A global survey of diagnostic practices in prosthetic joint infections

Shradha Subedi1, Patrick Na Harris2, Paul Chapman3

  • 1University of Queensland, UQ Centre for Clinical Research, Brisbane, Queensland, Australia; Sunshine Coast Hospital and Health Service, Queensland, Australia.

Insights

Global practices for diagnosing prosthetic joint infections (PJIs) vary significantly. This survey highlights differences in tissue sample collection, culture incubation, and identification methods, impacting PJI diagnosis accuracy.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Orthopedic Surgery

Background:

  • Prosthetic joint infections (PJIs) pose significant clinical and economic challenges.
  • Accurate microbiological diagnosis is essential for effective antimicrobial treatment of PJIs.
  • Current international guidelines offer limited clarity on optimal diagnostic practices for PJIs.

Purpose of the Study:

  • To survey and analyze global diagnostic practices for prosthetic joint infections (PJIs).
  • To identify variations in microbiological approaches used in different international healthcare settings.

Main Methods:

  • A global survey was conducted involving 107 hospitals across 24 countries.
  • Data collected included periprosthetic tissue sample collection, sonication, culture incubation periods, bacterial identification (MALDI-TOF), susceptibility testing (EUCAST), and PCR availability.

Main Results:

  • Significant variations were observed in the number of tissue samples collected (49.5% collected 5-6 samples, 11% collected <3).
  • Culture incubation periods varied, with 42% using ≤5 days, though 70% extended incubation when necessary.
  • Matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) was widely used for identification (74.8%), and EUCAST for susceptibility testing (64.5%), with intercontinental differences noted. Polymerase chain reaction (PCR) availability was limited (43%).

Conclusions:

  • Global diagnostic practices for PJIs are heterogeneous, affecting consistency in microbiological results.
  • Variations in sample handling, culture duration, and identification methods contribute to discrepancies in reported PJI etiology and culture-negative rates.
  • Standardization of diagnostic protocols is needed to improve the accuracy and comparability of PJI diagnosis worldwide.

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