Sydney Institute for Women, Children and their Families, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia,
Sydney Institute for Women, Children and their Families, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.
Fetal Diagn Ther. 2020;47(8):624-629. doi: 10.1159/000506541. Epub 2020 Apr 8.
Preterm prelabour rupture of membranes (PPRoM) is commonly associated with preterm delivery and affects up to 3% of all pregnancies. It is associated with high rates of morbidity and mortality for the mother and the newborn.
To identify risk factors for PPRoM and develop a model for first-trimester prediction of risk of PPRoM.
A retrospective analysis of a series of women who had first-trimester (11-13+6 weeks) screening for aneuploidy and pre-eclampsia and delivered in the same institution was performed. Univariate and multivariate logistic regression analyses were used to identify maternal and pregnancy factors and then develop a clinical prediction model for PPRoM.
10,280 women were screened between April 2010 and October 2016. 144 (1.4%) had PPRoM. Maternal factors predictive of PPRoM included nulliparity (parous women, OR 0.53; 95% CI 0.4-0.8), pre-existing diabetes mellitus (DM) (Type 1 DM, OR 6.7; 95% CI 2.3-19.4, Type 2 DM, OR 5.3; 95% CI 1.6-18.3), maternal age group (p = 0.004), and BMI category (p = 0.012). Uterine artery pulsatility index (UAPI) and biochemical parameters (PAPP-A, free βHCG) did not reach statistical significance. The predictive model had moderate efficacy with an area under the ROC curve of 0.67.
Several maternal characteristics collected during first-trimester screening predict PPRoM. Biomarkers currently measured during first-trimester screening (PAPP-A, βHCG, and UAPI) do not predict PPRoM. Whilst a predictive model can be generated with information currently collected at 11-13+6 weeks, this has only modest screening performance. First-trimester screening provides a structured framework where other predictors could improve model performance, and future studies should focus on the addition of other risk factors and biomarkers that may improve screening efficacy.
未足月胎膜早破(PPRoM)常与早产有关,影响多达 3%的所有妊娠。它与母亲和新生儿的高发病率和死亡率有关。
确定 PPRoM 的危险因素,并建立一种预测 PPRoM 风险的模型。
对在同一机构进行 11-13+6 周唐氏综合征和子痫前期筛查并分娩的一系列孕妇进行回顾性分析。采用单因素和多因素 logistic 回归分析确定母体和妊娠因素,然后建立 PPRoM 的临床预测模型。
2010 年 4 月至 2016 年 10 月,共有 10280 名妇女接受筛查。144 例(1.4%)发生 PPRoM。预测 PPRoM 的母体因素包括初产妇(经产妇,OR0.53;95%CI0.4-0.8)、孕前糖尿病(DM)(1 型 DM,OR6.7;95%CI2.3-19.4,2 型 DM,OR5.3;95%CI1.6-18.3)、母亲年龄组(p=0.004)和 BMI 类别(p=0.012)。子宫动脉搏动指数(UAPI)和生化参数(PAPP-A、游离βHCG)未达到统计学意义。预测模型效能中等,ROC 曲线下面积为 0.67。
在早孕筛查中收集的一些母体特征可预测 PPRoM。目前在早孕筛查中测量的生物标志物(PAPP-A、βHCG 和 UAPI)不能预测 PPRoM。虽然可以用 11-13+6 周时收集的信息生成预测模型,但该模型的筛查性能仅为中等。早孕筛查提供了一个结构化的框架,在这个框架中可以加入其他预测因素来提高模型性能,未来的研究应该侧重于添加其他可能提高筛查效果的危险因素和生物标志物。