• 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

满足患者对早孕期产前非整倍体筛查的教育和决策需求。

Meeting patients' education and decision-making needs for first trimester prenatal aneuploidy screening.

机构信息

Departments of Bioethics, Cleveland Clinic, Cleveland, OH 44195, USA.

出版信息

Prenat Diagn. 2011 Dec;31(13):1222-8. doi: 10.1002/pd.2867. Epub 2011 Oct 24.

DOI:10.1002/pd.2867
PMID:22024939
Abstract

OBJECTIVE

First trimester aneuploidy screening introduces unique challenges to patient education and informed decision-making. Our study assessed the decision-making process among those pregnant patients presenting for this new form of aneuploidy screening.

METHOD

A survey instrument was used to assess components of decision-making among women who presented for first trimester aneuploidy screening. Knowledge and leading factors in the decision-making process were measured.

RESULTS

Participants (n = 139) demonstrated understanding of the etiology of Down syndrome, but less understanding of its cognitive (65.2%) and physical manifestations (58.7%). Few were able to determine risk from first trimester screen results (36.7%). Participants were more familiar with amniocentesis (84.2%) than chorionic villus sampling (73.4%), though less familiar with procedural risks (29.5% and 28.1%, respectively). The majority of participants ranked the following as key information in their decision: knowledge of their intentions about the outcome of the pregnancy based on the test results (92.4%), knowledge of chorionic villus sampling to evaluate an abnormal result (92.0%), and values and beliefs about termination (89.1%).

CONCLUSION

First trimester aneuploidy screening generates education and decision-making benchmarks for patients and providers. It is important to address these barriers as this new screen becomes a growing part of current prenatal genetic testing offerings.

摘要

目的

早孕期非整倍体筛查给患者教育和知情决策带来了独特的挑战。我们的研究评估了那些接受这种新形式非整倍体筛查的孕妇的决策过程。

方法

使用调查工具评估了在早孕期非整倍体筛查中呈现的女性的决策过程的各个组成部分。衡量了知识和决策过程中的主要因素。

结果

参与者(n=139)对唐氏综合征的病因有一定的了解,但对其认知(65.2%)和身体表现(58.7%)的了解较少。很少有人能够从早孕期筛查结果中确定风险(36.7%)。参与者对羊膜穿刺术(84.2%)比绒毛膜取样(73.4%)更为熟悉,尽管对程序风险的了解较少(分别为 29.5%和 28.1%)。大多数参与者将以下内容列为决策的关键信息:根据测试结果了解自己对妊娠结果的意图(92.4%)、了解绒毛膜取样以评估异常结果(92.0%)以及对终止妊娠的价值观和信念(89.1%)。

结论

早孕期非整倍体筛查为患者和提供者提供了教育和决策基准。随着这种新筛查成为当前产前遗传检测服务的一部分,解决这些障碍非常重要。

相似文献

1
Meeting patients' education and decision-making needs for first trimester prenatal aneuploidy screening.满足患者对早孕期产前非整倍体筛查的教育和决策需求。
Prenat Diagn. 2011 Dec;31(13):1222-8. doi: 10.1002/pd.2867. Epub 2011 Oct 24.
2
Prenatal screening for fetal aneuploidy in singleton pregnancies.单胎妊娠胎儿非整倍体的产前筛查。
J Obstet Gynaecol Can. 2011 Jul;33(7):736-750. doi: 10.1016/S1701-2163(16)34961-1.
3
Risk and uncertainty: shifting decision making for aneuploidy screening to the first trimester of pregnancy.风险与不确定性:将非整倍体筛查的决策转移到孕早期。
Genet Med. 2011 May;13(5):429-36. doi: 10.1097/GIM.0b013e3182076633.
4
Prenatal screening for and diagnosis of aneuploidy in twin pregnancies.双胎妊娠非整倍体的产前筛查与诊断
J Obstet Gynaecol Can. 2011 Jul;33(7):754-67.
5
Decision-making for prenatal genetic screening: how will pregnant women navigate a growing number of aneuploidy and carrier screening options?产前基因筛查决策:孕妇将如何应对日益增多的非整倍体和携带者筛查选择?
BMC Pregnancy Childbirth. 2021 Dec 4;21(1):806. doi: 10.1186/s12884-021-04282-7.
6
Patient-centered prenatal counseling: aligning obstetric healthcare professionals with needs of pregnant women.以患者为中心的产前咨询:使产科医疗保健专业人员与孕妇需求相匹配。
Women Health. 2015;55(3):280-96. doi: 10.1080/03630242.2014.996724. Epub 2015 Mar 20.
7
Computerized prenatal genetic testing decision-assisting tool: a randomized controlled trial.计算机化产前基因检测决策辅助工具:一项随机对照试验。
Obstet Gynecol. 2009 Jan;113(1):53-63. doi: 10.1097/AOG.0b013e31818e7ec4.
8
Impact of first-trimester aneuploidy screening in a high-risk population.孕早期非整倍体筛查在高危人群中的影响。
Fetal Diagn Ther. 2009;26(1):29-34. doi: 10.1159/000236356. Epub 2009 Oct 10.
9
Screening for Down syndrome: practice patterns and knowledge of obstetricians and gynecologists.唐氏综合征筛查:产科医师和妇科医师的实践模式与知识水平
Obstet Gynecol. 2006 Jan;107(1):11-7. doi: 10.1097/01.AOG.0000190215.67096.90.
10
Preferences of pregnant women for amniocentesis or chorionic villus sampling for prenatal testing: comparison of patients' choices and those of a decision-analytic model.孕妇对羊膜穿刺术或绒毛取样进行产前检测的偏好:患者选择与决策分析模型选择的比较
J Clin Epidemiol. 1994 Nov;47(11):1215-28. doi: 10.1016/0895-4356(94)90126-0.

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
"Knowledge was clearly associated with education." epistemic positioning in the context of informed choice: a scoping review and secondary qualitative analysis.“知识显然与教育相关。” 知情选择背景下的认知定位:一项范围综述和二次定性分析。
BMC Med Ethics. 2025 Jan 9;26(1):1. doi: 10.1186/s12910-024-01144-7.
3
Disparities in access to reproductive genetic services associated with geographic location of residence and maternal race and ethnicity.
居住地的地理位置、产妇的种族和民族与获得生殖遗传服务的机会存在差异。
Genet Med. 2024 Nov;26(11):101221. doi: 10.1016/j.gim.2024.101221. Epub 2024 Jul 20.
4
Factors Influencing the Decision-Making Process for Undergoing Invasive Prenatal Testing.影响进行侵入性产前检测决策过程的因素。
Cureus. 2024 Apr 23;16(4):e58803. doi: 10.7759/cureus.58803. eCollection 2024 Apr.
5
Aspiring toward equitable benefits from genomic advances to individuals of ancestrally diverse backgrounds.力求让来自不同祖先背景的个人从基因组学进展中获得公平的益处。
Am J Hum Genet. 2024 May 2;111(5):809-824. doi: 10.1016/j.ajhg.2024.04.002. Epub 2024 Apr 19.
6
Pregnant Hispanic women's views and knowledge of prenatal genetic testing.西班牙语裔孕妇对产前基因检测的看法和了解。
J Genet Couns. 2021 Jun;30(3):838-848. doi: 10.1002/jgc4.1383. Epub 2021 Jan 26.
7
Decision-making factors in prenatal testing: A systematic review.产前检测中的决策因素:一项系统综述。
Health Psychol Open. 2021 Jan 13;8(1):2055102920987455. doi: 10.1177/2055102920987455. eCollection 2021 Jan-Jun.
8
Talking Points: Women's Information Needs for Informed Decision-Making About Noninvasive Prenatal Testing for Down Syndrome.要点:女性对于唐氏综合征无创产前检测知情决策的信息需求
J Genet Couns. 2018 Sep;27(5):1258-1264. doi: 10.1007/s10897-018-0250-8. Epub 2018 Mar 17.
9
Investigating Pregnancy Outcomes After Abnormal Cell-Free DNA Test Results.无细胞DNA检测结果异常后的妊娠结局调查。
J Genet Couns. 2018 Aug;27(4):902-908. doi: 10.1007/s10897-018-0219-7. Epub 2018 Jan 24.
10
The Legal Past, Present and Future of Prenatal Genetic Testing: Professional Liability and Other Legal Challenges Affecting Patient Access to Services.产前基因检测的法律过去、现在与未来:影响患者获得服务的职业责任及其他法律挑战
J Clin Med. 2014 Dec 15;3(4):1437-65. doi: 10.3390/jcm3041437.