全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
PLOS ONE  2012 

Drugs of Last Resort? The Use of Polymyxins and Tigecycline at US Veterans Affairs Medical Centers, 2005–2010

DOI: 10.1371/journal.pone.0036649

Full-Text   Cite this paper   Add to My Lib

Abstract:

Multidrug-resistant (MDR) and carbapenem-resistant (CR) Gram-negative pathogens are becoming increasingly prevalent around the globe. Polymyxins and tigecycline are among the few antibiotics available to treat infections with these bacteria but little is known about the frequency of their use. We therefore aimed to estimate the parenteral use of these two drugs in Veterans Affairs medical centers (VAMCs) and to describe the pathogens associated with their administration. For this purpose we retrospectively analyzed barcode medication administration data of parenteral administrations of polymyxins and tigecycline in 127 acute-care VAMCs between October 2005 and September 2010. Overall, polymyxin and tigecycline use were relatively low at 0.8 days of therapy (DOT)/1000 patient days (PD) and 1.6 DOT/1000PD, respectively. Use varied widely across facilities, but increased overall during the study period. Eight facilities accounted for three-quarters of all polymyxin use. The same statistic for tigecycline use was twenty-six VAMCs. There were 1,081 MDR or CR isolates during 747 hospitalizations associated with polymyxin use (1.4/hospitalization). For tigecycline these number were slightly lower: 671 MDR or CR isolates during 500 hospitalizations (1.3/hospitalization) (p = 0.06). An ecological correlation between the two antibiotics and combined CR and MDR Gram-negative isolates per 1000PD during the study period was also observed (Pearson’s correlation coefficient r = 0.55 polymyxin, r = 0.19 tigecycline). In summary, while polymyxin and tigecycline use is low in most VAMCs, there has been an increase over the study period. Polymyxin use in particular is associated with the presence of MDR Gram-negative pathogens and may be useful as a surveillance measure in the future.

References

[1]  Jain R, Kralovic SM, Evans ME, Ambrose M, Simbartl LA, et al. (2011) Veterans Affairs initiative to prevent methicillin-resistant Staphylococcus aureus infections. N Engl J Med 364: 1419–1430.
[2]  Kallen AJ, Mu Y, Bulens S, Reingold A, Petit S, et al. (2010) Health care-associated invasive MRSA infections, 2005–2008. JAMA 304: 641–648.
[3]  Wilson J, Guy R, Elgohari S, Sheridan E, Davies J, et al. (2011) Trends in sources of meticillin-resistant Staphylococcus aureus (MRSA) bacteraemia: data from the national mandatory surveillance of MRSA bacteraemia in England, 2006–2009. J Hosp Infect 79: 211–217.
[4]  Carlet J, Astagneau P, Brun-Buisson C, Coignard B, Salomon V, et al. (2009) French national program for prevention of healthcare-associated infections and antimicrobial resistance, 1992–2008: positive trends, but perseverance needed. Infect Control Hosp Epidemiol 30: 737–745.
[5]  Nordmann P, Naas T, Poirel L (2011) Global spread of Carbapenemase-producing Enterobacteriaceae. Emerg Infect Dis 17: 1791–1798.
[6]  Pfeifer Y, Cullik A, Witte W (2010) Resistance to cephalosporins and carbapenems in Gram-negative bacterial pathogens. Int J Med Microbiol 300: 371–379.
[7]  Gagliotti C, Balode A, Baquero F, Degener J, Grundmann H, et al. (2011) Escherichia coli and Staphylococcus aureus: bad news and good news from the European Antimicrobial Resistance Surveillance Network (EARS-Net, formerly EARSS), 2002 to 2009. Euro Surveill 16: pii. 19819 p.
[8]  Frank C, Werber D, Cramer JP, Askar M, Faber M, et al. (2011) Epidemic profile of Shiga-toxin-producing Escherichia coli O104:H4 outbreak in Germany. N Engl J Med 365: 1771–1780.
[9]  Nikaido H (2009) Multidrug resistance in bacteria. Annu Rev Biochem 78: 119–146.
[10]  Partridge SR (2011) Analysis of antibiotic resistance regions in Gram-negative bacteria. FEMS Microbiol Rev 35: 820–855.
[11]  Falagas ME, Karageorgopoulos DE, Nordmann P (2011) Therapeutic options for infections with Enterobacteriaceae producing carbapenem-hydrolyzing enzymes. Future Microbiol 6: 653–666.
[12]  Bertrand X, Dowzicky MJ (2012) Antimicrobial susceptibility among gram-negative isolates collected from intensive care units in North America, Europe, the Asia-Pacific Rim, Latin America, the Middle East, and Africa between 2004 and 2009 as part of the Tigecycline Evaluation and Surveillance Trial. Clin Ther 34: 124–137.
[13]  Tasina E, Haidich AB, Kokkali S, Arvanitidou M (2011) Efficacy and safety of tigecycline for the treatment of infectious diseases: a meta-analysis. Lancet Infect Dis 11: 834–844.
[14]  Yahav D, Lador A, Paul M, Leibovici L (2011) Efficacy and safety of tigecycline: a systematic review and meta-analysis. J Antimicrob Chemother 66: 1963–1971.
[15]  Prasad P, Sun J, Danner RL, Natanson C (2012) Excess Deaths Associated with Tigecycline After Approval Based on Non-Inferiority Trials. Clin Infect Dis. In press.
[16]  Li J, Nation RL, Turnidge JD, Milne RW, Coulthard K, et al. (2006) Colistin: the re-emerging antibiotic for multidrug-resistant Gram-negative bacterial infections. Lancet Infect Dis 6: 589–601.
[17]  Lim LM, Ly N, Anderson D, Yang JC, Macander L, et al. (2010) Resurgence of colistin: a review of resistance, toxicity, pharmacodynamics, and dosing. Pharmacotherapy 30: 1279–1291.
[18]  Yahav D, Farbman L, Leibovici L, Paul M (2012) Colistin: new lessons on an old antibiotic. Clin Microbiol Infect 18: 18–29.
[19]  Johnson CL, Carlson RA, Tucker CL, Willette C (2002) Using BCMA software to improve patient safety in Veterans Administration Medical Centers. J Healthc Inf Manag 16: 46–51.
[20]  Polk RE, Fox C, Mahoney A, Letcavage J, MacDougall C (2007) Measurement of adult antibacterial drug use in 130 US hospitals: comparison of defined daily dose and days of therapy. Clin Infect Dis 44: 664–670.
[21]  Jones M, DuVall SL, Spuhl J, Samore MH, Nielson C, et al. (2012) Identification of Methicillin-resistant Staphylococcus aureus within the Nation’s Veterans Affairs Medical Centers Using Natural Language Processing. BMC Med Inform Decis Mak. In press.
[22]  Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, et al. (2012) Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect 18: 268–281.
[23]  Bogdanovich T, Adams-Haduch JM, Tian GB, Nguyen MH, Kwak EJ, et al. (2011) Colistin-resistant, Klebsiella pneumoniae carbapenemase (KPC)-producing Klebsiella pneumoniae belonging to the international epidemic clone ST258. Clin Infect Dis 53: 373–376.
[24]  Marchaim D, Chopra T, Pogue JM, Perez F, Hujer AM, et al. (2011) Outbreak of colistin-resistant, carbapenem-resistant Klebsiella pneumoniae in metropolitan Detroit, Michigan. Antimicrob Agents Chemother 55: 593–599.
[25]  Chiang T, Mariano N, Urban C, Colon-Urban R, Grenner L, et al. (2007) Identification of carbapenem-resistant klebsiella pneumoniae harboring KPC enzymes in New Jersey. Microb Drug Resist 13: 235–239.
[26]  Endimiani A, Hujer AM, Perez F, Bethel CR, Hujer KM, et al. (2009) Characterization of blaKPC-containing Klebsiella pneumoniae isolates detected in different institutions in the Eastern USA. J Antimicrob Chemother 63: 427–437.
[27]  Hombach M, Bloemberg GV, Bottger EC (2012) Effects of clinical breakpoint changes in CLSI guidelines 2010/2011 and EUCAST guidelines 2011 on antibiotic susceptibility test reporting of Gram-negative bacilli. J Antimicrob Chemother 67: 622–632.
[28]  Trick WE, Zagorski BM, Tokars JI, Vernon MO, Welbel SF, et al. (2004) Computer algorithms to detect bloodstream infections. Emerg Infect Dis 10: 1612–1620.
[29]  Infectious Diseases Society of America (2010) The 10×'20 Initiative: pursuing a global commitment to develop 10 new antibacterial drugs by 2020. Clin Infect Dis 50: 1081–1083.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133