Journal Information
Vol. 15. Issue 4.
Pages 312-322 (July - August 2011)
Share
Share
Download PDF
More article options
Vol. 15. Issue 4.
Pages 312-322 (July - August 2011)
Original article
Open Access
Outbreaks, persistence, and high mortality rates of multiresistant Pseudomonas aeruginosa infections in a hospital with AIDS-predominant admissions
Visits
3226
Marisa Zenaide Ribeiro Gomes1,
Corresponding author
marisargomes@ioc.fiocruz.br

Correspondence to: Laboratório de Pesquisa em Infecção Hospitalar Instituto Oswaldo Cruz Fundação Oswaldo Cruz Avenida Brasil 4365, Pavilhão Rocha Lima - S319 Manguinhos, 21040-900, Rio de Janeiro, RJ Brazil Phone: 55 21 2598-4277, extension 319 Fax: +55 21 3322-0613.
, Carolina Romero Machado2, Magda de Souza da Conceição2, Jois Alves Ortega3, Sonia Maria Ferraz M Neves4, Maria Cristina da Silva Lourenço5, Marise Dutra Asensi6
1 Assistant Researcher, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (IOC/FIOCRUZ), RJ, Brazil; Visiting Scientist, University of Texas, MD Anderson Cancer Center, USA
2 Infectious Diseases Physician, Instituto de Pesquisa Clínica Evandro Chagas/FIOCRUZ, RJ, Brazil
3 Infectious Diseases Physician, Instituto de Pesquisa Clínica Evandro Chagas/FIOCRUZ, RJ, Brazil
4 Chairman of Hospital Infection Control Committee, Instituto de Pesquisa Clínica Evandro Chagas/FIOCRUZ, RJ, Brazil
5 Chairman of Laboratory of Bacteriology, Instituto de Pesquisa Clínica Evandro Chagas/FIOCRUZ, RJ, Brazil
6 Chairman of Nosocomial Infection Research Laboratory, IOC/FIOCRUZ, RJ, Brazil
This item has received

Under a Creative Commons license
Article information
Abstract
Bibliography
Download PDF
Statistics
Abstract
Introduction

Authors have reported increased incidence of multiresistant Pseudomonas aeruginosa (MR-PA) infections worldwide over the last decade. Researchers have proposed multifaceted approaches to control MR-PA infections, but none have been reported in the acquired immunodeficiency syndrome (AIDS) setting.

Objective and Methods

Herein we report the impact of a multifaceted intervention for controlling MR-PA over five years in a hospital with AIDS-predominant admissions and describe the clinical characteristics of MR-PA infection in our patient population. The clinical outcomes of infected patients and molecular characteristics of the isolated strains were used as tools for controlling MR-PA infection rates.

Results

Significant temporary decrease of new infections was achieved after intervention, although a high level of diagnostic suspicion of nosocomial infection was maintained. We obtained 35 P. aeruginosa isolates with multiresistant profiles from 13 infected and 3 colonized patients and 2 environmental samples. Most of the patients (94%) were immunocompromised with AIDS (n=10) or HTLV-1 infections (n=5). Of the followed patients, 67% had persistent and/or recurrent infections, and 92% died. We observed differences in the antibiotic-resistance pattern of MR-PA infection/colonization during two outbreaks, although the genetic profiles of the tested strains were identical.

Conclusions

Therefore, we concluded that early multidisciplinary interventions are essential for reducing the burden caused by this microorganism in patients with AIDS. Prolonged or suppressive antibiotic-based therapy should be considered for MR-PA infections in patients with AIDS because of the persistence characteristic of MR-PA in these patients.

Keywords:
Pseudomonas aeruginosa
disease outbreaks
infection control
molecular epidemiology
acquired immunodeficiency syndrome
Full text is only aviable in PDF
References
[1.]
A. Deplano, O. Denis, L. Poirel, et al.
Molecular characterization of an epidemic clone of panantibiotic-resistant Pseudomonas aeruginosa.
J Clin Microbiol, 43 (2005), pp. 1198-1204
[2.]
Y. Yakupogullari, B. Otlu, M. Dogukan, et al.
Investigation of a nosocomial outbreak by alginate-producing pan-antibioticresistant Pseudomonas aeruginosa.
Am J Infect Control, 36 (2008), pp. e13-e18
[3.]
J.A. Adachi, C. Perego, L. Graviss, et al.
The role of interventional molecular epidemiology in controlling clonal clusters of multidrug resistant Pseudomonas aeruginosa in critically ill cancer patients.
Am J Infect Control, 37 (2009), pp. 442-446
[4.]
S. Hota, Z. Hirji, K. Stockton, et al.
Outbreak of multidrug-resistant Pseudomonas aeruginosa colonization and infection secondary to imperfect intensive care unit room design.
Infect Control Hosp Epidemiol, 30 (2009), pp. 25-33
[5.]
J.A. Cortes, S.I. Cuervo, A.M. Urdaneta, et al.
Identifying and controlling a multiresistant Pseudomonas aeruginosa outbreak in a Latin-American cancer centre and its associated risk factors.
Braz J Infect Dis, 13 (2009), pp. 99-103
[6.]
R.C. Cezário, L. Duarte De Morais, J.C. Ferreira, et al.
Nosocomial outbreak by imipenem-resistant metallo-beta-lactamase-producing Pseudomonas aeruginosa in an adult intensive care unit in a Brazilian teaching hospital.
Enferm Infecc Microbiol Clin, 27 (2009), pp. 269-274
[7.]
O. Samuelsen, M.A. Toleman, A. Sundsfjord, et al.
Molecular epidemiology of metallo-beta-lactamase-producing Pseudomonas aeruginosa isolates from Norway and Sweden shows import of international clones and local clonal expansion.
Antimicrob Agents Chemother, 54 (2010), pp. 346-352
[8.]
A.P. Zavascki, C.G. Carvalhaes, R.C. Picão, A.C. Gales.
Multidrugresistant Pseudomonas aeruginosa and Acinetobacter baumannii: resistance mechanisms and implications for therapy.
Expert Rev Anti Infect Ther, 8 (2010), pp. 71-93
[9.]
P. Domingo, A. Ferré, M.A. Baraldès, et al.
Pseudomonas aeruginosa bronchopulmonary infection in patients with AIDS, with emphasis on relapsing infection.
Eur Respir J, 12 (1998), pp. 107-112
[10.]
D. Asboe, V. Gant, H.M. Aucken, et al.
Persistence of Pseudomonas aeruginosa strains in respiratory infection in AIDS patients.
AIDS, 12 (1998), pp. 1771-1775
[11.]
J.K. Johnson, S.M. Arduino, O.C. Stine, et al.
Multilocus sequence typing compared to pulsed-field gel electrophoresis for molecular typing of Pseudomonas aeruginosa.
J Clin Microbiol, 45 (2007), pp. 3707-3712
[12.]
G.H. Pereira, A.S. Levin, H.B. Oliveira, M.L. Moretti.
Controlling the clonal spread of Pseudomonas aeruginosa infection.
Infect Control Hosp Epidemiol, 29 (2008), pp. 549-552
[13.]
J.S. Garner, W.R. Jarvis, T.G. Emori, et al.
CDC definitions for nosocomial infections.
Am J Infect Control, 16 (1988), pp. 128-140
[14.]
T.G. Emori, D.H. Culver, T.C. Horan, et al.
National Nosocomial Infections Surveillance system (NNIS): description of surveillance methods.
Am J Infect Control, 19 (1991), pp. 19-35
[15.]
T.C. Horan, M. Andrus, M.A. Dudeck.
CDC/NHSN surveillance definition of health care-associated infection and criteria for specific types of infections in the acute care setting.
Am J Infect Control, 36 (2008), pp. 309-332
[16.]
R.B. Laing.
Nosocomial infections in patients with HIV disease.
J Hosp Infect, 43 (1999), pp. 179-185
[17.]
Clinical and Laboratory Standards Institute. Performance standards for antimicrobial susceptibility testing. 18th informational supplement. M100-S17. Wayne, PA: NCCLS, 2007.
[18.]
Y. Arakawa, N. Shibata, K. Shibayama, et al.
Convenient test for screening metallo-beta-lactamase-producing gram-negative bacteria by using thiol compounds.
J Clin Microbiol, 38 (2000), pp. 40-43
[19.]
C.M.C.P.A. Romão, Y.N. De Faria, L.R. Pereira, et al.
Susceptibility of clinical isolates of multiresistant Pseudomonas aeruginosa to a hospital disinfectant and molecular typing.
Mem Inst Oswaldo Cruz, 100 (2005), pp. 541-548
[20.]
F.C. Tenover, R.D. Arbeit, R.V. Goering, et al.
Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing.
J Clin Microbiol, 33 (1995), pp. 2233-2239
[21.]
G.H. Furtado, S.T. Martins, A.M. Machado, et al.
Clinical culture surveillance of carbapenem-resistant Pseudomonas aeruginosa and Acinetobacter species in a teaching hospital in Sao Paulo.
Brazil: a 7-year study. Infect Control Hosp Epidemiol, 27 (2006), pp. 1270-1273
[22.]
M. Thuong, K. Arvaniti, R. Ruimy, et al.
Epidemiology of Pseudomonas aeruginosa and risk factors for carriage acquisition in an intensive care unit.
J Hosp Infect, 53 (2003), pp. 274-282
[23.]
D. Lepelletier, A. Cady, N. Caroff, et al.
Imipenem-resistant Pseudomonas aeruginosa gastrointestinal carriage among hospitalized patients: risk factors and resistance mechanisms.
Diagn. Microbiol. Infect. Dis, 66 (2010), pp. 1-6
[24.]
C. Slekovec, J.C. Navellou, G. Blasco, et al.
Is surveillance of Pseudomonas aeruginosa carriage in intensive care units useful?.
Ann Fr Anesth Reanim, 29 (2010), pp. 279-282
[25.]
X. Bertrand, M. Thouverez, D. Talon, et al.
Endemicity, molecular diversity and colonisation routes of Pseudomonas aeruginosa in intensive care units.
Intensive Care Med, 27 (2001), pp. 1263-1268
[26.]
C.M. Fortaleza, L.C. Figueiredo, C.C. Beraldo, et al.
Risk factors of oropharyngeal carriage of Pseudomonas aeruginosa among patients from a Medical-Surgical Intensive Care Unit.
Braz J Infect Dis, 13 (2009), pp. 173-176
[27.]
S. Panagea, C. Winstanley, M.J. Walshaw, et al.
Environmental contamination with an epidemic strain of Pseudomonas aeruginosa in a Liverpool cystic fibrosis centre, and study of its survival on dry surfaces.
J Hosp Infect, 59 (2005), pp. 102-107
[28.]
I.J. Clifton, L.A. Fletcher, C.B. Beggs, et al.
A laminar flow model of aerosol survival of epidemic and non-epidemic strains of Pseudomonas aeruginosa isolated from people with cystic fibrosis.
BMC Microbiol, 8 (2008), pp. 105
[29.]
Z.G. Nunes, A.S. Martins, A.L. Altoe, et al.
Indoor air microbiological evaluation of offices, hospitals, industries, and shopping centers.
Mem Inst Oswaldo Cruz, 100 (2005), pp. 351-357
[30.]
L. Pagani, C. Colinon, R. Migliavacca, et al.
Nosocomial outbreak caused by multidrug-resistant Pseudomonas aeruginosa producing IMP-13 metallo-beta-lactamase.
J Clin Microbiol, 43 (2005), pp. 3824-3828
[31.]
D. Jonas, E. Meyer, F. Schwab, H. Grundmann.
Genodiversity of resistant Pseudomonas aeruginosa isolates in relation to antimicrobial usage density and resistance rates in intensive care units.
Infect Control Hosp Epidemiol, 29 (2008), pp. 350-357
[32.]
J. Quale, S. Bratu, J. Gupta, D. Landman.
Interplay of efflux system, ampC, and oprD expression in carbapenem resistance of Pseudomonas aeruginosa clinical isolates.
Antimicrob Agents Chemother, 50 (2006), pp. 1633-1641
[33.]
H. Pai, J.-W. Kim, J. Kim, et al.
Carbapenem resistance mechanisms in Pseudomonas aeruginosa clinical isolates.
Antimicrob Agents Chemother, 45 (2001), pp. 480-484
[34.]
T.P. Lodise, C.D. Miller, J. Graves, et al.
Clinical prediction tool to identify patients with Pseudomonas aeruginosa respiratory tract infections at greatest risk for multidrug resistance.
Antimicrob Agents Chemother, 51 (2007), pp. 417-422
[35.]
S.V. Bhat, A.Y. Peleg, T.P. Lodise, et al.
Failure of current cefepime breakpoints to predict clinical outcomes of bacteremia caused by gram-negative organisms.
Antimicrob Agents Chemother, 51 (2007), pp. 4390-4395
[36.]
J.L. Crandon, C.C. Bulik, J.L. Kuti, D.P. Nicolau.
Clinical pharmacodynamics of cefepime in patients infected with Pseudomonas aeruginosa.
Antimicrob Agents Chemother, 54 (2010), pp. 1111-1116
[37.]
E.N. Deal, S.T. Micek, R.M. Reichley, D.J. Ritchie.
Effects of an alternative cefepime dosing strategy in pulmonary and bloodstream infections caused by Enterobacter spp, Citrobacter freundii, and Pseudomonas aeruginosa: a single-center, openlabel, prospective, observational study.
[38.]
J.C. Davies.
Pseudomonas aeruginosa in cystic fibrosis: pathogenesis and persistence.
Paediatr Respir Rev, 3 (2002), pp. 128-134
[39.]
A.G. Ferreira, R.S. Leão, A.P. Carvalho-Assef, et al.
Influence of biofilm formation in the susceptibility of Pseudomonas aeruginosa from Brazilian patients with cystic fibrosis.
[40.]
E.L. Murphy, B. Wang, R.A. Sacher, et al.
Respiratory and urinary tract infections, arthritis, and asthma associated with HTLV-I and HTLV-II infection.
Emerg Infect. Dis, 10 (2004), pp. 109-116
[41.]
A.P. Zavascki, A.L. Barth, P.B. Gaspareto, et al.
Risk factors for nosocomial infections due to Pseudomonas aeruginosa producing metallo-beta-lactamase in two tertiary-care teaching hospitals.
J. Antimicrob. Chemother, 58 (2006), pp. 882-885
[42.]
C. Peña, C. Suarez, F. Tubau, et al.
Carbapenem-resistant Pseudomonas aeruginosa: factors influencing multidrug-resistant acquisition in non-critically ill patients.
Eur. J. Clin. Microbiol. Infect. Dis, 28 (2009), pp. 519-522
Copyright © 2011. Elsevier Editora Ltda.. All rights reserved
Download PDF
The Brazilian Journal of Infectious Diseases
Article options
Tools