
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
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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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