Improved detection rate of structural abnormalities in the first trimester using an extended examination protocol

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:2986148 17 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Improved detection rate of structural abnormalities in the first trimester using an extended examination protocol
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Objective: To assess the potential of first-trimester sonography in the detection of fetal abnormalities using an extended protocol that is achievable with reasonable resources of time, personnel and ultrasound equipment. Methods: This was a prospective two-center 2-year study of 5472 consecutive unselected pregnant women examined at 12 to 13 + 6 gestational weeks. Women were examined using an extended morphogenetic ultrasound protocol that, in addition to the basic evaluation, involved a color Doppler cardiac sweep and identification of early contingent markers for major abnormalities. Results: The prevalence of lethal and severe malformations was 1.39%. The first-trimester scan identified 40.6% of the cases detected overall and 76.3% of major structural defects. The first-trimester detection rate (DR) for major congenital heart disease (either isolated or associated with extracardiac abnormalities) was 90% and that for major central nervous system anomalies was 69.5%. In fetuses with increased nuchal translucency (NT), the first-trimester DR for major anomalies was 96%, and in fetuses with normal NT it was 66.7%. Most (67.1%) cases with major abnormalities presented with normal NT. Conclusions: A detailed first-trimester anomaly scan using an extended protocol is an efficient screening method to detect major fetal structural abnormalities in low-risk pregnancies. It is feasible at 12 to 13 + 6 weeks with ultrasound equipment and personnel already used for routine first-trimester screening. Rate of detection of severe malformations is greater in early- than in mid-pregnancy and on postnatal evaluation. Early heart investigation could be improved by an extended protocol involving use of color Doppler. Copyright © 2013 ISUOG. Published by John Wiley & Sons Ltd.
Έτος δημοσίευσης:
2013
Συγγραφείς:
Iliescu, D.
Tudorache, S.
Comanescu, A.
Antsaklis, P.
Cotarcea, S.
Novac, L.
Cernea, N.
Antsaklis, A.
Περιοδικό:
Ultrasound in Obstetrics and Gynecology
Τόμος:
42
Αριθμός / τεύχος:
3
Σελίδες:
300-309
Λέξεις-κλειδιά:
adult; central nervous system; clinical trial; congenital heart malformation; Doppler echocardiography; echography; feasibility study; female; fetus echography; first trimester pregnancy; human; multicenter study; pregnancy; procedures; prospective study; article; color ultrasound flowmetry; congenital disorder; congenital heart malformation; congenital malformation; Doppler echocardiography; echography; fetus echography; methodology; prenatal diagnosis; screening; ultrasound, Adult; Central Nervous System; Echocardiography, Doppler, Color; Feasibility Studies; Female; Heart Defects, Congenital; Humans; Pregnancy; Pregnancy Trimester, First; Prospective Studies; Ultrasonography, Prenatal, color Doppler; congenital abnormalities; first trimester; prenatal diagnosis; screening; ultrasound, Adult; Central Nervous System; Echocardiography, Doppler, Color; Feasibility Studies; Female; Heart Defects, Congenital; Humans; Pregnancy; Pregnancy Trimester, First; Prospective Studies; Ultrasonography, Prenatal
Επίσημο URL (Εκδότης):
DOI:
10.1002/uog.12489
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