Revisiting the Implications of a Wide or Narrow Fetal Cavum Septi Pellucidi

Author:

Sichitiu Joanna12ORCID,Ghannad‐Zadeh Kimia3,Van Mieghem Tim14,Toi Ants5,Greenfeld Elena6,Chitayat David7,Shinar Shiri14ORCID

Affiliation:

1. Fetal Medicine Unit, Department of Obstetrics and Gynaecology Mount Sinai Hospital and University of Toronto Toronto Ontario Canada

2. Woman‐Mother‐Child Department Lausanne University Hospital (CHUV) Lausanne Switzerland

3. Temerty Faculty of Medicine University of Toronto Toronto Ontario Canada

4. Ontario Fetal Centre Toronto Ontario Canada

5. Department of Radiology Mount Sinai Hospital, University of Toronto Toronto Ontario Canada

6. Division of Diagnostic Medical Genetics, Department of Pathology and Laboratory Medicine Mount Sinai Hospital, University of Toronto Toronto Ontario Canada

7. Prenatal Diagnosis and Medical Genetics, Department of Obstetrics and Gynecology Mount Sinai Hospital, University of Toronto Toronto Ontario Canada

Abstract

ObjectivesTo investigate short‐term neonatal developmental outcomes in fetuses with an isolated wide or narrow cavum septi pellucidi (CSP) using new reference ranges.MethodsA cross‐sectional study on fetuses at 16 + 0 to 36 + 6 weeks of gestation between December 2020 and January 2022. CSP width reference ranges were constructed from low‐risk pregnancies. Wide and narrow CSPs were defined as measurements above the 95th percentile and below the 5th percentile, respectively. For the primary outcome fetuses with normal neurosonograms were included. Neonatal developmental outcomes were assessed using the Survey of Well‐being of Young Children (SWYC).ResultsA total of 352 fetuses were included in this study, of whom 138 were healthy and had uncomplicated neonatal outcomes. These fetuses constituted the control group and were used to construct the CSP width reference ranges. Of 185 fetuses in the neurosonography group, 9.7% had wide and 7.6% had narrow CSPs, of whom 33.3% and 22.2%, respectively, scored below the SWYC threshold for expected developmental milestones, a rate similar to that reported in the general population.ConclusionsThe presence of a prenatally isolated wide or narrow CSP does not appear to increase the risk of neonatal neurodevelopmental delay.

Publisher

Wiley

Reference23 articles.

1. On the cavum septi pellucidi and the cavum vergae;Oteruelo FT;Anat Anz,1986

2. Long‐term postnatal outcome of fetuses with prenatally suspected septo‐optic dysplasia

3. The cavum septi pellucidi in euploid and aneuploid fetuses

4. Prenatal diagnosis of dilated cava septi pellucidi et vergae: associated anomalies, differential diagnosis, and pregnancy outcome;Bronshtein M;Obstet Gynecol,1992

5. Dilated cavum septi pellucidi in fetuses with microdeletion 22q11

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