• 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

Supporting Women's Autonomy in Prenatal Testing.

作者信息

Johnston Josephine, Farrell Ruth M, Parens Erik

机构信息

From the Hastings Center, Garrison, NY (J.J., E.P.); and the Ob/Gyn and Women's Health Institute and Department of Bioethics, Cleveland Clinic, Cleveland (R.M.F.).

出版信息

N Engl J Med. 2017 Aug 10;377(6):505-507. doi: 10.1056/NEJMp1703425.

DOI:10.1056/NEJMp1703425
PMID:28792882
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5688876/
Abstract
摘要

相似文献

1
Supporting Women's Autonomy in Prenatal Testing.在产前检查中支持女性自主权。
N Engl J Med. 2017 Aug 10;377(6):505-507. doi: 10.1056/NEJMp1703425.
2
Prenatal testing: Does reproductive autonomy succeed in dispelling eugenic concerns?产前检测：生殖自主权能否成功消除优生学担忧？
Bioethics. 2019 Oct;33(8):958-964. doi: 10.1111/bioe.12602. Epub 2019 Jul 2.
3
Supporting Patient Autonomy and Informed Decision-Making in Prenatal Genetic Testing.支持产前基因检测中的患者自主性和知情决策。
Cold Spring Harb Perspect Med. 2020 Jun 1;10(6):a036509. doi: 10.1101/cshperspect.a036509.
4
Should non-invasiveness change informed consent procedures for prenatal diagnosis?非侵入性检测是否应该改变产前诊断的知情同意程序？
Health Care Anal. 2011 Jun;19(2):122-32. doi: 10.1007/s10728-010-0146-8.
5
Legislating to preserve women's autonomy during pregnancy.立法保障女性孕期自主权。
Med Law. 1995;14(5-6):397-412.
6
Prenatal genetic testing kits sold at your local pharmacy: promoting autonomy or promoting confusion?在当地药店售卖的产前基因检测试剂盒：是促进了自主性还是加剧了困惑？
Bioethics. 2006 Sep;20(5):254-63. doi: 10.1111/j.1467-8519.2006.00502.x.
7
A Framework for Unrestricted Prenatal Whole-Genome Sequencing: Respecting and Enhancing the Autonomy of Prospective Parents.无限制产前全基因组测序框架：尊重和增强准父母的自主权。
Am J Bioeth. 2017 Jan;17(1):3-18. doi: 10.1080/15265161.2016.1251632.
8
Choices and rights: eugenics, genetics and disability equality.选择与权利：优生学、遗传学与残疾平等
Disabil Soc. 1998 Nov;13(5):665-81. doi: 10.1080/09687599826452.
9
Decision-making for non-invasive prenatal testing for Down syndrome: Hong Kong Chinese women's preferences for individual vs relational autonomy.唐氏综合征无创产前检测的决策：中国香港女性对个体自主与关系自主的偏好
Clin Genet. 2016 May;89(5):550-6. doi: 10.1111/cge.12743. Epub 2016 Mar 4.
10
Routine antenatal HIV testing and informed consent: an unworkable marriage?常规产前HIV检测与知情同意：一段无法维系的婚姻？
J Med Ethics. 2007 Aug;33(8):446-8. doi: 10.1136/jme.2006.018861.

引用本文的文献

1
Time for a New Norm: Experiences of 'Being Informed' and 'Having Choice' for Prenatal Screening for Chromosomal Conditions: A Qualitative Study.迎接新常态：染色体疾病产前筛查中“获得信息”与“拥有选择权”的体验：一项定性研究
Health Expect. 2025 Jun;28(3):e70292. doi: 10.1111/hex.70292.
2
The Current State and Challenges of Clinical Ethics Consultation for Prenatal Diagnosis: A Qualitative Study of Committee Employee Perspectives in China.产前诊断临床伦理咨询的现状与挑战：中国委员会工作人员视角的质性研究
Asian Bioeth Rev. 2024 Sep 5;17(1):73-90. doi: 10.1007/s41649-024-00303-7. eCollection 2025 Jan.
3
External Quality Assessment of Maternal Serum Levels of Alpha-Fetoprotein, Free Beta-Human Chorionic Gonadotropin, and Unconjugated Estriol in Detecting Down Syndrome and Neural Tube Defects in the Second Trimester of 87 Maternal Serum Samples, Based on 105-139 Days.基于 105-139 天的 87 例母血清样本，对甲胎蛋白、游离β-人绒毛膜促性腺激素和未结合雌三醇进行检测，以评估其在检测唐氏综合征和神经管缺陷中的外部质量。
Med Sci Monit. 2022 Apr 13;28:e935573. doi: 10.12659/MSM.935573.
4
Implementing Expanded Prenatal Genetic Testing: Should Parents Have Access to Any and All Fetal Genetic Information?实施扩展型产前基因检测：父母是否应该获取所有胎儿基因信息？
Am J Bioeth. 2022 Feb;22(2):4-22. doi: 10.1080/15265161.2020.1867933. Epub 2021 Jan 18.
5
Prenatal Genetic Screening and Potential Complicity in Abortion: Considerations for Catholic Health Care.产前基因筛查与堕胎中的潜在同谋关系：天主教医疗保健的考量
Linacre Q. 2020 May;87(2):206-217. doi: 10.1177/0024363919886515. Epub 2019 Nov 7.
6
Supporting Patient Autonomy and Informed Decision-Making in Prenatal Genetic Testing.支持产前基因检测中的患者自主性和知情决策。
Cold Spring Harb Perspect Med. 2020 Jun 1;10(6):a036509. doi: 10.1101/cshperspect.a036509.
7
Genetic Counseling and Genome Sequencing in Pediatric Rare Disease.儿科罕见病的遗传咨询和基因组测序。
Cold Spring Harb Perspect Med. 2020 Mar 2;10(3):a036632. doi: 10.1101/cshperspect.a036632.
8
Facilitating informed choice about non-invasive prenatal testing (NIPT): a systematic review and qualitative meta-synthesis of women's experiences.促进非侵入性产前检测（NIPT）知情选择：对女性体验的系统评价和定性元分析。
BMC Pregnancy Childbirth. 2019 Jan 14;19(1):27. doi: 10.1186/s12884-018-2168-4.
9
Ethical and counseling challenges in prenatal exome sequencing.产前外显子组测序的伦理和咨询挑战。
Prenat Diagn. 2018 Nov;38(12):897-903. doi: 10.1002/pd.5353. Epub 2018 Sep 11.
10
Genetic Counselors' Perspectives About Cell-Free DNA: Experiences, Challenges, and Expectations for Obstetricians.遗传咨询师对游离DNA的看法：产科医生的经验、挑战及期望
J Genet Couns. 2018 Dec;27(6):1374-1385. doi: 10.1007/s10897-018-0268-y. Epub 2018 Jun 27.

本文引用的文献

1
Expanding Use of cfDNA Screening in Pregnancy: Current and Emerging Ethical, Legal, and Social Issues.循环游离DNA筛查在孕期的应用拓展：当前及新出现的伦理、法律和社会问题
Curr Genet Med Rep. 2017 Mar;5(1):44-53. doi: 10.1007/s40142-017-0113-x. Epub 2017 Feb 11.
2
The Promise and Peril of Precision Medicine: Phenotyping Still Matters Most.精准医学的前景与风险：表型分型仍然最为重要。
Mayo Clin Proc. 2016 Oct 8. doi: 10.1016/j.mayocp.2016.08.008.
3
Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women.对从孕妇血液中分离出的胎儿细胞的DNA进行全基因组拷贝数分析。
Prenat Diagn. 2016 Dec;36(12):1127-1134. doi: 10.1002/pd.4948. Epub 2016 Nov 18.
4
Effect of enhanced information, values clarification, and removal of financial barriers on use of prenatal genetic testing: a randomized clinical trial.强化信息、价值观澄清及消除经济障碍对产前基因检测使用的影响：一项随机临床试验
JAMA. 2014 Sep 24;312(12):1210-7. doi: 10.1001/jama.2014.11479.
5
Women's experiences receiving abnormal prenatal chromosomal microarray testing results.女性接受异常产前染色体微阵列检测结果的体验。
Genet Med. 2013 Feb;15(2):139-45. doi: 10.1038/gim.2012.113. Epub 2012 Sep 6.