Teicoplanin Dosing Strategy for Treatment of Staphylococcus aureus in Korean Patients with Neutropenic Fever

被引:18
作者
Ahn, Byung-Jin [2 ]
Yim, Dong-Seok [3 ]
Lee, Dong-Gun [1 ]
Kwon, Jae-Cheol [1 ]
Kim, Si-Hyun [1 ]
Choi, Su-Mi [1 ]
机构
[1] Catholic Univ Korea, Coll Med, Dept Internal Med, Seoul 137701, South Korea
[2] Dongguk Univ, Grad Sch, Dept Med, Seoul, South Korea
[3] Catholic Univ Korea, Coll Med, Dept Pharmacol, Seoul 137701, South Korea
关键词
Teicoplanin; Staphylococcus aureus; neutropenia; pharmacokinetics; pharmacodynamics; VANCOMYCIN; PHARMACODYNAMICS; PHARMACOKINETICS; GLYCOPEPTIDES; THERAPY; SYSTEM;
D O I
10.3349/ymj.2011.52.4.616
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: The present study was conducted to determine and compare the target attainment rate (TAR) between microorganism-nonspecific (C-trough) and microorganism-specific (AUC(24)/MIC) targets over two weeks of teicoplanin administration according to several dose regimens for the treatment of Staphylococcus aureus in Korean patients with neutropenic fever. Materials and Methods: One thousand virtual concentrations were obtained for each dose using the population pharmacokinetic parameters of teicoplanin adopted from a published study. Simulation of 1,000 virtual MICs was performed using the MICs of 78 clinical isolates of S. aureus collected from a hospital in Korea. Thereafter, these simulated MICs were randomly allocated to 1,000 virtual patients in whom the TARs for AUC(24)/MIC >125 [or 345] and C-trough >10 [or 20] mg/L were determined. The relationship of the maintenance dose with the steady-state TAR was predicted with respect to the AUC(24)/MIC >125 [or 345] using logistic analysis. Results: The standard dose regimen of teicoplanin showed TARs of about 70% [or 33%] and 70% [or 20%] at steady-state in cases with AUC(24)/MIC >125 [or 345] and C-trough >10 [or 20] mg/L, respectively. Conclusion: The current standard dose regimen was predicted to be insufficient to adequately treat S. aureus in Korean patients with neutropenic fever. To assure at least an 80% TAR in this population, dose adjustment of teicoplanin should be considered.
引用
收藏
页码:616 / 623
页数:8
相关论文
共 26 条
[11]  
MacGowan Alasdair, 1996, J Infect Chemother, V2, P197, DOI 10.1007/BF02355116
[12]   Pharmacodynamics, pharmacokinetics, and therapeutic drug monitoring of glycopeptides [J].
MacGowan, AP .
THERAPEUTIC DRUG MONITORING, 1998, 20 (05) :473-477
[13]   Pharmacokinetic and pharmacodynamic issues in the treatment of bacterial infectious diseases [J].
McKinnon, PS ;
Davis, SL .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2004, 23 (04) :271-288
[14]   Area under the inhibitory curve and a pneumonia scoring system for predicting outcomes of vancomycin therapy for respiratory infections by Staphylococcus aureus [J].
Moise, PA ;
Forrest, A ;
Bhavnani, SM ;
Birmingham, MC ;
Schentag, JJ .
AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 2000, 57 (20) :S4-S9
[15]   Pharmacodynamics of vancomycin and other antimicrobials in patients with Staphylococcus aureus lower respiratory tract infections [J].
Moise-Broder, PA ;
Forrest, A ;
Birmingham, MC ;
Schentag, JJ .
CLINICAL PHARMACOKINETICS, 2004, 43 (13) :925-942
[16]  
Park SH, 2006, MOL CELLS, V21, P21
[17]   Teicoplanin therapeutic drug monitoring in critically ill patients: a retrospective study emphasizing the importance of a loading dose [J].
Pea, F ;
Brollo, L ;
Viale, P ;
Pavan, F ;
Furlanut, M .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 51 (04) :971-975
[18]   Teicoplanin in patients with acute leukaemia and febrile neutropenia - A special population benefiting from higher dosages [J].
Pea, F ;
Viale, P ;
Candoni, A ;
Pavan, F ;
Pagani, L ;
Damiani, D ;
Casini, M ;
Furlanut, M .
CLINICAL PHARMACOKINETICS, 2004, 43 (06) :405-415
[19]   Vancomycin Therapeutic Guidelines: A Summary of Consensus Recommendations from the Infectious Diseases Society of America, the American Society of Health-System Pharmacists, and the Society of Infectious Diseases Pharmacists [J].
Rybak, Michael J. ;
Lomaestro, Ben M. ;
Rotschafer, John C. ;
Moellering, Robert C., Jr. ;
Craig, Willam A. ;
Billeter, Marianne ;
Dalovisio, Joseph R. ;
Levine, Donald P. .
CLINICAL INFECTIOUS DISEASES, 2009, 49 (03) :325-327
[20]   Antimicrobial management strategies for Gram-positive bacterial resistance in the intensive care unit [J].
Schentag, JJ .
CRITICAL CARE MEDICINE, 2001, 29 (04) :N100-N107