Literature DB >> 2655521

Intestinal decontamination for control of nosocomial multiresistant gram-negative bacilli. Study of an outbreak in an intensive care unit.

C Brun-Buisson1, P Legrand, A Rauss, C Richard, F Montravers, M Besbes, J L Meakins, C J Soussy, F Lemaire.   

Abstract

STUDY
OBJECTIVE: To study the efficacy of intestinal decontamination by oral nonabsorbable antibiotic agents to control a nosocomial outbreak of intestinal colonization and infection with multiresistant Enterobacteriaceae, and to examine its effects on endemic nosocomial infection rates.
DESIGN: A 10-week prospective incidence study (group 1), and then an 8-week randomized, open trial of intestinal decontamination (groups 2 and 3).
SETTING: A medical intensive care unit of a tertiary care university hospital. PATIENTS: Consecutive patients with unit stay of over 2 days and a severity score at admission of more than 2; 124 patients were included in group 1, 50 in group 2 (control), and 36 in group 3 (intestinal decontamination).
INTERVENTIONS: Neomycin, polymyxin E, and nalidixic acid were given to group 3 patients throughout their stay in the unit.
MEASUREMENTS AND MAIN RESULTS: Intestinal colonization with multiresistant strains occurred in 19.6% of patients in group 1, at a mean of 16 days after admission, and preceded detection in clinical samples by a mean of 11 days. During the decontamination trial, intestinal colonization rates decreased to 10% (group 2), and 3% (group 3) (P = 0.12 and P less than 0.01, compared with group 1, respectively). Corresponding infection rates were 9% (group 1), 3% (group 2), and 0 (group 3). No new cases were detected in the following 4 months. The intestinal colonization rate with gram-positive cocci was higher in group 3 than group 2 (P less than 0.001). The overall rate of nosocomial infections was at 28% (group 1), 33% (group 2), and 32% (group 3).
CONCLUSIONS: Intestinal decontamination can help to control an outbreak of intestinal colonization and infection with multiresistant gram-negative bacilli in the intensive care unit, but should not be recommended for routine prevention of endemic nosocomial infections.

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Year:  1989        PMID: 2655521     DOI: 10.7326/0003-4819-110-11-873

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


  83 in total

1.  The epidemiology of antibiotic resistance in hospitals: paradoxes and prescriptions.

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Review 2.  All great truths are iconoclastic: selective decontamination of the digestive tract moves from heresy to level 1 truth.

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3.  Selective decontamination of the digestive tract: to stimulate or stifle?

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4.  History of recognition and measurement of colonization resistance of the digestive tract as an introduction to selective gastrointestinal decontamination.

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Journal:  Epidemiol Infect       Date:  1992-12       Impact factor: 2.451

Review 5.  Selective decontamination of the digestive tract in intensive care.

Authors:  S J Boom; G Ramsay
Journal:  Epidemiol Infect       Date:  1992-12       Impact factor: 2.451

Review 6.  Nosocomial pneumonia in the intensive care unit: mechanisms and significance.

Authors:  C A'Court; C S Garrard
Journal:  Thorax       Date:  1992-06       Impact factor: 9.139

Review 7.  Pharmacoeconomics of selective decontamination of the digestive tract in intensive care patients: a US perspective.

Authors:  S J Markowsky; J Christie
Journal:  Pharmacoeconomics       Date:  1994-05       Impact factor: 4.981

8.  Outbreak of nosocomial infections due to Klebsiella pneumoniae producing SHV-4 beta-lactamase.

Authors:  G Arlet; M J Sanson-le Pors; M Rouveau; G Fournier; O Marie; B Schlemmer; A Philippon
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1990-11       Impact factor: 3.267

9.  Selective decontamination of the digestive tract.

Authors: 
Journal:  BMJ       Date:  1990-02-17

10.  Selective decontamination of the digestive tract: effect of cessation of routine application at an ICU.

Authors:  H A Tissot van Patot; J A Leusink; J Roodenburg; B M de Jongh; H S Lau; S de Boer; A de Boer
Journal:  Pharm World Sci       Date:  1996-10
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