Sensitivity of prenatal ultrasound for detection of trisomy 18

J Matern Fetal Neonatal Med. 2019 Nov;32(22):3716-3722. doi: 10.1080/14767058.2018.1471460. Epub 2018 May 15.

Abstract

Objectives: To evaluate the sensitivity of prenatal ultrasound (US) for trisomy (T18) diagnosis and describe US findings in a large tertiary care institution in the USA. Materials and methods: This was a retrospective cohort of all T18 cases diagnosed at our institution from October 2004 to October 2014 based on prenatal or postnatal genetic diagnostic testing. We included all women with a fetus affected by T18 who had a comprehensive US by a maternal-fetal medicine specialist performed at our institution. US findings were reviewed, classified by organ system, and categorized as an anomaly or soft marker. Chi-square or t-test was used for statistical analysis. Results: We included 128 cases of T18 with confirmed cytogenetic analysis -110 (86%) of which were diagnosed prenatally or suspected by cell-free DNA and confirmed postnatally, and 18 of which underwent neonatal blood sampling alone. One hundred and twenty-one (95%) had at least one abnormal US finding. Anomalies were more frequently identified on US at ≥20 weeks as compared with <20 weeks (93% versus 76%; p = .004). The mean number of findings detected per fetus was 5.1 ± 3.0. Fetuses diagnosed by postnatal sampling alone had a similar number of US exams performed and number of abnormal findings compared to those diagnosed prenatally. Conclusion: Ninety-five percent of fetuses with T18 had at least one abnormal US finding. This sensitivity of is higher than reported in most prior studies, but is not 100%, and should be considered when counseling women regarding prenatal diagnosis of T18. Rationale: Historical detection rates for abnormal sonographic findings in trisomy 18 fetuses range from 70% to 100%. These studies are limited by small sample sizes. This is a contemporary study of ultrasound findings in a large group of women with confirmed trisomy 18 by prenatal or postnatal genetic diagnosis. We provide expansive detail on soft markers and anomalies broken down by organ-system and gestational age.

Keywords: Fetal anomaly; prenatal ultrasound; trisomy 18.

Publication types

  • Evaluation Study

MeSH terms

  • Adult
  • Female
  • Genetic Testing
  • Gestational Age
  • Humans
  • Predictive Value of Tests
  • Pregnancy
  • Pregnancy Outcome / epidemiology
  • Retrospective Studies
  • Sensitivity and Specificity
  • Trisomy 18 Syndrome / diagnosis*
  • Trisomy 18 Syndrome / epidemiology
  • Ultrasonography, Prenatal*