Evaluation of the Role for Synovial Aspiration in the Diagnosis of Aseptic Loosening After Total Knee Arthroplasty.

BACKGROUND Aseptic prosthetic loosening is known to be an inflammatory, cellular process. We hypothesized that the synovial cell count would significantly differ among normal controls, patients with aseptic loosening, and patients with other etiologies of aseptic failure after total knee arthroplasty and thus that the cell count would be useful in the diagnosis of aseptic loosening. METHODS Over a six-year time period, all patients undergoing revision total knee arthroplasties at our institution underwent prospective intraoperative aspiration by the two senior authors. Each patient was assigned to a failure category on the basis of a priori criteria: aseptic loosening, periprosthetic infection, component wear, periprosthetic fracture, component malposition, instability, stiffness, and extensor mechanism failure. Simultaneously, patients with well-functioning total knee replacements underwent aspiration as normal controls. Aspirate characteristics were then compared between groups. Receiver-operating characteristic curves were created to determine optimal white blood-cell cutoffs when periprosthetic infection was compared with each individual failure category. RESULTS Thirty normal control patients and 433 patients who underwent revision total knee arthroplasties were included in this study. The synovial white blood-cell count in the normal control group was 558 ± 522 cells/μL, which did not significantly differ (p = 0.091) from that taken from patients with aseptic loosening (947 ± 1027 cells/μL). However, normal controls had significantly higher white blood-cell counts than subjects with stiffness (367 ± 392 cells/μL; p = 0.002) and significantly lower white blood-cell counts than subjects with periprosthetic fractures (1687 ± 1613 cells/μL; p = 0.002). Subjects with aseptic loosening had significantly higher white blood-cell counts than subjects with component malpositioning (p = 0.002) or stiffness (p = 0.001). When individual aseptic failure categories were compared with periprosthetic infection, the optimal white blood-cell cutoff varied widely, including 2104 cells/μL for component malposition and 4697 cells/μL for periprosthetic fracture, and the optimal differential segmented cell count percentages varied from 47% to 83%. CONCLUSIONS Although synovial fluid aspirates in patients with aseptic loosening and those with normal total knee arthroplasties did not differ, synovial fluid aspirate characteristics differed among categories of aseptic failure. As a result, the optimal diagnosis of periprosthetic infection on the basis of synovial aspiration results may need to utilize different cutoff values depending on the alternative mode of failure being considered. Large prospective studies will be necessary to validate these threshold values.

[1]  C. Colwell,et al.  How Do Knee Implants Perform Past the Second Decade? Nineteen- to 25-year Followup of the Press-fit Condylar Design TKA , 2015, Clinical orthopaedics and related research.

[2]  K. Daniilidis,et al.  Diagnostic value of bone scintigraphy for aseptic loosening after total knee arthroplasty. , 2014, Technology and health care : official journal of the European Society for Engineering and Medicine.

[3]  Y. Konttinen,et al.  Characterization of macrophage polarizing cytokines in the aseptic loosening of total hip replacements , 2014, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[4]  T. Giese,et al.  Infectious versus non-infectious loosening of implants: activation of T lymphocytes differentiates between the two entities , 2014, International Orthopaedics.

[5]  J. Parvizi,et al.  The natural progression of synovial fluid white blood-cell counts and the percentage of polymorphonuclear cells after primary total knee arthroplasty: a multicenter study. , 2013, The Journal of bone and joint surgery. American volume.

[6]  Milan Raska,et al.  Macrophages-Key cells in the response to wear debris from joint replacements. , 2013, Journal of biomedical materials research. Part A.

[7]  V. Montori,et al.  Utility of intraoperative frozen section histopathology in the diagnosis of periprosthetic joint infection: a systematic review and meta-analysis. , 2012, The Journal of bone and joint surgery. American volume.

[8]  H. Kremers,et al.  Comparative long-term survivorship of uncemented acetabular components in revision total hip arthroplasty. , 2012, The Journal of bone and joint surgery. American volume.

[9]  S. Sporer,et al.  Serum and synovial fluid analysis for diagnosing chronic periprosthetic infection in patients with inflammatory arthritis. , 2012, The Journal of bone and joint surgery. American volume.

[10]  M. Keith,et al.  American Academy of Orthopaedic Surgeons clinical practice guideline on: the diagnosis of periprosthetic joint infections of the hip and knee. , 2011, The Journal of bone and joint surgery. American volume.

[11]  L. Bai,et al.  Polymethylmethacrylate and titanium alloy particles activate peripheral monocytes during periprosthetic inflammation and osteolysis , 2011, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[12]  J. Parvizi,et al.  Preoperative diagnosis of periprosthetic joint infection: role of aspiration. , 2011, AJR. American journal of roentgenology.

[13]  Thomas W. Bauer,et al.  Diagnosis of Periprosthetic Joint Infections of the Hip and Knee , 2010, The Journal of the American Academy of Orthopaedic Surgeons.

[14]  J. Parvizi,et al.  Cell count and differential of aspirated fluid in the diagnosis of infection at the site of total knee arthroplasty. , 2010, The Journal of bone and joint surgery. American volume.

[15]  C. Perka,et al.  Validity of Frozen Sections for Analysis of Periprosthetic Loosening Membranes , 2010, Clinical orthopaedics and related research.

[16]  S. Stea,et al.  Assessment of five interleukins in human synovial fluid as possible markers for aseptic loosening of hip arthroplasty. , 2009, Artificial organs.

[17]  S. Sporer,et al.  Perioperative testing for joint infection in patients undergoing revision total hip arthroplasty. , 2008, The Journal of bone and joint surgery. American volume.

[18]  R. Barrack,et al.  Cell count and differential of aspirated fluid in the diagnosis of infection at the site of total knee arthroplasty. , 2008, The Journal of bone and joint surgery. American volume.

[19]  T. Sculco,et al.  Expression profiling reveals alternative macrophage activation and impaired osteogenesis in periprosthetic osteolysis , 2008, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[20]  A. Rosenberg,et al.  Preoperative testing for sepsis before revision total knee arthroplasty. , 2007, The Journal of arthroplasty.

[21]  V. Jovaní,et al.  Synovial fluid analysis. , 2005, Best practice & research. Clinical rheumatology.

[22]  T. Holland-Letz,et al.  Comparison of subtraction arthrography, radionuclide arthrography and conventional plain radiography to assess loosening of total knee arthroplasty / Vergleich von Subtraktionsarthrographie, Radionuklidarthrographie und konventionellem Röntgen zur Erfassung von Prothesenlockerungen in der Knierevisi , 2005, Biomedizinische Technik. Biomedical engineering.

[23]  M. Wastie,et al.  Radionuclide bone scintigraphy in the detection of significant complications after total knee joint replacement. , 2001, Clinical radiology.

[24]  B. Marson,et al.  White blood cell counts and differential in synovial fluid of aseptically failed total knee arthroplasty. , 2000, The Journal of arthroplasty.

[25]  W. Maloney,et al.  Loosening and Osteolysis of Cemented Joint Arthroplasties: A Biologic Spectrum , 1997, Clinical orthopaedics and related research.

[26]  R. Deyo,et al.  Adapting a clinical comorbidity index for use with ICD-9-CM administrative databases. , 1992, Journal of clinical epidemiology.

[27]  P. Li,et al.  Different influence of Ti, PMMA, UHMWPE, and Co-Cr particles on peripheral blood monocytes during periprosthetic inflammation. , 2015, Journal of biomedical materials research. Part A.

[28]  S. Santavirta,et al.  Cathepsin G and alpha 1-antichymotrypsin in the local host reaction to loosening of total hip prostheses. , 1995, The Journal of bone and joint surgery. American volume.

[29]  C. Mackenzie,et al.  A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. , 1987, Journal of chronic diseases.

[30]  C. Mackenzie,et al.  Morbidity during hospitalization: can we predict it? , 1987, Journal of chronic diseases.

[31]  W. Youden,et al.  Index for rating diagnostic tests , 1950, Cancer.