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“我可以信任它”:相互易位携带者及其伴侣进行产前无细胞DNA筛查以检测不平衡易位的经历。

'I Could Trust It': Experiences of Reciprocal Translocation Carriers and Their Partners With Prenatal Cell-Free DNA Screening for Unbalanced Translocations.

作者信息

Cifuentes Ochoa Marta, Archibald Alison Dalton, Flowers Nicola Jane, Pertile Mark Domenic

机构信息

Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Parkville, Australia.

Department of Paediatrics, University of Melbourne, Parkville, Australia.

出版信息

Prenat Diagn. 2025 Feb;45(2):155-162. doi: 10.1002/pd.6696. Epub 2024 Nov 6.

Abstract

OBJECTIVE

To explore the experiences of people having cfDNA screening to detect unbalanced translocations, and to understand motivations for choosing this option.

METHODS

We used a qualitative approach with in-depth semi-structured interviews with reciprocal translocation carriers and their partners. People who underwent cfDNA screening with translocation analysis through Victorian Clinical Genetics Services between 2015 and 2019 were invited to take part. Purposive sampling based on the participant's geographic location, requesting practitioner specialty and cfDNA screening result was used to capture a range of experiences. Interview transcripts were analysed using thematic analysis.

RESULTS

Participants (n = 13) had complex reproductive journeys associated with the translocation and opted for cfDNA screening rather than prenatal diagnosis to avoid risk to their pregnancy. Participants benefited from having a result early in pregnancy and had sufficient confidence in the result to decline a diagnostic testing procedure.

CONCLUSION

Participants' experiences with cfDNA screening were intertwined with the experience of being a carrier of a reciprocal translocation. cfDNA screening with translocation analysis was perceived as an acceptable alternative to prenatal diagnosis and should be made more accessible to balanced translocation carriers. Access to specialist genetic counselling services is needed to ensure couples are provided with information about all prenatal testing options, including the benefits and limitations associated with cfDNA screening with translocation analysis.

摘要

目的

探讨进行循环游离DNA(cfDNA)筛查以检测不平衡易位的人群的经历,并了解他们选择这一检测方式的动机。

方法

我们采用定性研究方法,对相互易位携带者及其伴侣进行深入的半结构化访谈。邀请了2015年至2019年间通过维多利亚临床遗传学服务机构进行cfDNA筛查及易位分析的人群参与。基于参与者的地理位置、主诊医生专业以及cfDNA筛查结果进行目的抽样,以获取一系列不同的经历。使用主题分析法对访谈记录进行分析。

结果

参与者(n = 13)经历了与易位相关的复杂生育历程,选择cfDNA筛查而非产前诊断以避免对妊娠造成风险。参与者受益于在妊娠早期获得结果,并且对结果有足够信心从而拒绝诊断性检测程序。

结论

参与者进行cfDNA筛查的经历与作为相互易位携带者的经历相互交织。cfDNA筛查及易位分析被视为产前诊断的一种可接受替代方法,应让平衡易位携带者更容易获得。需要提供专业的遗传咨询服务,以确保为夫妇提供有关所有产前检测选项的信息,包括cfDNA筛查及易位分析的益处和局限性。

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