医学
胎儿
产科
胎龄
妊娠期
单脐动脉
脐动脉
小于胎龄
出生体重
怀孕
混淆
内科学
生物
遗传学
作者
Miguel Parra‐Saavedra,Serena Simeone,Stefania Triunfo,F. Crovetto,Francesc Botet,Alfons Nadal,E. Gratacós,F. Figueras
摘要
ABSTRACT Objective To investigate whether signs of placental underperfusion ( PUP ), defined as any maternal and/or fetal vascular pathology, confer an increased risk of neonatal morbidity in late‐onset small‐for‐gestational‐age ( SGA ) fetuses with normal umbilical artery ( UA ) Doppler indices. Methods A cohort of 126 SGA singleton fetuses with normal UA Doppler indices that were delivered after 34 weeks' gestation was studied. For each case, the placenta was evaluated histologically for signs of PUP using a hierarchical and standardized classification system. Neonatal morbidity was assessed according to the score calculated from the morbidity assessment index for newborns ( MAIN ), a validated outcome scale. The independent association between PUP and neonatal morbidity was evaluated using multivariable median regression analysis. Results In 84 (66.7%) placentae, 97 placental histological findings that qualified as signs of PUP were observed. These PUP cases had a significantly higher incidence of emergency Cesarean section for non‐reassuring fetal status (44.1% vs 21.4%, respectively; P = 0.013) and neonatal metabolic acidosis at birth (33.3% vs 14.3%, respectively; P = 0.023), than did those without PUP . The median MAIN score differed significantly between those with PUP and those without (89 vs 0, respectively; P = 0.025). This difference remained significant after adjustment for potential confounders. The proportion of cases with scores indicative of mild to severe morbidity was also significantly higher in the PUP group (31% vs 14.3%, respectively; P = 0.043). Conclusion In late‐onset SGA fetuses with normal UA Doppler indices, signs of PUP imply a higher neonatal morbidity. These findings allow the phenotypic profiling of fetal growth restriction among the general population of late‐onset SGA . Copyright © 2014 ISUOG. Published by John Wiley & Sons Ltd.
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