258 Infection 34 · 2006 · No. 5 © URBAN & VOGEL
Infection Clinical and Epidemiological Study
Influence of Prolonged Use of Intravenous
Administration Sets in Paediatric Cancer Patients
on CVAD-related Bloodstream Infection Rates
and Hospital Resources
A. Simon, G. Fleischhack, G. Wiszniewsky, C. Hasan, U. Bode, M. H. Kramer
Abstract
Background: To assess the effects of extending the routine
intravenous administration set (IVAS) change-interval from
72 h (group 1) to 7 days (group 2) on the incidence density
for central venous access device (CVAD)-related bloodstream
infections (BSIs) and on resource expenditures in a single-
centre pilot study.
Procedure: Prospective pre-/post-intervention comparison of
two consecutive 12-month surveillance periods (2001–2003)
in a 17-bed paediatric oncology tertiary care unit. IVAS
changes and nosocomial infections (NIs) were prospec-
tively analysed using a standardized unit-based surveillance
system (Oncopaed NI).
Results: All 175 eligible patients were enrolled, 96 in group
1 and 79 in group 2. Both groups had similar distributions
of primary diagnoses and risk factors. The proportion of
IVAS changes performed after 3 days increased from 5.6% to
22.5%, but only 8% of IVASs in group 2 were changed after
7 days. Most IVAS changes (64.8% in group 1 and 92.9%
in group 2) were done because of therapeutic interven-
tions (blood products, parenteral nutrition [TNP]) before the
scheduled endpoint. Overall, the rates and incidence densities
of NIs were significantly lower during the second period. The
corresponding results for CVAD-related BSIs did not show
significant differences. No death attributable to a NI occurred.
The ‘7-day’ strategy resulted in cost savings for devices
(3,300$/year) and of nursing time (23 working days/year).
Conclusions: Extending the routine IVAS change-interval from
3 days to 7 days appears to be safe and cost-effective in a
paediatric oncology unit with high infection control standards
and continuous surveillance for NIs. These results do not prove
that 7-day intervals prevent infections, but they do suggest
that this policy probably is not harmful and that a prospec-
tively randomized study with sufficient power is needed.
Infection 2006; 34: 258–263
DOI 10.1007/s15010-006-5646-y
Introduction
The use of long-term central venous access devices
(CVADs) in supportive care contributes to the intriguing
success of chemotherapy in paediatric oncology. However,
the use of CVADs also increases the risk for infection
[1, 2]. A reduced dose intensity due to a therapeutic delay
in patients with infectious complications negatively affects
the success of anticancer treatment and may increase mor-
tality [3]. Catheter-related infections result in an increased
length of hospital stay and in higher costs [4, 5] and drain
resources for nursing care, antimicrobials and for surgical
removal of the device in some cases [6]. Thus, the preven-
tion of CVAD-related bloodstream infections (BSIs) is an
issue of high priority in paediatric oncology. Therefore,
infection control advisory committees in the USA (since
1996) [7, 8] and in Germany (since 2002) [9] recommend
to extend the routine change-intervals of the intravenous
administration sets (IVAS) to 72 h, which was followed in
our department except for patients receiving blood prod-
ucts [10, 11] or TPN with iv lipids [12] (change after 6 h
and 24 h, respectively). The safety of extending the routine
IVAS change-interval beyond 96 h is still not fully inves-
tigated [13]. The only available prospectively randomized
study among adult oncology patients suggested an IVAS
change-interval of 7 days to be safe and cost-effective
for low risk patients [14] but, unlike in paediatric cancer
patients, more than 90% of the catheters in this study were
short-term, non-tunnelled devices. The principle aim of this
pilot study was to investigate the practical consequences of
extending the routine IVAS change-interval to 7 days in a
paediatric oncology unit.
A. Simon (corresponding author), G. Fleischhack, G. Wiszniewsky,
C. Hasan, U. Bode
Dept. of Paediatric Hematology and Oncology,
Children’s Hospital, Medical Center, University of Bonn,
Adenauerallee 119, 53113 Bonn, Germany;
Phone: (+49/228) 287-3254, Fax: -3301,
e-mail: asimon@ukb.uni-bonn.de
M. H. Kramer
Institute for Hygiene and Public Health, University of Bonn,
Bonn, Germany
Received: November 1, 2005 • Revision accepted: May 23, 2006
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