Antibiotic Selection for Respiratory Infections
For community-acquired lower respiratory tract infections, amoxicillin or amoxicillin-clavulanate should be the first-line antibiotic choice, with macrolides (azithromycin or clarithromycin) reserved for atypical pathogen coverage or penicillin allergy. 1
Community-Acquired Pneumonia (CAP)
Non-Severe CAP (Outpatient/Medical Ward)
First-line options include:
Duration: 7-10 days for uncomplicated bacterial CAP 1
Extended duration: 10-14 days for Mycoplasma pneumoniae or Chlamydophila pneumoniae; 21 days for Legionella pneumophila or Staphylococcus aureus 1
Severe CAP (ICU Admission)
- Recommended regimen: Third-generation cephalosporin (cefotaxime 1g IV every 8 hours or ceftriaxone 1g IV every 24 hours) PLUS macrolide 1
- Alternative: Third-generation cephalosporin PLUS respiratory fluoroquinolone (levofloxacin or moxifloxacin) 1
Pseudomonas Risk Factors Present
- Use: Anti-pseudomonal cephalosporin OR acylureidopenicillin/beta-lactamase inhibitor PLUS ciprofloxacin 1
- Alternative: Carbapenem PLUS ciprofloxacin 1
COPD Exacerbations
Mild COPD Exacerbation
- Antibiotics indicated when ≥2 of 3 Anthonisen criteria present: increased sputum purulence, increased sputum volume, increased dyspnoea 1
- First-line: Amoxicillin 500-1000 mg every 8 hours OR tetracyclines (doxycycline 100 mg every 12 hours) 1
- Alternatives: Amoxicillin-clavulanate, macrolides, levofloxacin, or moxifloxacin 1
Moderate/Severe COPD Exacerbation
COPD with Pseudomonas Risk
- Use: Ciprofloxacin 500 mg every 12 hours orally 1
Treatment Duration
- Standard: At least 7 days (except clarithromycin and azithromycin which have shorter courses) 1
- Legionella suspected: 21 days 1
Bronchiectasis
Acute Exacerbations
- No Pseudomonas risk: Amoxicillin-clavulanate, levofloxacin, or moxifloxacin 1
- Pseudomonas risk factors: Ciprofloxacin 1
Frequent Exacerbations (≥3 per year)
- If Pseudomonas aeruginosa isolated: Long-term inhaled anti-pseudomonal antibiotic OR long-term macrolide 1
- If other potentially pathogenic microorganisms: Long-term macrolides OR long-term oral/inhaled targeted antibiotic 1
- If no pathogen identified: Long-term macrolides (azithromycin 250 mg three times weekly as pragmatic starting dose) 1
Upper Respiratory Tract Infections
Acute Bacterial Rhinosinusitis
- Indications for antibiotics: Symptoms persisting >10 days without improvement, severe symptoms (fever >39°C with purulent discharge/facial pain ≥3 days), or "double sickening" pattern 4
- First-line: Amoxicillin-clavulanate 875/125 mg every 12 hours or 500/125 mg every 8 hours for 7-10 days 2, 4
- Alternatives: Doxycycline or respiratory fluoroquinolone (levofloxacin/moxifloxacin) 4
Streptococcal Pharyngitis
Pediatric Considerations
Acute Otitis Media (Children <3 years)
- High-dose amoxicillin-clavulanate: 80-100 mg/kg/day (amoxicillin component) divided into three doses for 10 days 2, 3
- Maximum daily dose: 3 g/day 4
Community-Acquired Pneumonia (Children)
- First-line: Amoxicillin-clavulanate 80-100 mg/kg/day (amoxicillin component) in three divided doses 2
- Children >3 years: Consider adding macrolide for atypical pathogen coverage 2
Monitoring and Response Assessment
Expected Response Timeline
- Fever resolution: Within 2-3 days of antibiotic initiation 1
- Clinical reassessment: If no improvement by 48-72 hours, consider alternative diagnosis, resistant pathogen, or complications 1, 2, 4
Route Switching
- IV to oral transition: When fever resolves and clinical condition stabilizes 1
Critical Pitfalls to Avoid
- Do not use first-generation cephalosporins (cephalexin) for respiratory infections due to inadequate activity against penicillin-resistant S. pneumoniae 4
- Do not substitute two 250/125 mg tablets for one 500/125 mg tablet of amoxicillin-clavulanate—they contain different clavulanate ratios 3
- Do not use fluoroquinolones inactive against pneumococci (ofloxacin, ciprofloxacin) or cefixime for pneumococcal infections 4
- Avoid macrolide monotherapy in areas with high pneumococcal macrolide resistance rates 1
- Consider local resistance patterns when selecting empiric therapy—national guidelines may not reflect regional antibiotic susceptibility 1