Table 1 |
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Antibiotics currently available for the treatment of serious methicillin-resistant S. aureus infections |
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|
Antibiotic |
Primary indications |
Daily dosea |
Volume of distribution (L/kg) |
Elimination half-life (hr) |
Protein binding (%) |
Main toxicity |
|
|
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|
Vancomycin |
Pneumonia |
30 mg/kg/day |
0.2 to 1.25 |
4 to 6 |
30 to 55 |
Nephrotoxicity (higher doses) |
|
Skin/soft tissues |
Thrombocytopenia |
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|
Bacteremia |
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|
Linezolid |
Pneumonia |
600 mg q 12 h |
0.5 - 0.6 |
5 |
31 |
Myelosuppression (prolonged duration generally >2 weeks) |
|
Skin/soft tissues |
Lactic acidosis |
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|
Peripheral and optic neuropathy |
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|
Serotonin syndrome |
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|
Tigecycline |
Skin/soft tissues |
100 mg load |
7 to 10 |
37 to 66 |
71 to 89 |
Nausea |
|
Intra-abdominal |
50 mg q 12 h |
Vomiting |
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|
Photosensitivity |
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|
Daptomycin |
Bacteremia |
Bacteremia: 6 mg/kg q 24 h |
0.09 |
8 to 9 |
92 |
Muscle toxicity |
|
Skin/soft tissues |
Skin/soft tissues: 4 mg/kg q 24 h |
CPK elevation |
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|
Quinupristin/dalfopristin |
Skin/soft tissues |
7.5 mg/kg q 8 h (via central vein) |
0.56 to 0.98 |
0.54 to 1.14 |
11 to 78 |
Phlebitis |
|
Arthralgias and myalgias |
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|
Ceftobiproleb |
Skin/soft tissues |
500 mg q 8 h |
0.25 to 0.30 |
3 to 4 |
16 |
Allergic reactions |
|
Ceftarolinec |
Skin/soft tissues Pneumonia |
600 mg q 12 h |
0.22 to 0.25 |
2.5 to 3 |
18 |
Allergic reactions |
|
Dalbavancinc |
Skin/soft tissues |
1,000 mg day 1 |
0.011 |
147 to 258 |
93 |
Nausea |
|
500 mg weekly |
Vomiting |
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|
Oritavancinc |
Skin/soft tissues |
1.5 to 3 mg/kg q 24 h |
0.65 to 1.92 |
195 |
90 |
Nausea |
|
Vomiting |
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|
Telavancinc |
Skin/soft tissues Pneumonia |
7.5 to 10 mg/kg day |
0.1 |
7 to 9 |
93 |
Renal thrombocytopenia |
|
Iclaprimd |
Skin/soft tissues |
0.8 mg/kg q 12 h |
1.15 |
2.5 to 4.1 |
93 |
|
|
|
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|
aDaily dose listed assumes normal kidney and liver function. bNot approved for clinical use in the US. Greater risk of clinical failure in ventilator-associated pneumonia compared to vancomycin plus ceftazadine. cNot approved for clinical use in the US at the time of writing. dNot approved for clinical use in the US. Failed to demonstrate non-inferiority against linezolid for treatment of complicated skin and skin structure infection. CPK, creatine phosphokinase. |
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Skrupky et al. Critical Care 2009 13:222 doi:10.1186/cc8028 |
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