Printer Friendly
The Free Library
22,741,889 articles and books

Multidrug-resistant Pseudomonas aeruginosa bloodstream infections: analysis of trends in prevalence and epidemiology. (Letters).



To the Editor: Multidrug-resistant (MDR MDR,
n See multidrug resistance.

MDR,
n the abbreviation for minimum daily requirement, specifically the Minimum Daily Requirements for Specific Nutrients compiled by the United States Food and Drug Administration.
) Pseudomonas aeruginosa Pseudomonas aeruginosa A normal soil inhabitant and human saprophyte that may contaminate various solutions in a hospital, causing opportunistic infection in weakened Pts Clinical Infective endocarditis in IVDAs, RTIs, UTIs, bacteremia, meningitis, 'malignant'  bloodstream infection has been described only in patients with cystic fibrosis (1) and in isolated outbreaks in intensive-care unit (ICU ICU intensive care unit.

ICU
abbr.
intensive care unit



ICU

see intensive care unit.

ICU 
) or neoplastic neoplastic /neo·plas·tic/ (ne?o-plas´tik)
1. pertaining to a neoplasm.

2. pertaining to neoplasia.


neoplastic

pertaining to neoplasia or a neoplasm.
 patients (2-4). We investigated the percentage and clinical findings of patients with P. aeruginosa bacteremia bacteremia: see septicemia.
bacteremia

Presence of bacteria in the blood. Short-term bacteremia follows dental or surgical procedures, especially if local infection or very high-risk surgery releases bacteria from isolated sites.
 having MDR strains in a 1,700-bed university hospital in Rome, Italy, over a 10-year period (1990-1999).

All consecutive patients with the first episode of community- or hospital-acquired P. aeruginosa bacteremia, according to the definition of the Centers for Disease Control and Prevention Centers for Disease Control and Prevention (CDC), agency of the U.S. Public Health Service since 1973, with headquarters in Atlanta; it was established in 1946 as the Communicable Disease Center.  (5), were included in the analysis. The term MDR P. aeruginosa covered resistance to ciprofloxacin ciprofloxacin /cip·ro·flox·a·cin/ (sip?ro-flok´sah-sin) a synthetic antibacterial effective against many gram-positive and gram-negative bacteria; used as the hydrochloride salt.

cip·ro·flox·a·cin
n.
, ceftazidime, imipenem, gentamicin gentamicin /gen·ta·mi·cin/ (jen?tah-mi´sin) an aminoglycoside antibiotic complex isolated from bacteria of the genus Micromonospora, , and piperacillin. In patients with P aeruginosa bacteremia, we evaluated age, gender, type of infection (hospital or community acquired), duration of hospitalization, risk factors, clinical findings, and outcome. Prognosis immediately before bacteremia developed was determined with the revised Acute Physiology and Chronic Health Evaluation (APACHE) III system (6).

Bacteria were identified by using API 20NE (Biomerieux, Marcyl'Etoile, France). MICs were determined by broth microdilution in accordance with the methods of the National Committee for Clinical Laboratory Standards. Contingency data were analyzed by the two-tailed chi-square test or Fisher's exact test Fisher's exact test

a statistical test for association in a two-by-two table based on the exact hypergeometric distribution of the frequencies within the table.
, and continuous data were analyzed by Student t test. Logistic regression analysis was used to determine which risk factors were independently significant. All statistical analysis was performed with the software program Statistics (Windows Systat Inc., Evanston, IL).

In the study period, P. aeruginosa was isolated from 358 of 379,190 hospitalized patients. Among 358 patients with P. aeruginosa bacteremia, 133 (37%) were hospitalized in medical wards, 103 (29%) in ICUs, 97 (27%) in surgical wards, and 25 (7%) in neonatology neonatology /neo·na·tol·o·gy/ (ne?o-na-tol´ah-je) the diagnosis and treatment of disorders of the newborn.

ne·o·na·tol·o·gy
n.
; 45 (12%) had HIV HIV (Human Immunodeficiency Virus), either of two closely related retroviruses that invade T-helper lymphocytes and are responsible for AIDS. There are two types of HIV: HIV-1 and HIV-2. HIV-1 is responsible for the vast majority of AIDS in the United States.  infection and 28 (8%) had hematologic malignancies.

For the study period, the overall hospital incidence of both nosocomial nosocomial /noso·co·mi·al/ (nos?o-ko´me-il) pertaining to or originating in a hospital.

nos·o·co·mi·al
adj.
1. Of or relating to a hospital.

2.
 and community-acquired P. aeruginosa bacteremia was 0.94 per 1,000 hospital admissions. In particular, the incidence increased from 9.7 to 24.7 per 1,000 hospital admissions (p <0.01; chi square for trend) in ICUs. In HIV-infected patients, the incidence increased from 1.5 to 12.4 per 1,000 hospital admissions until 1996 when, after highly active antiretroviral therapy Noun 1. highly active antiretroviral therapy - a combination of protease inhibitors taken with reverse transcriptase inhibitors; used in treating AIDS and HIV
drug cocktail, HAART
 was introduced, it decreased to 0.7 (p = 0.01, chi square for trend).

The first case of MDR P. aeruginosa strain was isolated in the hematologic hematological, hematologic

pertaining to or emanating from blood cells.


hematological tests
total and differential white cell counts, hematocrit estimation, erythrocyte count.
 unit in 1992. After that, the hospital prevalence of MDR strains increased significantly (p=0.03) from 8% (3/37) in 1993 to 17% (9/54) in 1999. Overall, we observed 51 (14% of 358) cases of MDR P. aeruginosa bloodstream infections; 49 (96%) were nosocomial. The prevalence of MDR among the total P. aeruginosa bacteremia cases per ward was as follows: medical wards 1 (2%) of 60 (95% confidence intervals [CI] = 0.05-10); surgical wards 7 (7%) of 97 (95% CI = 3-15); hematologic ward 3 (11%) of 28 (95% CI = 2-28); ICUs 22 (21%) of 103 (95% CI = 13-31); and infectious diseases ward (in HIV-infected patients only) 18 (40%) of 45 (95% CI = 26-54).

The mean age [+ or -] standard deviation of patients with MDR P. aeruginosa infections was 524 [+ or -] 12 years (range 29 to 77); 35 patients (69%) were men, and 9 (18%) were active intravenous drug abusers. The mean Apache III score at diagnosis of bacteremia was 41 [+ or -] 17 (95% CI = 39-56). The mean concentration of circulating polymorphonuclear polymorphonuclear /poly·mor·pho·nu·cle·ar/ (-noo´kle-er) having a nucleus so deeply lobed or so divided as to appear to be multiple.

pol·y·mor·pho·nu·cle·ar
adj.
Having a lobed nucleus.
 cells was 2,974 [+ or -] 2,790/ [mm.sup.3] (95% CI = 2,181-3,796). In HIV-infected patients, the mean number of peripheral CD4+ cells was 71 [+ or -] 104 / [mm.sup.3] (95% CI = 35-106). Advanced age (odds ratio [OR] = 1.07; 95% CI = 1.04-1.10, p<0.01), HIV infection (OR = 3.94; 95% CI = 1.10-14.11, p=0.03), intravenous drug abuse (OR=13.15; 95% CI=1.65-104.5; p=0.01), and previous therapy with quinolones (OR=3.21; 95% CI=2.14-23.33; p = 0.001) were independent risk factors on logistic regression analysis.

The overall mortality rate of patients with P. aeruginosa bacteremia was 31%; death rates were higher among patients with higher APACHE III score (mean 39 versus 27; p=0.01) and MDR P. aeruginosa infections (67% versus 23%; OR=15.13; 95% CI=1.90-323.13; p=0.001).

This prospective surveillance of P aeruginosa bloodstream infections clearly indicates, for the first time, that multidrug resistance is statistically associated with HIV infection, as already observed for cystic fibrosis (1). We also identified a significant correlation between MDR P. aeruginosa bacteremia and intravenous drug abuse, advanced age, and previous quinolone use.

The association between isolation of MDR strains, HIV infection, and intravenous drug abuse (the most important HIV risk factor in Italy) is not an unexpected result. We have already demonstrated that hospitalized HIV-infected patients are at increased risk of acquiring nosocomial bloodstream infections compared with other immunocompromised hosts (7). Age is a well-known predisposing factor for bacterial infections. In particular, older HIV-infected patients progress more rapidly to AIDS (8).

Resistance following treatment with a single antimicrobial agent may be due in some circumstances to synergy between enhanced production of beta-lactamases and diminished outer membrane permeability (9). More emphasis is now given, however, to the energy-dependent efflux efflux Medtalk That which flows outward  of antibiotics by P. aeruginosa. A single opening of a pump facilitates resistance to quinolones, beta-lactams, tetracycline tetracycline (tĕ'trəsī`klēn), any of a group of antibiotics produced by bacteria of the genus Streptomyces. They are effective against a wide range of Gram positive and Gram negative bacteria, interfering with protein , and chloramphenicol chloramphenicol (klōr'ămfĕn`əkŏl'), antibiotic effective against a wide range of gram-negative and gram-positive bacteria (see Gram's stain). It was originally isolated from a species of Streptomyces bacteria.  among the drug efflux (9). The recent characterization of a carbapenem-hydrolyzing metallo-beta-lactamase from P. aeruginosa opens new possibilities for reducing the spread of resistant strains (10).

One limitation of our study is the absence of genotypic analysis of MDR strains. However, we are confident that a general outbreak of MDR P aeruginosa did not occur in our hospital. Nevertheless, limited outbreaks involving few patients in different wards remain a possibility. In summary, the observation that 14% of P. aeruginosa bloodstream infections are multidrug resistant is worrisome and reflects the growing worldwide problem of antimicrobial resistance. In particular, the fact that HIV-infected patients are at increased risk, as are persons with cystic fibrosis, suggests the need for ongoing worldwide surveillance of P. aeruginosa in immunocompromised immunocompromised /im·mu·no·com·pro·mised/ (-kom´pro-mizd) having the immune response attenuated by administration of immunosuppressive drugs, by irradiation, by malnutrition, or by certain disease processes (e.g., cancer).  patients.

References

(1.) Aris RM, Gilligan PH, Neuringer IP, Gott KK, Rea J, Yakaskas JR. The effects of panresistant bacteria in cystic fibrosis on lung transplant outcome. Am J Respir Crit Care Med 1997; 155:1699-704.

(2.) Hsueh PR, Teng LJ, Yang PC, Chen YC, Ho SW, Luh KT. Persistence of a multidrug-resistant Pseudomonas aeruginosa clone in an intensive care burn unit. J Clin Microbiol 1998;36:1347-51.

(3.) Richard P, Le Floch R, Chamoux C, Pannier M, Espaze E, Richet H. Pseudomonas aeruginosa outbreak in a burn unit: role of antimicrobials in the emergence of multiply resistant strains. J Infect Dis 1994; 170:377-83.

(4.) Verweij PE, Bijl D, Melchere WJ, De Pauw BE, Meis JF, Hoogkamp-Korstanje JA, et al. Pseudo-outbreak of multiresistant Pseudomonas aeruginosa in a hematology unit. Infect Control Hosp Epidemiol 1997;18:128-31.

(5.) Garner JS, Jarvis WR, Emori TG, Horan TC, Hughes JM. CDC See Control Data, century date change and Back Orifice.

CDC - Control Data Corporation
 definition for nosocomial infections. Am J Infect Control 1988;16:128-40.

(6.) Knaus WA, Wagner DP, Draper EA, Zimmerman JE, Bergner M, Bostos PG, et al. The APACHE III prognostic system: risk prediction of hospital mortality for critically ill hospitalized adults. Chest 1991;100:1619-36.

(7.) Tumbarello M, Tacconelli E, de Gaetano K, Leone F, Morace G, Cauda R, et al. Nosocomial bloodstream infections in HIV-infected patients. Attributable mortality and extension of hospital stay. J Acquir Immune Defic Syndr 1998; 19:490-7.

(8.) Tumbarello M, Tacconelli E, Cauda R. Age as a prognostic factor in AIDS. Lancet 1996;348:623-4.

(9.) Poole K. Bacterial multidrug resistance-emphasis on efflux mechanisms and Pseudomonas aeruginosa. J Antimicrob Chemother 1994;34:453-6.

(10.) Poirel L, Naas T, Nicolas D, Collet L, Bellais S, Cavallo JD, et al. Characterization of VIM-2, a carbapenem-hydrolyzing metallo-[beta]-lactamase and its plasmid- and integron-borne gene from a Pseudomonas aeruginosa clinical isolate in France. Antimicrob Agents Chemother 2000;44;891-7.
Evelina Tacconelli, Mario
Tumbarello, Silvia Bertagnolio,
Rita Citton, Teresa Spanu,
Giovanni Fadda,
and Roberto Cauda
Catholic University, Rome, Italy
COPYRIGHT 2002 U.S. National Center for Infectious Diseases
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2002, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

 Reader Opinion

Title:

Comment:



 

Article Details
Printer friendly Cite/link Email Feedback
Author:Cauda, Roberto
Publication:Emerging Infectious Diseases
Article Type:Letter to the Editor
Geographic Code:4EUIT
Date:Feb 1, 2002
Words:1338
Previous Article:Medicine to kill, medicine to heal. (Another Dimension).
Next Article:Clinical issues in the prophylaxis, diagnosis, and treatment of anthrax. (Conference Summary).
Topics:



Related Articles
Reply to Drs. Angulo and Collignon.
Trends in Antimicrobial-Drug Resistance in Japan.
VEB-1-Like Extended-Spectrum [Beta]-Lactamases in Pseudomonas aeruginosa, Kuwait.
Changing Antibiotic Sensitivity Patterns at a University Hospital, 1992 Through 1999.
Multidrug-resistant pseudomonas aeruginosa producing PER-1 extended-spectrum serine-[beta]-lactamase and VIM-2 metallo-[beta]-lactamase. (Letters).
Surveillance for antimicrobial resistance in Croatia. (Synopsis).
Antimicrobial drug resistance in pathogens causing nosocomial infections at a University Hospital in Taiwan, 1981-1999. (Research).
Current status of antimicrobial resistance in Taiwan. (Synopsis).
Temporal changes in prevalence of antimicrobial resistance in 23 U.S. hospitals. (Research).
VIM- and IMP-Type Metallo-[beta]-lactamase--producing Pseudomonas spp. and Acinetobacter spp. in Korean hospitals. (Dispatches).

Terms of use | Copyright © 2014 Farlex, Inc. | Feedback | For webmasters