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PMID: 16322602 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A predominantly clonal multi-institutional outbreak of Clostridium difficile-associated diarrhea with high morbidity and mortality.

The New England journal of medicine ·Vol. 353 ·No. 23 ·2005-12-08 ·Pages 2442-9

Loo VG, Poirier L, Miller MA, Oughton M, Libman MD, Michaud S, Bourgault AM, Nguyen T, Frenette C, Kelly M, Vibien A, Brassard P, Fenn S, Dewar K, Hudson TJ, Horn R, René P, Monczak Y, Dascal A

Abstract

In March 2003, several hospitals in Quebec, Canada, noted a marked increase in the incidence of Clostridium difficile-associated diarrhea. In 2004 we conducted a prospective study at 12 Quebec hospitals to determine the incidence of nosocomial C. difficile-associated diarrhea and its complications and a case-control study to identify risk factors for the disease. Isolates of C. difficile were typed by pulsed-field gel electrophoresis and analyzed for binary toxin genes and partial deletions in the toxin A and B repressor gene tcdC. Antimicrobial susceptibility was evaluated in a subgroup of isolates. A total of 1703 patients with 1719 episodes of nosocomial C. difficile-associated diarrhea were identified. The incidence was 22.5 per 1000 admissions. The 30-day attributable mortality rate was 6.9 percent. Case patients were more likely than matched controls to have received fluoroquinolones (odds ratio, 3.9; 95 percent confidence interval, 2.3 to 6.6) or cephalosporins (odds ratio, 3.8; 95 percent confidence interval, 2.2 to 6.6). A predominant strain, resistant to fluoroquinolones, was found in 129 of 157 isolates (82.2 percent), and the binary toxin genes and partial deletions in the tcdC gene were present in 132 isolates (84.1 percent). A strain of C. difficile that was resistant to fluoroquinolones and had binary toxin and a partial deletion of the tcdC gene was responsible for this outbreak of C. difficile-associated diarrhea. Exposure to fluoroquinolones or cephalosporins was a risk factor.

MeSH Terms
Aged Aged, 80 and over Bacterial Proteins/genetics Bacterial Toxins/genetics Case-Control Studies Clostridioides difficile/classification,genetics,isolation & purification,pathogenicity Clostridium Infections/epidemiology,microbiology,mortality Cross Infection/epidemiology,microbiology,mortality Diarrhea/epidemiology,microbiology Disease Outbreaks Drug Resistance, Bacterial Female Fluoroquinolones/therapeutic use Gene Deletion Humans Incidence Male Microbial Sensitivity Tests Prospective Studies Quebec/epidemiology Repressor Proteins/genetics Risk Factors
Chemicals
Bacterial Proteins Bacterial Toxins Fluoroquinolones Repressor Proteins TcdC protein, Clostridium difficile
Authors & Affiliations
19 authors, click to expand affiliations / ORCID
Loo Vivian G
Department of Microbiology, McGill University Health Center, Montreal, Que., Canada. [email protected]
Poirier Louise
Miller Mark A
Oughton Matthew
Libman Michael D
Michaud Sophie
Bourgault Anne-Marie
Nguyen Tuyen
Frenette Charles
Kelly Mirabelle
Vibien Anne
Brassard Paul
Fenn Susan
Dewar Ken
Hudson Thomas J
Horn Ruth
René Pierre
Monczak Yury
Dascal André
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
1533-4406
Published
2005-12-08
Epub
2005-00-01
Pages
2442-9
Language
English
Region
United States
NLM ID
0255562
Subset
IM
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