{"title":"Development and validation of a risk prediction model for placental abruption in patients with preeclampsia","authors":"Mei Yang, Menghui Wang, Qing Zhu, Nanfang Li","doi":"10.1016/j.placenta.2025.03.005","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>To develop a validated risk prediction model for placental abruption in preeclamptic patients with singleton pregnancies firstly.</div></div><div><h3>Methods</h3><div>Data from 1448 preeclamptic patients with singleton pregnancies who delivered between January 2013 and December 2022 were reviewed. Variables, including demographic characteristics, laboratory test results, comorbidities, and aspirin use were collected and analyzed. The preeclamptic patients were divided into a training set and a validation set according to the time of delivery. Logistic regression with a backward stepwise elimination method was used for variable screening and nomogram construction. The area under the receiver operating characteristic curve and calibration curve were used to evaluate its accuracy. Decision curve analysis and clinical impact curves were conducted to assess predictive performance.</div></div><div><h3>Results</h3><div>Finally, 1448 preeclamptic patients were included. We collected 50 variables for further analysis. Multivariate logistic regression analysis revealed that severity, subtype, premature rupture of membranes, urinary casts, diastolic blood pressure, aspartate aminotransferase, serum potassium, and fibrin degradation product levels were predictors of placental abruption. These factors were used to construct the nomogram model, which showed good concordance and accuracy. The area under the receiver operating characteristic curve values of the training set and the validation set were 0.767 (95 % CI = 0.728–0.806, P < 0.001) and 0.800 (95 % CI = 0.728–0.872, P < 0.001). Calibration curves revealed significant agreement between the nomogram model and actual observations. Receiver operating characteristic curve analysis and decision curve analysis indicated that the nomogram had good predictive performance.</div></div><div><h3>Discussion</h3><div>The prediction model can accurately estimate the risk of placental abruption in preeclamptic patients.</div></div>","PeriodicalId":20203,"journal":{"name":"Placenta","volume":"164 ","pages":"Pages 1-9"},"PeriodicalIF":3.0000,"publicationDate":"2025-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Placenta","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0143400425000724","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
方法 回顾性分析 2013 年 1 月至 2022 年 12 月间分娩的 1448 例单胎妊娠先兆子痫患者的数据。收集并分析了包括人口统计学特征、实验室检查结果、合并症和阿司匹林使用情况在内的变量。根据分娩时间将先兆子痫患者分为训练集和验证集。在筛选变量和构建提名图时采用了后向逐步排除法的逻辑回归。采用接收者操作特征曲线下面积和校准曲线来评估其准确性。结果最终纳入了 1448 例先兆子痫患者。我们收集了 50 个变量进行进一步分析。多变量逻辑回归分析显示,严重程度、亚型、胎膜早破、尿铸型、舒张压、天冬氨酸氨基转移酶、血清钾和纤维蛋白降解产物水平是胎盘早剥的预测因素。利用这些因素构建的提名图模型显示出良好的一致性和准确性。训练集和验证集的接收者操作特征曲线下面积值分别为0.767(95 % CI = 0.728-0.806, P <0.001)和0.800(95 % CI = 0.728-0.872, P <0.001)。校准曲线显示,提名图模型与实际观察结果之间存在明显的一致性。讨论该预测模型可准确估计子痫前期患者发生胎盘早剥的风险。
Development and validation of a risk prediction model for placental abruption in patients with preeclampsia
Introduction
To develop a validated risk prediction model for placental abruption in preeclamptic patients with singleton pregnancies firstly.
Methods
Data from 1448 preeclamptic patients with singleton pregnancies who delivered between January 2013 and December 2022 were reviewed. Variables, including demographic characteristics, laboratory test results, comorbidities, and aspirin use were collected and analyzed. The preeclamptic patients were divided into a training set and a validation set according to the time of delivery. Logistic regression with a backward stepwise elimination method was used for variable screening and nomogram construction. The area under the receiver operating characteristic curve and calibration curve were used to evaluate its accuracy. Decision curve analysis and clinical impact curves were conducted to assess predictive performance.
Results
Finally, 1448 preeclamptic patients were included. We collected 50 variables for further analysis. Multivariate logistic regression analysis revealed that severity, subtype, premature rupture of membranes, urinary casts, diastolic blood pressure, aspartate aminotransferase, serum potassium, and fibrin degradation product levels were predictors of placental abruption. These factors were used to construct the nomogram model, which showed good concordance and accuracy. The area under the receiver operating characteristic curve values of the training set and the validation set were 0.767 (95 % CI = 0.728–0.806, P < 0.001) and 0.800 (95 % CI = 0.728–0.872, P < 0.001). Calibration curves revealed significant agreement between the nomogram model and actual observations. Receiver operating characteristic curve analysis and decision curve analysis indicated that the nomogram had good predictive performance.
Discussion
The prediction model can accurately estimate the risk of placental abruption in preeclamptic patients.
期刊介绍:
Placenta publishes high-quality original articles and invited topical reviews on all aspects of human and animal placentation, and the interactions between the mother, the placenta and fetal development. Topics covered include evolution, development, genetics and epigenetics, stem cells, metabolism, transport, immunology, pathology, pharmacology, cell and molecular biology, and developmental programming. The Editors welcome studies on implantation and the endometrium, comparative placentation, the uterine and umbilical circulations, the relationship between fetal and placental development, clinical aspects of altered placental development or function, the placental membranes, the influence of paternal factors on placental development or function, and the assessment of biomarkers of placental disorders.