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Pharmacokinetics of Vancomycin in Critically Ill Patients Undergoing Sustained Low-Efficiency Dialysis

机译:在患有持续低效率透析的危重患者中万古霉素的药代动力学

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Introduction Vancomycin pharmacokinetic data in critically ill patients receiving sustained low-efficiency dialysis (SLED) is limited. Published data using vancomycin with intermittent hemodialysis and continuous renal replacement therapy may not be applicable to hybrid dialysis modalities such as SLED. Current drug references lack recommendations for vancomycin dosing in patients receiving SLED. Objective The objective of this study was to determine vancomycin pharmacokinetics during SLED. Methods A total of 20 patients who were critically ill with oliguric or anuric renal failure who received vancomycin and SLED were included in the study. Surrounding one SLED session, serum vancomycin blood samples were drawn before the initiation of SLED, at the termination of SLED, and 4 hours after completion of SLED treatment. Following this, patients received vancomycin, dosed to target a goal peak of 20-30 mcg/ml. A vancomycin peak level was drawn 1 hour after the end of the infusion. SLED treatment duration was at least 7 hours. Continuous data are reported as median (interquartile range) and categorical data as percentage. Results The vancomycin elimination rate and half-life were 0.051 hours (0.042-0.074 hours) and 13.6 hours (9.4-16.6 hours), respectively. SLED reduced vancomycin serum concentrations by 35.4% (31.5-43.8%), and vancomycin rebound was 9.8% (2.5-13.7%). The vancomycin dose administered post-SLED was 1000 mg (875-1125 mg). For 18 patients, the patient-specific volume of distribution was 0.88 L/kg (0.67-1.1 L/kg), vancomycin clearance was 3.5 L/hr (2.2-5.2 L/hr), and the area under the concentration-time curve during the study time period was 280.8 mg center dot hr/L (254.7-297.3 mg center dot hr/L). Conclusion Vancomycin is significantly removed during SLED with little rebound in serum concentrations 4 hours after completion of SLED. Based on study findings, patients who are critically ill require additional vancomycin dosing after each SLED session to maintain therapeutic post-SLED vancomycin concentrations. Therapeutic drug monitoring of vancomycin is recommended during SLED.
机译:简介接受持续的低效率透析(雪橇)的重症患者中的万古霉素药代动力学数据受到限制。使用万古霉素与间歇性血液透析和持续肾脏替代疗法发布的数据可能不适用于混合透析模态(例如雪橇)。当前的药物参考缺乏接受雪橇的患者万古霉素给药的建议。目的本研究的目的是确定雪橇期间万古霉素药代动力学。该方法包括20例患有寡尿或高峰期肾衰竭的患者接受万古霉素和雪橇。周围的一个雪橇疗程,在雪橇终止之前,在雪橇终止之前以及完成雪橇治疗后4小时绘制血清万古霉素血液样本。此后,患者接受了万古霉素,靶向20-30 mcg/mL的目标峰值。输注结束后1小时,达到万古霉素峰值。雪橇治疗持续时间至少为7小时。连续数据报告为中位数(四分位间范围)和分类数据为百分比。结果,万古霉素的消除率和半衰期分别为0.051小时(0.042-0.074小时)和13.6小时(9.4-16.6小时)。雪橇降低了万古霉素的血清浓度35.4%(31.5-43.8%),而万古霉素的反弹为9.8%(2.5-13.7%)。送出后的万古霉素剂量为1000 mg(875-1125 mg)。对于18例患者,特定于患者的分布量为0.88 l/kg(0.67-1.1 l/kg),万古霉素清除率为3.5 l/hr(2.2-5.2 l/hr),浓度时间曲线下的面积为在研究期间为280.8 mg中心点HR/L(254.7-297.3 mg中心点HR/L)。结论在雪橇期间,万古霉素在雪橇群完成后4小时的血清浓度几乎没有反弹。根据研究结果,每次雪橇疗程后,病重病的患者需要额外的万古霉素剂量来维持治疗后的塞霉素浓度。在雪橇期间,建议对万古霉素进行治疗药物监测。

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