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Multiplex PCR Unyvero i60 ITI application improves detection of low-virulent microorganisms in periprosthetic joint
Irene Katharina Sigmund1, Reinhard Windhager2, Florian Sevelda2
1Department of Orthopaedics and Trauma Surgery, Medical University of Vienna, Spitalgasse 23, 1090, Vienna, Austria. irene.sigmund@meduniwien.ac.at.
Purpose:
The aim of this study was to evaluate the pre-operative performance of an automated multiplex PCR (mPCR) system in patients with suspected periprosthetic joint infection (PJI).
Methods:
Under sterile conditions, synovial fluid samples from patients with a suspected PJI were collected pre-operatively. One hundred eighty microliter of the aspirate was used for analysis in the mPCR. The remaining joint fluid was sent for microbiological analysis. PJI was diagnosed by using the Musculoskeletal Infection Society (MSIS) criteria. Total percentage agreement and Cohen's kappa coefficient were calculated to measure overall agreement.
Results:
Overall, 90 patients with a suspected PJI were included. Using MSIS criteria, 38 (42%) patients were classified as septic. Total percent agreement between mPCR and synovial fluid culture was 86% with a Cohen's kappa of 0.68. The mPCR and synovial fluid culture showed sensitivities of 71% and 84%, respectively. Combined evaluation provided an even higher sensitivity of 92%. While Cutibacterium spp. were detected five times by mPCR, it could only be cultured once. A higher detection rate of CoNS by mPCR (n = 7) compared to conventional culture (n = 5) was also demonstrated. In comparison to synovial fluid culture, the mPCR missed Staphylococcus aureus five times.
Conclusion:
With a moderate agreement between synovial fluid mPCR and culture, the mPCR system could be a useful adjunct in diagnosing a PJI pre-operatively. Due to faster availability of results and a higher detection rate of low-virulent microorganisms, it can complement conventional culture.
Insights
An automated multiplex PCR (mPCR) system shows moderate agreement with traditional cultures for diagnosing periprosthetic joint infection (PJI). This mPCR can be a useful adjunct, offering faster results and detecting more low-virulent organisms.
Area of Science:
- Orthopedics
- Infectious Diseases
- Molecular Diagnostics
Background:
- Periprosthetic joint infection (PJI) is a serious complication following joint replacement surgery.
- Accurate and timely diagnosis of PJI is crucial for effective treatment and patient outcomes.
- Conventional microbiological culture methods can be slow and may fail to detect certain pathogens, particularly low-virulent ones.
Purpose of the Study:
- To evaluate the pre-operative diagnostic performance of an automated multiplex PCR (mPCR) system for suspected PJI.
- To compare the mPCR system's results with conventional synovial fluid cultures.
- To assess the mPCR system's potential as an adjunct diagnostic tool for PJI.
Main Methods:
- Synovial fluid samples were collected pre-operatively from 90 patients with suspected PJI.
- Samples were analyzed using an automated multiplex PCR (mPCR) system.
- Conventional microbiological culture was performed on the remaining joint fluid.
- Diagnosis of PJI was based on the Musculoskeletal Infection Society (MSIS) criteria.
- Agreement was measured using total percentage agreement and Cohen's kappa coefficient.
Main Results:
- The mPCR system demonstrated 86% total agreement with synovial fluid culture (Cohen's kappa = 0.68).
- Sensitivities were 71% for mPCR and 84% for culture; combined evaluation reached 92% sensitivity.
- mPCR detected Cutibacterium spp. more frequently (5 vs. 1) and Coagulase-negative staphylococci (CoNS) more often (7 vs. 5) than culture.
- mPCR missed Staphylococcus aureus in five cases compared to culture.
Conclusions:
- The automated mPCR system shows moderate agreement with synovial fluid culture for pre-operative PJI diagnosis.
- mPCR can serve as a valuable adjunct to conventional culture due to faster results and improved detection of certain microorganisms.
- The system's ability to detect low-virulent organisms complements the limitations of traditional culture methods.
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