Fetal Structural Anomalies and Vasa Previa Newly Identified After an Unremarkable Mid-Trimester Systematic Ultrasound Screening: Clinical Significance and Follow-Up Findings in 47 Cases.
Sep 2026· Journal of Clinical Ultrasound· 0 citations· 28 references
Medicine
Abstract
Background
Some fetal structural anomalies and cases of vasa previa may not be detectable until after mid-trimester ultrasound screening. This study evaluated the spectrum, sonographic features, and perinatal outcomes of these newly detected abnormalities.
Methods
We retrospectively reviewed 14 579 singleton pregnancies that underwent standardized mid-trimester ultrasound screening with no structural abnormalities detected at that time. Among these, 47 fetuses had anomalies newly identified before delivery. One additional pregnancy, in which multiple malformations were already detected at mid-trimester screening, was encountered during the same period. Because this case did not meet the inclusion criterion of an unremarkable mid-trimester scan, it was not included in the primary cohort and is described separately.
Results
The detection proportion was 3.22 per 1000 pregnancies (47). Digestive and hepatobiliary anomalies accounted for 25.5% (12), followed by central nervous system anomalies 23.4% (11). Vasa previa was diagnosed in three pregnancies 6.4% (3). A total of 14 pregnancies were terminated. Four live-born infants died during the neonatal period; 21.3% (10) underwent surgery. A total of 8 of 10 surgically treated infants survived to hospital discharge. The overall survival to discharge was 61.7% (29).
Conclusions
Supplementary ultrasound after mid-trimester screening can identify additional fetal structural anomalies and vasa previa and may inform prenatal counseling, delivery planning, and neonatal management.
In a screening population with referral enrichment, about 1 in 57 pregnancies had a structural anomaly identified at the 11–13+6-week scan, dominated by cardiac and abdominal-wall defects, supporting the integration of systematic anatomical assessment and genetic evaluation into first-trimester screening.
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The value of serial prenatal ultrasonography in the diagnosis and longitudinal assessment of congenital pulmonary airway malformation is highlighted, and recognition of spontaneous regression during pregnancy may help avoid unnecessary intervention in appropriately selected cases.
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To retrospectively assess concordance in prenatal detection of craniofacial malformations (CFMs) between earlier fetal ultrasound (US) examinations performed at 13–17 weeks and routine second-trimester anomaly scans performed at 18–22 weeks, using a paired cohort with postnatal or fetopsy/autopsy confirmation....
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OBJECTIVE
To explore whether ultrasound can identify findings suggestive of fetal complex congenital heart disease in highly selected high-risk fetuses during the mid-first trimester.
METHODS
A retrospective analysis was conducted on 23 highly selected high-risk fetuses who related to CHD that underwent ultrasound ex...
Shui-Hua Yang, Yin-Bei Qin, Long-Bin Yang et al.· Journal of Clinical Ultrasou...· 0 citations
Background: Vasa previa is a rare but potentially life-threatening obstetric condition in which unprotected fetal vessels traverse the fetal membranes over or in close proximity to the internal cervical os. Prenatal diagnosis using grayscale ultrasonography and color Doppler allows identification of the aberrant fetal...