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The potential impact of universal screening for vasa previa in the prevention of stillbirths

  • Weiyu Zhang , Yinka Oyelese ORCID logo EMAIL logo , Ali Javinani ORCID logo , Alireza Shamshirsaz and Ranjit Akolekar
Published/Copyright: September 9, 2024

Abstract

Objectives

To estimate the number of pregnancies complicated by vasa previa annually in nine developed countries, and the potential preventable stillbirths associated with undiagnosed cases. We also assessed the potential impact of universal screening for vasa previa on reducing stillbirth rates.

Methods

We utilized nationally-reported birth and stillbirth data from public databases in the United States, United Kingdom, Canada, Germany, Ireland, Greece, Sweden, Portugal, and Australia. Using the annual number of births and the number and rate of stillbirths in each country, and the published incidence of vasa previa and stillbirth rates associated with the condition, we estimated the expected annual number of cases of vasa previa, those that would result in a livebirth, and the potential preventable stillbirths with and without prenatal diagnosis.

Results

There were 6,099,118 total annual births with 32,550 stillbirths, corresponding to a summary stillbirth rate of 5.34 per 1,000 pregnancies. The total expected vasa previa cases was estimated to be 5,007 (95 % CI: 3,208–7,201). The estimated number of livebirths would be 4,937 (95 % CI: 3,163–7,100) and 3,610 (95 % CI: 2,313–5,192) in pregnancies with and without a prenatal diagnosis of VP. This implies that prenatal diagnosis would potentially prevent 1,327 (95 % CI: 850–1,908) stillbirths in these countries, corresponding to a potential reduction in stillbirth rate by 4.72 % (95 % CI: 3.80–5.74) if routine screening for vasa previa was performed.

Conclusions

Our study highlights the importance of universal screening for vasa previa and suggests that prenatal diagnosis of prevention could potentially reduce 4–5 % of stillbirths.


Corresponding author: Yinka Oyelese, MD, Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Ave, KS3, Boston 02215, MA, USA; and Fetal Care and Surgery Center (FCSC), Division of Fetal Medicine and Surgery, Boston Children’s Hospital, Harvard Medical School, Boston, MA, USA, E-mail:
Weiyu Zhang and Yinka Oyelese share first authorship. Yinka Oyelese and Ranjit Akolekar share senior authorship.
  1. Research ethics: Not applicable.

  2. Informed consent: Not applicable.

  3. Author contributions: All the authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  4. Competing interests: Dr. Oyelese has received royalties for authorship from UpToDate and BMJ Best Practice. In addition, Dr. Oyelese is on the Scientific Advisory Board for Sonio LLC, for which he receives honoraria. The remaining authors report no conflict of interest.

  5. Research funding: None declared.

  6. Data availability: Not applicable.

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Received: 2024-05-05
Accepted: 2024-08-14
Published Online: 2024-09-09
Published in Print: 2024-11-26

© 2024 Walter de Gruyter GmbH, Berlin/Boston

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