Treatment of Preseptal Cellulitis in a Teenager as an Inpatient
For a hospitalized teenager with preseptal cellulitis, initiate IV vancomycin 15-20 mg/kg every 8-12 hours as first-line therapy, with clindamycin 600 mg IV every 8 hours as an alternative if local MRSA resistance is <10%. 1, 2
Initial Assessment and Risk Stratification
When a teenager presents with preseptal cellulitis requiring hospitalization, assess immediately for:
- Signs of systemic toxicity including fever, tachycardia, hypotension, or altered mental status, which mandate hospitalization and IV antibiotics 2
- Purulent drainage or exudate, which indicates possible MRSA involvement and necessitates MRSA-active therapy 1, 2
- Risk factors for MRSA including penetrating trauma, injection drug use, known MRSA colonization, or evidence of MRSA infection elsewhere 1, 2
- Potential progression to orbital cellulitis by evaluating for proptosis, ophthalmoplegia, pain with extraocular movements, or vision changes—these require emergent imaging and ophthalmology consultation 3
Blood cultures should be obtained in hospitalized patients, particularly those with severe systemic features, immunodeficiency, or malignancy 2
Antibiotic Selection Algorithm
First-Line IV Therapy
Vancomycin remains the gold standard for hospitalized patients with complicated skin and soft tissue infections, including preseptal cellulitis requiring admission 1, 2:
- Vancomycin 15-20 mg/kg IV every 8-12 hours (A-I level evidence) 1, 2
- This provides reliable MRSA coverage while also covering streptococci 1
Alternative IV Options (All A-I Evidence)
- Linezolid 600 mg IV twice daily 1, 2
- Clindamycin 600 mg IV every 8 hours (only if local MRSA clindamycin resistance <10%) 1, 2, 4
- Daptomycin 4 mg/kg IV once daily 1, 2
Clindamycin is particularly attractive because it covers both streptococci and MRSA with a single agent, avoiding the need for combination therapy 1, 2. However, this should only be used if your institution's antibiogram shows clindamycin resistance rates below 10% 1, 2.
When Beta-Lactam Monotherapy May Be Appropriate
If the preseptal cellulitis is nonpurulent (no drainage or exudate) and the patient lacks MRSA risk factors, IV cefazolin 1-2 g every 8 hours or ceftriaxone 1-2 g daily may be sufficient 2, 5. However, given that the patient requires hospitalization, there is likely concern for severity or complications, making MRSA coverage prudent in most cases 2.
Treatment Duration
- 7-14 days total therapy is recommended for complicated skin and soft tissue infections in hospitalized patients 1, 2
- Transition to oral therapy once clinical improvement is demonstrated (typically after minimum 4 days IV treatment) 2
- Oral options for step-down include clindamycin 300-450 mg every 6 hours, or doxycycline 100 mg twice daily plus a beta-lactam if streptococcal coverage is needed 1, 2
Critical Imaging Considerations
CT scan should be performed if there is any concern for orbital involvement or complications 3:
- In a pediatric study, CT was performed in 42.6% of preseptal cellulitis cases and identified sinusitis in 10.3% of patients 3
- Imaging helps distinguish preseptal from orbital cellulitis and identifies predisposing factors like sinusitis 3
Adjunctive Measures
- Elevation of the affected area promotes drainage and hastens improvement 2
- Examine for predisposing conditions including sinusitis (most common risk factor), odontogenic infections, insect bites, or periocular trauma 3
- Treat underlying sinusitis if present, as this is the most common predisposing factor in children and adolescents 3
Common Pitfalls to Avoid
- Do not reflexively add MRSA coverage simply because the patient is hospitalized—if the cellulitis is truly nonpurulent without risk factors, beta-lactam monotherapy may suffice 2
- Do not use doxycycline as monotherapy for preseptal cellulitis, as its activity against beta-hemolytic streptococci is unreliable 2
- Do not delay ophthalmology consultation if there is any concern for orbital extension—this can progress rapidly to vision-threatening complications 3
- Do not continue ineffective antibiotics beyond 48 hours—if the patient is not improving, reassess for resistant organisms, deeper infection, or misdiagnosis 2
When to Escalate Therapy
If the patient shows signs of rapid progression, severe systemic toxicity, or suspected necrotizing infection, escalate to broad-spectrum combination therapy 2:
- Vancomycin 15-20 mg/kg IV every 8-12 hours PLUS piperacillin-tazobactam 3.375-4.5 g IV every 6 hours 2
- This combination provides coverage for polymicrobial infection and anaerobes 2
- Obtain emergent surgical consultation if necrotizing fasciitis is suspected 2
Transition to Outpatient Management
Once clinical improvement is demonstrated (reduced erythema, edema, and systemic symptoms), transition to oral antibiotics and consider ambulatory IV therapy if continued parenteral treatment is needed 6: