4.2 Article

Bacterial biofilm formation on a human cochlear implant

Journal

OTOLOGY & NEUROTOLOGY
Volume 26, Issue 5, Pages 972-975

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/01.mao.0000169047.38759.8b

Keywords

bacterial biofilm; cochlear implant; implants

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Objective: To report the characteristics of a bacterial biofilm from the surface of a cochlear implant. Background: Bacterial biofilm formation on implanted devices causes intractable infections and device extrusions necessitating device removal, with loss of function. More information is needed about biofilm characteristics and interactions with the implant surface before better treatments can be designed. Study Design: A retrospective case review was combined with a descriptive histological study of the surface of an otologic device. Methods: The receiver/stimulator device removed from a cochlear implant patient because of intractable infection and partial device extrusion was fixed and processed for microscopic examination. Its surface and the material present on its surface were analyzed using light and electron microscopy, focusing on surface texture, cell types, and bacteria species and extracellular polymeric substances present within the biofilm. Results: Stereomicroscopic examination revealed extracellular polymeric substances, pinkish yellow in color, with spheres of uniform size scattered throughout, indicative of a biofilm containing Staphylococcus aureus. Biofilm density was greatest in depressions on the surface of the implant. Cross-sectional analysis revealed bacteria interspersed with polymorphonuclear leukocytes. Scanning electron microscopic examination demonstrated an amorphous layer of extracellular polymeric substances containing small filaments, bacteria, and inflammatory cells. Only Staphylococcus aureus was detected. Conclusion: Cochlear implant material can provide a surface for bacterial biofilm formation. Impressions can provide an environment conducive to biofilm establishment and growth, ultimately necessitating device removal, with loss of implant function. Biofilm characterization should aid in design of cochlear implant devices less susceptible to biofilm formation.

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