MICRO: Wound, Bone and Joint Infections Flashcards

1
Q

What pathogens most commonly cause SSIs (surgical site infections)?

A
  • Staphylococcus aureus (MSSA and MRSA)
  • Escherichia coli
  • Pseudomonas aeruginosa
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2
Q

What is the pathogenesis of SSIs?

A
  • Surgical site is contaminated
    • SSI risk increased if surgical site is contaminated with >105 microorganisms / gram of tissue
    • Lower dose required if foreign material present (i.e. silk suture)
  • Host immune response also plays a role in pathogenesis as well as the pathogenicity of the pathogen
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3
Q

What are the three levels of SSIs?

A
  • Superficial Incisional- skin and subcutaneous tissues
  • Deep Incisional - ascial and muscle layers
  • Organ/Space Infection - any part of the anatomy other than the incision
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4
Q
  • Case 1:
    • Admitted with SAH and sub-dural haemorrhage after a fall–> decompressive craniectomy
    • 2/12 later had a cranioplasty with titanium plate
    • 6/12 later admitted with large subdural collection and midline shift à abscess evacuation and infection
  • What is the organism?
    • Ecoli, enterobacter, MRSA, neisseria meningitides?
A

MRSA

Gram positive (dark purple, neg would be pale pink) and beta haemolytic

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5
Q

How can preventing SSIs be divided?

A
  1. Pre
  2. Intra
  3. Post - operative
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6
Q

What are the pre-operative measures to prevent SSIs?

A
  • Age (an independent risk factor) - increasing risk until 65 years
  • Treat all remote infection (e.g. pneumonia, UTI) before operation
  • Underlying illness risk factors (e.g. ASA score >3, diabetes, smoking)
  • Pre-operative Showering
    • Either chlorhexidine or normal detergent/bar soap (both same incidence of SSI)
    • Advised to showed with soap on the day of surgery or the day before
  • Hair removal
    • Shaving increases risk of SSI (micro-abrasions from shaving can multiply bacteria)
    • Electric clipper should be used instead on the day of surgery with a single-use head
  • Nasal Decontamination
    • Staphylococcus aureus is carried in the nostrils of 20-30%
      • SA carriage = MOST POWERFUL risk factor for SSI following cardiothoracic surgery
    • Nasal decontamination should be offered if they are found to be carrying S. aureus
  • Antibiotic Prophylaxisadminister at time of induction of anaesthesia:

To ensure bactericidal concentration in serum & tissue at time of incision

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7
Q

Which underlying conditions increase risk of SSIs?

A
  • ASA score >3
  • Diabetes (2-3x increased risk à control blood glucose, HbA1c <7)
  • Malnutrition
  • Low serum albumin
  • Radiotherapy and steroids
  • Rheumatoid arthritis (stoop DMARDs before operation)
  • Obesity (adipose poorly vascularised à poor access for immune system à risk of SSIs)
  • Smoking (nicotine delays wound healing and leads to PVD – see above poor vascularisation)
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8
Q

How does smoking increase risk of SSI?

A
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9
Q

Is shaving necessary to prevent SSIs?

A
  • Shaving with razor increases risk of SSI (micro-abrasions from shaving can multiply bacteria)
  • Electric clipper should be used instead on the day of surgery with a single-use head
  • Shaving should only be done if hair will interfere with the surgery
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10
Q

What kind of antibiotic prophylaxis can be given to prevent SSIs pre-op?

A
  • Antibiotic Prophylaxis – administer at time of induction of anaesthesia:
    • To ensure bactericidal concentration in serum & tissue at time of incision
    • Must have some bactericidal activity
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11
Q

What intra-op measures can be taken to prevent SSIs ?

A
  • Limit number of people in theatre (people shed skin cells)
  • Ventilation of theatre (positive pressure) –> laminar flow for orthopaedics
  • Sterilisation of Surgical Instruments
  • Skin Preparation:
    • Povidine-iodine
    • Chlorhexidine (in 70% alcohol)
  • Asepsis and Surgical Technique
    • Remove all dead tissue
    • IV devices should follow aseptic procedures
  • Normothermia (if <36C, consider warming):
  • Oxygenation
    • SpO2 >95%
    • Higher O2 saturations à reduced SSIs
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12
Q

What temperatures should be used intra-op?

A

Hypothermia –> increase risk of SSIs by causing vasoconstriction and decreasing oxygen delivery to wound space with impairment of neutrophil function

Measure the patient’s temperature before inducing anaesthesia

Start warming air if <36 degrees C

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13
Q

What oxygenation levels should be aimed for pre-op and why?

A
  • SpO2 >95%
  • Higher O2 saturations –> reduced SSIs
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14
Q

Why is it important to reduce theatre traffic intra-op?

A

One person sheds 1 billion skin cells per day - 10% of these carry bacteria

Microbial load in threatre is related to the number of people present

Theatre personnel should be kept to a minimum

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15
Q

How common is septic arthritis?

A
  • Incidence: 2-10 per 100,000
  • More common in patients with RhA; 28-38 per 100,000
  • Mortality 7-15% and morbidity 50%
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16
Q

Risk factors for septic arthritis?

A
  • Rheumatoid arthritis
  • Osteoarthritis
  • Crystal arthritis
  • Joint prosthesis
  • IVDU
  • Diabetes, chronic renal disease, chronic liver disease
  • Immunosuppression (e.g. steroids)
  • Trauma – intra-articular injection, penetrating injury
17
Q

What is the pathophysiology of septic arthritis?

A
  • Organisms adhere to synovium
  • Bacterial proliferation in synovial fluid –> host inflammatory response –> joint damage
  • Joint damage –> exposure of host derived protein (e.g. fibronectin) to which bacteria can adhere
18
Q

Which bacterial factors are important in septic arthirtis?

A
  • Bacterial Factors:
    • S. aureus has receptors such as fibronectin-binding protein that recognise selected host proteins
    • S. aureus (some strains) produce cytotoxin PVL (Panton-Valentine Leucocidin) à fulminant infection
    • Kingella kingae synovial adherence is via bacterial pili
19
Q

Which host factors are important in pathophysiology of septic arthritis?

A
  • Leucocyte derived proteases and cytokines can cause cartilage and bone damage
  • Raised intra-articular pressure impedes capillary blood flow –> cartilage and bone ischaemia/necrosis
  • Genetic deletion of macrophage-derived cytokines –> reduce host-response in S. aureus sepsis
  • Absence of IL-10 increases the severity of staphylococcus joint disease
20
Q

What are the most common organisms causing septic arthritis? Which is the single most common?

A
  • Staphylococcus aureus - 46%
  • Streptococci - 22%
    • Streptococcus pyogenes
    • Streptococcus pneumoniae
    • Streptococcus agalactiae
  • Gram-negative organisms:
    • Escherichia coli
    • Haemophilus influenzae
    • Neisseria gonorrhoea
    • Salmonella
  • Coagulase-negative staphylococci - 4%
  • Lyme disease, Brucellosis, Mycobacteria, Fungi - Rare
21
Q

Which investigations should be done for septic arthritis? What is the WCC in the synovium in this condition? Which imaging is useful?

A
  • Blood cultures (before ABx)
  • Synovial fluid aspiration MC&S- synovial count >50,000 WBC/mL is used to suggest septic arthritis
    • USS confirms and guides aspiration of fluid
  • ESR and CRP
  • CT – check for erosive bone change, periarticular soft tissue extension
  • MRI – joint effusion, articular cartilage destruction, abscess, contiguous osteomyelitis
22
Q

What is the management of septic arthritis?

A
  • ABx, 4-6 weeks (outpatient setting) - mostly IV
  • Drainage of the joint
23
Q

What are the most common causes of vertebral osteomyelitis?

A
  • Causes:
    • Acute haematogenous spread (bacteraemia)
    • Exogenous (after disc surgery, implant associated)
  • Causative organisms:
    • Staphylococcus aureus (48.3%)
    • Coagulase-negative staphylococcus
    • Gram-negative rods
    • Streptococcus
24
Q

Where is vertebral osteomeylitis most commonly located?

A
  • Lumbar (43.1%)
  • Cervical (10.6%)
  • Cervico-thoracic (0.4%)
25
Q

What are the symptoms of VO? What investigations should be done?

A
  • Symptoms:
    • Back pain
    • Fever
    • Neurological impairment
  • Investigations:
    • MRI (90% sensitive)
    • Blood cultures
    • CT-guided/open biopsy
26
Q

What is the management of vertebral osteomyelitis?

A
  • Treatment:
    • ABx, 6 weeks
27
Q
  • Case 1:
    • 76yo man, 4/12 hx of back pain with left leg radiation
    • WL 25kg over last 6/12
    • PMHx of fracture with metal plate insertion, arthritis R-knee, HTN, lived overseas until 1993
    • MRI: discitis of L2/L3–> spinal biopsy –> Coag -ve staph (staph epidermidis) grown –> histology shows vague granuloma
    • Anti-TB treatment started, empirical IV ceftriaxone started
    • Surgery debridement and stabilisation
    • No growth on agar of standard organisms and further PCR and IgG showed brucella

What is the causative organism? Staph aureus, salmonella, TB, brucella?

A

Brucella - commonly from unpasterised milk, cheese and eating meat.

  • Brucella IgG >1:2560
  • Brucella DNA using PCR was positive
  • Started on rifampicin, ciprofloxacin and doxycycline
28
Q

How does chronic osteomyelitis present?

A
  • Presentation:
    • Pain
    • Brodies abscess
    • Sinus tract

MRI of child shown

29
Q

How is chronic osteomyelitis diagnosed? How is it treated birefly?

A
  • Diagnosis
    • XR (often first line to screen; early changes take ~10 days)
    • MRI (much more sensitive for changes)
    • Bone biopsy (culture and histology)
  • Treatment = radical debridement to living bone and oral ABx (up to 6 weeks after discharge)
30
Q

What is the Papineau technique for chronic osteomyelitis?

A
  • Complete excision of infected tissue and necrotic bone
  • Followed by open cancellous bone grafting of the osseous defect
  • Split skin grafting is used to close the wound
  • Success rate of 89-93%
31
Q

What is the presentation of prosthetic joint infections?

A
  • Pain
  • Patient complain joint was ‘never right’ after the operation à early failure
  • Sinus tract releasing pus may be present
32
Q

What are the causative organisms of PJI?

A
  • Gram-positive cocci:
    • Coagulase-negative staphylococci > S. aureus
    • Streptococci
    • Enterococci
  • Aerobic Gram-negative bacilli:
    • Enterobacteriaceae
    • Pseudomonas aeruginosa
  • Anaerobes
  • Polymicrobials
  • Culture-negative
  • Fungi
33
Q

How are PJI diagnosed?

A
  • Radiology – loosening (bone loss along the cement-bone interface)
  • Raised CRP:
    • CRP >13.5 for prosthetic knee joint infection
    • CRP >5 for prosthetic hip joint infection
  • Joint Aspiration:
    • If >1,700 WCC/mL = knee PJI
    • If >4,200 WCC/mL = hip PJI
  • Intraoperative Microbiological Sampling:
    • Tissue specimens taken from at least 5 sites around the implant
    • Histopathology (if >3 specimens yield identical organisms –> suggestive of PJI)
34
Q

What is the management of PJI?

A
  • Single Stage Revision (i.e. Endo-Klinik):
    • Remove all foreign material and dead bone
    • Change gloves and drapes etc.
    • Re-implant new prosthesis with antibiotic impregnated cement and give IV antibiotics
    • ~89% success rate

OR…

  • Two Stage Revision:
      1. Remove prosthesis and put in a spacer (to take up the space of the prosthesis)
        * Take samples for microbiology and histology
        * Period of IV antibiotics (for 6 weeks) then stop antibiotics for 2 weeks
      1. Re-debride and sample at second stage
        * Re-implantation with antibiotic impregnated cement
        * NO further antibiotics needed if the samples are clear
        • If antibiotics are required, OPAT is used
35
Q

How many tissue samples should be sent from PJI? What is infection defined as on hitology in PJI? What about cultures?

A
36
Q

Case 3:

  • 70yo diabetic, 1994 right THR –> 1998 revision of acetabulum
  • X-ray = lysis around distal femoral component

Likely pathogen? CNS, H. influenzae, E coli or pseudomonas?

A

Coagulase negative staphylococci

IMPORTANT to send multiple specimens as this is commonly a skin contaminant

37
Q
A

Silvery white cultures = Brucella