Skin and soft tissue infection Flashcards

1
Q

What is included in soft tissues?

A
  • Skin commonly infected at various levels
  • connective tissues:
    • Fascia (rarely infected e.g. necrotising fasciitis) and synovial membranes (infective synovitis or bursitis).
    • also fat, tendons and ligaments (very rarely infected)
  • Also muscle (e.g. bacterial or viral myositis)
  • nerves (herpes, poliomyelitis)
  • blood vessels ( very rarely infected e.g. syphilis, typhus, viral vasculitis, endocarditis and vascular prosthesis infection).
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2
Q

Definitions:

Impetigo

Erysipelas

A

Impetigo = superficial skin infection that only affects the epidermis, usually staphylococcus.

Erysipelas = superficial skin infection that only affects the epidermis byt it tends to be streptococcal

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3
Q

Defnitions:

Cellulitis

A

Cellulitis = skin infection that gets into the dermis and possible into subcutaneous fat (but no further than that).

Most common can be caused by staphylocci or streptococci, or immune supression.

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4
Q

Definitions:

Furuncle

Carbuncle

A

Furuncle = deep infection of the hair follicle = Boil (usually straphyloccoccal)

Carbuncle = connecting collection of furuncles (usually staphylococcal).

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5
Q

Definitions:

Necrotising fasciitis

A

Necrotising fasciitis = deep infection that enters below epidermis/ dermis/ subcutaneous fat and into the fascia, with or without muscle involvement. Necrotising in nature, aggressive and lifethreatening.

Usually streptococcal or mixed bacteria if infection arises from the pelvis

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6
Q

Aetiology of skin/ soft tissue infections?

A
  1. Viruses
    • viral warts (skin warts, verrucas, genital warts)
    • herpes (labialis HSV 1 and HSV 2 genitalis)
    • viral exanthems (exanthem = rash) (chickenpox, shingles, measles).
    • Molluscum contagiosum (pox virus)
    • small pox
  2. Bacteria
    • ​​streptococcus and staphylococcus
    • opportunistic bacteria (e.g. immunocompromised, diabetic etc.. )
  3. Fungi
    • ​Tinea infections (tinea pedis = athletes foot, tinea corporis = of the head)
    • Serborrhoeic dermatitis (dandruff, fungus plays key role in initating the process).
  4. Protozoa, Hemlminths
  5. Ectoparasites –> scabies and cutaneous myiasis
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7
Q

Host microbe interactions

What interactions are there?

A
  • We are not sterile surfaces with only occasional and always pathological interactions with microbes
  • We are colonised by microorganisms, various interactions can occur:
    • Symbiotic interactions –> interaction between two organisms living in close physical association. Can be commensal, mutualistic or parasitic.
    • Commensal = symbiotic relationship between two different species where one derives some benefit and other is unaffected
    • Colonisation = when microbe grows on/ in another organism without causing disease
    • Pathogen = microbe able to cause disease
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8
Q

Define infection

A

Infection = invasion and multiplication of microbes in an area of the body where they are not normally present, usually leads to disease

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9
Q

Describe the host- microbe interactions that can occur on the skin:

What organisms are involved?

A
  • Skin bacteria can be either commensals or pathogens e.g. Staphylococcus species of bacteria
  • Staph. epidermidis and other staph species that are not staphylococcus aureus are usually called the coagulase negative staphylococci:
    • They lack an enzyme called coagulase and are therefore less aggressive towards humans
    • Colonise the skin of nearly all humans are are usally non pathogens
    • Unless they are able to reach an internal prosthetic surface where they can cause infection
  • Staphylococcus aureus = normally considered a pathogen, but can be commensal, has the potential to become a pathogen.
  • If colonised, risk of infection with staph. aureus increases. Especially if poor hygiene/ abnormal skin / immunocompromised
  • Still needs to invade and multiply to cause infection and so may remain as commensal bacteria
  • Hence “de- colonisation” treatment to sterilise skin may be beneficial prior to operation.
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10
Q

What is the pathogenesis of bacteria in skin and soft tissue infections?

A

AH AH Its MERDT

  • Access –> most bacteria causing SSTI found on skin as colonisers
  • Adherence –> have well developed adhesin molecules
  • Invasion -> most need a break in the skin, but some are highly invasive (PVL staph. aureus, aggresive staph aureus, Group A streptococcus more aggresive streptococcus.)
  • Multiplication –> colonisation of skin or wounds may precede infection
  • Evasion –> e.g. Staph catalase enzyme blocks free radials produced by neutrophils, Strep .M protein blocks complement
  • Resistance –> may bacteria causing SSTI have drug resistance (particularly methicillin resistant staph. aureus - MRSA)
  • Damage –> affects epidermis, dermis and deeper tissue and may lead to septicaemia
  • Transmission –> easily passed from skin by direct or indirect contact
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11
Q

What are some of the risk factors of skin and soft tissue infections?

A
  • Direct inoculation e.g. trauma, medical procedures or skin ulcers
  • Previous colonisation e.g. poor hygiene and Staph. aureus or MRSA
  • Immunosuppression e.g. diabetes mellitus or renal failure.
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12
Q

How do we clinically describe a lesion?

A
  • Shape and size
  • edge
  • colour
  • surface -> any breaks, vesicles etc
  • distribution
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13
Q

How do we diagnose skin and soft tissue infections?

A
  • Full History ->
  • Examination –> is this a localised infection, look for sepsis
  • Differentials and investigations –> body samples, imaging or physiology and histopathology. Body sample not always needed e.g. skin infection better to give empirical treatment
  • Diagnosis and then treatment
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14
Q

What investigations can be done in skin and soft tissue infection?

A
  • Swabs with furuncles and pus on the skin, or nore and throat if suspecting staphylococcus aureus colonisation
  • Body fluids -> pus, vescile fluid or blood
  • body tissue biposy but rare
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15
Q

Treatment of SSTIs

viral

bacterial

A
  • Viral skin infections are usually self limiting but ACICLOVIR and related drugs can be used for herpes, chickenpox and shingles
  • bacterial skin infections are rarely self limiting but:
    • Superificial infections e.g. impetigo can be treated with topical fuscidin
    • Staphyloccocus aureus is usually resistant to antibiotics (MRSA), therfore sampling recommedned and flucoxacillin often used initally
    • Streptococcus rarely resistant to antibiotics therefore penicillin is recommended (benzylpenicillin injected (penicillin g) , phenoxymethylpenicillin oral version (penicillin V) ).
  • If undecided if strep or staph, often used combination treatment
  • Opportunistic bacterial infections (diabetic ulcer) often polymicrobial , with anaerobic organisms –> sampling recommended
    • Co- amoxiclav used initially
  • Fungal infections usually superifical and rarely resistant
    • Topical terbinafine often used, can be oral if needed
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16
Q

What should be considered when choosing antibiotics?

A

Consider both the organism and the patient

Known organism? –> use sensitivies and resistance profile

Or most likely organism and the expected sensitivity and resistance

Take into account patient factors:

  • Allergies
  • renal and liver function
  • severity of infection or immunocompromisation
  • risk of antibiotic associate infection
  • route of admin
  • interactions with other medication
  • age and ethnicity
  • pregancy or breast feeding
  • oral contraception

Then choose antibiotic, route and duration

17
Q
A