POPULATION PHARMACOKINETICS AND RENAL FUNCTION-SPARING EFFECTS OF AMPHOTERICIN-B COLLOIDAL DISPERSION IN PATIENTS RECEIVING BONE-MARROW TRANSPLANTS

被引:39
作者
AMANTEA, MA
BOWDEN, RA
FORREST, A
WORKING, PK
NEWMAN, MS
MAMELOK, RD
机构
[1] FRED HUTCHINSON CANC RES CTR,SEATTLE,WA 98104
[2] SUNY BUFFALO,MILLARD FILLMORE HOSP,CLIN PHARMACOKINET LAB,BUFFALO,NY 14209
关键词
D O I
10.1128/AAC.39.9.2042
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The purpose of this study was to evaluate the pharmacokinetics of amphotericin B colloidal dispersion and its effect on creatinine clearance in bone marrow transplant patients with systemic fungal infections. Seventy-five patients (42 females and 33 males) with a median age of 34.5 years and a median weight of 70.0 kg were enrolled in the study, Patients received 1 of 15 dose levels (range, 0.5 to 8.0 mg/kg of body weight) daily for a mean duration of 28 days and a mean cumulative dose amount of 8 g. Plasma samples for amphotericin B determination (median number, 4; range, 2 to 30) and daily serum creatinine values were obtained for each patient. Iterative two-stage analysis, one of several approaches to population pharmacokinetic and pharmacodynamic modelling, was employed for the pharmacokinetic analysis, The plasma data were available for 51 of 75 patients and were best described by a two-compartment model, Both plasma clearance and volume of distribution increased with escalating doses; the overall average terminal elimination half-life was 29 h, Of the covariates studied, only body weight and dose size were significant. Serum creatinine values over the duration of therapy were available for 59 of 75 patients, Overall, there was no net change in renal function over the duration of therapy; 12 patients had >30% increases in creatinine clearance, whereas 13 had >30% decreases, No measure of amphotericin B colloidal dispersion exposure, demographic values, or concomitant treatment with other medications was related to changes in the creatinine clearance.
引用
收藏
页码:2042 / 2047
页数:6
相关论文
共 36 条
[1]  
AKAIKE H, 1979, BIOMETRIKA, V66, P237, DOI 10.1093/biomet/66.2.237
[2]   AMPHOTERICIN-B PHARMACOKINETICS IN HUMANS [J].
ATKINSON, AJ ;
BENNETT, JE .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1978, 13 (02) :271-276
[3]   INHIBITION OF THE INTERACTION BETWEEN LIPOPROTEINS AND AMPHOTERICIN-B BY SOME DELIVERY SYSTEMS [J].
BARWICZ, J ;
GAREAU, R ;
AUDET, A ;
MORISSET, A ;
VILLIARD, J ;
GRUDA, I .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 181 (02) :722-728
[4]  
CHIOU WL, 1975, J CLIN PHARMACOL, V45, P427
[5]   PROGRAM PACKAGE FOR SIMULATION AND PARAMETER-ESTIMATION IN PHARMACOKINETIC SYSTEMS [J].
DARGENIO, DZ ;
SCHUMITZKY, A .
COMPUTER PROGRAMS IN BIOMEDICINE, 1979, 9 (02) :115-134
[6]  
DARGENIO DZ, 1992, ADAPT USERS GUIDE BI
[7]   RELATIONSHIP OF PHARMACOKINETICS AND DRUG DISTRIBUTION IN TISSUE TO INCREASED SAFETY OF AMPHOTERICIN-B COLLOIDAL DISPERSION IN DOGS [J].
FIELDING, RM ;
SINGER, AW ;
WANG, LH ;
BABBAR, S ;
GUO, LSS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (02) :299-307
[8]   COMPARATIVE PHARMACOKINETICS OF AMPHOTERICIN-B AFTER ADMINISTRATION OF A NOVEL COLLOIDAL DELIVERY SYSTEM, ABCD, AND A CONVENTIONAL FORMULATION TO RATS [J].
FIELDING, RM ;
SMITH, PC ;
WANG, LH ;
PORTER, J ;
GUO, LSS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (06) :1208-1213
[9]  
FIELDS BT, 1971, APPL MICROBIOL, V2, P615
[10]   DEVELOPMENT OF A POPULATION PHARMACOKINETIC MODEL AND OPTIMAL SAMPLING STRATEGIES FOR INTRAVENOUS CIPROFLOXACIN [J].
FORREST, A ;
BALLOW, CH ;
NIX, DE ;
BIRMINGHAM, MC ;
SCHENTAG, JJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (05) :1065-1072