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a Department of Internal
Medicine, University Hospital Maastricht, Maastricht, The Netherlands, b Department of Internal Medicine,
University Hospital Utrecht, Utrecht, The Netherlands, c Department of Medical Microbiology, University Hospital
Maastricht, Maastricht, The Netherlands, d Department of Internal Medicine,
Eemland Hospital, Amersfoort, The Netherlands
Correspondence to: Dr D C J J Bergmans, Department of Internal Medicine, University Hospital Maastricht, P.O. Box 5800, 6202 AZ Maastricht, The Netherlands.
Received 9 February 1998; Returned to authors 18 May 1998; Revised version received 17 June 1998; Accepted for publication 6 July 1998
BACKGROUND
Ventilator-associated
pneumonia (VAP) caused by Pseudomonas aeruginosa is
usually preceded by colonisation of the respiratory tract. During
outbreaks, colonisation with P aeruginosa is mainly derived from exogenous sources. The relative importance of different pathways of colonisation of P aeruginosa has rarely been
determined in non-epidemic settings.
METHODS
In order to determine the
importance of exogenous colonisation, all isolates of P
aeruginosa obtained by surveillance and clinical cultures from
two identical intensive care units (ICUs) were genotyped with pulsed
field gel electrophoresis.
RESULTS
A total of 100 patients were
studied, 44 in ICU 1 and 56 in ICU 2. Twenty three patients were
colonised with P aeruginosa, seven at the start of the
study or on admission and 16 of the remaining 93 patients became
colonised during the study. Eight patients developed VAP due to P
aeruginosa. The incidence of respiratory tract colonisation and
VAP with P aeruginosa in our ICU was similar to that
before and after the study period, and therefore represents an endemic
situation. Genotyping of 118 isolates yielded 11 strain types: eight in
one patient each, two in three patients each, and one type in eight
patients. Based on chronological evaluation and genotypical identity of
isolates, eight cases of cross-colonisation were identified. Eight
(50%) of 16 episodes of acquired colonisation and two (25%) of eight
cases of VAP due to P aeruginosa seemed to be the result
of cross-colonisation.
CONCLUSIONS
Even in non-epidemic settings
cross-colonisation seems to play an important part in the epidemiology
of colonisation and infection with P aeruginosa.
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