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Guidelines for Cystic Fibrosis Carrier Screening in the Prenatal/Preconception Period

机译:产前/孕前囊性纤维化携带者筛查指南

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摘要

Cystic fibrosis (CF) is one of the most common autosomal recessive disorders. Carrier screening for CF should be offered to all women considering becoming pregnant or who are pregnant. Understanding the available screening tests, their limitations, and the benefits of screening is of paramount importance to the obstetrician-gynecologist. The objective is to review the current guidelines for CF carrier screening including the options for carrier screening, the potential complexities associated with carrier screening for CF, and indications for referral to certified genetic counselors or maternal-fetal medicine specialists. A MEDLINE search of “cystic fibrosis,” “cystic fibrosis carrier screening pregnancy,” and “inheritance of cystic fibrosis” in the review was performed. The evidence cited in this review includes 2 medical society committee opinions and 15 additional peer-reviewed journal articles that were original research or expert opinion summaries. The American College of Obstetricians and Gynecologists recommends that obstetricians offer CF carrier screening to all pregnant women or women considering becoming pregnant. Based on recent guidelines from ACMG, additional expanded carrier screening can be recommended to patients in the future, with additional CF variants and other autosomal or X-linked recessive conditions. It is important for the prenatal care provider to understand the guidelines for carrier screening as well as the potential complexities associated with carrier screening due to the multiple pathogenic variants in the CFTR gene that may be associated with varying phenotypes. With the options for CF carrier screening, screening performance in different populations, a basic understanding of the disease and interpretation of carrier screening results is of paramount importance to the prenatal care provider. Obstetrician-gynecologist, family medicine, or other practitioner(s) providing prenatal care After participating in this activity, physicians should be better able to define indications and the current guidelines for carrier testing for CF; compare types of CF carrier screening and describe potential results of the screening; propose patient counseling strategies regarding residual risk after negative CF carrier screening; and explain appropriate referral measures for patients with positive CF carrier screening results.
机译:囊性纤维化(CF)是最常见的常染色体隐性遗传病之一。应向所有考虑怀孕或怀孕的女性提供囊性纤维化携带者筛查。了解可用的筛查测试、它们的局限性以及筛查的好处对妇产科医生来说至关重要。目的是回顾当前的CF携带者筛查指南,包括携带者筛查的选择、与CF携带者筛查相关的潜在复杂性,以及转诊至认证遗传咨询师或母胎医学专家的适应症。在MEDLINE上检索了本综述中的“囊性纤维化”、“囊性纤维化携带者筛查妊娠”和“囊性纤维化的遗传”。本综述中引用的证据包括 2 篇医学会委员会意见和 15 篇额外的同行评审期刊文章,这些文章是原创研究或专家意见摘要。美国妇产科医师学会建议产科医生为所有孕妇或考虑怀孕的妇女提供囊性纤维化携带者筛查。根据 ACMG 最近的指南,未来可以建议患者进行额外的扩展携带者筛查,包括额外的 CF 变异和其他常染色体或 X 连锁隐性遗传病。对于产前保健提供者来说,了解携带者筛查指南以及与携带者筛查相关的潜在复杂性非常重要,因为 CFTR 基因中的多种致病变异可能与不同的表型有关。有了囊性纤维化携带者筛查的选择,不同人群的筛查表现,对疾病的基本了解和对携带者筛查结果的解释对产前保健提供者来说至关重要。妇产科医生、家庭医学医生或其他提供产前护理的从业者 参加这项活动后,医生应该能够更好地定义 CF 携带者检测的适应症和当前指南;比较CF携带者筛查的类型并描述筛查的潜在结果;提出有关CF携带者筛查阴性后残余风险的患者咨询策略;并解释CF携带者筛查结果呈阳性的患者的适当转诊措施。

著录项

  • 来源
    《Obstetrical and gynecological survey》 |2022年第10期|606-610|共5页
  • 作者单位

    Assistant Clinical Professor, Division of Maternal-Fetal Medicine, Women's Health Institute;

    Professor, Divisions of Reproductive Genetics and Maternal Fetal Medicine, Department of Obstetrics;

    Professor, Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Duke;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 英语
  • 中图分类 妇产科学;
  • 关键词

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