Serious infections associated with intravascular catheters are common. The
available data suggests there are likely to be more than 500 000 cases of c
atheter-associated bloodstream infections occurring annually in Western Eur
ope and the USA. These may be associated with as many as 100 000 deaths. Th
e pathophysiology of this common condition is still not fully elucidated. W
ith catheters that are in place for short periods (a few days), microbial m
igration down the outer surface of the device to the intravascular tip pred
ominates. For catheters that are in place for longer periods, migration occ
urs more often via the internal lumen. After being in place for more than 8
days, nearly all central vein catheters will have microorganisms embedded
in a biofilm within the catheter lumen. In some catheters, microorganisms w
ill proliferate to sufficient numbers for systemic sepsis to result. The oc
currence and rate of this proliferation is dependent on microbial virulence
factors, host factors, and characteristics of the catheter. Diagnosis of i
ntravascular device-associated sepsis remains problematic because the patho
physiology of the condition changes with time and because standard culture
techniques rarely detect organisms embedded in biofilms. The semiquantitati
ve roll method on blood agar remains in common use because of its simplicit
y. However, the method only samples the external surface of the catheter. F
or catheters that have been in place for extended periods of time, methods
that better sample the internal lumen, such as sonication and quantitative
broth methods, should be developed and used.