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A focus group study of consumer attitudes toward genetic testing and newborn screening for deafness.

机译:焦点小组研究消费者对基因检测和新生儿耳聋筛查的态度。

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PURPOSE: Progress in identifying genes for deafness together with implementation of universal audiologic screening of newborns has provided the opportunity for more widespread use of molecular tests to detect genetic forms of hearing loss. Efforts to assess consumer attitudes toward these advances have lagged behind. METHODS: Consumer focus groups were held to explore attitudes toward genetic advances and technologies for hearing loss, views about newborn hearing screening, and reactions to the idea of adding molecular screening for hearing loss at birth. Focus group discussions were recorded, transcribed and analyzed. RESULTS: Five focus groups with 44 participants including hearing parents of deaf children, deaf parents and young deaf adults were held. Focus group participants supported the use of genetic tests to identify the etiology of hearing loss but were concerned that genetic information might influence reproductive decisions. Molecular newborn screening was advocated by some; however, others expressed concern about its effectiveness. CONCLUSION: Documenting the attitudes of parents and other consumers toward genetic technologies establishes the framework for discussions on the appropriateness of molecular newborn screening for hearing loss and informs specialists about potential areas of public education necessary prior to the implementation of such screening.
机译:目的:在鉴定聋人基因方面的进展以及对新生儿的通用听力检查的实施为分子检测更广泛地用于检测遗传性听力损失提供了机会。评估消费者对这些进步的态度的努力已经落后。方法:举行了消费者焦点小组会议,探讨对遗传进步和听力损失技术的态度,对新生儿听力筛查的看法以及对增加分子筛查出生时听力损失的想法的反应。记录,记录和分析了焦点小组的讨论。结果:举行了五个重点小组,有44名参与者参加,其中包括聋人父母,聋人父母和年轻聋人成年人的听力。焦点小组参加者支持使用基因检测来确定听力损失的病因,但担心遗传信息可能会影响生殖决策。一些人主张进行分子新生儿筛查。但是,其他人对此表示关注。结论:记录父母和其他消费者对基因技术的态度,为讨论分子新生儿筛查听力损失的适当性建立了框架,并在实施筛查之前向专家们介绍了潜在的公共教育领域。

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