What is new for the prevention of catheter-related bloodstream infections?
Perspective

What is new for the prevention of catheter-related bloodstream infections?

Leonardo Lorente

Department of Critical Care, Hospital Universitario de Canarias, Ofra s/n, La Laguna 38320, Santa Cruz de Tenerife, Spain

Correspondence to: Leonardo Lorente, MD, PhD. Department of Critical Care, Hospital Universitario de Canarias, Ofra s/n, La Laguna 38320, Santa Cruz de Tenerife, Spain. Email: lorentemartin@msn.com.

Abstract: After the publication in 2011 of latest guidelines of the Centers for Disease Control and Prevention (CDC) for the prevention of catheter-related bloodstream infections (CRBSI) some interesting findings have been published in that field. There has been published that skin disinfection with chlorhexidine alcohol reduced the risk of CRBSI compared to skin disinfection with povidone iodine alcohol, that the implementation of quality improvement interventions reduced the incidence of CRBSI, that the use of chlorhexidine impregnated dressing compared to standard dressings reduced the risk of CRBSI and catheter related cost in an health economic model, and that the use of antimicrobial/antiseptic impregnated catheters reduced the incidence of CRBSI and catheter related cost in clinical studies.

Keywords: Central venous catheter (CVC); bacteremia; prevention; skin disinfection; impregnated catheter; impregnated dressing


Submitted Dec 04, 2015. Accepted for publication Feb 29, 2016.

doi: 10.21037/atm.2016.03.10


Different measures have been proposed for the prevention of catheter-related bloodstream infections (CRBSI) and have been revised by different scientific societies and the Centers for Disease Control and Prevention (CDC) (1). After the publication of those guidelines in 2011 some interesting articles have been published and could be considered in the prevention of CRBSI.

In this sense, one interesting article has been recently published in September of 2015 by Mimoz et al. studying the skin antisepsis (2). In this study were randomized 5,159 catheters to 4 groups of skin disinfection, 2% chlorhexidine and 70% isopropyl alcohol with scrubbing of the skin with detergent before antiseptic application (4% chlorhexidine), 2% chlorhexidine and 70% isopropyl alcohol without scrubbing of the skin with detergent before antiseptic application, 5% povidone iodine and 69% ethanol with detergent before antiseptic application (5% povidone iodine), or 5% povidone iodine and 69% ethanol without detergent before antiseptic application. The authors found that skin disinfection with chlorhexidine alcohol showed a lower risk of CRBSI that skin disinfection with povidone iodine alcohol, with or without scrubbing of the skin with detergent before antiseptic application. Previously, in a study published by Maki et al. in 1991 was found that the use of 2% aqueous chlorhexidine decreased the risk of catheter related infection compared to 10% povidone iodine or 70% alcohol (3). In other study by Mimoz et al. published in 1996 was found that the use of 0.25% chlorhexidine gluconate plus 0.025% benzalkonium chloride plus 4% benzylic alcohol for skin disinfection compared to 10% povidone iodine reduced the incidence of catheter colonization and catheter related sepsis (4). In a meta-analysis published in 2002 by Chaiyakunapruk et al. was found a lower risk of CRBSI with the skin disinfection with chlorhexidine gluconate compared to povidone iodine (5). In a study by Parienti et al. published in 2004 was found that the use of 5% povidone iodine in 70% ethanol compared with 10% aqueous povidone iodine for skin disinfection reduced the incidence of catheter colonization (6). In two studies, one published in 2007 and other in 2012, was found that the use of 0.25% chlorhexidine gluconate plus 0.025% benzalkonium chloride plus 4% benzylic alcohol for skin disinfection compared to 5% povidone iodine in 70% ethanol reduced significantly the risk of catheter colonization and non-significantly the risk of CRBSI (7,8). Thus, the new key points of the study by Mimoz et al. (2) compared with those two previous studies (7,8) were that skin disinfection with chlorhexidine alcohol showed a significantly lower incidence of CRBSI that skin disinfection with povidone iodine alcohol, and that in the chlorhexidine alcohol group were used only two compounds. However, that study by Mimoz et al. also has some limitations (2), such as the concentrations of antiseptic agents, and the type and concentrations of alcohol components were different in the different catheter groups. In the guidelines published in 2011 was recommended the use of >0.5% chlorhexidine preparation with alcohol for skin antisepsis (1). That recommendation (with category IA) was based in the findings of the two oldest studies previously commented (3,4). Thus, we think that there is enough evidence to recommend the use of >0.5% chlorhexidine preparation with alcohol for skin antisepsis.

Two other interesting articles has been the meta-analysis by Blot et al. (9) and the Spanish experience (10) reporting that the implementation of quality improvement interventions reduced the incidence of CRBSI. In 2014 was published a meta-analysis by Blot et al., which included 41 articles published between 1995 and 2012, reporting a reduction on CRBSI incidence with the implementation of quality improvement intervention for CRBSI prevention (9). In addition, Palomar et al. published in 2013 the Spanish Experience in 192 ICUs, and this Bacteremia Zero project decreased the overall median rate of CRBSI from 3.07 to 1.12 infections per 1,000 days of catheter (10). Those quality improvement interventions for CRBSI prevention were different in the different projects and included items as education, training, feedback, clinical reminders, bundle (hand hygiene, chlorhexidine skin antisepsis, maximal sterile barrier precautions, optimal catheter site selection, daily review of line necessity), checklist, empowerment to stop procedure, surveillance, leader designation, prepackaging of central venous catheter (CVC) materials, infrastructure changes, organizational changes. In the guidelines published in 2011 was recommended the use of hospital or collaborative improvement initiatives with the combination of different preventive measures (1). That recommendation (with category IB) was based in different experiences that reported a decrease in the CTBSI incidence after the implementation of those initiatives compared to before practice (11-14). Pronovost et al. reported in 2006 a reduction in the median incidence of CRBSI from 2.7 (mean of 7.7) infections per 1,000 days of catheter to 0 (mean, 2.3) after the implementation of the intervention in 103 intensive care units (ICUs) in the Michigan state (13). Thus, we think that there is enough evidence to recommend the implementation of quality improvement interventions; in this sense, we are implementing the Spanish Bacteremia Zero project.

Another two interesting articles have been a RCT by Timsit et al. (15) and the meta-analysis published by Safdar (16) reporting a reduction in CRBSI incidence with the use of chlorhexidine impregnated dressing. In the RCT published in 2012 by Timsit et al., which included 4,163 CVC and arterial catheters from critically ill patients, was reported a significant lower incidence of CRBSI with the use of chlorhexidine impregnated dressing compared to standard dressings (15). In a meta-analysis published by Safdar et al. in 2014, including 9 RCTs and 11,247 catheters, was found that the use of impregnated dressing reduced the risk of CRBSI (16). In addition, a cost-effectiveness analysis recently published in June of 2015 by Maunoury et al. found that antimicrobial chlorhexidine gluconate dressing is more cost-effective that non-antimicrobial transparent dressings using a health economic model (17). In the guidelines published in 2011 was recommended the use of chlorhexidine impregnated dressing if the CRBSI rate has not decreased after implementation of a strategy based in basic preventive measures (which include education, the use of a >0.5% chlorhexidine preparation with alcohol for skin antisepsis, and the use of maximal sterile barrier precautions) (1). That recommendation (with category IB) was based in a meta-analysis (18) and two RCTs (19,20). In the meta-analysis published by Ho et al. (18) in 2006, including 5 RCTs and 2,396 catheters (CVC and arterial catheters), was found a significant reduction in catheter colonization and a trend to lower incidence of CRBSI with the use of chlorhexidine impregnated dressing compared to standard dressings (18). In the RCT published in 2009 by Timsit et al., which included 3,778 CVC and arterial catheters from critically ill patients, was reported a significant lower incidence of CRBSI with the use of chlorhexidine impregnated dressing (19). In the RCT published in 2009 by Ruschulte et al., which included CVC and arterial catheters from 631 cancer patients, was reported that the use of chlorhexidine impregnated dressing reduced significantly the incidence of CRBSI (20). Thus, we think that the use of chlorhexidine impregnated dressing could reduce the incidence CRBSI and catheter related costs.

In respect to another measure for the prevention of CRBSI, such the use of antimicrobial/antiseptic impregnated catheters, our team has published the efficacy and efficiency of rifampicin-miconazole impregnated catheters and chlorhexidine-silver sulfadiazine (CHSS) impregnated catheters in different clinical circumstances (21-27). Different antimicrobial agents have been used for the impregnation, such as CHSS, rifampicin-minocycline, and rifampicin-miconazole. Veenstra et al. published in 1999 a meta-analysis, which included 11 RCTs and 2,603 catheters, reporting that catheters impregnated with CHSS on the external surface (first generation) reduced the risk of CRBSI compared with non-impregnated catheters (28). Later, a meta-analysis published in 2008 by Hockenhull et al., including 3 RCTs and 1,176 patients, reported that catheters impregnated in CHSS on external and internal surfaces (second generation) reduced the CRBSI incidence compared to standard catheters (29). In addition, in a meta-analysis by Falagas et al. published in 2007, including 3,452 CVCs from 8 RCTs (using rifampicin-minocycline impregnated catheters in 7 RCTs and rifampicin-miconazole impregnated catheters in 1 RCT), was found a reduction of CRBSI with the use of antimicrobial impregnated catheters compared with non-coated catheters (30). Besides, the use of antimicrobial impregnated catheters has been found to reduce the catheter related cost in some cost-effectiveness analyses (29,31,32). However, in all those cost-effectiveness analyses was included the cost associated with the increase of hospital stay. To simply the cost-effectiveness analyses, our team has carried out several studies to compare the immediate catheter related cost (including only the cost of CVC, diagnosis of CRBSI and antimicrobials for the treatment of CRBSI, and avoiding the cost due to increased hospital stay) using antimicrobial or antiseptic impregnated catheters or standard catheters (22-26). Initially, we found that the use of rifampicin miconazole impregnated catheters could reduce CRBSI incidence and catheter related cost in the jugular venous access with tracheostomy and in the femoral venous access (22,23). Afterwards, we found that the use of second generation of CHSS catheters could reduce CRBSI incidence and catheter related cost in femoral venous access, jugular venous access and subclavian access (24-26). In the guidelines published in 2011 was recommended the use of antimicrobial/antiseptic impregnated catheters (CHSS or rifampicin-minocycline impregnated catheters) if the CRBSI rate has not decreased after implementation of a strategy based in basic preventive measures (which include education, the use of a >0.5% chlorhexidine preparation with alcohol for skin antisepsis, and the use of maximal sterile barrier precautions) (1). This recommendation (with category IA) was based in 3 RCTs showed a reduction on the incidence of catheter tip colonisation with the use of second-generation CHSS-impregnated catheters (33-35) and two RCTs showing that rifampicin-minocycline impregnated catheters reduced the risk of CRBSI (36,37). We think that the use of antimicrobial/antiseptic impregnated catheters could reduce the incidence of CRBSI and catheter related costs.


Conclusions

After the publication in 2011 of latest CDC guidelines for the prevention of CRBSI some interesting findings have been published in that field. There has been published that skin disinfection with chlorhexidine alcohol reduced the risk of CRBSI compared to skin disinfection with povidone iodine alcohol, that the implementation of quality improvement interventions reduced the incidence of CRBSI, that the use of chlorhexidine impregnated dressing compared to standard dressings reduced the risk of CRBSI and catheter related cost in an health economic model, and that the use of antimicrobial/antiseptic impregnated catheters reduced the incidence of CRBSI and catheter related cost in clinical studies.

In our opinion, there is enough scientific evidence to recommend the use of a preparation with >0.5% chlorhexidine alcohol for skin disinfection and the implementation of quality improvement interventions. In addition, the use of chlorhexidine impregnated dressing or antimicrobial/antiseptic impregnated catheters could help in the reduction of CRBSI incidence and catheter related costs.


Acknowledgements

None.


Footnote

Conflicts of Interest: L Lorente has been a speaker invited by Teleflex.


References

  1. O'Grady NP, Alexander M, Burns LA, et al. Guidelines for the prevention of intravascular catheter-related infections. Clin Infect Dis 2011;52:e162-93. [Crossref] [PubMed]
  2. Mimoz O, Lucet JC, Kerforne T, et al. Skin antisepsis with chlorhexidine-alcohol versus povidone iodine-alcohol, with and without skin scrubbing, for prevention of intravascular-catheter-related infection (CLEAN): an open-label, multicentre, randomised, controlled, two-by-two factorial trial. Lancet 2015;386:2069-77. [Crossref] [PubMed]
  3. Maki DG, Ringer M, Alvarado CJ, et al. Prospective randomised trial of povidone-iodine, alcohol, and chlorhexidine for prevention of infection associated with central venous and arterial catheters. Lancet 1991;338:339-43. [Crossref] [PubMed]
  4. Mimoz O, Pieroni L, Lawrence C, et al. Prospective, randomized trial of two antiseptic solutions for prevention of central venous or arterial catheter colonization and infection in intensive care unit patients. Crit Care Med 1996;24:1818-23. [Crossref] [PubMed]
  5. Chaiyakunapruk N, Veenstra DL, Lipsky BA, et al. Chlorhexidine compared with povidone-iodine solution for vascular catheter-site care: a meta-analysis. Ann Intern Med 2002;136:792-801. [Crossref] [PubMed]
  6. Parienti JJ, du Cheyron D, Ramakers M, et al. Alcoholic povidone-iodine to prevent central venous catheter colonization: A randomized unit-crossover study. Crit Care Med 2004;32:708-13. [Crossref] [PubMed]
  7. Mimoz O, Villeminey S, Ragot S, et al. Chlorhexidine-based antiseptic solution vs alcohol-based povidone-iodine for central venous catheter care. Arch Intern Med 2007;167:2066-72. [Crossref] [PubMed]
  8. Girard R, Comby C, Jacques D. Alcoholic povidone-iodine or chlorhexidine-based antiseptic for the prevention of central venous catheter-related infections: in-use comparison. J Infect Public Health 2012;5:35-42. [Crossref] [PubMed]
  9. Blot K, Bergs J, Vogelaers D, et al. Prevention of central line-associated bloodstream infections through quality improvement interventions: a systematic review and meta-analysis. Clin Infect Dis 2014;59:96-105. [Crossref] [PubMed]
  10. Palomar M. Impact of a national multimodal intervention to prevent catheter-related bloodstream infection in the ICU: the Spanish experience. Crit Care Med 2013;41:2364-72. [Crossref] [PubMed]
  11. Eggimann P, Harbarth S, Constantin MN, et al. Impact of a prevention strategy targeted at vascular-access care on incidence of infections acquired in intensive care. Lancet 2000;355:1864-8. [Crossref] [PubMed]
  12. Frankel HL, Crede WB, Topal JE, et al. Use of corporate Six Sigma performance-improvement strategies to reduce incidence of catheter-related bloodstream infections in a surgical ICU. J Am Coll Surg 2005;201:349-58. [Crossref] [PubMed]
  13. Pronovost P, Needham D, Berenholtz S, et al. An intervention to decrease catheter-related bloodstream infections in the ICU. N Engl J Med 2006;355:2725-32. [Crossref] [PubMed]
  14. Galpern D, Guerrero A, Tu A, et al. Effectiveness of a central line bundle campaign on line-associated infections in the intensive care unit. Surgery 2008;144:492-5; discussion 495. [Crossref] [PubMed]
  15. Timsit JF, Mimoz O, Mourvillier B, et al. Randomized controlled trial of chlorhexidine dressing and highly adhesive dressing for preventing catheter-related infections in critically ill adults. Am J Respir Crit Care Med 2012;186:1272-8. [Crossref] [PubMed]
  16. Safdar N, O'Horo JC, Ghufran A, et al. Chlorhexidine-impregnated dressing for prevention of catheter-related bloodstream infection: a meta-analysis*. Crit Care Med 2014;42:1703-13. [Crossref] [PubMed]
  17. Maunoury F, Motrunich A, Palka-Santini M, et al. Cost-Effectiveness Analysis of a Transparent Antimicrobial Dressing for Managing Central Venous and Arterial Catheters in Intensive Care Units. PLoS One 2015;10:e0130439. [Crossref] [PubMed]
  18. Ho KM, Litton E. Use of chlorhexidine-impregnated dressing to prevent vascular and epidural catheter colonization and infection: a meta-analysis. J Antimicrob Chemother 2006;58:281-7. [Crossref] [PubMed]
  19. Timsit JF, Schwebel C, Bouadma L, et al. Chlorhexidine-impregnated sponges and less frequent dressing changes for prevention of catheter-related infections in critically ill adults: a randomized controlled trial. JAMA 2009;301:1231-41. [Crossref] [PubMed]
  20. Ruschulte H, Franke M, Gastmeier P, et al. Prevention of central venous catheter related infections with chlorhexidine gluconate impregnated wound dressings: a randomized controlled trial. Ann Hematol 2009;88:267-72. [Crossref] [PubMed]
  21. Lorente L, Lecuona M, Ramos MJ, et al. The use of rifampicin-miconazole-impregnated catheters reduces the incidence of femoral and jugular catheter-related bacteremia. Clin Infect Dis 2008;47:1171-5. [Crossref] [PubMed]
  22. Lorente L, Lecuona M, Ramos MJ, et al. Rifampicin-miconazole-impregnated catheters save cost in jugular venous sites with tracheostomy. Eur J Clin Microbiol Infect Dis 2012;31:1833-6. [Crossref] [PubMed]
  23. Lorente L, Lecuona M, Ramos MJ, et al. Lower associated costs using rifampicin-miconazole-impregnated catheters compared with standard catheters. Am J Infect Control 2011;39:895-7. [Crossref] [PubMed]
  24. Lorente L, Lecuona M, Jiménez A, et al. Chlorhexidine-silver sulfadiazine-impregnated venous catheters save costs. Am J Infect Control 2014;42:321-4. [Crossref] [PubMed]
  25. Lorente L, Lecuona M, Jiménez A, et al. Cost/benefit analysis of chlorhexidine-silver sulfadiazine-impregnated venous catheters for femoral access. Am J Infect Control 2014;42:1130-2. [Crossref] [PubMed]
  26. Lorente L, Lecuona M, Jiménez A, et al. Efficiency of chlorhexidine-silver sulfadiazine-impregnated venous catheters at subclavian sites. Am J Infect Control 2015;43:711-4. [Crossref] [PubMed]
  27. Lorente L, Lecuona M, Jiménez A, et al. Chlorhexidine-silver sulfadiazine- or rifampicin-miconazole-impregnated venous catheters decrease the risk of catheter-related bloodstream infection similarly. Am J Infect Control 2016;44:50-3. [Crossref] [PubMed]
  28. Veenstra DL, Saint S, Saha S, et al. Efficacy of antiseptic-impregnated central venous catheters in preventing catheter-related bloodstream infection: a meta-analysis. JAMA 1999;281:261-7. [Crossref] [PubMed]
  29. Hockenhull JC, Dwan K, Boland A, et al. The clinical effectiveness and cost-effectiveness of central venous catheters treated with anti-infective agents in preventing bloodstream infections: a systematic review and economic evaluation. Health Technol Assess 2008;12:iii-iv, xi-xii, 1-154.
  30. Falagas ME, Fragoulis K, Bliziotis IA, et al. Rifampicin-impregnated central venous catheters: a meta-analysis of randomized controlled trials. J Antimicrob Chemother 2007;59:359-69. [Crossref] [PubMed]
  31. Pai MP, Pendland SL, Danziger LH., et al. Antimicrobial-coated/bonded and -impregnated intravascular catheters. Ann Pharmacother 2001;35:1255-63. [Crossref] [PubMed]
  32. Saint S, Veenstra DL, Lipsky BA. The clinical and economic consequences of nosocomial central venous catheter-related infection: are antimicrobial catheters useful? Infect Control Hosp Epidemiol 2000;21:375-80. [Crossref] [PubMed]
  33. Brun-Buisson C, Doyon F, Sollet JP, et al. Prevention of intravascular catheter-related infection with newer chlorhexidine-silver sulfadiazine-coated catheters: a randomized controlled trial. Intensive Care Med 2004;30:837-43. [Crossref] [PubMed]
  34. Ostendorf T, Meinhold A, Harter C, et al. Chlorhexidine and silver-sulfadiazine coated central venous catheters in haematological patients--a double-blind, randomised, prospective, controlled trial. Support Care Cancer 2005;13:993-1000. [Crossref] [PubMed]
  35. Rupp ME, Lisco SJ, Lipsett PA, et al. Effect of a second-generation venous catheter impregnated with chlorhexidine and silver sulfadiazine on central catheter-related infections: a randomized, controlled trial. Ann Intern Med 2005;143:570-80. [Crossref] [PubMed]
  36. Raad I, Darouiche R, Dupuis J, et al. Central venous catheters coated with minocycline and rifampin for the prevention of catheter-related colonization and bloodstream infections. A randomized, double-blind trial. The Texas Medical Center Catheter Study Group. Ann Intern Med 1997;127:267-74. [Crossref] [PubMed]
  37. Hanna H, Benjamin R, Chatzinikolaou I, et al. Long-term silicone central venous catheters impregnated with minocycline and rifampin decrease rates of catheter-related bloodstream infection in cancer patients: a prospective randomized clinical trial. J Clin Oncol 2004;22:3163-71. [Crossref] [PubMed]
Cite this article as: Lorente L. What is new for the prevention of catheter-related bloodstream infections? Ann Transl Med 2016;4(6):119. doi: 10.21037/atm.2016.03.10

Download Citation