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囊性纤维化患者及其家庭成员对人群囊性纤维化产前和孕前携带者筛查的看法。

Perceptions of population cystic fibrosis prenatal and preconception carrier screening among individuals with cystic fibrosis and their family members.

作者信息

Maxwell Susannah J, Kyne Gaenor, Molster Caron, Barker Nigel M, Ormsby Jacqueline, O'Leary Peter

机构信息

Office of Population Health Genomics, Department of Health, Perth, Western Australia, Australia.

出版信息

Genet Test Mol Biomarkers. 2011 Mar;15(3):159-64. doi: 10.1089/gtmb.2010.0121. Epub 2011 Jan 4.

Abstract

AIM

Our study aimed to quantitatively explore the perceptions of individuals with cystic fibrosis (CF) and their family members toward population prenatal and preconception CF carrier screening, including perceived benefits, concerns, and the acceptability of offering screening.

METHOD

In November 2009, 258 members of the Cystic Fibrosis Association of Western Australia were invited via an e-mail newsletter to participate in a survey, with a link to an online survey tool. A further 246 members without e-mail access were mailed a paper copy of the survey.

RESULTS

Overall, we found the majority of individuals with CF (n=27) and their families (n=122) had positive views of population CF carrier screening. However, the small number of individuals with CF represented in the study limits the interpretation of these data.

CONCLUSION

From a public policy perspective, our findings overall suggest that in principle the views of family members are not a barrier to the introduction of population CF carrier screening. The views of individuals with CF warrant further investigation. Data such as ours should be used with other sources of information, such as economic evaluations and the perceptions of the general public, geneticists, and other medical practitioners to inform decisions regarding screening within the public health system.

摘要

目的

我们的研究旨在定量探究囊性纤维化(CF)患者及其家庭成员对人群产前和孕前CF携带者筛查的看法,包括感知到的益处、担忧以及对提供筛查的可接受性。

方法

2009年11月,通过电子邮件通讯邀请西澳大利亚囊性纤维化协会的258名成员参与一项调查,并提供在线调查工具的链接。另外,给246名没有电子邮件的成员邮寄了纸质调查问卷。

结果

总体而言,我们发现大多数CF患者(n = 27)及其家人(n = 122)对人群CF携带者筛查持积极看法。然而,参与研究的CF患者数量较少,限制了对这些数据的解读。

结论

从公共政策角度来看,我们的研究结果总体表明,原则上家庭成员的看法并非推行人群CF携带者筛查的障碍。CF患者的看法值得进一步研究。像我们这样的数据应与其他信息来源一起使用,如经济评估以及公众、遗传学家和其他医学从业者的看法,以便为公共卫生系统内的筛查决策提供参考。

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