Treatment of Community-Acquired Pneumonia in Inpatient Settings
For hospitalized non-ICU patients with community-acquired pneumonia (CAP), the recommended empiric treatment is a β-lactam (such as ceftriaxone, cefotaxime, ampicillin-sulbactam, or ceftaroline) plus a macrolide (such as azithromycin), or alternatively, a respiratory fluoroquinolone alone. 1, 2
Standard Treatment Regimens for Hospitalized Non-ICU Patients
Combination Therapy (Preferred):
- β-lactam plus macrolide combination:
Monotherapy Alternative:
- Respiratory fluoroquinolone: levofloxacin 750mg IV/oral daily or moxifloxacin 400mg IV/oral daily 1, 2
Treatment for ICU Patients
For ICU Patients without Risk Factors for Pseudomonas:
- β-lactam (cefotaxime, ceftriaxone, or ampicillin-sulbactam) plus either:
For ICU Patients with Risk Factors for Pseudomonas:
- Antipseudomonal β-lactam (piperacillin-tazobactam, cefepime, imipenem, or meropenem) plus either:
Special Considerations
MRSA Coverage:
- Add vancomycin or linezolid when community-acquired MRSA is suspected 2
- Risk factors include prior MRSA infection, recent hospitalization, or recent antibiotic use 2
Timing of Administration:
- First antibiotic dose should be administered while the patient is still in the emergency department 2, 4
- Early administration is associated with improved outcomes and reduced mortality 2
Duration of Therapy:
- Minimum duration of 5 days for most patients 2
- Patient should be afebrile for 48-72 hours and have no more than one sign of clinical instability before discontinuing therapy 2
- For uncomplicated S. pneumoniae pneumonia, 7-10 days is typically sufficient 2
- For severe pneumonia or specific pathogens like Legionella or staphylococcal infections, extend treatment to 14-21 days 2
Switching from IV to Oral Therapy:
- Transfer to oral regimen as soon as clinical improvement occurs and temperature has been normal for 24 hours 2
- For azithromycin, switch from IV to oral at physician's discretion based on clinical response 3
Clinical Rationale and Evidence
- Combination therapy with a β-lactam plus macrolide has been associated with lower mortality than monotherapy in bacteremic pneumococcal pneumonia 1
- The benefit of combination therapy is most pronounced in patients with severe illness 1
- Macrolides provide coverage for atypical pathogens (Mycoplasma, Chlamydophila, Legionella) and may have anti-inflammatory effects 5
- Respiratory fluoroquinolones offer the advantage of covering both typical and atypical pathogens as monotherapy 6
Common Pitfalls and Caveats
- Overreliance on fluoroquinolones can lead to resistance; they should be reserved for patients with β-lactam allergies or when specifically indicated 2
- Inadequate coverage for atypical pathogens should be avoided 2
- Failure to adjust therapy based on culture results can lead to unnecessary prolonged therapy 2
- Delaying antibiotic administration is associated with increased mortality, particularly in severe pneumonia 2, 4
- For patients who fail to improve as expected, conduct a careful review of the clinical history, examination, and consider additional investigations 2