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Pharmacokinetics of Doripenem During High Volume Hemodiafiltration in Patients With Septic Shock
被引:7
|作者:
Tamme, Kadri
[1
,2
]
Oselin, Kersti
[2
]
Kipper, Karin
[3
]
Low, Kaywei
[4
]
Standing, Joseph F.
[4
]
Metsvaht, Tuuli
[1
]
Karjagin, Juri
[1
,2
]
Herodes, Koit
[3
]
Kern, Hartmut
[1
,5
]
Starkopf, Joel
[1
,2
]
机构:
[1] Tartu Univ Hosp, Clin Anaesthesiol & Intens Care, EE-51014 Tartu, Estonia
[2] Univ Tartu, Dept Anaesthesiol & Intens Care, EE-50090 Tartu, Estonia
[3] Univ Tartu, Inst Chem, Testing Ctr, EE-50090 Tartu, Estonia
[4] UCL, Sch Pharm, London, England
[5] DRK Kliniken, Dept Anaesthesiol & Intens Care, Berlin, Germany
来源:
基金:
英国医学研究理事会;
关键词:
antibiotics;
carbapenems;
intensive care;
renal replacement therapy;
dosing;
CRITICALLY-ILL PATIENTS;
ORGAN FAILURE;
SEVERE SEPSIS;
PHARMACODYNAMICS;
RESISTANCE;
OPTIMIZATION;
GUIDELINES;
THERAPY;
D O I:
10.1002/jcph.432
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Pharmacokinetics (PK) of doripenem was determined during high volume hemodiafiltration (HVHDF) in patients with septic shock. A single 500 mg dose of doripenem was administered as a 1 hour infusion during HVHDF to 9 patients. Arterial blood samples were collected before and at 30 or 60 minute intervals over 8 hours (12 samples) after study drug administration. Doripenem concentrations were determined by ultrahigh performance liquid chromatography-tandem mass spectrometry. Population PK analysis and Monte Carlo simulation of 1,000 subjects were performed. The median convective volume of HVHDF was 10.3 L/h and urine output during the sampling period was 70 mL. The population mean total doripenem clearance on HVHDF was 6.82 L/h, volume of distribution of central compartment 10.8 L, and of peripheral compartment 12.1 L. Doses of 500 mg every 8 hours resulted in 88.5% probability of attaining the target of 50% time over MIC for bacteria with MIC = 2 mu g/mL at 48 hours, when doubling of MIC during that time was assumed. Significant elimination of doripenem occurs during HVHDF. Doses of 500 mu g every 8 hours are necessary for treatment of infections caused by susceptible bacteria during extended HVHDF.
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页码:438 / 446
页数:9
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