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Vol. 15. Issue 1.
Pages 1-5 (January - February 2011)
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Vol. 15. Issue 1.
Pages 1-5 (January - February 2011)
Original article
Open Access
Carbapenem stewardship – positive impact on hospital ecology
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Ana Lucia Lei Munhoz Lima1,
Corresponding author
ccih.iot@hcnet.usp.br

Correspondence to: Ovídio Pires de Campos, 333 - sala 311ª. 05403-010 - São Paulo Phone: (55 11) 30696900 Fax: (55 11) 30696900.
, Priscila Rosalba Domingos de, Oliveira2, Adriana Pereira de Paula3, Karine Dal-Paz4, João Nóbrega de Almeida Jr5, Cássia da Silva Félix6, Flávia Rossi7
1 Chief Physician, Infection Control Service, Institute of Orthopedics and Traumatology, Hospital das Clínicas, School of Medicine, Universidade de São Paulo - USP, Brazil
2 Assistant Physician, Infection Control Service, Microbiology Laboratory, LIM
3 Nurse, Infection Control Service, Hospital das Clínicas, School of Medicine, USP, Brazil
4 Pharmacist; Infection Service, Institute of Orthopedics and Traumatology, School of Medicine, USP, Brazil
5 Assistant Physician, Microbiology Laboratory, Hospital das Clínicas, Divisão de Laboratório Central, LIM 03, School of Medicine, USP, Brazil
6 Nurse, Infection Service, Institute of Orthopedics and Traumatology, Hospital das Clínicas, School of Medicine, USP, Brazil
7 Chief Physician, Microbiology Laboratory, Hospital das Clínicas, Divisão de Laboratório Central, LIM 03, School of Medicine, USP, Brazil
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Abstract
Introduction

Excessive group 2 carbapenem use may result in decreased bacterial susceptibility.

Objective

We evaluated the impact of a carbapenem stewardship program, restricting imipenem and meropenem use.

Methods

Ertapenem was mandated for ESBL-producing Enterobacteriaceae infections in the absence of non-fermenting Gram-negative bacilli (GNB) from April 2006 to March 2008. Group 2 carbapenems were restricted for use against GNB infections susceptible only to carbapenems and suspected GNB infections in unstable patients. Cumulative susceptibility tests were done for nosocomial pathogens before and after restriction using Clinical and Laboratory Standards Institute (CLSI) guidelines. Vitek System or conventional identification methods were performed and susceptibility testing done by disk diffusion according to CLSI. Antibiotic consumption (t-test) and susceptibilities (McNemar's test) were determined.

Results

The defined daily doses (DDD) of group 2 carbapenems declined from 61.1 to 48.7 DDD/1,000 patient-days two years after ertapenem introduction (p = 0.027). Mean ertapenem consumption after restriction was 31.5 DDD/1,000 patient-days. Following ertapenem introduction no significant susceptibility changes were noticed among Gram-positive cocci. The most prevalent GNB were P. aeruginosa, Klebsiella pneumoniae, and Acinetobacter spp. There was no change in P. aeruginosa susceptibility to carbapenems. Significantly improved P. aeruginosa and K. pneumoniae ciprofloxacin susceptibilities were observed, perhaps due to decreased group 2 carbapenem use. K. pneumoniae susceptibility to trimethoprim-sulfamethoxazole improved.

Conclusion

Preferential use of ertapenem resulted in reduced group 2 carbapenem use, with a positive impact on P. aeruginosa and K. pneumoniae susceptibility.

Keywords:
carbapenems
drug resistance
bacterial ecology
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References
[1.]
A. Apisarnthanarak, S. Danchaivijitr, T. Khawcharoenporn, et al.
Effectiveness of education and an antibiotic-control program in a tertiary care hospital in Thailand.
Clin Infect Dis, 42 (2006), pp. 768-775
[2.]
A. Brink, C. Feldman, D.C. Grolman, et al.
Appropriate use of the carbapenems.
S Afr Med J, 94 (2004), pp. 857-861
[3.]
Clinical Laboratory Standards Institute 2006.
Performance standards for antimicrobial susceptibility testing.
The Institute, (2006),
[4.]
M. DiNubile, I. Friedland, C.Y. Chan, et al.
Bowel colonization with resistant gram-negative bacilli after antimicrobial therapy of intra-abdominal infections: observations from two randomized comparative clinical trials of ertapenem therapy.
Eur J Clin Microbiol Infect Dis, 24 (2005), pp. 443-449
[5.]
European Antimicrobial Resistance Surveillance System (EARRS). http://www.rivm.nl/earss/result/Monitoring_reports/Annual_reports.jsp.Accessed 8 July 2009.
[6.]
D.A. Goff, J. Mangino.
Ertapenem: No effect on gram-negative susceptibilities to imipenem.
J Infect, 57 (2008), pp. 123-127
[7.]
E.J. Goldstein, D.M. Citron, V. Peraino, T. Elgourt, A.R. Miebohm, S. Lu.
Introduction of ertapenem onto a hospital formulary: Effect on antimicrobial usage improved in vitro susceptibility of Pseudomonas aeruginosa.
Antimicrob Agents Chemother, 53 (2009), pp. 5122-5126
[8.]
P.R. Hsueh, W.H. Chen, K.T. Luh.
Relationships between antimicrobial use and antimicrobial resistance in Gram-negative bacteria causing nosocomial infections from 1991–2003 at a university hospital in Taiwan.
Int J Antimicrob Agents, 26 (2005), pp. 463-472
[9.]
E. Iosifidis, C. Antachopoulos, M. Tsivitanidou, et al.
Differential correlation between rates of antimicrobial drug consumption and prevalence of antimicrobial resistance in a tertiary care hospital in Greece.
Infect Control Hosp Epidemiol, 29 (2008), pp. 615-622
[10.]
A.L. Lima, P.R. Oliveira, A.P. Paula, A.V. Zumiotti.
Influence of ertapenem administration on the incidence of carbapenem- resistant Pseudomonas aeruginosa.
Braz J Infect Dis, 12 (2008), pp. 105-106
[11.]
A.L. Lima, P.R. Oliveira, A.P. Paula, K. Dal-Paz, F. Rossi, A.V. Zumiotti.
The impact of ertapenem use on the susceptibility of Pseudomonas aeruginosa to imipenem: a hospital case study.
Infect Control Hosp Epidemiol, 30 (2009), pp. 487-490
[12.]
D. Livermore, S. Mushtaq, M. Warner.
Selectivity of ertapenem for Pseudomonas aeruginosa mutants cross-resistant to other carbapenems.
J Antimicrob Chemother, 55 (2005), pp. 306-311
[13.]
J.M. Loeffler, J. Garbino, D. Lew, S. Harbarth, P. Rohner.
Antibiotic consumption, bacterial resistance and their correlation in a Swiss University Hospital and its Adult Intensive Care Units.
Scand J Infect Dis, 35 (2003), pp. 843-850
[14.]
A.R. Marra, S.B. Wey, A. Castelo, et al.
Nosocomial bloodstream infections caused by Klebsiella pneumoniae: impact of extended- spectrum β-lactamase (ESBL) production on clinical outcome in a hospital with high ESBL prevalence.
BMC Infect Dis, 6 (2006), pp. 24-31
[15.]
J.L. Nouwen.
Controlling antibiotic use resistance.
Clin Infect Dis, 42 (2006), pp. 776-777
[16.]
P. Shah, R.D. Isaacs.
Ertapenem, the first of a new group of carbapenems.
J Antimicrob Chemother, 52 (2003), pp. 538-542
[17.]
E. Hirsch, V.H. Tam.
Detection and treatment options for Klebsiella pneumoniae carbapenemases (KPCs): an emerging cause of multidrug-resistant infection.
J Antimicrob Chemother, 65 (2010), pp. 1119-1125
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The Brazilian Journal of Infectious Diseases
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