Once-daily dosing of aminoglycosides: review and recommendations for clinical practice

被引:172
作者
Freeman, CD
Nicolau, DP
Belliveau, PP
Nightingale, CH
机构
[1] HARTFORD HOSP, DIV INFECT DIS, HARTFORD, CT 06115 USA
[2] UNIV MASSACHUSETTS, MED CTR, DEPT PHARM, WORCESTER, MA USA
[3] HARTFORD HOSP, DEPT RES, HARTFORD, CT 06115 USA
关键词
D O I
10.1093/jac/39.6.677
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The use of higher-dose, extended interval (i.e., once-daily) aminoglycoside regimens to optimize bacterial killing is justified by a pharmacodynamic principle of aminoglycosides, namely concentration-dependent killing, and by the partial attribution of the toxicity of aminoglycosides to prolonged serum concentrations. Numerous in-vitro and animal studies have supported using once-daily aminoglycoside dosing. Clinical studies show at least equal effectiveness and no greater toxicity when compared with traditional regimens. A dose of 5-7 mg/kg of gentamicin, tobramycin, or netilmicin, with at least a 24 h dosing interval should be employed and a similar regimen can be applied to amikacin dosing. As yet, there are some patient populations that have not been adequately studied to determine whether or not once-daily aminoglycoside dosing would be a better choice than traditional dosing regimens.
引用
收藏
页码:677 / 686
页数:10
相关论文
共 74 条
[1]   EXPERIENCE OF ONCE-DAILY AMINOGLYCOSIDE DOSING USING A TARGET AREA UNDER THE CONCENTRATION-TIME CURVE [J].
BARCLAY, ML ;
DUFFULL, SB ;
BEGG, EJ ;
BUTTIMORE, RC .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE, 1995, 25 (03) :230-235
[2]   COMPARISON OF GENTAMICIN DOSING REGIMENS USING AN INVITRO MODEL [J].
BEGG, EJ ;
PEDDIE, BA ;
CHAMBERS, ST ;
BOSWELL, DR .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1992, 29 (04) :427-433
[3]   A SUGGESTED APPROACH TO ONCE-DAILY AMINOGLYCOSIDE DOSING [J].
BEGG, EJ ;
BARCLAY, ML ;
DUFFULL, SB .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1995, 39 (06) :605-609
[4]  
BELLIVEAU PP, 1995, J INFECT DIS PHARMAC, V1, P11
[5]   MODIFICATION OF EXPERIMENTAL AMINOGLYCOSIDE NEPHROTOXICITY [J].
BENNETT, WM ;
WOOD, CA ;
HOUGHTON, DC ;
GILBERT, DN .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1986, 8 (05) :292-296
[6]   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
[7]   NEPHROTOXICITY, HIGH-FREQUENCY OTOTOXICITY, EFFICACY AND SERUM KINETICS OF ONCE VERSUS THRICE DAILY DOSING OF NETILMICIN IN PATIENTS WITH SERIOUS INFECTIONS [J].
BLASER, J ;
SIMMEN, HP ;
THURNHEER, U ;
KONIG, C ;
LUTHY, R .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1995, 36 (05) :803-814
[8]   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
[9]   SIMULATED HUMAN SERUM PROFILES OF ONE DAILY DOSE OF CEFTRIAXONE PLUS NETILMICIN IN TREATMENT OF EXPERIMENTAL STREPTOCOCCAL ENDOCARDITIS [J].
BLATTER, M ;
FLUCKIGER, U ;
ENTENZA, J ;
GLAUSER, MP ;
FRANCIOLI, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (09) :1971-1976
[10]   PHARMACOKINETICS OF TOBRAMYCIN IN PREGNANT-WOMEN - SAFETY AND EFFICACY OF A ONCE-DAILY DOSE REGIMEN [J].
BOURGET, P ;
FERNANDEZ, H ;
DELOUIS, C ;
TABURET, AM .
JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS, 1991, 16 (03) :167-176