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Microbiological Profi le of Periprosthetic Knee Infections in a Brazilian Unified Health System Hospital Specialized in Highly Complex Orthopedic Surgeries* * Study developed at Instituto Nacional de Traumatología e Ortopedia (INTO), Rio de Janeiro, Brazil.

Abstract

Objective

We studied the microbiological profile of periprosthetic knee infections treated in a Brazilian tertiary hospital.

Methods

The study included all patients undergoing revision surgery for total knee arthroplasty (RTKA) between November 2019 and December 2021, with a diagnosis of periprosthetic infection confirmed per the 2018 International Consensus Meeting (ICM) criteria.

Results

Sixty-two patients had a periprosthetic joint infection (PJI) per the 2018 ICM criteria. Cultures were monomicrobial in 79% and polymicrobial in 21% of cases. The most frequent bacterium in microbiological tissue and synovial fluid cultures was Staphylococcus aureus, observed in 26% of PJI patients. Periprosthetic joint infection with negative cultures occurred in 23% of patients.

Conclusion

Our results show the following: i) a high prevalence of Staphylococcus as an etiological agent for knee PJI; ii) a high incidence of polymicrobial infections in early infections; iii) the occurrence of PJI with negative cultures in approximately one fourth of the subjects.

arthroplasty; replacement; knee; postoperative complications; intraarticular injections; prosthesis-related infections

Resumo

Objetivo

Identificar o perfil microbiológico das infecções periprotéticas do joelho tratadas em um hospital terciário brasileiro.

Métodos

Todos os pacientes submetidos à cirurgia de revisão de artroplastia total do joelho (RATJ), no período compreendido entre novembro de 2019 e dezembro de 2021, e que tiveram o diagnóstico de infecção periprotética confirmado de acordo com critérios do International Consensus Meeting (ICM) 2018, foram incluídos no estudo.

Resultados

Sessenta e dois pacientes foram diagnosticados com infecção periprotética (IAP) pelos critérios do International Consensus Meeting 2018. Culturas monomicrobianas foram identificadas em 79% e polimicrobianas em 21% dos casos. A bactéria mais frequentemente identificada nas culturas microbiológicas de tecidos e líquido sinovial foi o Staphylococcus aureus, presente em 26% dos pacientes com infecção periprotética. Infecções periprotéticas com culturas negativas ocorreram em 23% dos pacientes.

Conclusão

Nossos resultados evidenciam: i) alta prevalência de bactérias do gênero Staphylococcus como causadores da IAP do joelho; ii) a alta incidência de infecções polimicrobianas nas infecções precoces e iii) IAP com culturas negativas ocorre em, aproximadamente, um quarto dos pacientes.

artroplastia do joelho; complicações pós-operatórias; injeções intra-articulares; infecções relacionadas à prótese

Introduction

Periprosthetic joint infection (PJI) represents a severe complication, with an incidence ranging from 1 to 4% after primary arthroplasties. However, this incidence can get up to 5 to 15% in high-risk patients and those undergoing revision surgery. Thus, in many series, PJI is the most significant cause for revision in modern knee arthroplasty.11 Delanois RE, Mistry JB, Gwam CU, Mohamed NS, Choksi US, Mont MA. Current Epidemiology of Revision Total Knee Arthroplasty in the United States. J Arthroplasty 2017;32(09):2663-2668

2 Evangelopoulos DS, Ahmad SS, Krismer AM, et al. Periprosthetic Infection: Major Cause of Early Failure of Primary and Revision Total Knee Arthroplasty. J Knee Surg 2019;32(10):941-946
-33 Meyer JA, Zhu M, Cavadino A, Coleman B, Munro JT, Young SW. Infection and periprosthetic fracture are the leading causes of failure after aseptic revision total knee arthroplasty. Arch Orthop Trauma Surg 2021;141(08):1373-1383

Early diagnosis and pathogen identification are critical for proper treatment and infection eradication. Nevertheless, PJI diagnosis is difficult because of its different clinical presentations and the lack of a single clinical test to confirm or rule out this complication. Thus, since 2011, several societies have proposed criteria to standardize PJI diagnosis.44 McNally M, Sousa R, Wouthuyzen-Bakker M, et al. The EBJIS definition of periprosthetic joint infection. Bone Joint J 2021; 103-B(01):18-25

5 Parvizi J, Tan TL, Goswami K, et al. The 2018 Definition of Periprosthetic Hip and Knee Infection: An Evidence-Based and Validated Criteria. J Arthroplasty 2018;33(05):1309-1314.e2
-66 Schwarz EM, Parvizi J, Gehrke T, et al. 2018 International Consensus Meeting on Musculoskeletal Infection: Research Priorities from the General Assembly Questions. J Orthop Res 2019;37 (05):997-1006

These criteria allow diagnostic confirmation of PJI, even in patients with negative microbiological cultures. However, pathogen identification remains a fundamental principle for treating these infections.55 Parvizi J, Tan TL, Goswami K, et al. The 2018 Definition of Periprosthetic Hip and Knee Infection: An Evidence-Based and Validated Criteria. J Arthroplasty 2018;33(05):1309-1314.e2, 77 Zimmerli W, Trampuz A, Ochsner PE. Prosthetic-joint infections. N Engl J Med 2004;351(16):1645-1654 Thus, this study aims to characterize the microbiological profile of periprosthetic knee infections treated in a Brazilian tertiary hospital.

Material and methods

Study subjects

This study included all patients undergoing revision surgery for total knee arthroplasty (RTKA) from November 2019 to December 2021 with a diagnosis of periprosthetic infection confirmed per the 2018 International Consensus Meeting (ICM) criteria. The Research Ethics Committee approved this research under number 20309419.0.0000.5273. Patients confirmed their participation in the study by signing an informed consent form.

Table 1 shows exclusion criteria.

Table 1
Exclusion criteria

The application of exclusion criteria resulted in a final sample of 62 patients diagnosed with a periprosthetic knee infection.

Surgical procedure and biological sampling

On the day before surgery, we collected peripheral blood from all patients for routine preoperative serological tests, including erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and D-dimer.

All patients underwent spinal anesthesia with a peripheral nerve block. We performed all procedures under ischemia with the pneumatic cuff inflated 100 mm Hg above the systolic blood pressure.

After limb exsanguination and surgical drapes placement, we performed an arthrocentesis with a 20G needle to get synovial fluid (SF) samples. The lack of surgical access or additional local anesthetic block minimized any chance of SF contamination by blood or other agents (►Fig. 1). If SF sampling was not feasible, we performed a second attempt by direct visualization after the medial parapatellar surgical approach.

Fig. 1
Surgical procedure and biological material sampling. (A) Anterior-posterior radiograph of the right knee showing failure of the total knee arthroplasty; (B) Arthrocentesis after sterile drapes placement and before the surgical incision to avoid synovial fluid contamination with blood, (C) Periprosthetic bone tissue sampling for microbiological analysis, (D) Periprosthetic membrane sampling for histopathological analysis.

We placed 1 to 2mL aliquots of SF in vacuum blood collection tubes containing ethylenediaminetetraacetic acid (EDTA). These samples went immediately to the laboratory for a total white cell count and determination of the percentage of polymorphonuclear cells in an Abbott Cell Dyn 3700 SL equipment (Abbott Laboratories, Chicago, IL,USA).

We inoculated 3 to 5 mL aliquots of SF into aerobic blood culture tubes and, if possible, the same amount into anaerobic blood culture tubes. Blood culture tubes were sent immediately for microbiological culture. All samples were cultured for 14 days.

After removing the prosthetic components, we collected the following samples for microbiological analysis: three samples of femoral bone tissue, three samples of tibial bone tissue, and a fragment of the periprosthetic membrane. If the obtention of a periprosthetic membrane fragment was not feasible, we collected a peri-implant soft-tissue sample. For histopathological analysis, we sampled the periprosthetic membranes from the femur and tibia. Antibiotic therapy started only after collecting all biological samples.

We placed the bone fragments in sterile tubes with 1 mL of 0.9% saline solution. The samples went immediately to the laboratory for microbiological cultures. All samples were cultured for 14 days.

For the histopathological examination, we collected one or two periprosthetic membrane fragments and stored them in flasks containing 10% formalin solution. Membrane classification followed the parameters proposed by Morawietz et al.88 Morawietz L, Tiddens O, Mueller M, et al. Twenty-three neutrophil granulocytes in 10 high-power fields is the best histopathological threshold to differentiate between aseptic and septic endopros-thesis loosening. Histopathology 2009;54(07):847-853

Diagnostic definition and group allotment

The following 2018 ICM criteria confirmed PJI diagnosis: i) growth of the same pathogen in two or more periprosthetic tissue cultures, or ii) presence of a fistula. These major criteria are enough for diagnostic confirmation. In addition, a score equal to or greater than 6 confirmed infections per the proposed algorithm (►Table 2).

Table 2
Criteria to diagnose a knee periprosthetic infection

Statistical analysis

Quantitative data, depicted as mean, standard deviation (SD), median, minimum, and maximum values, underwent descriptive analysis. The analysis of categorical variables, expressed as frequencies and percentages, used the chi-squared or Fisher exact test when necessary. We performed all analyses with the Med Calc and GraphPad Prism (Graph-Pad Software Inc., La Jolla, CA, USA) software. Significance was set at a p > 0.05 level.

Results

Study population

Based on clinical data and laboratory tests, we evaluated 84 patients who underwent RTKA for PJI diagnosis per the 2018 ICM criteria. In total, we included 62 patients with PJI in the study. Table 3 summarizes the demographic data from these patients.

Table 3
Demographics distribution

Fig. 2 shows the temporal evaluation (30 days) from infected patients.

Fig. 2
Distribution of patients with acute or chronic periprosthetic infection.

Pathogen identification

The microbiological cultures showed positive results, allowing pathogen identification in 77% (48 patients) of the cases. Cultures were monomicrobial in 79% and polymicrobial in 21% of the subjects. Periprosthetic joint infection with negative cultures occurred in 23% of patients.

We identified gram-negative agents in 24% of the cultures. Considering only monomicrobial infections, 86% of the patients presented gram-positive agents alone and 14% had exclusively gram-negative agents. The most frequent agent in cultures of periprosthetic tissues and SF samples was Staphylococcus aureus, present in 26% of patients with PJI. Fig. 3 reveals the bacteria identified at cultures from PJI patients and their rates.

Fig. 3
Distribution of culture-identified pathogens. S. aureus = S. aureus

When evaluating only patients with positive microbiological cultures, we found out that polymicrobial infections were significantly more frequent in early infections, that is, occurring up to 3 months after surgery, compared with intermediate or late infections (p = 0.02) (►Fig. 4). The distribution of PJI patients with negative cultures was similar in acute, intermediate, and chronic infections.

Fig. 4
Frequency of monomicrobial or polymicrobial infections

Discussion

Although the risk of periprosthetic infection after knee arthroplasty is low, the exponential boost in the amount of TKAs performed annually makes this complication a signifi-cant and increasingly frequent problem.

The 2018 ICM criteria for periprosthetic infection diagnosis allow its confirmation even in the absence of positive cultures. However, pathogen identification remains a fundamental principle for the proper diagnosis and treatment of bacterial diseases, including determining the most appropriate antibiotic agent. A significant issue with microbiological assays is their sensitivity since cultures fail to identify the etiological agent in 5 to 45% of periprosthetic infections.99 Kalbian I, Park JW, Goswami K, Lee YK, Parvizi J, Koo KH. Culture-negative periprosthetic joint infection: prevalence, aetiology, evaluation, recommendations, and treatment. Int Orthop 2020; 44(07):1255-1261

10 TanTL, Kheir MM, Shohat N, et al. Culture-Negative Periprosthetic Joint Infection: An Update on What to Expect. JBJS Open Access 2018;3(03):e0060
-1111 Palan J, Nolan C, Sarantos K, Westerman R, King R, Foguet P. Culture-negative periprosthetic joint infections. EFORT Open Rev 2019;4(10):585-594Negative cultures pose a critical challenge for treating periprosthetic infections since the lack of pathogen identification leads to the empirical use of antimicrobial agents, which may not be active against the actual infectious organism. In addition, they are associated with a 4.5-fold higher risk of reinfection when compared with cases with positive cul-tures.1212 Tarabichi M, Shohat N, Goswami K, et al. Diagnosis of Peripros-thetic Joint Infection: The Potential of Next-Generation Sequencing. J Bone Joint Surg Am 2018;100(02):147-154

13 Drago L, Clerici P, Morelli I, et al. The World Association against Infection in Orthopaedics and Trauma (WAIOT) procedures for Microbiological Sampling and Processing for Periprosthetic Joint Infections (PJIs) and other Implant-Related Infections. J Clin Med 2019;8(07):E933
-1414 Bémer P, LégerJ, Tandé D, et al; Centre de Référence des Infections Ostéo-articulaires du Grand Ouest (CRIOGO) Study Team. How Many Samples and How Many Culture Media To Diagnose a Prosthetic Joint Infection: a Clinical and Microbiological Prospective Multicenter Study. J Clin Microbiol 2016;54(02):385-391 Our findings show the microbiological profile of periprosthetic knee infections treated in a Brazilian tertiary hospital specialized in highly complex orthopedic surgery.

In our series, the most frequently identified pathogen was S. aureus, followed by coagulase-negative Staphylococcus. This finding is consistent with other series, in which these pathogens accounted for 50 to 60% of cases.1515 Tande AJ, Patel R. Prosthetic joint infection. Clin Microbiol Rev 2014;27(02):302-345,1616 Peel TN, Cheng AC, Buising KL, Choong PFM. Microbiological aetiology, epidemiology, and clinical profile of prosthetic joint infections: are current antibiotic prophylaxis guidelines effective? Antimicrob Agents Chemother 2012;56(05):2386-2391 Polymicrobial infections totaled 21% of the cases, especially early infections. Cobo et al.1717 Cobo J, Miguel LG, Euba G, et al. Early prosthetic joint infection: outcomes with debridement and implant retention followed by antibiotic therapy. Clin Microbiol Infect 2011;17(11): 1632-1637 had similar results, with an incidence of 32% of polymicrobial infections in subjects with early PJI. Other studies corroborate this finding, suggesting that this higher frequency of polymicrobial infections in early infections may reflect the inoculation of multiple organisms during surgery or contiguous dissemination from the surgical incision.1515 Tande AJ, Patel R. Prosthetic joint infection. Clin Microbiol Rev 2014;27(02):302-345,1818 Rieber H, Frontzek A, Heinrich S, et al. Microbiological diagnosis of polymicrobial periprosthetic joint infection revealed superiority of investigated tissue samples compared to sonicate fluid generated from the implant surface. Int J Infect Dis 2021;106:302-307,1919 Tsai Y, Chang CH, Lin YC, Lee SH, Hsieh PH, Chang Y. Differentmicrobiological profiles between hip and knee prosthetic joint infections. J Orthop Surg (Hong Kong) 2019;27(02): 2309499019847768

For Tan et al.,1010 TanTL, Kheir MM, Shohat N, et al. Culture-Negative Periprosthetic Joint Infection: An Update on What to Expect. JBJS Open Access 2018;3(03):e0060 the incidence of suspected culture-negative periprosthetic infection was 22%. However, according to the Musculoskeletal Infection Society (MSIS) diagnostic criteria, the incidence of infections with negative cultures was 6.4%. Per the 2018 ICM criteria, the actual rate of periprosthetic infection with negative cultures ranges from 7 to 15%.1111 Palan J, Nolan C, Sarantos K, Westerman R, King R, Foguet P. Culture-negative periprosthetic joint infections. EFORT Open Rev 2019;4(10):585-594 These findings reinforce the importance of differentiating whether periprosthetic infections with negative cultures are actually sterile or a false-negative result, that is, a failure to identify the organism infecting an implant.1111 Palan J, Nolan C, Sarantos K, Westerman R, King R, Foguet P. Culture-negative periprosthetic joint infections. EFORT Open Rev 2019;4(10):585-594

The main factors contributing to a negative culture are the following: (1) administration of antibiotic therapy before culture sampling, (2) using a culture medium inadequate for atypical or biofilm-encapsulated agents, (3) improper sample handling and transportation, (4) inadequate incubation time (especially for rare and indolent agents), (5) a limited number of samples or inadequate tissue collection, (6) delay in transportation to the laboratory, (7) infection by a low virulence organism.99 Kalbian I, Park JW, Goswami K, Lee YK, Parvizi J, Koo KH. Culture-negative periprosthetic joint infection: prevalence, aetiology, evaluation, recommendations, and treatment. Int Orthop 2020; 44(07):1255-1261

10 TanTL, Kheir MM, Shohat N, et al. Culture-Negative Periprosthetic Joint Infection: An Update on What to Expect. JBJS Open Access 2018;3(03):e0060
-1111 Palan J, Nolan C, Sarantos K, Westerman R, King R, Foguet P. Culture-negative periprosthetic joint infections. EFORT Open Rev 2019;4(10):585-594 It is important to emphasize that, unlike in other areas of microbiological diagnosis, there are no standardized culture methods for PJI diagnosis. The 2018 ICM recommends the collection of at least three and ideally five or more peri-implant tissue samples during revision surgeries, in addition to the synovial fluid sample. However, there is no consensus on the type of solid tissue most suitable for conventional cultures. Thus, further studies standardizing culture methods are required to optimize the efficiency of this test.1818 Rieber H, Frontzek A, Heinrich S, et al. Microbiological diagnosis of polymicrobial periprosthetic joint infection revealed superiority of investigated tissue samples compared to sonicate fluid generated from the implant surface. Int J Infect Dis 2021;106:302-307

Approximately one fourth of our patients had a negative biological culture. In these subjects, infection diagnosis was based on other tests from the ICM diagnostic criteria. Studies indicate that surgeons often minimize PJI and perform incomplete assessments for diagnosis confi rmation.2020 Li C, Renz N, Trampuz A, Ojeda-Thies C. Twentycommon errors in the diagnosis and treatment of periprosthetic joint infection. [published correction appears in Int Orthop 2019 Dec 10]Int Orthop 2020;44(01):3-14 In addition, we know that many of these tests are unavailable in Brazilian public hospitals. However, given this scenario, we emphasize the importance of adopting a careful routine to evaluate patients with a persistent exudative wound or a hot, swollen, or painful joint to rule out or confirm PJI diagnosis. This routine would allow for an early diagnosis and more effective treatment.

Limitations of this study include the lack of evaluation of the antibiotic resistance profile of the identified bacteria and the fact that it occurred during the pandemic, which may have impacted the profile of patients treated at our institute.

Conclusion

Our results show i) a high prevalence of Staphylococcus spp. as causes of knee PJI, ii) a high incidence of polymicrobial infections in early cases, and iii) the occurrence of PJI with negative culture in approximately one fourth of the patients.

References

  • 1
    Delanois RE, Mistry JB, Gwam CU, Mohamed NS, Choksi US, Mont MA. Current Epidemiology of Revision Total Knee Arthroplasty in the United States. J Arthroplasty 2017;32(09):2663-2668
  • 2
    Evangelopoulos DS, Ahmad SS, Krismer AM, et al. Periprosthetic Infection: Major Cause of Early Failure of Primary and Revision Total Knee Arthroplasty. J Knee Surg 2019;32(10):941-946
  • 3
    Meyer JA, Zhu M, Cavadino A, Coleman B, Munro JT, Young SW. Infection and periprosthetic fracture are the leading causes of failure after aseptic revision total knee arthroplasty. Arch Orthop Trauma Surg 2021;141(08):1373-1383
  • 4
    McNally M, Sousa R, Wouthuyzen-Bakker M, et al. The EBJIS definition of periprosthetic joint infection. Bone Joint J 2021; 103-B(01):18-25
  • 5
    Parvizi J, Tan TL, Goswami K, et al. The 2018 Definition of Periprosthetic Hip and Knee Infection: An Evidence-Based and Validated Criteria. J Arthroplasty 2018;33(05):1309-1314.e2
  • 6
    Schwarz EM, Parvizi J, Gehrke T, et al. 2018 International Consensus Meeting on Musculoskeletal Infection: Research Priorities from the General Assembly Questions. J Orthop Res 2019;37 (05):997-1006
  • 7
    Zimmerli W, Trampuz A, Ochsner PE. Prosthetic-joint infections. N Engl J Med 2004;351(16):1645-1654
  • 8
    Morawietz L, Tiddens O, Mueller M, et al. Twenty-three neutrophil granulocytes in 10 high-power fields is the best histopathological threshold to differentiate between aseptic and septic endopros-thesis loosening. Histopathology 2009;54(07):847-853
  • 9
    Kalbian I, Park JW, Goswami K, Lee YK, Parvizi J, Koo KH. Culture-negative periprosthetic joint infection: prevalence, aetiology, evaluation, recommendations, and treatment. Int Orthop 2020; 44(07):1255-1261
  • 10
    TanTL, Kheir MM, Shohat N, et al. Culture-Negative Periprosthetic Joint Infection: An Update on What to Expect. JBJS Open Access 2018;3(03):e0060
  • 11
    Palan J, Nolan C, Sarantos K, Westerman R, King R, Foguet P. Culture-negative periprosthetic joint infections. EFORT Open Rev 2019;4(10):585-594
  • 12
    Tarabichi M, Shohat N, Goswami K, et al. Diagnosis of Peripros-thetic Joint Infection: The Potential of Next-Generation Sequencing. J Bone Joint Surg Am 2018;100(02):147-154
  • 13
    Drago L, Clerici P, Morelli I, et al. The World Association against Infection in Orthopaedics and Trauma (WAIOT) procedures for Microbiological Sampling and Processing for Periprosthetic Joint Infections (PJIs) and other Implant-Related Infections. J Clin Med 2019;8(07):E933
  • 14
    Bémer P, LégerJ, Tandé D, et al; Centre de Référence des Infections Ostéo-articulaires du Grand Ouest (CRIOGO) Study Team. How Many Samples and How Many Culture Media To Diagnose a Prosthetic Joint Infection: a Clinical and Microbiological Prospective Multicenter Study. J Clin Microbiol 2016;54(02):385-391
  • 15
    Tande AJ, Patel R. Prosthetic joint infection. Clin Microbiol Rev 2014;27(02):302-345
  • 16
    Peel TN, Cheng AC, Buising KL, Choong PFM. Microbiological aetiology, epidemiology, and clinical profile of prosthetic joint infections: are current antibiotic prophylaxis guidelines effective? Antimicrob Agents Chemother 2012;56(05):2386-2391
  • 17
    Cobo J, Miguel LG, Euba G, et al. Early prosthetic joint infection: outcomes with debridement and implant retention followed by antibiotic therapy. Clin Microbiol Infect 2011;17(11): 1632-1637
  • 18
    Rieber H, Frontzek A, Heinrich S, et al. Microbiological diagnosis of polymicrobial periprosthetic joint infection revealed superiority of investigated tissue samples compared to sonicate fluid generated from the implant surface. Int J Infect Dis 2021;106:302-307
  • 19
    Tsai Y, Chang CH, Lin YC, Lee SH, Hsieh PH, Chang Y. Differentmicrobiological profiles between hip and knee prosthetic joint infections. J Orthop Surg (Hong Kong) 2019;27(02): 2309499019847768
  • 20
    Li C, Renz N, Trampuz A, Ojeda-Thies C. Twentycommon errors in the diagnosis and treatment of periprosthetic joint infection. [published correction appears in Int Orthop 2019 Dec 10]Int Orthop 2020;44(01):3-14
  • *
    Study developed at Instituto Nacional de Traumatología e Ortopedia (INTO), Rio de Janeiro, Brazil.
  • Financial Support: There was no financial support from public, commercial, or nonprofit sources.

Publication Dates

  • Publication in this collection
    24 July 2023
  • Date of issue
    May-Jun 2023

History

  • Received
    18 Apr 2022
  • Accepted
    12 Sept 2022
Sociedade Brasileira de Ortopedia e Traumatologia Al. Lorena, 427 14º andar, 01424-000 São Paulo - SP - Brasil, Tel.: 55 11 2137-5400 - São Paulo - SP - Brazil
E-mail: rbo@sbot.org.br