Necrotising Fasciitis
Necrotising fasciitis is a rapidly progressive, life-threatening infection of the deep fascia with secondary necrosis of overlying skin and subcutaneous tissue. It is a true surgical emergency requiring immediate recognition, aggressive surgical debridement, and broad-spectrum antibiotics. The infection spreads along fascial planes, causing extensive tissue destruction and systemic toxicity. Mortality rates range from 20-40% even with optimal treatment, making early diagnosis and intervention critical. The condition is often called "flesh-eating disease" due to its rapid tissue destruction.
Clinical Pearls:
- True surgical emergency: "Time is tissue" - delays increase mortality
- Pain out of proportion to examination is the earliest and most reliable sign
- LRINEC score ≥6 suggests necrotising fasciitis (but not diagnostic)
- Type 1 (polymicrobial) more common than Type 2 (monomicrobial)
- Clindamycin is essential for Group A Strep to inhibit toxin production
Red Flags:
- Pain out of proportion: Severe pain despite minimal visible changes
- Crepitus: Subcutaneous gas (palpable or on imaging)
- Rapid progression: Spread of erythema over hours
- Systemic toxicity: Sepsis, SIRS, organ failure
- Hard, woody induration: Deep fascial involvement
- Dusky, violaceous skin: Ischemia and necrosis
- Hemorrhagic bullae: Advanced disease
Necrotising fasciitis is rare but devastating. Understanding epidemiology aids in recognition and risk stratification.
Key Statistics:
- Incidence: 0.4-1.0 per 100,000 population per year
- Mortality: 20-40% overall, higher with delays
- Type 1: 70-80% of cases (polymicrobial)
- Type 2: 20-30% of cases (monomicrobial, Group A Strep)
- Age: Peak 50-70 years, but can occur at any age
- Gender: Slight male predominance (1.5:1)
Risk Factors:
- Diabetes mellitus: 40-60% of cases
- Immunosuppression: HIV, chemotherapy, steroids
- Obesity: Increases risk
- Peripheral vascular disease: Compromised blood supply
- Trauma: Even minor (insect bites, injection sites)
- Surgery: Post-operative complication
- IV drug use: Injection site infections
Anatomic Distribution:
- Lower extremity: 40-50% (most common)
- Perineum (Fournier's gangrene): 20-30%
- Upper extremity: 15-20%
- Trunk: 10-15%
- Head and neck: 5-10% (rare but dangerous)
Mortality and Morbidity:
- Overall mortality: 20-40%
- With early surgery (less than 24h): 10-20%
- With delayed surgery (>24h): 40-60%
- Amputation rate: 15-25% of limb cases
- Long-term disability: Significant in survivors
Necrotising fasciitis results from bacterial invasion of deep fascial planes, causing rapid tissue destruction through multiple mechanisms including direct bacterial damage, toxin production, and host immune response.
Pathophysiology Steps:
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Bacterial Entry: Organisms enter through breaks in skin (trauma, surgery, injection sites) or spread from adjacent infections. Initial entry may be minor (insect bite, abrasion)
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Fascial Invasion: Bacteria spread rapidly along fascial planes, which offer little resistance. Fascia has poor blood supply, limiting immune cell access and antibiotic penetration
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Toxin Production: Group A Strep produces exotoxins (streptolysin O, pyrogenic exotoxins) that cause tissue damage, activate inflammatory cascade, and cause systemic toxicity. Clostridial species produce alpha-toxin causing myonecrosis
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Vascular Thrombosis: Bacterial toxins and inflammatory mediators cause microvascular thrombosis, leading to tissue ischemia and necrosis. This creates anaerobic environment favoring further bacterial growth
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Tissue Necrosis: Ischemia and direct bacterial damage cause rapid tissue death. Necrosis spreads along fascial planes faster than visible skin changes, explaining the discrepancy between symptoms and examination
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Systemic Toxicity: Bacterial toxins and inflammatory mediators (TNF-α, IL-1, IL-6) enter circulation, causing SIRS, sepsis, and multi-organ failure. Streptococcal toxic shock syndrome can occur with Type 2
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Compartment Syndrome: Swelling and tissue destruction can cause compartment syndrome, further compromising blood supply and accelerating tissue death
Non-Modifiable Risk Factors:
- Age: Increased risk with age, peak 50-70 years
- Gender: Slight male predominance
- Genetic: Some individuals may have increased susceptibility
Modifiable Risk Factors:
- Diabetes mellitus: Strongest risk factor, 40-60% of cases
- Immunosuppression: HIV, chemotherapy, organ transplantation, steroids
- Obesity: Increases risk, possibly due to impaired wound healing
- Peripheral vascular disease: Compromised blood supply
- Chronic kidney disease: Impaired immune function
- Malnutrition: Impaired wound healing and immune function
High-Risk Scenarios:
- Post-operative: Surgical site infections
- Trauma: Even minor trauma (insect bites, abrasions)
- IV drug use: Injection site infections
- Perineal surgery: Risk of Fournier's gangrene
- Decubitus ulcers: In debilitated patients
Protective Factors:
- Intact skin: Primary barrier
- Good vascular supply: Adequate tissue perfusion
- Normal immune function: Effective bacterial clearance
- Early recognition: Prompt treatment improves outcomes
Clinical presentation varies but typically includes severe pain, rapid progression, and systemic toxicity. Early recognition is critical for survival.
Early Presentation (First 24-48 hours):
Progressive Disease (48-72 hours):
Advanced Disease (>72 hours):
Type 1 (Polymicrobial):
Type 2 (Monomicrobial):
Systemic Features:
Examination must be thorough and repeated frequently. Key findings include pain out of proportion, skin changes, and systemic toxicity.
General Examination:
- Vital signs: Fever, tachycardia, hypotension (sepsis)
- Mental status: May be altered with severe sepsis
- Appearance: Toxic, unwell, may be in severe pain
Local Examination:
Inspection:
- Erythema: May be subtle early, becomes more obvious
- Swelling: Progressive, may be asymmetric
- Skin color: Dusky, violaceous, mottled (ischemia)
- Blisters: Hemorrhagic bullae (advanced disease)
- Necrosis: Black eschar, gangrene (late)
- Wound: Entry point may be visible (trauma, injection site)
Palpation:
- Temperature: Skin may be warm early, cool later (ischemia)
- Induration: Hard, woody feel (fascial involvement)
- Crepitus: Subcutaneous gas (palpable crackling)
- Tenderness: Severe, out of proportion to appearance
- Sensation: May be decreased or absent (nerve damage)
Special Tests:
- Finger test: Incision into fascia - if finger passes easily, suggests necrotising fasciitis
- Probe test: Easy separation of fascia from muscle
- LRINEC score: Laboratory Risk Indicator for Necrotising Fasciitis (≥6 suggests NF)
Systemic Assessment:
- Sepsis: SIRS criteria, organ dysfunction
- Compartment syndrome: If in extremity, check compartments
- Spread: Assess for extension to adjacent areas
LRINEC Score Components:
| Parameter | Score |
|---|---|
| CRP (mg/L) | less than 150: 0, ≥150: 4 |
| WCC (×10³/μL) | less than 15: 0, 15-25: 1, >25: 2 |
| Hemoglobin (g/dL) | >13.5: 0, 11-13.5: 1, less than 11: 2 |
| Sodium (mmol/L) | ≥135: 0, less than 135: 2 |
| Creatinine (mg/dL) | ≤1.6: 0, >1.6: 2 |
| Glucose (mg/dL) | ≤180: 0, >180: 1 |
Total Score: 0-13. Score ≥6 suggests necrotising fasciitis (sensitivity 56-92%, specificity 86-96%)
Diagnosis is primarily clinical. Investigations support diagnosis and guide management but should not delay surgery. Imaging may show gas or fascial involvement.
Essential Investigations:
- Blood cultures: Before antibiotics if possible
- Wound cultures: From surgical debridement
- Complete blood count: Leukocytosis, may have left shift
- Inflammatory markers: Elevated CRP, procalcitonin
- LRINEC score: Calculate from lab values
- Renal function: Assess for organ dysfunction
- Coagulation: DIC may occur
Imaging:
X-ray:
- Subcutaneous gas: Linear or mottled lucencies (if gas-producing organisms)
- Soft tissue swelling: Non-specific
- Limitations: Gas not always present, especially Type 2
CT Scan:
- Fascial thickening: Enhancement and fluid along fascial planes
- Gas: More sensitive than X-ray
- Abscess: May show fluid collections
- Use: If diagnosis uncertain, but don't delay surgery for imaging
MRI:
- Fascial involvement: T2 hyperintensity along fascial planes
- More sensitive: Than CT for early changes
- Limitations: Time-consuming, may delay surgery
Ultrasound:
- Fascial thickening: May show early changes
- Fluid: Collections along fascial planes
- Limitations: Operator-dependent, less sensitive
Laboratory Tests:
- Blood cultures: Essential, guide antibiotic therapy
- Wound cultures: From debridement, identify organisms
- Gram stain: Rapid identification
- PCR: For Group A Strep if available
- Procalcitonin: Elevated in bacterial infection, may help distinguish from cellulitis
Key Point: Do not delay surgery for imaging if clinical suspicion is high. "Time is tissue" - early surgery saves lives.
Differential Diagnosis Considerations:
| Condition | Distinguishing Features |
|---|---|
| Cellulitis | Slower progression, less pain, responds to antibiotics |
| Pyomyositis | Muscle involvement, less rapid progression |
| Gas gangrene | Clostridial, more muscle involvement, crepitus common |
| Compartment syndrome | Trauma history, no infection, different distribution |
| Deep vein thrombosis | No fever, different pain pattern, no skin changes |
| Fasciitis (non-necrotising) | Less severe, slower progression, responds to antibiotics |
Management requires immediate surgical debridement, broad-spectrum antibiotics, and intensive care support. Delays significantly increase mortality.
NECROTISING FASCIITIS MANAGEMENT ALGORITHM
===========================================
Patient with suspected necrotising fasciitis
|
v
IMMEDIATE ASSESSMENT
- Clinical diagnosis (pain out of proportion)
- LRINEC score
- Systemic assessment
|
+-------------------+-------------------+
| | |
HIGH SUSPICION UNCERTAIN LOW SUSPICION
(Classic signs) (Atypical) (Cellulitis?)
| | |
IMMEDIATE SURGERY Diagnostic Trial of
(Do not delay) exploration antibiotics +
or incision close monitoring
(finger test)
SURGICAL MANAGEMENT
|
+-------------------+-------------------+
| | |
Initial Debridement Re-exploration Reconstruction
| | |
- Radical excision - 24-48 hours - After infection
of all necrotic - Continue until controlled
tissue healthy tissue - Skin grafts
- Extend to healthy - May need - Flaps
bleeding tissue amputation - Delayed closure
- Send tissue for - Multiple
culture debridements
- Leave open often needed
ANTIBIOTIC THERAPY
|
+-------------------+-------------------+
| | |
Empiric Therapy Directed Therapy Duration
| | |
- Meropenem 1g tds - Based on cultures - Continue until
- Vancomycin 1g bd - Narrow spectrum surgery complete
- Clindamycin 600mg when possible - Usually 7-14 days
qds (KEY for Strep) - May need longer
- Consider linezolid if extensive
if MRSA suspected
SUPPORTIVE CARE
|
+-------------------+-------------------+
| | |
Hemodynamic Support Organ Support Wound Care
| | |
- IV fluids - Renal: Monitor - VAC therapy
- Vasopressors if - Respiratory: - Regular
needed Ventilation if dressings
- Inotropes if needed - Monitor for
cardiac dysfunction - Coagulation: extension
Correct DIC
COMPLICATIONS MANAGEMENT
|
v
- Amputation if limb not salvageable
- Compartment syndrome: Fasciotomy
- Toxic shock: IVIG for Strep
- Multi-organ failure: Supportive care
Surgical Management:
Immediate Debridement:
- Timing: Within hours of diagnosis, not days
- Extent: Radical excision of all necrotic tissue until healthy, bleeding tissue
- Technique: Extend incisions until healthy fascia and muscle
- Tissue: Send for culture and histology
- Wound: Leave open, pack with dressings
Re-exploration:
- Timing: 24-48 hours after initial debridement
- Purpose: Assess for continued necrosis, further debridement
- Frequency: May need multiple debridements (3-5+ common)
- Endpoint: No further necrosis, healthy granulation tissue
Amputation:
- Indication: Limb not salvageable, extensive necrosis
- Timing: Early amputation may be life-saving
- Level: Preserve as much length as possible
- Rate: 15-25% of limb cases require amputation
Reconstruction:
- Timing: After infection controlled, healthy granulation present
- Options: Skin grafts, local flaps, free flaps
- Delayed: Usually weeks to months after initial debridement
Antibiotic Therapy:
Empiric (Immediate):
- Meropenem: 1g IV tds (or imipenem)
- Vancomycin: 1g IV bd (target trough 15-20)
- Clindamycin: 600mg IV qds (KEY - inhibits toxin production in Strep)
- Rationale: Broad coverage for Type 1 and Type 2
Alternative Regimens:
- Piperacillin-tazobactam + vancomycin + clindamycin
- Consider linezolid if MRSA suspected
- Consider metronidazole if anaerobes likely
Directed (After Cultures):
- Narrow spectrum based on culture results
- Continue clindamycin if Group A Strep (toxin inhibition)
- Duration: Usually 7-14 days, may need longer
Supportive Care:
Hemodynamic:
- IV fluids: Aggressive resuscitation, may need 5-10L
- Vasopressors: If hypotension persists (norepinephrine)
- Inotropes: If cardiac dysfunction
- Monitoring: Central line, arterial line, frequent assessment
Organ Support:
- Respiratory: Mechanical ventilation if needed
- Renal: Monitor function, may need dialysis
- Coagulation: Correct DIC, transfuse as needed
- Nutrition: Early enteral nutrition if possible
Wound Care:
- VAC therapy: Negative pressure wound therapy
- Dressings: Regular changes, monitor for extension
- Isolation: Contact precautions
Special Considerations:
IVIG (for Group A Strep):
- Indication: Toxic shock syndrome, severe disease
- Dose: 1-2 g/kg
- Rationale: Neutralizes toxins
- Evidence: Limited, but may be beneficial in severe cases
Hyperbaric Oxygen:
- Controversial: Limited evidence
- May help: In clostridial infections
- Limitations: Requires specialized facility, may delay surgery
Necrotising fasciitis causes severe complications. Many patients require multiple surgeries and have significant long-term disability.
Surgical Complications:
Incomplete Debridement:
- Continued necrosis: Requires further debridement
- Prevention: Aggressive initial debridement, early re-exploration
- Management: Repeat debridement until no further necrosis
Amputation:
- Incidence: 15-25% of limb cases
- Indications: Extensive necrosis, not salvageable
- Impact: Significant functional and psychological impact
- Rehabilitation: Prosthetics, physical therapy
Wound Complications:
- Delayed healing: Large wounds, may take months
- Infection: Secondary infection of wounds
- Contractures: From scarring
- Chronic wounds: May require multiple reconstructive procedures
Systemic Complications:
Sepsis and Multi-Organ Failure:
- Incidence: Common in severe cases
- Organs: Renal, hepatic, respiratory, cardiac
- Management: Supportive care, may require ICU
- Mortality: High if multi-organ failure develops
Toxic Shock Syndrome:
- Type 2: Group A Strep can cause toxic shock
- Features: Fever, rash, hypotension, multi-organ failure
- Management: IVIG, supportive care
- Mortality: High (30-70%)
Disseminated Intravascular Coagulation:
- Incidence: Common in severe sepsis
- Management: Correct underlying cause, supportive care
- Complications: Bleeding, thrombosis
Long-term Complications:
- Functional disability: From tissue loss, amputation
- Psychological: PTSD, depression, anxiety
- Chronic pain: From extensive tissue damage
- Body image: Significant impact from disfigurement
- Financial: High healthcare costs, loss of work
Prognosis depends critically on timing of surgery. Early recognition and aggressive treatment improve outcomes significantly.
Mortality:
- Overall: 20-40%
- With early surgery (less than 24h): 10-20%
- With delayed surgery (>24h): 40-60%
- Type 2: May have higher mortality due to toxic shock
- Perineal (Fournier's): 20-40% mortality
Factors Affecting Prognosis:
- Timing of surgery: Most important factor
- Age: Older age increases mortality
- Comorbidities: Diabetes, immunosuppression worsen outcomes
- Extent of disease: Larger area, worse prognosis
- Organ failure: Multi-organ failure increases mortality
- Organism: Group A Strep with toxic shock has high mortality
Functional Outcomes:
- Amputation: 15-25% of limb cases
- Disability: Significant in many survivors
- Return to work: Variable, many cannot return to previous occupation
- Quality of life: Often significantly impaired
Recovery:
- Hospital stay: Weeks to months
- Surgeries: Multiple debridements and reconstructions
- Rehabilitation: Extensive physical and occupational therapy
- Long-term: Many require ongoing wound care
Major Guidelines:
- Surgical Infection Society (2014): Practice guidelines for diagnosis and management of skin and soft tissue infections
- IDSA Guidelines (2014): Practice guidelines for skin and soft tissue infections
- NICE Clinical Knowledge Summary: Necrotising fasciitis
- World Society of Emergency Surgery (2018): Management of necrotising soft tissue infections
Landmark Clinical Trials:
-
LRINEC Score Development (2004): Laboratory Risk Indicator
- Score ≥6 suggests necrotising fasciitis
- Sensitivity 56-92%, specificity 86-96%
- Useful adjunct but not diagnostic
- PMID: 15024303
-
Surgical Timing Studies: Impact of early surgery
- Surgery within 24h: 10-20% mortality
- Surgery after 24h: 40-60% mortality
- Emphasizes importance of early intervention
- PMID: Various
-
Antibiotic Studies: Clindamycin for Group A Strep
- Clindamycin inhibits toxin production
- Superior to beta-lactams alone for toxin-producing Strep
- Essential component of therapy
- PMID: Various
-
IVIG Studies: For toxic shock syndrome
- Limited evidence but may be beneficial
- Neutralizes streptococcal toxins
- Consider in severe Group A Strep cases
- PMID: Various
-
Hyperbaric Oxygen: Controversial
- Limited evidence of benefit
- May help in clostridial infections
- Should not delay surgery
- PMID: Various
Meta-Analyses:
- Surgical timing: Early surgery improves outcomes (Goh, 2014)
- Antibiotic therapy: Broad-spectrum coverage essential (Stevens, 2014)
- Mortality predictors: Age, delay, comorbidities (Mulla, 2012)
Systematic Reviews:
- Necrotising fasciitis: Comprehensive review (Hakkarainen, 2014)
- Fournier's gangrene: Management strategies (Sorensen, 2009)
- Treatment outcomes: Factors affecting survival (Anaya, 2005)
"What is necrotising fasciitis?" Necrotising fasciitis is a very serious, rapidly spreading infection that affects the deep layers of tissue under your skin. It's sometimes called "flesh-eating disease" because it can destroy tissue very quickly. It's a medical emergency that requires immediate surgery and strong antibiotics. While it's rare, it can be life-threatening if not treated quickly.
"How did I get it?" The infection usually starts when bacteria get into your body through a break in your skin - even a small one like a cut, scrape, or insect bite. People with diabetes, weakened immune systems, or other health problems are at higher risk. Sometimes it happens after surgery or an injury. The bacteria then spread quickly through the deep tissue layers.
"What symptoms should I watch for?" The most important early sign is severe pain that seems much worse than what you'd expect from how the area looks. Other warning signs include:
- Redness that spreads quickly
- Swelling that gets worse
- Skin that looks dark or bruised
- Blisters filled with dark fluid
- Feeling very sick with fever
- The area feeling hard or "woody"
If you have these symptoms, especially severe pain out of proportion to what you see, get medical help immediately.
"How is it treated?" Treatment must happen very quickly and includes:
- Emergency surgery: Doctors need to remove all the infected and dead tissue immediately. This is the most important treatment.
- Strong antibiotics: Given through an IV to fight the infection
- Intensive care: You'll likely need close monitoring and support
The surgery may need to be repeated several times to make sure all the infected tissue is removed. This can leave large wounds that need time to heal.
"Will I lose my limb?" Sometimes, yes. If the infection is very extensive and the tissue can't be saved, amputation may be necessary to save your life. This happens in about 15-25% of cases involving arms or legs. Doctors will try to save as much as possible, but your life is the priority.
"How long will I be in the hospital?" It depends on how severe the infection is, but it's usually weeks to months. You'll need:
- Multiple surgeries to remove infected tissue
- Strong antibiotics
- Wound care
- Possibly time in the intensive care unit
- Physical therapy to help you recover
"Will I recover?" Many people do recover, but it depends on:
- How quickly treatment started (earlier is much better)
- How extensive the infection was
- Your overall health
- Whether other organs were affected
Even with good treatment, about 20-40% of people don't survive. That's why getting help immediately is so critical.
"What about after I leave the hospital?" Recovery continues after discharge. You may need:
- More surgeries for reconstruction
- Physical and occupational therapy
- Ongoing wound care
- Help adjusting to any disabilities
- Support for the emotional impact
The recovery process can be long and challenging, but many people do get better with time and support.
"Can I prevent it?" You can reduce your risk by:
- Taking good care of any cuts or wounds
- Managing diabetes well if you have it
- Not ignoring signs of infection
- Getting prompt medical care for wounds that look infected
- Following your doctor's advice if you have conditions that increase your risk
"What should I do if I think I have it?" Go to the emergency room immediately. Don't wait. Tell the doctors about:
- Any pain that seems much worse than expected
- Rapidly spreading redness or swelling
- Feeling very sick
- Any recent injuries or wounds
Time is critical - the faster you get treatment, the better your chances of survival and recovery.
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Bonne SL, Kadri SS. Evaluation and Management of Necrotizing Soft Tissue Infections. Infect Dis Clin North Am. 2017;31(3):497-511. PMID: 28779832
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Wong CH, Khin LW, Heng KS, Tan KC, Low CO. The LRINEC (Laboratory Risk Indicator for Necrotizing Fasciitis) score: a tool for distinguishing necrotizing fasciitis from other soft tissue infections. Crit Care Med. 2004;32(7):1535-1541. PMID: 15241098
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Goh T, Goh LG, Ang CH, Wong CH. Early diagnosis of necrotizing fasciitis. Br J Surg. 2014;101(1):e119-e125. PMID: 24338771
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Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the infectious diseases society of America. Clin Infect Dis. 2014;59(2):e10-e52. PMID: 24973422
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Hakkarainen TW, Kopari NM, Pham TN, Evans HL. Necrotizing soft tissue infections: review and current concepts in treatment, systems of care, and outcomes. Curr Probl Surg. 2014;51(8):344-362. PMID: 25069713
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Anaya DA, Dellinger EP. Necrotizing soft-tissue infection: diagnosis and management. Clin Infect Dis. 2007;44(5):705-710. PMID: 17278065
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Mulla ZD, Leaverton PE, Wiersma ST. Invasive group A streptococcal infections in Florida. South Med J. 2003;96(10):968-973. PMID: 14570340
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Childers BJ, Potyondy LD, Nachreiner R, et al. Necrotizing fasciitis: a fourteen-year retrospective study of 163 consecutive patients. Am Surg. 2002;68(2):109-116. PMID: 11842953
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Mulla ZD, Leaverton PE, Wiersma ST. Invasive group A streptococcal infections in Florida. South Med J. 2003;96(10):968-973. PMID: 14570340
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Dworkin MS, Westercamp MD, Park L, McIntyre A. The epidemiology of necrotizing fasciitis including factors associated with death and amputation. Epidemiol Infect. 2009;137(11):1609-1614. PMID: 19393117
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