Bedside Risk Scoring for Carbapenem-Resistant Gram-Negative Bacterial Infections in Patients with Hematological Malignancies.

IF 2.4 Q2 INFECTIOUS DISEASES
Sare Merve Başağa, Ayşegül Ulu Kılıç, Zeynep Ture, Gökmen Zararsız, Serra İlayda Yerlitaş
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引用次数: 0

Abstract

Background/objectives: This study aimed to create a 'carbapenem resistance score' with the risk factors of carbapenem-resistant Gram-negative bacterial infections (GNBIs) in patients with hematological malignancies.

Methods: Patients with carbapenem-resistant and susceptible GNBIs were included in this study and compared in terms of risk factors. Three models of "carbapenem resistance risk scores" were created with statistically significant variables.

Results: The study included 154 patients with hospital-acquired GNBIs, of whom 64 had carbapenem-resistant GNBIs and 90 had carbapenem-susceptible GNBIs. Univariate and multivariate analyses identified several statistically significant risk factors for carbapenem resistance, including transfer from another hospital or clinic (p = 0.038), prior use of antibiotics like fluoroquinolones (p = 0.009) and carbapenems (p = 0.001), a history of carbapenem-resistant infection in the last six months (p < 0.001), rectal Klebsiella pneumoniae colonization (p < 0.001), hospitalization for ≥30 days (p = 0.001), and the presence of a urinary catheter (p = 0.002). Notably, the 14-day mortality rate was significantly higher in the carbapenem-resistant group (p < 0.001). Based on these findings, three risk-scoring models were developed. Common factors in all three models were fluoroquinolone use in the last six months, rectal K. pneumoniae colonization, and the presence of a urinary catheter. The fourth variable was transfer from another hospital (Model 1), a history of carbapenem-resistant infection (Model 2), or hospitalization for ≥30 days (Model 3). All models demonstrated strong discriminative power (AUC for Model 1: 0.830, Model 2: 0.826, Model 3: 0.831). For all three models, a cutoff value of >2.5 was adopted as the threshold to identify patients at high risk for carbapenem resistance, a value which yielded high positive and negative predictive values.

Conclusions: This study successfully developed three practical risk-scoring models to predict carbapenem resistance in patients with hematological malignancies using common clinical risk factors. A cutoff score of >2.5 proved to be a reliable threshold for identifying high-risk patients across all models, providing clinicians with a valuable tool to guide appropriate empirical antibiotic therapy.

血液恶性肿瘤患者耐碳青霉烯革兰氏阴性细菌感染的床边风险评分
背景/目的:本研究旨在建立血液恶性肿瘤患者碳青霉烯耐药革兰氏阴性细菌感染(GNBIs)危险因素的“碳青霉烯耐药评分”。方法:将碳青霉烯耐药和敏感gnbi患者纳入研究,比较危险因素。建立3个“碳青霉烯耐药风险评分”模型,各变量具有统计学意义。结果:本研究纳入154例医院获得性gnbi患者,其中64例为碳青霉烯耐药gnbi, 90例为碳青霉烯敏感gnbi。单因素和多因素分析确定了碳青霉烯耐药的几个具有统计学意义的危险因素,包括从其他医院或诊所转院(p = 0.038)、以前使用过氟喹诺酮类抗生素(p = 0.009)和碳青霉烯类抗生素(p = 0.001)、过去6个月有碳青霉烯耐药感染史(p < 0.001)、直肠肺炎克雷伯菌定菌(p < 0.001)、住院≥30天(p = 0.001)。尿导管的存在(p = 0.002)。值得注意的是,碳青霉烯耐药组的14天死亡率明显更高(p < 0.001)。基于这些发现,开发了三种风险评分模型。所有三种模型的共同因素是过去六个月内使用氟喹诺酮类药物,直肠肺炎克雷伯菌定植和存在尿导管。第四个变量是其他医院转院(模型1)、碳青霉烯耐药感染史(模型2)或住院≥30天(模型3)。所有模型均表现出较强的判别能力(模型1的AUC为0.830,模型2为0.826,模型3为0.831)。三种模型均采用截断值bbbb2.5作为鉴别碳青霉烯类耐药高危患者的阈值,该值具有较高的阳性预测值和阴性预测值。结论:本研究成功建立了三个实用的风险评分模型,利用常见的临床危险因素预测血液恶性肿瘤患者的碳青霉烯耐药。截断分>2.5被证明是识别所有模型中高危患者的可靠阈值,为临床医生指导适当的经验性抗生素治疗提供了有价值的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Infectious Disease Reports
Infectious Disease Reports INFECTIOUS DISEASES-
CiteScore
5.10
自引率
0.00%
发文量
82
审稿时长
11 weeks
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