332
did not occur significantly more often for wound care procedures than for other procedures and patient care activities. Our study has some limitations. The study was conducted in a
setting with a predominantly male patient population, and most of the procedures and activities took place on medical-surgical wards. The number of procedures varied among participants and a multivariate analysis was not performed to assess risk factors for shedding given the small number of patients studied. Thus, addi- tional studies are needed to confirm the finding that wounds with MRSA may be associated with increased risk for shedding during procedures.Our observations suggest that shedding ofMRSAto sur- faces often occurred through direct transfer via the hands of person- nel or contaminated equipment used in procedures. However, we cannot exclude the possibility that airborne dispersal ofMRSA con- tributed to shedding during procedures. Others have demonstrated that airborne dispersal may occur during activities such as bedding changes.26 In a minority of cases isolates recovered from surfaces or equipment after procedures did notmatch the concurrent nasal iso- late. Thus, it is possible that some of the MRSA shed during proce- dures was derived from healthcare personnel or from other sources. In conclusion, our results suggest that environmental shedding
of MRSA occurs frequently during medical procedures and patient care activities. Such shedding could contribute to transmission of MRSA in healthcare facilities. Studies are needed to determine whether measures such as cleaning of surfaces and equipment after procedures can reduce the risk for transmission.
Acknowledgments. We would like to thank the nursing staff of the Cleveland VA Medical Center for assistance with coordination of research assessments during procedures and patient care activities.
Financial support. This work was supported by the Centers for Disease Control and Prevention (contract 2002011-42039 to M.S.) and by the Department of Veterans Affairs.
Conflicts of interest. C.J.D. has received research funding from Clorox, GOJO, PDI, Pfizer, Avery Dennison, and Boehringer Laboratories. All other authors report no potential conflicts.
References
1. Donskey CJ. Does improving surface cleaning and disinfection reduce health care-associated infections? Am J Infect Control 2013;41:S12–S19.
2. Stiefel U, Cadnum JL, Eckstein BC, Guerrero DM, Tima MA, Donskey CJ. Contamination of hands with methicillin-resistant Staphylococcus aureus after contact with environmental surfaces and after contact with the skin of colonized patients. Infect Control Hosp Epidemiol 2011; 32:185–187.
3. Weber DJ, Anderson D, Rutala WA. The role of the surface environment in healthcare-associated infections. Curr Opin Infect Dis 2013;26:338–344.
4. Cheng VC, Li IW, Wu AK, et al. Effect of antibiotics on the bacterial load of meticillin-resistant Staphylococcus aureus colonisation in anterior nares. J Hosp Infect 2008;70:27–34.
5. Livorsi DJ, Arif S, Garry P, et al. Methicillin-resistant Staphylococcus aureus (MRSA) nasal real-time PCR: a predictive tool for contamination of the hospital environment. Infect Control Hosp Epidemiol 2015;36:34–39.
6. Chang S, Sethi AK, Eckstein BC, Stiefel U,CadnumJL, Donskey CJ. Skin and environmental contamination with methicillin-resistant Staphylococcus aureus among carriers identified clinically versus through active surveil- lance. Clin Infect Dis 2009;48:1423–1428.
7. Bhalla A, Pultz NJ, Aron DC, Donskey CJ. Staphylococcus aureus intestinal colonization is associated with increased frequency of skin contamination in hospitalized patients. BioMed Central Infect Dis 2007;7:105.
Heba Alhmidi et al
8. Mody L, Maheshwari S, Galecki A, Kauffman CA, Bradley SF. Indwelling device use and antibiotic resistance in nursing homes: identifying a high- risk group. J Am Geriatr Soc 2007;55:1921–1926.
9. Boyce JM, Havill NL, Otter JA, Adams NM. Widespread environmental contamination associated with patients with diarrhea and methicillin- resistant Staphylococcus aureus colonization of the gastrointestinal tract. Infect Control Hosp Epidemiol 2007;28:1142–1147.
10. Pineles L, Morgan DJ, Lydecker A, et al. Transmission of methicillin- resistant Staphylococcus aureus to health care worker gowns and gloves dur- ing care of residents in Veterans Affairs nursing
homes.AmJ Infect Control 2017;45:947–953.
11. Kanwar A, Cadnum JL, Jencson AL, Donskey CJ. Impact of antibiotic treat- ment on the burden of nasal Staphylococcus aureus among hospitalized patients. Antimicrob Agents Chemother. 2018 Sep 24;62(10):e00609-18. doi: 10.1128/AAC.00609-18.
12. Endimiani A, Blackford M, Dasenbrook EC, et al. Emergence of linezolid- resistant Staphylococcus aureus after prolonged treatment of cystic fibrosis patients inCleveland, Ohio.AntimicrobAgents Chemother 2011;55: 1684–1692.
13. Faria NA, Carrico JA, Oliveira DC, Ramirez M, de Lencastre H. Analysis of typing methods for epidemiological surveillance of both methicillin- resistant and methicillin-susceptible Staphylococcus aureus strains. J Clin Microbiol 2008;46:136–144.
14. Carrel M, Perencevich EN, David MZ. USA300 Methicillin-resistant Staphylococcus aureus, United States, 2000–2013. Emerg Infect Dis 2015;11:1973–1980.
15. Donskey CJ, Deshpande A. Effect of chlorhexidine bathing in pre- venting infections and reducing skin burden and environmental contamination: a review of the literature. Am J Infect Control 2016; 44(5 suppl):e17–e21.
16. Kanwar A, Cadnum JL, Thakur M, Jencson AL, Donskey CJ. Contaminated clothing of methicillin-resistant Staphylococcus aureus carriers is a potential source of transmission. Am J Infect Control 2018;46:1414–1416.
17. Sunkesula VCK, Kundrapu S, Knighton S, Cadnum JL, Donskey CJ. A randomized trial to determine the impact of an educational patient hand-hygiene intervention on contamination of hospitalized patient’s hands with healthcare-associated pathogens. Infect Control Hosp Epidemiol 2017;38:595–597.
18. Sunkesula V, Kundrapu S, Macinga DR, Donskey CJ. Efficacy of alcohol gel for removal of methicillin-resistant Staphylococcus aureus from hands of colonized patients. Infect Control Hosp Epidemiol 2015;36:229–231.
19. Rutala WA, Weber DJ and the Healthcare Infection Control Practices Advisory Committee (HICPAC). Guideline for disinfection and sterilization in healthcare facilities, 2008. Centers for Disease Control and Preention website.
https://www.cdc.gov/hicpac/pdf/guidelines/Disinfection_Nov_2008. pdf. Published 2008. Accessed February 10, 2017.
20. Havill NL, Havill HL, Mangione E, Dumigan DG, Boyce JM. Cleanliness of portable medical equipment disinfected by nursing
staff.AmJ Infect Control 2011;39:602–604.
21. John A, Alhmidi H, Cadnum JL, Jencson AL, Donskey CJ. Contaminated portable equipment is a potential vector for dissemination of pathogens in the intensive care unit. Infect Control Hosp Epidemiol 2017;38:1247–1249.
22. Kundrapu S, Sunkesula V, Jury LA, Donskey CJ. A randomized trial of daily disinfection of high-touch surfaces in isolation rooms to reduce con- tamination of healthcare workers’ hands. Infect Control Hosp Epidemiol 2012;33:1039–1042.
23. Shen Z, Ning F, Zhou W, et al. Superspreading SARS events, Beijing, 2003. Emerg Infect Dis 2004;10:256–260.
24. James A, Pitchford JW, Plank MJ. An event-based model of superspreading in epidemics. Proc Biol Sci 2007;274:741–747.
25. Lloyd-Smith JO, Schreiber SJ, Kopp PE, Getz WM. Superspreading and the effect of individual variation on disease emergence. Nature 2005;438: 355–359.
26. Shiomori T, Miyamoto H, Makishima K, et al. Evaluation of bedmaking- related airborne and surface methicillin-resistant Staphylococcus aureus contamination. J Hosp Infect 2002;50:30–35.
Page 1 |
Page 2 |
Page 3 |
Page 4 |
Page 5 |
Page 6 |
Page 7 |
Page 8 |
Page 9 |
Page 10 |
Page 11 |
Page 12 |
Page 13 |
Page 14 |
Page 15 |
Page 16 |
Page 17 |
Page 18 |
Page 19 |
Page 20 |
Page 21 |
Page 22 |
Page 23 |
Page 24 |
Page 25 |
Page 26 |
Page 27 |
Page 28 |
Page 29 |
Page 30 |
Page 31 |
Page 32 |
Page 33 |
Page 34 |
Page 35 |
Page 36 |
Page 37 |
Page 38 |
Page 39 |
Page 40 |
Page 41 |
Page 42 |
Page 43 |
Page 44 |
Page 45 |
Page 46 |
Page 47 |
Page 48 |
Page 49 |
Page 50 |
Page 51 |
Page 52 |
Page 53 |
Page 54 |
Page 55 |
Page 56 |
Page 57 |
Page 58 |
Page 59 |
Page 60 |
Page 61 |
Page 62 |
Page 63 |
Page 64 |
Page 65 |
Page 66 |
Page 67 |
Page 68 |
Page 69 |
Page 70 |
Page 71 |
Page 72 |
Page 73 |
Page 74 |
Page 75 |
Page 76 |
Page 77 |
Page 78 |
Page 79 |
Page 80 |
Page 81 |
Page 82 |
Page 83 |
Page 84 |
Page 85 |
Page 86 |
Page 87 |
Page 88 |
Page 89 |
Page 90 |
Page 91 |
Page 92 |
Page 93 |
Page 94 |
Page 95 |
Page 96 |
Page 97 |
Page 98 |
Page 99 |
Page 100 |
Page 101 |
Page 102 |
Page 103 |
Page 104 |
Page 105 |
Page 106 |
Page 107 |
Page 108 |
Page 109 |
Page 110 |
Page 111 |
Page 112 |
Page 113 |
Page 114 |
Page 115 |
Page 116 |
Page 117 |
Page 118 |
Page 119 |
Page 120 |
Page 121 |
Page 122 |
Page 123 |
Page 124 |
Page 125 |
Page 126 |
Page 127 |
Page 128 |
Page 129 |
Page 130 |
Page 131 |
Page 132