Low Synovial Lymphocyte Percentage as a Novel Diagnostic Marker of Periprosthetic Joint Infection

Assil-Ramin Alimy1, Jonah Sijakov1, Nico Maximillian Jandl1

  • 1Department of Trauma and Orthopedic Surgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

JB & JS Open Access
|November 4, 2025
PubMed
Abstract

Insights

Low synovial lymphocyte percentage is a highly accurate marker for diagnosing periprosthetic joint infection (PJI). This finding could lead to earlier detection and improved treatment for patients with chronic PJI.

Area of Science:

  • Orthopedic surgery
  • Infectious diseases
  • Biomarker research

Background:

  • Periprosthetic joint infection (PJI) diagnosis is challenging, especially for chronic cases with subtle clinical signs.
  • Current diagnostic criteria for PJI lack sufficient sensitivity for chronic infections.

Purpose of the Study:

  • To identify accurate diagnostic markers for periprosthetic joint infection (PJI) in patients undergoing revision arthroplasty.
  • To evaluate serum and synovial fluid parameters for PJI detection.

Main Methods:

  • Retrospective analysis of 400 patients (145 with PJI, 255 with aseptic failure) undergoing hip or knee revision.
  • Diagnosis confirmed using 2018 International Consensus Meeting criteria.
  • Evaluation of serum and synovial biomarkers, including polymorphonuclear neutrophil (PMN) count and lymphocyte percentage, using receiver operating characteristic curves.

Main Results:

  • Synovial alpha-defensin and C-reactive protein were not superior to PMN count/percentage.
  • Low synovial lymphocyte percentage (<34.7%) showed high diagnostic accuracy for PJI (AUC=0.96, sensitivity=0.85, specificity=0.96).
  • A conditional inference tree model identified synovial lymphocyte percentage and PMN count as key for chronic PJI diagnosis (AUC=0.95).

Conclusions:

  • Low synovial lymphocyte percentage is a reliable diagnostic marker for PJI.
  • Incorporating synovial lymphocyte assessment may improve timely PJI diagnosis and treatment.
  • External validation is needed due to the single-center, hip/knee-specific nature of the study.

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