Pharmacokinetic-pharmacodynamic evaluation of daptomycin, tigecycline, and linezolid versus vancomycin for the treatment of MRSA infections in four western European countries

被引:37
作者
Canut, A. [2 ]
Isla, A. [3 ]
Betriu, C. [4 ]
Gascon, A. R. [1 ,3 ]
机构
[1] Univ Basque Country UPV EHU, Pharmacokinet Nanotechnol & Gene Therapy Grp, Vitoria 01006, Spain
[2] Hosp Univ Alava, Dept Microbiol, Vitoria, Spain
[3] Univ Basque Country UPV EHU, Fac Pharm, Vitoria 01006, Spain
[4] Hosp Clin San Carlos, Dept Microbiol, Madrid, Spain
关键词
RESISTANT STAPHYLOCOCCUS-AUREUS; PRACTICE GUIDELINES; DISEASES SOCIETY; MANAGEMENT; CARE; UK; SURVEILLANCE; BREAKPOINTS; BACTEREMIA; DIAGNOSIS;
D O I
10.1007/s10096-012-1560-7
中图分类号
R51 [传染病];
学科分类号
100201 [内科学];
摘要
Purpose To evaluate the usefulness of daptomycin, tigecycline, and linezolid for the treatment of MRSA infection compared with vancomycin in Belgium, the United Kingdom/Ireland, and Spain. Methods The methodology included the following steps: acquisition of microbiological and pharmacokinetic data, Monte Carlo simulation, estimation of the probability of target attainment (PTA), and calculation of the cumulative fraction of response (CFR). Results We showed that differences in the susceptibility of MRSA strains among countries may justify differences in the antibiotic dose selection. Two, 3, and 4 g daily of vancomycin seem be adequate in Belgium, Spain, and United Kingdom/Ireland respectively. The CFR obtained with 50 mg tigecycline every 12 h was higher in Spain than in Belgium and the United Kingdom/Ireland, but with the highest dose (100 mg q12h) the CFR was always 100%. At least 8 mg/kg daptomycin is necessary in United Kingdom/Ireland, but 4 mg/kg may be sufficient in Spain, and probably in Belgium. Six hundred mg q12h linezolid may be adequate in the four countries. Conclusion Our study reinforces the idea that the local MIC distribution must be considered in order to increase the probability of success of empirical treatment and must be periodically updated.
引用
收藏
页码:2227 / 2235
页数:9
相关论文
共 60 条
[1]
Application of patient population-derived pharmacokinetic-pharmacodynamic relationships to tigecycline breakpoint determination for staphylococci and streptococci [J].
Ambrose, Paul G. ;
Meagher, Alison K. ;
Passarell, Julie A. ;
Van Wart, Scott A. ;
Cirincione, Brenda B. ;
Bhavnani, Sujata M. ;
Ellis-Grosse, Evelyn .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2009, 63 (02) :155-159
[2]
Adequacy of Antimicrobial Treatment and Outcome of Staphylococcus aureus Bacteremia in 9 Western European Countries [J].
Ammerlaan, Heidi ;
Seifert, Harald ;
Harbarth, Stephan ;
Brun-Buisson, Christian ;
Torres, Antoni ;
Antonelli, Massimo ;
Kluytmans, Jan ;
Bonten, Marc .
CLINICAL INFECTIOUS DISEASES, 2009, 49 (07) :997-1005
[3]
In vivo pharmacodynamics of a new oxazolidinone (linezolid) [J].
Andes, D ;
van Ogtrop, ML ;
Peng, J ;
Craig, WA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (11) :3484-3489
[5]
[Anonymous], MICROBIOLOGICAL SURV
[6]
[Anonymous], CIRCULATION
[7]
[Anonymous], MICROBIOLOGICAL SURV
[8]
[Anonymous], REV ESP QUIMIOTER
[9]
Pharmacokinetics and tolerability of daptomycin at doses up to 12 milligrams per kilogram of body weight once daily in healthy volunteers [J].
Benvenuto, Mark ;
Benziger, David P. ;
Yankelev, Sara ;
Vigliani, Gloria .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (10) :3245-3249
[10]
A brief introduction to Monte Carlo simulation [J].
Bonate, PL .
CLINICAL PHARMACOKINETICS, 2001, 40 (01) :15-22