• 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

性染色体异常产前诊断后终止妊娠的决策:文献系统综述。

Decision to abort after a prenatal diagnosis of sex chromosome abnormality: a systematic review of the literature.

机构信息

Department of Health and Kinesiology, Texas A&M University, College Station, Texas, USA.

出版信息

Genet Med. 2012 Jan;14(1):27-38. doi: 10.1038/gim.0b013e31822e57a7. Epub 2011 Oct 7.

DOI:10.1038/gim.0b013e31822e57a7
PMID:22237429
Abstract

We performed a systematic review of factors affecting parental decisions to continue or terminate a pregnancy after prenatal diagnosis of a sex chromosome abnormality, as reported in published studies from 1987 to May 2011. Based on the Matrix Method for systematic reviews, 19 studies were found in five electronic databases, meeting specific inclusion/exclusion criteria. Abstracted data were organized in a matrix. Alongside the search for factors influencing parental decisions, each study was judged on its methodological quality and assigned a methodological quality score. Decisions either to terminate or to continue a sex chromosome abnormality-affected pregnancy shared five similar factors: specific type of sex chromosome abnormality, gestational week at diagnosis, parents' age, providers' genetic expertise, and number of children/desire for (more) children. Factors unique to termination decisions included parents' fear/anxiety and directive counseling. Factors uniquely associated with continuation decisions were parents' socioeconomic status and ethnicity. The studies' average methodological quality score was 10.6 (SD = 1.67; range, 8-14). Findings from this review can be useful in adapting and modifying guidelines for genetic counseling after prenatal diagnosis of a sex chromosome abnormality. Moreover, improving the quality of future studies on this topic may allow clearer understanding of the most influential factors affecting parental decisions.

摘要

我们对 1987 年至 2011 年 5 月期间已发表的研究报告进行了系统综述,分析了影响父母决定继续或终止产前诊断出性染色体异常胎儿妊娠的因素。根据系统综述矩阵方法,在五个电子数据库中找到了 19 项研究,这些研究符合特定的纳入/排除标准。提取的数据以矩阵形式组织。除了寻找影响父母决定的因素外,我们还根据方法学质量对每项研究进行了评估,并给出了方法学质量评分。决定终止或继续患有性染色体异常的妊娠有五个相似的因素:性染色体异常的具体类型、诊断时的孕周、父母的年龄、提供者的遗传专业知识,以及孩子的数量/(想要)孩子的数量。与终止决定相关的独特因素包括父母的恐惧/焦虑和指令性咨询。与继续决定相关的独特因素是父母的社会经济地位和种族。这些研究的平均方法学质量评分为 10.6(标准差=1.67;范围 8-14)。本综述的研究结果有助于适应和修改性染色体异常产前诊断后的遗传咨询指南。此外,提高未来关于这一主题的研究质量可能有助于更清楚地了解影响父母决定的最具影响力的因素。

相似文献

1
Decision to abort after a prenatal diagnosis of sex chromosome abnormality: a systematic review of the literature.性染色体异常产前诊断后终止妊娠的决策:文献系统综述。
Genet Med. 2012 Jan;14(1):27-38. doi: 10.1038/gim.0b013e31822e57a7. Epub 2011 Oct 7.
2
Factors that influence parents' and informal caregivers' views and practices regarding routine childhood vaccination: a qualitative evidence synthesis.影响父母和非正式照顾者对常规儿童疫苗接种看法和做法的因素:定性证据综合分析。
Cochrane Database Syst Rev. 2021 Oct 27;10(10):CD013265. doi: 10.1002/14651858.CD013265.pub2.
3
Parent training interventions for Attention Deficit Hyperactivity Disorder (ADHD) in children aged 5 to 18 years.针对5至18岁儿童注意力缺陷多动障碍(ADHD)的家长培训干预措施。
Cochrane Database Syst Rev. 2011 Dec 7;2011(12):CD003018. doi: 10.1002/14651858.CD003018.pub3.
4
Parents' and informal caregivers' views and experiences of communication about routine childhood vaccination: a synthesis of qualitative evidence.父母及非正式照料者关于儿童常规疫苗接种沟通的观点与经历:定性证据综述
Cochrane Database Syst Rev. 2017 Feb 7;2(2):CD011787. doi: 10.1002/14651858.CD011787.pub2.
5
Face-to-face interventions for informing or educating parents about early childhood vaccination.针对向父母宣传或教育幼儿疫苗接种情况的面对面干预措施。
Cochrane Database Syst Rev. 2018 May 8;5(5):CD010038. doi: 10.1002/14651858.CD010038.pub3.
6
Interventions from pregnancy to two years after birth for parents experiencing complex post-traumatic stress disorder and/or with childhood experience of maltreatment.针对经历复杂创伤后应激障碍和/或儿童期受虐待经历的父母,从怀孕到出生后两年的干预措施。
Cochrane Database Syst Rev. 2023 May 4;5(5):CD014874. doi: 10.1002/14651858.CD014874.pub2.
7
Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women.基于基因组学的非侵入性产前检测用于检测孕妇胎儿染色体非整倍体。
Cochrane Database Syst Rev. 2017 Nov 10;11(11):CD011767. doi: 10.1002/14651858.CD011767.pub2.
8
Cost-effectiveness of using prognostic information to select women with breast cancer for adjuvant systemic therapy.利用预后信息为乳腺癌患者选择辅助性全身治疗的成本效益
Health Technol Assess. 2006 Sep;10(34):iii-iv, ix-xi, 1-204. doi: 10.3310/hta10340.
9
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.系统性药理学治疗慢性斑块状银屑病:网络荟萃分析。
Cochrane Database Syst Rev. 2021 Apr 19;4(4):CD011535. doi: 10.1002/14651858.CD011535.pub4.
10
Dietary interventions for recurrent abdominal pain in childhood.儿童复发性腹痛的饮食干预措施
Cochrane Database Syst Rev. 2017 Mar 23;3(3):CD010972. doi: 10.1002/14651858.CD010972.pub2.

引用本文的文献

1
Prevalence of Differences of Sex Development Among Pediatric Endocrine Care Centers in Switzerland From 2000 to 2019.2000年至2019年瑞士儿科内分泌护理中心性发育差异的患病率
J Endocr Soc. 2025 Jun 20;9(8):bvaf099. doi: 10.1210/jendso/bvaf099. eCollection 2025 Aug.
2
Incidental finding of maternal sex chromosome aneuploidy from DMD carrier screening and single-nucleotide polymorphism (SNP)-based prenatal cell-free DNA screening.在杜氏肌营养不良症(DMD)携带者筛查和基于单核苷酸多态性(SNP)的产前游离DNA筛查中偶然发现母体性染色体非整倍体。
J Genet Couns. 2025 Jun;34(3):e70050. doi: 10.1002/jgc4.70050.
3
Reproductive outcomes after preimplantation genetic testing in couples with sex chromosome abnormalities: a retrospective cohort study of 83 couples.
性染色体异常夫妇进行植入前基因检测后的生殖结局:一项对83对夫妇的回顾性队列研究
J Assist Reprod Genet. 2024 Dec;41(12):3415-3421. doi: 10.1007/s10815-024-03303-6. Epub 2024 Oct 30.
4
Invited Perspective: Challenges and Opportunities in Evaluating the Effect of Chemical Mixtures on Congenital Chromosomal Abnormalities.特邀观点:评估化学混合物对先天性染色体异常影响中的挑战与机遇
Environ Health Perspect. 2024 Sep;132(9):91301. doi: 10.1289/EHP15799. Epub 2024 Sep 11.
5
Ethical Challenges in Information Disclosure and Decision-making in Prenatal Testing: A Focus Group Study of Chinese Health Professionals in Maternal and Child Health Services.产前检测中信息披露与决策的伦理挑战:一项针对中国妇幼保健服务领域卫生专业人员的焦点小组研究
J Bioeth Inq. 2024 Aug 20. doi: 10.1007/s11673-024-10376-6.
6
Gender and Sex Inclusive Approaches for Discussing Predicted Fetal Sex: A Call for Reflection and Research.讨论预测胎儿性别的性别与性取向包容方法:呼吁反思与研究。
J Midwifery Womens Health. 2024 Nov-Dec;69(6):821-825. doi: 10.1111/jmwh.13663. Epub 2024 Jul 18.
7
Clinical practice guidelines for the care of girls and women with Turner syndrome.特纳综合征患者的护理临床实践指南。
Eur J Endocrinol. 2024 Jun 5;190(6):G53-G151. doi: 10.1093/ejendo/lvae050.
8
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.
9
Prenatal diagnosis of sex chromosome aneuploidy-What do we tell the prospective parents?性染色体非整倍体的产前诊断-我们应该告诉准父母什么?
Prenat Diagn. 2023 Feb;43(2):250-260. doi: 10.1002/pd.6256. Epub 2022 Nov 9.
10
Positive predictive value of noninvasive prenatal testing for sex chromosome abnormalities.无创性产前检测性染色体异常的阳性预测值。
Mol Biol Rep. 2022 Oct;49(10):9251-9256. doi: 10.1007/s11033-022-07754-x. Epub 2022 Aug 12.