Purpose: In high-risk pregnancies, uterine artery (UtA) Doppler flow examination has been reported to be valuable for predicting pregnancy-induced hypertension (PIH) and fetal growth restriction (FGR). However, it has scarcely been evaluated in low-risk populations. The aim of this study is to analyze the association between abnormal UtA Doppler flow and adverse pregnancy outcomes in low-risk populations.
Subjects and Methods: This prospective observational study was conducted from 2009 to 2010. A total of 880 scans were obtained in the late second trimester. The inclusion criteria were as follows: (1) the neonate did not have congenital malformations; (2) the mother had a low-risk pregnancy, as determined by Japanese pregnancy risk score; and (3) the neonate was born in our institution. The UtA pulsatility index (PI) was measured on both sides, and the mean PI was calculated. An elevated UtA-PI was defined as a UtA-PI above the 95th percentile. Light-for-date (LFD) infants were defined as infants with birth weight below the 10th percentile according to Japanese standards. Statistical analysis was conducted by the χ
2 or Fisher’s exact tests. In addition, we performed multivariate logistic regression analysis to assess relative factors.
Results and Discussion: One hundred and seventy-three women with singleton pregnancies met the inclusion criteria. Three women had an elevated PI; none of these women developed PIH (p=0.978), and two gave birth to LFD infants (p=0.020). Elevated PIs were significantly related to giving birth to LFD infants, but no such relationship was observed in connection with PIH. Multivariate logistic regression analysis showed that elevated PI was the strongest risk factor involved with giving birth to LFD infants. In contrast, no risk factor was found to be associated with PIH.
Conclusion: In low-risk pregnancies, performing UtA Doppler flow velocimetry might predict LFD infants. No significant association was observed between elevated PI and PIH; this might be because there are only a few cases of PIH in low-risk populations.
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