2014, Number 1
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Medisur 2014; 12 (1)
Effectiveness of Increased Nuchal Translucency in Detecting Pregnancies at Risk for Chromosomal Abnormalities
González HL, Rodríguez RL, García RN, Valero AMP,Herrera MM, Jure RV
Language: Spanish
References: 25
Page: 63-76
PDF size: 253.81 Kb.
ABSTRACT
Background: assessment of embryonic anatomy by
ultrasound since early ages leads to the detection of
pregnancies at risk for chromosomal abnormalities. Advanced maternal age alone is not enough.
Objective: to assess the results of the nuchal translucency measurement at the first trimester ultrasound as a sonographic marker of chromosomal abnormalities.
Methods: a sample of 29 334 pregnant women was
studied from September 2006 to December 2010. General
performance of the sonographic marker was assessed
taking into account the years and maternal age.
Effectiveness of increased nuchal translucency in the
indirect detection of chromosomal abnormalities was
determined using the common parameters.
Results: the net number of increased nuchal
translucencies diminished over the years, as well as the
absolute amount of prenatal karyotypes performed; but its
proportion increased along with the positive prenatal
karyotypes among women with increased nuchal
translucency. Among the 71 fetuses with increased
translucency, seven cases of chromosomal abnormalities
were confirmed by other elements of the prenatal program.
The sensitivity of the isolated nuchal translucency was
14.6%; specificity was high (99.8%); positive and negative
predictive values were 18.4% and 99.9%, respectively.
Rates of false positives were very low.
Conclusions: high specificity reaffirms nuchal translucency as a good early marker of risk for chromosomal
abnormalities, particularly Down syndrome and Trisomy 18,
with a minimum rate of indications for invasive testing and
an extra increase in the detection of fetal defects.
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