Bacteria
Cellulitis
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Cellulitis
, Staphylococcal Cellulitis, Streptococcal Cellulitis
See Also
Skin Infection
Hand Infection
Nodular Lymphangitis
Erysipelas
Impetigo
Preseptal Cellulitis
and
Periorbital Cellulitis
Cellulitis in Diabetes Mellitus
Epidemiology
U.S, estimated 14 million cases per year
Accounts for 2% of all Emergency Department visits (3.5 Million cases per year in U.S. in 2005)
Risk factors
See
Skin Infection
Also see
Group A Streptococcus Cellulitis
(
Erysipelas
)
Trauma
Laceration
Puncture Wound
Post-operative infection at incision site
Underlying skin lesion
Superficial Folliculitis
or
Furuncle
(
Staphylococcus
infection)
Skin Ulcer
Fungal Dermatoses
Non-Group A Streptococcus Cellulitis
related lesions
Coronary Artery
bypass with saphenous vein graft
Radical pelvic surgery or radiation
Neoplasms
Lymph
atic Cutaneous metastases from neoplasms
Inflammatory
Breast Cancer
Carcinoma
Erysipeloid
es
Extremity Stasis or
Edema
Chronic
Dependent Edema
(may progress rapidly)
Peripheral Vascular Disease
Lymphedema
Perianal Streptococcal Cellulitis
(in children)
Diabetes Mellitus
See
Cellulitis in Diabetes Mellitus
Immunocompromised
patients
Causes
Gene
ral
Common (most Cellulitis cases)
Staphylococcal Cellulitis (typically with abscess)
Group A Streptococcus Cellulitis
(
Erysipelas
)
Less common Streptococcal infections
Pneumococcus
Non-Group A Streptococcus Cellulitis
Group C or G
Streptococcus
Cellulitis
Group B Streptococcus
Cellulitis in newborns
Rapidly progressive Cellulitis
See
Necrotizing Fasciitis
Vibrio Cellulitis
(
Vibrio vulnificus
)
Clostridium perfringens
Pasteurella
multocida
Aeromonas Hydrophila
Causes
Exposure
See
Nodular Lymphangitis
See
Pet-Borne Infection
See
Dermatologic Manifestations in Returning Traveler
Fish Handlers or water exposure (See
Marine Trauma
)
Erysipelothrix rhusiopathiae (
Erysipeloid
, fish handler's disease)
Mycobacterium marinum
(Fish tank exposure)
Aeromonas Hydrophila
Spines of stonefish (South Pacific) risk of serious systemic toxicity,
Pulmonary Edema
Vibrio vulnificus
(
Vibrio Cellulitis
, high risk of rapid progression)
Vibrio alginolyticus
Vibrio
parahaemolyticus
Streptococcus
iniae (from farmed tilapia)
Gardening or splinter exposure
See
Nodular Lymphangitis
Nocardia brasiliensis
(
Nocardiosis
)
Sporotrichosis
:
Sporothrix schenckii
(fungus)
Tetanus
Hospitalized patients
Methicillin Resistant Staphylococcus Aureus
(
MRSA
)
Pseudomonas
aeruginosa
Enterococcus
Escherichia coli
Animal Bite
s
See
Marine Envenomation
Cat Bite
s
Pasteurella
multocida
Dog Bite Infection
Mixed
Bacteria
l flora (
Staphylococcus
,
Streptococcus
,
Anaerobe
s)
Pasteurella
multocida
Capnocytophaga canimorsus (DF-2)
Staphylococcus
intermedius
Human Bite
s
See
Fight Bite
Mixed
Anaerobe
s and aerobes
Staphylococcus aureus
and
Streptococcus
Bacteroides
,
Fusobacterium
, Eikenella corrodens
Miscellaneous
Eosinophilic Cellulitis
Pseudomonas
aeruginosa
See
Water-borne Transmission
Sweaty Tennis Shoe Syndrome
Synthetics in moist environment (e.g.
Endotracheal Tube
)
Causes
Immunocompromised
Patients
See
Skin Infections in Diabetes Mellitus
Serratia
Proteus
Enterobacteriaceae
Cryptococcus
Legionella pneumophila
Associated with
Legionella pneumonia
Legionella
micdadei
Seen in
Renal Transplant
patients
Escherichia coli
Seen in children with relapsing
Nephrotic Syndrome
Symptoms
Inflamed
Skin Wound
develops rapidly days after injury (red, hot, swollen and painful)
Local tenderness
Pain (contrast with
Pruritus
of other skin conditions)
Erythema
Unilateral
Associated symptoms
Malaise
Fever
, chills
Signs
Draw margins of erythema with marker
Follow course of infection on
Antibiotic
s (but do not expect significant improvement in first 24 hours)
Wound
with contiguous inflammation
Erythema (Rubor)
Swelling (Tumor)
Local tenderness (Dolor)
Warm to touch (Calor)
Unilateral involvement
Contrast with stasis and edematous conditions which are bilateral
Abscess (or purulent drainage)
Hallmark of
Staphylococcus aureus
Peau d'orange Skin (orange-peel like skin)
Cellulitis results in edema including the fat layer
Hair Follicle
s remain anchored to the
Dermis
Results in an indentation or pitting at each
Hair Follicle
in the midst of edema of the surrounding tissue
Regional spread
Ascending lymphangitis
Regional Lymphadenopathy
Small patches of necrosis
Gram Negative
superinfection may also be present
Hemorrhagic and necrotic bullae (specific conditions)
Group A Streptococcal Cellulitis
Pseudomonas
Cellulitis
Vibrio Cellulitis
(
Vibrio vulnificus
)
Clostridium perfringens
Aeromonas Hydrophila
Bullous Impetigo
(not typically hemorrhagic)
Differential Diagnosis
Non-infectious Conditions (Pseudocellulitis)
Precautions
Cellulitis is overdiagnosed, with the risk of
Antibiotic
adverse effects (e.g.
Clostridium difficile
) and
Antibiotic Resistance
Consider alternative diagnoses (e.g.
Stasis Dermatitis
) when bilateral, pruritic, chronic, non-progressive
Vascular Conditions
Venous Insufficiency
and
Stasis Dermatitis
(most common)
Acute stasis appears with bilateral leg erythema (compare legs)
Lipodermatosclerosis
Panniculitis
with bilateral, medial ankle erythema
Superficial Thrombophlebitis
Deep Vein Thrombosis
Lymphedema
Dermatologic Conditions
Contact Dermatitis
Insect Bite
s
Acute
Drug Reaction
Eosinophilic Cellulitis
Sweet Syndrome
Shingles
Calciphylaxis
Calcium
deposition due to
ESRD
, DM,
Obesity
, liver disease,
Warfarin
Rheumatologic Condition
s
Gouty Arthritis
Relapsing Polychondritis
Miscellaneous
Edema
tous conditions (e.g. CHF,
Cirrhosis
)
Erythromelalgia
Inflammatory Carcinoma (metastatic cancer to skin)
Foreign body reaction (mesh, metal, silicone implant)
Familial Mediterranean fever
Erythema Migrans
(
Lyme Disease
)
References
Swadron and DeClerck in Herbert (2017) EM:Rap 17(5): 11-2
Vergidis (2005) Ann Intern Med 142:47-55 [PubMed]
Labs
See
Laboratory Risk Indicator for Necrotizing Fasciitis
(
LRINEC Score
)
Pustular drainage or abscess culture
Recommended if
Antibiotic
s are being used, systemic symptoms or severe localized findings
Blood Culture
(25%
Test Sensitivity
)
Not recommended in uncomplicated Cellulitis without associated systemic symptoms
Indications (risk of deep tissue involvement)
Severe infection or systemic symptoms or signs (lymphangitis,
Sepsis
)
Immunocompromised
patients or elderly
Patients requiring surgery
Recurrent, persistent or large abscess
Human Bite
or
Animal Bite
Lymphedema
Skin biopsy (25% sensitivity)
Indicated in necrotizing lesions (especially those requiring derbidement)
Obtain sample of leading margin of lesion
Fine Needle Aspiration
Saline injection and aspiration
Listed for historical purposes only (rarely done in clinical practice)
Technique
Leading edge injection and aspiration with saline
Efficacy
May assist diagnosis with Cellulitis, but yield is typically very low
Not useful in
Erysipelas
Test Sensitivity
may approach 30% from closed lesions
However overall
Test Sensitivity
may be as low as 5%
Indication
Unusual pathogens suspected
Cellulitis refractory to current
Antibiotic
s
Imaging
Soft tissue
Ultrasound
Test Sensitivity
94% and
Test Specificity
85% for abscess
Abcess formation is consistent with staphylococcal infection
Also confirms Cellulitis (cobblestoning)
Computed Tomography (CT)
Consider in suspicion of deep space infection
MRI
Consider in suspected
Necrotizing Fasciitis
Management
Gene
ral Care
Tetanus Prophylaxis
Clean wound site
Copious irrigation
Debride devitalized tissue
Incision and Drainage
Incision and Drainage
is the primary treatment for abscess (fluctuant pocket)
Compresses
Cool sterile saline dressings decrease pain
Later, moist heat helps localize infection
Consider immobilization and elevation of involved limb
Splinting
in a position of function may decrease swelling
Uncommonly done in practice
Consider
Corticosteroid
s in non-diabetic adults with Cellulitis (especially leg Cellulitis)
Associated with faster Cellulitis resolution
Dall (2005) Cutis 75(3): 177-80 +PMID:15839362 [PubMed]
Management
Factors affecting
Antibiotic
selection and course
Three decision points drive management
Purulent (abscess) or non-purulent (Cellulitis without abscess)
Staphylococcus aureus
coverage (including
MRSA
for purulent infections,
Penetrating Trauma
with abscess)
Abscesses are
MRSA
positive in 70% of U.S. isolates as of 2023
Streptococcus
coverage for non-purulent infections (no abscess, no significant
Penetrating Trauma
)
MRSA
accounts for only 4% of nonpurulent Cellulitis infections
Severe (infection with
SIRS
Criteria) or Mild (infection without
SIRS
Criteria)
Oral
Antibiotic
s for mild to moderate infections (no advantage to a single IV dose of
Antibiotic
)
IV
Antibiotic
s for moderate to severe infections (
SIRS
Criteria present)
See
Necrotizing Fasciitis
Modifying Factors
Specific exposures (see causes based on exposure as above)
See
Immunocompromised
patients as above
Deep space infection (e.g.
Necrotizing Fasciitis
)
Skin Infections in Diabetes Mellitus
Peripheral Arterial Disease
Intravenous Drug Abuse
(polymicrobial infections)
Chronic Wound
s or ulcerations (e.g.
Decubitus Ulcer
,
Diabetic Foot Ulcer
,
Venous Stasis Ulcer
)
See
Chronic Wound Infection
See
Chronic Osteomyelitis
Distinguish
Erysipelas
, abscess and Cellulitis
See
Necrotizing Fasciitis
Erysipelas
(superficial)
Sharply demarcated, bright red, indurated
Typically caused by
Group A Streptococcus
Although
Staphylococcus aureus
can have a similar appearance on the face
Cellulitis (deep, subcutaneous)
Abrupt onset of indistinct faint erythema with rapidly advancing border
Typically caused by group A.
Streptococcus
or Group G
Although
Staphylococcus
can cause this as well
Purulent Cellulitis
Cellulitis with pustular drainage or exudate without definitive, drainable abscess
Abscess
Hallmark of
Staphylococcus aureus
infection
Primary management is
Incision and Drainage
If
Antibiotic
s are needed (Cellulitis with abscess), then cover
MRSA
(see below)
Other
Bacteria
l
Skin Infection
s
Folliculitis
Impetigo
Consider exposures in
Antibiotic
selection
See causes based on exposure as above
Fresh water exposure
Fluoroquinolone
Salt water exposure
Doxycycline
Dog Bite
,
Cat Bite
or
Human Bite
Amoxicillin
-Clavulanate (
Augmentin
)
If
Penicillin Allergy
Clindamycin
or
Metronidazole
AND
Trimethoprim-Sulfamethoxazole or
Fluoroquinolone
Distinguish most likely organism:
Streptococcus
or
Staphylococcus
Streptococcus
(especially
Group A Streptococcus
)
Streptococcus
(especially Group A) is the most common cause of Cellulitis and
Erysipelas
Abrupt onset with rapid spread
May be associated with fever and ascending lymphangitis
Typically associated with an inciting
Skin Injury
with associated break in the skin (e.g.
Tinea Pedis
)
Staphylococcus aureus
(typically
MRSA
)
Less common cause of Cellulitis (causes only 14% of uncomplicated Cellulitis)
However, purulent drainage or abscess is typically caused by
Staphylococcus aureus
Typically presents without a primary
Skin Injury
site
Primary source is often a
Folliculitis
Abscess is often present (
Incision and Drainage
is primary treatment)
May present initially as pustular drainage or exudate (pustular Cellulitis)
Consider soft tissue
Ultrasound
if suspect occult abscess
Consider
Antibiotic Resistance
Avoid
Fluoroquinolone
s in Cellulitis due to high resistance
Staphylococcus aureus
infections are often due to
MRSA
Course: Uncomplicated
Historical: Standard course has been 10 days of
Antibiotic
s
Recommended: 5 day course is as effective as 10 day if uncomplicated
IDSA in 2020 recommends 5 day course in uncomplicated Cellulitis
Hepburn (2004) Arch Intern Med 164:1669-74 [PubMed]
Course: Complicated
Course 7-14 days (6 weeks if joint involvement)
Follow-up
Close interval follow-up
Avoid modifying therapy until 48 hours after last
Antibiotic
change
Patient should not expect improvement until >48 hours
Management
Emergency Department Approach
Factors associated with oral, outpatient treatment failure
Fever
with
Temperature
>38 C at triage (OR 4.3)
Chronic leg ulcers (OR 2.5)
Chronic edema or lympedema (OR 2.5)
Prior Cellulitis in the same area (OR 2.1)
Cellulitis at a wound site (OR 1.9)
Peterson (2014) Acad Emerg Med 21(5):526-31 +PMID:24842503 [PubMed]
Localized, uncomplicated Cellulitis without serious local or systemic findings
Start oral therapy without initial intravenous dose
Single intravenous dose prior to discharge on oral dosing does NOT speed resolution or improve efficacy
Most oral
Antibiotic
s used for
Skin Infection
s have excellent, rapid oral absorption
Cephalexin
(>90% GI absorption)
Clindamycin
(>90% GI absorption)
Doxycycline
(>90% GI absorption)
Bactrim
or
Septra
(>70% GI absorption)
Amoxicillin
(>75% GI absorption)
Oral
Antibiotic
s result in as good if not better efficacy than IV
Antibiotic
s
Faster resolution, shorter hospital stays and lower cost
IV
Antibiotic
selection may be ill fitted for convience (e.g.
Ceftriaxone
for once daily dosing)
IV
Antibiotic
s are associated with a higher rate of
Antibiotic Associated Diarrhea
Kilburn (2010) Cochrane Database Syst Rev 16(6): CD004299 +PMID:20556757 [PubMed]
Aboltins (2015) J Antimicrob Chemother 70(2): 581-6 [PubMed]
Do not empirically start
MRSA
for uncomplicated Cellulitis without abscess or purulent drainage
Majority of uncomplicated Cellulitis without abscess is caused by
Streptococcus
Cephalexin
alone has excellent coverage for
Streptococcus
and
MSSA
Added
MRSA
coverage (e.g.
Septra
) offers no benefit in non-purulent Cellulitis
Moran (2017) JAMA 317(20): 2088-96 +PMID:28535235 [PubMed]
Do not use a single
Vancomycin
dose prior to oral
Antibiotic
dosing
Vancomycin
serum concentrations after a single dose offer no benefit
Multiple doses are required to reach MIC
Only 3% of patients are therapeutic levels at 12 hours of single
Vancomycin
loading dose
Rosini (2015) Ann Pharmacother 49(1): 6-13 [PubMed]
Other risks of a single
Vancomycin
dose (beyond its lack of efficacy)
Will lengthen ED time by at least 60-90 minutes for the
Vancomycin
infusion alone
Increases the risk for
Antibiotic Resistance
and reactions
Localized Cellulitis with borderline indications for
Parenteral
Antibiotic
s
Start
Intravenous Fluid
s
Give initial oral
Antibiotic
dose
Administer
Analgesic
s
Reassess in 1 hour and reconsider
Parenteral
Antibiotic
s versus discharge on oral
Antibiotic
s
Localized Cellulitis with failure to respond to oral therapy
Consider Cellulitis Differential Diagnosis
Maintain same
Antibiotic
course for at least 24-48 hours (unless significant progression)
Cellulitis is unlikely to improve on any
Antibiotic
s regimen for the first 24 hours
Assess for Cellulitis with abscess
Consider soft tissue
Ultrasound
or attempt needle aspiration
Incision and Drainage
of abscess
Abscess complicating Cellulitis typically defines Staphylococcal Cellulitis (see
Antibiotic
selection below)
Consider broadening oral
Antibiotic
regimen
Include
MRSA
coverage if not already added (especially for purulent Cellulitis)
Parenteral
Antibiotic
s (esp. for serious findings such as
Necrotizing Fasciitis
,
Sepsis
)
See regimens below
Place and IV line and patient returns at intervals (typically every 12 hours) for next
Antibiotic
infusion
Patient returns to ED for infusion only RN visits with a planned recheck by a provider at 24-48 hours
RN alerts provider earlier if concerning findings at time of routine infusion
Admit or observe a patient developing systemic symptoms or other concerning findings
Consider
Consultation
Infectious Disease
Gene
ral Surgery
Consider inpatient management
See below
References
Morgenstern in Herbert (2019) EM:Rap 19(1): 14-5
Lin in Herbert (2014) EM:Rap 14(1): 6-7
Management
Inpatient
Indications
Cellulitis with serious associated findings or comorbidity
Severe extremity
Cellulitis in Diabetes Mellitus
Skin Abscess
involving the face, hands, genitalia
Sepsis
or other severe infection (e.g.
Necrotizing Fasciitis
)
Immunocompromised
state
Diagnostics
See
Laboratory Risk Indicator for Necrotizing Fasciitis
(
LRINEC Score
)
Complete Blood Count
(CBC)
C-Reactive Protein
Comprehensive metabolic panel
Blood Culture
s (in severe infections or
Immunocompromised
patients)
Wound
aspirate, culture or biopsy (advancing edge)
Imaging indications
Necrotizing Fasciitis
(MRI)
Other deep space infection (soft tissue
Ultrasound
or CT)
Consultation
Consider
Consultation
with infectious disease
Gene
ral surgery or orthopedic
Consultation
indications
Suspected
Necrotizing Fasciitis
Suspected
Gas Gangrene
Suspected other deep space infection
Suspected joint involvement
Approach
Admit
Incision and Drainage
of abscess
Debride necrotic tissue
Intravenous
Antibiotic
regimen as described below (typically with
MRSA
coverage)
Modify
Antibiotic
s based on wound culture results (if performed)
Transition to oral
Antibiotic
s
When tolerated and improving
Continue
Antibiotic
s for 7-14 day total course
Management
Extremity Infections (non-diabetic patients)
See
Skin Infections in Diabetes Mellitus
See
Necrotizing Fasciitis
See
Sepsis
Non-Purulent,
Erysipelas
(flat lesions, well demarcated and bright red):
Streptococcus
coverage
Treat as Cellulitis with broader coverage (see below) unless classic
Erysipelas
appearance
Only use
Streptococcus
specific
Antibiotic
s for classic
Erysipelas
appearance
In practice, most clinicians use broader Cellulitis coverage for both
Streptococcus
and
Staphylococcus
Mild infections (oral, outpatient management)
Penicillin VK
500 mg orally four times per day for 5-10 days OR
Amoxicillin
500 mg orally three times per day for 5-10 days OR
Cephalexin
500 mg orally four times per day for 5-10 days OR
Cefadroxil
500 to 1000 mg orally twice daily for 5 to 10 days OR
Mild Infections -
Penicillin
and
Cephalosporin
Allergy (oral, outpatient management)
Azithromycin
500 mg orally on day 1, then 250 mg orally on days 2-5
Clindamycin
300 mg orally four times per day for 5-10 days
Moderate infections (esp. with
SIRS
Criteria, requiring IV
Antibiotic
s)
Penicillin G
2 million units IV every 6 hours or
Nafcillin
1 to 2 g IV every 6 hours
Cefazolin
1 gram IV every 8 hours or
Clindamycin
600 mg IV every 8 hours or
Ceftriaxone
1 to 2 g IV every 24 hours
Severe Infections
See
Sepsis
See
Necrotizing Fasciitis
Severe, non-purulent Cellulitis is typically treated with combined regimen listed below
IDSA 2014 guidelines cover
Streptococcus
and
MRSA
in severe infections
Non-Purulent - Cellulitis (less distinct margins):
Streptococcus
and
Staphylococcus
coverage
First Line: Uncomplicated Cellulitis coverage for
Streptococcus
(most likely) and
MSSA
coverage
Mild Infections (Oral)
Cephalexin
500 mg orally four times per day for 5-10 days OR
Cefadroxil
500 to 1000 mg orally twice daily for 5 to 10 days OR
Dicloxacillin
500 mg orally four times per day for 5-10 days OR
Clindamycin
300 mg orally four times per day for 5-10 days OR
Amoxicillin
-Clavulanate (
Augmentin
) 875 mg orally twice per day for 5-10 days
Moderate Infections -
Parenteral
Antibiotic
s (esp. with
SIRS
Criteria, more severe infections)
Cefazolin
1 gram IV every 8 hours OR
Nafcillin
2 grams IV q4 hours OR
Oxacillin
2 grams IV q4 hours OR
Clindamycin
600 mg IV every 8 hours OR
Ceftriaxone
1 to 2 g IV every 24 hours
Moderate Infections - Outpatient
Parenteral
(adults, narrower spectrum
Parenteral
protocol)
Protocol: Both medications for 5-10 days
Cefazolin
2 gram IV q24 hours AND
Probenacid 1 gram PO q24 hours (Decreases
Cefazolin
excretion)
References
Grayson (2002) Clin Infect Dis 34:1440-8 [PubMed]
Second Line: Complicated, refractory or pustular Cellulitis coverage for
Streptococcus
and
MRSA
coverage
See
Methicillin Resistant Staphylococcus Aureus
(
MRSA
) for risk factors
Mild - Oral
Antibiotic
s (choose 1)
Trimethoprim Sulfamethoxazole
(
Septra
,
Bactrim
) DS
Dose: One DS tab orally twice daily
Use with
Penicillin
,
Amoxicillin
, or
Cephalexin
(see dosing above)
Some recommend 2 tabs if normal
Renal Function
, serious infections or weight >100 kg
However no advantage found clinically to the higher dosing
Cadena (2011) Antimicrob Agents Chemother 55(12):5430-2 +PMID: 21930870 [PubMed]
Clindamycin
Not typically recommended (Increasing
MRSA
resistance, and induced resistance)
Dosing: 300 mg orally four times per day for 7-10 days
Linezolid
Not typically used for mild infections (very expensive, but generic in 2017)
Dosing: 600 mg orally twice daily
Moderate to Severe -
Parenteral
Antibiotic
s (esp. with
SIRS
Criteria,
Sepsis
and other more severe infections)
See
Sepsis
This is the default multi-drug empiric protocol with severe non-purulent infection
Consider
Necrotizing Fasciitis
coverage
Antibiotic
1: Empiric
Gram Positive
,
Gram Negative
and
Anaerobe
Coverage
Piperacillin
/Tazobactam (
Zosyn
) 3.375 IV every 6 to 8 hours (preferred) OR
Meropenem
1 g IV every 8 hours OR
Imipenem
1 g IV every 8 hours OR
Cefepime
2 g IV every 12 hours AND
Metronidazole
500 mg IV every 6-8 hours
Antibiotic
2:
MRSA
Coverage (choose 1)
Vancomycin
15 mg/kg IV every 12 hours (adjusted for
Renal Function
) or
Linezolid
600 mg IV q12 hours or
Clindamycin
600-900 mg IV q8 hours
Lipoglycopeptides (
Dalbavancin
,
Oritavancin
)
Single dose/course, expensive agents with coverage similar to
Vancomycin
May be used in stable patients considered for ongoing IV
Antibiotic
course
Antibiotic
3: Adjunctive
Antibiotic
considerations
Consider
Clindamycin
900 mg every 8 hours
Indicated in suspected toxin release (
Necrotizing Fasciitis
, gangrene)
Purulent - Cellulitis with Abscess (or per
Gram Stain
):
Staphylococcus
coverage
See
Skin Abscess
Incision and Drainage
is primary treatment of solitary abscess (without accompanying Cellulitis)
Antibiotic
s are not uniformly required if no Cellulitis is present
Antibiotic
s may prevent Cellulitis (NNT 14), but also have adverse effects (NNH 23)
Gottlieb (2019) Ann Emerg Med 73(1):8-16 +PMID: 29530658 [PubMed]
Antibiotic
s are at the discretion of the provider and may be warranted despite lack of Cellulitis
Serious comorbidity such as
Diabetes Mellitus
,
Immunosuppression
or extremes of age
Multiple sites of infection
Systemic symptoms
Rapid progression with concurrent Cellulitis
Infection involving face, hand or genitalia
Associated septic phlebitis
Unreliable follow-up
Large abscess (e.g. 5 cm and greater,
Carbuncle
)
Failure to improve after
Incision and Drainage
Antibiotic
selection and course
Antibiotic
selection is the same as for abscess with Cellulitis (typically
MRSA
)
Choose a single agent (esp.
Septra
)
Course is brief in most cases (3-5 days)
Mild -
Staphylococcus
Cellulitis (purulent Cellulitis) present:
MRSA
coverage (choose 1)
Trimethoprim Sulfamethoxazole
(
Septra
,
Bactrim
) DS
Take one tab orally twice daily for 5-10 days
Consider 2 tabs if normal
Renal Function
, serious infections or weight >100 kg
Doxycycline
100 mg orally twice daily for 5-10 days
Linezolid
600 mg PO bid (very expensive, but generic as of 2017)
Clindamycin
is no longer recommended for
MRSA
coverage due to growing resistance
Historical dosing
Clindamycin
300 mg orally four times per day for 7-10 days
Moderate to Severe infections (esp. with
SIRS
Criteria)
See
Sepsis
Consider combined multi-drug regimen (e.g.
Vancomycin
and
Zosyn
) as above
Vancomycin
15 mg/kg IV every 12 hours (adjusted for
Renal Function
)
Linezolid
600 mg IV q12 hours (very expensive)
Daptomycin
4 mg/kg IV every 24 hours
Telavancin
Ceftaroline Fosamil
Management
Facial Erysipelas
Staphylococcus aureus
may be difficult to exclude (despite most cases being
Group A Streptococcus
)
Guidelines as of 2012 recommend covering for
MRSA
Sanford guide recommends Vancomycin
Parenteral
ly or
Linezolid
orally or IV
Mild to moderate infections
Clindamycin
300 mg orally four times per day or
Augmentin
high dose with
Septra
DS 2 tabs twice daily or
Severe infections
Vancomycin
15 mg/kg IV every 12 hours (adjusted for
Renal Function
) or
Linezolid
600 mg IV q12 hours
Management
Special circumstances (including complicated Cellulitis)
Cellulitis in comorbid
Diabetes Mellitus
See
Skin Infections in Diabetes Mellitus
Complicated skin and subcutaneous tissue infection (
SSTI
)
Indications
Deep soft tissue infection
Surgical or
Trauma
tic
Wound Infection
Infected ulcers or burns
Large abscess with Cellulitis
Management
Inpatient management is typically indicated
Consider surgical
Consultation
(and possibly infectious disease
Consultation
)
Obtain wound cultures
Initiate empiric broad spectrum
Antibiotic
coverage including
MRSA
Prevention
Recurrent skin and subcutaneous tissue infection (
SSTI
)
Recurrent infection definition
Two or more discrete episodes of active infection and different sites over a 6 month period
Recurrent abscess
See
Skin Abscess
for complete list of preventive strategies
Wash all sheets, towels and clothes after an episode
Dispose of used razors
Consider Antibacterial soap (e.g.
Chlorhexidine
)
Consider
Mupirocin
(
Bactroban
) in nares twice daily for 5 days (decolonization)
Dilute bleach bath
Dilute bleach: 1 teaspoon bleach per gallon water OR
One quarter cup bleach per 20 gallons water (or 1/4 tub of water)
Soak in the dilute bleach for 15 minutes twice weekly for 3 months
Shower to rinse off bleach completely
Make certain to rinse and dry feet before walking across carpet (and bleaching the carpet)
Recurrent Cellulitis
See measures above under
Recurrent Skin Abscess
Reduce
Peripheral Edema
(support stockings)
Weight loss
Treat underlying
Venous Insufficiency
Good skin hygiene
Prophylactic
Antibiotic
s are not recommended
Not typically effective, especially if there is an underlying predisposing condition
Strategies that have been used historically for 4-52 weeks (not recommended)
Penicllin G 1.2 MU IM every 4 weeks or
Penicillin V
250 mg orally twice daily
Macrolide
s (e.g.
Erythromycin
500 mg orally daily) was used as alternative in
Penicillin Allergy
Complications
Thrombophlebitis
in older patients
Necrotizing Fasciitis
References
May and Mason in Herbert (2021) EM:Rap 21(4): 4-5
Chan (2014) Crit Dec Emerg Med 28(9): 2-7
Gilbert (2011) Sanford Guide
Moran in Majoewsky (2013) EM:Rap 13(2): 11
Orman and Hayes in Herbert (2015) EM:Rap 15(4):4-6
Riekena, Naganathan and Mehkri (2022) Crit Dec Emerg Med 36(6): 4-11
Tamirian and Eyre (2024) Crit Dec Emerg Med 38(1): 24-5
Ramakrishnan (2015) Am Fam Physician 92(6): 474-83 [PubMed]
Stulberg (2002) Am Fam Physician 66(1):119-24 [PubMed]
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