Recommended Treatment for Pneumonia
The recommended first-line treatment for pneumonia depends on the setting, severity, and risk factors, with community-acquired pneumonia (CAP) typically treated with a β-lactam (such as amoxicillin) for mild cases, while moderate to severe cases require combination therapy with a β-lactam plus a macrolide or a respiratory fluoroquinolone. 1
Classification and Treatment Setting
Treatment approach should be based on:
- Type of pneumonia (community-acquired vs. hospital-acquired)
- Severity assessment (mild, moderate, severe)
- Risk factors for drug-resistant pathogens
- Patient characteristics
Community-Acquired Pneumonia (CAP)
Outpatient Treatment (Mild CAP)
- First choice: Amoxicillin 1 g three times daily 1
- Alternatives for penicillin allergy:
- Doxycycline 100 mg twice daily
- Respiratory fluoroquinolone (levofloxacin 750 mg daily or moxifloxacin 400 mg daily)
- Macrolide (if local pneumococcal resistance is low) 1
Hospitalized Non-ICU Patients (Moderate CAP)
- Standard regimen: β-lactam (ceftriaxone, cefotaxime, or ampicillin-sulbactam) plus either:
- Azithromycin 500 mg daily, or
- Respiratory fluoroquinolone 1
- Duration: 5-7 days (if afebrile for 48 hours and clinically stable) 1
ICU Patients (Severe CAP)
- No Pseudomonas risk: Non-antipseudomonal cephalosporin III + macrolide OR moxifloxacin/levofloxacin ± non-antipseudomonal cephalosporin III 2
- With Pseudomonas risk: Antipseudomonal cephalosporin OR acylureidopenicillin/β-lactamase inhibitor OR carbapenem PLUS ciprofloxacin OR macrolide + aminoglycoside 2
Hospital-Acquired Pneumonia (HAP)
Non-Ventilator-Associated HAP
Not at high risk of mortality and no MRSA risk factors:
- Piperacillin-tazobactam 4.5 g IV q6h, OR
- Cefepime 2 g IV q8h, OR
- Levofloxacin 750 mg IV daily, OR
- Imipenem 500 mg IV q6h, OR
- Meropenem 1 g IV q8h 2
Not at high risk of mortality but with MRSA risk factors:
- Above options PLUS vancomycin or linezolid 2
High risk of mortality:
- Two antibiotics from different classes (avoid two β-lactams)
- PLUS vancomycin 15 mg/kg IV q8-12h or linezolid 600 mg IV q12h 2
Specific Pathogen Considerations
Atypical Pathogens
- Chlamydophila pneumoniae: Doxycycline, macrolide, levofloxacin, or moxifloxacin 2
- Legionella spp.: Levofloxacin, moxifloxacin, or macrolide (azithromycin preferred) ± rifampicin 2
- Coxiella burnetii: Doxycycline, levofloxacin, or moxifloxacin 2
Drug-Resistant Pathogens
- MRSA: Vancomycin or linezolid 2, 1
- Pseudomonas aeruginosa: Antipseudomonal β-lactam (piperacillin-tazobactam, cefepime, imipenem, or meropenem) plus either ciprofloxacin/levofloxacin or aminoglycoside 1
Treatment Duration
- Standard duration: 5-7 days for most patients 1
- Minimum requirement for discontinuation: Afebrile for 48-72 hours and no more than one CAP-associated sign of clinical instability 1
- Biomarkers: Procalcitonin may guide shorter treatment duration 2
Monitoring and Follow-up
- Assess clinical response within 48-72 hours of initiating therapy 1
- Consider treatment failure if no improvement within 72 hours 1
- Clinical review at approximately 6 weeks after treatment 1
- Chest radiograph at 6 weeks for patients with persistent symptoms or signs, or those at higher risk of underlying malignancy 1
Common Pitfalls and Caveats
Delayed antibiotic administration: Antibiotics should be initiated immediately after diagnosis of CAP, especially in patients with septic shock 2
Inadequate coverage: Failure to consider local resistance patterns can lead to treatment failure
Excessive broad-spectrum use: Unnecessary broad-spectrum antibiotics contribute to antimicrobial resistance
Failure to adjust for renal impairment: Dose adjustments are necessary for patients with creatinine clearance ≤40 mL/min 3
Missing atypical pathogens: Consider coverage for atypical pathogens, especially in severe cases or when standard therapy fails
Inadequate duration: Premature discontinuation before clinical stability can lead to relapse
Overlooking complications: Monitor for complications such as empyema, lung abscess, or metastatic infections
By following these evidence-based recommendations and considering patient-specific factors, clinicians can optimize pneumonia treatment outcomes while practicing responsible antibiotic stewardship.