HOW VANCOMYCIN IS USED IN AUSTRALASIA - A SURVEY

被引:9
作者
DUFFULL, SB [1 ]
CHAMBERS, ST [1 ]
BEGG, EJ [1 ]
机构
[1] CHRISTCHURCH HOSP, DEPT INFECT DIS, CHRISTCHURCH, NEW ZEALAND
来源
AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE | 1993年 / 23卷 / 06期
关键词
VANCOMYCIN; THERAPEUTIC DRUG MONITORING; SURVEY;
D O I
10.1111/j.1445-5994.1993.tb04723.x
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background: Vancomycin serum concentrations have been monitored over the last 30 years in an attempt to avoid dose-dependent toxicity and enhance efficacy. Current literature recommendations for peak and trough concentrations are usually in the range of 20-40 mg/L and 5-10 mg/L, respectively. Literature recommendations regarding the time at which peak concentrations are measured are highly variable, ranging from immediately after the end of the infusion to three hours post-dose. Aims: To identify how vancomycin dosing is being monitored and assess variability in the current practice. Methods: A survey of microbiology departments and infectious disease physicians in major Australasian hospitals was undertaken. The variability in the current practice was assessed by fitting mean recommendations to a two compartment Bayesian model. Results: Of the 83 (70%) who replied 71 (86%) monitored vancomycin concentrations. Fifty-four percent targeted peak concentrations within the range of 20-40 mg/L, and 73% targeted trough concentrations less-than-or-equal-to 10 mg/L. The time of sampling of peak concentrations varied considerably ranging from immediately (12%) to 120 minutes (12%) post-infusion (median 30 minutes [40%]). The concentration-time curves resulting from three sets of mean recommendations ('peaks' drawn at: 0, 30 and 120 minutes aiming for a concentration of 35 mg/L with a trough concentration of 10 mg/L) were modelled using a two compartment Bayesian programme. The predicted true peak (maximum) concentrations ranged from 30 to 86 mg/L, despite aiming for identical target concentrations, indicating marked variation in the actual dosing practice. Conclusions: There is thus considerable variation in the practice of vancomycin therapeutic monitoring which has a major effect on dosing. The main contributing factor is the variable timing of sampling peak concentrations.
引用
收藏
页码:662 / 666
页数:5
相关论文
共 31 条
[1]
VANCOMYCIN - A REAPPRAISAL [J].
AHMAD, R ;
RAICHURA, N ;
KILBANE, V ;
WHITFIELD, E .
BRITISH MEDICAL JOURNAL, 1982, 284 (6333) :1953-1954
[2]
INDIVIDUALIZED AMINOGLYCOSIDE DOSAGE BASED ON PHARMACOKINETIC ANALYSIS IS SUPERIOR TO DOSAGE BASED ON PHYSICIAN INTUITION AT ACHIEVING TARGET PLASMA DRUG CONCENTRATIONS [J].
BEGG, EJ ;
ATKINSON, HC ;
JEFFERY, GM ;
TAYLOR, NW .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1989, 28 (02) :137-141
[3]
BOHLER J, 1992, EUR J CLIN PHARMACOL, V42, P635
[4]
RELATIONSHIP OF SERUM ANTIBIOTIC CONCENTRATIONS TO NEPHROTOXICITY IN CANCER-PATIENTS RECEIVING CONCURRENT AMINOGLYCOSIDE AND VANCOMYCIN THERAPY [J].
CIMINO, MA ;
ROTSTEIN, C ;
SLAUGHTER, RL ;
EMRICH, LJ .
AMERICAN JOURNAL OF MEDICINE, 1987, 83 (06) :1091-1097
[5]
PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE [J].
COCKCROFT, DW ;
GAULT, MH .
NEPHRON, 1976, 16 (01) :31-41
[6]
EDWARDS DJ, 1987, CLIN PHARMACY, V6, P652
[7]
RETROSPECTIVE STUDY OF THE TOXICITY OF PREPARATIONS OF VANCOMYCIN FROM 1974 TO 1981 [J].
FARBER, BF ;
MOELLERING, RC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1983, 23 (01) :138-141
[8]
SURVEY OF VANCOMYCIN MONITORING GUIDELINES IN ILLINOIS HOSPITALS [J].
FITZSIMMONS, WE ;
POSTELNICK, MJ ;
TORTORICE, PV .
DRUG INTELLIGENCE & CLINICAL PHARMACY, 1988, 22 (7-8) :598-600
[9]
GALLOWAY E, 1991, DIRECTORY NZ HOSPITA
[10]
GARRELTS JC, 1987, CLIN PHARMACY, V6, P795