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针对高危亲属群体,家庭和诊所式的检测前教育及囊性纤维化携带者检测所带来的心理社会和教育方面的结果。

Psychosocial and educational outcomes associated with home- and clinic-based pretest education and cystic fibrosis carrier testing among a population of at-risk relatives.

作者信息

Cheuvront B, Sorensen J R, Callanan N P, Stearns S C, DeVellis B M

机构信息

Department of Health Behavior and Health Education, School of Public Health, University of North Carolina, Chapel Hill 27599-7505, USA.

出版信息

Am J Med Genet. 1998 Feb 17;75(5):461-8.

PMID:9489788
Abstract

We report on the psychosocial and knowledge outcomes of two different approaches to cystic fibrosis (CF) gene pretest education and carrier testing offered to 288 proactively recruited first-, second-, and third-degree relatives of people with CF. One group received pretest education and gene testing in a clinical setting from a certified genetic counselor. The other group received pretest education in their homes from a specially prepared pamphlet and were asked to send in a buccal cell sample for genotyping. No statistically significant differences between groups were noted on measures of CF knowledge, anxiety, and positive or negative affect, either while waiting for their test results or within a few weeks after they had learned their results. At both measurement points, participants who had received home education and testing reported that the testing was more convenient, but that they had received less information than they would have liked, and they were more likely to report being confused by the testing, although their level of CF knowledge was comparable to that of people who had been seen by a genetic counselor. In light of the increasing interest in home-based medical testing of all kinds, this study suggests that CF carrier testing in the home warrants further consideration as one possible approach to facilitating access to testing.

摘要

我们报告了为288名主动招募的囊性纤维化(CF)患者的一级、二级和三级亲属提供的两种不同的CF基因检测前教育和携带者检测方法的心理社会和知识成果。一组在临床环境中由认证的遗传咨询师进行检测前教育和基因检测。另一组在家中通过一份特别编写的小册子接受检测前教育,并被要求寄送一份颊细胞样本进行基因分型。在等待检测结果期间或得知结果后的几周内,两组在CF知识、焦虑以及积极或消极情绪的测量上均未发现统计学上的显著差异。在两个测量点,接受家庭教育和检测的参与者报告称检测更方便,但他们获得的信息比期望的要少,并且他们更有可能报告对检测感到困惑,尽管他们的CF知识水平与接受遗传咨询师咨询的人相当。鉴于人们对各类家庭医疗检测的兴趣日益浓厚,本研究表明,家庭CF携带者检测作为一种促进检测可及性的可能方法值得进一步考虑。

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