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一项关于消费者对耳聋基因检测和新生儿筛查态度的焦点小组研究。

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

作者信息

Burton Sarah K, Withrow Kara, Arnos Kathleen S, Kalfoglou Andrea L, Pandya Arti

机构信息

Genetics Program, Department of Biology, Gallaudet University, Washington, DC, USA.

出版信息

Genet Med. 2006 Dec;8(12):779-83. doi: 10.1097/01.gim.0000250501.59830.ff.

Abstract

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.

摘要

目的

在确定致聋基因方面取得的进展,以及新生儿普遍听力筛查的实施,为更广泛地使用分子检测来检测遗传性听力损失提供了机会。评估消费者对这些进展态度的工作却滞后了。

方法

开展了消费者焦点小组讨论,以探讨对听力损失的基因进展和技术的态度、对新生儿听力筛查的看法,以及对在出生时增加听力损失分子筛查这一想法的反应。焦点小组讨论进行了录音、转录和分析。

结果

举办了五个焦点小组讨论,共有44名参与者,包括失聪儿童的听力正常父母、失聪父母和年轻失聪成年人。焦点小组参与者支持使用基因检测来确定听力损失的病因,但担心基因信息可能会影响生育决定。一些人主张进行新生儿分子筛查;然而,其他人对其有效性表示担忧。

结论

记录父母和其他消费者对基因技术的态度,为讨论新生儿听力损失分子筛查的适宜性建立了框架,并让专家了解在实施此类筛查之前有必要进行公众教育的潜在领域。

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