Analyze Diet
Acta veterinaria Scandinavica2012; 54(1); 14; doi: 10.1186/1751-0147-54-14

Infection prevention and control interventions in the first outbreak of methicillin-resistant Staphylococcus aureus infections in an equine hospital in Sweden.

Abstract: The first outbreak of methicillin-resistant Staphylococcus aureus (MRSA) infection in horses in Sweden occurred in 2008 at the University Animal Hospital and highlighted the need for improved infection prevention and control. The present study describes interventions and infection prevention control in an equine hospital setting July 2008 - April 2010. Methods: This descriptive study of interventions is based on examination of policy documents, medical records, notes from meetings and cost estimates. MRSA cases were identified through clinical sampling and telephone enquiries about horses post-surgery. Prospective sampling in the hospital environment with culture for MRSA and genotyping of isolates by spa-typing and pulsed-field gel electrophoresis (PFGE) were performed. Results: Interventions focused on interruption of indirect contact spread of MRSA between horses via staff and equipment and included: Temporary suspension of elective surgery; and identification and isolation of MRSA-infected horses; collaboration was initiated between authorities in animal and human public health, human medicine infection control and the veterinary hospital; extensive cleaning and disinfection was performed; basic hygiene and cleaning policies, staff training, equipment modification and interior renovation were implemented over seven months.Ten (11%) of 92 surfaces sampled between July 2008 and April 2010 tested positive for MRSA spa-type 011, seven of which were from the first of nine sampling occasions. PFGE typing showed the isolates to be the outbreak strain (9 of 10) or a closely related strain. Two new cases of MRSA infection occurred 14 and 19 months later, but had no proven connections to the outbreak cases. Conclusions: Collaboration between relevant authorities and the veterinary hospital and formation of an infection control committee with an executive working group were required to move the intervention process forward. Support from hospital management and the dedication of staff were essential for the development and implementation of new, improved routines. Demonstration of the outbreak strain in the environment was useful for interventions such as improvement of cleaning routines and interior design, and increased compliance with basic hygienic precautions. The interventions led to a reduction in MRSA-positive samples and the outbreak was considered curbed as no new cases occurred for over a year.
Publication Date: 2012-03-08 PubMed ID: 22401493PubMed Central: PMC3325856DOI: 10.1186/1751-0147-54-14Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research article examines the steps taken to manage the first occurrence of methicillin-resistant Staphylococcus aureus (MRSA) infection among horses in a Swedish equine hospital, emphasizing the importance of efficient infection control and prevention strategies.

Objective of the Study

  • The main objective is to delineate the control interventions employed in an equine hospital setting during the first outbreak of MRSA infection in Sweden.
  • The respective period of the study spans July 2008 – April 2010.

Methodology

  • The study is descriptive and its conclusions are drawn from analysis of policy documents, medical records, meeting notes, and cost estimates.
  • Identification of MRSA cases was executed through clinical sampling and telephone inquiries tracking horses post-surgery.
  • The researchers carried out environmental sampling in the hospital and included culture for MRSA and genotyping of isolates via spa-typing and pulsed-field gel electrophoresis (PFGE).

Interventions Deployed

  • Temporary suspension of elective surgery.
  • Identification and isolation of MRSA-contaminated horses.
  • Collaboration between animal and human public health authorities, infection control in human medicine, and the veterinary hospital.
  • Implementation of comprehensive cleaning and disinfection.
  • Introduction of basic hygiene, cleaning policies, staff training, equipment modification, and interior renovation over seven months.

Results

  • Ten out of ninety-two surfaces sampled tested positive for MRSA spa-type 011.
  • PFGE typing revealed the outbreak strain in nine of the ten cases, or a closely related strain.
  • Two new MRSA cases arose, fourteen and nineteen months later respectively, without proven connections to the initial outbreak cases.

Conclusions

  • For successful intervention, strategic collaboration is required between relevant authorities, the veterinary hospital, and the formation of an infection control committee with an executive working group.
  • The commitment of hospital management and staff is crucial for developing and implementing new, improved procedures.
  • Identifying the outbreak strain in the environment helps in refining cleaning routines, modifying interior design, and promoting compliance with basic hygiene measures.
  • The effective interventions enabled the reduction of MRSA-positive samples, with no new cases reported for over a year, which suggested that the outbreak was adequately contained.

Cite This Article

APA
Bergström K, Nyman G, Widgren S, Johnston C, Grönlund-Andersson U, Ransjö U. (2012). Infection prevention and control interventions in the first outbreak of methicillin-resistant Staphylococcus aureus infections in an equine hospital in Sweden. Acta Vet Scand, 54(1), 14. https://doi.org/10.1186/1751-0147-54-14

Publication

ISSN: 1751-0147
NlmUniqueID: 0370400
Country: England
Language: English
Volume: 54
Issue: 1
Pages: 14

Researcher Affiliations

Bergström, Karin
  • Department of Animal Environment and Health, Faculty of Veterinary Medicine and Animal Husbandry, Swedish University of Agricultural Sciences, Uppsala, Sweden. karin.bergstrom@sva.se
Nyman, Görel
    Widgren, Stefan
      Johnston, Christopher
        Grönlund-Andersson, Ulrika
          Ransjö, Ulrika

            MeSH Terms

            • Animals
            • Cross Infection / prevention & control
            • Cross Infection / veterinary
            • Genotype
            • Horse Diseases / microbiology
            • Horse Diseases / prevention & control
            • Horses
            • Hospitals, Animal / legislation & jurisprudence
            • Hospitals, Animal / standards
            • Infection Control / economics
            • Methicillin-Resistant Staphylococcus aureus / genetics
            • Methicillin-Resistant Staphylococcus aureus / isolation & purification
            • Staphylococcal Infections / microbiology
            • Staphylococcal Infections / prevention & control
            • Staphylococcal Infections / veterinary
            • Sweden

            References

            This article includes 47 references
            1. Otter JA, French GL. Molecular epidemiology of community-associated meticillin-resistant Staphylococcus aureus in Europe. Lancet Infect Dis 2010;10:227–239.
              doi: 10.1016/S1473-3099(10)70053-0pubmed: 20334846google scholar: lookup
            2. Deleo FR, Otto M, Kreiswirth BN, Chambers HF. Community-associated meticillin-resistant Staphylococcus aureus. Lancet 2010;375:1557–1568.
            3. Kock R, Becker K, Cookson B, van Gemert-Pijnen JE, Harbarth S, Kluytmans J, Mielke M, Peters G, Skov RL, Struelens MJ. Methicillin-resistant Staphylococcus aureus (MRSA): burden of disease and control challenges in Europe. Euro Surveill 2010;15:19688.
              pubmed: 20961515
            4. Cuny C, Friedrich A, Kozytska S, Layer F, Nubel U, Ohlsen K, Strommenger B, Walther B, Wieler L, Witte W. Emergence of methicillin-resistant Staphylococcus aureus (MRSA) in different animal species. Int J Med Microbiol 2009;300:109–117.
              pubmed: 20005777
            5. Vanderhaeghen W, Hermans K, Haesebrouck F, Butaye P. Methicillin-resistant Staphylococcus aureus (MRSA) in food production animals. Epidemiol Infect 2010;138:606–625.
              doi: 10.1017/S0950268809991567pubmed: 20122300google scholar: lookup
            6. Abbott Y, Leggett B, Rossney AS, Leonard FC, Markey BK. Isolation rates of meticillin-resistant Staphylococcus aureus in dogs, cats and horses in Ireland. Vet Rec 2010;166:451–455.
              pubmed: 20382932
            7. Cuny C, Nathaus R, Layer F, Strommenger B, Altmann D, Witte W. Nasal colonization of humans with methicillin-resistant Staphylococcus aureus (MRSA) CC398 with and without exposure to pigs. PLoS One 2009;4:1–6.
            8. Anzai TKMKT, Sugita S, Shimizu A, Higuchi T. Isolation of Methicillin-resistant Staphylococcus aureus (MRSA) from Mares with Metritis and its Zooepidemiology. J Equine Sci 1996;7:7–11.
              doi: 10.1294/jes.7.7google scholar: lookup
            9. Shimizu A, Kawano J, Yamamoto C, Kakutani O, Anzai T, Kamada M. Genetic analysis of equine methicillin-resistant Staphylococcus aureus by pulsed-field gel electrophoresis. J Vet Med Sci 1997;59:935–937.
              doi: 10.1292/jvms.59.935pubmed: 9362045google scholar: lookup
            10. Anderson ME, Lefebvre SL, Rankin SC, Aceto H, Morley PS, Caron JP, Welsh RD, Holbrook TC, Moore B, Taylor DR, Weese JS. Retrospective multicentre study of methicillin-resistant Staphylococcus aureus infections in 115 horses. Equine Vet J 2009;41:401–405.
              doi: 10.2746/042516408X345134pubmed: 19562904google scholar: lookup
            11. Weese JS, Rousseau J, Willey BM, Archambault M, McGeer A, Low DE. Methicillin-resistant Staphylococcus aureus in horses at a veterinary teaching hospital: frequency, characterization, and association with clinical disease. J Vet Intern Med 2006;20:182–186.
              pubmed: 16496939
            12. van Duijkeren E, Moleman M, Sloet van Oldruitenborgh-Oosterbaan MM, Multem J, Troelstra A, Fluit AC, van Wamel WJ, Houwers DJ, de Neeling AJ, Wagenaar JA. Methicillin-resistant Staphylococcus aureus in horses and horse personnel: an investigation of several outbreaks. Vet Microbiol 2010;141:96–102.
              doi: 10.1016/j.vetmic.2009.08.009pubmed: 19740613google scholar: lookup
            13. Van den Eede A, Martens A, Lipinska U, Struelens M, Deplano A, Denis O, Haesebrouck F, Gasthuys F, Hermans K. High occurrence of methicillin-resistant Staphylococcus aureus ST398 in equine nasal samples. Vet Microbiol 2009;133:138–144.
              doi: 10.1016/j.vetmic.2008.06.021pubmed: 18701224google scholar: lookup
            14. Fessler A, Scott C, Kadlec K, Ehricht R, Monecke S, Schwarz S. Characterization of methicillin-resistant Staphylococcus aureus ST398 from cases of bovine mastitis. J Antimicrob Chemother 2010;65:619–625.
              doi: 10.1093/jac/dkq021pubmed: 20164198google scholar: lookup
            15. Salmenlinna S, Lyytikainen O, Vainio A, Myllyniemi AL, Raulo S, Kanerva M, Rantala M, Thomson K, Seppanen J, Vuopio J. Human cases of methicillin-resistant Staphylococcus aureus CC398, Finland. Emerg Infect Dis 2010;16:1626–1629.
              pmc: PMC3294383pubmed: 20875297
            16. Witte W, Strommenger B, Stanek C, Cuny C. Methicillin-resistant Staphylococcus aureu ST398 in humans and animals, Central Europe. Emerg Infect Dis 2007;13:255–258.
              doi: 10.3201/eid1302.060924pmc: PMC2725865pubmed: 17479888google scholar: lookup
            17. Krziwanek K, Metz-Gercek S, Mittermayer H. Methicillin-Resistant Staphylococcus aureu ST398 from human patients, upper Austria. Emerg Infect Dis 2009;15:766–769.
              doi: 10.3201/eid1505.080326pmc: PMC2687006pubmed: 19402964google scholar: lookup
            18. Bengtsson B, Greko C, Groenlund-Andersson U. SVARM. Swedish Veterinary Antimicrobial Resistance Monitoring. 2007.
            19. Bengtsson B, Ericsson-Unnerstad H, Greko C, Groenlund-Andersson U, Landén A. Swedish Veterinary Antimicrobial Resistance Monitoring. 2010.
            20. van Loo I, Huijsdens X, Tiemersma E, de Neeling A, van de Sande-Bruinsma N, Beaujean D, Voss A, Kluytmans J. Emergence of methicillin-resistant Staphylococcus aureus of animal origin in humans. Emerg Infect Dis 2007;13:1834–1839.
              pmc: PMC2876750pubmed: 18258032
            21. Anderson ME, Lefebvre SL, Weese JS. Evaluation of prevalence and risk factors for methicillin-resistant Staphylococcus aureus colonization in veterinary personnel attending an international equine veterinary conference. Vet Microbiol 2008;129:410–417.
              doi: 10.1016/j.vetmic.2007.11.031pubmed: 18187274google scholar: lookup
            22. Wulf MW, Sorum M, van Nes A, Skov R, Melchers WJ, Klaassen CH, Voss A. Prevalence of methicillin-resistant Staphylococcus aureus among veterinarians: an international study. Clin Microbiol Infect 2008;14:29–34.
            23. . AFS 2005:1 Microbiological Work Environment Risks - Infection, Toxigenic Effect, Hypersensitivity. 2005.
            24. Korczak D, Schoffmann C. Medical and health economic evaluation of prevention-and control measures related to MRSA infections or -colonisations at hospitals. GMS Health Technol Assess 2010;6:Doc04.
              pmc: PMC3010887pubmed: 21289877
            25. Batra R, Cooper BS, Whiteley C, Patel AK, Wyncoll D, Edgeworth JD. Efficacy and limitation of a chlorhexidine-based decolonization strategy in preventing transmission of methicillin-resistant Staphylococcus aureus in an intensive care unit. Clin Infect Dis 2010;50:210–217.
              doi: 10.1086/648717pubmed: 20001537google scholar: lookup
            26. Wagenlehner FM, Naber KG, Bambl E, Raab U, Wagenlehner C, Kahlau D, Holler C, Witte W, Weidner W, Lehn N. Management of a large healthcare-associated outbreak of Panton-Valentine leucocidin-positive meticillin-resistant Staphylococcus aureus in Germany. J Hosp Infect 2007;67:114–120.
              doi: 10.1016/j.jhin.2007.07.006pubmed: 17900757google scholar: lookup
            27. Khoury J, Jones M, Grim A, Dunne WM Jr, Fraser V. Eradication of methicillin-resistant Staphylococcus aureus from a neonatal intensive care unit by active surveillance and aggressive infection control measures. Infect Control Hosp Epidemiol 2005;26:616–621.
              doi: 10.1086/502590pubmed: 16092741google scholar: lookup
            28. Kajita E, Okano JT, Bodine EN, Layne SP, Blower S. Modelling an outbreak of an emerging pathogen. Nat Rev Microbiol 2007;5:700–709.
              doi: 10.1038/nrmicro1660pubmed: 17703226google scholar: lookup
            29. Cimolai N. Methicillin-resistant Staphylococcus aureus in Canada: a historical perspective and lessons learned. Can J Microbiol 2010;56:89–120.
              doi: 10.1139/W09-109pubmed: 20237572google scholar: lookup
            30. Cuny C, Strommenger B, Witte W, Stanek C. Clusters of infections in horses with MRSA ST1, ST254, and ST398 in a veterinary hospital. Microb Drug Resist 2008;14:307–310.
              doi: 10.1089/mdr.2008.0845pubmed: 19025385google scholar: lookup
            31. Obee PGC, Cooper RA, Bennion NE. An evaluation of different methods for the recovery of meticillin-resistant Staphylococcus aureus from environmental surfaces. J Hosp Infect 2007;65:35–41.
              doi: 10.1016/j.jhin.2006.09.010pubmed: 17140698google scholar: lookup
            32. Weese JS DT, Button L, Goth K, Ethier M, Boehnke K. Isolation of methicillin-resistant Staphylococcus aureus from the environment in a veterinary teaching hospital. J Vet Intern Med 2004;18:468–470.
            33. EFSA. Analysis of the baseline survey on the prevalence of methicillin-resistant Staphylococcus aureus (MRSA) in holdings with breeding pigs, in the EU, 2008. EFSA Journal Vol. 8. Parma: EFSA; 2010; p. 1597. pp. 1597 [1567 pp.].
              pmc: PMC9579990pubmed: 36267542
            34. Tacconelli E. Antimicrobial use: risk driver of multidrug resistant microorganisms in healthcare settings. Curr Opin Infect Dis 2009;22:352–358.
              doi: 10.1097/QCO.0b013e32832d52e0pubmed: 19461514google scholar: lookup
            35. Sexton T, Clarke P, O'Neill E, Dillane T, Humphreys H. Environmental reservoirs of methicillin-resistant Staphylococcus aureus in isolation rooms: correlation with patient isolates and implications for hospital hygiene. J Hosp Infect 2006;62:187–194.
              doi: 10.1016/j.jhin.2005.07.017pubmed: 16290319google scholar: lookup
            36. Dancer SJ. Hospital cleaning in the 21st century. Eur J Clin Microbiol Infect Dis 2011;30:1473–1481.
              doi: 10.1007/s10096-011-1250-xpubmed: 21499954google scholar: lookup
            37. Bergström KAA, Landén A, Johnston C, Andersson UG. The first nosocomial outbreak of methicillin-resistant Staphylococcus aureus in horses in Sweden. Acta Vet Scand in press.
              pmc: PMC3348035pubmed: 22316072
            38. Nilsson O, Greko C, Bengtsson B. Environmental contamination by vancomycin resistant enterococci (VRE) in Swedish broiler production. Acta Vet Scand 2009;51:49.
              doi: 10.1186/1751-0147-51-49pmc: PMC2794861pubmed: 19954525google scholar: lookup
            39. Harmsen D, Claus H, Witte W, Rothganger J, Turnwald D, Vogel U. Typing of methicillin-resistant Staphylococcus aureus in a university hospital setting by using novel software for spa repeat determination and database management. J Clin Microbiol 2003;41:5442–5448.
            40. Murchan S, Kaufmann ME, Deplano A, de Ryck R, Struelens M, Zinn CE, Fussing V, Salmenlinna S, Vuopio-Varkila J, El Solh N. Harmonization of pulsed-field gel electrophoresis protocols for epidemiological typing of strains of methicillin-resistant Staphylococcus aureus: a single approach developed by consensus in 10 European laboratories and its application for tracing the spread of related strains. J Clin Microbiol 2003;41:1574–1585.
            41. Tenover FC, Arbeit RD, Goering RV, Mickelsen PA, Murray BE, Persing DH, Swaminathan B. Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J Clin Microbiol 1995;33:2233–2239.
              pmc: PMC228385pubmed: 7494007
            42. Weese JS, Lefebvre SL. Risk factors for methicillin-resistant Staphylococcus aureu colonization in horses admitted to a veterinary teaching hospital. Can Vet J 2007;48:921–926.
              pmc: PMC1950112pubmed: 17966332
            43. Weese JS, Rousseau J. Attempted eradication of methicillin-resistant Staphylococcus aureus colonisation in horses on two farms. Equine Vet J 2005;37:510–514.
              pubmed: 16295927
            44. Anderson ME, Weese JS. Evaluation of a real-time polymerase chain reaction assay for rapid identification of methicillin-resistant Staphylococcus aureus directly from nasal swabs in horses. Vet Microbiol 2007;122:185–189.
              doi: 10.1016/j.vetmic.2007.01.001pubmed: 17284351google scholar: lookup
            45. Cepeda JA, Whitehouse T, Cooper B, Hails J, Jones K, Kwaku F, Taylor L, Hayman S, Cookson B, Shaw S. Isolation of patients in single rooms or cohorts to reduce spread of MRSA in intensive-care units: prospective two-centre study. Lancet 2005;365:295–304.
              pubmed: 15664224
            46. Kramer A, Schwebke I, Kampf G. How long do nosocomial pathogens persist on inanimate surfaces? A systematic review. BMC Infect Dis 2006;6:130.
              doi: 10.1186/1471-2334-6-130pmc: PMC1564025pubmed: 16914034google scholar: lookup
            47. Socialstyrelsen. Förslag till utveckling av strategin mot antibiotikaresistens och vårdrelaterade infektioner. 2011; pp. 43–44.

            Citations

            This article has been cited 10 times.
            1. Alsing-Johansson T, Torstensson E, Bergström K, Sternberg-Lewerin S, Bergh A, Penell J. A comparison of two cleaning methods applied in a small animal hospital. BMC Vet Res 2025 Mar 15;21(1):171.
              doi: 10.1186/s12917-025-04631-0pubmed: 40089743google scholar: lookup
            2. Soza-Ossandón P, Rivera D, Allel K, González-Rocha G, Quezada-Aguiluz M, San Martin I, García P, Moreno-Switt AI. Mec-Positive Staphylococcus Healthcare-Associated Infections Presenting High Transmission Risks for Antimicrobial-Resistant Strains in an Equine Hospital. Antibiotics (Basel) 2022 May 4;11(5).
              doi: 10.3390/antibiotics11050621pubmed: 35625265google scholar: lookup
            3. Nielsen SS, Bicout DJ, Calistri P, Canali E, Drewe JA, Garin-Bastuji B, Gonzales Rojas JL, Gortázar C, Herskin M, Michel V, Miranda Chueca MÁ, Padalino B, Pasquali P, Roberts HC, Spoolder H, Ståhl K, Velarde A, Viltrop A, Winckler C, Baldinelli F, Broglia A, Kohnle L, Alvarez J. Assessment of listing and categorisation of animal diseases within the framework of the Animal Health Law (Regulation (EU) No 2016/429): antimicrobial-resistant Staphylococcus aureus in cattle and horses. EFSA J 2022 May;20(5):e07312.
              doi: 10.2903/j.efsa.2022.7312pubmed: 35582361google scholar: lookup
            4. Msimang V, Rostal MK, Cordel C, Machalaba C, Tempia S, Bagge W, Burt FJ, Karesh WB, Paweska JT, Thompson PN. Factors affecting the use of biosecurity measures for the protection of ruminant livestock and farm workers against infectious diseases in central South Africa. Transbound Emerg Dis 2022 Sep;69(5):e1899-e1912.
              doi: 10.1111/tbed.14525pubmed: 35306739google scholar: lookup
            5. Wierup M, Allard Bengtsson U, Vågsholm I. Biosafety considerations and risk reduction strategy for a new veterinary faculty building and teaching hospital in Sweden. Infect Ecol Epidemiol 2020 Jun 4;10(1):1761588.
              doi: 10.1080/20008686.2020.1761588pubmed: 32864050google scholar: lookup
            6. Rojas I, Barquero-Calvo E, van Balen JC, Rojas N, Muñoz-Vargas L, Hoet AE. High Prevalence of Multidrug-Resistant Community-Acquired Methicillin-Resistant Staphylococcus aureus at the Largest Veterinary Teaching Hospital in Costa Rica. Vector Borne Zoonotic Dis 2017 Sep;17(9):645-653.
              doi: 10.1089/vbz.2017.2145pubmed: 28816638google scholar: lookup
            7. Bortolami A, Williams NJ, McGowan CM, Kelly PG, Archer DC, Corrò M, Pinchbeck G, Saunders CJ, Timofte D. Environmental surveillance identifies multiple introductions of MRSA CC398 in an Equine Veterinary Hospital in the UK, 2011-2016. Sci Rep 2017 Jul 14;7(1):5499.
              doi: 10.1038/s41598-017-05559-8pubmed: 28710350google scholar: lookup
            8. Bergström K, Grönlund U. A pre- and post-intervention study of infection control in equine hospitals in Sweden. Acta Vet Scand 2014 Aug 22;56(1):52.
              doi: 10.1186/s13028-014-0052-4pubmed: 25146752google scholar: lookup
            9. Bengtsson B, Greko C. Antibiotic resistance--consequences for animal health, welfare, and food production. Ups J Med Sci 2014 May;119(2):96-102.
              doi: 10.3109/03009734.2014.901445pubmed: 24678738google scholar: lookup
            10. van Balen J, Mowery J, Piraino-Sandoval M, Nava-Hoet RC, Kohn C, Hoet AE. Molecular epidemiology of environmental MRSA at an equine teaching hospital: introduction, circulation and maintenance. Vet Res 2014 Mar 19;45(1):31.
              doi: 10.1186/1297-9716-45-31pubmed: 24641543google scholar: lookup