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

Author:

Kong Shao‐Min12,Gao Chang1,Yu Ang1,Lin Shan‐Shan1,Wei Dong‐Mei13,Wang Cheng‐Rui14,Lu Jin‐Hua13,Zeng Ding‐Yuan5,Zhang Jun6,He Jian‐Rong137,Qiu Xiu137ORCID

Affiliation:

1. Division of Birth Cohort Study, Guangzhou Women and Children's Medical Center Guangzhou Medical University Guangzhou China

2. Haizhu District Center for Disease Control and Prevention Guangzhou China

3. Department of Women's Health, Guangdong Provincial Key Clinical Specialty of Women and Child Health, Guangzhou Women and Children's Medical Center Guangzhou Medical University Guangzhou China

4. State Key Laboratory of Dampness Syndrome of Chinese Medicine The Second Affiliated Hospital of Guangzhou University of Chinese Medicine Guangzhou China

5. Liuzhou Maternity and Child Healthcare Hospital Affiliated Women and Children's Hospital of Guangxi University of Science and Technology Liuzhou China

6. Ministry of Education‐Shanghai Key Laboratory of Children's Environmental Health, Xinhua Hospital, Affiliated with School of Medicine Shanghai Jiao Tong University Shanghai China

7. Guangdong Provincial Clinical Research Center for Child Health, Guangzhou Women and Children's Medical Center Guangzhou Medical University Guangzhou China

Abstract

AbstractObjectiveTo construct a simple term small‐for‐gestational‐age (SGA) neonate prediction model that is clinically practical.MethodsThis 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.ResultsThe 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.ConclusionA prediction model derived from fetal biometrics in early third trimester is satisfactory to predict SGA.

Funder

Guangdong Provincial Department of Science and Technology

Guangzhou Municipal Science and Technology Bureau

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Basic and Applied Basic Research Foundation of Guangdong Province

Publisher

Wiley

Subject

Obstetrics and Gynecology,General Medicine

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