Department of Pharmacy, The University of Tokyo Hospital, Tokyo, Japan.
The Education Center for Clinical Pharmacy, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
J Antimicrob Chemother. 2023 May 3;78(5):1231-1240. doi: 10.1093/jac/dkad079.
Limited evidence is available regarding alternative therapeutic agents to vancomycin in treating glycopeptide-susceptible Enterococcus faecium (GSEF) bacteraemia. This study assessed the effectiveness and safety of teicoplanin compared with vancomycin for treating GSEF bacteraemia.
This was a retrospective, non-inferiority cohort study. Patients aged ≥18 years who developed GSEF bacteraemia and received either teicoplanin or vancomycin were included. The primary effectiveness outcome was the clinical success at the end of treatment, with a generalized linear model using the propensity score for selecting the agent as a covariate. We used an absolute difference of 20% in clinical success as the non-inferiority margin. Using multivariable logistic regression, the primary safety outcome was the incidence of acute kidney injury (AKI).
In total, 164 patients (74 and 90 in the teicoplanin and vancomycin groups, respectively) were included. Overall, 64.9% (48/74) and 48.9% (44/90) of patients in the teicoplanin and vancomycin groups, respectively, achieved the primary effectiveness outcome. A generalized linear analysis showed an adjusted effectiveness difference of 9.9% (95% CI, -0.9% to 20.0%; P = 0.07), indicating non-inferiority of teicoplanin versus vancomycin. The incidence of AKI was 8.1% (6/74) and 24.4% (22/90) in the teicoplanin and vancomycin groups, respectively, with an adjusted OR of 0.242 (95% CI, 0.068 to 0.864; P = 0.029), indicating significantly lower AKI risk in the teicoplanin than in the vancomycin group.
Teicoplanin is a safe and useful alternative therapeutic agent for treating GSEF bacteraemia.
治疗糖肽类敏感性粪肠球菌(GSEF)菌血症时,万古霉素的替代治疗药物的证据有限。本研究评估了替考拉宁与万古霉素治疗 GSEF 菌血症的有效性和安全性。
这是一项回顾性非劣效性队列研究。纳入年龄≥18 岁、发生 GSEF 菌血症且接受替考拉宁或万古霉素治疗的患者。主要有效性结局为治疗结束时的临床疗效,采用广义线性模型,将倾向评分作为选择药物的协变量。我们使用临床疗效的 20%绝对差异作为非劣效性边界。使用多变量逻辑回归,主要安全性结局为急性肾损伤(AKI)的发生率。
共纳入 164 例患者(替考拉宁组 74 例,万古霉素组 90 例)。总体而言,替考拉宁组和万古霉素组分别有 64.9%(48/74)和 48.9%(44/90)的患者达到主要有效性结局。广义线性分析显示,调整后的疗效差异为 9.9%(95%CI,-0.9%至 20.0%;P=0.07),表明替考拉宁与万古霉素相比非劣效。替考拉宁组和万古霉素组 AKI 的发生率分别为 8.1%(6/74)和 24.4%(22/90),调整后的 OR 为 0.242(95%CI,0.068 至 0.864;P=0.029),表明替考拉宁组 AKI 风险显著低于万古霉素组。
替考拉宁是治疗 GSEF 菌血症的一种安全有效的替代治疗药物。