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SSTI: Antibiotic Dosing

 

Penicillin allergies: For risk stratification see Penicillin ADR (HISTORICAL) Clinical Pathway

  • For patients with a low risk of IgE-mediated reaction to penicillin, consider observed oral dose of the recommended treatment and continue therapy if tolerated.
  • For patients with a high risk of IgE-mediated or severe delayed reaction to penicillin, refer to guidance below.

Cephalosporin allergies: For patients with history of anaphylaxis or severe delayed reaction, refer to guidance below.

Place in Therapy

Recommended Treatment

Additional Considerations

Paronychia

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.

Folliculitis

First-line

Topical mupirocin x 5 days

If concurrent cellulitis, refer to cellulitis or erysipelas management.

Mild Impetigo

First-line

Topical mupirocin x 5 days

 

Extensive Impetigo (i.e. > 5 lesions, covering large areas of the body, or near the mouth)

First-line

 

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.

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.

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 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

 

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.

Cellulitis or Erysipelas

First-line

 

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.

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.

Alternative

 

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.

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.

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.

Abscess

First-line

 

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.

Trimethoprim-sulfamethoxazole 4 - 6 mg/kg/dose PO q12h x 5 days (max 160 mg/dose)

Dosed on trimethoprim component.

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.