Optimal Timing and Antibiotic Prophylaxis in Periprosthetic Joint Infection: Literature Review and World Consensus (Part Two)

Parvizi, Javad; Ghazavi, Mohammad; Committee of the Consensus Meeting, Members of Pre-Op Antibiotics

doi:10.17795/soj-445

Volume 2, Issue 1 (2-2015) J. Res. Orthop. Sci. 2015, 2(1): 0-0 | Back to browse issues page

‎ 10.17795/soj-445

Mendeley

Zotero

RefWorks

Parvizi J, Ghazavi M, Committee of the Consensus Meeting M O P A. Optimal Timing and Antibiotic Prophylaxis in Periprosthetic Joint Infection: Literature Review and World Consensus (Part Two). J. Res. Orthop. Sci. 2015; 2 (1)
URL: http://jros.iums.ac.ir/article-1-143-en.html

Optimal Timing and Antibiotic Prophylaxis in Periprosthetic Joint Infection: Literature Review and World Consensus (Part Two)

Javad Parvizi

¹, Mohammad Ghazavi²

, Members of Pre-Op Antibiotics Committee of the Consensus Meeting³

1- Rothman Institute, Thomas Jefferson University, Philadelphia, PA, USA
2- Scarborough Hospital, Toronto, Ontario, Canada
3- William Arnold MD PhD; Katherine Belden MD; Goran Bicanic; Stefano Bini MD; Fabio Catani MD; Jiying Chen MD PhD; Mohammad Ghazavi MD FRCSC; Karine M. Godefroy MD; Erik Hansen MD; Paul Holham MD; Hamid Hosseinzadeh MD; Kang II Kim MD; Klaus Kirketerp-Moller MD; Lars Lidgren MD PhD; Jian Hao Lin MD; Jess H Lonner MD; Christopher Moore MD; Panayiotis Papagelopoulos MD; Lazaros Poultsides MD MSc PhD; Khalid Saleh MD MSC FRCSC MHCM; Julia V Salmon MD; Edward Schwarz PhD; Randi Silibovsky MD (US); Jose Stuyck MD; Markus Vogt MD (International); Annette W Dahl MD; Koji Yamada MD

Keywords: Infection, Periprosthetic, Joints, Arthroplasty, Penicillin, Vancomycin

Full-Text [PDF 88 kb] (438 Downloads) | Abstract (HTML) (824 Views)

Full-Text: (335 Views)

Abstract

Results: The choice of antibiotics for patients with preexisting prostheses, such as heart valves, is similar to that for routine elective arthroplasty. Currently, teicoplanin and vancomycin are reasonable alternatives when routine antibiotic prophylaxis cannot be administered. In a patient with a known anaphylactic reaction to penicillin, vancomycin or clindamycin should be administered as prophylaxis. Teicoplanin is an option only in countries where it is available. In a patient with a reported non-anaphylactic reaction to penicillin, a second generation cephalosporin can be used safely, as there is limited cross-reactivity. Penicillin skin testing may be helpful in certain situations to clarify whether the patient has a true penicillin allergy.

Copyright © 2015, Iran University of Medical Sciences. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

1. Context

Decision making in selecting the best choice of antibiotic prophylaxis for periprosthetic joint infection (PJI) is a challenge for all arthroplasty surgeons. There are special situations where routine use of first-generation cephalosporins is not sufficient, appropriate, or it is even contraindicated. In these situations, e.g. patients with prostheses in other parts of their body, such as heart valves or patients who are allergic to penicillin, the best or most effective antibiotic prophylaxis must be chosen. All delegates of the consensus meeting on PJI voted on the following statements regarding the choice of antibiotic prophylaxis in special situations at the time of hip or knee arthroplasties.

2. Evidence Acquisition

From November 2012 until August 2013, 400 delegates from all over the world formed 15 workgroups to review the current literature and find high level evidence for all issues related to PJI. Workgroup No. 3 (authors) was assigned to review the current literature on perioperative antibiotics. The goal was to find answers and recommendations for more than 264 questions, based on the high level evidence, if present, or reach to a consensus, when there is a lack of high level evidence.

After 10 months of hard work by the delegates from 58 countries and 100 societies, relevant publications reviewed and communications exchanged, finally, a draft was prepared to be presented for vote at the final meeting on 1st of August 2013. The draft included recommendations for management on the basis of high level of evidence if present. Otherwise the cumulative wisdom of 400 delegates from 58 countries and over 100 societies used to reach a consensus about practices lacking higher level of evidence.

3. Results

Question 3: What is the choice of antibiotic in patients who have preexisting prostheses, such as heart valves?

Consensus: The choice of antibiotics for patients with preexisting prostheses, such as heart valves, is the same as that for routine elective arthroplasty.

Delegate Vote: Agree: 94%, Disagree: 3%, Abstain: 3% (Strong Consensus)

Justification: Patients with preexisting prostheses, such as heart valves, are at risk for infective endocarditis due to bacteremia, which although is relatively rare, it can lead to catastrophic complications and death. Guidelines for the prevention of infective endocarditis have been published by the American Heart Association (AHA) for more than 50 years. The first nine guidelines (published between 1955 and 1997) were based on low-level evidence; only more recently have the guidelines been stratified based upon the lifetime risk of infective endocarditis. Similar to the change in recommendations regarding dental prophylaxis for patients undergoing total join arthroplasty (TJA), the 2007 antibiotic prophylaxis guidelines for infective endocarditis from the AHA and the Infectious Disease Society of America (IDSA) recommend antibiotic prophylaxis only for patients at the highest risk of infective endocarditis and only for selected dental procedures (e.g. those that involve manipulation of gingival tissue or the periapical region of teeth or perforation of the oral mucosa) (1).

Infections that complicate heart valve replacement and prosthetic joint replacement have several features in common. Staphylococcus aureus (S. aureus) and Staphylococcus epidermidis (S. epidermidis) are common pathogens and infection rates are similar (2, 3). It is generally accepted that antimicrobial prophylaxis reduces the frequency of early postoperative infections; however, when such infections do occur, they are difficult to control without removing the prosthesis. The antibiotics that are recommended for endocarditis prophylaxis are similar to those of prophylaxis against PJI. Also, when an infection is known or suspected to be caused by S. aureus, the antibiotic regimen should contain an antistaphylococcal penicillin or a cephalosporin; whereas vancomycin should be used in those in whom an infection is known or suspected to be caused by methicillin resistant S. aureus (MRSA) (4).

While there is literature to support the use of prophylactic antibiotics for up to 48 hours postoperatively in cardiac surgery, to prevent deep and superficial sternal wound infection, this is not relevant to our discussion of TJA surgery in a patient with a preexisting heart valve (4, 5). Interestingly, there have been several studies showing an increase in the routine use of vancomycin for routine valve surgery prophylaxis over the past years. Haydon et al. reviewed the national practice patterns for antibiotic prophylaxis in cardiac surgery in Australia and found that between 2004 and 2008, there was a doubling in the proportion of cardiac units using vancomycin for routine prophylaxis from 31% to 62% (P <; 0.001) (6).

Question 4: What alternatives are available for routine prophylaxis when cephalosporins are not an option?

Consensus: Currently teicoplanin and vancomycin are reasonable alternatives when routine antibiotic prophylaxis cannot be administered.

Delegate Vote: Agree: 73%, Disagree: 22%, Abstain: 5% (Strong Consensus)

Justification: Teicoplanin has proven to be an effective and safe prophylactic agent in prosthetic implant surgery in Europe, but is not yet available in the US, Canada, or China (7-10). Due to the increased frequency of MRSA and MRSE infections in recent years, the prophylactic use of alternative antibiotics such as glycopeptides (vancomycin and teicoplanin) in hospitals where MRSA/MRSE are prevalent may be justified (11). As vancomycin is more difficult to administer and has a shorter half-life and poorer tolerability profile than teicoplanin, the latter may be a better choice in these settings. Teicoplanin is notable for having a long half-life (70-100 hours), low toxicity, and good tissue penetration, which allows it to achieve therapeutic concentrations in bone and surrounding soft tissues (11-13).

Ceftaroline (fifth generation cephalosporin) has the same spectrum of activity as ceftriaxone with additional MRSA activity. The US Food and Drug Administration and the European Medicines Agency have provided indications for the use of ceftaroline for treatment of complicated skin and soft tissue infections only, and not for prophylaxis.

In one multicenter Randomized Controlled Trial (RCT), Periti et al. compared the administration of a single dose of teicoplanin (400 mg intravenous (IV) bolus at time of anesthesia) versus that of five doses of cefazolin over a 24 hours period (2 g at induction and 1 g every 6 hours postoperatively) as prophylaxis in patients undergoing TJA. They randomized 846 patients and noted that six patients (1.5%) in the teicoplanin group and seven patients (1.7%) in the cefazolin group developed a surgical wound infection during their hospital stay, which was a non-significant difference. Additionally, an insignificant difference in adverse events was recorded in the two groups, with three (0.7%) of the teicoplanin patients and nine (2.1%) of the cefazolin patients (10).

Question 5A: What antibiotic should be administered in a patient with a known anaphylactic penicillin allergy?

Consensus: In a patient with a known anaphylactic reaction to penicillin, vancomycin or clindamycin should be administered as prophylaxis. Teicoplanin is an option in countries where it is available.

Delegate Vote: Agree: 88%, Disagree: 10%, Abstain: 2% (Strong Consensus)

Question 5B: What antibiotic should be administered in a patient with a known non-anaphylactic penicillin allergy?

Consensus: In a patient with a reported non-anaphylactic reaction to penicillin, a second generation cephalosporin can be used safely, as there is limited cross-reactivity. Penicillin skin testing may be helpful in certain situations to clarify whether the patient has a true penicillin allergy.

Delegate Vote: Agree: 87%, Disagree: 9%, Abstain: 4% (Strong Consensus)

Justification: When patients present with a penicillin allergy, further information should be obtained to determine whether an immunoglobulin E (IgE)-mediated response (anaphylaxis) occurred. In patients with a documented IgE-mediated response to penicillin, third and fourth generation cephalosporins can be used. First and second generation cephalosporins with R1 side chains, similar to that of penicillin (cefaclor, cefadroxil, cefatrizine, cefprozil, cephalexin, or cephradine) should be avoided; first and second generation cephalosporins with different R1 side chains can be prescribed.

Vancomycin and clindamycin are recommended as alternative agents for patients who have a true type I β-lactam allergy, manifested by immediate urticaria, laryngeal edema, or bronchospasm (14). Clindamycin is the preferred alternative for persons with an established β-lactam allergy or with contraindications to its use and at institutions with low rates of MRSA infection. Clindamycin has good bioavailability and at 30 minutes after infusion has been shown to exceed the MICs for S. aureus in both animal and human cortical bone samples (15). However, clindamycin is a bacteriostatic agent. In addition, vancomycin alone has a relatively poor activity against S. aureus and clinical studies suggest that vancomycin, as prophylaxis alone, increases the risk for surgical site infection (SSI). Therefore, a second agent should be considered (levofloxacin, moxifloxacin) in addition to vancomycin (16).

Cross-reactivity between penicillin and cephalosporin is overestimated and much lower than reported in earlier studies. The 10% risk estimate of for allergic reactions to cephalosporins in penicillin-allergic patients is based on data collected and reviewed in the 1960s and 1970s. It is due, in large part, to the widely referenced reviews of Dash and Petz, which reported allergic reactions in 7.7% and 8.1%, respectively, of penicillin-allergic patients (allergy was based on patient history) and only included first generation cephalosporins and second generation cefamandole (17, 18). The high cross-reactivity found in earlier studies may be due, in part, to the contamination of the study drugs with penicillin during the manufacturing process (19). Moreover, the authors of the early studies had a broader definition of allergy and did not account for the fact that penicillin-allergic patients have an increased risk of adverse reactions to any medication (20, 21). Skin testing in penicillin-allergic patients cannot reliably predict an allergic response to a cephalosporin, particularly to compounds with dissimilar side chains (22). However, skin testing may be useful in determining whether a true allergy to penicillin exists (23).

Twenty-seven articles on the topic of the cross-reactivity of penicillin and cephalosporin were reviewed, of which two were meta-analyses, 12 were prospective cohorts, three were retrospective cohorts, two were surveys, and nine were laboratory studies. The authors demonstrated that penicillin has a cross-allergy with first generation cephalosporins (OR 4.8; 95% CI 3.7-6.2) and a negligible cross-allergy with second generation cephalosporins (OR 1.1; 95% CI 0.6-2.1). Moreover, laboratory and cohort studies indicate that the R1 side chain, not the β-lactam ring, is responsible for this cross-reactivity. The authors conclude that the overall cross-reactivity between penicillin and cephalosporin is lower than previously reported, at 10%, although there is a strong association between amoxicillin and ampicillin with first and second generation cephalosporins that share a similar R1 side chain. The overall cross-reactivity between penicillin and cephalosporin in individuals who report a penicillin allergy is of approximately 1% and in those with a confirmed penicillin allergy, 2.55%, respectively. For penicillin-allergic patients, the use of third or fourth generation cephalosporin (such as cefuroxime and ceftriaxone), with dissimilar side chains than the offending penicillin, carries a negligible risk for cross allergy (24).

A similar review of 44 articles on the evidence of cross-reactivity between cephalosporin and penicillin in human and animal studies supports the finding that cephalosporin can be safely prescribed to a patient with a non-life threatening reaction to penicillin (including type I anaphylaxis, Stevens-Johnson syndrome, toxic epidermal necrolysis, and angioedema) (25). The relative risk of an anaphylactic reaction to cephalosporin ranges from 1:1000 to 1:1000000 and this risk is increased by a factor of 4 in patients with a history of penicillin allergy (26).

Based on an analysis of nine articles that compare allergic reactions to a cephalosporin in penicillin-allergic and non-penicillin-allergic subjects, Pichichero et al. found that first generation cephalosporins have a cross-allergy with penicillin, but cross-allergy is negligible with second and third generation cephalosporins. Specifically, a significant increase in allergic reactions to cephalothin (OR 2.5, 95% CI 1.1-5.5), cephaloridine (OR 8.7, 95% CI 5.9-12.8), and cephalexin (OR 5.8, 95% CI 3.6-9.2) and all first generation cephalosporins plus cefamandole (OR 4.8, 95% CI 3.7-6.2) were observed in penicillin-allergic patients; no increase was observed with second generation cephalosporin (OR 1.1, 95% CI 0.6-2.1) or third generation cephalosporin (OR 0.5, CI 0.2-1.1) (21,22).

In a retrospective cohort of 2933 patients who received a cephalosporin (usually cefazolin) during their procedure, including 413 who were allergic to penicillin, only one of the penicillin-allergic patients may have had an allergic reaction to the cephalosporin; and one of the non-penicillin-allergic patients developed a rash, while the antibiotic was infused, requiring discontinuation of the antibiotic (27).

In a large, retrospective review of 534810 patients who received penicillin, followed by a cephalosporin at least 60 days later, Apter et al. noted that a total of 3877 patients had an allergic-like event (ALE) after penicillin administration, but only 43 (1.1%) experienced a second ALE after receiving cephalosporin (unadjusted risk ratio (RR) 10.0; 95% CI 7.4‒13.6). Interestingly, in a separate analysis reviewing sulfonamide antibiotics, 1.6% of penicillin sensitive patients experienced a second ALE after receiving a sulfonamide (7.2; 95% CI 3.8‒12.5), suggesting that patients who are allergic to penicillin are at a higher likelihood of being allergic to other medications in general, not necessarily indicating that cross-reactivity had occurred (28).

Park et al. performed a retrospective cohort study to determine whether patients with a penicillin allergy were at an increased risk of adverse drug reactions when administered cephalosporin. Eighty-five patients with a history of penicillin allergy and positive penicillin skin test and 726 patients with a history of penicillin allergy and a negative penicillin skin test were administered a first generation cephalosporin. Five (6%) of the 85 cases had an adverse drug reaction to cephalosporin, compared to five (0.7%) of 726 of the control population (P = 0.0019). The rate of presumed IgE-mediated adverse drug reactions to the cephalosporin among the cases was 2 (2%) of 85 compared to 1 (0.1%) of 726 among the reference population (P = 0.03) (29).

4. Conclusions

Question 3: What is the choice of antibiotics in patients who have preexisting prostheses, such as heart valves?

Consensus: The choice of antibiotics for patients with preexisting prostheses, such as heart valves, is the same as that for routine elective arthroplasty.

Question 4: What alternatives are available for routine prophylaxis when cephalosporins are not an option?

Consensus: Currently teicoplanin and vancomycin are reasonable alternatives when routine antibiotic prophylaxis cannot be administered.

Question 5A: What antibiotic should be administered in a patient with a known anaphylactic penicillin allergy?

Question 5B: What antibiotic should be administered in a patient with a known non-anaphylactic penicillin allergy?

Consensus: In a patient with a reported non-anaphylactic reaction to penicillin, a second generation cephalosporin can be used safely as there is limited cross-reactivity. Penicillin skin testing may be helpful in certain situations to clarify whether the patient has a true penicillin allergy.

References

1. Enzler MJ, Berbari E, Osmon DR. Antimicrobial prophylaxis in adults. Mayo Clin Proc. 2011; 86(7): 686-701[DOI][PubMed]
2. Stefansdottir 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(11-12): 831-40[DOI][PubMed]
3. Wilson W, Taubert KA, Gewitz M, Lockhart PB, Baddour LM, Levison M, et al. Prevention of infective endocarditis: guidelines from the American Heart Association: a guideline from the American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee, Council on Cardiovascular Disease in the Young, and the Council on Clinical Cardiology, Council on Cardiovascular Surgery and Anesthesia, and the Quality of Care and Outcomes Research Interdisciplinary Working Group. Circulation. 2007; 116(15): 1736-54[DOI][PubMed]
4. Eagle KA, Guyton RA, Davidoff R, Edwards FH, Ewy GA, Gardner TJ, et al. ACC/AHA 2004 guideline update for coronary artery bypass graft surgery: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to Update the 1999 Guidelines for Coronary Artery Bypass Graft Surgery). Circulation. 2004; 110(14)-437[PubMed]
5. Edwards FH, Engelman RM, Houck P, Shahian DM, Bridges CR, Society of Thoracic S. The Society of Thoracic Surgeons Practice Guideline Series: Antibiotic Prophylaxis in Cardiac Surgery, Part I: Duration. Ann Thorac Surg. 2006; 81(1): 397-404[DOI][PubMed]
6. Haydon TP, Presneill JJ, Robertson MS. Antibiotic prophylaxis for cardiac surgery in Australia. Med J Aust. 2010; 192(3): 141-3[PubMed]
7. Mollan RA, Haddock M, Webb CH. Teicoplanin vs cephamandole for antimicrobial prophylaxis in prosthetic joint implant surgery: (preliminary results). Eur J Surg Suppl. 1992; (567): 19-21[PubMed]
8. Lazzarini L, Pellizzer G, Stecca C, Viola R, de Lalla F. Postoperative infections following total knee replacement: an epidemiological study. J Chemother. 2001; 13(2): 182-7[DOI][PubMed]
9. Periti P, Pannuti F, Cuna GRD, Mazzei T, Mini E, Martoni A, et al. Combination Chemotherapy with Cyclophosphamide, Fluorouracil, and Either Epirubicin or Mitoxantrone: a Comparative Randomized Multicenter Study in Metastatic Breast Carcinoma. Cancer Invest. 1991; 9(3): 249-55[DOI]
10. Periti P, Stringa G, Mini E. Comparative multicenter trial of teicoplanin versus cefazolin for antimicrobial prophylaxis in prosthetic joint implant surgery. Italian Study Group for Antimicrobial Prophylaxis in Orthopedic Surgery. Eur J Clin Microbiol Infect Dis. 1999; 18(2): 113-9[PubMed]
11. Brogden RN, Peters DH. Teicoplanin. A reappraisal of its antimicrobial activity, pharmacokinetic properties and therapeutic efficacy. Drugs. 1994; 47(5): 823-54[PubMed]
12. Wood MJ. The comparative efficacy and safety of teicoplanin and vancomycin. J Antimicrob Chemother. 1996; 37(2): 209-22[PubMed]
13. Wilson AP. Antibiotic prophylaxis in cardiac surgery. J Antimicrob Chemother. 1988; 21(5): 522-4[PubMed]
14. Weed HG. Antimicrobial prophylaxis in the surgical patient. Med Clin North Am. 2003; 87(1): 59-75[PubMed]
15. Bratzler DW, Houck PM, Surgical Infection Prevention Guidelines Writers W, American Academy of Orthopaedic S, American Association of Critical Care N, American Association of Nurse A, et al. Antimicrobial prophylaxis for surgery: an advisory statement from the National Surgical Infection Prevention Project. Clin Infect Dis. 2004; 38(12): 1706-15[DOI][PubMed]
16. Darley ES, MacGowan AP. Antibiotic treatment of gram-positive bone and joint infections. J Antimicrob Chemother. 2004; 53(6): 928-35[DOI][PubMed]
17. Dash CH. Penicillin allergy and the cephalosporins. J Antimicrob Chemother. 1975; 1(3 Suppl): 107-18[PubMed]
18. Petz LD. Immunologic cross-reactivity between penicillins and cephalosporins: a review. J Infect Dis. 1978; 137 Suppl-9[PubMed]
19. Kelkar PS, Li JT. Cephalosporin allergy. N Engl J Med. 2001; 345(11): 804-9[DOI][PubMed]
20. Saxon A, Beall GN, Rohr AS, Adelman DC. Immediate hypersensitivity reactions to beta-lactam antibiotics. Ann Intern Med. 1987; 107(2): 204-15[PubMed]
21. Pichichero ME. Use of selected cephalosporins in penicillin-allergic patients: a paradigm shift. Diagn Microbiol Infect Dis. 2007; 57(3 Suppl): 13S-8S[DOI][PubMed]
22. Pichichero ME, Casey JR. Safe use of selected cephalosporins in penicillin-allergic patients: a meta-analysis. Otolaryngol Head Neck Surg. 2007; 136(3): 340-7[DOI][PubMed]
23. Audicana M, Bernaola G, Urrutia I, Echechipia S, Gastaminza G, Munoz D, et al. Allergic reactions to betalactams: studies in a group of patients allergic to penicillin and evaluation of cross-reactivity with cephalosporin. Allergy. 1994; 49(2): 108-13[PubMed]
24. Solensky R, Earl HS, Gruchalla RS. Lack of penicillin resensitization in patients with a history of penicillin allergy after receiving repeated penicillin courses. Arch Intern Med. 2002; 162(7): 822-6[PubMed]
25. Campagna JD, Bond MC, Schabelman E, Hayes BD. The use of cephalosporins in penicillin-allergic patients: a literature review. J Emerg Med. 2012; 42(5): 612-20[DOI][PubMed]
26. DePestel DD, Benninger MS, Danziger L, LaPlante KL, May C, Luskin A, et al. Cephalosporin use in treatment of patients with penicillin allergies. J Am Pharm Assoc (2003). 2008; 48(4): 530-40[DOI][PubMed]
27. Platt R. Adverse effects of third-generation cephalosporins. J Antimicrob Chemother. 1982; 10 Suppl C: 135-40[PubMed]
28. Apter AJ, Kinman JL, Bilker WB, Herlim M, Margolis DJ, Lautenbach E, et al. Is there cross-reactivity between penicillins and cephalosporins? Am J Med. 2006; 119(4): 354 e11-9[DOI][PubMed]
29. Park MA, Koch CA, Klemawesch P, Joshi A, Li JT. Increased adverse drug reactions to cephalosporins in penicillin allergy patients with positive penicillin skin test. Int Arch Allergy Immunol. 2010; 153(3): 268-73[PubMed]

Subject: Knee surgery
Received: 2019/09/9 | Accepted: 2015/02/15 | Published: 2015/02/15

Rights and permissions
	This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Designed & Developed by : Yektaweb