Importance of a detailed anomaly scan after a cfDNA test indicating fetal trisomy 21, 18 or 13.

Fetal defects NIPT Trisomy Ultrasound examination cfDNA

Journal

Archives of gynecology and obstetrics
ISSN: 1432-0711
Titre abrégé: Arch Gynecol Obstet
Pays: Germany
ID NLM: 8710213

Informations de publication

Date de publication:
13 Dec 2023
Historique:
received: 22 10 2023
accepted: 15 11 2023
medline: 13 12 2023
pubmed: 13 12 2023
entrez: 13 12 2023
Statut: aheadofprint

Résumé

To investigate the effect of the presence or absence of fetal anomalies and soft markers diagnosed by ultrasound on positive predictive value (PPV) 21, 18 and 13 in pregnancies with a high-risk cfDNA result. Retrospective study including singleton pregnancies with high-risk NIPT results for common trisomies followed by invasive testing. The cases were grouped by gestational age at the time of invasive testing and by the presence or absence of fetal abnormalities or soft markers. The ultrasound was considered abnormal if at least one major defect or a soft marker was detected. A total of 173 women were included. Median maternal and gestational age was 37.7 years and 14.0 weeks, respectively. CfDNA test result showed high-risk for trisomy 21 and trisomy 18 or 13 in 119 and 54 cases, respectively. The "pre-ultrasound" PPV for trisomy 21 and for trisomy 18 or 13 were 98.3% and 68.4%, respectively. In case of a high-risk result for trisomy 21 and no fetal anomalies, the PPV was 86.7% while it was 100% if there were anomalies or markers present. In the case of a high-risk result for trisomy 18 or 13, the PPV was 9.5% if the ultrasound examination was normal and 100% if the ultrasound examination was abnormal. This study suggests that a detailed ultrasound examination performed after a cfDNA result that is high-risk for one of the common autosomal trisomies adds significantly to establishing an individualized risk assessment. This is particularly true in cases with a high-risk result for trisomies 18 or 13.

Identifiants

pubmed: 38091054
doi: 10.1007/s00404-023-07311-2
pii: 10.1007/s00404-023-07311-2
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023. The Author(s).

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Auteurs

Tobias Spingler (T)

Department of Women's Health, University of Tuebingen, Calwerstrasse 7, 72076, Tübingen, Germany.

Jiri Sonek (J)

Fetal Medicine Foundation USA, Dayton, OH, USA.
Division of Maternal Fetal Medicine, Wright State University, Dayton, OH, USA.

Markus Hoopmann (M)

Department of Women's Health, University of Tuebingen, Calwerstrasse 7, 72076, Tübingen, Germany.

Natalia Prodan (N)

Department of Women's Health, University of Tuebingen, Calwerstrasse 7, 72076, Tübingen, Germany.

Gertruda Jonaityte (G)

Department of Women's Health, University of Tuebingen, Calwerstrasse 7, 72076, Tübingen, Germany.

Tania Elger (T)

Department of Women's Health, University of Tuebingen, Calwerstrasse 7, 72076, Tübingen, Germany.

Karl Oliver Kagan (KO)

Department of Women's Health, University of Tuebingen, Calwerstrasse 7, 72076, Tübingen, Germany. KOKagan@gmx.de.

Classifications MeSH