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. 2007 Jul;20(3):391–408. doi: 10.1128/CMR.00047-06

TABLE 3.

Prospective clinical studies of PK/PD parameters

Agent Infection(s)c PK/PD parameter selected Magnitude of parameter for maximum efficacy (clinical cure rate)f Reference(s)
β-Lactams
    Cefmenoxime Nosocomial pneumonia Time above DRCa 70-100% 118
    Cefepime Hospitalized, various Time above 4.3× MIC 100% 126
    Penicillins and cephalosporinsb Otitis media caused by Streptococcus pneumoniae or Haemophilus influenzae Time above MIC 60% 38
Fluoroquinolones
    Ciprofloxacin Mainly nosocomial pneumonia AUC24/MIC ratio ≥125 71
    Levofloxacin Serious community-acquired infection Cmax/MIC ratio ≥12.2 111
    Gatifloxacin and levofloxacin Streptococcus pneumoniae community-acquired pneumonia and AECB fuAUC24/MIC ratiod ≥33.7 1
    Grepafloxacin AECB AUC24/MIC ratio ≥175 72
    Garenoxacin Community-acquired pneumonia, AECB, and sinusitis Nonee 133
    Levofloxacin Nosocomial pneumonia AUC24/MIC ratio ≥87 59
    Ciprofloxacin Pseudomonas aeruginosa bacteremia Cmax/MIC ratio ≥8 143
Other agents
    Gentamicin Nosocomial pneumonia Cmax/MIC ratio ≥10 85
    Gentamicin and tobramycin Pseudomonas aeruginosa bacteremia Cmax/MIC ratio ≥8 143
    Vancomycin Staphylococcus aureus lower respiratory tract infection AUC24/MIC ratio ≥350 101, 102
a

DRC was used as a surrogate of the MIC per reference 128.

b

This was an analysis of data from multiple clinical studies.

c

AECB, acute exacerbations of chronic bronchitis.

d

fu, fraction unbound.

e

Due to the very high activity of the agent, fuAUC24/MIC ratios were >200 in more than 90% of patients.

f

Magnitudes are expressed in terms of total drug, rather than unbound drug, unless stated otherwise.