Feasibility, accuracy and safety of chorionic villus sampling: a report of 10 741 cases

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Abstract
Objectives To evaluate the feasibility, accuracy and safety of chorionic villus sampling (CVS). Methods Ten thousand seven hundred and forty one singleton pregnancies at risk of chromosome abnormalities (96.3%) and gene disorders (2.8%) were referred from 1990 to 1999 to the fetal medicine unit of a teaching hospital. CVS was performed transabdominally after 11 weeks, using a modified freehand ultrasonographically guided technique by 5 operators. Fetal karyotyping was obtained using a direct method before 1995 and was completed by cell culture after 1996. Failed results, feto‐placental discrepancy and fetal loss were assessed. Results Villi were sampled using extra‐amniotic puncture (89.4%) and one sampling‐device insertion (92.3%). The mean weight of the specimen was 15.2 ± 6.0 mg. All attempts at sampling were successful, except eight (0.07%). The number of failed results following direct preparation, cell culture and both methods was 20 (0.19%), 23 (0.21%) and 2 (0.02%), respectively. Light maternal cell contamination occurred in less than 1% of the samplings after microscopic selection of the villi, and never interfered with the assessment of karyotyping. All 3 false‐negative results (0.03%) were recorded after direct preparation and 2 were corrected by culture. The rate of chromosomal abnormalities confined to the placenta decreased from 1.08% before 1995 to 0.73% after 1996. True fetal mosaicisms were recorded in 7 cases (0.06%). The rate of fetal loss at <28 weeks was 1.64% in all pregnancies and 1.92% when CVS was performed before 13 weeks. Advanced maternal age was the single factor significantly associated with fetal loss. Conclusions CVS was feasible, accurate and safe in our institution, as a result of the increasing experience of the operators and the cytogeneticists. Copyright © 2003 John Wiley & Sons, Ltd.