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Why Do People Choose Not to Have Screening for Hemochromatosis?

机译:人们为什么选择不筛查血色素沉着病?

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摘要

Aim: Hemochromatosis is a common disorder of iron overload most commonly due to homozogosity for the HFE C282Y substitution. A workplace-screening program was conducted in which over 11,000 individuals were screened for this mutation. A substudy of this project was to ascertain why people chose not to attend information and screening sessions offered in their workplace. Method: Staff were recruited by email, questionnaires in common areas, and direct approach. A purpose-designed questionnaire sought the reasons for not attending information and screening sessions. Results: The nonattender questionnaire was distributed at 24 workplaces and completed by 872 individuals. The most common reason for not attending sessions, accounting for 70.1%, was practical (e.g., unaware of session, too busy, or unavailable). Other relatively common reasons were that the individual had low iron levels or were a blood donor (14.9%), or that hemochromatosis was considered unimportant (12.2%). Insurance concerns were very rarely cited as the reason for nonattendance (1.0%). Conclusion: The nonattender data presented here indicate that concerns about insurance, anxiety, and use of genetic information are not major factors for why people did not attend workplace information and screening sessions for hereditary hemochromatosis. Practical barriers were the major reasons identified. This highlights that when implementing screening programs, as many practical barriers as possible need to be overcome, so that a maximum number of people who would like to be informed about screening are given the opportunity to do so.
机译:目的:血色素沉着病是铁超负荷的常见疾病,最常见的原因是HFE C282Y替代的同源性。进行了一项工作场所筛选计划,其中筛选了超过11,000个人的这种突变。该项目的子研究是确定为什么人们选择不参加其工作场所提供的信息和筛选会议。方法:通过电子邮件,公共区域问卷和直接方法招募员工。专门设计的问卷调查了不参加信息和筛选会议的原因。结果:无人参与调查问卷在24个工作场所分发,由872个人完成。不参加会议的最常见原因是实用的(例如,不知道会议,太忙或不可用),占70.1%。其他相对常见的原因是,个体铁水平低或是献血者(14.9%),或血色素沉着病被认为不重要(12.2%)。很少有人将保险问题作为缺勤的原因(1.0%)。结论:此处提供的非参与人数据表明,对于保险,焦虑和遗传信息的使用并不是人们不参加工作场所信息和遗传性血色素沉着病筛查的主要原因。实际障碍是确定的主要原因。这突出表明,在实施筛查计划时,需要克服尽可能多的实际障碍,以便使有大量希望了解筛查信息的人有机会这样做。

著录项

  • 来源
    《Genetic testing and molecular biomarkers》 |2013年第1期|21-24|共4页
  • 作者单位

    Murdoch Childrens Research Institute, Parkville, Australia;

    Murdoch Childrens Research Institute, Parkville, Australia,Cold Spring Harbor Laboratory, DNA Learning Center, Cold Spring Harbor, New York;

    Murdoch Childrens Research Institute, Parkville, Australia,Department of Pediatrics, The University of Melbourne, Parkville, Australia;

    Murdoch Childrens Research Institute, Parkville, Australia,Department of Pediatrics, The University of Melbourne, Parkville, Australia;

    Murdoch Childrens Research Institute, Parkville, Australia;

    Murdoch Childrens Research Institute, Parkville, Australia,Department of Pediatrics, The University of Melbourne, Parkville, Australia,Royal Children's Hospital, Parkville, Australia;

    Murdoch Childrens Research Institute Flemington Road Parkville Victoria 3052 Australia;

  • 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
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