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Published on: February 6, 2020
Absolute synovial polymorphonuclear neutrophil cell count as a biomarker of periprosthetic joint infection
Nico M Jandl1, Sebastian Kleiss1, Haider Mussawy1
1Department of Trauma and Orthopaedic Surgery, Division of Orthopaedics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Abstract:
The aim of this study was to evaluate the diagnostic accuracy of the absolute synovial polymorphonuclear neutrophil cell (PMN) count for the diagnosis or exclusion of periprosthetic joint infection (PJI) after total hip (THA) or knee arthroplasty (TKA). In this retrospective cohort study, 147 consecutive patients with acute or chronic complaints following THA and TKA were included. Diagnosis of PJI was established based on the 2018 International Consensus Meeting criteria. A total of 39 patients diagnosed with PJI (32 chronic and seven acute) and 108 patients with aseptic complications were surgically revised. Using receiver operating characteristic curves and calculating the area under the curve (AUC), an optimal synovial cut-off value of 2,000 PMN/µl was determined (AUC 0.978 (95% confidence interval (CI) 0.946 to 1)). Using this cut-off, sensitivity and specificity of absolute synovial PMN count for PJI were 97.4% (95% CI 91.2 to 100) and 93.5% (95% CI 88.9 to 98.1), respectively. Positive and negative predictive value were 84.4% (95% CI 72.7 to 93.9) and 99.0% (95% CI 96.7 to 100), respectively. Exclusion of 20 patients with acute complications improved specificity to 97.9% (95% CI 94.6 to 100). Different cut-off values for THA (< 3,600 PMN/µl) and TKA (< 2,000 PMN/µl) were identified. Absolute synovial PMN count correlated strongly with synovial alpha-defensin (AD) (r = 0.759; p < 0.001). With a positive AD result, no additional PJI could be identified in any case. Absolute synovial PMN count is a widely available, rapid, cost-effective, and accurate marker in PJI diagnostics, whereas synovial AD appears to be a surrogate parameter of absolute synovial PMN count. Despite limitations in the early postoperative phase, wear, and rheumatic diseases in confirming PJI, an absolute synovial PMN count below 2,000/µl is highly suitable for ruling out PJI, with specific cut-off values for THA and TKA.
Insights
The absolute synovial polymorphonuclear neutrophil (PMN) count accurately diagnoses periprosthetic joint infection (PJI) after hip or knee arthroplasty. A cut-off of 2,000 PMN/µl effectively rules out PJI, with specific values for hip and knee replacements.
Area of Science:
- Orthopedics
- Infectious Diseases
- Diagnostic Medicine
Background:
- Periprosthetic joint infection (PJI) is a serious complication following arthroplasty.
- Accurate and timely diagnosis of PJI is crucial for effective treatment and patient outcomes.
- Synovial fluid analysis is a key component in PJI diagnostics.
Purpose of the Study:
- To evaluate the diagnostic accuracy of absolute synovial polymorphonuclear neutrophil (PMN) cell count for diagnosing or excluding PJI.
- To determine an optimal cut-off value for PMN count in PJI diagnosis.
- To compare PMN count with synovial alpha-defensin (AD) levels.
Main Methods:
- Retrospective cohort study of 147 patients with hip or knee arthroplasty complications.
- Diagnosis of PJI based on 2018 International Consensus Meeting criteria.
- Receiver operating characteristic (ROC) curve analysis to determine optimal PMN cut-off values.
Main Results:
- An optimal synovial cut-off value of 2,000 PMN/µl was determined (AUC 0.978).
- Sensitivity and specificity for PJI were 97.4% and 93.5%, respectively, using the 2,000 PMN/µl cut-off.
- Absolute synovial PMN count showed strong correlation with synovial alpha-defensin (r = 0.759, p < 0.001).
- Specific cut-off values identified for total hip arthroplasty (< 3,600 PMN/µl) and total knee arthroplasty (< 2,000 PMN/µl).
Conclusions:
- Absolute synovial PMN count is a rapid, cost-effective, and accurate marker for PJI diagnostics.
- A synovial PMN count below 2,000/µl is highly suitable for ruling out PJI.
- Synovial alpha-defensin may serve as a surrogate marker for absolute synovial PMN count.

