Assessment of a Patient with Facial Cellulitis
The assessment of facial cellulitis requires prompt identification of causative pathogens (primarily beta-hemolytic streptococci and Staphylococcus aureus) and evaluation for systemic toxicity to guide appropriate antibiotic therapy and determine the need for hospitalization. 1, 2
Clinical Assessment
Key Diagnostic Features
- Acute onset of erythema, warmth, swelling, and tenderness in the facial region
- Well-demarcated borders (especially in erysipelas)
- Pain disproportionate to physical findings (may indicate deeper infection)
- Lymphangitis and regional lymphadenopathy
- Systemic symptoms (fever, chills, malaise)
Severity Assessment
- Mild: Localized infection without systemic signs
- Moderate: More extensive infection with systemic signs (fever, tachycardia)
- Severe: Significant systemic toxicity, hemodynamic instability, altered mental status
Red Flags Requiring Immediate Attention
- Violaceous bullae
- Cutaneous hemorrhage
- Skin sloughing
- Skin anesthesia
- Rapid progression
- Gas in tissue
- Hypotension (systolic BP <90 mmHg)
- Tachycardia (>100 beats/min)
- Fever or hypothermia 1
Laboratory Evaluation
For patients with systemic toxicity, obtain:
- Blood cultures
- Complete blood count with differential (marked left shift suggests severe infection)
- Creatinine, bicarbonate levels
- Creatine phosphokinase (elevated levels 2-3× normal suggest deeper infection)
- C-reactive protein (>13 mg/L suggests severe infection) 1
Differential Diagnosis
Rule out non-infectious mimics:
Special Considerations for Facial Cellulitis
- Higher risk of complications due to proximity to central nervous system
- More commonly caused by beta-hemolytic streptococci
- Potential for rapid spread to orbital or intracranial structures
- Lower threshold for hospitalization and IV antibiotics
Treatment Approach
Antibiotic Selection
First-line (mild cases): Oral antibiotics active against streptococci and MSSA
For moderate to severe cases: Parenteral therapy
- Vancomycin 15-20 mg/kg/dose IV every 8-12 hours (if MRSA suspected)
- Clindamycin IV 600-900mg every 8 hours 2
Treatment Duration
Hospitalization Criteria
- Presence of SIRS (Systemic Inflammatory Response Syndrome)
- Altered mental status
- Hemodynamic instability
- Concern for deeper or necrotizing infection
- Poor adherence to therapy
- Severe immunocompromise
- Failure of outpatient treatment 1
Prevention of Recurrence
Identify and treat predisposing conditions:
For patients with 3-4 episodes per year despite addressing predisposing factors, consider prophylactic antibiotics:
Common Pitfalls to Avoid
- Misdiagnosing non-infectious mimics as cellulitis, leading to unnecessary antibiotic use
- Failing to recognize signs of deeper infection requiring surgical consultation
- Inadequate coverage for potential pathogens based on risk factors
- Not addressing underlying predisposing factors, leading to recurrence
- Delaying treatment in facial cellulitis, which can lead to rapid spread and complications 4, 5