scholarly journals VP47.08: Interest of first trimester ultrasound in the early diagnosis of fetal malformation: the experience of Nabul prenatal diagnostic centre

2021 ◽  
Vol 58 (S1) ◽  
pp. 301-301
Author(s):  
C. Mrazguia ◽  
A. Hammami ◽  
M. Souissi ◽  
E. Fenina ◽  
S. Azzerz ◽  
...  
Keyword(s):  
Early Diagnosis ◽  
First Trimester ◽  
Fetal Malformation ◽  
Prenatal Diagnostic ◽  
Diagnostic Centre ◽  
First Trimester Ultrasound

scholarly journals Detection of Single Umbilical Artery in the First Trimester Ultrasound: Its Value as a Marker of Fetal Malformation

2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Cristina Martínez-Payo ◽  
Elena Cabezas ◽  
Yolanda Nieto ◽  
Miguel Ruiz de Azúa ◽  
Fátima García-Benasach ◽  
...  
Keyword(s):  
Umbilical Artery ◽  
False Positive Rate ◽  
False Negative ◽  
False Negative Rate ◽  
First Trimester ◽  
University Hospital ◽  
Fetal Malformation ◽  
Single Umbilical Artery ◽  
Sensitivity Specificity ◽  
First Trimester Ultrasound

Introduction. The value of a single umbilical artery (SUA) in first trimester ultrasound is not well established. The aim of our study was to determinate the relevance of diagnosis of single umbilical artery in first trimester ultrasound as an early marker suggesting the presence of malformations or associated chromosomopathies.Material and Methods. Retrospective study of clinical cases of SUA diagnosed at the University Hospital Puerta de Hierro in Madrid (Spain) during the first trimester ultrasound between September 2008 and September 2012.Results. Prevalence of SUA was 1.1% in single pregnancies and 3.3% in twin pregnancies. Sensitivity, specificity, false positive rate, and false negative rate for the finding in the first trimester were 84.2, 99.8, 0.2, and 15.7%, respectively. 17.6% of cases had associated malformations. With an ultrasound in the 16th week most of the cases with significant fetal malformation were diagnosed.Discussion. SUA is a useful marker in the first trimester for fetal malformation pathology, as it will allow detecting a large number of cases with malformations before 20 weeks of gestation.

scholarly journals P01.13: Detection of single umbilical artery in first trimester ultrasound: its value as a marker of fetal malformation

2014 ◽  
Vol 44 (S1) ◽  
pp. 185-185
Author(s):  
E. Cabezas ◽  
C. Martínez-Payo ◽  
Y. Chiverto ◽  
Y. Nieto Jimenez ◽  
M. Ruiz de Azúa ◽  
...  
Keyword(s):  
Umbilical Artery ◽  
First Trimester ◽  
Fetal Malformation ◽  
Single Umbilical Artery ◽  
First Trimester Ultrasound

Crown–rump length measurement: a new age for first‐trimester ultrasound?

2021 ◽  
Author(s):  
J. Stirnemann ◽  
M. Massoud ◽  
N. Fries ◽  
C. Dumont ◽  
G. Haddad ◽  
...  
Keyword(s):  
First Trimester ◽  
New Age ◽  
Length Measurement ◽  
Crown Rump Length ◽  
First Trimester Ultrasound

415: The utility of first trimester ultrasound for women with a negative free fetal DNA

2015 ◽  
Vol 212 (1) ◽  
pp. S216-S217
Author(s):  
Emily Reiff ◽  
Bryann Bromley ◽  
Lori Dobson ◽  
Sarah Little
Keyword(s):  
First Trimester ◽  
Fetal Dna ◽  
First Trimester Ultrasound

Current relevance of non-invasive prenatal study of cell-free fetal DNA in the mother’s blood and prospects for its application in mass screening of pregnant women in the Russian Federation

2021 ◽  
Vol 70 (1) ◽  
pp. 19-50
Author(s):  
Elena A. Kalashnikova ◽  
Andrey S. Glotov ◽  
Elena N. Andreyeva ◽  
Ilya Yu. Barkov ◽  
Galina Yu. Bobrovnik ◽  
...  
Keyword(s):  
Mass Screening ◽  
Russian Federation ◽  
Prenatal Screening ◽  
First Trimester ◽  
Screening Programs ◽  
Non Invasive ◽  
Fetal Dna ◽  
Prenatal Diagnostic ◽  
Cell Free Fetal Dna ◽  
The Russian Federation

This review article offers an analysis of application of cell-free fetal DNA non-invasive prenatal screening test for chromosome abnormalities in the mothers blood in different countries. The diagnostic capacities of the method, its limitations, execution models and ethical aspects pertinent to its application are discussed. The data for the discordant results is shown and analyzed. The advantages of the genome-wide variant of cell-free fetal DNA analysis and the problems concerning its application in the mass screening are described. The main suggestion is to implement the contingent cell-free fetal DNA testing model for the common trisomies (for the chromosomes 21, 18 and 13) into the prenatal diagnostic screening programs in the Russian Federation. This novel model is based on the results of the mass combined first trimester prenatal screening in four federal subjects of the country completed by 2019 and is offered as an additional screening in the mid-level risk group (with cut-off from 1 : 100 to 1 : 500 or from 1 : 100 to 1 : 1000) defined according to the first trimester prenatal screening results. The basic requirements for the implementation of the contingent model in the Russian Federation are stated.

When diamniotic twins suddenly become monoamniotic twins: spontaneous septostomy of the dividing membrane

2021 ◽  
Vol 14 (7) ◽  
pp. e243513
Author(s):  
Angela Vidal ◽  
Cristina Nastasia ◽  
Markus Hodel ◽  
Joachim Kohl
Keyword(s):  
Twin Pregnancy ◽  
Rare Condition ◽  
First Trimester ◽  
Sonographic Diagnosis ◽  
Sudden Failure ◽  
Reliable Diagnosis ◽  
Accepted Standard ◽  
Perinatal Management ◽  
Twin Pregnancies ◽  
First Trimester Ultrasound

In twin pregnancies, amnionicity and chorionicity are crucial as they strongly determine prenatal and perinatal management. First trimester ultrasound allows a highly reliable diagnosis of amnionicity and chorionicity, making it an internationally accepted standard in antenatal care. However, in rare cases, amnionicity can change from diamniotic to monoamniotic throughout pregnancy, substantially impacting perinatal management. We report the case of a confirmed monochorionic diamniotic twin pregnancy with a diagnosis of spontaneous septostomy of the dividing membrane (SSDM) at 28 weeks of gestation, resulting in a pseudomonoamniotic pregnancy. Even though SSDM is a rare condition and its sonographic diagnosis might be challenging, it should be considered if, in a known diamniotic pregnancy, there is a sudden failure to visualise the intertwin membrane truly separating both twins.

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