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作 者:郭敏珊 陈小燕[3] 梁伟 马金香[4] 贾亦真 Guo Minshan;Chen Xiaoyan;Liang Wei;Ma Jinxiang;Jia Yizhen(Guangzhou Medical University,Guangzhou 511436,China;Department of Endocrine,the University of HongKong-Shenzhen Hospital,Shenzhen 518053,China;Department of Endocrine,the First Affiliated Hospital of Guangzhou Medical University,Guangzhou 510120,China;Department of Statistics,Guangzhou Medical University,Guangzhou 510030,China;Department of Core Laboratory,the University of HongKong-Shenzhen Hospital,Shenzhen 518053,China)
机构地区:[1]广州医科大学,511436 [2]香港大学深圳医院内分泌科,518053 [3]广州医科大学附属第一医院内分泌科,510120 [4]广州医科大学统计学院,510030 [5]香港大学深圳医院中心实验室,518053
出 处:《国际内分泌代谢杂志》2022年第5期349-353,386,共6页International Journal of Endocrinology and Metabolism
摘 要:目的构建妊娠期糖尿病(GDM)启动药物干预的风险模型。方法回顾性分析2015年3月至2017年4月香港大学深圳医院GDM患者669例,比较药物干预组(n=110)和生活方式干预组(n=559)各临床指标的差异,利用logistic回归建立风险模型,应用受试者工作特征(ROC)曲线及Hosmer-Lemeshow拟合优度检验(HL检验)进行评价,并选取75例GDM进行内部验证。结果本研究纳入孕28周前的孕期体重增加(ΔW)、孕前体重指数(BMI)、口服糖耐量试验(OGTT)-0 h、OGTT-2 h共4个危险因素,建立风险模型:Z=0.270×ΔW+0.167×孕前BMI+1.768×OGTT-0 h+0.371×OGTT-2 h-18.787。模型ROC曲线下面积为0.809,HL检验P>0.05。内部验证结果:模型灵敏度64.7%,特异度79.3%,准确率76.0%。结论本模型有一定临床参考价值,但其泛化能力及模型的稳定性和适用性有待进一步验证。Objective To establish a risk model of pharmacological intervention for gestational diabetes mellitus(GDM).Methods We retrospectively analyzed the data of 669 GDM in the University of HongKong-Shenzhen Hospital from Mar.2015 to Apr.2017.And indicators of pharmacological intervention group(n=110)and lifestyle intervention group(n=559)were compared.Logistic regression was used to establish a risk model.The ROC curve and Hosmer-Lemeshow goodness of fit test were used to test the model′s efficiency.A total of 75 GDM patients were selected to evaluate the model′s effect as internal validation.Results The four risk factors including weight gain during the first and second trimester(Δweight),pre-pregnancy BMI,OGTT-0 h and OGTT-2 h were included in the risk model.The model formula was:Z=0.270×Δweight+0.167×BMI+1.768×OGTT-0 h+0.371×OGTT-2 h-18.787.The AUC was 0.809,with Hosmer-Lemeshow goodness of fit test P>0.05.The internal validation showed the sensitivity,specificity,and the accuracy of this model were 64.7%,79.3%and 76.0%,respectively.Conclusion The risk model has certain clinical reference value,but its generalization ability and the stability and applicability of the model need further verification.
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