Issue
SICOT-J
Volume 7, 2021
Special Issue: "SICOT Education Academy Collection" Guest Editor: H. Said
Article Number 54
Number of page(s) 10
Section Knee
DOI https://doi.org/10.1051/sicotj/2021054
Published online 01 November 2021

© The Authors, published by EDP Sciences, 2021

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Introduction

Total joint arthroplasty is one of the most common orthopedic procedures performed in the United States. More than a million patients undergo total hip and knee arthroplasties (THA and TKA) per year [1]. The statistics are predicted to surge in the coming years [2], and with that, the complications associated with joint replacements. Periprosthetic joint infection (PJI) is one of the most dreadful complications after THA and TKA, its incidence roughly varies between 1% and 2% [3, 4]. From the standpoint of quality of life, infected arthroplasty results in a significant decrease in affected patients when compared to the general population [5]. Even though prevention is of utmost importance in the management of PJI, the first step to solve a problem is always “identification,” and the last decade has seen many remarkable developments in the diagnosis of PJI. These developments include the introduction of several standardized PJI diagnostic definitions from the national scientific societies and organizations [69], and later, biomarkers and better culture techniques [10] to improve the diagnostic capabilities. The second step after identification is “solution,” and depending on the specific clinical situation, treatment options for PJI include irrigation and debridement, one-stage exchange arthroplasty, or two-stage exchange arthroplasty, just to name a few. While two-stage revision has traditionally been the treatment of choice in the United States [11], there has been a growing body of evidence framing one-stage revision as a comparable choice [1214].

Despite the best efforts and advances about the diagnosis and treatment of the infected arthroplasty, there is no gold standard diagnostic test or treatment. The evidence on these subjects is developing incessantly, the evidence is growing. Thus, in our review, our objective is to summarize the pertinent information on the diagnosis of PJI and synthesize literature on the different available treatment methods currently used in clinical practice.

Diagnosis

Over the years, multiple definitions and markers have been proposed to define periprosthetic joint infection. Hereafter, we discuss the most relevant proposed PJI diagnostic criteria and biomarkers used for that purpose.

One of the first and most accepted PJI diagnostic definitions was developed by the Musculoskeletal Infection Society (MSIS) in 2011 [6], which was later modified in the 2013 International Consensus Meeting (ICM) [7]. The application of these criteria require a physical examination, preoperative serum, synovial laboratory tests including cultures, and intraoperative frozen sections with histology. Based on this consensus-based PJI definition (Table 1), the presence of two positive periprosthetic cultures with phenotypically identical organisms, or a sinus tract communicating with the joint, or positive three out of five minor criteria are considered diagnostic of PJI. The minor criteria include: (i) erythrocyte sedimentation rate (ESR) more than 30 mm/h and C-reactive protein (CRP) more than 10 mg/L, (ii) more than 3000 WBCs/μL/positive leukocyte esterase, (iii) polymorphonuclear (PMN)% more than 80%, (iv) one positive culture with the identified organism, and (v) more than five neutrophils per high power field (HPF) in five HPFs on the histologic analysis [7]. It needs to be acknowledged that even if three criteria are not met, PJI might still be existent. In addition, each batch of 3–5 tissue/fluid samples needs to be taken with a different set of sterile instruments. When the required number of criteria are not met, some conclusions could be drawn from the virulence of cultured organisms (if any). If it is a low virulence organism (Corynebacterium, Cutibacterium acnes, or coagulase-negative Staphylococcus), this might not signify PJI. However, if it is a single virulent organism (Staphylococcus aureus), this may characterize infection [7]. The 2013 ICM definition is the most commonly used PJI definition. Nevertheless, this definition has shown poor performance for diagnosing infection in some circumstances [1520]. For instance, in patients with metal-on-metal implants, this criterion is associated with high false-positive results [1517]. In the setting of two-stage revision, the 2013 ICM definition has shown low sensitivity (0–25%) to confirm infection control and predict failure of reimplantation [1820]. Thus, this definition appears to have limited screening capability for infection at the time of reimplantation.

Table 1

2013 International Consensus Meeting (ICM) modified Musculoskeletal Infection Society (MSIS) consensus-based criteria for the diagnosis of periprosthetic joint infection (PJI).

Another set of clinical practice guidelines were proposed by the Infectious Diseases Society of America (IDSA) for PJI diagnosis [8]. According to these recommendations, when a sinus tract communicating with the prosthesis or purulence without any other known cause is present, there is a definitive PJI diagnosis. Further, two or more pre-/intraoperative cultures of the same organism were also deemed as definitive PJI. Similar to the aforementioned ICM definition, a single virulent organism (S. aureus) might represent PJI. Any signs of acute inflammation on histopathologic examination of tissue samples were considered indicative of infection. This set of recommendations have not been investigated in their ability to diagnose PJI as such [8].

Due to low sensitivity to rule out infection using traditional WBC-count and PMN% thresholds (3000/μL and 80%, respectively) in the widely used 2013 ICM definition, several thresholds of WBC-count and PMN% have also been tested to determine improvements in diagnostic accuracy. New thresholds of these markers to detect infection (ranges: WBC-count = 970/μL to 4450/μL, and PMN% = 56–80%) have been proposed with variable sensitivities (ranges: WBC-count = 39.1–92.9%; PMN% = 67–76%) and specificities (ranges: WBC-count = 10–76%; PMN% = 56–80%) [2126].

To improve the PJI diagnostic accuracy, several serum and synovial tests/biomarkers have been investigated [10]. Among the synovial markers, alpha-defensins, CRP, leukocyte esterase, IL-6, IL-1β, and IL-17 have been demonstrated to have high odds ratios in patients with PJI [10]. Out of all these, alpha-defensin has the best ability to diagnose PJI, with 748.3 times more odds of positive test results in patients with infection versus those without it [10]. Several meta-analyses have pooled data from multiple studies to assess the predictive ability of alpha-defensin and leukocyte esterase. The results from three meta-analyses on this subject demonstrated alpha-defensin and leukocyte esterase to pooled PJI diagnostic sensitivities/specificities ranging from 87% to 100%/96% to 97% and 81% to 90%/96% to 97%, respectively [2729]. Overall, both synovial markers seem to have high PJI diagnostic accuracy. Recently, alpha-defensins has been tested against the 2013 ICM and IDSA definitions of PJI. This synovial marker exhibited high specificity of more than 95% (better than both definitions) and sensitivity of 84% (better than 2013 ICM) and IDSA (67%), showing potential as an affirmative rather than a screening test [30]. D-Dimer, a serum-marker, is promising for diagnosing PJI in an initial investigation. Serum D-Dimer threshold of 850 ng/mL demonstrated better sensitivity (89%) and specificity (93%) than ESR and CRP (ESR: 73%/79% and CRP: 78%/80%, respectively) [31]. Notwithstanding, conflicting results have been found with many studies regarding its performance in diagnosing PJI [32, 33].

The search for an actual “gold standard” definition/criteria for PJI diagnosis led to the development of the new PJI diagnostic criteria [9]. With the incorporation of promising diagnostic tests such as synovial alpha-defensin and serum D-Dimer, the new 2018 ICM definition of PJI has been recently proposed (Table 2) [9]. While most previous PJI definitions were consensus-based, this recent definition was evidence-based with a weight-adjusted scoring system for underlying criteria/biomarkers and internal and external validation of the definition in a series of patients. Under this PJI diagnostic definition, two positive cultures of the same organism or a sinus tract communicating with the joint or exposure of the prosthesis are deemed as definitive PJI diagnoses (major criteria). “Minor criteria” includes both preoperative and intraoperative tests/criteria, with a scoring system to define PJI. A total score ≥ 6 represented PJI, a score of 2–5 is indecisive and needs the consideration of intraoperative criteria to confirm/refute infection diagnosis, and a score of 0 or 1 does not define PJI (Table 2). This new definition revealed a sensitivity and specificity of 97.7% and 99.5, respectively. When compared to the 2013 ICM definition, the 2018 definition showed much higher sensitivity (2018 ICM [97.7%] vs. 2013 ICM [86.9%]), even though both had similar specificity [9].

Table 2

The new evidence-based 2018 International Consensus Meeting (ICM) definition for diagnosing periprosthetic joint infection (knee and hips).

Recognizing the fact that the 2018 ICM definition of PJI was supported by only 68% of meeting delegates and also not endorsed by MSIS, yet another most recent PJI definition has been recently proposed by the European Bone and Joint Infection Society (EBJIS) (Table 3) [34]. The EBJIS definition categorizes scenarios into three: infection unlikely, infection likely, and infection confirmed. The details on these categories and their underlying tests have been presented in Table 3. Based on their significance, different tests and their values have been grouped differently [34]. For instance, for “infection unlikely” result, there shall be no positive suggestive or confirmatory test, and for “infection confirmed”, even one positive test under this category can define the presence of infection. The middle category of “infection likely” covers all likelihood situations of infection and when additional investigations should be considered. Of note, even in the case of multiple positive test results under this category, a confirmatory test under “infection confirmed” category is required to establish the diagnosis of PJI [34]. While this new EBJIS is backed by the selective arthroplasty community, its performance remains to be widely investigated in PJI patient populations. It is important to note that the evolution of PJI definitions from 2011, 2013 MSIS to 2018 ICM to the most recent EBJIS definition might confuse surgeons while choosing the right definition in their clinical practice. At the time of this writing, the 2013 MSIS definition is still the most commonly used among surgeons until robust evidence emanates on the superiority of the newly proposed definitions. Each definition has its limitations, and the researchers have tried to improve upon the diagnostic performance over the years.

Table 3

The European Bone and Joint Infection Society (EBJIS) definition for diagnosing periprosthetic joint infection (knee and hips).

One of the oldest diagnostic tests is also important: frozen section (operator-dependent test), which is a minor criterion under various PJI definitions. The performance of intraoperative frozen section in PJI diagnosis has been recently investigated in a meta-analysis of 26 studies with a total of 3269 patients [35]. The frozen section (>5 PMNs per HPF) demonstrated 52.6 times more odds of getting a positive test result in cases with PJI than in those with no PJI. The testing of frozen section against the 2013 ICM criteria showed high specificity of 98.8% and moderate sensitivity of 73.7%, supporting its role as a rule-in or confirmatory test [36].

Treatment (Figure 1)

DAIR

DAIR is an acronym for debridement, antibiotics, and implant retention. While both two-stage and one-stage revision involve the removal and implantation of a new prosthesis, DAIR involves the retention of the implant secured to the bone, with the removal of just polyethylene (PE) insert/liner and all the remaining modular parts followed by a thorough radical debridement, and re-insertion of a new insert/liner. This approach is simple, preserves bone stock, reduces costs, and decreases morbidity compared to the implant exchange revisions [37]. However, the success rate in the setting of PJI is variable. Timing and causing organisms of the infection to seem to impact the outcomes achieved with DAIR. Di Benedetto et al. found this procedure more useful in the setting of early acute or acute, delayed PJIs [38]. With respect to the profile of the infecting organism, DAIR is considered more suitable in the case of early and sensitive Staphylococcal infections (<7 days symptoms or drainage) [39]. However, in PJI, where methicillin-resistant Staphylococcus aureus is the causative organism, this treatment method has been shown to fail in 84% of the cases [40]. While DAIR should not be performed for PJI with organisms like MRSA, delay in treatment until culture results (48 h or more) is debatable. A recent investigation compared the success with DAIR between two timelines: more than two days of symptom onset until cultures versus within two days of symptom onset. DAIR was indicated in these patients based on decision-making algorithms [41]. Bedair et al. did not find any differences and determined DAIR to be successful in only 57% of non-Staphylococcal PJI cases [41]. They found the infecting organism to be a significant predictor of treatment success. While the overall success of this procedure ranges from 20% to 75% in knee PJIs [4244], 80% success rate has been reported in hip PJIs by Rava et al. [45]. The use of systemic antibiotics and long-term chronic oral antibiotic suppression in patients undergoing this procedure has been shown to reduce the failure rates [46]. In the literature, several scoring systems (KLIC and CRIME80 score) have been proposed to predict the success of DAIR in late acute PJIs [47, 48]. These scores are based on preoperative risk factors, including comorbidities, inflammatory markers, type of prosthesis, etc. KLIC-score includes five preoperative risk factors and stands for Kidney (score = 2), Liver (1.5), Index surgery (1.5), Cemented prosthesis (2), and C-reactive protein > 115 mg/L (2.5) [47]. In the study by Tornero et al., patients with KLIC-scores of two and seven had failure rates of 4.5% and 100%, respectively. Beginning at a KLIC score of 4, DAIR success rate is <45% [48]. CRIME80 score is used for hematogenous infections covering seven preoperative risk factors and stands for chronic obstructive pulmonary disease (COPD) (score = 2), CRP > 150 mg/L (1), rheumatoid arthritis (RA) (3), index surgery (following fractures) (3), male (1), polyethylene exchange (−1), and 80 years of age (2). There have been mixed results on their performance. A CRIME-80 score ≥ 3 reduces the probability of surgical success to <40% [48].

thumbnail Figure 1

An algorithm of the management of periprosthetic joint infection (PJI) – acute and chronic.

One-stage revision arthroplasty

In the setting of PJI, even though two-stage revision is the treatment of choice in the United States [11], this is not the only option. The literature reports a mortality rate of 26% at five years in patients undergoing two surgeries in a two-stage revision [49]. This implies that surgeons must consider a single surgery (one-stage revision) as the indicated procedure in a selected group of patients. One stage exchange arthroplasty involves removing the implants, performing a thorough radical debridement, mechanical and chemical disruption of the biofilm, and placing new implants all during the same surgical episode.

While multiple investigations have demonstrated success rates ranging from 75% to 100% for the two-stage treatment [5054], it was determined in the 2013 ICM that the actual success rate (no reinfection, no reoperation/surgical intervention and no adverse mechanical outcome) of this treatment approach was just 65% [55]. On top of that, recent studies have revealed comparable reinfection rates in patients undergoing one-versus two-stage revision with rather a drift towards superior functional clinical outcomes in those who had one-stage procedures [14, 56]. Haddad et al. compared the one-stage and two-stage revision treatments. For 102 chronic knee PJI patients, the authors devised strict selection criteria to indicate one-stage revision. The selection criteria were as follows: minimal-moderate bone loss, absence of immunocompromising conditions, healthy soft tissues (extremity grade 1), and a known organism with known sensitivities for which appropriate antibiotics were available for addition to the cement at the time of reimplantation, and after that, for chronic oral suppression. Not a single one-stage patient developed a recurrent infection, but five two-stage patients had reinfection at a minimum follow-up of three years. Furthermore, one-stage patients had superior knee society scores as compared to those who underwent two-stage treatment [14].

For one-stage revision THA, Singer et al. demonstrated a success rate of 95% on the exclusion of those hips that cultured MRSA [57]. In a recent report, the success rate of 100% for PJI has been demonstrated in the case of one-stage hip and knee revisions [58]. Thus, one-stage revision should be considered in patients who meet strict selection criteria: no sinus tract, proper soft tissue available for wound closure, appropriate bone stock, a favorable identifiable organism with encouraging antibiotic sensitivities (for cement and oral suppression later), and robust immunological status. Since the studies show that the success of repeated revision arthroplasties goes down along the curve to 60%, choosing the right procedure at the time of presentation is the key [14, 56, 59].

Two-stage exchange arthroplasty

Two-stage revision is the treatment of choice for chronic PJI in the United States [11]. This procedure involves surgery in two stages with a time interval between the two. The first stage of two-stage revision comprises the removal of the prosthesis, a thorough irrigation, and debridement, mechanical and chemical disruption of the biofilm, subsequently followed by the insertion of antibiotic-eluding cement spacer (static or articulating) with a new set of clean drapes and instruments. The role of spacers is to maintain the joint space and motion (articulating spacer) while PJI is being treated with antibiotic therapy and until the infection control and subsequent final reimplantation [60]. Overall, articulating spacers have been known to result in a better range of motion and outcomes than the static spacer. Nevertheless, in cases with ligamentous instability, widespread bone loss, or compromised soft tissue coverage, static spacers are a better choice to provide stability, reduced soft tissue tension, and reduced bone loss rate [60]. In addition to preoperative work-up, intraoperative tissue samples are recommended for cultures. It is paramount to give prophylactic antibiotics to the patient before incision, as withholding antibiotics before collecting culture samples has been shown not to increase the likelihood of obtaining positive cultures [61, 62]. After confirmation of infection control, the second stage of two-stage revision involves removing the cement spacer, followed by reimplantation of the new prosthesis. In the time interval between the two stages, antibiotic therapy is indicated for approximately six weeks. In the setting of PJI, mostly parenteral antibiotic therapy is traditionally used [63]. However, studies have shown that transition to oral antibiotic therapy after an initial short course of intravenous antibiotic therapy is effective. In the study by Ascione et al. on 122 PJI patients who underwent two-stage revision, 52 patients received intravenous antibiotic therapy in the entire interim period before reimplantation and 70 patients were administered two weeks of intravenous antibiotic therapy with transition to oral antibiotic therapy in the remaining interim period [64]. They found that the use of oral antibiotics (Odds ratio = 5.3; p = 0.02) was significantly associated with treatment success of two-stage revision [64]. An investigation by Darley et al. in the setting of hip PJIs also found that an early switch from intravenous (for 10–14 days) to oral antibiotics (6–8 weeks) is a viable option [65]. An antibiotic holiday of two weeks is customary before reimplantation, but the evidence is limited to support the need or duration of this period (agreed by 92% delegates in the ICM) [7]. The primary reason is to measure serum ESR, CRP and test synovial fluid for indicators of infection such as WBC counts, PMN%, and to perform cultures [66]. This time-off antibiotics before reimplantation to identify persistent infection has been controversial. A study by Tan et al. on 409 two-stage revisions that were performed after the first stage with no interim procedures with a treatment success rate of 84.4% demonstrated no changes in treatment failure rates with variable duration of antibiotic-free periods (one week, two weeks, four weeks) before reimplantation [67]. On the contrary, on comparing the reimplantations in which continuous antibiotic therapy was instituted versus those in which antibiotic holiday of two weeks was implemented, Ascione et al. determined continuous antibiotic treatment in the interim between the first and second stage as a significant predictor of treatment success (Odds ratio = 3.32; p = 0.02) [68]. Furthermore, they found that compared to the patients who had an antibiotic-free interval before reimplantation, the continuous antibiotic treatment led to a significantly higher treatment success rate in immunocompromised patients (46 patients vs. 31 patients; p = 0.02) [68]. In general, choosing the antibiotic-free interval or not is mostly based on the surgeon’s experience and preference with no one definitive answer.

The importance of the confirmation of infection control before reimplantation cannot be overemphasized. When it comes to accurate criteria or definition to rule out infection at the time of reimplantation, we run out of options due to the low sensitivity (0–25%) of the most accepted 2013 ICM criteria. Due to high specificity, the combination of 2013 ICM criteria and frozen sections are often recommended during reimplantation [18, 69]. Several biomarkers such as alpha defensin have been investigated to confirm infection control. Since alpha defensin has not been validated for diagnosing PJI in patients with cement spacers, its reliability either alone or together with results of preoperative aspiration is questionable to confirm control of infection before reimplantation [70, 71]. The importance of synovial fluid aspiration before reimplantation has been controversial. The chief reason being that these patients on cement spacers (after first stage) have smaller amount of synovial fluid and lower WBC thresholds as compared to standard total joint prosthesis [72]. Thus, not even a single definition/test/criterion is conclusive of infection status to decide the right time of reimplantation in two-stage revision. Clinical examination and varying test combinations, mainly cultures, are used for surgical decision-making at the time of reimplantation.

Two-stage revision might be more appropriate for patients infected with more virulent and/resistant bacteria, soft tissue deficiencies, and reduced bone stock [57]. The bacteria which are difficult to treat (Methicillin-resistant Staphylococcus aureus (MRSA), Enterococcus, or gram-negative bacteria) are associated with a lower rate of infection control after surgery, significantly predictive of surgical failure [73]. Disadvantages of two-stage arthroplasty include increased cost, cement spacer morbidity with decreased quality of life, joint contractures, disuse osteopenia, muscle atrophy, and increased mortality [7477]. Such adverse outcomes should always be discussed with the patient before embarking on such treatment.

In the clinical set-up, there are patients who are either frail as determined by the surgeon or do not want to proceed with the second stage, in these patients, retention of the spacer is an option. In a recent case series, 35 out of 94 patients retained the spacer for more than one year, and 31 out of these 35 patients did not develop a recurrent infection or need any additional surgical intervention at a follow-up of three years [78].

Antibiotic suppression alone

Antibiotic suppression is not a first-line treatment and is offered to PJI patients who have been through multiple unsuccessful revisions and is reserved for those who cannot tolerate another procedure or those who refuse further surgical intervention. Extended oral antibiotics were recently shown to be associated with a significant reduction in failure rate after DAIR (hazard ratio: 2.47) compared to only intravenous antibiotics [79]. The recommended duration of antibiotic administration in patients is variable, but intake beyond one year in knee PJIs was not found to have a significant advantage versus less than one year by Shah et al. [61]. The success of oral antibiotic suppression is also dictated by the type of infecting organism. Leijtens et al. studied 23 patients with hip PJI treated with antibiotic suppressive therapy for a mean duration of 38 months and found the overall failure rate to be 43.5% [80]. In their patient cohort, PJIs with Staphylococcus aureus had a failure rate of 80% compared to 33% in the case of PJI with any other causative organism [80]. In another investigation, Siqueira et al. documented a marked increase in infection-free survival (68.5%) with the use of chronic antibiotic suppression (minimum six months) versus lack thereof (41.1%) in hip or knee PJI patients who underwent irrigation and debridement with polyethylene exchange or two-stage revision [46]. Patients who had irrigation and debridement with polyethylene exchange (64.7%) and those who had PJI caused by S. aureus (57.4%) showed the highest increase in survival with chronic oral antibiotic suppression [46]. With patients put on prolonged antibiotic suppressive therapy for PJI, Prendki et al. conducted a nationwide database study to ascertain the clinical outcomes and adverse events in 136 elderly patients (>75 years of age) with PJI [81]. Out of 136, 25 patients had an adverse drug reaction which led to discontinuation or change of prescription, eight had eventual sepsis, and 13 patients died. The failure-free survival with no event at a follow-up of two years was 61% [81]. It is noteworthy that with infection-free survival reaching 60%, numbers in chronic antibiotic suppression are not far from two-stage revision (true success rate of approximately 65%) [55]. Another study by Sandiford et al. evaluated 26 patients receiving prolonged antibiotic suppression therapy and showed a success rate as high as 84% [82]. In their study, only four patients had an event, two had persistent symptoms and underwent amputation, and two had sepsis successfully managed with intravenous antibiotics [82]. Prolonged suppressive antibiotic therapy seems to be a viable option for selected patients with PJI.

Last resort: resection arthroplasty (girdlestone) or arthrodesis

For a set of patients who develop a recalcitrant periprosthetic joint infection, surgeons unsuccessfully try DAIR or multiple two revisions. However, nothing seems to work in this particular patient population resulting in difficult treatment decision-making. In this circumstance, there are not many salvage options available. Resection arthroplasty (Girdlestone) [83] and arthrodesis [84] are the salvage procedures available. Girdlestone is hardly used nowadays for knee due to resultant poor outcomes and continuing pain. Nevertheless, results from an infection control standpoint in a recent study by Goldman et al. are rather encouraging [85]. They evaluated 25 knees in which resection arthroplasty was performed over four decades with a mean follow-up of four years. Interestingly, at follow-up, 21 out of 25 knees (84%) were infection-free even though all patients required bracing and assistive devices [86]. More than three decades ago, Bourne et al. investigated 33 Girdlestones in the setting of hip PJI at a mean follow-up of 6.2 years and found similar results [86]. While satisfactory pain relief was achieved in 91% of patients and infection control in 97%, limited functional ability (58%), and leg-length discrepancy were the shortcomings. The authors concluded Girdlestone as a reasonable treatment to salvage repeatedly infected arthroplasty resistant to previous approaches [86]. Arthrodesis is another salvage option that can provide more stability and superior functional outcomes versus resection arthroplasty after failed two-stage knee reimplantation [84]. This surgery can be performed with several techniques: external fixation, intramedullary nail, fixation with cannulated screw, and dual plating with locking compression plate [8790]. While infection control and eventual rate of union are not different between external fixation and intramedullary nail fixation [87, 90], external fixation is mostly chosen in patients with PJI [89]. Even the fusion can fail in cases with unremitted infection, and treatment involves explantation of the construct, followed by thorough debridement with insertion of antibiotic spacer. On confirmation of the infection control [91], arthrodesis can be attempted again in these patients [92], even though arthrodesis is a complex procedure [93]. In the worst scenario, if local infection spreads systemically increasing the risk of septic shock or severe soft tissue compromise makes the limb unsalvagable, amputation or hip disarticulation could be indicated. Schwartz et al. evaluated the National Inpatient Sample database to determine factors associated with a higher frequency of hip disarticulation and found age under 65 years without private insurance, diabetes with chronic complications, and peripheral vascular disease as the significant risk factors [94].

Conclusion

In patients with a history of total hip or knee arthroplasty, diligent screening and evaluation are extremely important at the follow-up to achieve an early diagnosis of periprosthetic joint infection. There are many existing PJI diagnostic definitions and markers, the 2013 ICM criteria are the most widely accepted and used criteria for diagnosing an infected arthroplasty. In confirmed infections, two-stage exchange arthroplasty is the treatment of choice in the United States. Encouraging evidence in favor of one-stage revision comes from Europe. This treatment modality is recommended in patients with healthy soft tissues, fair bone stock, and no immunocompromising risk factors. There is a dire need for a randomized controlled trial comparing one- versus two-stage revision, which is already underway in the United States. In a small set of patients in whom no treatment works, and infection recurs after repeated surgeries, salvage procedures are the last resort.

Conflict of interest statement

The work under consideration for publication: no relevant conflicts of interest. Dr. Higuera reports personal fees and others from KCI, PSI, CD Diagnostics, Cymedica, Ferring Pharmaceuticals, Lyfstone, OREF, Orthofix, Inc., Stryker, Zimmer, American Journal of Orthopedics, Journal of Arthroplasty, Journal of Hip Surgery, Journal of Knee Surgery, American Association of Hip and Knee Surgeons, Mid-American Orthopaedic Association, Musculoskeletal Infection Society, and the work submitted outside. Dr. Pannu and Dr. Villa have nothing to disclose.

Funding

This research did not receive any specific funding.

Ethical approval

Ethical approval was not required.

Informed consent

This article does not contain any studies involving human subjects.

Author contributions

Tejbir S. Pannu: Conception/design of the work, writing, revising, final approval of the manuscript.

Jesus M. Villa: Conception/design of the work, writing, revising, final approval of the manuscript.

Carlos A. Higuera: Conception/design of the work, writing, revising, final approval of the manuscript.

Acknowledgments

There are no acknowledgements to disclose.

References

  1. Steiner C, Andrews R, Barrett M, Weiss A (2012) HCUP projections: Mobility/orthopedic procedures 2003 to 2012. HCUP projections report # 2012-03. U.S. Agency for Healthcare Research and Quality. http://hcup-us.ahrq.gov/reports/projections/2012-03.pdf. Accessed 2021 Feb 10. [Google Scholar]
  2. Kurtz S, Ong K, Lau E, Mowat F, Halpern M (2007) Projections of primary and revision hip and knee arthroplasty in the United States from 2005 to 2030. J Bone Joint Surg Am 89(4), 780–785. [CrossRef] [PubMed] [Google Scholar]
  3. Wang FD, Wang YP, Chen CF, Chen HP (2018) The incidence rate, trend and microbiological aetiology of prosthetic joint infection after total knee arthroplasty: A 13 years’ experience from a tertiary medical center in Taiwan. J Microbiol Immunol Infect 51(6), 717–722. [CrossRef] [PubMed] [Google Scholar]
  4. Pulido L, Ghanem E, Joshi A, Purtill JJ, Parvizi J (2008) Periprosthetic joint infection: the incidence, timing, and predisposing factors. Clin Orthop Relat Res 466(7), 1710–1715. [CrossRef] [PubMed] [Google Scholar]
  5. Helwig P, Morlock J, Oberst M, Hauschild O, Hübner J, Borde J, Südkamp NP, Konstantinidis L (2014) Periprosthetic joint infection – effect on quality of life. Int Orthop 38(5), 1077–1081. [CrossRef] [PubMed] [Google Scholar]
  6. Parvizi J, Zmistowski B, Berbari EF, Bauer TW, Springer BD, Della Valle CJ, Garvin KL, Mont MA, Wongworawat MD, Zalavras CG (2011) New definition for periprosthetic joint infection: From the Workgroup of the Musculoskeletal Infection Society. Clin Orthop Relat Res 469, 2992–2994. [CrossRef] [PubMed] [Google Scholar]
  7. Parvizi J, Gehrke T (2014) International Consensus Group on Periprosthetic Joint Infection. Definition of periprosthetic joint infection. J Arthroplasty 29(7), 1331. [CrossRef] [PubMed] [Google Scholar]
  8. Osmon DR, Berbari EF, Berendt AR, Lew D, Zimmerli W, Steckelberg JM, Rao N, Hanssen A, Wilson WR, Infectious Diseases Society of America (2013) Diagnosis and management of prosthetic joint infection: Clinical practice guidelines by the Infectious Diseases Society of America. Clin Infect Dis 56(1), e1–e25. [CrossRef] [PubMed] [Google Scholar]
  9. Parvizi J, Tan TL, Goswami K, Higuera C, Della Valle C, Chen AF, Shohat N (2019) The 2018 definition of periprosthetic hip and knee infection: An evidence-based and validated criteria. J Arthroplasty 33(5), 1309.e2–1314.e2. [Google Scholar]
  10. Saleh A, Ramanathan D, Siqueira MBP, Klika AK, Barsoum WK, Higuera Rueda CA (2017) The diagnostic utility of synovial fluid markers in periprosthetic joint infection: A systematic review and meta-analysis. J Am Acad Orthop Surg 25, 763–772. [CrossRef] [PubMed] [Google Scholar]
  11. Insall JN, Thompson FM, Brause BD (1983) Two-stage reimplantation for the salvage of infected total knee arthroplasty. J Bone Joint Surg Am 65(8), 1087–1098. [CrossRef] [PubMed] [Google Scholar]
  12. Leonard HA, Liddle AD, Burke O, Murray DW, Pandit H (2014) Single- or two-stage revision for infected total hip arthroplasty? A systematic review of the literature. Clin Orthop Relat Res 472(3), 1036–1042. [CrossRef] [PubMed] [Google Scholar]
  13. Bedair H, Ting N, Bozic KJ, Della Valle CJ, Sporer SM (2011) Treatment of early postoperative infections after THA: A decision analysis. Clin Orthop Relat Res 469(12), 3477–3485. [CrossRef] [PubMed] [Google Scholar]
  14. Haddad FS, Sukeik M, Alazzawi S (2015) Is single-stage revision according to a strict protocol effective in treatment of chronic knee arthroplasty infections? Clin Orthop Relat Res 473(1), 8–14. [CrossRef] [PubMed] [Google Scholar]
  15. Wyles CC, Larson DR, Houdek MT, Sierra RJ, Trousdale RT (2019) Utility of synovial fluid aspirations in failed metal-on-metal total hip arthroplasty. J Arthroplasty 28(5), 818–823. [Google Scholar]
  16. Wyles C, Van Demark RE III, Sierra RJ, Trousdale RT (2014) High rate of infection after aseptic revision of failed metal-on-metal total hip arthroplasty. Clin Infect Dis 472(2), 509–516. [Google Scholar]
  17. Judd KT, Noiseux N (2011) Concomitant infection and local metal reaction in patients undergoing revision of metal on metal total hip arthroplasty. Iowa Orthop J 31, 59–63. [PubMed] [Google Scholar]
  18. George J, Kwiecien G, Klika AK, Ramanathan D, Bauer TW, Barsoum WK, Higuera CA (2016) Are frozen sections and MSIS criteria reliable at the time of reimplantation of two-stage revision arthroplasty? Clin Orthop Relat Res 474(7), 1619–1626. [CrossRef] [PubMed] [Google Scholar]
  19. Frangiamore SJ, Siqueira MBP, Saleh A, Daly T, Higuera CA, Barsoum WK (2016) Synovial cytokines and the MSIS criteria are not useful for determining infection resolution after periprosthetic joint infection explantation. Clin Orthop Relat Res 474(7), 1630–1639. [CrossRef] [PubMed] [Google Scholar]
  20. Kheir MM, Ackerman CT, Tan TL, Benazzo A, Tischler EH, Parvizi J (2019) Leukocyte esterase strip test can predict subsequent failure following reimplantation in patients with periprosthetic joint infection. J Arthroplasty 32(6), 1976–1979. [Google Scholar]
  21. Boelch SP, Roth M, Arnholdt J, Rudert M, Luedemann M (2018) Synovial fluid aspiration should not be routinely performed during the two-stage exchange of the knee. Biomed Res Int 2018, 6720712. [PubMed] [Google Scholar]
  22. Hoell S, Moeller A, Gosheger G, Hardes J, Dieckmann R, Schulz D (2016) Two-stage revision arthroplasty for periprosthetic joint infections: What is the value of cultures and white cell count in synovial fluid and CRP in serum before second stage reimplantation? Arch Orthop Trauma Surg 136(4), 447–452. [CrossRef] [PubMed] [Google Scholar]
  23. Newman JM, George J, Klika AK, Hatem SF, Barsoum WK, Trevor North W, Higuera CA (2017) What is the diagnostic accuracy of aspirations performed on hips with antibiotic cement spacers? Clin Orthop Relat Res 475(1), 204–211. Erratum in: Clin Orthop Relat Res, 475(6):1755. [CrossRef] [PubMed] [Google Scholar]
  24. Zmistowski BM, Clyde CT, Ghanem ES, Gotoff JR, Deirmengian CA, Parvizi J (2017) Utility of synovial white blood cell count and differential before reimplantation surgery. J Arthroplasty 32(9), 2820–2824. [CrossRef] [PubMed] [Google Scholar]
  25. Kusuma SK, Ward J, Jacofsky M, Sporer SM, Della Valle CJ (2011) What is the role of serological testing between stages of two-stage reconstruction of the infected prosthetic knee? Clin Orthop Relat Res 469(4), 1002–1008. [CrossRef] [PubMed] [Google Scholar]
  26. Shukla SK, Ward JP, Jacofsky MC, Sporer SM, Paprosky WG, Della Valle CJ (2010) Perioperative testing for persistent sepsis following resection arthroplasty of the hip for periprosthetic infection. J Arthroplasty 25(6 Suppl), 87–91. [Google Scholar]
  27. Wyatt MC, Beswick AD, Kunutsor SK, Wilson MJ, Whitehouse MR, Blom AW (2016) The alpha-defensin immunoassay and leukocyte esterase colorimetric strip test for the diagnosis of periprosthetic infection: A systematic review and meta-analysis. J Bone Joint Surg Am 98(12), 992–1000. [CrossRef] [PubMed] [Google Scholar]
  28. Chen Y, Kang X, Tao J, Zhang Y, Ying C, Lin W (2019) Reliability of synovial fluid alpha-defensin and leukocyte esterase in diagnosing periprosthetic joint infection (PJI): A systematic review and meta-analysis. J Orthop Surg Res 14(1), 453. [CrossRef] [PubMed] [Google Scholar]
  29. Li Z, Zhang Q, Shi L, Gao F, Sun W, Li Z (2020) Alpha-defensin versus leukocyte esterase in periprosthetic joint infection: An updated meta-analysis. Biomed Res Int 2020, 3704285. [PubMed] [Google Scholar]
  30. Renz N, Yermak K, Perka C, Trampuz A (2018) Alpha defensin lateral flow test for diagnosis of periprosthetic joint infection. J Bone Joint Surg Am 100(9), 742–750. [CrossRef] [PubMed] [Google Scholar]
  31. Shahi A, Kheir MM, Tarabichi M, Hosseinzadeh HRS, Tan TL, Parvizi J (2017) Serum D-Dimer test is promising for the diagnosis of periprosthetic joint infection and timing of reimplantation. J Bone Joint Surg Am 99(17), 1419–1427. [CrossRef] [PubMed] [Google Scholar]
  32. Xu H, Xie J, Huang Q, Lei Y, Zhang S, Pei F (2019) Plasma fibrin degradation product and D-Dimer are of limited value for diagnosing periprosthetic joint infection. J Arthroplasty 34(10), 2454–2460. [CrossRef] [PubMed] [Google Scholar]
  33. Pannu TS, Villa JM, Patel PD, Riesgo AM, Barsoum WK, Higuera CA (2020) The utility of serum D-Dimer for the diagnosis of periprosthetic joint infection in revision total hip and knee arthroplasty. J Arthroplasty 35(6), 1692–1695. [CrossRef] [PubMed] [Google Scholar]
  34. McNally M, Sousa R, Wouthuyzen-Bakker M, Chen AF, Soriano A, Vogely HC, Clauss M, Higuera CA, Trebše R (2021) The EBJIS definition of periprosthetic joint infection. Bone Joint J 103-B(1), 18–25. [Google Scholar]
  35. Tsaras G, Maduka-Ezeh A, Inwards CY, Mabry T, Erwin PJ, Murad MH, Montori VM, West CP, Osmon DR, Berbari EF (2012) Utility of intraoperative frozen section histopathology in the diagnosis of periprosthetic joint infection: A systematic review and meta-analysis. J Bone Joint Surg Am 94(18), 1700–1711. [CrossRef] [PubMed] [Google Scholar]
  36. Kwiecien G, George J, Klika AK, Zhang Y, Bauer TW, Rueda CA (2019) Intraoperative frozen section histology: Matched for musculoskeletal infection society criteria. J Arthroplasty 32(1), 223–227. [Google Scholar]
  37. Jiranek WA, Waligora AC, Hess SR, Golladay GL (2015) Surgical treatment of prosthetic joint infections of the hip and knee: Changing paradigms? J Arthroplasty 30(6), 912–918. [CrossRef] [PubMed] [Google Scholar]
  38. Di Benedetto P, Di Benedetto ED, Salviato D, Beltrame A, Gissoni R, Cainero V, Causero A (2017) Acute periprosthetic knee infection: Is there still a role for DAIR? Acta Biomed, 88(2S), 84–91. [PubMed] [Google Scholar]
  39. Odum SM, Fehring TK, Lombardi AV, Zmistowski BM, Brown NM, Luna JT, Fehring KA, Hansen EN (2011) Irrigation and debridement for periprosthetic infections: Does the organism matter? J Arthroplasty 26(6 Suppl), 114–118. [CrossRef] [PubMed] [Google Scholar]
  40. Bradbury T, Fehring TK, Taunton M, Hanssen A, Azzam K, Parvizi J, Odum SM (2009) The fate of acute methicillin-resistant Staphylococcus aureus periprosthetic knee infections treated by open debridement and retention of components. J Arthroplasty 24(6 Suppl), 101–104. [Google Scholar]
  41. Bedair HS, Katakam A, Bedeir YH, Yeroushalmi D, Schwarzkopf R (2020) A decision analysis of treatment strategies for acute periprosthetic joint infection: Early irrigation and debridement versus delayed treatment based on organism. J Orthop 22, 246–250. [CrossRef] [PubMed] [Google Scholar]
  42. Johns BP, Loewenthal MR, Davis JS, Dewar DC (2020) Open debridement is superior to arthroscopic debridement for the infected total knee arthroplasty. J Arthroplasty 35(12), 3716–3723. [CrossRef] [PubMed] [Google Scholar]
  43. Fehring TK, Odum SM, Berend KR, Jiranek WA, Parvizi J, Bozic KJ, Della Valle CJ, Gioe TJ (2013) Failure of irrigation and debridement for early postoperative periprosthetic infection. Clin Orthop Relat Res 471(1), 250–257. [CrossRef] [PubMed] [Google Scholar]
  44. Kunutsor SK, Beswick AD, Whitehouse MR, Wylde V, Blom AW (2018) Debridement, antibiotics and implant retention for periprosthetic joint infections: A systematic review and meta-analysis of treatment outcomes. J Infect 77(6), 479–488. [CrossRef] [PubMed] [Google Scholar]
  45. Rava A, Bruzzone M, Cottino U, Enrietti E, Rossi R (2019) Hip spacers in two-stage revision for periprosthetic joint infection: A review of literature. Joints 7(2), 56–63. [Google Scholar]
  46. Siqueira MB, Saleh A, Klika AK, O’Rourke C, Schmitt S, Higuera CA, Barsoum WK (2015) Chronic suppression of periprosthetic joint infections with oral antibiotics increases infection-free survivorship. J Bone Joint Surg Am 97(15), 1220–1232. [CrossRef] [PubMed] [Google Scholar]
  47. Tornero E, Morata L, Martínez-Pastor JC, Bori G, Climent C, García-Velez DM, García-Ramiro S, Bosch J, Mensa J, Soriano A (2015) KLIC-score for predicting early failure in prosthetic joint infections treated with debridement, implant retention and antibiotics. Clin Microbiol Infect 21(8), 786.e9–786.e17. [CrossRef] [Google Scholar]
  48. Boyer B, Cazorla C (2021) Methods and probability of success after early revision of prosthetic joint infections with debridement, antibiotics and implant retention. Orthop Traumatol Surg Res 107(1S), 102774. [CrossRef] [PubMed] [Google Scholar]
  49. Zmistowski B, Tetreault MW, Alijanipour P, Chen AF, Della Valle CJ, Parvizi J (2013) Recurrent periprosthetic joint infection: Persistent or new infection? J Arthroplasty 28(9), 1486–1489. [CrossRef] [PubMed] [Google Scholar]
  50. Bejon P, Berendt A, Atkins BL, Green N, Parry H, Masters S, McLardy-Smith P, Gundle R, Byren I (2010) Two-stage revision for prosthetic joint infection: Predictors of outcome and the role of reimplantation microbiology. J Antimicrob Chemother 65(3), 569–575. [CrossRef] [PubMed] [Google Scholar]
  51. Biring GS, Kostamo T, Garbuz DS, Masri BA, Duncan CP (2009) Two-stage revision arthroplasty of the hip for infection using an interim articulated Prostalac hip spacer: A 10- to 15-year follow-up study. J Bone Joint Surg Br 91(11), 1431–1437. [PubMed] [Google Scholar]
  52. Chen SY, Hu CC, Chen CC, Chang YH, Hsieh PH (2015) Two-stage revision arthroplasty for periprosthetic hip infection: Mean follow-up of ten years. Biomed Res Int 2015, 345475. [PubMed] [Google Scholar]
  53. Mortazavi SM, Molligan J, Austin MS, Purtill JJ, Hozack WJ, Parvizi J (2011) Failure following revision total knee arthroplasty: Infection is the major cause. Int Orthop 35(8), 1157–1164. [CrossRef] [PubMed] [Google Scholar]
  54. Westrich GH, Walcott-Sapp S, Bornstein LJ, Bostrom MP, Windsor RE, Brause BD (2010) Modern treatment of infected total knee arthroplasty with a 2-stage reimplantation protocol. J Arthroplasty 25(7), 1015–1021, 1021.e1–e2. [CrossRef] [PubMed] [Google Scholar]
  55. Parvizi J, Gehrke T, Chen AF (2013) Proceedings of the International Consensus on Periprosthetic Joint Infection. Bone Joint J 95B(11), 1450–1452. [Google Scholar]
  56. Leonard HA, Liddle AD, Burke O, Murray DW, Pandit H (2014) Single- or two-stage revision for infected total hip arthroplasty? A systematic review of the literature. Clin Orthop Relat Res 472(3), 1036–1042. [CrossRef] [PubMed] [Google Scholar]
  57. Singer J, Merz A, Frommelt L, Fink B (2012) High rate of infection control with one-stage revision of septic knee prostheses excluding MRSA and MRSE. Clin Orthop Relat Res 470(5), 1461–1471. [CrossRef] [PubMed] [Google Scholar]
  58. George DA, Konan S, Haddad FS (2015) Single-stage hip and knee exchange for periprosthetic joint infection. J Arthroplasty 30(12), 2264–2270. [CrossRef] [PubMed] [Google Scholar]
  59. Winkler H, Stoiber A, Kaudela K, Winter F, Menschik F (2008) One stage uncemented revision of infected total hip replacement using cancellous allograft bone impregnated with antibiotics. J Bone Joint Surg Br 90(12), 1580–1584. [PubMed] [Google Scholar]
  60. Limtong J, Pannu TS, Villa JM, Riesgo AM, Higuera CA (2021) Comparison of outcomes between static spacers versus articulating spacers in the setting of revision periprosthetic knee infections: A systematic review. Ann Joint 6, 3. [CrossRef] [Google Scholar]
  61. Burnett RS, Aggarwal A, Givens SA, McClure JT, Morgan PM, Barrack RL (2009) Prophylactic antibiotics do not affect cultures in the treatment of an infected TKA: A prospective trial. Clin Orthop Relat Res 468(1), 127–134. [PubMed] [Google Scholar]
  62. Bedenčič K, Kavčič M, Faganeli N, Mihalič R, Mavčič B, Dolenc J, Bajc Z, Trebše R (2016) Does preoperative antimicrobial prophylaxis influence the diagnostic potential of periprosthetic tissues in hip or knee infections? Clin Orthop Relat Res 474(1), 258–264. [CrossRef] [PubMed] [Google Scholar]
  63. Esposito S, Leone S, Bassetti M, Borrè S, Leoncini F, Meani E, Venditti M, Mazzotta F, Bone Joint Infections Committee for the Italian Society of Infectious Tropical Diseases (SIMIT) (2009) Italian guidelines for the diagnosis and infectious disease management of osteomyelitis and prosthetic joint infections in adults. Infection 37(6), 478–496. [CrossRef] [PubMed] [Google Scholar]
  64. Ascione T, Pagliano P, Balato G, Mariconda M, Rotondo R, Esposito S (2017) Oral therapy, microbiological findings, and comorbidity influence the outcome of prosthetic joint infections undergoing 2-stage exchange. J Arthroplasty 32(7), 2239–2243. [CrossRef] [PubMed] [Google Scholar]
  65. Darley ES, Bannister GC, Blom AW, Macgowan AP, Jacobson SK, Alfouzan W (2011) Role of early intravenous to oral antibiotic switch therapy in the management of prosthetic hip infection treated with one- or two-stage replacement. J Antimicrob Chemother 66(10), 2405–2408. [CrossRef] [PubMed] [Google Scholar]
  66. Ghanem E, Azzam K, Seeley M, Joshi A, Parvizi J (2009) Staged revision for knee arthroplasty infection: what is the role of serologic tests before reimplantation? Clin Orthop Relat Res 467(7), 1699–1705. [CrossRef] [PubMed] [Google Scholar]
  67. Tan TL, Kheir MM, Rondon AJ, Parvizi J, George J, Higuera CA, Shohat N, Chen AF (2018) Determining the role and duration of the “Antibiotic Holiday” period in periprosthetic joint infection. J Arthroplasty 33(9), 2976–2980. [CrossRef] [PubMed] [Google Scholar]
  68. Ascione T, Balato G, Mariconda M, Rotondo R, Baldini A, Pagliano P (2019) Continuous antibiotic therapy can reduce recurrence of prosthetic joint infection in patients undergoing 2-stage exchange. J Arthroplasty 34(4), 704–709. [CrossRef] [PubMed] [Google Scholar]
  69. Bori G, Soriano A, Garcia S, Mallofre C, Riba J, Mensa J (2007) Usefulness of histological analysis for predicting the presence of microorganisms at the time of reimplantation after hip resection arthroplasty for the treatment of infection. J Bone Joint Surg Am 89(6), 1232–1237. [CrossRef] [PubMed] [Google Scholar]
  70. Kanwar S, Al-Mansoori AA, Chand MR, Villa JM, Suarez JC, Patel PD (2018) What is the optimal criteria to use for detecting periprosthetic joint infections before total joint arthroplasty? J Arthroplasty 33(7S), S201–S204. [CrossRef] [PubMed] [Google Scholar]
  71. Samuel LT, Sultan AA, Kheir M, Villa J, Patel P, Parvizi J, Higuera CA (2019) Positive alpha-defensin at reimplantation of a two-stage revision arthroplasty is not associated with infection at 1 year. Clin Orthop Relat Res 477(7), 1615–1621. [CrossRef] [PubMed] [Google Scholar]
  72. Newman JM, George J, Klika AK, Hatem SF, Barsoum WK, Trevor North W, Higuera CA (2016) What is the diagnostic accuracy of aspirations performed on hips with antibiotic cement spacers? Clin Orthop Relat Res 475(1), 204–211. [PubMed] [Google Scholar]
  73. Kurd MF, Ghanem E, Steinbrecher J, Parvizi J (2010) Two-stage exchange knee arthroplasty: Does resistance of the infecting organism influence the outcome? Clin Orthop Relat Res 468(8), 2060–2066. [CrossRef] [PubMed] [Google Scholar]
  74. Parisi TJ, Konopka JF, Bedair HS (2017) What is the long-term economic societal effect of periprosthetic infections after THA? A Markov analysis. Clin Orthop Relat Res 475(7), 1891–1900. [CrossRef] [PubMed] [Google Scholar]
  75. Berend KR, Lombardi AV Jr, Morris MJ, Bergeson AG, Adams JB, Sneller MA (2013) Two-stage treatment of hip periprosthetic joint infection is associated with a high rate of infection control but high mortality. Clin Orthop Relat Res 471(2), 510–518. [CrossRef] [PubMed] [Google Scholar]
  76. Hanssen AD (2002) Managing the infected knee: As good as it gets. J Arthroplasty 17(4 Suppl 1), 98–101. [CrossRef] [PubMed] [Google Scholar]
  77. Fehring TK, Odum S, Calton TF, Mason JB (2000) Articulating versus static spacers in revision total knee arthroplasty for sepsis. The Ranawat Award. Clin Orthop Relat Res 380, 9–16. [CrossRef] [Google Scholar]
  78. Lee KJ, Min BW, Bae KC, Cho CH, Son ES, Lee SW, Lee SJ, Kang MK (2020) Unintended retention of temporary articulating spacers in the treatment of periprosthetic hip joint infection. Orthopedics 43(4), e251–e257. [PubMed] [Google Scholar]
  79. Shah NB, Hersh BL, Kreger A, Sayeed A, Bullock AG, Rothenberger SD, Klatt B, Hamlin B, Urish KL (2020) Benefits and adverse events associated with extended antibiotic use in total knee arthroplasty periprosthetic joint infection. Clin Infect Dis 70(4), 559–565. [CrossRef] [PubMed] [Google Scholar]
  80. Leijtens B, Weerwag L, Schreurs BW, Kullberg BJ, Rijnen W (2019) Clinical outcome of antibiotic suppressive therapy in patients with a prosthetic joint infection after hip replacement. J Bone Jt Infect 4(6), 268–276. [CrossRef] [PubMed] [Google Scholar]
  81. Prendki V, Ferry T, Sergent P, Oziol E, Forestier E, Fraisse T, Tounes S, Ansart S, Gaillat J, Bayle S, Ruyer O, Borlot F, Le Falher G, Simorre B, Dauchy FA, Greffe S, Bauer T, Bell EN, Martha B, Martinot M, Froidure M, Buisson M, Waldner A, Lemaire X, Bosseray A, Maillet M, Charvet V, Barrelet A, Wyplosz B, Noaillon M, Denes E, Beretti E, Berlioz-Thibal M, Meyssonnier V, Fourniols E, Tliba L, Eden A, Jean M, Arvieux C, Guignery-Kadri K, Ronde-Oustau C, Hansmann Y, Belkacem A, Bouchand F, Gavazzi G, Herrmann F, Stirnemann J, Dinh A (2017) Prolonged suppressive antibiotic therapy for prosthetic joint infection in the elderly: A national multicentre cohort study. Eur J Clin Microbiol Infect Dis 36(9), 1577–1585. [CrossRef] [PubMed] [Google Scholar]
  82. Sandiford NA, Hutt JR, Kendoff DO, Mitchell PA, Citak M, Granger L (2020) Prolonged suppressive antibiotic therapy is successful in the management of prosthetic joint infection. Eur J Orthop Surg Traumatol 30(2), 313–321. [CrossRef] [PubMed] [Google Scholar]
  83. Wroblewski BM (1990) Girdlestone pseudarthrosis for a failed total hip arthroplasty. London, Revision Surgery in Total Hip Arthroplasty, Springer, pp. 217–219. [Google Scholar]
  84. Wu CH, Gray CF, Lee GC (2014) Arthrodesis should be strongly considered after failed two-stage reimplantation TKA. Clin Orthop Relat Res 472(11), 3295–3304. [CrossRef] [PubMed] [Google Scholar]
  85. Goldman AH, Clark NJ, Taunton MJ, Lewallen DG, Berry DJ, Abdel MP (2020) Definitive resection arthroplasty of the knee: A surprisingly viable treatment to manage intractable infection in selected patients. J Arthroplasty 35(3), 855–858. [CrossRef] [PubMed] [Google Scholar]
  86. Bourne RB, Hunter GA, Rorabeck CH, Macnab JJ (1984) A six-year follow-up of infected total hip replacements managed by Girdlestone’s arthroplasty. J Bone Joint Surg Br 66(3), 340–343. [CrossRef] [PubMed] [Google Scholar]
  87. Kuo AC, Meehan JP, Lee M (2005) Knee fusion using dual platings with the locking compression plate. J Arthroplasty 20(6), 772–776. [CrossRef] [PubMed] [Google Scholar]
  88. Lim HC, Bae JH, Hur CR, Oh JK, Han SH (2009) Arthrodesis of the knee using cannulated screws. J Bone Joint Surg Br 91(2), 180–184. [PubMed] [Google Scholar]
  89. Van Rensch PJ, Van de Pol GJ, Goosen JH, Wymenga AB, De Man FH (2014) Arthrodesis of the knee following failed arthroplasty. Knee Surg Sports Traumatol Arthrosc 22(8), 1940–1948. [CrossRef] [PubMed] [Google Scholar]
  90. Mabry TM, Jacofsky DJ, Haidukewych GJ, Hanssen AD (2007) Comparison of intramedullary nailing and external fixation knee arthrodesis for the infected knee replacement. Clin Orthop Relat Res 464, 11–15. [CrossRef] [PubMed] [Google Scholar]
  91. Sukeik M, Haddad FS (2019) Periprosthetic joint infections after total hip replacement: An algorithmic approach. SICOT J 5, 5. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  92. Cavadas PC, Thione A, Perez-Garcia A, Lorca-Garcia C, Aranda-Romero F (2014) Salvage of infected intramedullary knee arthrodesis with vascularized free fibula and staged fixation. Injury 45(11), 1772–1775. [CrossRef] [PubMed] [Google Scholar]
  93. Ferry T, Batailler C, Brosset S, Kolenda C, Goutelle S, Sappey-Marinier E, Josse J, Laurent F, Lustig S, Lyon BJI Study Group (2020) Medical innovations to maintain the function in patients with chronic PJI for whom explantation is not desirable: a pathophysiology-, multidisciplinary-, and experience-based approach. SICOT J 6, 26. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  94. Schwartz AJ, Trask DJ, Bews KA, Hanson KT, Etzioni DA, Habermann EB (2020) Hip disarticulation for periprosthetic joint infection: frequency, outcome, and risk factors. J Arthroplasty 35(11), 3269.e3–3273.e3. [Google Scholar]

Cite this article as: Pannu TS, Villa JM & Higuera CA (2021) Diagnosis and management of infected arthroplasty. SICOT-J 7, 54

All Tables

Table 1

2013 International Consensus Meeting (ICM) modified Musculoskeletal Infection Society (MSIS) consensus-based criteria for the diagnosis of periprosthetic joint infection (PJI).

Table 2

The new evidence-based 2018 International Consensus Meeting (ICM) definition for diagnosing periprosthetic joint infection (knee and hips).

Table 3

The European Bone and Joint Infection Society (EBJIS) definition for diagnosing periprosthetic joint infection (knee and hips).

All Figures

thumbnail Figure 1

An algorithm of the management of periprosthetic joint infection (PJI) – acute and chronic.

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