Department of Infection Control and Prevention, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.
Department of Infection Control and Prevention, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan; Department of Clinical Infectious Diseases, Tokoname City Hospital, Tokoname, Aichi, Japan.
J Infect Chemother. 2022 Feb;28(2):232-237. doi: 10.1016/j.jiac.2021.10.023. Epub 2021 Nov 27.
Because of its lower risk of renal toxicity than vancomycin, teicoplanin is the preferred treatment for methicillin-resistant Staphylococcus aureus infection in patients undergoing continuous venovenous haemodiafiltration (CVVHDF) in whom renal function is expected to recover. The dosing regimen for achieving a trough concentration (C) of ≥20 μg/mL remains unclear in patients on CVVHDF using the low flow rate adopted in Japan.
The study was conducted in patients undergoing CVVHDF with a flow rate of <20 mg/kg/h who were treated with teicoplanin. We adopted three loading dose regimens for the initial 3 days: the conventional regimen, a high-dose regimen (four doses of 10 mg/kg), and an enhanced regimen (four doses of 12 mg/kg). The initial C was obtained at 72 h after the first dose.
Overall, 60 patients were eligible for study inclusion. The proportion of patients achieving the C target was significantly higher for the enhanced regimen than for the high-dose regimen (52.9% versus 8.3%, p = 0.003). In multivariate analysis, the enhanced regimen (odds ratio [OR] = 39.93, 95% confidence interval [CI] = 5.03-317.17) and hypoalbuminaemia (OR = 0.04, 95% CI = 0.01-0.44) were independent predictors of the achievement of C ≥ 20 μg/mL.
An enhanced teicoplanin regimen was proposed to treat complicated or invasive infections by methicillin-resistant Staphylococcus aureus in patients receiving CVVHDF even with a low flow rate.
替考拉宁的肾毒性低于万古霉素,因此在预计肾功能恢复的接受连续性静脉-静脉血液透析滤过(CVVHDF)的患者中,替考拉宁是治疗耐甲氧西林金黄色葡萄球菌感染的首选药物。在日本采用的低流速下,对于接受 CVVHDF 的患者,达到谷浓度(C)≥20μg/mL 的剂量方案仍不清楚。
本研究纳入了接受流速<20mg/kg/h 的 CVVHDF 治疗的替考拉宁治疗患者。我们在最初的 3 天采用了三种负荷剂量方案:常规方案、高剂量方案(4 剂 10mg/kg)和强化方案(4 剂 12mg/kg)。首次给药后 72 小时获得初始 C。
共有 60 名患者符合研究纳入标准。与高剂量方案相比,强化方案达到 C 目标的患者比例显著更高(52.9%比 8.3%,p=0.003)。多变量分析显示,强化方案(比值比[OR] 39.93,95%置信区间[CI] 5.03-317.17)和低白蛋白血症(OR 0.04,95%CI 0.01-0.44)是达到 C≥20μg/mL 的独立预测因素。
对于接受 CVVHDF 的患者,即使采用低流速,替考拉宁强化方案也可用于治疗复杂或侵袭性耐甲氧西林金黄色葡萄球菌感染。