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唐氏高风险胎儿孕中期超声筛查的研究分析 被引量:1

The Study and Analysis of Ultrasound Screening in Middle Stage of Pregnancy for Down's High-risk Fetal
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摘要 目的探讨孕中期超声筛查在诊断唐氏高风险胎儿中的作用和意义。方法对15~20周孕妇抽血进行血清标记物甲胎蛋白(AFP)、β绒毛膜促性腺激素(β-hCG)筛查,以1:300为切割值,对唐氏高风险者建议孕中期超声筛查及羊膜腔穿刺。结果血清筛查唐氏高风险682例,其中184例同意羊水穿刺,发现21三体4例,阳性率2.17%。孕中期超声筛查635例,发现胎儿异常标记37例,异常检出率5.83%。其中21例分娩,16例引产。结论孕中期超声筛查可检出胎儿结构畸形和软指标异常,联合血清标记物和羊水穿刺可有效减少唐氏儿的出生。 Objective To investigate the function and significance of ultrasound screening for detecting Down's high-risk fetal during the second trimester. Methods The examinations of serum markers of alpha-fetal protein(AFP)and human chorionic gonadotrophin(尾-hCG)were given to pregnant women with a gestational age of 15-20 weeks. When the number exceed 1:300,it was regarded as high risk of Down's. Every high-risk fetal was suggested to have ultrasound screening and amniocentesis in middle stage of pregnancy. Results Of the 682 cases received serum screening, 184 cases accepted amniocentesis. Among them, 4 cases were found with 21-trisomy syndrome,the positive rate was 2.17%. Of the 635 cases received ultrasound screening during the second trimester,37 fetals were found with abnormal markers,the detection rate was 5.83%. Of which, there were 21 cases of delivery and 16 cases of induced labor. Conclusion Ultrasound screening in the second trimester can detect fetal structure malformation and soft marker abnormalities,which combined with the examination of serum markers and amniocentesis can reduce the birth of Down's fetal effectively.
出处 《中外医疗》 2013年第27期18-19,共2页 China & Foreign Medical Treatment
关键词 唐氏高风险 胎儿 孕中期 超声筛查 Down's high risk fetal middle stage of pregnancy ultrasound screening
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  • 1黄燕,税青林,赵小平,余红.21-三体综合征患儿发病与母亲年龄和环境因素的关系[J].中国妇幼保健,2006,21(2):246-247. 被引量:9
  • 2赵灵琴,郁凯明.母体叶酸缺乏与胎儿21-三体综合征关系的研究[J].中国妇幼健康研究,2006,17(4):305-307. 被引量:8
  • 3钱敏,孙燕,吴青青,马玉庆,陈焰.11~14周正常胎儿心脏超声检查[J].中国医学影像技术,2007,23(2):268-271. 被引量:34
  • 4张俊玲,王建秀.933例21-三体综合征筛查[J].中国生育健康杂志,2007,18(3):171-172. 被引量:6
  • 5Raniga S,Desai PD,Parikh H,et al.Ultrasonographic soft markere of aneuploidy in second trimester:are we lest?[J].Med Gen Med,2006,11 (1):9-24.
  • 6Tongsons T,Sirichotiyakul S,Wanapirak C,et al.Sonographic features of trisomy 13 at midpregnancy[J].Int J Gynecol Obstet,2006,16(2):143-148.
  • 7Tongsons T,Sirichotiyakul S,Wanapirak C,et al.Sonographic features of trisomy 18 at midpregnancy[J].J Obstet Gynecol Kes,2002,28 (5):245-250.
  • 8Benacerruf BR.The role of the second-trimester genetic sonogram in screening for fetal Down syndrome[J].Semin Perinatol,2005,29(6):386-394.
  • 9Nicolaides KH.Screening for chromosomal defects[J].Ultrasound Obstet Gyneeol,2003,21:313-321.
  • 10Krantz DA,Hallahan TW,Macri VJ,et al.Genetia sonography after first-trimester Down syndrome screening[J].Ultrasound Obstet Gynecol,2007,29:666-670.

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  • 1Van den Hof Michiel C,Wilson R Douglas.Fetal soft markers in obstetric ultrasound. Journal of obstetrics and gynaecology Canada : JOGC = Journal d’obstétrique et gynécologie du Canada : JOGC . 2005
  • 2Halliday J,Lumley J,Bankier A.Karyotype abnormalities in fetuses diagnosed as abnormal on ultrasound before 20 weeks’ gestational age. Prenatal Diagnosis . 1994
  • 3Nicolaides K H,Snijders R J,Gosden C M,Berry C,Campbell S.Ultrasonographically detectable markers of fetal chromosomal abnormalities. The Lancet . 1992
  • 4Jiang Tao,Lv Ling,Yang Bing,Sun Yijun,Zhang Xiaojuan,Sun Yun,Xu Qianjun,Xu Zhengfeng.(Second trimester screening for trisomy 21 using ADAM12-S as a maternal serum marker)Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics . 2012
  • 5JULIESANFORD HANNA,RICHARD L.NEU,DAVID H.LOCKWOOD.??PRENATAL CYTOGENETIC RESULTS FROM CASES REFERRED FOR 44 DIFFERENT TYPES OF ABNORMAL ULTRASOUND FINDINGS(J)Prenat. Diagn. . 1999 (2)
  • 6NICOLARIZZO,MARIA CARLAPITTALIS,GIANLUIGIPILU,ANTONELLAPEROLO,CRISTINABANZI,ANTONELLAVISENTIN,LUCIANOBOVICELLI.??DISTRIBUTION OF ABNORMAL KARYOTYPES AMONG MALFORMED FETUSES DETECTED BY ULTRASOUND THROUGHOUT GESTATION(J)Prenat. Diagn. . 1999 (2)
  • 7Michael L.Begleiter,Molly M.Lund,Andrea M.Atherton,Janda D.Buchholz,Holly H.Ardinger.??Maternal serum screening and 22q11.2 deletion syndrome(J)Am. J. Med. Genet. . 2007 (4)
  • 8Positive biochemical screening for trisomy 18: on the path of trisomy 9(J)Prenat. Diagn. . 2008 (2)
  • 9Aysel Uysal Derbent,Filiz Fatma Yanik,&Idot,lknur &Idot,neg?,l Gü,mü,&scedil,Serap Simavli,Nilgü,n ?,ztü,rk Turhan.??Impact of inherited thrombophilias on first and second trimester maternal serum markers for aneuploidy(J)Journal of Maternal-Fetal and Neonatal Medicine . 2012 (11)
  • 10田晓先,陈科,黎新艳,林莲恩,晁桂华,杜娟,李雪芹,黄飞雪,周璇.中孕期胎儿超声软指标筛查21-三体综合征的意义分析[J].中国妇幼保健,2011,26(12):1809-1811. 被引量:11

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