恶性血液病碳青霉烯类耐药革兰阴性菌血流感染预后预测模型构建及验证

Development and validation of a prognostic prediction model for carbapenem-resistant gram-negative bacteria bloodstream infection in patients with hematological malignancies

  • 摘要:
    目的 探讨恶性血液病(HMs)患者合并碳青霉烯类耐药革兰阴性菌(GNB)血流感染(BSI)及预后的危险因素, 并构建列线图预测模型。
    方法 选择2017年1月-2022年12月西安交通大学第一附属医院收治的316例HMs合并GNB-BSI患者作为训练集, 2023年1月-2024年10月收治的106例患者作为验证集。通过lasso回归和多因素logistic回归进行变量筛选, 并构建nomogram模型, 分别采用受试者工作特征(ROC)曲线、校准曲线和临床决策曲线(DCA)对预测模型进行内部验证。
    结果 粒细胞缺乏≥7 d(OR=14.525)、BSI前30 d内使用头孢菌素/β内酰胺酶抑制剂(OR=3.510)、碳青霉烯类抗菌药物暴露史(OR=4.840)及白蛋白 < 30 g/L(OR=2.697)是HMs患者发生碳青霉烯类耐药革兰阴性菌血流感染(CR-GNB BSI)的危险因素(P<0.05)。脓毒症休克(OR=6.934)、中心静脉置管(OR=5.586)、不恰当的经验性抗菌药物治疗(OR=4.744)、CR-GNB感染(OR=2.916)及白蛋白<30 g/L(OR=3.324)是HMs患者GNB-BSI 30 d死亡的危险因素(P<0.05), 基于这些指标, 构建了两个nomogram模型。内部验证集ROC曲线下面积(AUC)分别为0.775和0.849。校准曲线显示预测模型具有较高的预测效能(P=0.998和0.660), DCA显示两种模型的临床应用价值较高。
    结论 本研究基于多因素分析构建的nomogram预测模型, 不仅预测价值良好, 而且临床效能显著, 有助于临床早期识别高危患者从而进行针对性治疗。

     

    Abstract:
    OBJECTIVE To investigate the risk factors for carbapenem-resistant gram-negative bacteria (GNB) bloodstream infection (BSI) in patients with hematological malignancies (HMs) and their prognosis, and to develop a nomogram prediction model.
    METHODS A total of 316 patients with HMs and GNB-BSI admitted to the First Affiliated Hospital of Xi′an Jiaotong University from Jan. 2017 to Dec. 2022 were selected as the training set, and 106 patients admitted from Jan. 2023 to Oct. 2024 were selected as the validation set. Variables were selected by lasso regression and multifactor logistic regression, and a nomogram model was constructed. The prediction model was internally validated by the receiver operating characteristic (ROC) curve, calibration curve and decision curve analysis (DCA), respectively.
    RESULTS Granulocytopenia for ≥7 days (OR=14.525), use of cephalosporins/β-lactamase inhibitors within 30 days before BSI (OR=3.510), exposure history of carbapenem antibacterial drug (OR=4.840) and albumin < 30 g/L (OR=2.697) were risk factors for CR-GNB BSI in patients with HMs (P < 0.05). Septic shock (OR=6.934), central venous catheterization (OR=5.586), inappropriate empirical antibacterial drug therapy (OR=4.744), CR-GNB infection (OR=2.916) and albumin < 30 g/L (OR=3.324) were risk factors for 30-day mortality in patients with HMs and GNB-BSI (P < 0.05). Based on these indicators, two nomogram models were constructed. The areas under the ROC curve (AUC) for the internal validation set were 0.775 and 0.849, respectively. The calibration curves demonstrated high predictive performance for the prediction models (P=0.998 and 0.660, respectively), and DCA showed high clinical application value for both models.
    CONCLUSION The nomogram prediction model constructed in this study based on multifactor analysis not only demonstrates good predictive value but also exhibits significant clinical efficacy, aiding in the early identification of high-risk patients for targeted therapy.

     

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