Significant Difference in Antimicrobial Resistance of Bacteria in Septic Revision between Total Knee Arthroplasty and Total Hip Arthroplasty
by
,
Stella Stevoska
*, 
Felix Himmelbauer
,
Julian Stiftinger
,
Christian Stadler
,
Lorenz Pisecky
,
Tobias Gotterbarm
and
Antonio Klasan
Department for Orthopaedics and Traumatology, Kepler University Hospital GmbH, Johannes Kepler University Linz, Krankenhausstrasse 9, 4020 Linz and Altenberger Strasse 69, 4040 Linz, Austria
*
Author to whom correspondence should be addressed.
Antibiotics 2022, 11(2), 249; https://doi.org/10.3390/antibiotics11020249
Submission received: 25 December 2021
/
Revised: 10 February 2022
/
Accepted: 11 February 2022
/
Published: 14 February 2022
Abstract
:Antimicrobial resistance (AMR) aggravates the already difficult treatment of periprosthetic joint infections (PJI). Due to many factors influencing AMR, the correct choice of antimicrobial management remains arguable. The primary purpose of this retrospective study was to identify and compare bacteria and their antibiotic resistance profile between septic revision total knee arthroplasty (TKA) and septic revision total hip arthroplasty (THA). A review of all revision TKAs and revision THAs, undertaken between 2007 and 2020 in a tertiary referral hospital, was performed. Included were cases meeting the consensus criteria for PJI, in which an organism has been identified. There were no major differences in tissue sampling between revision TKAs and revision THAs over time. A total of 228 bacterial strains, isolated after revision TKA and THA, were analysed for their resistance to 20 different antibiotics. There was a statistically significant higher occurrence of Gram-negative bacteria identified after revision THAs compared to TKA (p = 0.002). The comparison of antibiotic resistance between revision TKAs and revision THAs was statistically significant in 9 of 20 analysed antibiotics. This has implications for the choice of empirical antibiotic in revision surgery as well as prophylactic antibiotic in primary surgery, depending on the joint that is to be replaced.
1. Introduction
The number of patients undergoing total knee arthroplasty (TKA) and total hip arthroplasty (THA) around the world is increasing due to higher life expectancy of the population, and further increase is expected [1,2]. Although the overall incidence of periprosthetic joint infection (PJI) is relatively low, 1% to 2% [3,4,5,6], it remains one of the biggest challenges and represents an enormous economic burden [7,8]. It occurs in approximately 0.97% of primary THA and 1.03% of primary TKA [6]. Eradication of an implant-associated infection is best achieved by a combination of both an appropriate surgical procedure and a prolonged antibiotic treatment, adjusted depending on antimicrobial susceptibility of the pathogen [9]. An emergence of antimicrobial resistance (AMR), especially to antibiotic classes commonly used in PJI, aggravates the already difficult treatment of PJI [3,10].
Antimicrobial resistance (AMR) has become one of the greatest global health issues of the 21st century [11]. It occurs naturally; however, excessive antibiotic use and misuse of antibiotics accelerates the process [12,13,14]. The prevalence of drug-resistant pathogens varies across countries [12,13,14] and changes over time [10,15,16]. Initiatives, such as ResistanceMap (resistancemap.org) and the World Health Organization’s (WHO) Global Antimicrobial Resistance Surveillance System (GLASS), document the geographic trends in antimicrobial resistance [12]. However, not all pathogens commonly isolated in PJI are included yet [12,13,14]. Studies focused on time-varying resistance mostly described an increase in AMR in PJI [15,16].
The most common bacteria causing periprosthetic joint infections are coagulase-negative staphylococci (CNS) in Europe [3,17,18,19,20] and Asia [21] and Staphylococcus aureus in the USA [20]. Additionally, there are microbiological differences reported depending on the joint infected [3,22,23,24]. Polymicrobial infections, anaerobes, and enteric Gram-negative bacteria are more commonly involved in the revision THA than in the revision of TKA [3,22,23,24,25]. In this context, only one study has descriptively compared antibiotic resistance incidence between revision TKA and revision THA [3]. The current literature comparing AMR regarding the joint location, therefore, remains scarce.
The aim of this retrospective clinical study was to identify and compare causative bacteria and to compare the incidence of antibiotic resistance between septic revision TKA and septic revision THA. Additionally, using a cluster analysis, two chronological time periods were created and the antibiotic resistance of the identified bacteria between these two clusters was evaluated.
2. Results
A total of 228 bacterial strains were analysed for their resistance—99 strains were isolated after revision TKA and 129 strains after revision THA. Coagulase-negative staphylococci (CNS) were the most common Gram-positive bacteria as well as the most common causative bacteria in both groups—in 56.6% (56 of 99 cultures) after revision TKAs and in 43.4% (56 of 129 cultures) after revision THAs. There was a statistically significant higher occurrence of Gram-negative bacteria identified after revision THAs compared to TKA (p = 0.002). This difference was mostly influenced by the occurrence of Escherichia coli after revision THAs, in 4.7% (6 of 129 cultures). Additionally, significantly higher occurrence of Gram-positive Enteroccoccus spp. after revision THA was detected (p = 0.026). On the contrary, an occurrence of Streptococcus spp. was significantly higher in revision TKA (p = 0.002) (Table 1).
The resistance occurrence after revision TKAs and THAs was analysed for a total of 20 different antibiotics: ampicillin, cefazolin, cefuroxime, ciprofloxacin, clindamycin, co-trimoxazole, erythromycin, Fosfomycin, fucidin acid, imipenem, levofloxacin, linezolid, moxifloxacin, oxacillin, penicillin, rifampicin, teicoplanin, tetracycline, tigecycline, vancomycin (Table 2).
In both groups, the strains were mostly resistant to penicillins, between 33.8% and 60.7% after revision TKAs and between 51.3% and 68.1% after revision THAs. In the THA group, high resistance was also detected against fluoroquinolones, between 42.6% and 61.9%, and against macrolide and erythromycin in 53.2%. Rifampicin resistance was observed in 22.2% in the THA group and only in 2.0% in the TKA group. There was almost no resistance to glycopeptides, teicoplanin, or vancomycin detected (Table 2).
The most effective antibiotics in the TKA group were glycopeptides-teicoplanin and vancomycin, imipenem, and linezolid, all with fully preserved sensitivity. Other antibiotics with almost entirely preserved sensitivity in the TKA group were tetracyclines and rifampicin (Table 2). Glycopeptides and linezolid were also very effective antibiotics in the THA group, with 98.8% and 98.9% sensitivity, respectively. However, the most sensitive antibiotic in the THA group was tigecycline with completely maintained sensitivity (Table 2).
The comparison of antibiotic resistance between revision TKAs and revision THAs was statistically significant in 9 of 20 analysed antibiotics: oxacillin (p = 0.03), ciprofloxacin (p < 0.001), levofloxacin (p < 0.001), moxifloxacin (p = 0.005), clindamycin (p < 0.001), co-trimoxazole (p < 0.001), imipenem (p = 0.01), rifampicin (p = 0.005), and tetracycline (p = 0.009). The difference in the resistance of strains was not statistically significant for ampicillin, penicillin, cefazolin, cefuroxime, erythromycin, Fosfomycin, fucidin acid, linezolid, tigecycline, teicoplanin, or vancomycin (Table 2).
Gram-positive bacteria isolated after the revision of THA were statistically significantly more resistant to ciprofloxacin (p < 0.001), levofloxacin (p < 0.001), moxifloxacin (p = 0.003), oxacillin (p = 0.03), and rifampicin (p = 0.002) (Table 3). If Gram-negative bacteria were isolated, a susceptibility to fluoroquinolones (ciprofloxacin, moxifloxacin), carbapenem (imipenem), co-trimoxazole, Fosfomycin, and tigecycline was primarily tested. No statistically significant difference in antibiotic resistance of Gram-negative bacteria was observed (Table 4).
3. Discussion
The most common bacteria causing PJI in this study, carried out in a European tertiary referral hospital, were CNS, without any substantial difference between revision TKA and revision THA, 56.6% and 43.4%, respectively. However, the results of the present study show a statistically significantly higher occurrence of Gram-negative bacteria (p = 0.002) and Enterococcus species (p = 0.026) after revision THAs compared to revision TKAs (Table 1). In the present study, a statistically significant difference was detected in 9 of 20 analysed antibiotics. Pathogens isolated after revision THA were much more resistant compared to pathogens isolated after TKA. Resistance in revision THAs was significantly higher to oxacillin (p = 0.03), ciprofloxacin (p < 0.001), levofloxacin (p < 0.001), moxifloxacin (p = 0.005), clindamycin (p < 0.001), co-trimoxazole (p < 0.001), imipenem (p = 0.01), rifampicin (p = 0.005), and tetracycline (p = 0.009). There was no significantly higher resistance of pathogens isolated after revision TKAs detected (Table 2). No statistically significant difference in antibiotic resistance of Gram-negative bacteria between revision TKA and revision THA was observed (Table 4). Additionally, there was a statistically significant increase in antibiotic resistance of pathogens to rifampicin and ciprofloxacin observed (Table 5).
The proportion of detected CNS bacteria detected in the present study is comparable to the results reported in previous European studies, where CNS bacteria represented between 43.4% and 46.6% of isolated pathogens [3,10,15]. Gram-negative bacteria and Enterococcus species, isolated after THA, represent, with 18.6% and 10.9%, respectively, a substantial portion of causative pathogens in this study. Higher prevalence of enteric Gram-negative bacteria in revision THAs PJI may be due to its proximity to the gastrointestinal tract with the colonisation of enteric microorganisms around the hip and inguinal area [22,23].
Few other studies have focused on the comparison of microbiological profiles between revision TKA and revision THA. Tsai et al. [22] reported a statistically significant higher occurrence of anaerobes and polymicrobial pathogens in revision THA. In the present study, the occurrence of anaerobes after revision THA was not statistically significantly higher, however, it showed a greater tendency compared to revision TKA (Table 1). Preobrazhensky et al.’s [26] study also revealed changes in the distribution of microorganisms between revision TKA and revision THA. The proportions of Staphylococcus aureus and CNS were significantly higher in revision TKA and Streptococcus spp. in revision THA. On the contrary, Aggarwal et al. [20] and Drago et al. [3] found no significant differences in the microbiological profile between revision TKA and revision THA within each of their institutions. Nevertheless, Drago et al. [3], observed some differences in antibiotic resistance between revision TKA and revision THA, but did not statistically compare them.
On the other hand, studies regarding AMR differences between pathogens isolated after revision THA and revision TKA are scarce [3]. The present study showed an alarmingly high resistance of pathogens, isolated after revision THA, especially to fluoroquinolones (42.6% to 61.9%), a cornerstone therapy for Gram-negative PJI. The detected resistance to ciprofloxacin (50.5%) was much higher than the resistance recorded from Drago et al. (37.5%). Furthermore, the resistance to ciprofloxacin has statistically significantly increased in recent years (p = 0.03) (Table 5).
Currently, multi drug resistant (MDR) Gram-negative bacteria are on the rise around the globe [27], even in the orthopaedic field [28]. PJI due to Gram-negative pathogens is more difficult to treat and is associated with limited success [25,29]. Therefore, a comparison of the resistance of Gram-negative bacteria isolated after revision THA and revision TKA was additionally performed (Table 4). Resistance to fluoroquinolones, ciprofloxacin, and moxifloxacin, was higher after revision THA, 29.2% and 33.3%, respectively, compared to revision TKA, where no resistance was detected. The higher resistance of Gram-negative bacteria was, however, not statistically significant. Nevertheless, resistance to fluoroquinolones (e.g., ciprofloxacin) raises some concerns. There are still some alternative therapeutic strategies available. As such, there has been a resurgence of old antibiotics (e.g., Fosfomycin) and a development of a variety of new drugs and new drug combinations. Another area of promising research, also in the orthopaedic field, is a resurgence of an older antimicrobial treatment strategy: bacteriophage therapy [27]. In the present study, a low bacterial resistance of Gram-negative bacteria to carbapenems (imipenem), 9.5%, is still maintained. However, the resistance of Gram-negative bacteria to Fosfomycin is high, 66.7% after revision TKA and 38.5% after revision THA (Table 4). Therefore, an alternative therapy with Fosfomycin in the analysed referral hospital, does not seem like a viable option.
As in previous studies [3,10], a relevantly high resistance to the penicillin group of antibiotics was detected (Table 2). Pathogens isolated after THA revision were significantly more resistant to oxacillin/methicillin (p = 0.03), in 51.3%, compared to after TKA revision, in 33.8%. The methicillin resistant bacteria do not respond to cefuroxime, cefazolin or any of the other numerous b-lactam drugs [30,31]. Although a cefuroxime sensitivity seems to be maintained, it was not as commonly tested as oxacillin (Table 2). Therefore, in patients, who are carriers of methicillin resistant bacteria, a prophylactic antibiotic treatment with glycopeptides, such as vancomycin and teicoplanin, can be considered. Both showed maintained susceptibility in revision TKA and revision THA in the present study (Table 2). However, an improper or unnecessary widespread use carries the risk of developing glycopeptide resistance [3,31,32] and is, therefore, not widely supported. Nevertheless, vancomycin use as an empirical antibiotic or as a part of dual empirical antibiotic therapy, at least in revision THA, where methicillin-resistant pathogens seem to be more common, remains reasonable.
Rifampicin, as a biofilm active antibiotic, plays a major role in the treatment of staphylococcal periprosthetic joint infections [4,9,10,33]. A significantly higher resistance to rifampicin after revision THA, 22.2%, compared to resistance of only 2.0% after revision TKA in this referral hospital, is worrying. On the other hand, Drago et al. reported a higher rifampicin resistance after revision TKA (between 12.5% and 30.5%) compared to revision THA (between 10.4% and 21.2%) [3]. The risk of developing rifampicin resistance is known to be high due to its structure and incorrect clinical use [33,34]. Such infections are difficult to eradicate and with statistically significant increasing rifampicin resistance (p = 0.02), as reported in this study, fewer patients with PJI would be able to benefit from orthopaedic implant retention (Table 5).
This study has several limitations. Owing to its retrospective design, there is a collection and selection bias. Due to a wide catchment area, the exact history of each patient could not be accounted for. Any previous surgical or antibiotic treatment that was used outside of in this study investigated institutions is unknown and, therefore, the potential influence of this on the resistance was not reviewed. Additionally, the study was conducted at a single referral hospital, which may cause selection bias. Moreover, there might have been changes in microbiology protocols in the included years unknown to authors of this study. Secondly, polymicrobial pathogens were not excluded and were not separately analysed. Additionally, not every isolated pathogen was tested on every antibiotic included in this study. For example, if Gram-negative bacteria were isolated, a susceptibility to fluoroquinolones, carbapenem, co-trimoxazole, Fosfomycin, and tigecycline was primarily tested. Finally, the study was conducted on the groups of causative pathogens and, therefore, lacking on data about antibiotic resistance of single species.
4. Methods
This retrospective, single-centre cohort study included all revision TKAs and revision THAs undertaken between 2007 and 2020 in a tertiary referral hospital. The study was approved by the University’s Ethics Board (1253/2020). Included were all cases meeting the consensus criteria for PJI, in which an organism has been identified [35]. Retrospective information was collected on the choice of empiric antibiotic treatment and microbiology. The microbiological database was searched for the pathogens detected intraoperatively and for antimicrobial susceptibility testing.
4.1. Surgical Treatment
All patients presenting with possible PJI due to an elevated CRP and/or signs of local inflammation underwent a sterile aspiration of synovial fluid and microbiological analysis. No later than six weeks after the aspiration, the revision procedure was performed. All the revisions were either two-stage or multiple-stage procedures. In the first stage, all components, including cement, if present, were removed and multiple deep intra-operative tissue samples from different areas were obtained. After an aggressive debridement and irrigation, a static or mobile antibiotic-loaded cement spacer was implanted. Systemic antibiotics were administered for six weeks. In patients with low CRP < 20 mg/L and no local signs of infection, the second stage, where new components and renewed postoperative antibiotic therapy were introduced, followed. If there was any suspicion of persistent infection, a repeat debridement with spacer exchange was undertaken. The technique for performing revision TKA and THA for PJI remained the same throughout the study period.
4.2. Microbiology
Routinely, at each stage, at least three tissue samples and one sample of synovial fluid were obtained for culture. Synovial fluid was aseptically inoculated into aerobic and anaerobic blood culture bottles (BACTEC, Beckton Dickinson, Franklin Lakes, NJ, USA) and incubated for 14 days. Tissue samples were obtained from the subfascial tissue and the proximal and distal interfaces of the prosthesis. Each culture was transported, processed, and analysed according to international standards and the definitions of the European Committee on Antimicrobial Susceptibility Testing (EUCAST) [36]. Tissues were inoculated onto Columbia agar, chocolate agar, McConkey agar and Schädler agar and into Brain-Heart-Infusion (BHI) broth. The broth was subcultured the next day. All culture media were incubated for 14 days and inspected every day for bacterial growth. Antibiotic susceptibility testing was performed using the disk-diffusion technique and presented according to the EUCAST criteria that were valid at the time of testing.
Additionally, sonication of the explanted prosthetic components was performed. The explanted components were placed in sterile polypropylene containers and in the laboratory immersed in Ringer’s solution. After 5 min of vigorous manual shaking, explanted prosthetic components were sonicated for 5 min followed by an additional 5 min of vigorous shaking. 500 µL were directly applied onto Columbia agar and Schädler agar. 50 mL of sonication fluid was centrifuged at 3000 U for 5 min. The supernatant was aspirated, and the sediment was inoculated into BHI broth. All culture media were incubated for 14 days and inspected every day for bacterial growth.
Oxacillin resistance was used to classify organisms as resistant to methicillin. There were no major differences in tissue sampling between revision TKAs and revision THAs over time.
4.3. Antibiotic Treatment
The chosen prophylactic antibiotic used before the primary non-revision surgery was a single shot of 1500 mg intravenous cefuroxime. In the case of the history of penicillin and/or cephalosporin hypersensitivity, antibiotic prophylaxis has been adapted accordingly and was usually replaced by a single preoperative shot of clindamycin.
In revision surgery, in case of suspected PJI, an intravenous antibiotic therapy of wide antimicrobial-spectrum was started intraoperatively directly after tissue sampling. The usual empiric preoperative antibiotic therapy used was ampicillin/sulbactam. In septic patients, known MRSA-carriers, or patients with suspected low-grade infection, vancomycin, as a monotherapy or as an addition to ampicillin/sulbactam was usually initiated. Once pathogens were known, and the antimicrobial susceptibility was available, antibiotic therapy was adapted to the resistance situation in collaboration with microbiologists. If possible, rifampicin, effective against biofilm, was added to the treatment in cases of infection with Gram-positive bacteria as soon as the skin wound showed no drainage. In case of resistance to rifampicin, or in the case of isolation of Gram-negative bacteria, a further therapy was determined individually with the microbiologists for each patient.
4.4. Outcome Measures
The main outcome measure of this retrospective study was to identify and compare bacteria and their antibiotic resistance profile between septic revision TKA and septic revision THA. Additionally, using a cluster analysis, two chronological time periods were created and the antibiotic resistance of the identified bacteria between these two clusters was evaluated.
4.5. Statistical Analysis
Data were collected using Microsoft Excel (Redmond, WA, USA) and analysed with SPSS v.24 (IBM, Armonk, New York, NY, USA). The study cohort was described using descriptive statistics. Overall antibiotic resistance was calculated by determining the number of antibiotics to which each culture was sensitive. A formal power analysis using an alfa level of 0.05 and beta level of 0.8 estimated the minimum sample size of at least 15 cultures per group. Antibiotics with insufficient analysis power were excluded. Chronological groups were created using a two-step cluster analysis. First, a hierarchical cluster analysis of the number of cases per year was performed to determine the number of clusters, after which k-means cluster analysis was performed to identify the cases in each cluster. The differences between the groups were analysed using the chi-squared test. A p-value of < 0.05 was considered statistically significant.
5. Conclusions
The occurrence and the resistance of bacteria to antibiotics differs significantly between revision TKAs and revision THAs. Based on these findings, a referral hospital should continuously monitor their microbiological cultures, differentiating between the hips and knees, as this has significant implications on the choice of empirical antibiotic in revision surgery as well as prophylactic antibiotics in primary surgery, depending on the joint that is to be replaced.
Author Contributions
Conceptualization, S.S., T.G. and A.K.; methodology, F.H. and J.S.; validation, C.S.; formal analysis, A.K. and C.S.; investigation F.H. and J.S.; data curation, S.S. and L.P.; writing—original draft preparation, S.S. and F.H.; writing—review and editing, S.S. and A.K.; visualization, L.P.; supervision, A.K. and T.G.; project administration, S.S. and C.S. All authors have read and agreed to the published version of the manuscript.
Funding
This research did not receive any specific grant from funding agencies belonging to the public, commercial, or not-for-profit sectors. Open Access Funding by the University of Linz.
Institutional Review Board Statement
The study was conducted according to the guidelines of the Declaration of Helsinki and has been approved by the Ethics Committee of Johannes Kepler University Linz, Austria, study number 1253/2020.
Informed Consent Statement
Informed consent for study participation was not necessary according to our institution’s guidelines for a retrospective non-interventional study as hereby presented and was waived by the Ethics Committee of Johannes Kepler University Linz, Austria.
Data Availability Statement
The data presented in this study are available upon request from the corresponding author.
Acknowledgments
We would like to thank the Department for Microbiology and Hospital Hygiene for their help with the study. Open Access Funding by the University of Linz.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Leitner, L.; Türk, S.; Heidinger, M.; Stöckl, B.; Posch, F.; Maurer-Ertl, W.; Leithner, A.; Sadoghi, P. Trends and Economic Impact of Hip and Knee Arthroplasty in Central Europe: Findings from the Austrian National Database. Sci. Rep. 2018, 8, 6–10. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Anzahl der Implantationen Künstlicher Hüftgelenke in Ausgewählten OECD-Ländern in den Jahren 2013 bis 2017. Wurden in Deutschland Durchschnittlich, Höchste Rate Derartiger Eingriffe Weltweit. Available online: https://de.statista.com/statistik/daten/studie/182669/umfrage/hueftgelenksoperationen-in-ausgewaehlten-oecd-laendern/#:~:text=2017 (accessed on 15 December 2021).
- Drago, L.; De Vecchi, E.; Bortolin, M.; Zagra, L.; Romanò, C.L.; Cappelletti, L. Epidemiology and Antibiotic Resistance of Late Prosthetic Knee and Hip Infections. J. Arthroplast. 2017, 32, 2496–2500. [Google Scholar] [CrossRef] [PubMed]
- Gehrke, T.; Alijanipour, P.; Parvizi, J. The management of an infected total knee arthroplasty. Bone Jt. J. 2015, 97-B, 20–29. [Google Scholar] [CrossRef] [PubMed]
- Ahmed, S.S.; Haddad, F.S. Prosthetic joint infection. Bone Jt. Res. 2019, 8, 570–572. [Google Scholar] [CrossRef] [PubMed]
- Springer, B.D.; Cahue, S.; Etkin, C.D.; Lewallen, D.G.; McGrory, B.J. Infection burden in total hip and knee arthroplasties: An international registry-based perspective. Arthroplast. Today 2017, 3, 137–140. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Premkumar, A.; Kolin, D.A.; Farley, K.X.; Wilson, J.M.; McLawhorn, A.S.; Cross, M.B.; Sculco, P.K. Projected Economic Burden of Periprosthetic Joint Infection of the Hip and Knee in the United States. J. Arthroplast. 2020, 36, 1484–1489. [Google Scholar] [CrossRef]
- Faschingbauer, M.; Bieger, R.; Kappe, T.; Weiner, C.; Freitag, T.; Reichel, H. Difficult to treat: Are there organism-dependent differences and overall risk factors in success rates for two-stage knee revision? Arch. Orthop. Trauma Surg. 2020, 140, 1595–1602. [Google Scholar] [CrossRef]
- Trampuz, A.; Widmer, A.F. Infections associated with orthopedic implants. Curr. Opin. Infect. Dis. 2006, 19, 349–356. [Google Scholar] [CrossRef]
- Klasan, A.; Schermuksnies, A.; Gerber, F.; Bowman, M.; Fuchs-Winkelmann, S.; Heyse, T.J. Development of antibiotic resistance in periprosthetic joint infection after total knee arthroplasty. Bone Jt. J. 2021, 103-B, 171–176. [Google Scholar] [CrossRef]
- Munita, J.; Arias, C. Mechanisms of antibiotic resistance. Microbiol. Spectr. 2016, 4. [Google Scholar] [CrossRef] [Green Version]
- Frost, I.; Van Boeckel, T.P.; Pires, J.; Craig, J.; Laxminarayan, R. Global geographic trends in antimicrobial resistance: The role of international travel. J. Travel Med. 2019, 26. [Google Scholar] [CrossRef] [PubMed]
- ECDC. Antimicrobial Resistance Tackling the Burden in the European Union. Eur. Cent. Dis. Prev. Control 2019, 1–20. Available online: https://www.oecd.org/health/health-systems/AMR-Tackling-the-Burden-in-the-EU-OECD-ECDC-Briefing-Note-2019.pdf (accessed on 15 December 2021).
- Arrouas, M.; Herzog, U. Resistance Report Austria AURES; Federal Ministry of Health and Women’s Affairs: Wien, Austria, 2018. [Google Scholar]
- Mohanty, S.S.; Kay, P.R. Infection in total joint replacements. J. Bone Jt. Surgery. Br. Vol. 2004, 86, 266–268. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Hu, L.; Fu, J.; Zhou, Y.; Chai, W.; Zhang, G.; Hao, L.; Chen, J. Trends in microbiological profiles and antibiotic resistance in periprosthetic joint infections. J. Int. Med. Res. 2021, 49, 03000605211002784. [Google Scholar] [CrossRef] [PubMed]
- Stefánsdóttir, A.; Johansson, D.; Knutson, K.; Lidgren, L.; Robertsson, O. Microbiology of the infected knee arthroplasty: Report from the Swedish Knee Arthroplasty Register on 426 surgically revised cases. Scand. J. Infect. Dis. 2009, 41, 831–840. [Google Scholar] [CrossRef]
- Nickinson, R.S.J.; Board, T.N.; Gambhir, A.K.; Porter, M.L.; Kay, P.R. The microbiology of the infected knee arthroplasty. Int. Orthop. 2009, 34, 505–510. [Google Scholar] [CrossRef] [Green Version]
- Hickson, C.J.; Metcalfe, D.; Elgohari, S.; Oswald, T.; Masters, J.P.; Rymaszewska, M.; Reed, M.R.; Sprowson, A.P. Prophylactic antibiotics in elective hip and knee arthroplasty: An analysis of organisms reported to cause infections and national survey of clinical practice. Bone Jt. Res. 2015, 4, 181–189. [Google Scholar] [CrossRef] [Green Version]
- Aggarwal, V.; Bakhshi, H.; Ecker, N.U.; Parvizi, J.; Gehrke, T.; Kendoff, D. Organism Profile in Periprosthetic Joint Infection: Pathogens Differ at Two Arthroplasty Infection Referral Centers in Europe and in the United States. J. Knee Surg. 2014, 27, 399–406. [Google Scholar] [CrossRef] [Green Version]
- Gao, Z.; Du, Y.; Piao, S.; Sun, J.; Li, X.; Zhou, Y. Comparison between the Staphylococci aureus and coagulase-negative staphylococci infected total joint arthroplasty treated by two-stage revision: A retrospective study with two year minimum follow-up. J. Orthop. Sci. 2018, 24, 109–115. [Google Scholar] [CrossRef]
- Tsai, Y.; Chang, C.-H.; Lin, Y.-C.; Lee, S.-H.; Hsieh, P.-H.; Chang, Y. Different microbiological profiles between hip and knee prosthetic joint infections. J. Orthop. Surg. 2019, 27, 2309499019847768. [Google Scholar] [CrossRef] [Green Version]
- Tande, A.J.; Patel, R. Prosthetic Joint Infection. Clin. Microbiol. Rev. 2014, 27, 302–345. [Google Scholar] [CrossRef] [Green Version]
- Marculescu, C.E.; Cantey, R.J. Polymicrobial Prosthetic Joint Infections: Risk Factors and Outcome. Clin. Orthop. Relat. Res. 2008, 466, 1397–1404. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Zmistowski, B.; Fedorka, C.J.; Sheehan, E.; Deirmengian, G.; Austin, M.S.; Parvizi, J. Prosthetic Joint Infection Caused by Gram-Negative Organisms. J. Arthroplast. 2011, 26, 104–108. [Google Scholar] [CrossRef] [PubMed]
- Preobrazhensky, P.; Bozhkova, S.; Kochish, A.; Tikhilov, R.; Kazemirsky, A. Comparative analysis of pathogen structure in patients with PJI after primary total hip and knee arthroplasty. Arch. Orthop. Trauma. Surg. 2021, 141, 1963–1969. [Google Scholar] [CrossRef] [PubMed]
- Morris, S.; Cerceo, E. Trends, Epidemiology, and Management of Multi-Drug Resistant Gram-Negative Bacterial Infections in the Hospitalized Setting. Antibiotics 2020, 9, 196. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Benito, N.; Franco, M.; Ribera, A.; Soriano, A.; Rodriguez-Pardo, D.; Sorlí, L.; Fresco, G.; Fernández-Sampedro, M.; Dolores del Toro, M.; Guío, L.; et al. Time trends in the aetiology of prosthetic joint infections: A multicentre cohort study. Clin. Microbiol. Infect. 2016, 22, 732.e1–732.e8. [Google Scholar] [CrossRef] [Green Version]
- Da Silva, R.; Salles, M. Outcomes and Risk Factors in Prosthetic Joint Infections by multidrug-resistant Gram-negative Bacteria: A Retrospective Cohort Study. Antibiotics 2021, 10, 340. [Google Scholar] [CrossRef]
- Campoccia, D.; Montanaro, L.; Arciola, C.R. The significance of infection related to orthopedic devices and issues of antibiotic resistance. Biomaterials 2006, 27, 2331–2339. [Google Scholar] [CrossRef]
- Nodzo, S.R.; Boyle, K.K.; Frisch, N.B. Nationwide Organism Susceptibility Patterns to Common Preoperative Prophylactic Antibiotics: What Are We Covering? J. Arthroplast. 2019, 34, S302–S306. [Google Scholar] [CrossRef]
- Bull, A.L.; Worth, L.J.; Richards, M.J. Impact of Vancomycin Surgical Antibiotic Prophylaxis on the Development of Methicillin-Sensitive Staphylococcus aureus Surgical Site Infections: Report from Australian surveillance data (VICNISS). Ann. Surg. 2012, 256, 1089–1092. [Google Scholar] [CrossRef]
- Livermore, D.M. Antibiotic resistance in staphylococci. Int. J. Antimicrob. Agents 2000, 16, 3–10. [Google Scholar] [CrossRef]
- Achermann, Y.; Eigenmann, K.; Ledergerber, B.; Derksen, L.; Rafeiner, P.; Clauss, M.; Nüesch, R.; Zellweger, C.; Vogt, M.; Zimmerli, W. Factors associated with rifampin resistance in staphylococcal periprosthetic joint infections (PJI): A matched case–control study. Infection 2012, 41, 431–437. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Parvizi, J.; Gehrke, T.; Chen, A.F. Proceedings of the International Consensus on Periprosthetic Joint Infection. Bone Jt. J. 2013, 95-B, 1450–1452. [Google Scholar] [CrossRef] [PubMed]
- Leclercq, R.; Cantón, R.; Brown, D.; Giske, C.; Heisig, P.; MacGowan, A.; Mouton, J.; Nordmann, P.; Rodloff, A.; Rossolini, G.M.; et al. EUCAST expert rules in antimicrobial susceptibility testing. Clin. Microbiol. Infect. 2013, 19, 141–160. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Table 1.
List of bacteria identified in the cultures.
| Bacteria | Occurrence in TKA: n (%) | Occurrence in THA: n (%) | p-Value (Significant < 0.05) |
|---|---|---|---|
| Gram-positive | 94 (94.9) | 105 (81.4) | p = 0.002 |
| CPS | 16 (16.2) | 23 (17.8) | p = 0.740 |
| Staphylococcus aureus | 15 (15.2) | 22 (17.1) | |
| MRSA | 0 | 1 (0.8) | |
| Staphylococcus pseudintermedius | 1 (1.0) | 0 | |
| CNS | 56 (56.6) | 56 (43.4) | p = 0.049 |
| Staphylococcus capitis | 1 (1.0) | 3 (2.3) | |
| Staphylococcus caprae | 1 (1.0) | 0 | |
| Staphylococcus cohnii | 1 (1.0) | 0 | |
| Staphylococcus epidermidis | 42 (42.4) | 42 (32.6) | |
| Staphylococcus haemolyticus | 3 (3.0) | 8 (6.2) | |
| Staphylococcus hominis | 4 (4.0) | 0 | |
| Staphylococcus lugdunensis | 3 (3.0) | 2 (1.6) | |
| Staphylococcus saccharolyticus | 0 | 1 (0.8) | |
| Staphylococcus saprophyticus | 1 (1.0) | 0 | |
| Streptococcus spp. | 13 (13.1) | 3 (2.3) | p = 0.002 |
| Streptococcus agalactiae | 3 (3.0) | 2 (1.6) | |
| Streptococcus gordonii | 1 (1.0) | 0 | |
| Streptococcus oralis | 1 (1.0) | 0 | |
| β-haemolytic streptococci group G | 8 (8.0) | 1 (0.8) | |
| Anaerobes | 3 (3.0) | 9 (7.1) | p = 0.190 |
| Propionibacterium | 3 (3.0) | 6 (4.7) | |
| Cutibacterium acnes | 0 | 1 (0.8) | |
| Finegoldia magna | 0 | 1 (0.8) | |
| Peptostreptococcus magnus | 0 | 1 (0.8) | |
| Enterococcus spp. | 3 (3.0) | 14 (10.9) | p = 0.026 |
| Enterococcus faecalis | 2 (2.0) | 13 (10.1) | |
| Enterococcus faecium | 1 (1.0) | 1 (0.8) | |
| Corynebacterium | 3 (3.0) | 0 | |
| Gram-negative | 5 (5.1) | 24 (18.6) | p = 0.002 |
| Acinetobacter baumannii | 0 | 1 (0.8) | |
| Citrobacter koseri | 0 | 2 (1.6) | |
| Enterobacter cloacae | 2 (2.0) | 3 (2.3) | |
| Escherichia coli | 1 (1.0) | 6 (4.7) | |
| Klebsiella pneumoniae | 0 | 4 (3.1) | |
| Klebsiella variicola | 0 | 1 (0.8) | |
| Morganella morganii | 0 | 2 (1.6) | |
| Pseudomonas aeruginosa | 2 (2.0) | 5 (3.9) | |
| Total number | 99 | 129 |
CPS, coagulase-positive staphylococci; MRSA, methicillin-resistant Staphylococcus aureus; CNS, coagulase-negative staphylococci; n, number; TKA, total knee arthroplasty; THA, total hip arthroplasty.
Table 2.
Antibiotic resistance of 20 different types of antibiotics and its statistical significance, comparing revision TKA and revision THA.
Table 2.
Antibiotic resistance of 20 different types of antibiotics and its statistical significance, comparing revision TKA and revision THA.
| Type of Antibiotic | TKA (n = 99) | THA (n = 129) | p-Value (Significant < 0.05) | ||
|---|---|---|---|---|---|
| S | R | S | R | ||
| Penicillin grp. | |||||
| Ampicillin | 14/30 (46.7%) | 16/30 (53.3%) | 14/35 (40.0%) | 21/35 (60.0%) | 0.751 |
| Oxacillin | 49/74 (66.2%) | 25/74 (33.8%) | 39/80 (48.8%) | 41/80 (51.3%) | 0.03 |
| Penicillin | 35/89 (39.3%) | 54/89 (60.7%) | 29/91 (31.9%) | 62/91 (68.1%) | 0.3 |
| Cephalosporins | |||||
| Cefazolin | 14/21 (66.7%) | 7/21 (33.3%) | 11/17 (64.7%) | 6/17 (35.3%) | 0.270 |
| Cefuroxime | 20/27 (74.1%) | 7/27 (25.9%) | 12/20 (60.0%) | 8/20 (40.0%) | 0.055 |
| Fluoroquinolones | |||||
| Ciprofloxacin | 62/82 (75.6%) | 20/82 (24.4%) | 52/105 (49.5%) | 53/105 (50.5%) | <0.001 |
| Levofloxacin | 24/31 (77.4%) | 7/31 (22.6%) | 24/63 (38.1%) | 39/63 (61.9%) | <0.001 |
| Moxifloxacin | 66/85 (77.7%) | 19/85 (22.3%) | 58/101 (57.4%) | 43/101 (42.6%) | 0.005 |
| Lincosamide | |||||
| Clindamycin | 60/90 (66.7%) | 30/90 (33.3%) | 47/89 (52.8%) | 42/89 (47.2%) | <0.001 |
| Sulfonamide | |||||
| Co-trimoxazole | 32/40 (80.0%) | 8/40 (20.0%) | 59/90 (65.6%) | 31/90 (34.4%) | <0.001 |
| Macrolide | |||||
| Erythromycin | 36/62 (58.1%) | 26/62 (41.9%) | 36/77 (46.8%) | 41/77 (53.2%) | 0.373 |
| Phosphonic acid | |||||
| Fosfomycin | 56/76 (73.7%) | 20/76 (26.3%) | 56/92 (60.9%) | 36/92 (39.1%) | 0.138 |
| Fusidane class | |||||
| Fusidic acid | 57/74 (77.0%) | 17/74 (23.0%) | 60/80 (75.0%) | 20/80 (25.0%) | 0.121 |
| Carbapenem | |||||
| Imipenem | 15/15 (100.0%) | 0/15 (0.0%) | 38/41 (92.7%) | 3/41 (7.3%) | 0.010 |
| Oxazolidinone | |||||
| Linezolid | 63/63 (100.0%) | 0/63 (0.0%) | 88/89 (98.9%) | 1/89 (1.1%) | 0.490 |
| Antimycobacterial | |||||
| Rifampicin | 49/50 (98.0%) | 1/50 (2.0%) | 56/72 (77.8%) | 16/72 (22.2%) | 0.005 |
| Tetracycline grp. | |||||
| Tetracycline | 35/36 (97.2%) | 1/36 (2.8%) | 64/72 (88.9%) | 8/72 (11.1%) | 0.009 |
| Tigecycline | 61/62 (98.4%) | 1/62 (1.6%) | 102/102 (100.0%) | 0/102 (0.0%) | 0.015 |
| Glycopeptides | |||||
| Teicoplanin | 60/60 (100.0%) | 0/60 (0.0%) | 82/83 (98.8%) | 1/83 (1.2%) | 0.590 |
| Vancomycin | 72/72 (100.0%) | 0/72 (0.0%) | 85/86 (98.8%) | 1/86 (1.2%) | 0.403 |
TKA, total knee arthroplasty; THA, total hip arthroplasty; n, number; S, sensitive; R, resistant; grp., group.
Table 3.
Antibiotic resistance of 20 different types of antibiotics to Gram-positive bacteria and its statistical significance, comparing revision TKA and revision THA.
Table 3.
Antibiotic resistance of 20 different types of antibiotics to Gram-positive bacteria and its statistical significance, comparing revision TKA and revision THA.
| Type of Antibiotic | TKA (n = 94) | THA (n = 105) | p-Value (Significant < 0.05) | ||
|---|---|---|---|---|---|
| S | R | S | R | ||
| Ampicillin | 14/27 (51.9%) | 13/27 (48.1%) | 13/17 (76.5%) | 4/17 (23.5%) | 0.10 |
| Oxacillin | 49/74 (66.2%) | 25/74 (33.8%) | 39/80 (48.8%) | 41/80 (51.3%) | 0.03 |
| Penicillin | 35/89 (39.3%) | 54/89 (60.7%) | 29/91 (31.9%) | 62/91 (68.1%) | 0.3 |
| Cefazolin | 14/20 (70.0%) | 6/20 (30%) | 11/17 (64.7%) | 6/17 (35.3%) | 0.73 |
| Cefuroxime | 18/24 (75.0%) | 6/24 (25.0%) | 3/5 (60%) | 2/5 (40%) | 0.49 |
| Ciprofloxacin | 57/77 (74.0%) | 20/77 (15.4%) | 35/81 (43.2%) | 46/81 (56.8%) | <0.001 |
| Levofloxacin | 23/29 (79.3) | 6/29 (20.7%) | 24/63 (38.1%) | 39/63 (61.9%) | <0.001 |
| Moxifloxacin | 65/84 (77.4%) | 19/84 (22.6%) | 46/83 (55.4%) | 37/83 (44.6%) | 0.003 |
| Clindamycin | 60/90 (66.7%) | 30/90 (33.3%) | 47/89 (52.8%) | 42/89 (47.2%) | 0.06 |
| Co-trimoxazole | 30/37 (81.1%) | 7/37 (18.9%) | 46/71 (64.8%) | 25/71 (35.2%) | 0.08 |
| Erythromycin | 36/61 (59.0%) | 25/61 (41.0%) | 36/77 (46.8%) | 41/77 (53.2%) | 0.15 |
| Fosfomycin | 55/73 (75.3%) | 18/73 (24.7%) | 48/79 (60.8%) | 31/79 (39.2%) | 0.06 |
| Fucidin acid | 57/74 (77.0%) | 17/74 (23.0%) | 60/80 (75.0%) | 20/80 (25.0%) | 0.77 |
| Imipenem | 10/10 (100.0%) | 0/10 (0.0%) | 19/20 (95.0%) | 1/20 (5.0%) | 0.47 |
| Linezolid | 62/62 (100.0%) | 0/62 (0.0%) | 88/89 (98.9%) | 1/89 (1.1%) | 0.4 |
| Rifampicin | 48/49 (98.0%) | 1/49 (2.0%) | 56/72 (77.8%) | 16/72 (22.2%) | 0.002 |
| Tetracycline | 34/35 (97.1%) | 1/35 (2.9%) | 64/72 (88.9%) | 8/72 (11.1%) | 0.15 |
| Tigecycline | 60/60 (100.0%) | 0/60 (0.0%) | 89/89 (100.0%) | 0/89 (0.0%) | NA |
| Teicoplanin | 59/59 (100.0%) | 0/59 (0.0%) | 82/83 (98.8%) | 1/83 (1.2%) | NA |
| Vancomycin | 71/71 (100.0%) | 0/71 (0.0%) | 85/86 (98.8%) | 1/86 (1.2%) | 0.36 |
TKA, total knee arthroplasty; THA, total hip arthroplasty; n, number; S, sensitive; R, resistant; NA, not available.
Table 4.
Antibiotic resistance of 20 different types of antibiotics to Gram-negative bacteria and its statistical significance, comparing revision TKA and revision THA.
Table 4.
Antibiotic resistance of 20 different types of antibiotics to Gram-negative bacteria and its statistical significance, comparing revision TKA and revision THA.
| Type of Antibiotic | TKA (n = 5) | THA (n = 24) | p-Value (Significant < 0.05) | ||
|---|---|---|---|---|---|
| S | R | S | R | ||
| Ampicillin | 0/3 (0.0%) | 3/3 (100.0%) | 1/18 (5.6%) | 17/18 (94.4%) | 0.68 |
| Oxacillin | NA | NA | NA | NA | NA |
| Penicillin | NA | NA | NA | NA | NA |
| Cefazolin | 0/1 (0.0%) | 1/1 (100.0%) | NA | NA | NA |
| Cefuroxime | 2/3 (66.7%) | 1/3 (33.3%) | 9/15 (60%) | 6/15 (40%) | 0.83 |
| Ciprofloxacin | 5/5 (100.0%) | 0/5 (0.0%) | 17/24 (70.8%) | 7/24 (29.2%) | 0.17 |
| Levofloxacin | 1/2 (50.0%) | 1/2 (50.0%) | NA | NA | NA |
| Moxifloxacin | 1/1 (100.0%) | 0/1 (0.0%) | 12/18 (66.7%) | 6/18 (33.3%) | 0.49 |
| Clindamycin | NA | NA | NA | NA | NA |
| Co-trimoxazole | 2/3 (66.7%) | 1/3 (33.3%) | 13/19 (68.4%) | 6/19 (31.6%) | 0.95 |
| Erythromycin | 0/1 (0.0%) | 1/1 (100.0%) | NA | NA | NA |
| Fosfomycin | 1/3 (33.3%) | 2/3 (66.7%) | 8/13 (61.5%) | 5/13 (38.5%) | 0.37 |
| Fucidin acid | NA | NA | NA | NA | NA |
| Imipenem | 5/5 (100.0%) | 0/5 (0.0%) | 19/21 (90.5%) | 2/21 (9.5%) | NA |
| Linezolid | 1/1 (100.0%) | 0/1 (0.0%) | NA | NA | NA |
| Rifampicin | 1/1 (100.0%) | 0/1 (0.0%) | NA | NA | NA |
| Tetracycline | 1/1 (100.0%) | 0/1 (0.0%) | NA | NA | NA |
| Tigecycline | 1/2 (50.0%) | 1/2 (50.0%) | 13/13 (100.0%) | 0/13 (0.0%) | 0.01 |
| Teicoplanin | 1/1 (100.0%) | 0/1 (0.0%) | NA | NA | NA |
| Vancomycin | 1/1 (100.0%) | 0/1 (0.0%) | NA | NA | NA |
TKA, total knee arthroplasty; THA, total hip arthroplasty; n, number; S, sensitive; R, resistant; NA, not available.
Table 5.
Antibiotic resistance of 17 different types of antibiotics and the statistical significance, comparing two chronological groups.
Table 5.
Antibiotic resistance of 17 different types of antibiotics and the statistical significance, comparing two chronological groups.
| Type of Antibiotic | 2007–2016 (n = 90) | 2017–2020 (n = 138) | p-Value (Significant < 0.05) | ||
|---|---|---|---|---|---|
| S | R | S | R | ||
| Penicillin grp. | |||||
| Ampicillin | 14/33 (42.4%) | 19/33 (57.6%) | 14/32 (43.8%) | 18/32 (56.2%) | 0.91 |
| Oxacillin | 40/67 (59.7%) | 27/67 (40.3%) | 48/87 (55.2%) | 39/87 (44.8%) | 0.57 |
| Penicillin | 33/81 (40.7%) | 48/81 (59.3%) | 31/99 (31.3%) | 68/99 (68.7%) | 0.19 |
| Cephalosporins | |||||
| Cefuroxime | 21/30 (70.0%) | 9/30 (30.0%) | 11/17 (64.7%) | 6/17 (35.3%) | 0.71 |
| Fluoroquinolones | |||||
| Ciprofloxacin | 51/72 (70.8%) | 21/72 (29.2%) | 63/115 (54.8%) | 52/115 (45.2%) | 0.03 |
| Moxifloxacin | 57/77 (74.0%) | 20/77 (26.0%) | 67/109 (61.5%) | 42/109 (38.5%) | 0.07 |
| Lincosamide | |||||
| Clindamycin | 52/80 (65.0%) | 28/80 (35.0%) | 55/99 (55.6%) | 44/99 (44.4%) | 0.20 |
| Sulfonamide | |||||
| Co-trimoxazole | 20/29 (69.0%) | 9/29 (31.0%) | 71/101 (70.3%) | 30/101 (29.7%) | 0.89 |
| Macrolide | |||||
| Erythromycin | 26/51 (51.0%) | 25/51 (49.0%) | 46/88 (52.3%) | 42/88 (47.7%) | 0.88 |
| Phosphonic acid | |||||
| Fosfomycin | 45/70 (64.3%) | 25/70 (35.7%) | 67/98 (68.4%) | 31/98 (31.4%) | 0.58 |
| Fusidane class | |||||
| Fusidic acid | 53/67 (79.1%) | 14/67 (20.9%) | 64/87 (73.6%) | 23/87 (26.4%) | 0.43 |
| Oxazolidinone | |||||
| Linezolid | 49/49 (100.0%) | 0 | 102/103 (99.0%) | 1 (1.0%) | 0.49 |
| Antimycobacterial | |||||
| Rifampicin | 35/36 (97.2%) | 1/36 (2.8%) | 70/86 (81.4%) | 16/86 (18.6%) | 0.02 |
| Tetracycline grp. | |||||
| Tetracycline | 23/24 (95.8%) | 1/24 (4.2%) | 76/84 (90.5%) | 8/84 (9.5%) | 0.40 |
| Tigecycline | 51/52 (98.1%) | 1 (1.9%) | 112/112 (100.0%) | 0 | 0.14 |
| Glycopeptides | |||||
| Teicoplanin | 48/48 (100.0%) | 0 | 94/95 (99.0%) | 1/95 (1.0%) | 0.48 |
| Vancomycin | 57/57 (100.0%) | 0 | 100/101 (99.0%) | 1/101 (1.0%) | 0.45 |
S, sensitive; R, resistant; n, number; grp., group.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
MDPI and ACS Style
Stevoska, S.; Himmelbauer, F.; Stiftinger, J.; Stadler, C.; Pisecky, L.; Gotterbarm, T.; Klasan, A. Significant Difference in Antimicrobial Resistance of Bacteria in Septic Revision between Total Knee Arthroplasty and Total Hip Arthroplasty. Antibiotics 2022, 11, 249. https://doi.org/10.3390/antibiotics11020249
AMA Style
Stevoska S, Himmelbauer F, Stiftinger J, Stadler C, Pisecky L, Gotterbarm T, Klasan A. Significant Difference in Antimicrobial Resistance of Bacteria in Septic Revision between Total Knee Arthroplasty and Total Hip Arthroplasty. Antibiotics. 2022; 11(2):249. https://doi.org/10.3390/antibiotics11020249
Chicago/Turabian StyleStevoska, Stella, Felix Himmelbauer, Julian Stiftinger, Christian Stadler, Lorenz Pisecky, Tobias Gotterbarm, and Antonio Klasan. 2022. "Significant Difference in Antimicrobial Resistance of Bacteria in Septic Revision between Total Knee Arthroplasty and Total Hip Arthroplasty" Antibiotics 11, no. 2: 249. https://doi.org/10.3390/antibiotics11020249
Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.
