13/10/2010
13/10/2010
• NECROTIZING SOFT-TISSUE INFECTIONS (NSTI) comprise a
spectrum of disease entities that are characterized by extensive ,
rapidly progressive soft-tissue necrosis that usually involve deep
subcutaneous tissue, superficial or deep fascia, or muscle, or
any combination of the three.
• Necrotizing soft-tissue infections are classified as fasciitis , or
myositis, based on the principal soft-tissue layer involved with
necrosis
.CELLULITIS
Is a soft tissue infection with an
intact blood supply and viable
tissue
Marked by an acute inflammatory
response with small vessel
engorgement and stasis,
endothelial leakage with interstitial
edema, and leukocyte infiltration
It is typically located in a more
superficial plane.
ABSCESS
An infectious process characterized
by a necrotic center, without a blood
supply
Composed of debris from local
tissues, dead and dying WBC’s,
components of blood and plasma,
and bacteria.
Pus is surrounded by a vascularized
zone of inflammatory tissue.
NON NECROTISING SOFT TISSUE INFECTIONNSTI VS
13/10/2010
First reported by Hippocrates as “flesh, sinews, and bones fell away in large
quantities...There were many deaths.”2
They were labeled as Streptococcal gangrene, Phagedena, and Phagedena
gangrenosum
An army surgeon was the first to report a necrotizing infection in the United
States in 1871
In 1883, FOURNIER described a gangrenous infection of the scrotum
In 1924, MELENEY documented the pathogenic role of streptococci in soft
tissue infection.
In 1952, Wilson coined the term necrotizing fasciitis
13/10/2010
A substantial number of classifications based on anatomic location,
microbiology, and depth of infection have been described.
The wide range of classifications makes understanding of this entity
rather confusing, when the only important factor to be determined is
the presence or absence of a necrotic component requiring surgical
intervention
13/10/2010
Necrotizing soft tissue infections types:
1) Necrotizing fasciitis type I (Polymicrobial),
2) Necrotizing fasciitis type II (Group A streptococcal),
3) Necrotising fasciitis type III(marine vibrios)
4) Specfic syndromes:
a. Clostridial myonecrosis
b. Fourniers gangrene
13/10/2010
Usually occurs after trauma or surgery
Subcutaneous fat and fascia overlying muscle are prominently
involved
Primarily includes 3 categories (locations) of infection
Diabetes Mellitus- infections of the feet
Cervical necrotizing fasciitis- infection of the neck
Fournier’s Gangrene- infection of the perineum
Course of disease is usually somewhat slower than that seen with
type II (streptococcal) necrotizing fasciitis and clostridial
myonecrosis,
 2/3 of cases have mixed aerobic and anaerobic infections
The bugs: The average case had 4-6 isolates
•Staphylococcus aureus
•Streptococci
•Enterococci
•Escherichia coli
•Peptostreptococcus
•Preveoella and Porphyromonas
•Bacteroides fragilis
•Clostridium
13/10/2010
Caused by virulent subtypes of streptococcus pyogenes.
The bacteria is often referred to as a flesh-eating bacteria.
The incidence of this infection increased in the last two decades,
• Improvements in diagnosis and reporting.
• Result of an organism virulence
The presence of the M1 and M3 proteins is associated with virulent
infection.
C/F
Most of the general features of NSTI
the presence of gas in tissues is unusual.
 Third type
 Caused by the marine vibrios(gram
negative rods)
 Vibrio vulnificus, vibrio parahemolyticus,
vibrio damsela, vibrio alginolyticus
 Puncture wound from fish, cut or insect
bite exposed to sea water, shellfish or fish
in tropical water
 Synthesize an extracellular toxin
 This bacteria has an alarming mortality
rate of 50%.
 First described by French verenologist JEAN
ALFRED FOURNIER who witnessed a rapidly
progressing gangrene of the penis and scrotum of 5
previously healthy young men.
 A polymicrobial necrotizing fasciitis (NF) of the
perinium, perianal area, or genitals. It may involve
either men or women.
 Mostly age 30-60, although all ages have been
reported
I (EARLY)
Tenderness to palpation (beyond area of
cellulitis)
Erythema/warmth
Edema
II (INTERMEDIATE)
Bullae formation
Skin fluctuation or induration
III (LATE)
Hemorrhagic bullae or skin necrosis
Crepitus
Skin anesthesia
 Fever
 Tachycardia
 Hypotension
 Tense edema around involved skin
 Disproportionate pain
 Blisters/ bullae
 Crepitus (present 10% of time)
 Subcutaneous gas
• These are all fairly specific, but have a sensitivity of
only 10-40%
 Skin findings
• May be erythematous, edematous, cyanotic, bronzed,
indurated, blistered, or frankly gangrenous.
• Generally the appearance of the skin underestimates
the degree of underlying disease.
 Diabetes mellitus (present in up to 60% of cases)
 Drug use
 Obesity
 Immunosuppresion
 Malnutrition
 HIV infection
 Alcoholism
13/10/2010
Established by making a small skin incision and passing a haemostat or probe
through the subcutaneous tissues.
In necrotizing fasciitis the subcutaneous and fascial layers lack resistance to this
manoeuvre, a feature that indicates widespread tissue necrosis underneath seemingly
viable skin.
Gas may or may not be present in the soft tissues
HISTOLOGY
Shows widespread necrosis of subcutaneous fat and fascia, with relative sparing of
muscle.
An acute inflammatory reaction, with many Polymorphonuclear cells,
 Thrombosis of blood vessels and abundant Bacteria
1. Blood samples-for TLC,DLC
2. Testing for elevated or lowered creatinine, glucose, CPK,
bicarbonate, albumin, and calcium levels.
3. X-ray
4. CT, and MRI scanning in advanced cases
5. And most importantly antibiotic culture and sensitivity tests
13/10/2010
13/10/2010
This score allows early classification of patients according to disease severity
identify patients at high risk of death
Identify a high-risk patients in whom surgical decision making debridement vs
amputaion.
Control or attempts at limb salvage with repeat operative debridements.
A prognostic score which allow weigh the relative risks and benefits of an
intervention better
Score can be used for comparisons across institutions and over time, providing a
more formal means to assess the impact of interventions
13/10/2010
 Early and aggressive surgical exploration and debridement
 This should be done in the first 24 hours of symptoms
 Surgical mortality 6% (<24hrs), 24% (>24hrs)
 Repeat debridement should be repeated daily until all necrotic tissue
has been removed (typically 2-4 times)
 Fourneir’s Gangrene may require cystostomy, colostomy, or
orchiectomy (although this is rare).
• Virtually 100% of patients will die on antibiotics without
surgical debridement
• Antibiotics should be broad-spectrum until cultures return
• Type 1- ampicillin or ampicillin-sulbactam and clindamycin
or metronidazole. For patients with prior hospitalization
substitute ticarcillin-clavulanate or piperacillin-tazobactam
for ampicillin-sulbactam
• Type 2- penicillin group + clindamycin. Add vancomycin to
cover for MRSA
• Type 2
• In the case of streptococcal toxic shock massive amounts of fluid (10-20
L/day) may be necessary to maintain perfusion. Pressors such as
dopamine may also be required
• IV Ig has also been used to neutralize the streptococcal superantigens,
however no studies have been done to support this use
• NF can progress rapidly leading to amputation or death
• A degree of suspicion is necessary to get a patient to surgery for
diagnosis and treatment
• Treatment primarily involves surgery ,surgery , and only surgery and
antibiotics
• Even with rapid treatment mortality remains high
13/10/2010
13/10/2010

NECROTISING SOFT TISSUE INFECTION- Dr. Kiran Kumar G.

  • 1.
  • 2.
    13/10/2010 • NECROTIZING SOFT-TISSUEINFECTIONS (NSTI) comprise a spectrum of disease entities that are characterized by extensive , rapidly progressive soft-tissue necrosis that usually involve deep subcutaneous tissue, superficial or deep fascia, or muscle, or any combination of the three. • Necrotizing soft-tissue infections are classified as fasciitis , or myositis, based on the principal soft-tissue layer involved with necrosis
  • 3.
    .CELLULITIS Is a softtissue infection with an intact blood supply and viable tissue Marked by an acute inflammatory response with small vessel engorgement and stasis, endothelial leakage with interstitial edema, and leukocyte infiltration It is typically located in a more superficial plane. ABSCESS An infectious process characterized by a necrotic center, without a blood supply Composed of debris from local tissues, dead and dying WBC’s, components of blood and plasma, and bacteria. Pus is surrounded by a vascularized zone of inflammatory tissue. NON NECROTISING SOFT TISSUE INFECTIONNSTI VS
  • 4.
    13/10/2010 First reported byHippocrates as “flesh, sinews, and bones fell away in large quantities...There were many deaths.”2 They were labeled as Streptococcal gangrene, Phagedena, and Phagedena gangrenosum An army surgeon was the first to report a necrotizing infection in the United States in 1871 In 1883, FOURNIER described a gangrenous infection of the scrotum In 1924, MELENEY documented the pathogenic role of streptococci in soft tissue infection. In 1952, Wilson coined the term necrotizing fasciitis
  • 5.
    13/10/2010 A substantial numberof classifications based on anatomic location, microbiology, and depth of infection have been described. The wide range of classifications makes understanding of this entity rather confusing, when the only important factor to be determined is the presence or absence of a necrotic component requiring surgical intervention
  • 6.
    13/10/2010 Necrotizing soft tissueinfections types: 1) Necrotizing fasciitis type I (Polymicrobial), 2) Necrotizing fasciitis type II (Group A streptococcal), 3) Necrotising fasciitis type III(marine vibrios) 4) Specfic syndromes: a. Clostridial myonecrosis b. Fourniers gangrene
  • 7.
    13/10/2010 Usually occurs aftertrauma or surgery Subcutaneous fat and fascia overlying muscle are prominently involved Primarily includes 3 categories (locations) of infection Diabetes Mellitus- infections of the feet Cervical necrotizing fasciitis- infection of the neck Fournier’s Gangrene- infection of the perineum Course of disease is usually somewhat slower than that seen with type II (streptococcal) necrotizing fasciitis and clostridial myonecrosis,
  • 8.
     2/3 ofcases have mixed aerobic and anaerobic infections The bugs: The average case had 4-6 isolates •Staphylococcus aureus •Streptococci •Enterococci •Escherichia coli •Peptostreptococcus •Preveoella and Porphyromonas •Bacteroides fragilis •Clostridium
  • 9.
    13/10/2010 Caused by virulentsubtypes of streptococcus pyogenes. The bacteria is often referred to as a flesh-eating bacteria. The incidence of this infection increased in the last two decades, • Improvements in diagnosis and reporting. • Result of an organism virulence The presence of the M1 and M3 proteins is associated with virulent infection. C/F Most of the general features of NSTI the presence of gas in tissues is unusual.
  • 10.
     Third type Caused by the marine vibrios(gram negative rods)  Vibrio vulnificus, vibrio parahemolyticus, vibrio damsela, vibrio alginolyticus  Puncture wound from fish, cut or insect bite exposed to sea water, shellfish or fish in tropical water  Synthesize an extracellular toxin  This bacteria has an alarming mortality rate of 50%.
  • 11.
     First describedby French verenologist JEAN ALFRED FOURNIER who witnessed a rapidly progressing gangrene of the penis and scrotum of 5 previously healthy young men.  A polymicrobial necrotizing fasciitis (NF) of the perinium, perianal area, or genitals. It may involve either men or women.  Mostly age 30-60, although all ages have been reported
  • 12.
    I (EARLY) Tenderness topalpation (beyond area of cellulitis) Erythema/warmth Edema II (INTERMEDIATE) Bullae formation Skin fluctuation or induration III (LATE) Hemorrhagic bullae or skin necrosis Crepitus Skin anesthesia
  • 13.
     Fever  Tachycardia Hypotension  Tense edema around involved skin  Disproportionate pain  Blisters/ bullae  Crepitus (present 10% of time)  Subcutaneous gas • These are all fairly specific, but have a sensitivity of only 10-40%  Skin findings • May be erythematous, edematous, cyanotic, bronzed, indurated, blistered, or frankly gangrenous. • Generally the appearance of the skin underestimates the degree of underlying disease.
  • 14.
     Diabetes mellitus(present in up to 60% of cases)  Drug use  Obesity  Immunosuppresion  Malnutrition  HIV infection  Alcoholism
  • 15.
    13/10/2010 Established by makinga small skin incision and passing a haemostat or probe through the subcutaneous tissues. In necrotizing fasciitis the subcutaneous and fascial layers lack resistance to this manoeuvre, a feature that indicates widespread tissue necrosis underneath seemingly viable skin. Gas may or may not be present in the soft tissues HISTOLOGY Shows widespread necrosis of subcutaneous fat and fascia, with relative sparing of muscle. An acute inflammatory reaction, with many Polymorphonuclear cells,  Thrombosis of blood vessels and abundant Bacteria
  • 16.
    1. Blood samples-forTLC,DLC 2. Testing for elevated or lowered creatinine, glucose, CPK, bicarbonate, albumin, and calcium levels. 3. X-ray 4. CT, and MRI scanning in advanced cases 5. And most importantly antibiotic culture and sensitivity tests
  • 17.
  • 18.
    13/10/2010 This score allowsearly classification of patients according to disease severity identify patients at high risk of death Identify a high-risk patients in whom surgical decision making debridement vs amputaion. Control or attempts at limb salvage with repeat operative debridements. A prognostic score which allow weigh the relative risks and benefits of an intervention better Score can be used for comparisons across institutions and over time, providing a more formal means to assess the impact of interventions
  • 19.
  • 20.
     Early andaggressive surgical exploration and debridement  This should be done in the first 24 hours of symptoms  Surgical mortality 6% (<24hrs), 24% (>24hrs)  Repeat debridement should be repeated daily until all necrotic tissue has been removed (typically 2-4 times)  Fourneir’s Gangrene may require cystostomy, colostomy, or orchiectomy (although this is rare).
  • 21.
    • Virtually 100%of patients will die on antibiotics without surgical debridement • Antibiotics should be broad-spectrum until cultures return • Type 1- ampicillin or ampicillin-sulbactam and clindamycin or metronidazole. For patients with prior hospitalization substitute ticarcillin-clavulanate or piperacillin-tazobactam for ampicillin-sulbactam • Type 2- penicillin group + clindamycin. Add vancomycin to cover for MRSA
  • 22.
    • Type 2 •In the case of streptococcal toxic shock massive amounts of fluid (10-20 L/day) may be necessary to maintain perfusion. Pressors such as dopamine may also be required • IV Ig has also been used to neutralize the streptococcal superantigens, however no studies have been done to support this use
  • 23.
    • NF canprogress rapidly leading to amputation or death • A degree of suspicion is necessary to get a patient to surgery for diagnosis and treatment • Treatment primarily involves surgery ,surgery , and only surgery and antibiotics • Even with rapid treatment mortality remains high
  • 24.
  • 25.