Literature DB >> 2563000

Multicentre randomised clinical trial of chorion villus sampling and amniocentesis. First report. Canadian Collaborative CVS-Amniocentesis Clinical Trial Group.

.   

Abstract

2787 women who were aged 35 years or more at expected date of delivery were randomised to chorionic villus sampling (CVS) at 9-12 weeks gestation or amniocentesis at 15-17 weeks for the detection of a chromosomal abnormality in the fetus. 396 women were excluded after randomisation because of a non-viable fetus, a multiple pregnancy, or infection or because the pregnancy was too far advanced (more than 12 completed weeks). Among all women eligible at the time of the first study procedure there were 89/1169 (7.6%, 95% confidence interval [CI] 6.2-9.3%) total losses (spontaneous and induced abortions and late losses) in the CVS group and 82/1174 (7.0%, CI 5.6-8.6%) in the amniocentesis group for an excess of 0.6% for those women undergoing CVS, with a tendency to later losses in the CVS group. Approximate 95% CIs indicate that this difference is most unlikely to be greater than 2.7%. Mean birthweights for each week of gestation were similar in both groups, with no evidence of excess small-for-gestational age babies in the CVS group. The proportion of preterm births were similar in both groups. Perinatal mortality was greater in the CVS group, the greatest imbalance being beyond 28 weeks. Preliminary analysis has not disclosed an obvious recurrent event in the CVS group which might explain a cause-and-effect relationship for these late fetal losses. There is no evidence of any excess intrauterine growth retardation babies in the CVS group. Maternal morbidity was similar in both groups. 103/1037 (9.9%) women eligible for CVS had a further amniocentesis; 32 of these second procedures were needed to complete the cytogenetic diagnosis. More problems such as confined mosaicism and maternal cell contamination occurred in the interpretation of the CVS samples, but these were clarified by amniocentesis when appropriate.

Entities:  

Mesh:

Year:  1989        PMID: 2563000

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  37 in total

1.  Oxalate, livers, and kidneys.

Authors:  R W Watts; M A Mansell
Journal:  BMJ       Date:  1990-10-06

Review 2.  The prenatal diagnosis of genetic diseases.

Authors:  Peter Wieacker; Johannes Steinhard
Journal:  Dtsch Arztebl Int       Date:  2010-12-03       Impact factor: 5.594

3.  Tissue extraction of DNA and RNA and analysis by the polymerase chain reaction.

Authors:  D P Jackson; F A Lewis; G R Taylor; A W Boylston; P Quirke
Journal:  J Clin Pathol       Date:  1990-06       Impact factor: 3.411

4.  Association between Helicobacter pylori infection and serum pepsinogen concentrations in gastroduodenal disease.

Authors:  K Matsumoto; N Konishi; M Ohshima; Y Hiasa; E Kimura; T Samori
Journal:  J Clin Pathol       Date:  1996-12       Impact factor: 3.411

Review 5.  Tobacco and the Third World.

Authors:  J Crofton
Journal:  Thorax       Date:  1990-03       Impact factor: 9.139

Review 6.  The preimplantation genetic diagnosis of genetic diseases.

Authors:  Y Verlinsky; E Pergament; C Strom
Journal:  J In Vitro Fert Embryo Transf       Date:  1990-02

7. 

Authors:  G Hebisch
Journal:  Arch Gynecol Obstet       Date:  1995-12       Impact factor: 2.344

Review 8.  Helicobacter pylori (formerly Campylobacter pyloridis/pylori) 1986-1989: a review.

Authors:  A C Maddocks
Journal:  J Clin Pathol       Date:  1990-05       Impact factor: 3.411

Review 9.  Amniocentesis and chorionic villus sampling for prenatal diagnosis.

Authors:  Zarko Alfirevic; Kate Navaratnam; Faris Mujezinovic
Journal:  Cochrane Database Syst Rev       Date:  2017-09-04

10.  Distribution of Helicobacter pylori colonisation and associated gastric inflammatory changes: difference between patients with duodenal and gastric ulcers.

Authors:  J A Louw; V Falck; C van Rensburg; J Zak; G Adams; I N Marks
Journal:  J Clin Pathol       Date:  1993-08       Impact factor: 3.411

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.