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让消费者参与囊性纤维化携带者筛查教育项目的开发。

Involving consumers in the development of an educational program for cystic fibrosis carrier screening.

作者信息

Myers M F, Bernhardt B A, Tambor E S, Holtzman N A

机构信息

University of Cincinnati.

出版信息

Am J Hum Genet. 1994 Apr;54(4):719-26.

Abstract

Input from consumers of health care was sought in developing an educational program to be provided to individuals who are considering carrier testing for cystic fibrosis (CF). In addition, we assessed the ability of health professionals to predict consumers' priorities with regard to such information. A focus group of six middle school teachers formulated questions that they would ask in trying to decide whether they wanted carrier screening for CF. Then, other adults with (n = 39) and without (n = 60) a family history of CF were presented with the questions and were asked to select the questions in the order in which they would want them answered if offered the carrier test. After each question was answered, they were asked whether they would want the carrier test if it were offered to them. CF clinic staff, clinical geneticists, and genetic counselors (n = 31) were asked to select the questions in the order in which they believed that an adult from the general population would want them answered. There were no differences in the order in which adults with and without a family history of CF would want questions answered. Consumers would want to learn about the carrier test as well as their risk of being a carrier and of having a child with CF, before receiving information on reproductive options and the effect that a child with CF would have on the family. Of the 44% of consumers who changed their mind about wanting screening during the course of selecting questions, 52% did so after the first question that they selected.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在制定一项将提供给考虑进行囊性纤维化(CF)携带者检测的个人的教育计划时,征求了医疗保健消费者的意见。此外,我们评估了医疗专业人员预测消费者对这类信息优先考虑事项的能力。一个由六名中学教师组成的焦点小组拟定了他们在试图决定是否想要进行CF携带者筛查时会提出的问题。然后,向其他有CF家族史(n = 39)和没有CF家族史(n = 60)的成年人展示这些问题,并要求他们按照如果提供携带者检测他们希望得到解答的顺序选择问题。在每个问题得到回答后,询问他们如果提供携带者检测是否愿意接受检测。要求CF诊所工作人员、临床遗传学家和遗传咨询师(n = 31)按照他们认为普通人群中的成年人希望得到解答的顺序选择问题。有CF家族史和没有CF家族史的成年人希望得到问题解答的顺序没有差异。在获得关于生殖选择以及患有CF的孩子对家庭的影响的信息之前,消费者希望了解携带者检测以及他们成为携带者和生育患有CF孩子的风险。在选择问题过程中改变了对筛查意愿的44%的消费者中,52%是在他们选择的第一个问题之后改变想法的。(摘要截短于250字)

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