Anesthesiology and Critical Care Department, CHU Bordeaux, 33000, Bordeaux, France.
Anesthesiology and Critical Care Department, CHU Bordeaux, 33000, Bordeaux, France.
Int J Antimicrob Agents. 2018 Mar;51(3):443-449. doi: 10.1016/j.ijantimicag.2017.11.013. Epub 2017 Nov 24.
This study assessed whether augmented renal clearance (ARC) impacts negatively on antibiotic concentrations and clinical outcomes in patients treated by high-dose β-lactams administered continuously. Over a 9-month period, all critically ill patients without renal impairment treated by one of the monitored β-lactams for a documented infection were eligible. During the first 3 days of antibiotic therapy, every patient underwent 24-h CL measurements and therapeutic drug monitoring. The main outcome was the rate of β-lactam underdosing, defined as a free drug concentration <4 × MIC of the known pathogen. Secondary outcomes were rates of subexposure for β-lactams and therapeutic failure. The performance of CL in predicting underdosing was assessed by a ROC curve, and multivariable logistic regression was performed to determine risk factors for subexposure and therapeutic failure. A total of 79 patients were included and 235 samples were analysed. The rate of underdosing was 12%, with a significant association with CL (P <0.0001). A threshold of CL ≥ 170 mL/min had a sensitivity and specificity of 0.93 (95% CI 0.77-0.99) and 0.65 (95% CI 0.58-0.71) for predicting β-lactam underdosing. Mean CL values ≥170 mL/min were significantly associated with subexposure [OR = 10.1 (2.4-41.6); P = 0.001]. Patients with subexposure presented higher rates of therapeutic failure [OR = 6.3 (1.2-33.2); P = 0.03]. Mean CL values ≥170 mL/min remain a risk factor for subexposure to β-lactams despite high doses of β-lactams administered continuously. β-Lactam subexposure was associated with higher rates of therapeutic failure in septic critically ill patients.
这项研究评估了增强的肾清除率(ARC)是否会对接受高剂量连续β-内酰胺类药物治疗的患者的抗生素浓度和临床结局产生负面影响。在 9 个月的时间内,所有无肾功能损害且接受监测的β-内酰胺类药物治疗的确诊感染患者均符合条件。在抗生素治疗的前 3 天,每位患者均进行了 24 小时 CL 测量和治疗药物监测。主要结局是β-内酰胺类药物剂量不足的发生率,定义为游离药物浓度<已知病原体 MIC 的 4 倍。次要结局是β-内酰胺类药物亚暴露率和治疗失败率。通过 ROC 曲线评估 CL 预测剂量不足的性能,并进行多变量逻辑回归以确定亚暴露和治疗失败的危险因素。共纳入 79 例患者,分析了 235 个样本。剂量不足的发生率为 12%,与 CL 显著相关(P<0.0001)。CL≥170mL/min 的阈值对预测β-内酰胺类药物剂量不足的灵敏度和特异性分别为 0.93(95%CI 0.77-0.99)和 0.65(95%CI 0.58-0.71)。CL 值平均值≥170mL/min 与亚暴露显著相关[OR=10.1(2.4-41.6);P=0.001]。亚暴露患者的治疗失败率更高[OR=6.3(1.2-33.2);P=0.03]。尽管连续给予高剂量的β-内酰胺类药物,但 CL 值平均值≥170mL/min 仍然是β-内酰胺类药物亚暴露的危险因素。β-内酰胺类药物亚暴露与脓毒症危重症患者的治疗失败率升高相关。