Peri-prosthetic joint infection



Definitions

Prosthetic joint infection (PJI) is an infrequent but serious complication of joint arthroplasty. PJI affect approximately 2% of total knee arthroplasty (TKA) and total hip arthroplasty (THA).

Types

  • Early/Post-operative
  • Late/Haematogenous
  • Chronic

Definitions

Clinical:

  • Sinus tract communicating with prosthesis
  • Purulence surrounding prosthetic joint

Microbiological:

  • Presence of 2 phenotypically indistinguishable organisms recovered from joint tissue/fluid specimens OR single virulent organism (e.g. S. aureus)

Histological:

  • Acute inflammation on histopathological examination of periprosthetic tissue

Diagnosis

  • Dx and Mx PJI dependent on microbiological sampling
  • Separate instruments should be used to minimize contamination. Each tissue sampled should be transferred to a separate sterile container and labeled
  • Recommended sample sites: capsular tissue, acetabular membrane (for THA), femoral membrane, tibial membrane (for TKA), other tissue (i.e. granulation tissue)
  • ID of the causative organism may be optimized by the addition of enrichment cultures (i.e. blood culture specimen bottles/other enrichment media)
  • For chronic PJI, consider peri-prosthetic biopsy or aspirate in advance of surgery

Antimicrobial therapy

  • In general, systemically stable patients with chronic PJI should not receive any antibiotics for 2 weeks prior to operative sampling to optimize culture yield
  • Surgical prophylaxis should not be given in theatre
  • I.D. should be consulted for all patients with PJI

Preoperative care


Treatment AFTER sampling

Empiric therapy

  • Early active antimicrobial therapy is associated better outcomes in PJI treated with debridement, antibiotics and implant retention (DAIR)
  • All patients should receive empiric coverage for gram-positive and gram-negative organisms after sampling
  • Gram-negative cover (i.e. Piperacillin/tazobactam or ceftriaxone as per above algorithms) should be continued for 48 hours after surgery. If no gram-negative organisms are grown at 48 hours, gram-negative cover can be discontinued
  • Gram-positive cover (i.e. vancomycin) should be continued for 7 days until reviewed by ID or until results from sampling are available
  • For patients with chronic PJI and a known organism, empiric regimen should include an antibiotic with activity against that organism

Local antimicrobial therapy

  • There is evidence that use of antibiotic-loaded spacers improves outcomes in PJI
  • Surgical team should ensure that an antibiotic with appropriate cover for the isolated organism is used. Consult I.D. for further guidance

Monitoring

  • All patients receiving antimicrobial therapy as an inpatient should have twice weekly FBC, renal/liver profile, CRP
  • Drug specific monitoring:
    • Vancomycin – twice weekly trough levels if within range (refer to Vancomycin dosing and monitoring on nchd.ie)
    • Daptomycin – weekly CK levels and to hold statins
    • Gentamicin – daily trough level prior to antibiotic admin.
    • Rifampicin – Pharmacy review due to multiple drug-drug interactions. Weekly LFTs
    • Antifungals – weekly renal/liver profiles

Micro interpretation

  • A positive microbiology result is the isolate of either:
    • At least 2 phenotypically indistinguishable organisms (e.g. S. hominis)
    • 1 virulent organism (e.g. S. aureus)
  • Surgical team should ensure that an antibiotic with appropriate cover for the isolated organism is used. Consult Infectious Diseases for further guidance


Content by Dr Íomhar O' Sullivan. Last review Dr ÍOS 18/07/24.