Bacterial Skin Infections Flashcards

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1
Q

What is cellulitis?

A

Acute infection of the lower dermis and subcutaneous (soft) tissues caused by beta-haemolytic streptococcus ± staphylococcus

=> localised area of red, painful, swollen skin, and systemic symptoms

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2
Q

Who is at risk of cellulitis?

*Same as erysipelas

A

Previous episode(s) of cellulitis

Fissuring of toes or heels, eg due to athlete’s foot, tinea pedis or cracked heels

Venous disease, eg gravitational eczema, leg ulceration, and/or lymphoedema

Injury, eg trauma, surgical wounds, radiotherapy

Immunodeficiency, eg HIV

Immune suppressive medications

Diabetes

Chronic kidney disease

Chronic liver disease

Obesity

Pregnancy

Alcoholism

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3
Q

What organism causes cellulitis?

A

Most common bacteria = Streptococcus pyogenes (2/3) and Staphylococcus aureus (1/3).

Rare causes of cellulitis include:
=> Pseudomonas aeruginosa, usually in a puncture wound of foot or hand

=> Haemophilus influenzae, in children with facial cellulitis

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4
Q

What is the clinical presentation of cellulitis?

A

Cellulitis can affect any site, most often a limb

=> Usually unilateral

=> Feeling unwell, fever, chills and rigors = first signs of illness due to bacteraemia

=> Systemic symptoms are soon followed by localised area of painful, red, swollen skin

Other signs include:

=> Dimpled skin (peau d’orange)

=> Warmth

=> Blistering

=> Erosions and ulceration

=> Abscess formation

=> Purpura: petechiae, ecchymoses, or haemorrhagic bullae

*may be associated with lymphangitis and lymphadenitis

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5
Q

What are the complications of cellulitis?

A

Severe or rapidly progressive cellulitis may lead to:

  1. Necrotising fasciitis (serious soft tissue infection = severe pain, skin pallor, loss of sensation, purpura, ulceration and necrosis)
  2. Gas gangrene
  3. Severe sepsis (fever, malaise, loss of appetite, nausea, lethargy, headache, aching muscles & joints, hypotention, reduced capillary refill, heart failure, renal failure)
  4. Infection of other organs, eg pneumonia, osteomyelitis, meningitis
  5. Endocarditis
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6
Q

How is cellulitis diagnosed?

A

Diagnosis based on clinical features.

Investigations may reveal:
=> Leukocytosis raised WCC
=> Raised CRP
=> Causative organism from blood culture or lesion swab culture

=> Chest X-ray in case of heart failure or pneumonia

=> Doppler ultrasound to look for blood clots (deep vein thrombosis)

=> MRI in case of necrotising fasciitis.

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7
Q

What is the treatment for cellulitis?

A

Cellulitis is potentially serious.

=> Rest and elevate the affected limb

=> Edge of the involved area of swelling should be marked to monitor progression/regression of infection

=> Benzylpenicillin + Flucloxacillin (erythromycin if penicillin allergy)

*Management of cellulitis = more complicated due to rising rates of MRSA and macrolide- or erythromycin-resistant Streptococcus pyogenes

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8
Q

What is the treatment for cellulitis?

A

Cellulitis is potentially serious.

=> Rest and elevate the affected limb

=> Edge of the involved area of swelling should be marked to monitor progression/regression of infection

=> Benzylpenicillin Flucloxacillin (erythromycin if penicillin allergy)

*Management of cellulitis = more complicated due to rising rates of MRSA and macrolide- or erythromycin-resistant Streptococcus pyogenes

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9
Q

What is the treatment of uncomplicated cellulitis?

A

No signs of systemic illness or extensive cellulitis

=> patients treated with oral antibiotics for 5–10 days or until all signs of infection have cleared (redness, pain and swelling)

=> Analgesia to reduce pain

=> Adequate water/fluid intake

=> Management of co-existing skin conditions like venous eczema or tinea pedis

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10
Q

What is the treatment for complicated / severe cellulitis?

A

Severe cellulitis and systemic symptoms treated with fluids, intravenous antibiotics and oxygen.

=> Penicillin-based antibiotics are often chosen (eg penicillin G or flucloxacillin)

=> Amoxicillin and clavulanic acid provide broad-spectrum cover if unusual bacteria are suspected

=> Cephalosporins eg ceftriaxone, cefotaxime or cefazolin

=> Clindamycin, sulfamethoxazole / trimethoprim, doxycycline and vancomycin used in patients with penicillin or cephalosporin allergy, or if MRSA infection

Treatment may be switched to oral antibiotics when the fever has settled, cellulitis has regressed, and CRP is reducing.

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11
Q

What is erysipelas?

A

Erysipelas is a superficial form of cellulitis, affecting upper dermis and extends into superficial cutaneous lymphatics.

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12
Q

What causes erysipelas?

A

Similar to cellulitis

Almost all erysipelas is caused by
=> Group A haemolytic streptococci i.e. streptococcus pyogenes

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13
Q

What are the clinical features of erysipelas?

A

=> Abrupt onset

=> Fevers, chills and shivering

=>Predominantly affects lower limb skin

=> Butterfly rash when it involves the face

=> Affected skin = very sharp, raised border

=> Bright red, firm and swollen

=> It may be finely dimpled (p’eau de orange)

=> Blistered and if severe = necrotic

=>Purpura

=> Pain and increased warmth in both cellulitis and erysipelas

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14
Q

What are the complications of erysipelas?

A

Erysipelas recurs in 1/3 of patients due to:

=> Persistence of risk factors
=> Lymphatic damage (hence impaired drainage of toxins)

Complications are rare but can include:

=> Abscess

=> Gangrene

=> Thrombophlebitis

=> Chronic leg swelling

=> Infections distant to the site of erysipelas
Infective endocarditis (heart valves)

=> Septic arthritis

=> Bursitis

=> Tendonitis

=> Post-streptococcal glomerulonephritis (a kidney condition affecting children)

=> Streptococcal toxic shock syndrome (rare).

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15
Q

Differential diagnosis of erysipelas same as cellulitis.

How is erysipelas diagnosed?

A

Erysipelas is usually diagnosed by the characteristic rash. History of a relevant injury.

Tests may reveal:

=> Raised white cell count

=> Raised CRP

=> Positive blood culture identifying the organism.

=> MRI and CT are undertaken in case of deep infection.

=> Skin biopsy

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16
Q

How is erysipelas treated?

A

General:
=> Cold packs and analgesics

=> Elevation of an infected limb to reduce local swelling

=> Compression stockings

=> Wound care with saline dressings that are frequently changed.

Antibiotics:
=> Oral or intravenous penicillin (1st line)

=> Erythromycin in patients with penicillin allergy

=> Vancomycin is used for facial erysipelas caused by MRSA

=> Treat for 10–14 days

17
Q

What is impetigo?

How does it present?

Who does it affect?

A

Impetigo is a highly contagious superficial bacterial skin infection (pyoderma) spread by direct contact.

Very common in children.

Inflamed, erythamatous pustules with a golden, crusted surface, most common around mouth and nose.

18
Q

What causes impetigo?

A

Staphylococcus aureus
*toxin producing strains of staph. aureus can cause blisters => bulbous impetigo

Streptococcus pyogens

19
Q

What predisposes to impetigo?

A

Atopic eczema

Scabies

Skin trauma i.e. chickenpox, insect bite, abrasion, burn, dermatitis, surgical wound

20
Q

What is the clinical presentation of impetigo?

A

Primary impetigo: affects exposed areas i.e. face and hands, trunk, perineum

=> Single or multiple, irregular bouts of irritable superficial plaques

=> Plaques extend as they heal, forming annular or arcuate lesions

=> Lymphadenopathy, mild fever and malaise may occur

  1. Nonbullous impetigo:

=> starts as a pink macule - evolves into a vesicle or pustule and then into crusted erosions

=> untreated impetigo resolves within 2 to 4 weeks without scarring

  1. Ecthyma:
    => starts as nonbullous impetigo but develops into a punched-out necrotic ulcer

=> heals slowly, leaving a scar

  1. Bullous impetigo:
    => small vesicles evolves into flaccid transparent bullae

=> heals without scarring

21
Q

How is impetigo diagnosed?

A

Impetigo is diagnosed clinically but can be confirmed by bacterial swabs sent for microscopy (gram-positive cocci are observed), culture and sensitivity.

Bloods: neutrophil leucocytosis if impetigo widespread

22
Q

How is impetigo managed?

A

Topical fusidic acid

Mupirocin for MRSA cases

Oral antibiotics for 7 days i.e. flucloxacillin or erythromycin if patient has penicillin allergy => for widespread or bullous impetigo

Avoid school until lesions are dry or 48hrs after starting antibiotics