Mezam地区妊娠期高血压预测模型的建立与验证

Nkem Ernest Njukang, Thomas Obinchemti EGBE, Nicolas Tendongfor, Tah Aldof Yoah, Kah Emmanuel Nji, M. Sama, Fidelis Atabon AKO, J. Kamgno
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摘要

目的:本研究旨在建立并验证喀麦隆西北地区Mezam地区妊娠期高血压(GH)风险增加的预测模型。方法:采用回顾性队列设计。1183名参与者的数据随机分为衍生(n = 578)和验证(n = 585)数据集。纳入标准为无慢性高血压的女性。主要结局是妊娠期高血压。采用问卷调查和数据抽象化表格进行数据收集。采用χ2检验、独立样本t检验和多元logistic回归(建立预测模型)进行数据分析。对于每个重要变量,通过将系数(β)乘以100并四舍五入到最接近的整数来计算得分。利用c统计量估计歧视。结果:舒张压、收缩压、妊娠史高血压、压力和吸烟(评分分别为10、6、210、56和18)是GH发生的预测因素。以受试者工作特征曲线下面积(AUC)评价模型精度,最佳截断值为936。使用衍生数据集,模型的灵敏度为75.9%,特异性为80.8%,AUC为0.828 (95% CI 0.772-0.884)。通过将综合得分分为低、中、高三个区间,计算其累计发生率,对模型进行验证;在衍生数据集中,分别为3.5%、6.1%和39.4%;在验证数据集中,分别为4.7%、6.2%和30.2%。两个队列的校准都很好。发展队列中GH高风险妇女的阴性预测值为92.0%,而验证队列为94.0%。结论:该预测模型在独立队列验证后显示出足够的性能,可用于将女性分为高、中、低GH风险。它有助于努力提供临床决策支持,以改善产妇保健和分娩结果。
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Development and Validation of a Prediction Model for Gestational Hypertension in Mezam Division
Objective: Our study aimed to develop and validate a prediction model for identifying women at increased risk of developing gestational hypertension (GH) in Mezam division, Northwest Region (NWR) of Cameroon. Method: A retrospective cohort design was employed. Data for a cohort of 1183 participants were randomly divided into derivation (n = 578) and validation (n = 585) datasets. Inclusion criterion was women without chronic hypertension. Primary outcome was Gestational hypertension. A questionnaire and data abstraction form were used for data collection. Chi square (χ2) test, independent sample t-test and multivariate logistic regression (to derive the prediction model) were used for data analysis. For each significant variable, a score was calculated by multiplying coefficient (β) by 100 and rounding to the nearest integer. Discrimination was estimated by used of the c-statistic. Results: DBP, SBP, hypertension in previous pregnancy, stress and smoking (scores 10, 6, 210, 56 and 18, respectively) were predictors of incident GH. The model accuracy was assessed by the area under the receiver operating characteristic curve (AUC), with optimal cut-off value 936. With the derivation dataset, sensitivity, specificity and AUC of the model were 75.9%, 80.8% and 0.828 (95% CI 0.772–0.884) respectively. The model was validated by dividing the aggregated scores into three ranges (low, moderate and high) and their cumulative incidence calculated which were; 3.5%, 6.1% and 39.4%, respectively, in the derivation dataset and 4.7%, 6.2% and 30.2%, respectively, in the validation dataset. Calibration was good in both cohorts. The negative predictive value of women in the development cohort at high risk of GH was 92.0% compared to 94.0% in the validation cohort. Conclusions: The prediction model revealed adequate performance after validation in an independent cohort and can be used to classify women into high, moderate or low risk of developing GH. It contributes to efforts to provide clinical decision-making support to improve maternal health and birth outcomes.
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