TY - JOUR
T1 - Study protocol for first national vasa previa perinatal registry
AU - Paulosky, Kayla E.
AU - Santos-Roca, Antonio
AU - Corbetta-Rastelli, Chiara
AU - Cudjoe, Efe
AU - Esterquest, David
AU - Fadairo, Oluwaseun
AU - Fickau, Brittany A.
AU - Funfar, Brenna
AU - Perelman, Allison
AU - Ross, Naima
AU - Sibbald, Carrie A.
AU - Todhunter, Logan
AU - Waites, Bethany T.
AU - Chon, Andrew H.
AU - DeBolt, Chelsea A.
AU - Drennen, Kathryn
AU - Hanks, Laura
AU - Jelin, Angie C.
AU - Kush, Michelle
AU - Lynch, Tara
AU - Malshe, Amol
AU - Miller, Lauren A.
AU - Munoz, Jessian L.
AU - Norton, Mary E.
AU - Rincon, Monica
AU - Roman, Ashley S.
AU - Russo, Melissa
AU - St. Onge, Rachelle
AU - Oyelese, Yinka
AU - Steinberg, Guy
AU - Toscano, Marika
N1 - Publisher Copyright:
© 2026, Paulosky et al. This is an open access article distributed under the terms of the Creative Commons Attribution License https://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2026
Y1 - 2026
N2 - Vasa previa is a rare but potentially catastrophic obstetric condition characterized by unprotected fetal blood vessels over or adjacent to the internal cervical os. Although advances in prenatal ultrasound have dramatically improved neonatal survival through planned cesarean delivery, many aspects of vasa previa remain poorly understood. Existing studies are limited by small sample sizes, single-center designs, heterogeneous diagnostic criteria, and inconsistent reporting of clinical outcomes, highlighting the need for large, systematically collected multicenter datasets. Here we describe, to our knowledge, the first United States multicenter registry of pregnancies complicated by vasa previa without concurrent placenta previa, the U.S. Vasa Previa Registry (US-VPR). This report outlines the rationale, design, and implementation of a large, multicenter, retrospective registry developed to characterize patient demographics, risk factors, placental pathology, natural history, antenatal management, maternal outcomes, neonatal outcomes, and healthcare utilization associated with vasa previa. The US-VPR includes contributions from 15 tertiary referral centers and represents the largest multicenter cohort of pregnancies complicated by vasa previa without concurrent placenta previa reported to date. By leveraging multicenter collaboration and standardized data collection, the registry provides a unique opportunity to characterize variation in clinical practice and outcomes across referral centers, strengthen the evidence base for this rare condition, and inform future prospective studies and evidence-based patient counseling.
AB - Vasa previa is a rare but potentially catastrophic obstetric condition characterized by unprotected fetal blood vessels over or adjacent to the internal cervical os. Although advances in prenatal ultrasound have dramatically improved neonatal survival through planned cesarean delivery, many aspects of vasa previa remain poorly understood. Existing studies are limited by small sample sizes, single-center designs, heterogeneous diagnostic criteria, and inconsistent reporting of clinical outcomes, highlighting the need for large, systematically collected multicenter datasets. Here we describe, to our knowledge, the first United States multicenter registry of pregnancies complicated by vasa previa without concurrent placenta previa, the U.S. Vasa Previa Registry (US-VPR). This report outlines the rationale, design, and implementation of a large, multicenter, retrospective registry developed to characterize patient demographics, risk factors, placental pathology, natural history, antenatal management, maternal outcomes, neonatal outcomes, and healthcare utilization associated with vasa previa. The US-VPR includes contributions from 15 tertiary referral centers and represents the largest multicenter cohort of pregnancies complicated by vasa previa without concurrent placenta previa reported to date. By leveraging multicenter collaboration and standardized data collection, the registry provides a unique opportunity to characterize variation in clinical practice and outcomes across referral centers, strengthen the evidence base for this rare condition, and inform future prospective studies and evidence-based patient counseling.
UR - https://www.scopus.com/pages/publications/105047644965
U2 - 10.1371/journal.pone.0355045
DO - 10.1371/journal.pone.0355045
M3 - Article
C2 - 42607098
AN - SCOPUS:105047644965
SN - 1932-6203
VL - 21
JO - PLOS One
JF - PLOS One
IS - 8
M1 - e0355045
ER -