Cellulitis - Treatment I (Generalized and Individualized Approaches)

Generalized Approach

               The existing treatment paradigm is that empiric therapy should provide coverage for the most commonly involved gram-positive cocci. The presence or absence of an abscess as well as recent antibiotic exposures also impacts empiric treatment in light of issues regarding CA-MRSA. Treatment options and common pathogens are detailed in Table 1 for different cellulitis syndromes. Algorithms 1-4 provide extensive detail on dealing with the various types of cellulitis and associated conditions. Whether initial empiric therapy administered parenterally or orally is based on the clinician’s decision and not on evidence-based data which are not available. A list of indications for inpatient antibiotic treatment are listed in Table 4 and includes: comorbidities, signs of systemic toxicity (tachycardia, hypotension), those who cannot tolerate oral antibiotics or those who are not reliable for early follow up should be hospitalized and treated with parenteral therapy. Once symptomatic improvement occurs, therapy can be switched to oral (usually within 2-5 days) to complete 10-14 days course.

Individualized Approach

              Although the antibiotic regimens listed in Algorithms 1-4 should be efficacious in most cases of cellulitis in the immunocompetent patient; pivotal epidemiologic and host factors must be reviewed case-by-case so that therapy for less frequent or more resistant pathogens is provided when unique factors are present. In each case, however, empiric coverage should be selected that will provide coverage for beta-hemolytic streptococci and methicillin-sensitive Staphylococcus aureus. The following sections address treatment options in those cases where epidemiologic or host-related factors impact choice of empiric therapy of cellulitis. Treatment options are detailed in Table 1.

Recurrent Abscesses

               The major method of controlling recurrent abscesses is the use of antibacterial agents to eradicate staphylococcal carriage. There is scant data available on the efficacy of the various decolonization regimens. Mupirocin (bactroban) is the most commonly utilized topical antibiotic, often applied to the nares on the first 5 days of each month for 6 consecutive months. Chlorhexedine body wash is often used in conjunction with mupirocin, but tolerating it is challenging due to drying and irritation of the skin. Decolonization of household contacts may decrease recurrent episodes and should be considered. If these regimens fail, then low dose systemic antibiotics may be employed. Daily single dose clindamycin (150 mg) for 3 months has been shown to be 80% effective in decreasing staphylococcal colonization. Single dose TMP-SMX or doxycycline for 3 months has also been used, though clinical data is scarce. Some endorse the previous mentioned systemic antibiotics combined with rifampin for a shorter course of therapy to attempt to eradicate colonization. Several small studies have shown that tea tree oil (4% nasal ointment and 5% body wash) is at least as effective as a mupirocin based regimen. Polysporin may also have a role in the decolonization process.

50 year old male with MRSA abscess of his thigh

Algorithm 1:  Empiric Intravenous Antibacterial Agent Therapy Based on Anatomic Site.

Algorithm 2:  Empiric Intravenous Antibacterial Therapy for Community-Acquired Cellulitis Based on Host Status and in Patients without Preceding Antibiotic Therapy.

Algorithm 3:  Empiric Intravenous Antibacterial Therapy for Cellulitis Based on Degree of Immunosuppression.

 

Algorithm 4:  Empiric Antibacterial Agent Therapy Based on Type of Exposure.

Table 1: Specific Cellulitis Syndromes: Organisms and Empirical Therapy.

 

Syndrome

Location

Likely organisms

Source

Empiric parenteral therapy

Oral regimens

Abdominal wall cellulitis

Abdominal wall, may extend to thighs

Beta-hemolytic streptococci

Morbid obesity, abdominal wall lymphedema

Same as extremity cellulitis

 

Same as extremity cellulitis

 

Aquaculture cellulitis

Varies

Streptococcus iniae

Fish

Penicillin G but empiric coverage is same as extremity cellulitis

Penicillin V but empiric coverage is same as extremity cellulitis

 

Bacterial cellulitis in the immunosuppressed patient

Varies

Group A streptococci, S aureus, P. aeruginosa, Serratia, Proteus,  and the Enterobacteriaciae

 

Immunosuppression, bacteremia

Cefepime

OR

imipenem

OR

piperacillin-tazobactam

 

In penicillin-allergic*

[aztreonam + MRSA agent]

 

Consider the addition of tobramycin or ciprofloxacin to above until pathogen identified

 

In patients with possible MRSA: Same as extremity cellulitis with abscess

Not recommended initially

Dog and cat bite cellulitis

Varies

Pasteurella , S. aureus, streptococci, Capnocytophaga Bacteroides species, Fusobacterium, Porphyromonas species, Prevotella heparinolytica, Proprionibacterium, and Peptostreptococcus

Oral organisms and skin flora

Ampicillin-sulbactam

OR

ertapenem

OR

[clindamcyin  + levofloxacin]

OR

[metronidazole + levofloxacin]

Amoxicillin-clavulonate

OR

moxifloxacin

OR

[clindamycin  + TMP/SX]

OR

[levofloxacin + metronidazole]

Erysipelas

Face and lower extremity

Group A streptococci

Antecedent streptococcal respiratory tract infection, skin ulcers, local trauma or abrasions, psoriatic or eczematous lesions

Same as extremity cellulitis without abscess

 

 

Same as extremity cellulitis without abscess

Extremity cellulitis with abscess

Lower extremity

MRSA

Nasal colonization

Daptomycin

OR

vancomycin

OR

linezolid

TMP/SMZ

OR

doxycycline

OR

linezolid

OR

clindamycin

Fresh water exposure cellulitis

Varies

Aeromonas hydrophilia

Fresh water

Levofloxacin

OR

cefepime

OR

carbapenems

Same fluoroquinolones as listed for “parenteral”

Human bite cellulitis

Varies

Normal oral flora of biter: Streptococci (especially viridans streptococci), S. aureus, Haemophilus, Eikenella and anaerobes

Oral organisms and skin flora

Same as dog and cat bite cellulitis

Same as dog and cat bite cellulitis

Meat  handling cellulitis

Hands

Erysipelothrix rhusiopathiae

Meat, poultry, hides, saltwater fish and shellfish

Penicillin G

OR

ceftriaxone

OR

imipenem

 

If penicillin* allergic:

levofloxacin

OR

clindamycin

Penicillin V

 

If penicillin* allergic:

ciprofloxacin

OR

clindamycin

OR

azithromycin

Orbital cellulitis

Orbital

Streptococci, S. aureus, and non-spore-forming anaerobes

Sinusitis, orbital trauma with fracture or foreign body, dacryocystitis, and infection of the teeth, middle ear, or face

Same as preseptal cellulitis

Same as preseptal cellulitis

Perineal or post-gynecologic surgery cellulitis

Abdominal wall, inguinal area, and/or the proximal thigh

Non-group A beta-hemolytic streptococci, Staphylococcus aureus, enterococci, Escherichia coli, Peptostreptococcus, Prevotella and Porphyromonas, Bacteroides fragilis group, and Clostridium.

Surgical procedures with local lymph node dissection and radiation for several types of gynecologic cancer

Same as preseptal cellulitis

Same as preseptal cellulitis

Post-lumpectomy cellulitis

Ipsilateral breast

(may extend to  shoulder, back, and arm)

Non-group A beta-hemolytic streptococci

Complication of surgeries which involve limited lymph node dissection and breast conservation and radiation

Same as extremity cellulitis without abscess

 

Same as extremity cellulitis without abscess

 

 

Post-mastectomy cellulitis

Ipsilateral arm

Non-group A beta-hemolytic streptococci

Complication of surgeries which involve lymph node dissection

Same as extremity cellulitis without abscess

 

Same as extremity cellulitis without abscess

 

Post-saphenous venectomy cellulitis

Lower extremity

Beta-hemolytic streptococci

Occur months to years after saphenous venectomy: Disruption of the cutaneous barrier, lymphedema, venous insufficiency

Same as extremity cellulitis without an abscess

 

Same as extremity cellulitis without an abscess

 

Preseptal cellulitis

Periorbital

Streptococcus pneumoniae, Staphylococcus aureus, coagulase-negative Staphylococcus, and anaerobes,

Haemophilus influenzae type b, S. pyogenes

Contiguous infection of the soft tissues of the face and eyelids secondary to local trauma, insect bites, or foreign bodies

[Ceftriaxone  + metronidazole +/- vancomycin]

OR

[ertapenem  +/- vancomycin]

OR

moxifloxacin

Amoxicillin-clavulanate

OR

[levofloxacin + metronidazole]

OR

moxifloxacin

 

Saltwater exposure cellulitis

Varies

Vibrio species, particularly V. vulnificus

Saltwater, ingestion of raw or undercooked seafood

[Minocycline

+ cefotaxime]

OR

levofloxacin

Minocycline

+

levofloxacin

 

*Immediate-type hypersensitivity reaction

+ Nafcillin and oxacillin can be used interchangeably

 

Table 4:  Indications for Inpatient Treatment of Cellulitis

  • Hemodynamic instability
  • Evidence of systemic toxicity or inability to stabilize signs of toxicity rapidly with fluid, intravenous antibiotics and other supportive measures
  • Altered mental status
  • Concern for a deep space infection (i.e. necrotizing fasciitis)
  • Inability to ensure prompt outpatient follow-up
  • Marked elevation in temperature and/or rigors
  • Inability to tolerate oral antibiotics
  • Complex constellation of comorbidities
  • Already failed appropriate oral antibiotics