Hostname: page-component-5c6d5d7d68-wtssw Total loading time: 0 Render date: 2024-08-19T03:05:47.688Z Has data issue: false hasContentIssue false

Rapid Inactivation of Infectious Pathogens by Chlorhexidine-Coated Gloves

Published online by Cambridge University Press:  21 June 2016

Shanta Modak*
Affiliation:
Department of Surgery, Columbia University College of Physicians and Surgeons, New York, New York
Lester Sampath
Affiliation:
Department of Surgery, Columbia University College of Physicians and Surgeons, New York, New York
Harvey S.S. Miller
Affiliation:
Daltex Medical Sciences, Inc., Fairfield, New Jersey
Irving Millman
Affiliation:
Fox Chase Cancer Center, Divisions of Population, Oncology, and Clinical Research, Philadelphia, Annsylvania
*
Dept. of Surgery, Black Bldg. Rm. 1734, Columbia University, College of Physicians and Surgeons, 630 W 168th St., New York, NY 10032

Abstract

Objective:

Gloves containing chlorhexidine gluconate in an instant-release matrix on their inner surface (CHG gloves) were tested to determine their ability to rapidly inactivate infectious pathogens that may permeate or leak through the latex surface.

Design:

CHG gloves were exposed for 1 to 10 minutes to blood or media containing infectious pathogens (e.g., bacteria, fungi, parasites, and viruses) as well as to lymphocytes and macrophages that are known to be the primary carriers of human immunodeficiency virus (HIV). Inactivation of pathogens was determined either by in vitro assay or in vivo infectivity. Stressed control and CHG glove fingers were submerged in a viral pool (retrovirus or bacteriophage) and after a set time, the glove interiors were checked for presence of permeated viz-ions.

Results:

CHG gloves rapidly inactivate all the pathogens tested including retrovirus and hepatitis B virus (90% to 100%). In the stressed glove fingers, live virus was detected in 26% of the control group but not in any of the CHG group.

Conclusions:

The use of CHG gloves may reduce the risk of exposure to infectious fluidborne pathogens should the integrity of the latex barrier be compromised by overt failure or by permeation of viruses. Rapid destruction of lymphocytes and macrophages may facilitate inactivation of HIV associated with these cells. Tests have shown that CHG coating does not alter physical properties of the glove, and, furthermore, CHG gloves do not show potential for dermal irritation or sensitization.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1992

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Kotilainen, HR, Blinker, JP, Avato, JL, Gantz, NM. Latex and vinyl examination gloves: quality control procedures and implications for health care workers. Arch Intern Med. 1989:149:27492753.CrossRefGoogle ScholarPubMed
2. Russell, TR, Roque, FE, Miller, FA. A new method for detection of the leaky glove: a study on incidence of defective gloves and bacterial growth from surgeon's hands. Arch Surg. 1966;93:245249.CrossRefGoogle Scholar
3. Church, J, Sanderson, I? Surgical gloves puncture. /Hosp Infect. 1980;1:84.CrossRefGoogle Scholar
4. Paulsen, J, Eidem, T, Kristiansen, R. Perforations in surgeons' gloves. J Hosp Infect. 1988;11:8285.CrossRefGoogle Scholar
5. Dodds, RDA, Guy, PJ. Surgical glove perforation. By J Surg. 1988,75:966968.Google ScholarPubMed
6. Miller, JM, Collier, CS, Griffith, NM. Permeability of surgical rubber gloves. Am J Surg. 1972;124:5759.CrossRefGoogle ScholarPubMed
7. Hochreiter, MC, Barton, LL. Epidemiology of needlestick injury in emergency medical service personnel. J Emerg Med. 1988;6:912.CrossRefGoogle ScholarPubMed
8. Peterson, AF, Rosenberg, A, Alatary, SD. Comparative evaluation of surgical scrub preparations. Surg Gynecol Obstet. 1978;146:6365.Google ScholarPubMed
9. Rosenberg, A, Alatary, SD, Peterson, AF. Safety and efficacy of the antiseptic chlorhexidine gluconate. Surg Gynecol Obstet. 1976;143:789792.Google ScholarPubMed
10. Denton, GW. Chlorhexidine. In: Block, SS ed. D&infection, Sterilization, and Preservation. Philadelphia, Pa: Lea & Febiger; 1991:274289.Google Scholar
11. Schiott, CR Effect of chlorhexidine on the microflora of the oral cavity. J Periodont Res. 1973;8:710.Google Scholar
12. Loe, H. Chlorhexidine in the prophylaxis of dental diseases. Introduction. J Periodont Res. 1973;8:56.CrossRefGoogle Scholar
13. Cumming, BR, Loe, H. Optimal dosage and method of delivering chlorhexidine solutions for the inhibition of dental plaque. J Periodont Res. 1973;8:5762.CrossRefGoogle ScholarPubMed
14. Schiott, , Loe, H. The sensitivity of oral streptococci to chlorhexidine. J Periodont Res. 1972:7:192194.CrossRefGoogle ScholarPubMed
15. Hannah, WJ. Prevention of urinary tract infections after vaginal surgery. Can Med Assoc J. 1963;88:802805.Google ScholarPubMed
16. Bastable, JRG, Peel, RN, Birch, DM, Richards, B. Continuous irrigation of the bladder after prostatectomy: its effect on post-prostatectomy infection. Br J Urol. 1977;49:689693.CrossRefGoogle ScholarPubMed
17. Benson, L, Bush, L, LeBlanc, D. Importance of neutralizers in the stripping fluid in a simulated healthcare personnel handwash. Infect Control Hosp Epidemiol. 1990;11:595599.Google Scholar
18. Millman, I, Southam, L, Halbherr, T, Simmons, H. Kang, CM. Woodchuck hepatitis virus; experimental infection and natural occurrence. Hepatology. 1984;4:817823.CrossRefGoogle ScholarPubMed
19. Sinclair, JF, Tzagoloff, A, Levine, D, Mindich, L. Proteins of bacteriophage 06. J Virol. 1975;16:685695.CrossRefGoogle Scholar
20. Olkkonen, VM. Gottlieb, P. Strassman, I. Qiao, X. Bamford, DH. Mindich, L. In vitro assembly of infectious nucleocapsids of bacteriophage 06: formation of a recombinant double-stranded RNA virus. Proc Natl Acad Sci. 1990;87:91739177.CrossRefGoogle Scholar
21. Gottlieb, P, Strassman, J, Qiao, X, Frucht, A, Mindich, L. In vitro replication, packaging, and transcription of the segmented double-stranded RNA genome of bacteriophage 06 studies with procapsids assembled from plasmid-encoded proteins. 1 Bact. 1990;172:57745782.CrossRefGoogle Scholar
22. Montefiori, DC, Robinson, WE, Modliszewski, A, Mitchell, WM. Effective inactivation of human immunodeficiency virus with chlorhexidine antiseptics containing detergents and alcohol. J Hosp Infect. 1990;15:279282.CrossRefGoogle ScholarPubMed
23. Bernstein, D, Schiff, G, Echler, G, et al. In vitro virucidal effectiveness of a 0.12%-chlorhexidine gluconate mouthrinse. J Dent Res. 1990;69:874876.CrossRefGoogle ScholarPubMed
24. Modak, MJ, Marcus, S. Purification and properties of Rauscher leukemia virus DNA polymerase. J Biol Chem. 1977;252:1119.CrossRefGoogle ScholarPubMed
25. Ruprecht, RM, Rossoni, LD, Haseltine, WA, Broder, S. Suppression of retroviral propagation and disease by suramin in murine system. Proc Natl Acad Sci. 1985;82:77337737.CrossRefGoogle Scholar
26. Ruprecht, RM, O'Brien, LG, Rossoni, LD, Nusinoff-Lehrman, S. Suppression of mouse viraemia and retroviral disease by 3’azido-3’-deoxythymidine. Nature. 1986;323:467469.CrossRefGoogle Scholar
27. Murine lentivirus model concept and others ok'd by NIAID advisors. AIDS Update. 1989;2:12.Google Scholar
28. Gallo, RC, Salahuddin, SZ, Popovic, M, et al. Human lymphotropic virus. HTL VIII. isolated from AIDS patients and donors at risk for AIDS. Science. 1984;224:500503..Google Scholar
29. Geddes, AM. Risks of AIDS to health care workers. Br Med J. 1986;292:711712.CrossRefGoogle ScholarPubMed
30. Weiss, SH, Goedert, JJ, Gartner, S, et al. Risk of human immunodeficiency virus (HTV1). Infection among laboratory workers. Science. 1988;239:68.CrossRefGoogle Scholar
31. Newsom, SWB, Rowland, C, Wells, FC. What is in the surgeon's glove? J Hosp Infect. 1988;11(suppl A):244259.CrossRefGoogle ScholarPubMed
32. Dalgleish, AG, Malkousky, M. Latex gloves not enough to exclude viruses . Br J Surg. 1988;76:171172.Google Scholar
33. Reingold, AL, Kane, MA, Hightower, AW. Failure of gloves and other protective devices to prevent transmission of hepatitis B virus to oral surgeons. JAMA. 1988;259:25582560.CrossRefGoogle ScholarPubMed
34. Albin, MS, Bunegin, L, Duke, ES, Ritter, RR, Page, CI? Anatomy of a defective barrier: sequential glove leak detection in a surgical and dental environment. Crit Cure Med. 1992;20:170.CrossRefGoogle Scholar
35. Quebbeman, EJ, Telford, GL, Hubbard, S, et al. Risk of blood contamination and injury to operating room personnel. Ann Surg. 1991;214:614620.CrossRefGoogle ScholarPubMed
36. Groopman, JE, Salahuddin, SZ. Sarngadharan, MG. Markham, PD. Gonda, M, Sliski, A, Gallo, Rd. HTLV-III in saliva' of people with AIDS related complex and healthy homosexual men at risk for AIDS. Science. 1984;226:447449.CrossRefGoogle Scholar
37. Ho, DD, Moudgil, T, Alam, M. Quantitation of human immunodeficiency virustype 1 in the blood of infected persons. N Engl J Med. 1989;321:16211625.CrossRefGoogle Scholar
38. Harbison, MA, Hammer, SM. Inactivation of human immunodeficiency virus by betadine products and chlorhexidine. J Acquired Immune Deficiency Syndromes. 1989;2:1620.Google ScholarPubMed
39. Dienstag, JL, Ryan, DM. Occupational exposure to hepatitis B virus in hospital personnel. Am J Epidemiol. 1982;115:2639.CrossRefGoogle ScholarPubMed
40. Burnie, JP. Candida and hands. J Hosp Infect. 1986;8:14.CrossRefGoogle Scholar
41. Stickler, DJ. Chlohexidine resistance to Proteus mirabilis . J Clin Path. 1974;27:284287.CrossRefGoogle Scholar
42. Pitt, TL, Gaston, MA, Hoffman, PN. In vitro susceptibility of hospital isolates of various bacterial genera to chlorhexidine. J Hosp Infect. 1983;4:173176.CrossRefGoogle ScholarPubMed
43. Russell, AD. Chlorhexidine: antibacterial action and bacterial resistance. Comment. Infection. 1986;14:212215.CrossRefGoogle Scholar