Table 1: Indications of prenatal invasive procedures for fetal karyotyping according to AC and CVS.
Indication of prenatal invasive procedures for fetal karyotyping AC (n=500) CVS (n=224) Total (n=724)
Suspicious first trimester screening 120 145 265
Increased nuchal translucency 19 36 55
Suspicious biochemistry 79 46 125
Combined elevated risk 22 63 85
Maternal age 223 33 256
Suspicious genetic history 50 41 91
Suspicious ultrasound findings 95 18 113
Other indications (request, infections, etc.) 23 0 23
* Total number of indications larger than total population due to double indication