首页|ICU产超广谱β-内酰胺酶肺炎克雷伯菌医院感染预测模型构建

ICU产超广谱β-内酰胺酶肺炎克雷伯菌医院感染预测模型构建

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目的 探讨重症监护室(ICU)内产超广谱β-内酰胺酶肺炎克雷伯菌(ESBLs-KP)医院感染预测模型。方法 选取2019年1月—2022年12月于济宁市第一人民医院ICU发生肺炎克雷伯菌医院感染的157例患者,其中71例产ESBLs-KP医院感染患者为感染组,其余86例为非感染组,分析标本来源、耐药性,多因素Logistic回归分析产ESBLs-KP医院感染因素并构建列线图风险预测模型,使用Hosmer-Lemeshow评估风险模型拟合度,使用受试者工作特征(ROC)曲线下面积(AUC)、校准曲线评价模型并进行验证。结果 157例KP医院感染患者标本以呼吸道标本为主,占39。49%,产ESBLs-KP医院感染以泌尿道感染为主(33例,46。48%);发生医院感染的产ESBLs菌株对碳青霉烯类及阿米卡星抗菌药物较为敏感,对大部分抗菌药物的耐药率普遍高于非ES-BLs菌株(P<0。05);多因素分析结果显示,ICU入住天数、头孢类及喹诺酮类抗菌药物用药史、低蛋白血症是ICU内产ESBLs-KP医院感染的危险因素(P<0。05);据此构建医院感染风险列线图模型,Hosmer-Lemeshow检验该风险预测模型的拟合度良好(P=0。226),AUC为0。785(95%CI:0。712~0。857),敏感度为83。70%,特异度为63。40%,与校准曲线均显示模型区分度和校准度良好。结论 产ESBLs-KP耐药性仍较高,基于产ES-BLs-KP医院感染危险因素构建的列线图风险预测模型具有良好的区分度和校准度。
Construction of a predictive model for nosocomial infection of ESBLs-producing Klebsiella pneumoniae in ICU
OBJECTIVE To explore the predictive model for nosocomial infection of extended-spectrum-β-lactamase-producing(ESBLs-producing)Klebsiella pneumoniae in intensive care unit(ICU).METHODS A total of 157 pa-tients who developed nosocomial infection of Klebsiella pneumoniae in the ICU of Jining NO.1 People's Hospital from Jan.2019 to Dec.2022 were selected,of which 71 patients with ESBLs-KP hospital acquired infection were in the infection group and the remaining 86 cases were in the non-infection group.The source of specimens and drugs resistance were analyzed,and multivariate logistic regression analysis was used to analyze the factors of nos-ocomial infection with ESBLs-producing Klebsiella pneumoniae,and a risk predictive model of nomogram was constructed.Hosmer-Lemeshow was used to assess the risk model fit,and the model was evaluated and validated using the area under the curve of the receiver operating characteristic(ROC)curve and calibration curves.RESULTS Specimens from 157 patients with KP hospital infections were predominantly respiratory tract speci-mens,accounting for 39.49%and ESBLs-producing Klebsiella pneumoniae nosocomial infections were predomi-nantly urinary tract infections(33 cases,46.48%).The ESBLs producing strains of nosocomial infection were more sensitive to carbapenems and amikacin antibiotics,and the resistance rate of ESBLs-producing strains to most antimicrobial drugs was generally higher than that of ESBLs non-producing strains(P<0.05).Multivariate logistic regression analysis indicated that days of ICU stay,history of use of cephalosporin and quinolone,and hy-poproteinemia were independent risk factors for nosocomial infection of ESBLs-producing Klebsiella pneumoniae in ICU(P<0.05).Based on which,the nomogram risk prediction model was constructed,and th Hosmer-Leme-show test showed that the fitting degree of the risk prediction model was good(P=0.226),with an AUC of 0.785(95%CI:0.712-0.857),a sensitivity of 83.70%,a specificity of 63.40%,and the calibration curves showed that the risk prediction model was well differentiated and well calibrated.CONCLUSION The drug resist-ance of ESBLs-producing Klebsiella pneumoniae was still very high,and the nomogram risk prediction model constructed on the basis of the risk factors of ESBLs-producing Klebsiella pneumoniae nosocomial infection had good discrimination and calibration.

Extended-spectrum-β-lactamase-producingKlebsiella pneumoniaeInfectionDurg resistanceRisk prediction modelNomogramICU

李元叶、茹义福、曹晓花、邱瑞霞

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济宁市第一人民医院感染管理部,山东济宁 272000

济宁市第一人民医院重症医学科,山东济宁 272000

产超广谱β-内酰胺酶 肺炎克雷伯菌 感染 耐药性 风险预测模型 列线图 ICU

山东省医药卫生科技发展计划基金资助项目

202003100526

2024

中华医院感染学杂志
中华预防医学会 中国人民解放军总医院

中华医院感染学杂志

CSTPCD北大核心
影响因子:1.885
ISSN:1005-4529
年,卷(期):2024.34(4)
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