only 51 (19.7%) had previous knowledge of their carrier status, while the rest were unaware. When reading the letter with the provisional diagnostic result of their child, emotions that could be considered undesirable were present in about 60% of the cases. Nevertheless, the information was experienced as welcome, clear, and useful by 100% of the participants. When asked about the option of prenatal diagnosis (PD) in case of genetic risk, 85.7% and 87.5% of the autochthonous and allochthonous interviewed declared either to be in favor or to eventually consider PD, while only 14.3% and 12.5% would not consider it for various reasons. Discussion: During our study, we registered undesirable feelings as well as welcome reactions: the first being experienced during the very first reading of the letter and the second after reflection on and understanding of the content during the visit to the center later on. Significantly, satisfaction and understanding of the advantage of knowledge was registered in 100% of the cases during our enquiry.
机译:目的:记录(假定)未意识到的健康血红蛋白病携带者的意见和感受,并接收有关其携带者状态的信息。方法:在中部地区(意大利中部)的公共卫生保健计划进行的常规学校筛查活动中,他们的孩子被临时诊断为血红蛋白病携带者后,我们从中学生的父母那里收集了259次访谈。在对孩子进行筛查之后,所有父母均收到一封标准的放心信件,告知他们有关孩子的假定健康携带者状况,并应邀确认该特征并在需要时进行进一步解释。结果:我们分析了来自土著居民的219次访谈(占84.5%)和来自新移民或异性恋夫妇的40次来自外来人口(占15.5%)的访谈。父母的平均年龄为45.5岁。以前只有51个(19.7%)知道他们的携带者身分,而其余人则不知道。当阅读带有孩子临时诊断结果的信时,大约60%的病例中出现了被认为是不良的情绪。但是,100%的参与者对这些信息感到欢迎,清晰和有用。当被问及有遗传风险时是否可以进行产前诊断(PD)时,接受采访的85.7%和87.5%的本地和异源宣布赞成或最终考虑使用PD,而只有14.3%和12.5%的人不考虑出于各种原因。讨论:在研究过程中,我们记录了不良的感受和可喜的反应:第一次读信时经历了第一次,第二次对中心的内容进行了反思和理解之后,第二次经历了。重要的是,在我们的查询过程中,有100%的案例记录了对知识优势的满意和理解。

著录项

  • 来源
    《Genetic testing and molecular biomarkers》 |2012年第7期|p.734-738|共5页
  • 作者单位

    Associazione Nazionale Microcitemie Italia (ANMI ONLUS), Centro Studi Microcitemie di Roma (CSMR), Rome, Italy;

    Associazione Nazionale Microcitemie Italia (ANMI ONLUS), Centro Studi Microcitemie di Roma (CSMR), Rome, Italy;

    Associazione Nazionale Microcitemie Italia (ANMI ONLUS), Centro Studi Microcitemie di Roma (CSMR), Rome, Italy;

    Associazione Nazionale Microcitemie Italia (ANMI ONLUS), Centro Studi Microcitemie di Roma (CSMR), Rome, Italy;

    Hemoglobinopathies Laboratory, Human and Clinical Genetics Department, Leiden University Medical Center, Leiden, The Netherlands;

    Hemoglobinopathies Laboratory Human and Clinical Genetics Department Leiden University Medical Center O&O Building, Einthovenweg 20 Leiden 2333 ZC, P.O. Box 9600 2300 RC Leiden The Netherlands;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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