Abstract
Study design:
Retrospective observational study of bacterial susceptibilities in Veterans with SCI/D as compared to a general patient population.
Objectives:
The purpose of this project was to evaluate the prevalence and susceptibility of bacteria isolated from spinal cord injury and disorder (SCI/D) patients as compared with a general patient population and determine whether a SCI/D-specific antibiogram, a report of bacterial susceptibilities used to guide empiric antibiotic selection, would be a useful stewardship tool.
Setting:
Veterans Affairs Medical Center located in Cook county, IL, USA.
Methods:
Microbiology reports from 1 October 2012 to 30 September 2013 were compiled into a SCI/D-specific antibiogram and compared to a non-SCI/D antibiogram.
Results:
Persons with positive cultures and SCI/D were younger and had a higher Charlson Index as compared to non-SCI/D patients (P<0.0001 for both). Five thousand one hundred and thirty-one unique isolate cultures were evaluated (SCI/D=23.0%). Frequencies of pathogens isolated in SCI/D and non-SCI/D differed. Methicillin-resistant Staphylococcus aureus occurred more frequently in SCI/D (27.8% vs 55.4%; P<0.0001). Gram-negatives had generally lower susceptibilities in SCI/D and a higher frequency of organisms producing extended-spectrum Beta-lactamases (17.6% vs 5.0%; P<0.0001), carbapenem-resistant Enterobacteriaceae (2.4% vs 0.5%; P<0.0001), carbapenem resistance (7.6% vs 2.4%; P<0.0001) and isolates resistant to ⩾3 antibiotic classes (60.7% vs 28.0%; P=0.0001).
Conclusion:
Different pathogens with poorer susceptibilities are isolated in SCI/D. Thus an SCI/D-specific antibiogram reflective of resistance patterns in these patients may increase the appropriateness of empiric antibiotic selection. The frequency of multi-drug resistant organisms in cultures obtained from patients with SCI/D is worrisome.
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References
Costelloe C, Metcalfe C, Lovering A, Mant D, Hay AD . Effect of antibiotic prescribing in primary care on antimicrobial resistance in individual patients: systematic review and meta-analysis. BMJ 2010; 340: c2096.
Ibrahim EH, Sherman G, Ward S, Fraser VJ, Kollef MH . The influence of inadequate antimicrobial treatment of bloodstream infections on patient outcomes in the ICU setting. Chest 2000; 118: 146–155.
McDonald JR, Friedman ND, Stout JE, Sexton DJ, Kaye KS . Risk factors for ineffective therapy in patients with bloodstream infection. Arch Intern Med 2005; 165: 308–313.
Leibovici L, Konisberger H, Pitlik SD, Samra Z, Drucker M . Patients at risk for inappropriate antibiotic treatment of bacteraemia. J Intern Med 1992; 231: 371–374.
Leibovici L, Paul M, Paznanski O, Drucker M, Samra Z, Konigsberger H et al. Monotherapy versus beta-lactam-aminoglycoside combination treatment for Gram-negative bacteremia: a prospective, observational study. Antimicrob Agents Chemother 1997; 41: 1127–1133.
Leibovici L, Shraga I, Drucker M, Konigsberger H, Samra Z, Pitlik SD . The benefit of appropriate empirical antibiotic treatment in patients with bloodstream infection. J Intern Med 1998; 244: 379–386.
Zaragoza R, Artero A, Camarena JJ, Sancho S, Gonzalex R, Nogueira JM . The influenza of inadequate empirical antimicrobial treatment on patients with bloodstream infections in an intensive care unit. Clin Microbiol Infect 2003; 9: 412–418.
Chaubey VP, Pitout JD, Dalton B, Ross T, Church DL, Gregson DB et al. Clinical outcomes of empiric antimicrobial therapy of bacteremia due to extended-spectrum beta-lactamase producing Escherichia coli and Klebsiella pneumonia. BMC Res Notes 2010; 3: 116.
Kang CI, Kim SH, Kim HB, Park SW, Choe YJ, Oh MD et al. Pseudomonas aeruginosa bacteremia: risk factors for mortality and influence of delayed receipt of effective antimicrobial therapy on clinical outcome. Clin Infect Dis 2003; 37: 745–751.
Kang CI, Kim SH, Park WB, Lee KD, Kim HB, Kim EC et al. Bloodstream infections caused by antibiotic-resistant Gram-negative bacilli: risk factors for mortality and impact of inappropriate initial antimicrobial therapy on outcome. Antimicrob Agents Chemother 2005; 49: 760–766.
Harbarth S, Garbino J, Pugin J, Romand JA, Lew D, Pittet D . Inappropriate initial antimicrobial therapy and its effect on survival in a clinical trial of immunomodulating therapy for severe sepsis. Am J Med 2003; 115: 529–535.
Micek ST, Lloyd AE, Ritchie DJ, Reichley RM, Fraser VJ, Kollef MH . Pseudomonas aeruginosa bloodstream infection: importance of appropriate initial antimicrobial treatment. Antimicrob Agents Chemother 2005; 49: 1306–1311.
Tumbarello M, Spanu T, Bidino RD, Marchetti M, Ruggeri M, Trecarichi EM et al. Costs of bloodstream infections caused by Escherichia coli and influence of extended-spectrum-beta-lactamases production and inadequate initial antibiotic therapy. Antimicrob Agents Chemother 2010; 54: 4085–4091.
Imamura T, Ohta B, Tanaka E, Branch J . Prognosis of urosepsis patients who are treated by inappropriate initial antimicrobial therapy in the emergency department. Ann Emerg Med 2009; 54: S38–S39.
Xu R, Polk RE, Stencel L, Lowe DK, Guharoy R, Duggal RW et al. Antibiogram compliance in University HealthSystem Consortium participating hospitals with Clinical and Laboratory Standards Institute guidelines. Am J Health Syst Pharm 2012; 69: 598–606.
Fridkin SK, Edwards JR, Tenover FC, Gaynes RP, McGowan JE Jr for the ICARE Project and NNIS. Antimicrobial resistance prevalence rates in hospital antibiograms reflect prevalence rates among pathogens associated with hospital-acquired infections. Clin Infect Dis 2001; 33: 324–329.
Kaufman D, Haas CE, Edinger R, Hollick G . Antibiotic susceptibility in the surgical intensive care unit compared with the hospital-wide antibiogram. Arch Surg 1998; 133: 1041–1045.
Draper HM, Farland JB, Heidel RE, May LS, Suda KJ . Comparison of bacteria isolated from emergency department patients versus hospitalized patients. Am J Health Syst Pharm 2013; 70: 2124–2128.
Healthcare Analysis and Information Group (HAIG) Office of the Assistant Deputy Under Secretary for Health for Policy and Planning. 2012 Survey of Antimicrobial Stewardship in VHA. Department of Veterans Affairs, Washington, DC, USA, May 2013.
Binkley S, Fisherman NO, LaRosa LA, Marr AM, Nachamkin I, Wordell D et al. Comparison of unit-specific and hospital-wide antibiograms potential implications for selection of empirical antimicrobial therapy. Infect Control Hosp Epidemiol 2006; 27: 682–687.
Pogue JM, Alaniz C, Carver PL, Pleva M, Newton D, DePestel DD . Role of unit-specific combination antibiograms for improving the selection of appropriate empiric therapy for Gram-negative pneumonia. Infect Control Hosp Epidemiol 2011; 32: 289–292.
Swami SK, Banerjee R . Comparison of hospital-wide and age and location-stratified antibiograms of S. aureus E. coli, and S. pneumoniae: age-and location-stratified antibiograms. SpringerPlus 2013; 2: 63.
Montgomerie JZ . Infections in patients with spinal cord injuries. Clin Infect Dis 1997; 25: 1285–1290.
Evans CT, LaVela SL, Weaver FM, Priebe M, Sandford P, Niemiec P et al. Epidemiology of hospital-acquired infections in Veterans with spinal cord injury and disorder. Infect Control Hosp Epidemiol 2008; 29: 234–242.
Evans CT, Rogers TJ, Burns SP, Lopansri B, Weaver FM . Knowledge and use of antimicrobial stewardship resources by spinal cord injury providers. PM R 2011; 3: 619–623.
Goff DA . Antimicrobial stewardship: bridging the gap between quality care and cost. Curr Opin Infect Dis 2011; 24: S11–S20.
Hindler JF, Stelling J . Analysis and presentation of cumulative antibiograms: a new consensus guideline from the Clinical and Laboratory Standards Institute. Clin Infect Dis 2007; 44: 867–873.
Smith B, Evans CT, Ullrich P, Burns S, Guihan M, Miskevics S et al. Using VA data for research in persons with spinal cord injuries and disorders: lessons from SCI QUERI. J Rehabil Res Dev 2010; 47: 679–688.
CLSI. Analysis and Presentation of Cumulative Antimicrobial Susceptibility Test Data, 3rd edn, Guideline M39-A3. Clinical and Laboratory Standards Institute: Wayn, PA, USA, 2009.
Clinical and Laboratory Standards Institute (CLSI) Performance Standards for Antimicrobial Susceptibility Testing; Twenty-third Informational Supplement M100-S23. CLSI: Wayne, PA, USA. 2013.
Clinical and Laboratory Standards Institute Interpretive Criteria for Carbapenems and Enterobacteriaceae M100-S22. CLSI: Wayne, PA, USA. 2012.
Dellit TH, Owens RC, McGowan JE Jr, Gerding DN, Weinstein RA, Burke JP et al. Infectious Diseases Society of America; Society for Healthcare Epidemiology of America. Infectious Diseases Society of America and Society for Healthcare Epidemioloogy of America guidelines for developing an institutional program to enhance antimicrobial stewardship. Clin Infect Dis 2007; 44: 159–177.
Yoon SB, Lee BS, Lee KD, Hwang SI, Lee HJ, Han ZA . Comparison of bacterial strains and antibiotic susceptibilities in urinary isolates of spinal cord injury patients from the community and hospital. Spinal Cord 2014; 52: 298–301.
Waites KB, Chen Y, DeVivo MJ, Canupp KC, Moser SA . Antimicrobial resistance in Gram-negative bacteria isolated from the urinary tract in community-residing person with spinal cord injury. Arch Phys Med Rehabil 2000; 81: 764–769.
Hinkel A, Finke W, Botel U, Gatermann SG, Pannek J . Increasing resistance against antibiotics in bacteria isolated from the lower urinary tract of an outpatient population of spinal cord injury patients. Urol Int 2004; 73: 143–148.
Montgomerie JAZ, Chan E, Gilmore DS, Canawati HN, Sapico FL . Low mortality among patients with spinal cord injury and bacteremia. Rev Infect Dis 1991; 13: 867–871.
Evans CT, Burns SP, Chin A, Weaver FM, Hershow RC . Predictors and outcomes of antibiotic adequacy for bloodstream infections in Veterans with spinal cord injury. Arch Phys Med Rehabil 2009; 90: 1364–1370.
Acknowledgements
The views expressed in this article are those of the authors and do not necessarily represent the views of the Department of Veterans Affairs, the Health Services Research and Development Service or the United States government. This work was supported by the US Department of Veterans Affairs as a QUERI center grant (SCI 98-001) and QUERI LIP (QLP 97-009).
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This project was presented, in part, as a poster at the Infectious Disease Society of America Annual Meeting in Philadelphia, PA, USA, October 2014.
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Suda, K., Patel, U., Sabzwari, R. et al. Bacterial susceptibility patterns in patients with spinal cord injury and disorder (SCI/D): an opportunity for customized stewardship tools. Spinal Cord 54, 1001–1009 (2016). https://doi.org/10.1038/sc.2016.38
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DOI: https://doi.org/10.1038/sc.2016.38
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