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Frequent Acquisition of Multiple Strains of Methicillin-Resistant Staphylococcus aureus by Healthcare Workers in an Endemic Hospital Environment

Published online by Cambridge University Press:  21 June 2016

Steven M. Opal*
Affiliation:
Infectious Disease Service, Memorial Hospital and Brown University Program in Medicine, Providence, Rhode Island
Kenneth H. Mayer
Affiliation:
Infectious Disease Service, Memorial Hospital and Brown University Program in Medicine, Providence, Rhode Island
Marjorie J. Stenberg
Affiliation:
Infection Control and Laboratory Service, VA Medical Center, Providence, Rhode Island
Julia E. Blazek
Affiliation:
Infection Control and Laboratory Service, VA Medical Center, Providence, Rhode Island
Dennis J. Mikolich
Affiliation:
Infection Control and Laboratory Service, VA Medical Center, Providence, Rhode Island
David L. Dickensheets
Affiliation:
Infection Control and Laboratory Service, VA Medical Center, Providence, Rhode Island
Lisa W. Lyhte
Affiliation:
Infectious Disease Service, Memorial Hospital and Brown University Program in Medicine, Providence, Rhode Island
Ronald R. Trudel
Affiliation:
Infectious Disease Service, Memorial Hospital and Brown University Program in Medicine, Providence, Rhode Island
James M. Musser
Affiliation:
Department of Biology, Mueller Laboratory, Pennsylvania State University, University Park, Pennsylvania
*
Memorial Hospital of Rhode Island, 111 Brewster Street, Pawtucket, RI 02860

Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) has been an endemic nosocomial pathogen at the VA medical center (VAMC) in Providence, Rhode Island since 1981. From 1985 to 1987, more than 30% of all unique S aureus isolates were methicillin resistant. To evaluate the frequency of acquisition of MRSA isolates by healthcare workers, we compared the antimicrobial susceptibility patterns, multilocus enzyme genotypes and plasmid profiles of isolates recovered from nasal and hand cultures from VAMC nurses and house staff on rotation at the VAMC with those of clinical isolates from patients at the VAMC and four other affiliated hospitals. Fifty-six percent of ward nurses cultured (n = 112) were colonized with S aureus, of which 65% was methicillin resistant. Six isolates of MRSA were identified on the initial culturing of house staff (n=65); 16 MRSA isolates were recovered at the end of a four-week rotation (p<.02). Phenotypic and genotypic analyses demonstrated that numerous distinct MRSA strains were recovered in the study period. The incidence of MRSA among clinical isolates at the VAMC and affiliated institutions was remarkably constant throughout the three-year study period. Moreover, despite regularly sharing resident physicians, interns and medical students, MRSA isolates were uncommonly recovered at the other university-affiliated hospitals. Our study failed to reveal evidence of significant interhospital transmission of MRSA isolates by healthcare workers. While healthcare workers may contribute to the dissemination of MRSA within institutions, they appear to be less important in spreading MRSA between institutions (Infect Control Hosp Epidemiol. 1990;11:479-485.).

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1990

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References

1. Bell, SM. Recommendations for controlling the spread of methicillin-resistant Staphylococcus aureus infection: based on 18 years' experience in a group of teaching hospitals. Med J Aust. 1982;l:472474.10.5694/j.1326-5377.1982.tb132420.xGoogle Scholar
2. Boyce, JM, White, RL, Causey, WA, Lockwood, WR. Bum units as a source of methicillin-resistant Staphylococcus aureus infections. JAMA. 1983;249:28032807.10.1001/jama.1983.03330440041029Google Scholar
3. Brumfitt, W, Hamilton-Miller, J. Methicillin-resistant Staphylococcus aureus. N Engl J Med. 1989;320:11881196.10.1056/NEJM198905043201806Google Scholar
4. Haley, RW, Hightower, AW, Khabbaz, RF, et al. The emergence of methicillin-resistant Staphylococcus aureus infections in United States hospitals, possible role of the house staff-patient transfer circuit. Ann Intern Med. 1982;97:297308.10.7326/0003-4819-97-3-297CrossRefGoogle ScholarPubMed
5. Roccaforte, JS, Bittner, MJ, Stumpf, CA, Preheim, LC. Attempts to eradicate methicillin-resistant Staphylococcus aureus colonization with the use of trimethoprim-sulfamethoxazole, rifampin, and bacitracin. Am J Infect Control. 1988;16:141146.10.1016/0196-6553(88)90024-7Google Scholar
6. Thompson, RL, Cabezudo, I, Wenzel, RP. Epidemiology of nosocomial infections caused by methicillin-resistant Staphylococcus aureus . Ann Intern Med. 1982;97:309317.10.7326/0003-4819-97-3-309CrossRefGoogle ScholarPubMed
7. Bartzokas, CA, Paton, JH, Gibson, MF, Graham, R, McLoughlin, GA, Croton, RS. Control and eradication of methicillin-resistant Staphylo-coccus aureus on a surgical unit. N Engl J Med. 1984;311:14221425.10.1056/NEJM198411293112207CrossRefGoogle Scholar
8. Boyce, JM. Methicillin-resistant Staphylococcus aureus: detection, epidemiology, and control measures. Infect Dis Clin North Am. 1989;3:901913.10.1016/S0891-5520(20)30313-5CrossRefGoogle ScholarPubMed
9. Rhinehart, E, Shales, DM, Keys, TF, et al. Nosocomial clonal dissemination of methicillin-resistant Staphylococcus aureus; elucidation by plasmid analysis. Arch Intern Med. 1987;147:521524.10.1001/archinte.1987.00370030125024Google Scholar
10. Shanson, DC, McSwiggan, DA. Operating theatre stain of Staphylococcus aureus: outbreaks in two hospitals attributable to one surgeon. J Hosp Infect. 1980;1:171172.10.1016/0195-6701(80)90050-XCrossRefGoogle Scholar
11. Gamer, JS, Favero, MS. Centers for Disease Control: guidelines for handwashing in hospital environmental control: section I: handwashing. In: Guidelines for the Prevention and Control of Nosocomial Infections. Atlanta, Ga: Centers for Disease Control. 1985;120.Google Scholar
12. Lynch, P, Jackson, MM, Cummings, MJ, Stamm, WE. Rethinking the role of isolation practices in the prevention of nosocomial infections. Ann Intern Med. 1987;107:243246.10.7326/0003-4819-107-2-243Google Scholar
13. Mayer, JA, Dubbert, PM, Miller, M, Burkett, PA, Champman, SW. Increasing handwashing in an intensive care unit. Infect Control. 1986;7:259262.10.1017/S0195941700064171Google Scholar
14. Albert, RK, Condie, F. Hand-washing patterns in a medical intensive-care unit. N Engl J Med.1981;304:14651466.10.1056/NEJM198106113042404Google Scholar
15. Preston, GA, Larson, EL, Stamm, WE. The effect of private isolation rooms on patient care practices, colonization and infection in an intensive care unit, Am J Med. 1981;70:641645.10.1016/0002-9343(81)90588-XGoogle Scholar
16. Benner, EJ, Kayser, FH. Growing clinical significance of methicillin-resistant Staphylococcus aureus. Lancet. 1968;ii:741744.10.1016/S0140-6736(68)90947-1Google Scholar
17. Jevons, MP. “Celbenin”-resistant Staphylococci. Br Med J. 1961;1:124125.10.1136/bmj.1.5219.124-aCrossRefGoogle Scholar
18. Centers for Disease Control. Nosocomial infection surveillance. MMWR. 1984;36:17SS29SS.Google Scholar
19. Hsu, CCS, Macaluso, CP, Speical, L, Hubble, RH. High rate of methicillin-resistance of Staphylococcus aureus isolated from hospitalized nursing home patients. Arch Intern Med. 1988;148:569570.10.1001/archinte.1988.00380030075016Google Scholar
20. Peacock, JE Jr, Marsik, FJ, Wenzel, RP. Methicillin-resistant Staphylococcus aureus: introduction and spread within a hospital, Ann Intern Med. 1980;93:526532.10.7326/0003-4819-93-4-526Google Scholar
21. Preheim, LC, Rimland, D, Bittner, MJ. Methicillin-resistant Staphylococcus aureus in Veteran's Administration Medical Centers. Infect Control. 1987;8:191194.10.1017/S0195941700065929Google Scholar
22. Saraglou, G, Cramer, M, Bisno, AL. Methicillin-resistant Staphylococcus aureus: interstate spread of nosocomial infections with emergence of gentamicin-methicillin-resistant strains. Infect Control. 1980;1:8189.10.1017/S0195941700052590CrossRefGoogle Scholar
23. Trallero, EP, Garcia Arenzana, JM, Equiluz, GC, Cancer, RC. Prevalence of methicillin-resistant Staphylococcus aureus in a Spanish hospital. Rev Infect Dis. 1988;10:627628.10.1093/clinids/10.3.627Google Scholar
24. Craven, DE, Rixinger, AI, Goularte, TA, McCabe, WR. Methicillin-resistant Staphylococcus aureus bacteremia linked to intravenous drug users using a “shooting gallery.” Am J Med. 1986;80:770776.10.1016/0002-9343(86)90614-5CrossRefGoogle Scholar
25. Saravolatz, LD, Pohlod, DJ, Arkling, LM. Community-acquired methicillin-resistant Staphylococcus aureus infections: a new source of nosocomial outbreaks. Ann Intern Med. 1982;97:325329.10.7326/0003-4819-97-3-325Google Scholar
26. McDougal, LK, Thornsberry, C. New recommendations for disk diffusion antimicrobial susceptibility test for methicillin-resistant (heter-oresistant) staphylococci. J Clin Microbiol. 1984;19:482488.10.1128/jcm.19.4.482-488.1984Google Scholar
27. McDougal, LK, Thornsberry, C. The role of β-lactamase in staphylococcal resistance to penicillinase-resistant penicillins and cephalosporins. J Clin Microbiol. 1986;23:832839.10.1128/jcm.23.5.832-839.1986Google Scholar
28. Selander, RK, Caugant, DA, Ochman, H, Musser, JM, Gilmour, MN, Whittam, TS. Methods of multilocus enzyme electmphoresis for bacterial population genetics and systematics. Appl Environ Microbiol. 1986;7:15131523.Google Scholar
29. Birnboim, HC, Doly, J. A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res. 1979;7: 15131523.10.1093/nar/7.6.1513Google Scholar
30. Ballou, WR. Gross, AS, Wiffiams, DY, Keiser, J, Zierdt, CH. Colonization of newly arrived house staff by virulent staphylococcal phage types endemic to a hospital environment. J Clin Microbiol. 1986;23:10301033.10.1128/jcm.23.6.1030-1033.1986Google Scholar
31. Ward, TT, Winn, RE, Hartstein, AL, et al. Observations relating to an inter-hospital outbreak of methicillin-resistant Staphylococcus aureus: role of antimicrobial therapy in infection control. Infect Control. 1981;2:453459.10.1017/S0195941700055715Google Scholar
32. Boyce, JM, Lytle, LS, Walsh, DA. Detection of methicillin-resistant Staphylococcus aureus by microdilution and disk elution susceptibility systems. J Clin Microbiol. 1984;20:10681075.10.1128/jcm.20.6.1068-1075.1984Google Scholar
33. Cookson, B, Peters, B, Webster, M, Phillips, I, Rahman, M, Noble, W. Staff carriage of epidemic methicillin-resistant Staphylococcus aureus. J Clin Microbiol. 1989;27:14711476.10.1128/jcm.27.7.1471-1476.1989Google Scholar
34. Coia, JE, Norr-Hussain, I, Platt, DJ. Plasmid profiles and restriction enzyme fragmentation patterns of plasmids of methicillin-sensitive and methicillin-resistant isolates of Staphylococcus aureus from hospitals and the community. J Med Microbiol.1988;27:271276.10.1099/00222615-27-4-271Google Scholar
35. Kozarksy, PE, Rimland, D, Terry, PM, Wachsmuth, K. Plasmid analysis of simultaneous nosocomial outbreaks of methicillin-resistant Staphylococcus aureus . Infect Control. 1986;7:577580.Google Scholar
36. Weinstein, RA, Kabins, SA. Strategies for prevention and control of multiple drug-resistant nosocomial infection. Am J Med. 1981;70:449454.10.1016/S0002-9343(81)80001-0CrossRefGoogle ScholarPubMed
37. Shanson, DC, Kensit, JC, Duke, R. Outbreak of hospital infection with a strain of Staphylococcus aureus resistant to gentamicin and methicillin. Lancet. 1976;ii: 13471348.10.1016/S0140-6736(76)91986-3Google Scholar
38. Ribner, BS, Landry, MN, Gholoson, CL. Strict versus modified isolation for prevention of nosocomial transmission of methicillin-resistant Staphylococcus aureus . Infect Control. 1986;7:317320.10.1017/S0195941700064341Google Scholar