耐碳青霉烯类肠杆菌科血流感染临床特征及预后模型构建

Clinical characteristics and construction of prognostic model for carbapenem-resistant Enterobacteriaceae bloodstream infections

  • 摘要:
    目的 探讨耐碳青霉烯类肠杆菌科细菌(CRE)血流感染患者的临床特征,筛选危险因素,构建预后模型,为早期识别高危患者及优化临床干预策略提供参考。
    方法 回顾性分析2016年1月-2025年6月天津市第三中心医院收治的190例CRE血流感染患者的临床资料,收集人口学特征、基础疾病、侵入性操作等相关指标。根据确诊后30 d全因死亡情况,将患者分为生存组(n=68)与死亡组(n=122)。采用多因素logistic回归模型归纳危险因素,并构建预后模型。采用C指数、受试者工作特征(ROC)曲线下面积(AUC)、校准曲线及决策曲线分析(DCA)评估模型的区分度、校准度及临床实用性,并通过Bootstrap法进行内部验证。
    结果 CRE血流感染患者检出主要致病菌为肺炎克雷伯菌(90.53%)。泌尿系统疾病(OR=3.822,95%CI:1.601~9.476,P=0.003)和机械通气(OR=8.737,95%CI:2.789~30.356,P<0.001)是CRE血流感染患者预后不良的危险因素。模型的C指数为0.819(验证后0.818),AUC为0.819。校准效果满意,决策曲线分析显示具有临床净获益。
    结论 肺炎克雷伯菌是CRE血流感染的主要病原体,泌尿系统疾病与机械通气是预后不良的危险因素,在重症患者中尤为显著。基于此构建的预后模型性能良好,具备较高的临床应用价值,能为早期风险分层提供重要依据,并有望为指导个体化临床干预、改善患者预后提供支持。

     

    Abstract:
    OBJECTIVE  To investigate the clinical characteristics of patients with carbapenem-resistant Enterobacteriaceae (CRE) Bloodstream Infections (BSI), identify risk factors and construct a prognostic model, thereby providing a reference for early identification of high-risk patients and optimization of clinical intervention strategies.
    METHODS  A retrospective analysis was conducted on the clinical data of 190 patients with CRE BSI admitted to Tianjin Third Central Hospital from Jan. 2016 to Jun. 2025. Demographic characteristics, underlying diseases, invasive procedures and other relevant indicators were collected. Patients were classified as 30-day survivors (n=68) and 30-day non-survivors (n=122) based on all-cause mortality within 30 days after diagnosis. A multivariate logistic regression model was used to summarize risk factors and construct a prognostic model. The model's discrimination, calibration and clinical utility were evaluated through the C-index, area under the curve (AUC)—receiver operating characteristic (ROC), calibration curve, and decision curve analysis (DCA). Internal validation was performed via the Bootstrap method.
    RESULTS  The primary pathogenic bacterium detected in patients with CRE-BSI was Klebsiella pneumoniae (90.53%). Urinary system diseases (OR=3.822, 95%CI: 1.601-9.476, P=0.003) and mechanical ventilation (OR=8.737, 95%CI: 2.789-30.356, P<0.001) were identified as risk factors for poor prognosis in patients with CRE-BSI. The model's C-index was 0.819 (0.818 after validation), and the AUC was 0.819. The calibration was satisfactory, and decision curve analysis demonstrated clinical net benefit.
    CONCLUSIONS  K. pneumoniae is the primary pathogenic bacterium of CRE BSI, and urinary system diseases and mechanical ventilation are risk factors for poor prognosis, particularly in critical patients. The constructed prognostic model demonstrates good performance and high clinical utility. It provides an important basis for early risk stratification and has the potential to guide individualized clinical interventions, ultimately improving patient prognosis.

     

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