Chlorhexidine Sponge Dressing
Chlorhexidine Sponge Dressing
Chlorhexadine is an antiseptic that has broad spectrum effect against both gram-positive and gram-negative bacteria. Use of a foam dressing containing chlorhexadine for central lines was examined in patients with cancer for prevention of central line infection.
Effectiveness Not Established
Research Evidence Summaries
Chambers, S.T., Sanders, J., Patton, W.N., Ganly, P., Birch, M., Crump, J.A., & Spearing, R.L. (2005). Reduction of exit-site infections of tunnelled intravascular catheters among neutropenic patients by sustained-release chlorhexidine dressings: Results from a prospective randomized controlled trial. Journal of Hospital Infection, 61, 53–61.doi: 10.1016/j.jhin.2005.01.023
The purpose of the study was to evaluate the efficacy of sustained-release chlorhexidine (CHX) dressings versus standard dressings.
Intervention Characteristics/Basic Study Process:
All adult patients admitted under the hematology service that were to receive chemotherapy and had a tunneled cuffed central intravascular catheter inserted were eligible for inclusion. After insertion, all tunneled intravascular catheters were randomized, but they were treated in the same manner with a sterile gauze and porous adhesive dressings until the exit site was dry and free from ooze. Those randomized to standard catheter exit-site treatment (control group) received no dressing in accordance with BCHS guidelines. The CHX group (intervention group) were treated with CHX dressings consisting of a 2.5 cm hydrophilic polyurethane foam disk containing CHX gluconate in a sustained-release formulation. These were applied to the exit site as soon the oozing had stopped following intravascular catheter insertion, and changed as needed or weekly until the catheter was removed. The same treatment was continued for the life of the catheter but if an intravascular catheter was removed and replaced, the new catheter was randomized. Exit site and tunnels were routinely examined on a weekly basis.
The primary endpoint of this study was the development of exit-site and/or tunnel infection. The secondary endpoint was removal of the catheter for infection. In total, 114 tunneled intravascular catheters in 95 patients were randomized from August 1998 to December 2001.
- The total sample consisted of 95 patients.
- Mean age of the control group was 49 years (range = 16–70); mean age of the CHX group was 50 years (range = 15–68).
- Chemotherapy infusion was a key disease characteristic
- Total catheters in the control group were 43.
- Total catheters in the CHX group were 52.
Malignancies: acute nyeloid leukemia (17% control, 17% CHX), non-Hodgkin lymphoma (9% control, 11% CHX), myeloma (5% control, 9% CHX), acute lymphoblastic leukemia (3% control, 6% CHX), breast (2% control, 1% CHX), chronic myeloid leukemia (2% control, 1% CHX). Other malignancies (amyloidosis, Ewing sarcoma, renal cell carcinoma, myelodysplasia and aplastic anemia) accounted for 6% of the CHX group.
A single-site inpatient hematology unit
Phase of Care and Clinical Applications:
- There were multiple phases of care
Clinical applications were for late effects and survivorship
All patients received a 10F vascular catheter with a surecuff tissue ingrowth, vitacuff antimicrobial cuff inserted percutaneously by a radiologist using the Seldinger technique.
- Exit site infection: redness, pain, and tenderness at the exit site less than 2 cm from the skin along the intravascular catheter of sufficient degree to warrant antimicrobial therapy as judged by the attending medical team.
- Tunnel infection: pain, tenderness, and swelling over the subcutaneous tunnel more than 2 cm from the exit site.
- Bacteraemia: presence of one or more species of organism in two sets of blood cultures within 24 hours (both sets from peripheral vein or one set from peripheral vein and one from central catheter).
- Intravascular catheter-related bacteraemia: evidence of bacteraemia in the presence of fever but no recognized focus of infection, with the same organism recovered from the catheter tip as from the blood cultures or exit site.
- Suspected intravascular catheter infection: positive blood cultures drawn in the presence of fever (single measure higher than 38.5ºC or two measures higher than 38ºC) with no other recognized focus of infection, causing the catheter to be removed prematurely.
- Intravascular catheter infection: suspected catheter infection in which the culture of the tip yielded more than 15 colonies of the same organism as was found in the blood cultures drawn from either the catheter or from the periphery.
- Neutropenia: less than 0.5 x 109 neutrophils/L
This study has shown that the use of CHX dressings was associated with less exit site infections (OR = 0.13, 95% CI [0.04, 0.37], p < 0.001). The rate of premature catheter removal for these infections was reduced approximately three fold in the CHX group (OR = 0.23, 95% CI [0.07, 0.77]). The failures of the CHX dressing group were associated either with a very early occurrence after insertion of the catheter, suggesting that the infecting organisms were implanted at the time of catheter insertion, or with delays in application of the CHX dressing. Positive blood cultures occurred in fewer patients in the control group (p < 0.01) with less isolates of gram-positive organisms in the control group (p < 0.05).
This study demonstrated that use of the sustained-release CHX dressing was associated with reduced extralumenal catheter infections; however, it was not associated with fewer blood stream infections.
- Small sample size (less than 100 participants)
- There was a risk of bias favoring the CHX group because the clinical team was not blinded to treatment.
- Results were reported in terms of patients and various time points and could have been more clear if reported in terms of total or cumulative patient catheter days.
- No results of defined outcomes such as suspected catheter infection, etc., were reported.
It is unclear how immunosuppressed the sample was in order to draw relevant conclusions.
Sustained-release CHX dressings may help to reduce some central line-associated infections in patients with cancer who are at risk and in whom other aspects of catheter insertion and care are in place. Further well-designed research in this area is warranted.
O’Grady, N.P., Alexander, M., Burns, L.A., Dellinger, E.P., Garland, J., Heard, S.O., . . . Healthcare Infection Control Practices Advisory Committee (HICPAC). (2011). Guidelines for the prevention of intravascular catheter-related infections, 2011. Retrieved from http://www.cdc.gov/hicpac/pdf/guidelines/bsi-guidelines-2011.pdf
PROFESSIONAL GROUPS: Healthcare Infection Control Practices Advisory Committee (HICPAC), Center for Disease Control (CDC)
Purpose & Patient Population:
To provide evidence-based recommendations for the prevention of intravascular catheter-related infections for healthcare personnel who insert and care for intravascular catheters and for those responsible for surveillance and infection control in hospital, outpatient, and home health settings. Patients addressed in the guidelines were adult and pediatric patients with intravascular catheters.
Type of Resource/Evidence-Based Process:
The resource is comprised of evidence-based guidelines. For the development process, evidence was categorized as category 1A to category 2 based on strength of recommendation and support from clinical or epidemiological studies.
Phase of Care and Clinical Applications:
- Patients were undergoing multiple phases of care.
- The study has clinical applicability for pediatrics.
Results Provided in the Reference:
The results were not summarized.
Guidelines & Recommendations:
The guidelines provided extensive recommendations regarding the education and training of staff; selection of catheters and sites, including avoidance of the femoral vein for central venous access and use of the central venous catheter with the minimum number of ports needed; hand hygiene; use of maximal sterile barrier precautions for insertion; skin preparation with alcohol, iodine, or chlorhexidine; use of standard catheter site dressing regimens; specific aspects of care for umbilical and dialysis catheters; and use of piggybacks, stopcocks, and catheter flushing. Guideline recommendations include a bundling of multiple recommendations: antimicrobial-impregnated catheters and cuffs are recommended in patients with long-term use if the organizational central line-associated blood stream infection (CLABSI) rate is not decreasing despite the implementation of comprehensive strategies for improvement. Lower-level (category II) recommendations include the use of prophylactic antimicrobial lock solutions in patients with long-term catheters who have a history of CLABSIs despite optimal aseptic technique as well as daily cleansing of patients in the intensive care unit with 2% chlorhexidine-impregnated washcloths. Recommends changing IV administration sets no more often than every 96 hours unless used for blood products. For needleless components, recommends changing according to administration set timing as above, and states no benefit to changing more than every 72 hours.
Provides extensive recommendations for management of all types of intravenous catheters and system components. Nurses should refer to the full set of guidelines for all specific aspects of care.