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A Cluster of Mycobacterium wolinskyi Surgical Site Infections at an Academic Medical Center

Published online by Cambridge University Press:  10 May 2016

Avish Nagpal*
Affiliation:
Division of Infectious Diseases, Mayo Clinic, Rochester, Minnesota
Jean E. Wentink
Affiliation:
Infection Prevention and Control, Mayo Clinic, Rochester, Minnesota
Elie F. Berbari
Affiliation:
Division of Infectious Diseases, Mayo Clinic, Rochester, Minnesota Infection Prevention and Control, Mayo Clinic, Rochester, Minnesota
Kimberly C. Aronhalt
Affiliation:
Infection Prevention and Control, Mayo Clinic, Rochester, Minnesota
Alan J. Wright
Affiliation:
Division of Infectious Diseases, Mayo Clinic, Rochester, Minnesota Infection Prevention and Control, Mayo Clinic, Rochester, Minnesota
Dale A. Krageschmidt
Affiliation:
Industrial Hygiene, Mayo Clinic, Rochester, Minnesota
Nancy L. Wengenack
Affiliation:
Division of Microbiology, Mayo Clinic, Rochester, Minnesota
Rodney L. Thompson
Affiliation:
Division of Infectious Diseases, Mayo Clinic, Rochester, Minnesota Infection Prevention and Control, Mayo Clinic, Rochester, Minnesota
Pritish K. Tosh
Affiliation:
Division of Infectious Diseases, Mayo Clinic, Rochester, Minnesota
*
Division of Infectious Diseases, Mayo Clinic, Rochester, MN 55905 (tosh.pritish@mayo.edu).

Extract

Objective

To study a cluster of Mycobacterium wolinskyi surgical site infections (SSIs).

Design

Observational and case-control study.

Setting

Academic hospital.

Patients.

Subjects who developed SSIs with M. wolinskyi following cardiothoracic surgery.

Methods

Electronic surveillance was performed for case finding as well as electronic medical record review of infected cases. Surgical procedures were observed. Medical chart review was conducted to identify risk factors. A case-control study was performed to identify risk factors for infection; Fisher exact or Kruskal-Wallis tests were used for comparisons of proportions and medians, respectively. Patient isolates were studied using pulsed-field gel electrophoresis (PFGE). Environmental microbiologic sampling was performed in operating rooms, including high-volume water sampling.

Results

Six definite cases of M. wolinskyi SSI following cardiothoracic surgery were identified during the outbreak period (October 1, 2008–September 30, 2011). Having cardiac surgery in operating room A was significantly associated with infection (odds ratio, 40; P = .0027). Observational investigation revealed a cold-air blaster exclusive to operating room A as well a microbially contaminated, self-contained water source used in heart-lung machines. The isolates were indistinguishable or closely related by PFGE. No environmental samples were positive for M. wolinskyi.

Conclusions

No single point source was established, but 2 potential sources, including a cold-air blaster and a microbially contaminated, self-contained water system used in heart-lung machines for cardiothoracic operations, were identified. Both of these potential sources were removed, and subsequent active surveillance did not reveal any further cases of M. wolinskyi SSI.

Infect Control Hosp Epidemiol 2014;35(9):1169-1175

Type
Original Article
Copyright
© 2014 by The Society for Healthcare Epidemiology of America. All rights reserved.

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References

1. Foz, A, Roy, C, Jurado, J, Arteaga, E, Ruiz, JM, Moragas, A. Mycobacterium chelonei iatrogenic infections. J Clin Microbiol 1978;7(3):319321.CrossRefGoogle ScholarPubMed
2. Safranek, TJ, Jarvis, WR, Carson, LA, et al. Mycobacterium chelonae wound infections after plastic surgery employing contaminated gentian violet skin-marking solution. New Engl J Med 1987;317(4):197201.CrossRefGoogle ScholarPubMed
3. Soto, LE, Bobadilla, M, Villalobos, Y, et al. Post-surgical nasal cellulitis outbreak due to Mycobacterium chelonae. J Hosp Infect 1991;19(2):99106.CrossRefGoogle ScholarPubMed
4. Chadha, R, Grover, M, Sharma, A, et al. An outbreak of post-surgical wound infections due to Mycobacterium abscessus. Pediatr Surg Int 1998;13(56):406410.Google Scholar
5. Lee, YS, Nam, SW, Park, YS, Lee, BK. Mycobacterium wolinskyi infection after total knee arthroplasty in a healthy woman. J Orthop Sci 2013. doi:10.1007/s00776-013-0422-1.Google Scholar
6. Santos Lima, A, Carneiro Neves, MM, Machado Gomes, K, et al. First case report of infection by Mycobacterium wolinskyi after mammoplasty in Brazil. Infect Dis Rep 2013;5(2):e12.Google Scholar
7. Yoo, SJ, Lee, KH, Jung, SN, Heo, ST. Facial skin and soft tissue infection caused by Mycobacterium wolinskyi associated with cosmetic procedures. BMC Infect Dis 2013;13:479.CrossRefGoogle ScholarPubMed
8. Ariza-Heredia, EJ, Dababneh, AS, Wilhelm, MP, Wengenack, NL, Razonable, RR, Wilson, JW. Mycobacterium wolinskyi: a case series and review of the literature. Diagn Microbiol and Infect Dis 2011;71(4):421427.Google Scholar
9. Fisher, RA. On the interpretation of χ2 from contingency tables, and the calculation of P. J R Stat Soc 1922;85(1):8794.Google Scholar
10. Kruskal, WH, Wallis, WA. Use of ranks in one-criterion variance analysis. J Am Stat Assoc 1952;47(260):583621.Google Scholar
11. Centers for Disease Control and Prevention (CDC). Procedures for the recovery of Legionella from the environment manual. 2005. http://www.cdc.gov/legionella/specimen-collect-mgmt/procedures-manual.html. Accessed December 30, 2012.Google Scholar
12. Brown, BA, Springer, B, Steingrube, VA, et al. Mycobacterium wolinskyi sp. nov. and Mycobacterium goodii sp. nov., two new rapidly growing species related to Mycobacterium smegmatis and associated with human wound infections: a cooperative study from the International Working Group on Mycobacterial Taxonomy. Int J Syst Bacteriol 1999;49(4):14931511.Google Scholar
13. Tenover, FC, Arbeit, RD, Goering, RV, et al. Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J Clin Microbiol 1995;33(9):22332239.Google Scholar
14. Milano, CA, Kesler, K, Archibald, N, Sexton, DJ, Jones, RH. Mediastinitis after coronary artery bypass graft surgery: risk factors and long-term survival. Circulation 1995;92(8):22452251.Google Scholar
15. Ottino, G, De Paulis, R, Pansini, S, et al. Major sternal wound infection after open-heart surgery: a multivariate analysis of risk factors in 2,579 consecutive operative procedures. Ann Thorac Surg 1987;44(2):173179.CrossRefGoogle Scholar
16. Peters, M, Muller, C, Rusch-Gerdes, S, et al. Isolation of atypical mycobacteria from tap water in hospitals and homes: is this a possible source of disseminated MAC infection in AIDS patients? J Infect 1995;31(1):3944.Google Scholar
17. Phillips, MS, von Reyn, CF. Nosocomial infections due to nontuberculous mycobacteria. Clin Infect Dis 2001;33(8):13631374.Google Scholar
18. Leao, SC, Viana-Niero, C, Matsumoto, CK, et al. Epidemic of surgical-site infections by a single clone of rapidly growing mycobacteria in Brazil. Future Microbiol 2010;5(6):971980.Google Scholar
19. Lim, JM, Kim, JH, Yang, HJ. Management of infections with rapidly growing mycobacteria after unexpected complications of skin and subcutaneous surgical procedures. Arch Plast Surg 2012;39(1):1824.Google Scholar
20. CDC. Rapidly growing mycobacterial infection following liposuction and liposculpture: Caracas, Venezuela, 1996–1998. MMWR Morb Mortal Wkly Rep 1998;47(49):10651067.Google Scholar
21. Marchandin, H, Battistella, P, Calvet, B, et al. Pacemaker surgical site infection caused by Mycobacterium goodii. J Med Microbiol 2009;58(4):517520.Google Scholar
22. Wallace, RJ Jr, Musser, JM, Hull, SI, et al. Diversity and sources of rapidly growing mycobacteria associated with infections following cardiac surgery. J Infect Dis 1989;159(4):708716.CrossRefGoogle ScholarPubMed