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BJOG. 2022 Jan;129(1):e1-e15. doi: 10.1111/1471-0528.16821. Epub 2021 Oct 24.
2
Intertwin discordance in fetal size at 11-13 weeks' gestation and pregnancy outcome.11-13 孕周胎儿大小的相间不协调性与妊娠结局。
Ultrasound Obstet Gynecol. 2020 Feb;55(2):189-197. doi: 10.1002/uog.21923.
3
Maternal age and risk for adverse outcomes.母亲年龄与不良结局风险。
Am J Obstet Gynecol. 2018 Oct;219(4):390.e1-390.e15. doi: 10.1016/j.ajog.2018.08.034. Epub 2018 Aug 25.
4
Association between very advanced maternal age and adverse pregnancy outcomes: a cross sectional Japanese study.超高龄产妇与不良妊娠结局的相关性:一项日本的横断面研究。
BMC Pregnancy Childbirth. 2017 Oct 10;17(1):349. doi: 10.1186/s12884-017-1540-0.
5
Amniocentesis and chorionic villus sampling for prenatal diagnosis.用于产前诊断的羊膜穿刺术和绒毛取样。
Cochrane Database Syst Rev. 2017 Sep 4;9(9):CD003252. doi: 10.1002/14651858.CD003252.pub2.
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J Obstet Gynaecol Can. 2017 Sep;39(9):e347-e361. doi: 10.1016/j.jogc.2017.06.015.
7
First trimester ultrasound tests alone or in combination with first trimester serum tests for Down's syndrome screening.孕早期单独进行超声检查或与孕早期血清检查联合用于唐氏综合征筛查。
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韩国母胎医学会产前非整倍体筛查和诊断检测临床实践指南:(2)胎儿染色体异常的有创性诊断检测。

Clinical Practice Guidelines for Prenatal Aneuploidy Screening and Diagnostic Testing from Korean Society of Maternal-Fetal Medicine: (2) Invasive Diagnostic Testing for Fetal Chromosomal Abnormalities.

机构信息

Department of Obstetrics and Gynecology, CHA Bundang Medical Center, CHA University School of Medicine, Seongnam, Korea.

Department of Obstetrics and Gynecology, College of Medicine, The Catholic University of Korea, Seoul, Korea.

出版信息

J Korean Med Sci. 2021 Jan 25;36(4):e26. doi: 10.3346/jkms.2021.36.e26.

DOI:10.3346/jkms.2021.36.e26
PMID:33496085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7834898/
Abstract

The Korean Society of Maternal Fetal Medicine proposed the first Korean guideline on prenatal aneuploidy screening and diagnostic testing, in April 2019. The clinical practice guideline (CPG) was developed for Korean women using an adaptation process based on good-quality practice guidelines, previously developed in other countries, on prenatal screening and invasive diagnostic testing for fetal chromosome abnormalities. We reviewed current guidelines and developed a Korean CPG on invasive diagnostic testing for fetal chromosome abnormalities according to the adaptation process. Recommendations for selected 11 key questions are: 1) Considering the increased risk of fetal loss in invasive prenatal diagnostic testing for fetal genetic disorders, it is not recommended for all pregnant women aged over 35 years. 2) Because early amniocentesis performed before 14 weeks of pregnancy increases the risk of fetal loss and malformation, chorionic villus sampling (CVS) is recommended for pregnant women who will undergo invasive prenatal diagnostic testing for fetal genetic disorders in the first trimester of pregnancy. However, CVS before 9 weeks of pregnancy also increases the risk of fetal loss and deformity. Thus, CVS is recommended after 9 weeks of pregnancy. 3) Amniocentesis is recommended to distinguish true fetal mosaicism from confined placental mosaicism. 4) Anti-immunoglobulin should be administered within 72 hours after the invasive diagnostic testing. 5) Since there is a high risk of vertical transmission, an invasive prenatal diagnostic testing is recommended according to the clinician's discretion with consideration of the condition of the pregnant woman. 6) The use of antibiotics is not recommended before or after an invasive diagnostic testing. 7) The chromosomal microarray test as an alternative to the conventional cytogenetic test is not recommended for all pregnant women who will undergo an invasive diagnostic testing. 8) Amniocentesis before 14 weeks of gestation is not recommended because it increases the risk of fetal loss and malformation. 9) CVS before 9 weeks of gestation is not recommended because it increases the risk of fetal loss and malformation. 10) Although the risk of fetal loss associated with invasive prenatal diagnostic testing (amniocentesis and CVS) may vary based on the proficiency of the operator, the risk of fetal loss due to invasive prenatal diagnostic testing is higher in twin pregnancies than in singleton pregnancies. 11) When a monochorionic twin is identified in early pregnancy and the growth and structure of both fetuses are consistent, an invasive prenatal diagnostic testing can be performed on one fetus alone. However, an invasive prenatal diagnostic testing is recommended for each fetus in cases of pregnancy conceived via in vitro fertilization, or in cases in which the growth of both fetuses differs, or in those in which at least one fetus has a structural abnormality. The guidelines were established and approved by the Korean Academy of Medical Sciences. This guideline is revised and presented every 5 years.

摘要

韩国母胎医学会于 2019 年 4 月提出了首份产前非整倍体筛查和诊断检测的韩国指南。该临床实践指南(CPG)是基于在其他国家制定的、关于产前筛查和胎儿染色体异常的有创诊断检测的高质量实践指南,为韩国女性量身定制。我们复习了现有的指南,并根据适应过程制定了韩国胎儿染色体异常有创诊断检测的 CPG。针对 11 个关键问题提出了以下建议:1. 鉴于有创产前诊断检测胎儿遗传性疾病的胎儿丢失风险增加,不建议所有年龄超过 35 岁的孕妇进行。2. 因为在妊娠 14 周前进行早期羊膜腔穿刺术会增加胎儿丢失和畸形的风险,所以对于在妊娠早期将进行胎儿遗传性疾病有创诊断检测的孕妇,推荐进行绒毛膜绒毛取样(CVS)。然而,妊娠 9 周前进行 CVS 也会增加胎儿丢失和畸形的风险。因此,建议在妊娠 9 周后进行 CVS。3. 羊膜腔穿刺术有助于鉴别真正的胎儿嵌合体与局限的胎盘嵌合体。4. 应在有创诊断检测后 72 小时内给予抗免疫球蛋白。5. 鉴于垂直传播的风险较高,应根据孕妇的情况并由临床医生判断是否进行有创产前诊断检测。6. 不建议在有创诊断检测前或后使用抗生素。7. 不建议将染色体微阵列检测作为常规细胞遗传学检测的替代方法用于所有将进行有创诊断检测的孕妇。8. 不建议在妊娠 14 周前进行羊膜腔穿刺术,因为它会增加胎儿丢失和畸形的风险。9. 不建议在妊娠 9 周前进行 CVS,因为它会增加胎儿丢失和畸形的风险。10. 尽管与有创产前诊断检测(羊膜腔穿刺术和 CVS)相关的胎儿丢失风险可能因操作者的熟练程度而异,但在双胎妊娠中,与单胎妊娠相比,有创产前诊断检测导致的胎儿丢失风险更高。11. 当在早期妊娠中发现单绒毛膜双胎且两个胎儿的生长和结构一致时,可以单独对一个胎儿进行有创产前诊断检测。然而,如果是通过体外受精受孕的妊娠,或者两个胎儿的生长存在差异,或者至少一个胎儿存在结构异常,则建议对每个胎儿进行有创产前诊断检测。该指南由韩国医学科学院制定和批准。本指南每 5 年修订和发布一次。