Abstract

BackgroundHypertensive disorders complicating pregnancy (HDCP) continues to be a leading cause of maternal and neonatal mortality and morbidity. The clinical value of placental three-dimensional power Doppler (3DPD) in assessing HDCP requires further confirmation. The research was developed to assess changes of placental vascularity in HDCP using 3DPD and to investigate the placental vascularity in small for gestational age (SGA) compared with not-SGA in patients with HDCP.MethodsThere were 126 normotensive and 128 hypertensive pregnant women included in this prospective case–control study from March 2011 to March 2013. Pregnant women underwent 3DPD. Vascularization index (VI), flow index (FI) and vascularization flow index (VFI) were obtained. The placental 3DPD indices, umbilical artery systolic and diastolic ratio (S/D) and pregnancy outcomes were compared between the groups.ResultsThe placental VI and VFI were significantly lower in hypertensive women compared with normotensive women (P < 0.001 and P = 0.014, respectively), and these parameters were significantly reduced in severe preeclampsia (P < 0.001 and P = 0.003, respectively). A weak correlation was found between VI and umbilical artery S/D in HDCP group (r = -0.277, P = 0.001). In HDCP population, neonates who were postnatally diagnosed with SGA had lower VI (P = 0.041) and higher S/D (P < 0.001).DiscussionThe placental vascularity indices decreased in hypertensive women and the reduction inplacental perfusion was consistent with the severity of the hypertensive disorder. The associations betweenplacental vascularization and umbilical artery impedance may be valuable for further researches and arerequired confirmation. The significant differences in the 3DPD placental vascularization between SGA andnot-SGA in hypertensive pregnancy population may show some clinical importance that we could use tobetter assess or predict the progression and adverse outcomes in the future. Although 3DPD quantificationhas been widely used in multiple publications, we have to acknowledge its limitations.ConclusionsThe intraplacental vascularization was poor in HDCP, and especially in severe preeclampsia. Neonates with SGA had poor placental vascularization and higher umbilical artery S/D. Further studies should focus on the clinical assessment of placental 3DPD as well as a combination of placental 3DPD and other fetal Doppler indices to better predict the development and outcomes of preeclampsia.

Highlights

  • Hypertensive disorders complicating pregnancy (HDCP) continues to be a leading cause of maternal and neonatal mortality and morbidity

  • The intraplacental vascularization was poor in HDCP, and especially in severe preeclampsia

  • Further studies should focus on the clinical assessment of placental Three-dimensional power Doppler (3DPD) as well as a combination of placental 3DPD and other fetal Doppler indices to better predict the development and outcomes of preeclampsia

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Summary

Introduction

Hypertensive disorders complicating pregnancy (HDCP) continues to be a leading cause of maternal and neonatal mortality and morbidity. The clinical value of placental three-dimensional power Doppler (3DPD) in assessing HDCP requires further confirmation. Multiple tests and combination tests have been developed as screening methods for preeclampsia, including maternal serum biomarkers and Doppler parameters. Placental dysfunction and hypo-perfusion play an important role in HDCP pathophysiology and are considered to be responsible for pathologic pregnancy outcomes, such as fetal growth restriction and perinatal loss [7,8,9]. Three-dimensional power Doppler (3DPD) has been a focal point of recent placental research; it is superior to 2D Doppler in several ways, including its ability to detect the secondary and tertiary stem vessels in the placenta and intraplacental vessel characteristics, such as the vessel density, branching, caliber changes and tortuosity, which can be shown using 3DPD [8, 10, 11]. Quantitative 3DPD analysis has been used to assess placental perfusion and vascularization indices, which potentially reflect both utero-placental and feto-placental blood perfusion [10]

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