Indication for Therapy | Usual Causative Organisms | Antimicrobials Regimens |
---|---|---|
Outpatient treatment
|
S. pneumoniae, M. pneumoniae, C. pneumoniae, H. influenzae, M. catarrhalis Legionella spp., Enterobacterales |
amoxicillin/clavulanate 875/125 mg PO q12h OR amoxicillin/clavulanate 875/125 mg PO q12h |
β-lactam allergy (anaphylaxis): moxifloxacin 400 mg PO q24h |
||
Inpatient admission (non-ICU) | S. pneumoniae, M. pneumoniae, C. pneumoniae, H. influenzae, Legionella spp. | cefTRIAXone 1 g IV q24h OR cefTRIAXone 1 g IV q24h +/- doxycycline 100 mg PO q12h x 7 days* |
β-lactam allergy (anaphylaxis): moxifloxacin 400 mg IV/PO q24h |
||
Options for oral step-down therapy from cefTRIAXone includes one of: amoxicillin/clavulanate 875/125 mg PO q12h OR cefuroxime 500 mg PO q12h |
||
Inpatient ICU admission
|
S. pneumoniae, S. aureus, Legionella spp., Gram-negative bacilli, H. influenzae | cefTRIAXone 1 g IV q24h + azithromycin 500 mg IV q24h |
β-lactam allergy (anaphylaxis): moxifloxacin 400 mg IV q24h |
||
Influenza suspected | Influenza A or B | Add oseltamavir 75 mg PO q12h x 5 days |
Macroaspiration suspected | Oral anaerobes | cefTRIAXone 1g IV q24h (CTX has adequate oral anaerobic coverage and may be used alone). In the setting of severe anaerobic pulmonary infection (e.g. lung abscess, empyema): metroNIDAZOLE 500 mg IV/PO q12h may be added. |
amoxicillin/clavulanate 875/125 mg PO q12h | ||
MRSA suspected | Methicillin-resistant Staphylococcus aureus | Add vancomycin 15 mg/kg IV q12h (Dose as per hospital guidelines) |
Pseudomonas suspected | Pseudomonas aeruginosa | Refer to Hospital Acquired Pneumonia Guidelines |
* Consider adding atypical coverage when “enhanced surveillance directive” from Public Health has been issued or when patients have not responded to drug therapy after 48 hours.
If the patient has received antibiotics within the last 3 months, consideration should be given to prescribing an agent from a different class.
Minimum of 3 days. Patients should be afebrile for 48h and clinically stable before discontinuation of therapy.
Mandell LA et al. Infectious Diseases Society of America/American Thoracic Society Consensus Guidelines on the Management of Community-Acquired Pneumonia in Adults. Clin Infect Dis. 2007;44:S27-72.
Ruhe JJ and Hasbun R. Streptococcus pneumoniae Bacteremia: Duration and Previous Antibiotic Use and Association with Penicillin Resistance. Clin Infect Dis. 2003;36:1132-38.
Leroy O, Saux P, Bedos JP, Caulin E. Comparison of Levofloxacin and Cefotaxime Combined With Ofloxacin for ICU Patients With Community-Acquired Pneumonia Who Do Not Require Vasopressors. CHEST. 2005;128:172-83.
Doernberg SB, Winston LG, Deck DH, Chambers HF. Does doxycycline protect against development of Clostridium difficile Infection? Clin Infect Dis. 2012:55:615-620.
El Moussaoui R, De Borgie CAMJ, Van Den Broek P, et al. (2006). Effectiveness of discontinuing antibiotic treatment after three days versus eight days in mild to moderate-severe community acquired pneumonia: randomised, double blind study. BMJ. 332(7554):1355.