Variability of linezolid concentrations after standard dosing in critically ill patients: a prospective observational study

被引:94
作者
Zoller, Michael [1 ]
Maier, Barbara [2 ]
Hornuss, Cyrill [1 ]
Neugebauer, Christina [1 ]
Doebbeler, Gundula [1 ]
Nagel, Dorothea [2 ]
Holdt, Lesca Miriam [2 ]
Bruegel, Mathias [2 ]
Weig, Thomas [1 ]
Grabein, Beatrice [3 ,4 ]
Frey, Lorenz [1 ]
Teupser, Daniel [2 ]
Vogeser, Michael [2 ]
Zander, Johannes [2 ]
机构
[1] Hosp Ludwig Maximilians Univ Munich, Dept Anesthesiol, D-81377 Munich, Germany
[2] Hosp Ludwig Maximilians Univ Munich, Inst Lab Med, D-81377 Munich, Germany
[3] Hosp Ludwig Maximilians Univ Munich, Dept Clin Microbiol, D-81377 Munich, Germany
[4] Hosp Ludwig Maximilians Univ Munich, Hosp Hyg, D-81377 Munich, Germany
关键词
CONTINUOUS VENOVENOUS HEMOFILTRATION; RESISTANT STAPHYLOCOCCUS-AUREUS; GRAM-POSITIVE INFECTIONS; PHARMACOKINETIC/PHARMACODYNAMIC PROFILE; ANTIMICROBIAL THERAPY; UNITED-STATES; SEVERE SEPSIS; SEPTIC SHOCK; PHARMACOKINETICS; EPIDEMIOLOGY;
D O I
10.1186/cc13984
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Introduction: Severe infections in intensive care patients show high morbidity and mortality rates. Linezolid is an antimicrobial drug frequently used in critically ill patients. Recent data indicates that there might be high variability of linezolid serum concentrations in intensive care patients receiving standard doses. This study was aimed to evaluate whether standard dosing of linezolid leads to therapeutic serum concentrations in critically ill patients. Methods: In this prospective observational study, 30 critically ill adult patients with suspected infections received standard dosing of 600 mg linezolid intravenously twice a day. Over 4 days, multiple serum samples were obtained from each patient, in order to determine the linezolid concentrations by liquid chromatography tandem mass spectrometry. Results: A high variability of serum linezolid concentrations was observed (range of area under the linezolid concentration time curve over 24 hours (AUC(24)) 50.1 to 453.9 mg/L, median 143.3 mg*h/L; range of trough concentrations (C-min) < 0.13 to 14.49 mg/L, median 2.06 mg/L). Furthermore, potentially subtherapeutic linezolid concentrations over 24 hours and at single time points (defined according to the literature as AUC(24)<200 mg*h/L and C-min < 2 mg/L) were observed for 63% and 50% of the patients, respectively. Finally, potentially toxic levels (defined as AUC(24)>400 mg*h/L and C-min > 10 mg/L) were observed for 7 of the patients. Conclusions: A high variability of linezolid serum concentrations with a substantial percentage of potentially subtherapeutic levels was observed in intensive care patients. The findings suggest that therapeutic drug monitoring of linezolid might be helpful for adequate dosing of linezolid in critically ill patients.
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页数:11
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共 54 条
[1]   Linezolid pharmacokinetic/pharmacodynamic profile in critically ill septic patients: intermittent versus continuous infusion [J].
Adembri, Chiara ;
Fallani, Stefania ;
Cassetta, Maria Iris ;
Arrigucci, Silvia ;
Ottaviano, Alessandra ;
Pecile, Patrizia ;
Mazzei, Teresita ;
De Gaudio, Raffaele ;
Novelli, Andrea .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2008, 31 (02) :122-129
[2]  
Alvarez-Lerma F, 2012, REV ESP QUIM, V25, P65
[3]   Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care [J].
Angus, DC ;
Linde-Zwirble, WT ;
Lidicker, J ;
Clermont, G ;
Carcillo, J ;
Pinsky, MR .
CRITICAL CARE MEDICINE, 2001, 29 (07) :1303-1310
[4]   The emergence of vancomycin-intermediate and vancomycin-resistant Staphylococcus aureus [J].
Appelbaum, PC .
CLINICAL MICROBIOLOGY AND INFECTION, 2006, 12 :16-23
[5]   Trends in antimicrobial-drug resistance in Japan [J].
Arakawa, Y ;
Ike, Y ;
Nagasawa, M ;
Shibata, N ;
Doi, Y ;
Shibayama, K ;
Yagi, T ;
Kurata, T .
EMERGING INFECTIOUS DISEASES, 2000, 6 (06) :572-575
[6]  
Bodmann KF, 2010, CHEMOTHER J, V19, P179
[7]   Pharmacokinetics and intrapulmonary concentrations of linezolid administered to critically ill patients with ventilator-associated pneumonia [J].
Boselli, E ;
Breilh, D ;
Rimmelé, T ;
Djabarouti, S ;
Toutain, A ;
Chassard, D ;
Saux, MC ;
Allaouchiche, B .
CRITICAL CARE MEDICINE, 2005, 33 (07) :1529-1533
[8]   Linezolid Pharmacokinetics in Patients With Acute Renal Failure Undergoing Continuous Venovenous Hemodiafiltration [J].
Carcelero, Esther ;
Soy, Dolors ;
Guerrero, Laura ;
Poch, Esteban ;
Fernandez, Javier ;
Castro, Pedro ;
Ribas, Jose .
JOURNAL OF CLINICAL PHARMACOLOGY, 2012, 52 (09) :1430-1435
[9]   Linezolid plasma concentrations and occurrence of drug-related haematological toxicity in patients with Gram-positive infections [J].
Cattaneo, Dario ;
Orlando, Giovanna ;
Cozzi, Valeria ;
Cordier, Laura ;
Baldelli, Sara ;
Merli, Stefania ;
Fucile, Serena ;
Gulisano, Cecilia ;
Rizzardini, Giuliano ;
Clementi, Emilio .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2013, 41 (06) :586-589
[10]   Linezolid versus teicoplanin in the treatment of Gram-positive infections in the critically ill: a randomized, double-blind, multicentre study [J].
Cepeda, JA ;
Whitehouse, T ;
Cooper, B ;
Hails, J ;
Jones, K ;
Kwaku, F ;
Taylor, L ;
Hayman, S ;
Shaw, S ;
Kibbler, C ;
Shulman, R ;
Singer, M ;
Wilson, APR .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2004, 53 (02) :345-355