This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Carmeli, Y.
Right arrow Articles by Samore, M. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Carmeli, Y.
Right arrow Articles by Samore, M. H.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, June 1999, p. 1379-1382, Vol. 43, No. 6
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Emergence of Antibiotic-Resistant Pseudomonas aeruginosa: Comparison of Risks Associated with Different Antipseudomonal Agents

Yehuda Carmeli,* Nicolas Troillet, George M. Eliopoulos, and Matthew H. Samore

Division of Infectious Diseases, Beth Israel Deaconess Medical Center, and Harvard Medical School, Boston, Massachusetts

Received 24 November 1998/Returned for modification 13 January 1999/Accepted 17 March 1999

Pseudomonas aeruginosa is a leading cause of nosocomial infections. The risk of emergence of antibiotic resistance may vary with different antibiotic treatments. To compare the risks of emergence of resistance associated with four antipseudomonal agents, ciprofloxacin, ceftazidime, imipenem, and piperacillin, we conducted a cohort study, assessing relative risks for emergence of resistant P. aeruginosa in patients treated with any of these drugs. A total of 271 patients (followed for 3,810 days) with infections due to P. aeruginosa were treated with the study agents. Resistance emerged in 28 patients (10.2%). Adjusted hazard ratios for the emergence of resistance were as follows: ceftazidime, 0.7 (P = 0.4); ciprofloxacin, 0.8 (P = 0.6); imipenem, 2.8 (P = 0.02); and piperacillin, 1.7 (P = 0.3). Hazard ratios for emergence of resistance to each individual agent associated with treatment with the same agent were as follows: ceftazidime, 0.8 (P = 0.7); ciprofloxacin, 9.2 (P = 0.04); imipenem, 44 (P = 0.001); and piperacillin, 5.2 (P = 0.01). We concluded that there were evident differences among antibiotics in the likelihood that their use would allow emergence of resistance in P. aeruginosa. Ceftazidime was associated with the lowest risk, and imipenem had the highest risk.


* Corresponding author. Mailing address: Division of Infectious Diseases, Tel Aviv Medical Center, 6 Weizman St., Tel Aviv 64239, Israel. Phone: (972) 3 697-3317. Fax: (972) 3 697-4996. E-mail: ycarmeli{at}mailexcite.com.


Antimicrobial Agents and Chemotherapy, June 1999, p. 1379-1382, Vol. 43, No. 6
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • El Solh, A. A., Alhajhusain, A. (2009). Update on the treatment of Pseudomonas aeruginosa pneumonia. J Antimicrob Chemother 64: 229-238 [Abstract] [Full Text]  
  • Baughman, R. P. (2009). The Use of Carbapenems in the Treatment of Serious Infections. J Intensive Care Med 24: 230-241 [Abstract]  
  • Gelfand, M. S., Cleveland, K. O., Mazumder, S. A. (2009). Successful treatment with doripenem and tobramycin of ventriculitis due to imipenem- and meropenem-resistant Pseudomonas aeruginosa. J Antimicrob Chemother 63: 1297-1299 [Full Text]  
  • Crandon, J. L, Kuti, J. L, Jones, R. N, Nicolau, D. P (2009). Comparison of 2002-2006 OPTAMA Programs for US Hospitals: Focus on Gram-Negative Resistance. The Annals of Pharmacotherapy 43: 220-227 [Abstract] [Full Text]  
  • Cirioni, O., Silvestri, C., Ghiselli, R., Orlando, F., Riva, A., Mocchegiani, F., Chiodi, L., Castelletti, S., Gabrielli, E., Saba, V., Scalise, G., Giacometti, A. (2008). Protective effects of the combination of {alpha}-helical antimicrobial peptides and rifampicin in three rat models of Pseudomonas aeruginosa infection. J Antimicrob Chemother 62: 1332-1338 [Abstract] [Full Text]  
  • Moya, B., Juan, C., Alberti, S., Perez, J. L., Oliver, A. (2008). Benefit of Having Multiple ampD Genes for Acquiring {beta}-Lactam Resistance without Losing Fitness and Virulence in Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 52: 3694-3700 [Abstract] [Full Text]  
  • El Solh, A. A., Akinnusi, M. E., Wiener-Kronish, J. P., Lynch, S. V., Pineda, L. A., Szarpa, K. (2008). Persistent Infection with Pseudomonas aeruginosa in Ventilator-associated Pneumonia. Am. J. Respir. Crit. Care Med. 178: 513-519 [Abstract] [Full Text]  
  • Henrichfreise, B., Wiegand, I., Luhmer-Becker, I., Wiedemann, B. (2007). Development of Resistance in Wild-Type and Hypermutable Pseudomonas aeruginosa Strains Exposed to Clinical Pharmacokinetic Profiles of Meropenem and Ceftazidime Simulated In Vitro. Antimicrob. Agents Chemother. 51: 3642-3649 [Abstract] [Full Text]  
  • Plasencia, V., Borrell, N., Macia, M. D., Moya, B., Perez, J. L., Oliver, A. (2007). Influence of High Mutation Rates on the Mechanisms and Dynamics of In Vitro and In Vivo Resistance Development to Single or Combined Antipseudomonal Agents. Antimicrob. Agents Chemother. 51: 2574-2581 [Abstract] [Full Text]  
  • Cirioni, O., Ghiselli, R., Silvestri, C., Kamysz, W., Orlando, F., Mocchegiani, F., Di Matteo, F., Riva, A., Lukasiak, J., Scalise, G., Saba, V., Giacometti, A. (2007). Efficacy of Tachyplesin III, Colistin, and Imipenem against a Multiresistant Pseudomonas aeruginosa Strain. Antimicrob. Agents Chemother. 51: 2005-2010 [Abstract] [Full Text]  
  • Pena, C., Guzman, A., Suarez, C., Dominguez, M. A., Tubau, F., Pujol, M., Gudiol, F., Ariza, J. (2007). Effects of Carbapenem Exposure on the Risk for Digestive Tract Carriage of Intensive Care Unit-Endemic Carbapenem-Resistant Pseudomonas aeruginosa Strains in Critically Ill Patients. Antimicrob. Agents Chemother. 51: 1967-1971 [Abstract] [Full Text]  
  • Siempos, I. I., Vardakas, K. Z., Manta, K. G., Falagas, M. E. (2007). Carbapenems for the treatment of immunocompetent adult patients with nosocomial pneumonia. Eur Respir J 29: 548-560 [Abstract] [Full Text]  
  • Lodise, T. P., Miller, C. D., Graves, J., Furuno, J. P., McGregor, J. C., Lomaestro, B., Graffunder, E., McNutt, L.-A. (2007). Clinical Prediction Tool To Identify Patients with Pseudomonas aeruginosa Respiratory Tract Infections at Greatest Risk for Multidrug Resistance. Antimicrob. Agents Chemother. 51: 417-422 [Abstract] [Full Text]  
  • Cirioni, O., Giacometti, A., Silvestri, C., Della Vittoria, A., Licci, A., Riva, A., Scalise, G. (2006). In Vitro Activities of Tritrpticin Alone and in Combination with Other Antimicrobial Agents against Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 50: 3923-3925 [Abstract] [Full Text]  
  • Juan, C., Moya, B., Perez, J. L., Oliver, A. (2006). Stepwise Upregulation of the Pseudomonas aeruginosa Chromosomal Cephalosporinase Conferring High-Level {beta}-Lactam Resistance Involves Three AmpD Homologues.. Antimicrob. Agents Chemother. 50: 1780-1787 [Abstract] [Full Text]  
  • Macia, M. D., Borrell, N., Segura, M., Gomez, C., Perez, J. L., Oliver, A. (2006). Efficacy and Potential for Resistance Selection of Antipseudomonal Treatments in a Mouse Model of Lung Infection by Hypermutable Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 50: 975-983 [Abstract] [Full Text]  
  • Aloush, V., Navon-Venezia, S., Seigman-Igra, Y., Cabili, S., Carmeli, Y. (2006). Multidrug-Resistant Pseudomonas aeruginosa: Risk Factors and Clinical Impact. Antimicrob. Agents Chemother. 50: 43-48 [Abstract] [Full Text]  
  • Juan, C., Macia, M. D., Gutierrez, O., Vidal, C., Perez, J. L., Oliver, A. (2005). Molecular Mechanisms of {beta}-Lactam Resistance Mediated by AmpC Hyperproduction in Pseudomonas aeruginosa Clinical Strains. Antimicrob. Agents Chemother. 49: 4733-4738 [Abstract] [Full Text]  
  • Hsu, D. I., Okamoto, M. P., Murthy, R., Wong-Beringer, A. (2005). Fluoroquinolone-resistant Pseudomonas aeruginosa: risk factors for acquisition and impact on outcomes. J Antimicrob Chemother 55: 535-541 [Abstract] [Full Text]  
  • Giacometti, A., Cirioni, O., Kamysz, W., D'Amato, G., Silvestri, C., Prete, M. S. D., Licci, A., Riva, A., Lukasiak, J., Scalise, G. (2005). In Vitro Activity of the Histatin Derivative P-113 against Multidrug-Resistant Pathogens Responsible for Pneumonia in Immunocompromised Patients. Antimicrob. Agents Chemother. 49: 1249-1252 [Abstract] [Full Text]  
  • Mushtaq, S., Ge, Y., Livermore, D. M. (2004). Doripenem versus Pseudomonas aeruginosa In Vitro: Activity against Characterized Isolates, Mutants, and Transconjugants and Resistance Selection Potential. Antimicrob. Agents Chemother. 48: 3086-3092 [Abstract] [Full Text]  
  • Zelenitsky, S. A., Harding, G. K. M., Sun, S., Ubhi, K., Ariano, R. E. (2003). Treatment and outcome of Pseudomonas aeruginosa bacteraemia: an antibiotic pharmacodynamic analysis. J Antimicrob Chemother 52: 668-674 [Abstract] [Full Text]  
  • Chamot, E., Boffi El Amari, E., Rohner, P., Van Delden, C. (2003). Effectiveness of Combination Antimicrobial Therapy for Pseudomonas aeruginosa Bacteremia. Antimicrob. Agents Chemother. 47: 2756-2764 [Abstract] [Full Text]  
  • Brun-Buisson, C. (2003). Antibiotic Therapy of Ventilator-Associated Pneumonia: In Search of the Magic Bullet. Chest 123: 670-673 [Full Text]  
  • Jonas, D., Engels, I., Hartung, D., Beyersmann, J., Frank, U., Daschner, F. D. (2003). Development and mechanism of fluoroquinolone resistance in Legionella pneumophila. J Antimicrob Chemother 51: 275-280 [Abstract] [Full Text]  
  • Van Eldere, J. (2003). Multicentre surveillance of Pseudomonas aeruginosa susceptibility patterns in nosocomial infections. J Antimicrob Chemother 51: 347-352 [Abstract] [Full Text]  
  • Lepper, P. M., Grusa, E., Reichl, H., Hogel, J., Trautmann, M. (2002). Consumption of Imipenem Correlates with {beta}-Lactam Resistance in Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 46: 2920-2925 [Abstract] [Full Text]  
  • Peacock, J. E. Jr., Herrington, D. A., Wade, J. C., Lazarus, H. M., Reed, M. D., Sinclair, J. W., Haverstock, D. C., Kowalsky, S. F., Hurd, D. D., Cushing, D. A., Harman, C. P., Donowitz, G. R. (2002). Ciprofloxacin plus Piperacillin Compared with Tobramycin plus Piperacillin as Empirical Therapy in Febrile Neutropenic Patients: A Randomized, Double-Blind Trial. ANN INTERN MED 137: 77-87 [Abstract] [Full Text]  
  • Giamarellou, H. (2002). Prescribing guidelines for severe Pseudomonas infections. J Antimicrob Chemother 49: 229-233 [Full Text]  
  • Le Thomas, I., Couetdic, G., Clermont, O., Brahimi, N., Plesiat, P., Bingen, E. (2001). In vivo selection of a target/efflux double mutant of Pseudomonas aeruginosa by ciprofloxacin therapy. J Antimicrob Chemother 48: 553-555 [Abstract] [Full Text]  
  • Kaye, K. S., Cosgrove, S., Harris, A., Eliopoulos, G. M., Carmeli, Y. (2001). Risk Factors for Emergence of Resistance to Broad-Spectrum Cephalosporins among Enterobacter spp.. Antimicrob. Agents Chemother. 45: 2628-2630 [Abstract] [Full Text]  
  • Henwood, C. J., Livermore, D. M., James, D., Warner, M., Pseudomonas Study Group, t. (2001). Antimicrobial susceptibility of Pseudomonas aeruginosa: results of a UK survey and evaluation of the British Society for Antimicrobial Chemotherapy disc susceptibility test. J Antimicrob Chemother 47: 789-799 [Abstract] [Full Text]  
  • Livermore, D. M. (2001). Of Pseudomonas, porins, pumps and carbapenems. J Antimicrob Chemother 47: 247-250 [Full Text]  
  • Lynch, J. P. III (2001). Hospital-Acquired Pneumonia : Risk Factors, Microbiology, and Treatment. Chest 119 : 373S-384S [Abstract] [Full Text]  
  • (1999). Pseudomonas Aeruginosa Develops Resistance to Imipenem. JWatch Infect. Diseases 1999: 7-7 [Full Text]  
  • Tranier, S., Bouthors, A.-T., Maveyraud, L., Guillet, V., Sougakoff, W., Samama, J.-P. (2000). The High Resolution Crystal Structure for Class A beta -Lactamase PER-1 Reveals the Bases for Its Increase in Breadth of Activity. J. Biol. Chem. 275: 28075-28082 [Abstract] [Full Text]