VALUE OF THE COMBINED TEST IN PRENATAL DIAGNOSTICS
Lončar D
*Corresponding Author: Dragan Lončar, Gynecology and Obstetrics Clinic, Clinical Center Kragujevac , Vojislava Kalanovića 1A/3, 34000 Kragujevac, Serbia; Tel.: +381-64-616-8999; E-mail: drloncar@sezampro.rs
page: 53

MATERIALS AND METHODS

The prospective, observational study was conducted at the Gynecology and Obstetrics Clinic at the Clinical Center Kragujevac (GOC, CC Kragujevac, Kragujevac, Serbia) during 2008 and 2009 on singleton intrauterine pregnancies in the first trimester of pregnancy. The clinical and experimental model of study was used throughout the research. The Ethics Committee at the CC Kragujevac confirmed the correctness of this study and authorized its conduct. Three hundred and seventeen pregnant women were included in the examination and observed by the Board of Genetic Counseling at GOC, CC Kragujevac. An informed consent form was signed by all participants. All ultrasound examinations were conducted on the Aloka Prosound 3500 Ultrasound Machine Package with UST-9124 (Aloka, Seoul, South Korea) at GOC, CC Kragujevac. Pregnancy was 11-13+6 weeks of gestation. The crown-rump length (CRL) of the fetus was between 45 and 84 mm. While measuring fetal nuchal translucency (NT), we used the ultrasound apparatus of high resolution with the option“cine loop” so that the image could be turned by calipers that allow measurement of one decimal point. The screen image on which NT was measured, encompassed only the head and the upper part of fetal rib cage. We used the maximum enlargement, so that small movements of the caliper altered the diameter by only 0.1 mm. The NT was measured by transvaginal approach of color Doppler technique with the fetus in a neutral position. We measured the maximal thickness of subcutaneous illumination between the skin and soft tissue located above the cervical part of the fetal spine. We set the calipers on lines that define the fold, so that they were barely visible on the white limit line of the accumulation behind the neck. During the examinations we conducted more measurements and took into consideration only the highest thickness of the NT. We carried out the quantitative settings of free β-HCG and PAPP-A from venous blood of patients by applying commercial tests from DPC. Tests were based on the analytical immunochemiluminescence assay and were realized by using the automated analyzer IMMULITE 2000 (DPC). All the pregnant women included in this study underwent amniocentesis by a standard transabdominal procedure with the ultrasound control using the “free hand” technique at 16 to 17+6 weeks of gestation. We performed the amniocentesis by needles with mandrene of 20-22G thickness and aspirated 15-20 mL of amniotic fluid into a syringe without a rubber seal. The amniotic fluid sample was delivered to the Cytogenetics Laboratory at GOC, CC Kragujevac, and all results received were deposited into the unique database with required logistic control.



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