Discrepant karyotypes after second- and third-trimester combined placentacentesis/amniocentesis

Cytogenetic data are presented from a total of 1306 consecutive pregnancies with successful diagnosis obtained from both chorionic villi after short‐time culture (CVS‐SC) and amniotic fluid cell cultures (AC); samples had been taken simultaneously at combined placentacentesis (placental biopsy) and amniocentesis during the second (92·8 per cent) and third (7·2 per cent) trimesters. Concordant results were obtained in 1218 pregnancies with a normal karyotype and in 62 pregnancies with an aberrant fetal karyotype. Discrepant, i. e. false‐positive and false‐negative, results were found in 26 cases (2 per cent). From these data the accuracy of CVS‐SC, defined as the proportion of all correct diagnoses, is calculated to be 98 per cent. Three non‐mosaic and 14 mosaic false‐positive results obtained after CVS‐SC could not be confirmed by AC. Related to 1235 true normal fetal karyotypes, the specificity of CVS‐SC, i.e. the proportion of normal karyotypes correctly diagnosed, amounts to 98·6 per cent. In nine pregnancies, an aberrant fetal karyotype detected after AC was missed by CVS‐SC. The sensitivity of CVS‐SC, i.e. the proportion of abnormal fetuses correctly diagnosed (62 out of 71), amounts to 87·3 per cent in our study group.