Fetal Medicine Unit, Department of Obstetrics and Gynaecology, Hospital Universitario 12 de Octubre, Instituto de Investigación Hospital 12 de Octubre (imas12), Madrid, Spain.
Primary Care Interventions to Prevent Maternal and Child Chronic Diseases of Perinatal and Developmental Origin (RICORS network), Instituto de Salud Carlos III, Madrid, Spain.
Ultrasound Obstet Gynecol. 2023 Feb;61(2):181-190. doi: 10.1002/uog.26116.
To analyze the ability to predict perinatal survival and severe neonatal morbidity of cases with early-onset fetal growth restriction (eoFGR) using maternal variables, ultrasound parameters and angiogenic markers at the time of diagnosis.
This was a prospective observational study in a cohort of singleton pregnancies with a diagnosis of eoFGR (< 32 weeks of gestation). At diagnosis of eoFGR, complete assessment was performed, including ultrasound examination (anatomy, biometry and Doppler assessment) and maternal serum measurement of the angiogenic biomarkers, soluble fms-like tyrosine kinase-1 (sFlt-1) and placental growth factor (PlGF). Logistic regression models for the prediction of perinatal survival (in cases diagnosed at < 28 weeks) and severe neonatal morbidity (in all liveborn cases) were calculated.
In total, 210 eoFGR cases were included, of which 185 (88.1%) survived perinatally. The median gestational age at diagnosis was 27 + 0 weeks. All cases diagnosed at ≥ 28 weeks survived. In cases diagnosed < 28 weeks, survivors (vs non-survivors) had a higher gestational age (26.1 vs 24.4 weeks), estimated fetal weight (EFW; 626 vs 384 g), cerebroplacental ratio (1.1 vs 0.9), PlGF (41 vs 18 pg/mL) and PlGF multiples of the median (MoM; 0.10 vs 0.06) and lower sFlt-1/PlGF ratio (129 vs 479) at the time of diagnosis (all P < 0.001). The best combination of two variables for predicting perinatal survival was provided by EFW and PlGF MoM (area under the receiver-operating-characteristics curve (AUC), 0.84 (95% CI, 0.75-0.92)). These were also the best variables for predicting severe neonatal morbidity (AUC, 0.73 (95% CI, 0.66-0.80)).
A model combining EFW and maternal serum PlGF predicts accurately perinatal survival in eoFGR cases diagnosed before 28 weeks of gestation. Prenatal prediction of severe neonatal morbidity in eoFGR cases is modest regardless of the model used. © 2022 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.
分析在诊断时使用母体变量、超声参数和血管生成标志物预测早发型胎儿生长受限(eoFGR)围产儿生存和严重新生儿发病率的能力。
这是一项在单胎妊娠队列中进行的前瞻性观察性研究,这些妊娠被诊断为 eoFGR(<32 孕周)。在诊断为 eoFGR 时,进行了完整的评估,包括超声检查(解剖学、生物测量和多普勒评估)和母体血清测量血管生成生物标志物可溶性 fms 样酪氨酸激酶-1(sFlt-1)和胎盘生长因子(PlGF)。计算了预测围产儿生存(在诊断为 <28 周的病例中)和严重新生儿发病率(在所有活产病例中)的逻辑回归模型。
共纳入 210 例 eoFGR 病例,其中 185 例(88.1%)围产儿存活。诊断时的中位孕龄为 27+0 周。所有诊断为≥28 周的病例均存活。在诊断为<28 周的病例中,幸存者(与非幸存者相比)的胎龄更高(26.1 周 vs 24.4 周),估计胎儿体重(EFW;626 克 vs 384 克),脑胎盘比(1.1 比 0.9),PlGF(41 皮克/毫升 vs 18 皮克/毫升)和 PlGF 中位数倍数(0.10 比 0.06),sFlt-1/PlGF 比值较低(129 比 479)(均 P<0.001)。预测围产儿生存的两个变量的最佳组合是 EFW 和 PlGF MoM(受试者工作特征曲线下面积(AUC),0.84(95%CI,0.75-0.92))。这些变量也是预测严重新生儿发病率的最佳变量(AUC,0.73(95%CI,0.66-0.80))。
在诊断为<28 周的 eoFGR 病例中,联合 EFW 和母体血清 PlGF 的模型可准确预测围产儿生存。无论使用哪种模型,对 eoFGR 病例严重新生儿发病率的产前预测都只是中等水平。