Prospective Determination of Serum Ceftazidime Concentrations in Intensive Care Units

被引:33
作者
Aubert, Gerald [1 ]
Carricajo, Anne [2 ]
Coudrot, Maud [3 ]
Guyomarc'h, Stephane [3 ]
Auboyer, Christian [4 ]
Zeni, Fabrice [3 ]
机构
[1] Ctr Hosp Univ, North Hosp, Antibiol Lab, St Etienne, France
[2] Ctr Hosp Univ, North Hosp, Bacteriol Lab, St Etienne, France
[3] Ctr Hosp Univ, North Hosp, Intens Med Care Unit, St Etienne, France
[4] Ctr Hosp Univ, North Hosp, Intens Surg Care Unit, St Etienne, France
关键词
therapeutic drug monitoring; PK/PD; ceftazidime; dosage; Pseudomonas aeruginosa; CRITICALLY-ILL PATIENT; PHARMACODYNAMICS; PHARMACOKINETICS; INFECTIONS; INFUSION;
D O I
10.1097/FTD.0b013e3181e60ca6
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Introduction: The purpose of this study was to assess the value of a serum assay for ceftazidime (CAZ) in patients in the intensive care unit (ICU) of the Saint-Etienne University Teaching Hospital and in other ICUs in the region to optimize therapy. Material and Methods: Between November 1, 2005, and February 29, 2008, for patients hospitalized in ICUs not on dialysis and undergoing continuous CAZ infusion, serum assay of the antibiotic was performed 36 to 48 hours after the start of treatment using a single serum sample. The target serum CAZ concentration was 40 +/- 10 mg/L with a concentration/minimum inhibitory concentration ratio of 5 or greater x minimum inhibitory concentration of CAZ when a strain was isolated. Results: Serum CAZ concentration was determined in 92 patients (28 females, 64 males) receiving CAZ by continuous infusion. The mean age was 66 years (range, 19-89 years) and the mean weight was 73 kg (range, 33-122 kg). The CAZ dose was between 1 g and 6 g/24 hours. The mean serum CAZ concentration was 46.9 mg/L (range, 7.4-162.3 mg/L). Serum CAZ concentrations were as follows: 30 to 50 mg/L in 35.9% of patients, less than 30 mg/L in 36.9%, and greater than 50 mg/L in 27.2%. Infection was documented in 51 patients, with 42 strains of Pseudomonas aeruginosa being detected. The serum concentration/minimum inhibitory concentration ratio was 5 or greater for 84.3%. Antibiotic dosage was adjusted based on the CAZ assay results. Conclusion: Our study suggests that CAZ measurement is needed in ICUs to achieve adequate CAZ concentrations to avoid treatment toxicity and to achieve efficacy as rapidly as possible, particularly in strains having limited susceptibility to antibiotics.
引用
收藏
页码:517 / 519
页数:3
相关论文
共 13 条
[1]   Is there a pharmacodynamic need for the use of continuous versus intermittent infusion with ceftazidime against Pseudomonas aeruginosa?: An in vitro pharmacodynamic model [J].
Alou, L ;
Aguilar, L ;
Sevillano, D ;
Giménez, MJ ;
Echeverría, O ;
Gómez-Lus, ML ;
Prieto, J .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 55 (02) :209-213
[2]   Treatment of infections with ESBL-producing organisms: pharmacokinetic and pharmacodynamic considerations [J].
Andes, D ;
Craig, WA .
CLINICAL MICROBIOLOGY AND INFECTION, 2005, 11 :10-17
[3]   Imipenem levels are not predictable in the critically ill patient [J].
Belzberg, H ;
Zhu, J ;
Cornwell, EE ;
Murray, JA ;
Sava, J ;
Salim, A ;
Velmahos, GC ;
Gill, MA .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 2004, 56 (01) :111-117
[4]   Pharmacokinetics of ceftazidime in serum and peritoneal exudate during continuous versus intermittent administration to patients with severe intra-abdominal infections [J].
Buijk, SLCE ;
Gyssens, IC ;
Mouton, JW ;
Van Vliet, A ;
Verbrugh, HA ;
Bruining, HA .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 49 (01) :121-128
[5]   PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE [J].
COCKCROFT, DW ;
GAULT, MH .
NEPHRON, 1976, 16 (01) :31-41
[6]   INTERRELATIONSHIP BETWEEN PHARMACOKINETICS AND PHARMACODYNAMICS IN DETERMINING DOSAGE REGIMENS FOR BROAD-SPECTRUM CEPHALOSPORINS [J].
CRAIG, WA .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1995, 22 (1-2) :89-96
[7]   Continuous infusion ceftazidime in intensive care: a randomized controlled trial [J].
Lipman, J ;
Gomersall, CD ;
Gin, T ;
Joynt, GM ;
Young, RJ .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1999, 43 (02) :309-311
[8]   Optimizing ceftazidime pharmacodynamics in patients with acute exacerbation of severe chronic bronchitis [J].
Lubasch, A ;
Lück, S ;
Lode, H ;
Mauch, H ;
Lorenz, J ;
Bölcskei, P ;
Welte, T .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 51 (03) :659-664
[9]   Concentration-effect relationship of ceftazidime explains why the time above the MIC is 40 percent for a static effect in vivo [J].
Mouton, Johan W. ;
Punt, Nieko ;
Vinks, Alexander A. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (09) :3449-3451
[10]   Continuous versus intermittent administration of ceftazidime in intensive care unit patients with nosocomial pneumonia [J].
Nicolau, DP ;
McNabb, J ;
Lacy, MK ;
Quintiliani, R ;
Nightingale, CH .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2001, 17 (06) :497-504