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E. Carlos Rodríguez-Merchán Sam Oussedik Editors T he Infected Total Knee Arthroplasty Prevention, Diagnosis, and Treatment 123 The Infected Total Knee Arthroplasty E. Carlos Rodríguez-Merchán Sam Oussedik Editors The Infected Total Knee Arthroplasty Prevention, Diagnosis, and Treatment Editors E. Carlos Rodríguez-Merchán Sam Oussedik Department of Orthopaedic Surgery University College London Hospitals La Paz University Hospital London Madrid UK Spain ISBN 978-3-319-66729-4 ISBN 978-3-319-66730-0 (eBook) https://doi.org/10.1007/978-3-319-66730-0 Library of Congress Control Number: 2017959149 © Springer International Publishing AG 2018 This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. The use of general descriptive names, registered names, trademarks, service marks, etc. in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. The publisher, the authors and the editors are safe to assume that the advice and information in this book are believed to be true and accurate at the date of publication. Neither the publisher nor the authors or the editors give a warranty, express or implied, with respect to the material contained herein or for any errors or omissions that may have been made. The publisher remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Printed on acid-free paper This Springer imprint is published by Springer Nature The registered company is Springer International Publishing AG The registered company address is: Gewerbestrasse 11, 6330 Cham, Switzerland Preface Patients presenting for total knee arthroplasty (TKA) have one goal in mind— to return to “normal” knee function, however they choose to define this. Postoperative complications are understood to be a risk, but one worth taking for all patients who consent to undergo the procedure. The diagnosis of infection following TKA is devastating and represents the most cruel betrayal of this dream of normal knee function. Both patients and clinicians alike may experience the classical grief response, journeying from denial through anger and guilt to acceptance. Differentiating periprosthetic joint infection (PJI) from other causes of postoperative pain is the surgeon’s first challenge. Infection does not always declare itself overtly and so a knowledge of the latest diagnostic strategies is vital. From this diagnosis flows the appropriate treatment strategy. Here again, risk of failure must be navigated, both in terms of recurrent infection and poor knee function. Unfortunately, while offering the possibility of retaining good function, less invasive procedures also run a greater risk of failing to clear the infection. As with many medical conditions, the key to obtaining a good outcome is rapid diagnosis which then enables the timely deployment of the correct treatment strategy. In the chapters of this book we have collected the current evidence regard- ing the best management of PJI, drawing on the most experienced clinicians in the field from Europe and the United States. It is our hope that our readers will gain the information they need to help their patients achieve their goals. Madrid, Spain E. Carlos Rodríguez-Merchán London, UK Sam Oussedik v Contents 1 Epidemiology of the Infected Total Knee Arthroplasty: Incidence, Causes, and the Burden of Disease . . . . . . . . . . . . . . 1 E. Carlos Rodríguez-Merchán and Alexander D. Liddle 2 Microbiological Concepts of the Infected Total Knee Arthroplasty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11 E. Carlos Rodríguez-Merchán and Alexander D. Liddle 3 Preoperative Optimization to Prevent an Infected Total Knee Arthroplasty: Host Factors . . . . . . . . . . . . . . . . . . . . 19 Sven E. Putnis and Sam Oussedik 4 Depilation and Skin Preparation to Prevent an Infected Total Knee Arthroplasty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31 Carlos Kalbakdij-Sánchez, Gregorio Arroyo- Salcedo, and E. Carlos Rodríguez-Merchán 5 Antibiotic Prophylaxis to Prevent Infection in Total Knee Arthroplasty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35 Alfonso Vaquero-Picado and E. Carlos Rodríguez-Merchán 6 Preoperative Screening and Eradication of Infection . . . . . . . . 47 Alexander D. Liddle and E. Carlos Rodríguez-Merchán 7 Clinical Diagnosis of the Infected Total Knee Arthroplasty . . . 55 Stephen M. Petis and Matthew P. Abdel 8 Diagnosis by Imaging of the Infected Total Knee Arthroplasty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61 Carmen Martín-Hervás and E. Carlos Rodríguez-Merchán 9 Serological Markers of Infection in the Infected Total Knee Arthroplasty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71 Alexander J. Rondon, Timothy L. Tan, and Javad Parvizi 10 The Role of Knee Aspiration in the Infected Total Knee Arthroplasty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79 Juan S. Ruiz-Pérez, Mercedes Agüera-Gavaldá, and E. Carlos Rodríguez-Merchán vii viii Contents 11 Polymerase Chain Reaction (PCR) in the Infected Total Knee Arthroplasty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87 Andrea Volpin and Sujith Konan 12 Histological Diagnosis in the Infected Total Knee Arthroplasty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 97 Paddy Subramanian and Rahul Patel 13 Intraoperative Cultures for the Suspected Total Knee Arthroplasty Infection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 105 Antony C. Raymond and Sam Oussedik 14 Sonication of Removed Implants in the Infected Total Knee Arthroplasty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 117 Enrique Gómez-Barrena and Eduardo García-Rey 15 Antibiotic Suppression in the Infected Total Knee Arthroplasty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 123 José A. García-Ramos García, Alicia Rico-Nieto, and E. Carlos Rodríguez-Merchán 16 Arthroscopic Debridement of Infected Total Knee Arthroplasty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 127 Jonathan Miles and Michael T. Parratt 17 Open Debridement and Polyethylene Exchange (ODPE) in the Infected Total Knee Arthroplasty . . . . . . . . . . . . . . . . . . . 133 Carlos A. Encinas-Ullán, Ángel Martínez-Lloreda, and E. Carlos Rodríguez-Merchán 18 One-Stage Revision Arthroplasty in the Infected Total Knee Arthroplasty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 139 Jurek R.T. Pietrzak, David A. George, and Fares S. Haddad 19 Two-Stage Revision of Infected Total Knee Arthroplasty . . . . . 151 Agustín Garabito-Cociña, Primitivo Gómez-Cardero, and E. Carlos Rodríguez-Merchán 20 Knee Arthrodesis in the Infected Total Knee Arthroplasty . . . 165 Nima Razii, Rahul Kakar, and Rhidian Morgan-Jones 21 Above Knee Amputation in the Treatment of Failed Septic Total Knee Arthroplasty . . . . . . . . . . . . . . . . . . . . . . . . . . 181 E. Carlos Rodríguez-Merchán, Hortensia de la Corte-Rodriguez, and Juan M. Román-Belmonte 1 Epidemiology of the Infected Total Knee Arthroplasty: Incidence, Causes, and the Burden of Disease E. Carlos Rodríguez-Merchán and Alexander D. Liddle Abstract Periprosthetic joint infection (PJI) after total knee arthroplasty (TKA) is a severe complication. The purpose of this chapter is to review the inci- dence, causes, and burden of PJI after TKA. At 30 days, the overall rate of surgical site infection (SSI) is 1.1%, while the reported rate of deep infec- tion is 0.1%. The lifetime incidence of PJI after TKA ranges from 0.7 to 4.6%. Many related and predisposing factors have been identified. These can be classified as preoperative, intraoperative, postoperative, and late infections. The preoperative factors are previous knee surgery, inflamma- tory arthritis, and the use of glucocorticoids and immunosuppressants. The intraoperative factors are prolonged surgical time, inadequate antibiotic prophylaxis, and intraoperative fractures. The postoperative factors are wound drainage for longer than 10 days, reoperation and deep venous thrombosis. Factors related to late infections include cutaneous infections, urinary tract infections, lower respiratory tract infections, abdominal infections, and generalized sepsis. Patients with PJIs have significantly longer hospitalizations (5.3 vs. 3 days), more readmissions (3.6 vs. 0.1), and more clinic visits (6.5 vs. 1.3) when compared to a matched control group. The mean annual cost is significantly higher in patients who have PJIs ($116,383 on average) when compared to the matched control group ($28,249 on average). Hospital costs are between 2- and 24-fold higher in patients with PJI than in those without PJI. PJIs following TKA represent a huge burden for the patient, for the surgeon, and for the health-care economy. E.C. Rodríguez-Merchán (*) A.D. Liddle Department of Orthopaedic Surgery, University College London Institute of Orthopaedics “La Paz” University Hospital-IdiPaz, and Musculoskeletal Science, Royal National Paseo de la Castellana 261, 28046 Orthopaedic Hospital, Brockley Hill, Stanmore, Madrid, Spain Middlesex HA7 4LP, UK e-mail: [email protected] e-mail: [email protected] © Springer International Publishing AG 2018 1 E.C. Rodriguez-Merchan, S. Oussedik (eds.), The Infected Total Knee Arthroplasty, https://doi.org/10.1007/978-3-319-66730-0_1 2 E.C. Rodríguez-Merchán and A.D. Liddle 1.1 Introduction reported rate of 0.67%, meaning that the rate was underestimated by over a third [5]. Similar find- Periprosthetic joint infection (PJI) after total ings were reported by audits of the Danish and knee arthroplasty (TKA) is a severe complication Swedish joint registries with the rates being which has significant personal and financial costs underestimated by 40% and 33%, respectively [6, [1]. In this chapter, we discuss the burden of PJI 7]. Reasons for underreporting may include the worldwide and aim to define the risk factors for fact that some reoperations do not class as revi- the development of PJI following TKA. sion surgery (such as debridement and exchange of modular components) or that revisions for infection are not recognized and are therefore not 1.2 Incidence reported. The most common causative organisms for PJI The development of institutional and national are staphylococci [8, 9], although gram-n egative joint registries has allowed us to define the inci- organisms are becoming more common as are dence and prevalence of PJI with greater accu- multidrug resistant organisms. The incidence of racy than was previously possible. Pugely et al. infection with lower virulence organisms such as [2], in a study of 23,128 joint replacements (pri- propionibacteria may be underreported as they mary and revision total knee and hip arthro- require prolonged incubation periods for cultures plasty), estimated that the rate of surgical site to be isolated [10, 11]. infection (SSI) at 30 days was 1.1%, with the rate of deep infection being 0.1% at the same time point. Infection is now the most common reason 1.3 Risk Factors for Prosthetic for revision in the National Joint Registry for Joint Infection Following England, Wales, and Northern Ireland, reporting TKA a patient-time incidence rate (PTIR) of 1.05 revi- sions for infection per 1000 patient years [3]. Several authors have attempted to delineate the While improvements in implant design, materi- principal risk factors for PJI after TKA. Kunutsor als, and instrumentation have reduced the rate of et al. [12] conducted a meta-analysis examining aseptic loosening and other “technical” compli- risk factors for infection after primary hip and cations, no such improvement has been demon- knee replacement and reported a higher risk of strated in the rate of infection. As a result, the rate PJI in men compared to women and in smokers of revision for infection is increasing relative to compared to nonsmokers. Diabetes, rheumatoid other reasons for revision. It is not clear whether arthritis, corticosteroids, and previous surgery to the absolute rate of PJI is increasing; Dale et al. the joint in question were all reported to increase studied the rate of revision in four Nordic arthro- the risk of PJI as did frailty, but alcohol intake, plasty registers and reported that the risk of PJI age, hypertension, or previous intra-articular ste- increased between 1995 and 2009 in all countries roid injection was not found to be associated [4]. There were no significant changes in risk fac- with PJI. tors during that time period, but the increase may Tayton et al. analyzed data on 64,566 cases simply indicate improvements in diagnosis and from the New Zealand Joint Registry, using revi- reporting. sion surgery for PJI at 6 and 12 months after sur- Overall, however, it is likely that the reported gery as primary outcome measures [13]. Again, rates of infection represent an underestimate. Zhu male gender was a significant risk factor for et al. cross-referenced 4009 records from the infection. Other factors included previous sur- New Zealand Joint Registry with records from gery (osteotomy, ligament reconstruction), the three tertiary hospitals, finding that the rate of use of laminar flow, and the use of antibiotic- revision for infection was 1.1%, compared to the laden cement. There was a trend toward signifi- 1 Epidemiology of the Infected Total Knee Arthroplasty: Incidence, Causes, and the Burden of Disease 3 cance at 6 months with the use of surgical helmet deep infections, the remaining 45 were superficial systems. These findings showed that patient fac- and were treated successfully with antibiotics tors remain the most important in terms of pre- with or without surgical debridement. Six patients dicting early PJI following TKA and suggested required superficial debridement (in all cases the that some factors previously identified as being infection was superficial to the fascia); the mean protective (such as laminar flow and exhaust sys- duration of antibiotic treatment was 16.5 days. At tems) may in fact increase the risk of PJI. Jamsen almost 6 years, 6 patients had died of unrelated et al. [14] analyzed 7181 TKAs and total hip causes, and 3 were revised for other causes; none arthroplasties (THAs) from a single center, find- of the 45 patients had a deep infection [16]. ing an increased risk of PJI with diabetes (odds ratio, OR, 2.3 compared to nondiabetics) and obesity (OR 6.4 in the morbidly obese). Patients 1.3.2 Previous Arthroscopy with both diabetes and morbid obesity had a 10% and Intra-articular Injection rate of PJI. In the study of Pugely et al., risk fac- tors were body mass index (BMI) > 40, hyperten- Werner et al. [17] found that the incidence of sion, prolonged operative time, electrolyte infection was higher in patients who underwent disturbance, and previous infection [2]. TKA within 6 months after knee arthroscopy A number of smaller studies have supported compared to controls. There was no increase in these findings and identified further risk factors. infection when TKA was performed more than 6 De Dios and Cordero [15] performed a case- months after knee arthroscopy. control study comparing 32 consecutive knee Cancienne et al. [18] investigated the associa- infections with 100 matched controls. The signifi- tion between intra-articular injection of glucocor- cant factors were classified as pre-, intra-, or post- ticoids and infection in subsequent ipsilateral operative. Preoperative factors included previous TKA. In patients who had undergone steroid knee surgery, use of glucocorticoids, immunosup- injections less than 3 months prior to surgery, the pressants, and a diagnosis of inflammatory rate of infection was higher than controls at both arthropathy. Intraoperative factors included pro- 3 and 6 months post-TKA (with infection being longed surgical time, inadequate antibiotic pro- twice as likely as controls at 3 months and 50% phylaxis, and intraoperative fracture. Postoperative more likely than in controls at 6). If more than 3 factors included wound drainage longer than months had elapsed between injection and TKA, 10 days, the presence of a hematoma, the need for there was no increased risk of infection compared early reoperations, a diagnosis of deep vein throm- to controls. bosis (DVT), and the presence of distant infections This association was supported by a study of in the skin, respiratory, or urinary tract. In the 83,684 patients, of whom 35% had previously cohort study of Lee et al. [9], significant risk fac- had an ipsilateral injection of corticosteroid [15]. tors included young age and comorbidities such as Those patients who had undergone injection were diabetes, anemia, thyroid disease, heart disease, stratified into 12 groups on the basis of the num- lung disease, and prolonged operating time. ber of months prior to TKA that the injection was performed. The proportion of TKAs who went on to develop PJI was higher in knees that received 1.3.1 Superficial Wound Infection an injection before TKA than in controls (4.4% vs. 3.6%; OR = 1.2, p < 0.001), as were the pro- Properly treated, a superficial postoperative infec- portion who required further surgery for infec- tion should not lead to later deep PJI. Guirro et al. tion (1.49% vs. 1.04%; OR 1.4, p < 0.001). Time [16] reviewed a cohort of 3000 TKAs, 63 of to TKA analysis suggested that the effect of whom were diagnosed with an acute infection. injection remained significant up to 6 months While 18 of these were considered to be acute with respect to any infection and 7 months with

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