[Application and evaluation of invasive prenatal diagnostic techniques and analysis of chromosomal karyotype]
- PMID: 23645241
- DOI: 10.3969/j.issn.1672-7347.2013.04.011
[Application and evaluation of invasive prenatal diagnostic techniques and analysis of chromosomal karyotype]
Abstract
Objective: To evaluate the safety, effectiveness and complications of serial invasive prenatal diagnostic techniques, and to investigate the prenatal diagnosis indication as well as to analyze the abnormal chromosomal karyotype.
Methods: We retrospectively studied all patients from March 2005 to May 2012 who received amniocentesis and cordocentesis in the prenatal diagnosis center of Second Xiangya Hospital. The indication of the procedure, successful rate and complications were evaluated, and 25 abnormal chromosome nuclear types were analyzed.
Results: A total of 669 patients received invasive prenatal diagnosis from March 2005 to May 2012 in Second Xiangya Hospital: 598 received amniocentesis and 71 cordocentesis carried out. Compared with the cordocentesis group, the amniocentesis group had higher achievement ratio (91.54% vs 100%, P<0.05), lower spontaneous abortion rate (1.41% vs 0.33%, P<0.05), fewer abnormal karyotypes (11.27% vs 2.84%, P<0.05) and lower expenditure (880 yuan vs 800 yuan, P<0.05). Positive screening, advanced maternal age, and ultrasonography abnormality were the top 3 indications of amniocentesis and cordocentesis. We found 25 abnormal karyotypes, including 6 cases of trisomy 21, 4 sex chromosomal abnormalities, 7 autosomal balanced translocations, 1 marker chromosome, and 7 mosaics.
Conclusion: As a widely used invasive prenatal diagnosis, amniocentesis is safe and effective. The complications of cordocentesis are much higher than those of amniocentesis, which is not a proper routine procedure for prenatal diagnosis of abnormal karyotype. The analysis of karyotype not only can identify fetal chromosome abnormality, but also provide the scientific basis for pregnancy continuation, thus reducing the ratio of birth defect.
Similar articles
-
[Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].Zhonghua Fu Chan Ke Za Zhi. 2011 Sep;46(9):644-8. Zhonghua Fu Chan Ke Za Zhi. 2011. PMID: 22176986 Chinese.
-
[Value of detection of cell-free fetal DNA in maternal plasma in the prenatal diagnosis of chromosomal abnormalities].Zhonghua Fu Chan Ke Za Zhi. 2012 Nov;47(11):808-12. Zhonghua Fu Chan Ke Za Zhi. 2012. PMID: 23302119 Chinese.
-
Karyotype analysis with amniotic fluid in 12365 pregnant women with indications for genetic amniocentesis and strategies of prenatal diagnosis.J Obstet Gynaecol. 2016;36(3):293-6. doi: 10.3109/01443615.2015.1041889. Epub 2015 Oct 7. J Obstet Gynaecol. 2016. PMID: 26445265
-
[Clinical approach to prenatal diagnosis of chromosome abnormalities].Reprod Nutr Dev. 1990;Suppl 1:139s-145s. Reprod Nutr Dev. 1990. PMID: 2206291 Review. French.
-
Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review.Taiwan J Obstet Gynecol. 2011 Sep;50(3):331-8. doi: 10.1016/j.tjog.2011.07.013. Taiwan J Obstet Gynecol. 2011. PMID: 22030049 Review.
Cited by
-
Karyotype analysis of amniotic fluid cells and report of chromosomal abnormalities in 15,401 cases of Iranian women.Sci Rep. 2021 Sep 30;11(1):19402. doi: 10.1038/s41598-021-98928-3. Sci Rep. 2021. PMID: 34593920 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Medical
Research Materials