Alfirevic Z
Department of Obstetrics and Gynaecology, University of Liverpool, Liverpool, UK, L69 3BX.
Cochrane Database Syst Rev. 2000;1999(2):CD000077. doi: 10.1002/14651858.CD000077.
A major disadvantage of amniocentesis is that test results are usually available only after 18 weeks gestation. Early amniocentesis can now be done between 9 to 14 weeks gestation.
The objective was to assess the safety and accuracy of early amniocentesis compared with chorion villus sampling.
The Cochrane Pregnancy and Childbirth Group trials register and the Cochrane Controlled Trials Register were searched. Date of last search: October 1998.
Randomised trials comparing early amniocentesis with transabdominal chorion villus sampling.
One reviewer assessed eligibility and trial quality.
Three studies were included. Sampling failure was 0.4% in the early amniocentesis group compared to 2% in the chorion villus group (relative risk 0.23, 95% confidence interval 0.08 to 0.65). Consequently, more women in the chorion villus sampling group needed a second prenatal diagnostic test (relative risk 0.43, 95% confidence interval 0.21 to 0.88). There were no statistically significant differences in the laboratory failures (relative risk 0.43, 95% confidence interval 0. 17 to 1.10) or number of women with various chromosomal abnormalities (relative risk 0.51, 95% confidence interval 0.26 to 1. 04). Combined total pregnancy loss in the early amniocentesis group was 6.2% (57/915) compared with 5% (46/917) in the chorion villus sampling group (relative risk 1.24, 95% confidence interval 0.85 to 1.81). There were more spontaneous miscarriages after early amniocentesis (4.4% versus 2.3%, relative risk 1.92, 95% confidence interval 1.14 to 3.23). There was no difference in the incidence of neonatal respiratory distress and anomalies in the newborn infants. The incidence of talipes was greater in the early amniocentesis group, although haemangiomas were more common in the chorion villus sampling group.
REVIEWER'S CONCLUSIONS: Current data suggest that early amniocentesis is associated with a greater risk of spontaneous miscarriage and neonatal talipes compared to transabdominal chorion villus sampling. An increased risk of these complications needs to be weighed against fewer technical difficulties and the possibility of fewer neonatal haemangiomas.
羊膜穿刺术的一个主要缺点是通常要在妊娠18周后才能得到检测结果。现在可在妊娠9至14周进行早期羊膜穿刺术。
目的是评估早期羊膜穿刺术与绒毛取样相比的安全性和准确性。
检索了Cochrane妊娠与分娩组试验注册库和Cochrane对照试验注册库。最后检索日期:1998年10月。
比较早期羊膜穿刺术与经腹绒毛取样的随机试验。
一名评价者评估了研究的合格性和试验质量。
纳入了三项研究。早期羊膜穿刺术组的取样失败率为0.4%,而绒毛取样组为2%(相对危险度0.23,95%可信区间0.08至0.65)。因此,绒毛取样组中更多的妇女需要进行第二次产前诊断检测(相对危险度0.43,95%可信区间0.21至0.88)。实验室检测失败率(相对危险度0.43,95%可信区间0.17至1.10)或患有各种染色体异常的妇女数量(相对危险度0.51,95%可信区间0.26至1.04)无统计学显著差异。早期羊膜穿刺术组的总妊娠丢失率为6.2%(57/915),而绒毛取样组为5%(46/917)(相对危险度1.