SSTI: Antibiotic Dosing
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Penicillin allergies: For risk stratification see Penicillin ADR (HISTORICAL) Clinical Pathway
Cephalosporin allergies: For patients with history of anaphylaxis or severe delayed reaction, refer to guidance below. |
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Place in Therapy |
Recommended Treatment |
Additional Considerations |
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Paronychia |
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First-line |
Incision and drainage + warm compresses PLUS Topical mupirocin three times daily x 5 days |
If concurrent cellulitis, refer to cellulitis or erysipelas management. |
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Folliculitis |
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First-line |
Topical mupirocin x 5 days |
If concurrent cellulitis, refer to cellulitis or erysipelas management. |
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Mild Impetigo |
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First-line |
Topical mupirocin x 5 days |
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Extensive Impetigo (i.e. > 5 lesions, covering large areas of the body, or near the mouth) |
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First-line
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Cephalexin 17 mg/kg/dose PO q8h x 7 days (max 500 mg/dose) |
Cephalexin can be used in patients with penicillin allergies at a low risk for IgE-mediated reactions. Refer to Penicillin ADR Clinical Pathway for more information. |
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Cefazolin 25 mg/kg/dose IV q8h (max 2000 mg/dose); transition to PO at earliest opportunity to complete 7 days |
Cefazolin can be used in patients with penicillin allergies at a low OR high risk for IgE-mediated reactions. Refer to Penicillin ADR Clinical Pathway for more information. |
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MRSA risk factor OR Penicillin allergy at a high risk for IgE-mediated or severe delayed reaction
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Clindamycin 10 mg/kg/dose PO q8h x 7 days (max 450 mg/dose) Clindamycin 10 mg/kg/dose IV q8h (max 600 mg/dose); transition to PO at earliest opportunity to complete 7 days |
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Trimethoprim-sulfamethoxazole 4 - 6 mg/kg/dose PO q12h x 7 days (max 160 mg/dose) |
Dosed on trimethoprim component. Controversial coverage of S. pyogenes. |
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Cellulitis or Erysipelas |
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First-line
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Cephalexin 17 mg/kg/dose PO q8h x 5 days (max 500 mg/dose) |
Cephalexin can be used in patients with penicillin allergies at a low risk for IgE-mediated reactions. Refer to Penicillin ADR Clinical Pathway for more information. |
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Cefazolin 25 mg/kg/dose IV q8h x 5 days (max 2000 mg/dose); transition to PO at earliest opportunity to complete 5 days |
Cefazolin can be used in patients with penicillin allergies at a low OR high risk for IgE-mediated reactions. Refer to Penicillin ADR Clinical Pathway for more information. |
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Alternative
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Amoxicillin-clavulanate 22.5 mg/kg/dose PO q12h x 5 days (max 875 mg/dose) |
Dosed on amoxicillin component. Refer to the Outpatient Antimicrobial Handbook's Dosing of Amoxicillin/Clavulanate guide (page 31) for which formulation to use. |
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Ampicillin-sulbactam 50 mg/kg/dose IV q6h (max 2000 mg/dose); transition to PO at earliest opportunity to complete 5 days |
Dosed on ampicillin component. |
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MRSA risk factor OR Penicillin allergy at a high risk for IgE-mediated or severe delayed reaction |
Clindamycin 10 mg/kg/dose PO q8h x 5 days (max 450 mg/dose) Clindamycin 10 mg/kg/dose IV q8h (max 600 mg/dose); transition to PO at earliest opportunity to complete 5 days |
Clindamycin resistance for S. aureus and S. pyogenes has been increasing. Consider selecting an alternative if patient has a history of clindamycin-resistant S. aureus or changing to a narrow spectrum antibiotic if culture results show MSSA or S. pyogenes. |
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Abscess |
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First-line
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Clindamycin 10 mg/kg/dose PO q8h x 5 days (max 450 mg/dose) Clindamycin 10 mg/kg/dose IV q8h (max 600 mg/dose); transition to PO at earliest opportunity to complete 5 days |
Clindamycin resistance for S. aureus and S. pyogenes has been increasing. Consider selecting an alternative if patient has a history of clindamycin-resistant S. aureus or changing to a narrow spectrum antibiotic if culture results show MSSA or S. pyogenes. |
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Trimethoprim-sulfamethoxazole 4 - 6 mg/kg/dose PO q12h x 5 days (max 160 mg/dose) |
Dosed on trimethoprim component. |
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These pathways do not establish a standard of care to be followed in every case. It is recognized that each case is different, and those individuals involved in providing health care are expected to use their judgment in determining what is in the best interests of the patient based on the circumstances existing at the time. It is impossible to anticipate all possible situations that may exist and to prepare a pathway for each. Accordingly, these pathways should guide care with the understanding that departures from them may be required at times.