First-trimester prediction of preterm prelabour rupture of membranes incorporating cervical length measurement

医学 产科 逻辑回归 胎膜早破 接收机工作特性 怀孕 回顾性队列研究 膜破裂 妇科 试验预测值 妊娠期 外科 内科学 生物 遗传学
作者
Line Rode,C. B. Wulff,Charlotte Kvist Ekelund,Eva Hoseth,Olav Bjørn Petersen,Ann Tabor,Vanessa El-Achi,Jon Hyett,A. McLennan
出处
期刊:European Journal of Obstetrics & Gynecology and Reproductive Biology [Elsevier]
卷期号:284: 76-81
标识
DOI:10.1016/j.ejogrb.2023.03.003
摘要

To examine early pregnancy risk factors for preterm prelabour rupture of membranes (PPROM) and develop a predictive model.Retrospective analysis of a cohort of mixed-risk singleton pregnancies screened in the first and second trimesters in three Danish tertiary fetal medicine centres, including a cervical length measurement at 11-14 weeks, at 19-21 weeks and at 23-24 weeks of gestation. Univariable and multivariable logistic regression analyses were employed to identify predictive maternal characteristics, biochemical and sonographic factors. Receiver operating characteristic (ROC) curve analysis was used to determine predictors for the most accurate model.Of 3477 screened women, 77 (2.2%) had PPROM. Maternal factors predictive of PPROM in univariable analysis were nulliparity (OR 2.0 (95% CI 1.2-3.3)), PAPP-A < 0.5 MoM (OR 2.6 (1.1-6.2)), previous preterm birth (OR 4.2 (1.9-8.9)), previous cervical conization (OR 3.6 (2.0-6.4)) and cervical length ≤ 25 mm on transvaginal imaging (first-trimester OR 15.9 (4.3-59.3)). These factors all remained statistically significant in a multivariable adjusted model with an AUC of 0.72 in the most discriminatory first-trimester model. The detection rate using this model would be approximately 30% at a false-positive rate of 10%. Potential predictors such as bleeding in early pregnancy and pre-existing diabetes mellitus affected very few cases and could not be formally assessed.Several maternal characteristics, placental biochemical and sonographic features are predictive of PPROM with moderate discrimination. Larger numbers are required to validate this algorithm and additional biomarkers, not currently used for first-trimester screening, may improve model performance.
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