NEPHROTOXICITY, HIGH-FREQUENCY OTOTOXICITY, EFFICACY AND SERUM KINETICS OF ONCE VERSUS THRICE DAILY DOSING OF NETILMICIN IN PATIENTS WITH SERIOUS INFECTIONS

被引:13
作者
BLASER, J [1 ]
SIMMEN, HP [1 ]
THURNHEER, U [1 ]
KONIG, C [1 ]
LUTHY, R [1 ]
机构
[1] INSELSPITAL BERN,ANNA SEILER HAUS,CH-3010 BERN,SWITZERLAND
关键词
D O I
10.1093/jac/36.5.803
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The effect of dosing regimen on nephrotoxicity, high frequency ototoxicity, efficacy and serum kinetics was studied in a prospective, randomised clinical study. Therapy was started with total daily doses of 6 mg/kg given once (od) or thrice (tid) daily to 56 and 57 patients, respectively. Subsequent doses were adjusted according to serum levels. No major differences in toxicity or efficacy were noticed between od and tid regimens: clinical failures occurred in two and two patients, four and five patients suffered from a decrease of greater than or equal to 20 dB at least unilaterally at one frequency between 8 and 18 kHz, six and seven patients had a > 25 mu mol/L or > 25% increase in serum creatinine, respectively. Serum creatinine or creatinine clearance did not change significantly during either therapy. Major differences between the two study groups were limited to pharmacokinetic parameters. Od dosing resulted in higher peak (mean of 21.6 vs 7.2mg/L) and lower trough levels (0.5 vs 1.4mg/L). Half-lives of netilmicin determined between 1 and 8h increased significantly during therapy with tid (from a mean of 2.75 to a mean of 3.33 h, P<0.01) but not significantly with od (rise from 2.8 to 3.03 h). Much longer half-lives were determined between 8 and 24 h in the od group (mean of 5.7 h, P<0.01). In conclusion, only minimal differences in toxicity and efficacy were observed. Their clinical relevance appears to be minimal.
引用
收藏
页码:803 / 814
页数:12
相关论文
共 20 条
[1]   INFLUENCE OF DOSAGE REGIMEN ON EXPERIMENTAL GENTAMICIN-NEPHROTOXICITY - DISSOCIATION OF PEAK SERUM LEVELS FROM RENAL-FAILURE [J].
BENNETT, WM ;
PLAMP, CE ;
GILBERT, DN ;
PARKER, RA ;
PORTER, GA .
JOURNAL OF INFECTIOUS DISEASES, 1979, 140 (04) :576-580
[2]   COMPARATIVE-STUDY WITH ENOXACIN AND NETILMICIN IN A PHARMACODYNAMIC MODEL TO DETERMINE IMPORTANCE OF RATIO OF ANTIBIOTIC PEAK CONCENTRATION TO MIC FOR BACTERICIDAL ACTIVITY AND EMERGENCE OF RESISTANCE [J].
BLASER, J ;
STONE, BB ;
GRONER, MC ;
ZINNER, SH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1987, 31 (07) :1054-1060
[3]   MONITORING SERUM CONCENTRATIONS FOR ONCE-DAILY NETILMICIN DOSING REGIMENS [J].
BLASER, J ;
KONIG, C ;
SIMMEN, HP ;
THURNHEER, U .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1994, 33 (02) :341-348
[4]   PHARMACODYNAMICS OF AMIKACIN INVITRO AND IN MOUSE THIGH AND LUNG INFECTIONS [J].
CRAIG, WA ;
REDINGTON, J ;
EBERT, SC .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1991, 27 :29-40
[5]  
DEVRIES PJ, 1990, EUR J CLIN MICROBIOL, V9, P161
[6]   IMPORTANCE OF THE AMINOGLYCOSIDE DOSING REGIMEN IN THE PENICILLIN-NETILMICIN COMBINATION FOR TREATMENT OF ENTEROCOCCUS-FAECALIS-INDUCED EXPERIMENTAL ENDOCARDITIS [J].
FANTIN, B ;
CARBON, C .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (12) :2387-2391
[7]   ANTIBIOTIC-THERAPY OF INFECTIONS DUE TO PSEUDOMONAS-AERUGINOSA IN NORMAL AND GRANULOCYTOPENIC MICE - COMPARISON OF MURINE AND HUMAN PHARMACOKINETICS [J].
GERBER, AU ;
BRUGGER, HP ;
FELLER, C ;
STRITZKO, T ;
STALDER, B .
JOURNAL OF INFECTIOUS DISEASES, 1986, 153 (01) :90-97
[8]   ONCE-DAILY AMINOGLYCOSIDE THERAPY [J].
GILBERT, DN .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (03) :399-405
[9]   LONG-TERM ACCURACY OF FLUORESCENCE POLARIZATION IMMUNOASSAYS FOR GENTAMICIN, TOBRAMYCIN, NETILMICIN AND VANCOMYCIN [J].
JOOS, B ;
LUTHY, R ;
BLASER, J .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1989, 24 (05) :797-803
[10]   SINGLE, LARGE, DAILY DOSING VERSUS INTERMITTENT DOSING OF TOBRAMYCIN FOR TREATING EXPERIMENTAL PSEUDOMONAS PNEUMONIA [J].
KAPUSNIK, JE ;
HACKBARTH, CJ ;
CHAMBERS, HF ;
CARPENTER, T ;
SANDE, MA .
JOURNAL OF INFECTIOUS DISEASES, 1988, 158 (01) :7-12