PRESENTED BY,
Mrs. Rijo Lijo.
Lecturer.
CELLULITIS
DEFINITION
Cellulitis is a bacterial infection involving the
inner layers of the skin. It specifically affects the dermis
and subcutaneous fat.
INCIDENCE
The cellulitis incidence rate of 24.6/1000 person-
years, with a higher incidence among males and individu
als aged 45-64 years. The most common site of infection
was the lower extremity (39.9%).
ETIOLOGY
 Staphylococcus.
 Streptococcus Group A β.
 H. Influenza (periorbital cellulitis).
 Facial cellulitis in children < 3 years old.
 Streptococcus pneumonia.
RISK FACTORS
 Local trauma (e.g., lacerations, insect bites, wounds).
 Skin infections such as impetigo, scabies etc.
 Underlying skin ulcer.
 Fragile skin.
 Immunocompromised host.
 Diabetes mellitus.
 Inflammation (e.g., eczema).
 Edema secondary to venous insufficiency or lymphe
dema.
PATHOPHYSIOLOGY
CLINICAL MANIFESTATIONS
 pain and tenderness in the affected area.
 redness or inflammation of your skin.
 a skin sore or rash that grows quickly.
 tight, glossy, swollen skin.
 a feeling of warmth in the affected area.
 an abscess with pus.
 fever.
DIAGNOSTIC FINDINGS
 History collection.
 Physical examination.
 culture and sensitivity:
Swab any wound discharge for culture and sensitivity.
Blood culture If:
1. Systemic toxicity (fever, chills, tachycardia).
2. Extensive skin or soft tissue involvement.
3. Underlying comorbidities (lymphedema, malignancy,
neutropenia, immunodeficiency, splenectomy, diabetes).
4. Special exposures (animal bite).
5. Persistent cellulitis.
 Radiographic examination:
US (skin abscess), MRI (osteomyelitis), CT (necrotizing
faciatious).
 A skin biopsy if the diagnosis is uncertain.
 Cultures of swabs from intact skin are not helpful.
MANAGEMENT AND
INTERVENTIONS
GOALS OF TREATMENT FOR
MILD CELLULITIS
Goals of Treatment for Mild Cellulitis
 Resolve infection.
 Identify formation of abscess.
 Check tetanus prophylaxis.
MEDICAL MANAGEMENT
 Mild cases of cellulitis can be treated on an outpatient
basis with oral antibiotic therapy with Dicloxacillin, Amo
xicillin, or Cephalexin.
 If the cellulitis is severe, the patient is hospitalized and
treated with intravenous antibiotics for at least 7 to 14 d
ays.
 Immobilize the part and elevate the extremity above the
level of heart.
 Provide moist heat to promote wound healing.
 Patients with known community acquired MRSA or pu
rulent cellulitis:
trimethoprim-sulfamethoxazole 8-12 mg / kg per
day for 7 days (dosing is based on trimethoprim).
NON PHARMACOLGICAL
MANAGEMENT
 Apply warm or, if more comfortable, cool saline
compresses to affected areas for 15 minutes.
 Mark border of erythema with pen to monitor spread.
 Elevate, rest and gently splint the affected limb.
COMPLICATIONS
 Blood infection (septicemia).
 Bone infection (osteomyelitis).
 Inflammation of the lymph vessels (lymphangitis).
 Inflammation of the heart (endocarditis).
 Meningitis.
 Shock.
 Tissue death (gangrene).
Cellulitis

Cellulitis

  • 1.
    PRESENTED BY, Mrs. RijoLijo. Lecturer. CELLULITIS
  • 2.
    DEFINITION Cellulitis is abacterial infection involving the inner layers of the skin. It specifically affects the dermis and subcutaneous fat.
  • 3.
    INCIDENCE The cellulitis incidencerate of 24.6/1000 person- years, with a higher incidence among males and individu als aged 45-64 years. The most common site of infection was the lower extremity (39.9%).
  • 4.
    ETIOLOGY  Staphylococcus.  StreptococcusGroup A β.  H. Influenza (periorbital cellulitis).  Facial cellulitis in children < 3 years old.  Streptococcus pneumonia.
  • 5.
    RISK FACTORS  Localtrauma (e.g., lacerations, insect bites, wounds).  Skin infections such as impetigo, scabies etc.  Underlying skin ulcer.  Fragile skin.  Immunocompromised host.  Diabetes mellitus.  Inflammation (e.g., eczema).  Edema secondary to venous insufficiency or lymphe dema.
  • 6.
  • 7.
    CLINICAL MANIFESTATIONS  painand tenderness in the affected area.  redness or inflammation of your skin.  a skin sore or rash that grows quickly.  tight, glossy, swollen skin.  a feeling of warmth in the affected area.  an abscess with pus.  fever.
  • 8.
    DIAGNOSTIC FINDINGS  Historycollection.  Physical examination.  culture and sensitivity: Swab any wound discharge for culture and sensitivity.
  • 9.
    Blood culture If: 1.Systemic toxicity (fever, chills, tachycardia). 2. Extensive skin or soft tissue involvement. 3. Underlying comorbidities (lymphedema, malignancy, neutropenia, immunodeficiency, splenectomy, diabetes). 4. Special exposures (animal bite). 5. Persistent cellulitis.
  • 10.
     Radiographic examination: US(skin abscess), MRI (osteomyelitis), CT (necrotizing faciatious).  A skin biopsy if the diagnosis is uncertain.  Cultures of swabs from intact skin are not helpful.
  • 11.
  • 12.
    GOALS OF TREATMENTFOR MILD CELLULITIS Goals of Treatment for Mild Cellulitis  Resolve infection.  Identify formation of abscess.  Check tetanus prophylaxis.
  • 13.
    MEDICAL MANAGEMENT  Mildcases of cellulitis can be treated on an outpatient basis with oral antibiotic therapy with Dicloxacillin, Amo xicillin, or Cephalexin.  If the cellulitis is severe, the patient is hospitalized and treated with intravenous antibiotics for at least 7 to 14 d ays.  Immobilize the part and elevate the extremity above the level of heart.  Provide moist heat to promote wound healing.
  • 14.
     Patients withknown community acquired MRSA or pu rulent cellulitis: trimethoprim-sulfamethoxazole 8-12 mg / kg per day for 7 days (dosing is based on trimethoprim).
  • 15.
    NON PHARMACOLGICAL MANAGEMENT  Applywarm or, if more comfortable, cool saline compresses to affected areas for 15 minutes.  Mark border of erythema with pen to monitor spread.  Elevate, rest and gently splint the affected limb.
  • 16.
    COMPLICATIONS  Blood infection(septicemia).  Bone infection (osteomyelitis).  Inflammation of the lymph vessels (lymphangitis).  Inflammation of the heart (endocarditis).  Meningitis.  Shock.  Tissue death (gangrene).