First-Trimester Ultrasound Screening in Routine Obstetric Practice
- PMID: 38723258
- DOI: 10.1097/AOG.0000000000005594
First-Trimester Ultrasound Screening in Routine Obstetric Practice
Abstract
Technologic advances and ultrasonographer-physician experience in fetal imaging have led to significant improvements in our ability to distinguish between normal and abnormal fetal structural development in the latter part of the first trimester. As a critical component of pregnancy care, assessment of fetal anatomy at the end of the first trimester with a standardized imaging protocol should be offered to all pregnant patients regardless of aneuploidy screening results because it has been demonstrated to identify approximately half of fetal structural malformations. Early identification of abnormalities allows focused genetic counseling, timely diagnostic testing, and subspecialist consultation. In addition, a normal ultrasound examination result offers some degree of reassurance to most patients. Use of cell-free DNA alone for aneuploidy screening while foregoing an accompanying early anatomic evaluation of the fetus will result in many anomalies that are typically detected in the first trimester not being identified until later in pregnancy, thus potentially diminishing the quality of obstetric care for pregnant individuals and possibly limiting their reproductive options, including pregnancy termination.
Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc.
Conflict of interest statement
Financial Disclosure Dr. Platt serves as a consultant for General Electric Healthcare and serves on the advisory board for Natera, Pulsenmore, Nuvocares, Mahmee, and Triceimaging. Dr. Bromley did not report any potential conflicts of interest.
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