IF 2.7 2区 医学 Q2 GENETICS & HEREDITY Prenatal Diagnosis Pub Date : 2025-01-24 DOI:10.1002/pd.6751
Stina Lou, Anna Ryberg, Naja Becher, Ida Charlotte Bay Lund, Ida Vogel
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引用次数: 0

摘要

目的产前在绒毛膜采样(CVS)结果中发现 16 三体嵌合体(MosT16)可能会导致胎儿畸形和胎儿生长受限(FGR)的风险,这可能会让准父母非常焦虑。本研究旨在调查怀孕期间收到 MosT16 结果的妇女的经历和决策:对收到 MosT16 CVS 结果的八名丹麦妇女进行了深入的半结构式访谈。采用反思性主题分析法对访谈进行分析:结果:四名妇女在得到 MosT16 CVS 结果后终止了妊娠,她们强调了等待羊水穿刺的精神负担以及对胎儿受累和 FGR 风险的担忧。四名妇女选择等待羊膜腔穿刺,其中一人因胎儿受累而终止妊娠,三人继续妊娠(一名结果正常,两名胎儿受累比例较低)。在怀孕期间,所有三个胎儿的胎龄都较小,对其成长的担忧给准父母带来了负担。两名妇女早产,但三人均称自己的婴儿健康:结论:产前 MosT16 CVS 结果是一个关键的决策点,需要同时考虑胎儿受累和 FGR 风险。因此,遗传咨询应与产科/胎儿医学专家的咨询相结合。
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Making Sense of a Prenatal Detection of Trisomy 16 Mosaicism in the Placenta: A Qualitative Study of Pregnant Women's Decision Making.

Objective: Prenatal detection of Trisomy 16 mosaicism (MosT16) in a Chorionic Villus Sample (CVS) results may cause significant anxiety for expectant parents due to the risk of fetal malformation and fetal growth restriction (FGR). The aim of this study was to investigate the experiences and decision-making of women receiving a MosT16 results during pregnancy.

Methods: In-depth, semi-structured interviews with eight Danish women who received a MosT16 CVS results. Interviews were analyzed using reflexive thematic analysis.

Results: Four women terminated pregnancy following the MosT16 CVS result, emphasizing the emotional burden of waiting for amniocentesis and concerns about fetal involvement and FGR risk. Four women opted to await amniocentesis following which one terminated pregnancy due to fetal involvement, while three continued their pregnancies (one normal result, two low-percentage fetal involvement results). During pregnancy, all three fetuses were small for gestational age, and the concerns about their growth were burdensome for expectant parents. Two women delivered prematurely, but all three described their babies as healthy.

Conclusion: The prenatal MosT16 CVS result represents a critical decision point, requiring consideration of both fetal involvement and FGR risk. Thus, genetic counseling should be combined with counseling from obstetrics/fetal medicine specialists.

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来源期刊
Prenatal Diagnosis
Prenatal Diagnosis 医学-妇产科学
CiteScore
5.80
自引率
13.30%
发文量
204
审稿时长
2 months
期刊介绍: Prenatal Diagnosis welcomes submissions in all aspects of prenatal diagnosis with a particular focus on areas in which molecular biology and genetics interface with prenatal care and therapy, encompassing: all aspects of fetal imaging, including sonography and magnetic resonance imaging; prenatal cytogenetics, including molecular studies and array CGH; prenatal screening studies; fetal cells and cell-free nucleic acids in maternal blood and other fluids; preimplantation genetic diagnosis (PGD); prenatal diagnosis of single gene disorders, including metabolic disorders; fetal therapy; fetal and placental development and pathology; development and evaluation of laboratory services for prenatal diagnosis; psychosocial, legal, ethical and economic aspects of prenatal diagnosis; prenatal genetic counseling
期刊最新文献
Chromosomal Aberrations in Fetuses With Isolated Persistent Right Umbilical Vein-A Nationwide Study. Advances in Prenatal Cell-Free DNA Screening for Dominant Monogenic Conditions: A Review of Current Progress and Future Directions in Clinical Implementation. Making Sense of a Prenatal Detection of Trisomy 16 Mosaicism in the Placenta: A Qualitative Study of Pregnant Women's Decision Making. Outcomes of Intrauterine Interventions in Twin Reversed Arterial Perfusion (TRAP) Sequence: A Systematic Review of the Literature Over the Past 35 Years. Prenatal Diagnosis of Caroli's Disease by Ultrasound and MRI Imaging.
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