Treatment for Acute Bacterial Sinus Infection
For an otherwise healthy adult with acute bacterial sinusitis, prescribe amoxicillin-clavulanate 875 mg/125 mg twice daily for 5–10 days as first-line therapy, achieving 90–92% predicted clinical efficacy against the major pathogens. 1, 2
Confirm the Diagnosis Before Prescribing Antibiotics
Before initiating antibiotics, verify that the patient meets at least one of three diagnostic criteria for acute bacterial rhinosinusitis (ABRS):
- Persistent symptoms ≥10 days without improvement: purulent nasal discharge plus either nasal obstruction or facial pain/pressure/fullness. 1, 2
- Severe symptoms ≥3–4 consecutive days: fever ≥39°C (102.2°F) with purulent nasal discharge and facial pain at illness onset. 1, 2
- "Double sickening": initial improvement from a viral upper respiratory infection followed by new or worsening fever, nasal discharge, or cough within 10 days. 1, 2
Critical context: Approximately 98–99.5% of acute rhinosinusitis episodes are viral and resolve spontaneously within 7–10 days without antibiotics. 1, 2 Do not prescribe antibiotics for symptoms lasting <10 days unless the severe criteria above are met. 1, 2
First-Line Antibiotic Regimen
- Amoxicillin-clavulanate 875 mg/125 mg orally twice daily for 5–10 days (or until symptom-free for 7 consecutive days, typically 10–14 days total). 1, 2, 3
- This regimen provides 90–92% predicted clinical efficacy against Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis. 1, 2, 4
- The clavulanate component is essential because 30–40% of H. influenzae and 90–100% of M. catarrhalis produce β-lactamase, rendering plain amoxicillin ineffective. 2
High-dose regimen (2 g amoxicillin/125 mg clavulanate twice daily) is indicated when any of the following risk factors are present: recent antibiotic use within the past 4–6 weeks, age >65 years, daycare exposure, moderate-to-severe symptoms, comorbidities (diabetes, chronic cardiac/hepatic/renal disease), or immunocompromised state. 2, 4
Alternatives for Penicillin-Allergic Patients
Non-Severe (Non-Type I) Penicillin Allergy
- Use a second- or third-generation cephalosporin for 10 days: cefuroxime-axetil, cefpodoxime-proxetil, cefdinir, or cefprozil. 1, 2, 3
- Cross-reactivity with penicillins is negligible (<1%). 2
Severe (Type I/Anaphylactic) Penicillin Allergy
- Levofloxacin 500 mg once daily for 10–14 days or moxifloxacin 400 mg once daily for 10 days. 1, 2, 5, 4
- Both achieve 90–92% predicted efficacy against multidrug-resistant S. pneumoniae and β-lactamase-producing organisms. 2, 4
- Reserve fluoroquinolones for severe penicillin allergy or documented treatment failure to limit resistance development. 1, 2
Suboptimal Alternative
- Doxycycline 100 mg once daily for 10 days offers lower efficacy (77–81%) and a 20–25% bacteriologic failure rate due to limited activity against H. influenzae. 2, 3
- Use only when cephalosporins and fluoroquinolones are contraindicated. 2
- Contraindicated in children <8 years due to tooth enamel discoloration. 2
Essential Adjunctive Therapies (Add to All Patients)
- Intranasal corticosteroids (mometasone, fluticasone, or budesonide) twice daily significantly reduce mucosal inflammation and accelerate symptom resolution; supported by strong evidence from multiple randomized controlled trials. 1, 2
- Saline nasal irrigation 2–3 times daily provides symptomatic relief and aids mucus clearance. 1, 2, 6
- Analgesics (acetaminophen or ibuprofen) for pain and fever control. 1, 2, 6
Watchful-Waiting Strategy
- For uncomplicated ABRS with reliable follow-up, initial observation without antibiotics is appropriate. 1, 2
- Initiate antibiotics only if no improvement by day 7 or if symptoms worsen at any time. 1, 2
- The number needed to treat (NNT) with antibiotics is 10–15 to achieve one additional cure compared with placebo. 2
Monitoring and Reassessment
- Reassess at 3–5 days: If no clinical improvement (persistent purulent drainage, unchanged facial pain, or worsening), switch to high-dose amoxicillin-clavulanate (2 g/125 mg twice daily) or a respiratory fluoroquinolone (levofloxacin or moxifloxacin). 1, 2, 4
- Reassess at 7 days: Persistent or worsening symptoms warrant confirmation of diagnosis, exclusion of complications (orbital cellulitis, meningitis, intracranial abscess), and consideration of imaging or ENT referral. 1, 2
- Expected timeline: Noticeable improvement within 3–5 days of appropriate therapy, with complete resolution by 10–14 days or when symptom-free for 7 consecutive days. 2
Antibiotics to Avoid
- Macrolides (azithromycin, clarithromycin): 20–25% resistance rates in S. pneumoniae and H. influenzae; the American Academy of Pediatrics explicitly contraindicates azithromycin for ABRS. 1, 2, 3
- Trimethoprim-sulfamethoxazole: ≈50% resistance in S. pneumoniae and ≈27% in H. influenzae. 2
- First-generation cephalosporins (e.g., cephalexin): Inadequate coverage since ≈50% of H. influenzae strains produce β-lactamase. 2
Referral to Otolaryngology
Refer immediately if any of the following occur:
- No improvement after 7 days of appropriate second-line antibiotic therapy. 1, 2
- Worsening symptoms at any point (increasing facial pain, fever, purulent drainage). 1, 2
- Signs of complications: severe headache, visual changes, periorbital swelling/erythema, proptosis, diplopia, altered mental status, or cranial nerve deficits. 1, 2
- Recurrent sinusitis (≥3 episodes per year) requiring evaluation for underlying allergic rhinitis, immunodeficiency, or anatomic abnormalities. 1, 2
Common Pitfalls to Avoid
- Do not prescribe antibiotics for symptoms <10 days unless severe features (fever ≥39°C with purulent discharge for ≥3 consecutive days) are present. 1, 2
- Avoid routine imaging (X-ray or CT) for uncomplicated ABRS; up to 87% of viral upper-respiratory infections show sinus abnormalities on imaging, leading to unnecessary interventions. 2
- Ensure adequate treatment duration (≥5 days for adults) to prevent relapse. 2, 7
- Fluoroquinolones should not be used as first-line therapy in patients without documented β-lactam allergy to limit resistance development. 1, 2
- Gastrointestinal adverse effects with amoxicillin-clavulanate are common: diarrhea in 40–43% of patients, severe diarrhea in 7–8%. 2