Approach to Surgical Infections (Wound vs Prosthetic) Flashcards

1
Q

def of a wound infection

A

Within 30 days after surgery, only include skin, subcut tissues, deep layers or distant organs and have purulent drainage or organisms isolated from the wound site

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2
Q

what is considered a prosthetic?

A

Prosthesis: foreign body

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3
Q

the viral load amount to infect a prosthetic joint vs a native joint is _____________

A

lower

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4
Q

RF for a prosthetic joint infection

A

Preop RF: hx of prior surgery at arthroplasty site, current bacteremia/sepsis, prev/active infection at current surg site, hx of multiple arthroplasties, a prev joint infection, intra-articular injections within the 3M before surgery

Modifiable RF: smoking, alcohol, IV drug use, poor oral hygiene, malnutrition, poor preop glycemic control, obesity, poorly controlled comorbidities (DM, liver, kidney, HIV, use of immunosuppressants)

Nonmodifiable RF: genetics → first- or second-degree relative with a hx of joint infection

Operative RF: ↑ surgical time and complexity

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5
Q

common bacteria for early, delayed, and late prosthetic infections

A

early (within 4wks) - Staphylococcus aureus – high virulence so can infect early

delayed (3-12M postop) - staphylococcus epidermidis

late (2-3Y) - staph aureus

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6
Q

typical pathogenesis entry point for pathogen for early, delayed, and late prosthetic infections

A

early - localized dissemination

delayed - localized or hematogenous

late - hematogenous spread

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7
Q

what makes prosthetic infections so difficult to treat?

A

biofilms

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8
Q

why are biofilms more difficult to target?

A

acts as a barrier vs antimicrobial agents and host immune response, so a higher concentration of abx is required to achieve bactericidal activity

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9
Q

how are biofilms created?

A
  1. free floating bacteria have surface contact and adhere to the surface
  2. there is irreversible attachment and they begin to form/produce biofilm matrix in a single layer
  3. they mature and form multilayer microcolonies
  4. a matured biofilm has characteristic “mushroom” shape which can burst and allow for the bacteria to disperse and start the process again

*within the mushroom shape the bacteria can communicate and share resistance genes

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10
Q

what is a biofilm?

A

a community of surface-attached or non-surface attached bacteria ➔ bacterial aggregates

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11
Q

how does someone with a prosthetic joint infection present? s/s

A

pain w/ affected joint – may be very red, w/ persistent wound drainage and decrease ROM (5 signs of inflammation)

*may lack systemic s/s and fever

there is a specific criteria for dx - not needed to know

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12
Q

how do you work up a sus prosthetic joint infection?

A

standard w/u: blood culture, CRSP, ESR, WBC count, Xray
➔ sus persists: bone/soft tissue biopsy/aspiration + advanced imaging tests (MRI bone scan or Indium/WBC nuclear med scan)

  1. Find the source!
    - blood culture, synovial fluid culture, surgical wound swabbing for C&S and gram stain, tissue culture
  2. Bloodwork: CBC w/diff, inflammatory markers (CRP, ESR), glucose
  3. imaging - xray, indium scan (WBCs will travel potentially travel to source of inflammation), bone scan
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13
Q

what preventative steps can we take to stop a prosthetic joint infection from occuring?

A
  1. good surgical infection prevention (scrub, disinfectants, OR traffic)
  2. prophylactic abx - cefazolin for gen pop; add vanco for increase risk of MRSA
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14
Q

how do we tx prosthetic joint infections?

A
  1. surgical debridement or removal of hardware – refer to ortho for options
  2. antibiotic tx for >=6wks

*aim to target S. aureus, MRSA, and GN bacilli

in prosthetic joint infections, rifampin and fluoroquniolones are often used as empiric bc it penetrates biofilms well

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