How to enhance the applicability of a risk prediction model for term small‐for‐gestational‐age neonates in clinical settings?

医学 逻辑回归 胎龄 百分位 小于胎龄 人口 生物识别 产科 预测建模 队列 怀孕 独生子女 期限(时间) 统计 内科学 人工智能 计算机科学 数学 物理 环境卫生 生物 量子力学 遗传学
作者
Shao‐Min Kong,Chang Gao,Ang Yu,Shanshan Lin,Dongmei Wei,Cheng‐Rui Wang,Jinhua Lu,Dingyuan Zeng,Jun Zhang,Jianrong He,Xiu Qiu
出处
期刊:International journal of gynaecology and obstetrics [Wiley]
卷期号:165 (3): 1104-1113
标识
DOI:10.1002/ijgo.15268
摘要

Abstract Objective To construct a simple term small‐for‐gestational‐age (SGA) neonate prediction model that is clinically practical. Methods This analysis was based on the Born in Guangzhou Cohort Study (BIGCS). Mothers who had a singleton pregnancy, delivered a term neonate, and had an ultrasonography within 30 + 0 to 32 + 6 weeks of gestation were included. Term SGA was defined with customized population percentiles. Prediction models were constructed with backward selection logistic regression in a four‐step approach, where model 1 contained fetal biometrics only, models 2 and 3 included maternal features and a time factor (weeks between ultrasonography and delivery), respectively; and model 4 contained all features mentioned. The prediction performance of individual models was evaluated based on area under the curve (AUC) and a calibration test was performed. Results The prevalence of SGA in the study population of 21 346 women was 11.5%. With a complete‐case analysis approach, data of 19 954 women were used for model construction and validation. The AUC of the four models were 0.781, 0.793, 0.823, and 0.834, respectively, and all were well‐calibrated. Model 3 consisted of fetal biometrics and corrected for time to delivery was chosen as the final model to build risk prediction graphs for clinical use. Conclusion A prediction model derived from fetal biometrics in early third trimester is satisfactory to predict SGA.

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