TABLE 1.
Indication | Infecting pathogen | Restrictions | Dose (IV or PO) | Duration of therapy† |
---|---|---|---|---|
Skin and soft tissue infections (complicated and uncomplicated) | Methicillin-susceptible Staphylococcus aureus | Allergy or resistance to other first-line agents for which culture and sensitivity is reported by the institution’s microbiology laboratory (beta-lactams, cephalosporins, clindamycin, cotrimoxazole, fluoroquinolones, macrolides, tetracyclines), including allergy or intolerance to vancomycin | ≤30 kg adult 300 mg every 12 h, >30 kg adult 600 mg every 12 h | ≤28 days |
Methicillin-resistant S aureus | Allergy or resistance to other first-line agents for which culture and sensitivity is reported by the institution’s microbiology laboratory (fusidic acid combination therapy, rifampin combination therapy [unless there is rifampin drug interaction], cotrimoxazole, clindamycin), including allergy or intolerance to vancomycin | |||
Pneumonia | Pneumonia (PSSP, PRSP and multiresistant species) | Allergy or resistance to other first-line agents for which culture and sensitivity is reported by the institution’s microbiology laboratory (beta-lactams, cephalosporins, cotrimoxazole, fluoroquinolones, macrolides, tetracyclines), including allergy or intolerance to vancomycin | ≤30 kg adult 300 mg every 12 h, >30 kg adult 600 mg every 12 h | ≤28 days |
Methicillin-susceptible S aureus | Allergy or resistance to other first-line agents for which culture and sensitivity is reported by the institution’s microbiology laboratory (beta-lactams, cephalosporins, clindamycin, cotrimoxazole, fluoroquinolones, macrolides, tetracyclines), including allergy or intolerance to vancomycin | |||
Methicillin-resistant S aureus | Allergy or resistance to other first-line agents for which culture and sensitivity is reported by the institution’s microbiology laboratory (fusidic acid combination therapy, rifampin combination therapy [unless there is rifampin drug interaction], cotrimoxazole, clindamycin), including allergy or intolerance to vancomycin | |||
Infection (including osteomyelitis and prosthetic joint infection) | Vancomycin-resistant enterococci | Infectious diseases specialist consultation required | ≤30 kg adult 300 mg every 12 h, >30 kg adult 600 mg every 12 h | ≤28 days |
Osteomyelitis and prosthetic joint infection | Methicillin-resistant S aureus or coagulase-negative methicillin-resistant staphylococci | Allergy or resistance to other first-line agents for which culture and sensitivity is reported by the institution’s microbiology laboratory (fusidic acid combination therapy, rifampin combination therapy [unless rifampin drug interaction], cotrimoxazole, clindamycin), including allergy or intolerance to vancomycin | ≤30 kg adult 300 mg every 12 h, >30 kg adult 600 mg every 12 h | ≤28 days |
Please see disclaimer at the end of the article;
Could be longer, if clinically necessary. IV Intravenous form; PO Oral form; PRSP Penicillin-resistant Streptococcus pneumoniae; PSSP Penicillin-susceptible S pneumoniae