首页|期刊导航|山西医科大学学报|基于回顾性队列的替加环素相关肝损伤危险因素分析

基于回顾性队列的替加环素相关肝损伤危险因素分析OA

A retrospective cohort study on risk factors for Tigecycline-associated liver injury

中文摘要英文摘要

目的 探讨替加环素(TGC)相关药物性肝损伤(DILI)的发生率及其独立危险因素,为临床优化给药方案、建立风险预警体系提供依据.方法 收集在山西省人民医院接受TGC治疗≥3 d的成年患者临床资料,根据患者是否发生肝损伤分为肝损伤组和肝未损伤组,对比两组患者的人口学特征、用药情况和实验室检验指标等临床信息,采用单因素和多因素Logistic回归分析TGC相关肝损伤的独立危险因素,并通过受试者工作特征曲线(ROC)确定独立危险因素的阈值.结果 共纳入375例接受TGC治疗≥3 d的成年患者,TGC相关DILI发生率为14.4%(54/375).肝损伤组和肝未损伤组患者的人口学信息、感染灶、基础疾病、基线肝脏生化指标等临床资料差异无统计学意义(P>0.05).单因素及多因素Logistic回归分析结果显示,年龄≥60岁(OR=2.163,95%CI:1.179~3.969,P=0.013)、TGC用药时长(OR=1.102,95%CI:1.030~1.178,P=0.005)为TGC相关DILI的独立危险因素,而PLT水平(OR=0.997,95%CI:0.994~0.999,P=0.008)为TGC相关DILI的保护因素.ROC分析提示TGC用药时长>13 d时DILI风险显著升高(AUC=0.623).结论 TGC用药疗程超过13 d且≥60岁的成年患者更可能发生TGC相关DILI,临床用药应密切监测此类患者肝功能变化,以保障TGC安全合理用药.

Objective To investigate the incidence and independent risk factors of Tigecycline(TGC)-associated drug-induced liver injury(DILI)for providing evidence for optimizing dosing strategies and risk early-warning systems.Methods Clinical data were col-lected from adult patients who received TGC for more than three days in Shanxi Provincial People's Hospital.Based on the occurrence of liver injury,the patients were divided into liver injury group and non-liver injury group.Demographic characteristics,medication details,laboratory parameters,and other clinical variables were compared between the two groups.Univariate and multivariate Logistic regression analyses were employed to identify independent risk factors for TGC-associated liver injury,and the cutoffs for the indepen-dent risk factors were determined using receiver operating characteristic(ROC)curve analysis.Results A total of 375 adult patients were included in this study.The incidence of TGC-associated DILI was 14.4%(54/375).No significant differences were observed in demographic data,infection sites,comorbidities,baseline liver biochemistry,or other clinical characteristics between the two groups(all P>0.05).Univariate and multivariate Logistic regression analyses identified age≥60 years(OR=2.163,95%CI:1.179-3.969,P=0.013)and duration of TGC therapy(OR=1.102,95%CI:1.030-1.178,P=0.005)as independent risk factors for TGC-associated DILI.The baseline PLT count was identified as a protective factor(OR=0.997,95%CI:0.994-0.999,P=0.008).ROC curve analysis indicated a significant increase in DILI risk when the duration of TGC therapy exceeded 13 d(AUC=0.623).Conclusion Patients aged≥60 years treated with TGC for more than 13 days are at an increased risk of developing TGC-associated DILI.Therefore,close monitoring of liver function is recommended in these patients to ensure the safe and effective use of TGC.

赵倩倩;周敏;曲婷丽

山西医科大学药学院,太原 030001||山西省人民医院药学部山西省人民医院药学部山西医科大学药学院,太原 030001

医药卫生

替加环素药物性肝损伤危险因素Logistic回归分析药物联用

Tigecyclinedrug-induced liver injuryrisk factorsLogistic regression analyzedrug combination

《山西医科大学学报》 2026 (3)

319-324,6

山西省科技厅基础研究项目(20210302124586)

10.13753/j.issn.1007-6611.2026.03.010

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