Literature DB >> 25690169

Twenty Percent of Patients May Remain Colonized With Methicillin-resistant Staphylococcus aureus Despite a Decolonization Protocol in Patients Undergoing Elective Total Joint Arthroplasty.

Michael D Baratz1, Ruth Hallmark, Susan M Odum, Bryan D Springer.   

Abstract

BACKGROUND: Staphylococcus aureus is the most commonly isolated organism in periprosthetic joint infection (PJI). Resistant strains such as methicillin-resistant S aureus (MRSA) are on the rise, and many programs have instituted decolonization protocols. There are limited data on the success of S aureus nasal decolonization programs and their impact on PJI. QUESTIONS/PURPOSES: The purposes of this study were to (1) determine the proportion of patients successfully decolonized using a 2-week protocol; (2) compare infection risks between our surveillance and decolonization protocol group against a historical control cohort to evaluate changes in proportions of S aureus infections; and (3) assess infection risk based on carrier type, comparing S aureus carriers with noncarrier controls.
METHODS: We retrospectively evaluated a group of 3434 patients who underwent elective primary and revision hip and knee arthroplasty over a 2-year period; each patient in the treatment group underwent a surveillance protocol, and a therapeutic regimen of mupurocin and chlorhexidine was instituted when colonization criteria were met. A 2009 to 2010 comparative historical cohort was chosen as the control group. We compared risks of infection between our treatment group and the historical control cohort. Furthermore, in patients who developed surgical site infections (SSIs), we compared the proportions of each S aureus type between the two cohorts. Finally, we compared infection rates based on carrier status. Surveillance for infection was carried out by the hospital infection control coordinator using the Centers for Disease Control and Prevention (CDC) criteria. During the time period of this study, the CDC defined hospital-acquired infection related to a surgical procedure as any infection diagnosed within 1 year of the procedure. With the numbers available, we had 41% power to detect a difference of 0.3% in infection rate between the treatment and control groups. To achieve 80% power, a total of 72,033 patients would be needed.
RESULTS: Despite the protocol, 22% (26 of 121) of patients remained colonized with MRSA. With the numbers available, there were no differences in infection risk between the protocoled group (27 of 3434 [0.8%]) and the historical control group (33 of 3080 [1.1%]; relative risk [RR], 0.74; 95% confidence interval [CI], 0.44-1.22; p = 0.28). In terms of infecting organism in those who developed SSI, S aureus risk decreased slightly (treatment: 13 of 3434 patients [0.38%]; control: 21 of 3080 patients [0.68%]; RR, 0.56; CI, 0.28-1.11; p = 0.11). Within the protocoled group, carriers had a slightly higher risk of developing SSI (carrier: seven of 644 [1.1%]; noncarrier: 18 of 2763 [0.65%]; RR, 1.77; CI, 0.74-4.24; p = 0.20).
CONCLUSIONS: The screening and decolonization protocol enabled a substantial reduction in nasal carriage of MRSA, but some patients remained colonized. However, our nasal decolonization protocol before elective total joint arthroplasty did not demonstrate a decrease in the proportion of patients developing SSI. Future meta-analyses and systematic reviews will be needed to pool the results of studies like these to ascertain whether small improvements in infection risk are achieved by protocols like ours and to determine whether any such improvements warrant the costs and potential risks of surveillance and intervention. LEVEL OF EVIDENCE: Level III, therapeutic study.

Entities:  

Mesh:

Year:  2015        PMID: 25690169      PMCID: PMC4457751          DOI: 10.1007/s11999-015-4191-3

Source DB:  PubMed          Journal:  Clin Orthop Relat Res        ISSN: 0009-921X            Impact factor:   4.176


  34 in total

1.  The relation between the nasal-staphylococcal-carrier state and the incidence of postoperative complications.

Authors:  H J WEINSTEIN
Journal:  N Engl J Med       Date:  1959-06-25       Impact factor: 91.245

2.  Preoperative screening/decolonization for Staphylococcus aureus to prevent orthopedic surgical site infection: prospective cohort study with 2-year follow-up.

Authors:  Nalini Rao; Barbara A Cannella; Lawrence S Crossett; Adolph J Yates; Richard L McGough; Cindy W Hamilton
Journal:  J Arthroplasty       Date:  2011-04-19       Impact factor: 4.757

3.  The impact of infection after total hip arthroplasty on hospital and surgeon resource utilization.

Authors:  Kevin J Bozic; Michael D Ries
Journal:  J Bone Joint Surg Am       Date:  2005-08       Impact factor: 5.284

4.  The burden of Staphylococcus aureus infections on hospitals in the United States: an analysis of the 2000 and 2001 Nationwide Inpatient Sample Database.

Authors:  Gary A Noskin; Robert J Rubin; Jerome J Schentag; Jan Kluytmans; Edwin C Hedblom; Maartje Smulders; Elizabeth Lapetina; Eric Gemmen
Journal:  Arch Intern Med       Date:  2005 Aug 8-22

5.  In vivo transfer of high-level mupirocin resistance from Staphylococcus epidermidis to methicillin-resistant Staphylococcus aureus associated with failure of mupirocin prophylaxis.

Authors:  Julian G Hurdle; Alex J O'Neill; Lona Mody; Ian Chopra; Suzanne F Bradley
Journal:  J Antimicrob Chemother       Date:  2005-11-07       Impact factor: 5.790

6.  Preoperative chlorhexidine preparation and the incidence of surgical site infections after hip arthroplasty.

Authors:  Aaron J Johnson; Jacqueline A Daley; Michael G Zywiel; Ronald E Delanois; Michael A Mont
Journal:  J Arthroplasty       Date:  2010-05-31       Impact factor: 4.757

7.  Emerging elevated mupirocin resistance rates among staphylococcal isolates in the SENTRY Antimicrobial Surveillance Program (2000): correlations of results from disk diffusion, Etest and reference dilution methods.

Authors:  L M Deshpande; A M Fix; M A Pfaller; R N Jones
Journal:  Diagn Microbiol Infect Dis       Date:  2002-04       Impact factor: 2.803

8.  Efficient detection and long-term persistence of the carriage of methicillin-resistant Staphylococcus aureus.

Authors:  M D Sanford; A F Widmer; M J Bale; R N Jones; R P Wenzel
Journal:  Clin Infect Dis       Date:  1994-12       Impact factor: 9.079

9.  Periprosthetic infection due to resistant staphylococci: serious problems on the horizon.

Authors:  Javad Parvizi; Khalid Azzam; Elie Ghanem; Matthew S Austin; Richard H Rothman
Journal:  Clin Orthop Relat Res       Date:  2009-05-01       Impact factor: 4.176

Review 10.  The fate of acute methicillin-resistant Staphylococcus aureus periprosthetic knee infections treated by open debridement and retention of components.

Authors:  Thomas Bradbury; Thomas K Fehring; Michael Taunton; Arlen Hanssen; Khalid Azzam; Javad Parvizi; Susan M Odum
Journal:  J Arthroplasty       Date:  2009-06-24       Impact factor: 4.757

View more
  13 in total

Review 1.  Community-associated methicillin-resistant Staphylococcus aureus infection: Literature review and clinical update.

Authors:  Kassandra Loewen; Yoko Schreiber; Mike Kirlew; Natalie Bocking; Len Kelly
Journal:  Can Fam Physician       Date:  2017-07       Impact factor: 3.275

2.  Editor's Spotlight/Take 5: Addition of Vancomycin to Cefazolin Prophylaxis Is Associated With Acute Kidney Injury After Primary Joint Arthroplasty.

Authors:  M Daniel Wongworawat
Journal:  Clin Orthop Relat Res       Date:  2015-04-25       Impact factor: 4.176

3.  Greater Rates of Acute Kidney Injury in African American Total Knee Arthroplasty Patients.

Authors:  Tanner N Womble; John D King; Dustin H Hamilton; Max A Shrout; Cale A Jacobs; Stephen T Duncan
Journal:  J Arthroplasty       Date:  2019-01-31       Impact factor: 4.757

4.  "Recommendations for periprosthetic joint infections (PJI) prevention: the European Knee Associates (EKA)-International Committee American Association of Hip and Knee Surgeons (AAHKS)-Arthroplasty Society in Asia (ASIA) survey of members".

Authors:  Pier Francesco Indelli; F Iannotti; A Ferretti; R Valtanen; P Prati; D Pérez Prieto; N P Kort; B Violante; N R Tandogan; A Schiavone Panni; G Pipino; M T Hirschmann
Journal:  Knee Surg Sports Traumatol Arthrosc       Date:  2021-09-13       Impact factor: 4.342

5.  Screening of MRSA colonization in patients undergoing total joint arthroplasty.

Authors:  A M Valverde Villar; J Gutiérrez Del Álamo Oms; I Neira Borrajo; S de Miguel Fernández; P Flox Benítez; R Llopis Miró
Journal:  J Infect Prev       Date:  2021-06-23

6.  CORR Insights®: Preoperative Colonization With Staphylococcus Aureus in THA is Associated With Increased Length of Stay.

Authors:  Geert Meermans
Journal:  Clin Orthop Relat Res       Date:  2022-03-08       Impact factor: 4.755

7.  Calcium sulphate mixed with antibiotics does not decrease efficacy against Cutibacterium acnes (formerly Propionibacterium acnes), in vitro study.

Authors:  Anne Couture; Valéry Lavergne; Emilie Sandman; Jean-Michel Leduc; Benoit Benoit; Stéphane Leduc; Dominique M Rouleau
Journal:  J Orthop       Date:  2019-11-28

Review 8.  Prophylaxis with nasal decolonization in patients submitted to total knee and hip arthroplasty: systematic review and meta-analysis.

Authors:  David Sadigursky; Henrique Santos Pires; Saulo Américo Caldas Rios; Francisco Luiz Borja Rodrigues Filho; Gustavo Castro de Queiroz; Mateus Lemos Azi
Journal:  Rev Bras Ortop       Date:  2017-10-27

9.  Employing high-frequency alternating magnetic fields for the non-invasive treatment of prosthetic joint infections.

Authors:  Rajiv Chopra; Sumbul Shaikh; Yonatan Chatzinoff; Imalka Munaweera; Bingbing Cheng; Seth M Daly; Yin Xi; Chenchen Bing; Dennis Burns; David E Greenberg
Journal:  Sci Rep       Date:  2017-08-08       Impact factor: 4.379

Review 10.  Total knee arthroplasty and infection: how surgeons can reduce the risks.

Authors:  Nicola Ratto; Chiara Arrigoni; Federica Rosso; Matteo Bruzzone; Federico Dettoni; Davide Edoardo Bonasia; Roberto Rossi
Journal:  EFORT Open Rev       Date:  2017-03-13
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.