首页|期刊导航|中国感染控制杂志|医院获得性耐碳青霉烯类肺炎克雷伯菌血流感染预测模型的构建与验证

医院获得性耐碳青霉烯类肺炎克雷伯菌血流感染预测模型的构建与验证OA

Development and validation of prediction model for hospital-acquired carbapenem-resistant Klebsiella pneumoniae bloodstream infection

中文摘要英文摘要

目的 分析耐碳青霉烯类肺炎克雷伯菌(CRKP)所致医院获得性血流感染的危险因素,并构建列线图预测模型.方法 回顾性收集川北医学院附属医院2020年1月1日—2025年12月31日期间,由肺炎克雷伯菌(KP)引起的医院获得性血流感染病例147例.根据 KP对碳青霉烯类抗生素的药敏结果,将病例分为CRKP组(n=59)和碳青霉烯类敏感肺炎克雷伯菌(CSKP)组(n=88).首先采用LASSO回归筛选潜在危险因素,随后通过多因素Logistic回归确定独立危险因素,并基于此构建列线图预测模型.通过Brier评分、受试者工作特征曲线下面积(AUC)、Hosmer-Lemeshow检验、校准曲线及决策曲线分析综合评估模型效能,并采用Bootstrap内部验证法(重复抽样1 000次)对模型进行内部验证.结果 多因素Logistic回归分析显示,使用碳青霉烯类抗生素、使用喹诺酮类抗菌药物、入住ICU及合并其他部位多重耐药菌感染是医院获得性CRKP血流感染的独立危险因素(均P<0.05).基于上述变量构建的列线图预测模型表现出良好的区分度与校准度,Brier评分为0.100,AUC为0.923(95%CI:0.880~0.967),Hosmer-Lemeshow检验差异无统计学意义(χ2=4.552,P=0.208),校准曲线接近理想曲线,决策曲线分析表明模型阈值概率约0.1~0.8时具有临床净获益.经 Bootstrap内部验证校正后,AUC为0.913(95%CI:0.882~0.967),AUC衰减率为1.08%,进一步证实模型稳定性良好.结论 使用碳青霉烯类抗生素、使用喹诺酮类抗菌药物、入住ICU及合并其他部位多重耐药菌感染是医院获得性CRKP血流感染的独立危险因素.基于上述变量构建的列线图预测模型具有良好的判别效能和临床实用性,可为医院获得性CRKP血流感染高危患者的早期识别与干预提供参考.

Objective To analyze the risk factors for hospital-acquired bloodstream infections(BSIs)caused by carbapenem-resistant Klebsiella pneumoniae(CRKP)and to develop a nomogram prediction model.Methods A retrospective study was conducted at the Affiliated Hospital of North Sichuan Medical College from January 1,2020,to December 31,2025.A total of 147 cases of hospital-acquired BSIs caused by Klebsiella pneumoniae(KP)were included.Cases were divided into CRKP(n=59)and carbapenem-sensitive KP(CSKP)(n=88)groups based on susceptibility to carbapenem antibiotics.Potential risk factors were initially screened using LASSO regres-sion,followed by multivariate logistic regression to identify independent risk factors.A nomogram prediction model was then constructed based on these factors.The model's performance was evaluated using Brier score,area under the receiver operating characteristic curve(AUC),Hosmer-Lemeshow test,calibration curve,and decision curve analysis(DCA).Bootstrap internal validation with 1 000 resamplings was performed to assess model stability.Results Multivariate logistic regression analysis identified the following as independent risk factors for hospital-acquired CRKP BSIs:use of carbapenem antibiotics,use of quinolone antibiotics,admission to ICU,and co-infection with multidrug-resistant organisms(MDROs)at other sites(all P<0.05).The nomogram model demonstrated good discrimination and calibration:Brier score was 0.100,AUC was 0.923(95%CI:0.880-0.967),the Hosmer-Lemeshow test was not statistically significant(χ2=4.552,P=0.208),the calibration curve closely approximated the ideal curve,and DCA indicated a clinical net benefit at a threshold probability of approximately 0.1-0.8.After bootstrap internal validation,the AUC was 0.913(95%CI:0.882-0.967),with an AUC decay of 1.08%,which further confirmed the model's stability.Conclusion Carbapenem use,quinolone antibiotic use,ICU admission,and concomitant multidrug-resistant organism infection at other sites are independent risk factors for hospital-acquired CRKP BSIs.The nomogram prediction model constructed based on these factors exhibits good discriminative ability and clinical utility,and may inform the early identification and intervention of patients at high risk of hospital-acquired CRKP BSIs.

郭杨柳;庞若楠;张红;刘婧;岳瑾熙;谢宁;廖涛

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医药卫生

碳青霉烯类耐药肺炎克雷伯菌血流感染预测模型

Carbapenem resistanceKlebsiella pneumoniaeBloodstream infectionPrediction model

《中国感染控制杂志》 2026 (8)

1148-1156,9

四川省自然科学基金面上项目(2024NSFSC0760)

10.12138/j.issn.1671-9638.20264253

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