• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

术前和术后咨询需要哪些内容?

What are the required components of pre- and post-test counseling?

机构信息

Mount Carmel Health Systems, 6001 East Broad Street Columbus, Ohio 43213, United States; Division of Maternal-Fetal Medicine, Duke University Medical Center, United States.

Mount Carmel Health Systems, 6001 East Broad Street Columbus, Ohio 43213, United States; Division of Maternal-Fetal Medicine, Duke University Medical Center, United States.

出版信息

Semin Perinatol. 2018 Aug;42(5):287-289. doi: 10.1053/j.semperi.2018.07.005. Epub 2018 Jul 26.

DOI:10.1053/j.semperi.2018.07.005
PMID:30107889
Abstract

Prenatal care providers are faced with a myriad of decisions about how to offer genetic screening and testing in ways that are appropriate to their patient population and their workflow. Among the critical issues brought to the forefront of rapidly advancing genetic and genomic technologies is the importance of pre- and post-test counseling. This document is a synthesis of proceedings of a workshop sponsored by the American College of Obstetricians and Gynecologists, the American College of Medical Genetics and Genomics, and the Society for Maternal-Fetal Medicine, on January 24-25, 2017, during which invited experts discussed required components of pre- and post-test counseling and associated concerns in the provision of prenatal care.

摘要

产前护理提供者面临着如何以适合患者人群和工作流程的方式提供遗传筛查和检测的众多决策。在快速发展的遗传和基因组技术将一系列关键问题推到前沿的过程中,产前和产后咨询的重要性尤为突出。本文件是美国妇产科医师学院、美国医学遗传学与基因组学学院和母胎医学学会于 2017 年 1 月 24 日至 25 日联合举办的一次研讨会的会议记录,会上邀请的专家讨论了产前护理中提供产前和产后咨询以及相关问题所需的组成部分。

相似文献

1
What are the required components of pre- and post-test counseling?术前和术后咨询需要哪些内容?
Semin Perinatol. 2018 Aug;42(5):287-289. doi: 10.1053/j.semperi.2018.07.005. Epub 2018 Jul 26.
2
Prenatal genetic carrier screening in the genomic age.基因组时代的产前遗传携带者筛查。
Semin Perinatol. 2018 Aug;42(5):303-306. doi: 10.1053/j.semperi.2018.07.019. Epub 2018 Jul 26.
3
Joint SOGC-CCMG Opinion for Reproductive Genetic Carrier Screening: An Update for All Canadian Providers of Maternity and Reproductive Healthcare in the Era of Direct-to-Consumer Testing.加拿大妇产科医师学会(SOGC)和加拿大医学遗传学会(CCMG)关于生殖遗传携带者筛查的联合意见:面向直接面向消费者检测时代所有加拿大孕产妇和生殖健康护理提供者的最新信息。
J Obstet Gynaecol Can. 2016 Aug;38(8):742-762.e3. doi: 10.1016/j.jogc.2016.06.008.
4
Implementing Group Prenatal Counseling for Expanded Noninvasive Screening Options.实施针对扩展的非侵入性筛查选项的团体产前咨询。
J Genet Couns. 2018 Aug;27(4):894-901. doi: 10.1007/s10897-017-0178-4. Epub 2017 Dec 15.
5
Introducing new and emerging genetic tests into prenatal care.将新的和新兴的基因检测引入产前保健。
Semin Perinatol. 2018 Aug;42(5):283-286. doi: 10.1053/j.semperi.2018.07.004. Epub 2018 Jul 26.
6
Optimizing use of existing prenatal genetic tests: Screening and diagnostic testing for aneuploidy.优化现有产前遗传检测的应用:非整倍体的筛查和诊断检测。
Semin Perinatol. 2018 Aug;42(5):296-302. doi: 10.1053/j.semperi.2018.07.014. Epub 2018 Jul 26.
7
Screening for Fetal Chromosomal Abnormalities: ACOG Practice Bulletin Summary, Number 226.胎儿染色体异常筛查:ACOG 实践公告摘要,第 226 号。
Obstet Gynecol. 2020 Oct;136(4):859-867. doi: 10.1097/AOG.0000000000004107.
8
Expanded Carrier Screening.扩展型携带者筛查。
Obstet Gynecol Clin North Am. 2018 Mar;45(1):103-112. doi: 10.1016/j.ogc.2017.10.005.
9
Screening for Fetal Chromosomal Abnormalities: ACOG Practice Bulletin, Number 226.筛查胎儿染色体异常:ACOG 实践公告,第 226 号。
Obstet Gynecol. 2020 Oct;136(4):e48-e69. doi: 10.1097/AOG.0000000000004084.
10
Pre- and post-test genetic counseling for chromosomal and Mendelian disorders.针对染色体疾病和孟德尔遗传病的检测前和检测后遗传咨询。
Semin Perinatol. 2016 Feb;40(1):44-55. doi: 10.1053/j.semperi.2015.11.007. Epub 2015 Dec 21.

引用本文的文献

1
Is intermediate risk really intermediate? Comparison of karyotype and non-invasive prenatal testing results of pregnancies at intermediate risk of trisomy 21 on maternal serum screening.中度风险真的是中度吗?对孕中期血清筛查中21三体中度风险妊娠的核型与无创产前检测结果的比较。
J Genet Couns. 2025 Apr;34(2):e1973. doi: 10.1002/jgc4.1973. Epub 2024 Oct 4.
2
Validation of the "Perceptions Regarding pRE-Symptomatic Alzheimer's Disease Screening" (PRE-ADS) Questionnaire in the German Population: Attitudes, Motivations, and Barriers to Pre-Symptomatic Dementia Screening.验证“关于预症状期阿尔茨海默病筛查的认知”(PRE-ADS)问卷在德国人群中的适用性:对预症状期痴呆筛查的态度、动机和障碍。
J Alzheimers Dis. 2024;97(1):309-325. doi: 10.3233/JAD-230961.
3
Attitudes toward pre-symptomatic screening for Alzheimer's dementia in five European countries: a comparison of family members of people with Alzheimer's dementia non-family members.五个欧洲国家对阿尔茨海默病痴呆症症状前筛查的态度:阿尔茨海默病痴呆症患者家庭成员与非家庭成员的比较
Front Genet. 2023 Dec 15;14:1305107. doi: 10.3389/fgene.2023.1305107. eCollection 2023.
4
Predictors of genetic beliefs toward cancer risk perceptions among adults in the United States: Implications for prevention or early detection.美国成年人对癌症风险认知的遗传信念预测因素:对预防或早期检测的启示。
J Genet Couns. 2020 Aug;29(4):494-504. doi: 10.1002/jgc4.1228. Epub 2020 Feb 27.