Division of Infectious Diseases and Hospital Epidemiology, University Hospital of Zurich, Raemistrasse 100, 8091, Zurich, Switzerland.
Infection. 2013 Apr;41(2):553-7. doi: 10.1007/s15010-012-0300-3. Epub 2012 Jul 21.
For critically ill patients undergoing continuous renal replacement therapy (CRRT), daptomycin dosing recommendations are scarce. We, therefore, retrospectively assessed routinely measured daptomycin plasma concentrations, daptomycin dose administered and microbiological data in 11 critically ill patients with Gram-positive infections that had received daptomycin once daily.
The retrospective analysis included critically ill patients treated at the intensive care unit (ICU) who had daptomycin plasma concentrations measured.
Daptomycin dose ranged from 3 to 8 mg/kg/q24 h in patients undergoing CRRT (n = 7) and 6 to 10 mg/kg/q24 h in patients without CRRT (n = 4). Peak and trough concentrations showed a high intra- and inter-patient variability in both groups, independent of the dosage per kg body weight. No drug accumulation was detected in CRRT patients with once-daily daptomycin dosing. Causative pathogens were Enterococcus faecium (n = 6), coagulase-negative Staphylococcus (n = 2), Staphylococcus aureus (n = 2) and unknown in one patient. Microbiological eradication was successful in 8 of 11 patients. Two of three patients with unsuccessful microbiological eradication and fatal outcome had an Enterococcus faecium infection.
In critically ill patients undergoing CRRT, daptomycin exposure with once-daily dosing was similar to ICU patients with normal renal function, but lower compared to healthy volunteers. Our data suggest that daptomycin once-daily dosing is appropriate in patients undergoing CRRT.
对于接受连续肾脏替代治疗(CRRT)的危重症患者,达托霉素的给药推荐意见很少。因此,我们回顾性评估了 11 例接受每日 1 次达托霉素治疗的革兰阳性感染的危重症患者的常规测量的达托霉素血浆浓度、给予的达托霉素剂量和微生物学数据。
该回顾性分析包括在重症监护病房(ICU)接受治疗且测量了达托霉素血浆浓度的危重症患者。
接受 CRRT 的患者(n = 7)的达托霉素剂量为 3 至 8 mg/kg/q24 h,未接受 CRRT 的患者(n = 4)的达托霉素剂量为 6 至 10 mg/kg/q24 h。两组患者的峰浓度和谷浓度均表现出很高的个体内和个体间变异性,与每公斤体重的剂量无关。在接受每日 1 次达托霉素给药的 CRRT 患者中未检测到药物蓄积。致病病原体分别为屎肠球菌(n = 6)、凝固酶阴性葡萄球菌(n = 2)、金黄色葡萄球菌(n = 2)和 1 例未知。11 例患者中有 8 例微生物学清除成功。2 例微生物学清除失败且死亡的患者均感染粪肠球菌。
在接受 CRRT 的危重症患者中,每日 1 次给药时的达托霉素暴露与肾功能正常的 ICU 患者相似,但低于健康志愿者。我们的数据表明,在接受 CRRT 的患者中,每日 1 次达托霉素给药是合适的。