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Control of endemic nosocomial Legionnaires' disease by using sterile potable water for high risk patients

Published online by Cambridge University Press:  15 May 2009

T. J. Marrie ,
D. Haldane ,
S. Macdonald ,
K. Clarke ,
C. Fanning ,
S. Le Fort-Jost ,
G. Bezanson  and
J. Joly
T. J. Marrie
Affiliation:
Departments of Medicine, Dalhousie University and the Victorial General Hospital, Halifax Department of Microbiology, Dalhousie University and the Victoria General Hospital, Halifax
D. Haldane
Affiliation:
Department of Microbiology, Dalhousie University and the Victoria General Hospital, Halifax
S. Macdonald
Affiliation:
The Infection Control Department Victoria General Hospital, Halifax
K. Clarke
Affiliation:
The Infection Control Department Victoria General Hospital, Halifax
C. Fanning
Affiliation:
The Infection Control Department Victoria General Hospital, Halifax
S. Le Fort-Jost
Affiliation:
The Infection Control Department Victoria General Hospital, Halifax
G. Bezanson
Affiliation:
Department of Microbiology, Dalhousie University and the Victoria General Hospital, Halifax
J. Joly
Affiliation:
Nova Scotia and Department of Microbiology Université Laval, Quebec City, Quebec
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In a setting where potable water is contaminated with Legionella pneumophila serogroup 1, we performed two case control studies. The first case control study consisted of 17 cases of nosocomial Legionnaires' disease (LD) and 33 control (the patients who were admitted to the ward where the case was admitted immediately before and after the case) subjects. Cases had a higher mortality rate 65% vs 12% (P < 0.004); were more likely to have received assisted ventilation (P < 0.00001); to have nasogastric tubes (P < 0.0004) and to be receiving corticosteroids or other immunosuppressive therapy (P < 0.0001). Based on the results of this study, sterile water was used to flush nasogastric tubes and to dilute nasogastric feeds. Only 3 cases of nosocomial LD occurred during the next year compared with 12 the previous year (P < 0.0001). Nine cases subsequently occurred and formed the basis for the second case-control study. Eighteen control subjects were those patients admitted to the same unit where the case developed LD, immediately before and after the case. The mortality rate for the cases was 89% vs 6% for controls (P < 0.00003). The only other significant difference was that cases were more likely to be receiving corticosteroids or other immunosuppressive therapy 89% vs 39% ( < 0.01). We hypothesized that microaspiration of contaminated potable water by immunocompromised patients was a risk factor for nosocomial Legionnaires' disease. From 17 March 1989 onwards such patients were given only sterile potable water. Only two cases of nosocomial LD occurred from June 1989 to September 1990 and both occurred on units where the sterile water policy was not in effect. We conclude that aspiration of contaminated potable water is a possible route for acquisition of nosocomial LD in our hospital and that provision of sterile potable water to high risk patients (those who are receiving corticosteroids or other immunosuppressive drugs; organ transplant recipients or hospitalized in an intensive care unit) should be mandatory.

Type
Research Article
Information
Epidemiology & Infection , Volume 107 , Issue 3 , December 1991 , pp. 591 - 605
Copyright
Copyright © Cambridge University Press 1991

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