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Long-Lasting Contamination of a Vitrectomy Apparatus With Serratia marcescens

Published online by Cambridge University Press:  02 January 2015

Ines Kappstein*
Affiliation:
Institute of Environmental Medicine and Hospital Epidemiology, University Hospital, Freiburg, Germany
Christian M. Schneider
Affiliation:
Institute of Environmental Medicine and Hospital Epidemiology, University Hospital, Freiburg, Germany
Hajo Grundmann
Affiliation:
Institute of Environmental Medicine and Hospital Epidemiology, University Hospital, Freiburg, Germany
Regina Scholz
Affiliation:
Institute of Environmental Medicine and Hospital Epidemiology, University Hospital, Freiburg, Germany
Peter Janknecht
Affiliation:
Department of Ophthalmology, University Hospital, Freiburg, Germany
*
Technische Univesität, Abteilung, für Infektionshygiene, Klinikum rechts der Isar, Troggerstrasse 32, 81675 München, Germany

Abstract

Objective:

To investigate the contamination of a vitrectomy apparatus with Serratia marcescens.

Design:

Descriptive microbiological and molecular environmental study.

Setting:

An 1,800-bed university hospital.

Results:

S marcescens was found inside the vitrectomy apparatus at the pressure transducer. Molecular typing by randomly amplified polymorphic DNA-automated laser flourescence analysis and pulsed-field gel electrophoresis identified a single pattern for all strains isolated from the apparatus. Surprisingly, the contaminating strain was identical to two strains of S marcescens isolated nearly 2 years earlier from two patients who were involved in a small outbreak of acute postoperative endophthalmitis following cataract surgery at another hospital. The emergency vitrectomies in these patients were performed at our hospital with the same apparatus that was found to be contaminated 2 years later.

Conclusion:

Performing a systematic environmental search for the assumed bacterial reservoir within the system of the vitrectomy apparatus finally made it possible to find and eliminate the nidus for the gram-negative rod. Molecular typing demonstrated that all isolates belonged to a single genotype, and revealed unexpectedly a link to two vitrectomies performed 2 years earlier. The data support the hypothesis that the source of the contamination was one of these patients, and thus contamination of the apparatus was present for almost 2 years.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1999

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References

1. Puliafito, CA, Baker, AS, Haaf, J, Forster, CS. Infectious endophthalmitis: review of 36 cases. Ophthalmology 1982;89:921929.Google Scholar
2. Forster, RK, Abbott, KL, Gelender, H. Management of infectious endophthalmitis. Ophthalmology 1980;87:313319.Google Scholar
3. Liu, PY, Lau, YJ, Hu, BS, Shir, JM, Cheung, MH, Shi, ZY, Tsai, WS. Use of PCR to study epidemiology of Serratia marcescens isolates in nosocomial infection. J Clin Microbiol 1994;32:19351938.CrossRefGoogle ScholarPubMed
4. Grundmann, H, Schneider, C, Tichy, HV, Simon, R, Klare, I, Hartung, D, et al. Automated laser fluorescence analysis of randomly amplified polymorphic DNA a rapid method for investigating nosocomial transmission of Acinetobacter baumannii . J Med Microbiol 1995;43:446451.CrossRefGoogle ScholarPubMed
5. Matushek, MG, Bonten, MJM, Hayden, MK. Rapid preparation of bacterial DNA for pulsed-fleld gel electrophoresis. J Clin Microbiol 1996;34:25982600.Google Scholar
6. Traub, WH, Eiden, A, Leonhard, B, Bauer, D. Typing of nosocomial strains of Serratia marcescens: comparison of restriction enzyme cleaved genomic DNA fragment (PFGE) analysis with bacteriocin typing, biochemical profiles and serotyping. Zentralblatt fir Bakteriologie 1996;284:93106.Google Scholar
7. Ariyasu, RG, Nakamura, T, Trousdale, MD, Smith, RE. Intraoperative bacterial contamination of the aqueous humour. Ophthalmic Surgery 1993;24:367373.Google Scholar
8. Dhaliwal, DK, Kowalski, RP, Donahue, SP, Doft, BH, Karenchak, LM. Evaluation of vitrectomy machines as a source of false-positive culture contamination in endophthalmitis. Am J Ophthalmol 1995;119:6264.CrossRefGoogle ScholarPubMed
9. de Courten, C, Sancho, P, BenEzra, D. Metastatic Serratia marcescens endophthalmitis. J Pediatr Ophthalmol Strabismus 1988;25:4547.Google Scholar
10. Joondeph, HC, Nothnagel, AF. Serratia rubidea endophthalmitis following penetrating ocular injury. Ann Ophthalmol 1983;15:11381140.Google Scholar
11. McCray, E, Rampell, N, Solomon, SL, Bond, WW, Marrone, WJ, O'Day, D. Outbreak of Candida parapsilosis endophthalmitis after cataract extraction and intraocular lens implantation. J Clin Microbiol 1986;24:625628.Google Scholar