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. Author manuscript; available in PMC: 2010 Oct 12.
Published in final edited form as: J Antimicrob Chemother. 2008 Feb 4;61(3):621–628. doi: 10.1093/jac/dkm536

Table 3.

PTA at existing CLSI breakpointsa

Antimicrobial and dosing regimen PTA (%)
Piperacillin-tazobactam
 3.375 g every 4 h 91
 3.375 g every 6 h 6
 4.5 g every 6 h 21
Cefepime
 1 g every 12 h 2
 1 g every 8 h 57
 2 g every 12 h 21
 2 g every 8 h 87
Ceftizoxime
 1 g every 8 h 5
Ceftriaxone
 1 g every 24 h 0
 2 g every 24 h 17
Ceftazidime
 1 g every 8 h 68
 2 g every 8 h 98
Ertapenem
 1 g every 24 h 59
Imipenem
 500 mg every 6 h 99
Meropenem
 1 g every 8 h 98
Aztreonam
 1 g every 8 h 26
 2 g every 8 h 90
Gentamicin
 5 mg/kg every 24 h 20
Tobramycin
 5 mg/kg every 24 h 20
Ciprofloxacin
 400 mg every 8 h 0
 400 mg every 12 h 0
Levofloxacin
 500 mg every 24 h 0
 750 mg every 24 h 0
a

The CLSI breakpoints are consistent for all antibiotics evaluated against Enterobacteriaceae, P. aeruginosa and A. baumannii, except for piperacillin-tazobactam (breakpoint for P. aeruginosa, 64 mg/L). Table 3 reflects the PTA for piperacillin-tazobactam when a breakpoint of 16 mg/L was used. If a breakpoint of 64 mg/L were used instead (i.e. P. aeruginosa), the corresponding probabilities of target attainment for piperacillin-tazobactam would be: 3.375 g every 4 h (0%), 3.375 g every 6 h (0%) and 4.5 g every 6 h (0%).