Wound, bone, joint Infections Flashcards
Major pathogens causing Surgical site infections (SSI)
o Staphylococcus aureus (MSSA and MRSA)
o Escherichia coli
o Pseudomonas aeruginosa
Three levels of SSIs
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
Preventing SSIs pre-operatively
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
Intra-operative prevention of SSIs
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
Pathophysiology of septic arthritis
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
Bacterial factors allowing septic arthritis
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
Host factors allowing septic arthritis
Genetic deletion of macrophage-derived cytokines reduce host-response in S. aureus sepsis
Absence of IL-10 increases the severity of staphylococcus joint disease
Organisms causing septic arthritis
o Staphylococcus aureus 46% o Streptococci: 22% Streptococcus pyogenes Streptococcus pneumoniae Streptococcus agalactiae
Investigations of septic arthritis
o Blood cultures (before ABx)
o Synovial fluid aspiration MC&S synovial count >50,000 WBC/mL is used to suggest septic arthritis
Management of SA
o ABx, 4-6 weeks (outpatient setting)
o Drainage of the joint
Causes of vertebral osteomyelitis
o Acute haematogenous spread (bacteraemia) o Exogenous (after disc surgery, implant associated)
Causative organisms of VO
o Staphylococcus aureus (48.3%)
o Coagulase-negative staphylococcus
o Gram-negative rods
o Streptococcus
Main location of VO
o Lumbar (43.1%) o Cervical (10.6%) o Cervico-thoracic (0.4%)
Ix for VO
• Investigations:
o MRI (90% sensitive)
o Blood cultures
o CT-guided/open biopsy
Tx of VO
o ABx, 6 weeks
Diagnosis of chronic osteomyelitis
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)
Treatment of chronic OM
Radical debridement to living bone
Oral ABx 6 weeks
Papineau Technique
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%
Causative organisms of Prosthetic joint infections
Coagulase-negative staphylococci > S. aureus
Features of PJI
o Pain
o Patient complain joint was ‘never right’ after the operation early failure
o Sinus tract
Diagnosis of PJI
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
Tx of PJI
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