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Infection Protection 
Catheter site dressings and infection control
by
Cynthia T. Crosby
Vice President, Clinical Affairs, Medi-Flex,Inc.

Infection
Protection is a monthly column dedicated to education about infection
control issues. This month’s column discusses catheter site dressing
materials and antisepsis. Every fourth issue includes a Q&A forum to
answer questions you have about the infection control information
presented here. If you have a question, please submit it to jakridge@hpnonline.com
or call (941)927-9345 ext. 202.
Introduction
The Guidelines for the Prevention of Intravascular Catheter-Related
Infections published by the Centers for Disease Control (CDC) provide
evidence-based recommendations for reducing the incidence of
catheter-related bloodstream infections (CRBSIs).1 One of the
recommendations concerns the use of transparent, semi-permeable
polyurethane dressings. Compared to gauze, the transparency of
polyurethane dressings provides the advantage of visual inspection of
the catheter site without removing the dressing. Polyurethane dressings
also do not need to be changed as often as gauze.
Polyurethane dressings and infection risk
An early study of transparent dressings compared to gauze conducted in
1987 demonstrated that cutaneous bacterial colonization and
catheter-related infection were similarly low for both types of
dressings. Neither type of dressing resulted in bacteremia.2 However, a
meta-analysis of infection risk associated with various central venous
catheter dressings revealed a slight increase of bacteremia and catheter
sepsis associated with transparent dressings compared to gauze.3 A
prospective, randomized study comparing gauze, conventional polyurethane
transparent dressing and highly permeable transparent dressings used for
pulmonary artery catheters also demonstrated that the highest risk of
cutaneous bacterial colonization occurred under conventional
polyurethane dressings. The risk for any infection among the three
groups was extremely low, however, and there were no cases of CRBSIs.
Permeable polyurethane was associated with a lower risk of colonization
than conventional polyurethane.4
Several additional studies have
been conducted to compare infection rates associated with various types
of transparent polyurethane dressings and traditional gauze. Infection
rates appear to be generally comparable,5 but moisture accumulation
under conventional polyurethane dressings contributes to increased risk
for cutaneous infection. Therefore, a higher moisture vapor transmission
rate for transparent dressings was suggested,4 and several highly
permeable transparent dressings are now available. Infection rate
results from studies of these highly permeable transparent dressings
vary. A review of several prospective studies suggests that there is no
significant difference in clinical outcomes when highly permeable
dressings are used,5 although one retrospective study demonstrated a
significant 25% decrease in catheter-related infections associated with
highly permeable dressings and associated cost savings of $69,814 due to
the decrease in infection care costs and fewer hospital days.5,6 The CDC
guidelines for catheter-related infections conclude that CRBSI rates do
not differ significantly by type of dressing, and the choice of dressing
material can be a matter of preference. In addition, the CDC guidelines
describe advantageous effects of using chlorhexidine as part of the
dressing regimen to reduce infection rates.1
Chlorhexidine dressings
A prospective study evaluated the efficacy of a chlorhexidine dressing
in reducing microbial flora at catheter insertion sites. The dressing
was constructed of a urethane sponge composite to which chlorhexidine
gluconate was chemically bound. The dressing matrix was semi-permeable
and non-occlusive with a higher vapor transmission rate than skin. An
initial pilot study with 17 patients was conducted to determine the
amount of catheter-site colonization that occurred with a control
dressing. The pilot study was followed by a randomized study of 57
patients who received either a chlorhexidine dressing or a control
dressing. The pilot study of the control dressing produced positive
cultures in 29.4% of patients. Similarly, in the randomized arm of the
study, the control group had a 29% rate of colonization. In contrast,
the rate of infection among patients in the chlorhexidine dressing group
was statistically significantly lower at only 3.8%. There were no
adverse effects reported among patients in the chlorhexidine dressing
group.7 Similar positive results have been demonstrated elsewhere. A
prospective, randomized study evaluating the use of a chlorhexidine
impregnated dressing (Biopatch; Johnson & Johnson, Arlington, TX) in 55
patients found positive cultures in 40.1% of the control group (11/27
patients) compared to 3.4% of the chlorhexidine group (1/29 patients).8
These results are illustrated in
(Figure 1.)
Cutaneous antisepsis with dressings
A "best practices" study of hemodialysis catheter care compared 2%
chlorhexidine plus 70% isopropyl alcohol used with a transparent
dressing to povidine with either gauze, transparent dressings, or
transparent anti-microbial polyhexamethylene dressings. A total of 150
patients were evaluated for 30 days. All povidine dressing were changed
three times per week. Chlorhexidine dressings were changed once per week
unless they were soiled or stopped adhering. Staff and patients were
surveyed regarding their preferences. Use of chlorhexidine dressings
resulted in better staff and patient satisfaction, reduced nursing time,
and decreased costs. The use of a 2% chlorhexidine/isopropyl alcohol
skin antisepsis and transparent dressing was preferred for hemodialysis
catheter care.9 A case report of an increase in CRBSIs in another
hemodialysis center described an intervention designed to decrease
infection rates. Staff members were educated about central venous
catheter care, chlorhexidine replaced povidone iodine for cutaneous
antisepsis, gauze was used instead of transparent dressings, and the use
of antimicrobial ointments containing polyethylene glycol was
discontinued. The 6-month intervention program decreased the CRBSI rate
from 4.1 per 100 patient-months to1 per 100 patient-months. The use of
optimal antisepsis contributed to the decrease in CRBSI rates.10
Cost savings with chlorhexidine
A randomized cost-benefit analysis including patients from all
Philadelphia area hospitals and one academic center compared
chlorhexidine dressings to standard treatment without chlorhexidine. The
estimated annual cost benefit of using chlorhexidine dressings ranged
from $275 million to approximately $1.97 billion, depending on baseline
CRBSI rates, incremental costs of treating CRBSI, and the number of
catheters used. Preventable mortality ranged from 329 to 3906 deaths
annually, assuming nationwide use of chlorhexidine in the United
States.11
Conclusion
Study results regarding the superiority of transparent polyurethane
dressings compared to gauze vary, although semi-permeable transparent
dressings appear to provide benefits over standard transparent
polyurethane by decreasing moisture under the dressings. The difference
in clinical outcomes is not statistically significant; therefore, choice
of dressing should be based on preference.1 However, study results
demonstrate that the addition of a chlorhexidine dressing and/or
chlorhexidine for cutaneous antisepsis around catheter insertion sites
significantly decreases infection rates. Chlorhexidine is recommended by
the CDC for catheter care and has been shown in best practices and
infection intervention analyses to reduce infection rates.
HPN
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Figure 1 Legend:
Two prospective, randomized studies of chlorhexidine (CHX) dressings
compared to control groups demonstrated statistically significant
reductions in infection rates with chlorhexidine. |
References
1.Centers for Disease Control and Prevention. Guidelines for the
Prevention of Intravascular Catheter-Related Infections. MMWR.
2002;51(RR-10). Available at:
http://www.cdc.gov/mmwr/preview
/mmwrhtml/rr5110a1.htm. Accessed on December 27, 2004.
2.Maki DG, Ringer M. Evaluation of dressing regimens for prevention of
infection with peripheral intravenous catheters. Gauze, a transparent
polyurethane dressing, and an iodophor-transparent dressing. JAMA.
1987;258(17):2396-2403.
3.Hoffmann KK, Weber DJ, Samsa GP, Rutala WA. Transparent polyurethane
film as an intravenous catheter dressing. A meta-analysis of the
infection risks. JAMA. 1992;267(15):2072-2076.
4.Maki DG, Stolz SS, Wheeler S, Mermel LA. A prospective, randomized
trial of gauze and two polyurethane dressings for site care of pulmonary
artery catheters: implications for catheter management. Crit Care Med.
1994;22(11):1729-1737.
5.Zitella L. Central venous catheter site care for blood and marrow
transplant recipients. Clin J Oncol Nurs. 2003;7(3):289-298.
6.Treston-Aurand J, Olmsted RN, Allen-Bridson K, Craig CP. Impact of
dressing materials on central venous catheter infection rates. J
Intraven Nurs. 1997;20(4):201-206.
7.Shapiro JM, Bond EL, Garman JK. Use of a chlorhexidine dressing to
reduce microbial colonization of epidural catheters. Anesthesiology.
1990;73:625-631.
8.Mann TJ, Orlikowski CE, Gurrin LC, Keil AD. The effect of the biopatch,
a chlorhexidine impregnated dressing, on bacterial colonization of
epidural catheter exit sites. Anaesth Intensive Care.
2001;29(6):600-603.
9.Balovlenkov EK. Developing a CQI model to identify best practices in
hemodialysis catheter care using a 2% chlorhexidine (CHG) and 70%
isopropyl alcohol (IPA) no touch applicator [abstract]. Presented at:
The 35th annual meeting of the American Nephrology Nurses’ Association;
April 15-18, 2004: Washington, DC.
10.Price CS, Hacek D, Noskin GA, Peterson LR. An outbreak of bloodstream
infections in an outpatient hemodialysis center. Infect Control Hosp
Epidemiol. 2002;23(12):725-729.
11.Crawford AG, Fuhr JP Jr, Rao B. Cost-benefit analysis of
chlorhexidine gluconate dressing in the prevention of catheter-related
bloodstream infections. Infect Control Hosp Epidemiol. 2004
Aug;25(8):668-674. 12.Figure 1. Infection rates from two randomized
studies7,8 |
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February 2005


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