Wound, bone, joint Infections Flashcards

1
Q

Major pathogens causing Surgical site infections (SSI)

A

o Staphylococcus aureus (MSSA and MRSA)
o Escherichia coli
o Pseudomonas aeruginosa

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2
Q

Three levels of SSIs

A

o Superficial Incisional skin and subcutaneous tissues
o Deep Incisional fascial and muscle layers
o Organ/Space Infection any part of the anatomy other than the incision

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3
Q

Preventing SSIs pre-operatively

A

 Treat all remote infection (e.g. pneumonia, UTI) before operation
 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%
 Antibiotic Prophylaxis

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4
Q

Intra-operative prevention of SSIs

A

 Limit number of people in theatre
 Ventilation of theatre (positive pressure)
 Sterilisation of Surgical Instruments
 Skin Preparation:
• Povidine-iodine
• Chlorhexidine (in 70% alcohol)
 Normothermia (if <36C, consider warming):
• 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
 Asepsis and Surgical Technique
• Remove all dead tissue

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5
Q

Pathophysiology of septic arthritis

A

o Organisms adhere to synovium
o Bacterial proliferation in synovial fluid  host inflammatory response  joint damage
o Joint damage  exposure of host derived protein (e.g. fibronectin) to which bacteria can adhere

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6
Q

Bacterial factors allowing septic arthritis

A

 S. aureus has receptors such as fibronectin-binding protein that recognise selected host proteins
 S. aureus (some strains) produce cytotoxin PVL (Panton-Valentine Leucocidin)  fulminant infection
 Kingella kingae synovial adherence is via bacterial pili

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7
Q

Host factors allowing septic arthritis

A

 Genetic deletion of macrophage-derived cytokines  reduce host-response in S. aureus sepsis
 Absence of IL-10 increases the severity of staphylococcus joint disease

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8
Q

Organisms causing septic arthritis

A
o	Staphylococcus aureus 						46%
o	Streptococci: 								22%
	Streptococcus pyogenes
	Streptococcus pneumoniae
	Streptococcus agalactiae
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9
Q

Investigations of septic arthritis

A

o Blood cultures (before ABx)

o Synovial fluid aspiration MC&S synovial count >50,000 WBC/mL is used to suggest septic arthritis

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10
Q

Management of SA

A

o ABx, 4-6 weeks (outpatient setting)

o Drainage of the joint

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11
Q

Causes of vertebral osteomyelitis

A
o	Acute haematogenous spread (bacteraemia)
o	Exogenous (after disc surgery, implant associated)
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12
Q

Causative organisms of VO

A

o Staphylococcus aureus (48.3%)
o Coagulase-negative staphylococcus
o Gram-negative rods
o Streptococcus

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13
Q

Main location of VO

A
o	Lumbar 			(43.1%)
o	Cervical 				(10.6%)
o	Cervico-thoracic 			(0.4%)
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14
Q

Ix for VO

A

• Investigations:
o MRI (90% sensitive)
o Blood cultures
o CT-guided/open biopsy

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15
Q

Tx of VO

A

o ABx, 6 weeks

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16
Q

Diagnosis of chronic osteomyelitis

A
o	XR (often first line to screen; early changes take ~10 days)
o	MRI (much more sensitive for changes)
o	Bone biopsy (culture and histology)
17
Q

Treatment of chronic OM

A

Radical debridement to living bone

Oral ABx 6 weeks

18
Q

Papineau Technique

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%

19
Q

Causative organisms of Prosthetic joint infections

A

 Coagulase-negative staphylococci > S. aureus

20
Q

Features of PJI

A

o Pain
o Patient complain joint was ‘never right’ after the operation  early failure
o Sinus tract

21
Q

Diagnosis of PJI

A

o Radiology – loosening (bone loss along the cement-bone interface)
o Raised CRP:
 CRP >13.5 for prosthetic knee joint infection
 CRP >5 for prosthetic hip joint infection
o Joint Aspiration:
 If >1,700 WCC/mL  knee PJI
 If >4,200 WCC/mL  hip PJI

22
Q

Tx of PJI

A

o 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

o Two Stage Revision:
 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
 Re-debride and sample at second stage
 Re-implantation with antibiotic impregnated cement