Dustin Williams

Dr. Dustin Williams

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Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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31 January 2012 in Journal of Orthopaedic Research
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Journal Article
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SJSujee Jeyapalina
Sujee Jeyapalina
JBJames Peter Beck
James Peter Beck
KBKent N. Bachus
Kent N. Bachus
DWDustin Williams
Dustin Williams
RBRoy D. Bloebaum
Roy D. Bloebaum
Infections of percutaneous osseointegrated prostheses (POP) cause prolonged morbidity and device failure because once established, they are refractory to antibiotic therapy. To date, only limited translational animal studies have investigated the efficacy of POP designs in preventing infections. We developed an animal model to evaluate the efficacy of a porous‐coated titanium (Ti) subdermal barrier to achieve skin–implant integration and to prevent periprosthetic infection. In a single‐stage “amputation and implantation” surgery, 14 sheep were fitted with percutaneous devices with an attached porous‐coated Ti subdermal barrier. Nine sheep were implanted with a smooth Ti subdermal barrier construct and served as controls, with one control sheep removed from the study due to a fractured bone. Clinical, microbiological, and histopathological data showed that the porous Ti barrier prevented superficial and deep tissue infections in all animals (14/14, 100%) at the 9‐month endpoint. In contrast, animals with the smooth Ti implant construct had a 25% (2/8) infection rate. Survival analysis indicated a significant difference between the groups (log‐rank test,p = 0.018). Data also indicated that although skin marsupialization was evident in both implant types, animals in the control group had a four times greater marsupialization rate. We concluded that osseointegrated implants incorporating porous‐coated Ti subdermal barriers may have the ability to prevent infection by maintaining a healthy, biologically attached epithelial barrier at the skin–implant interface in load‐bearing animals up to a 9‐month terminus. © 2012 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 30:1304–1311, 2012

1 November 2012 in Biomaterials
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Journal Article
Closed access
DWDustin Williams
Dustin Williams
BHBryan S. Haymond
Bryan S. Haymond
JBJames P. Beck
James P. Beck
PSPaul B. Savage
Paul B. Savage
VCVinod Chaudhary
Vinod Chaudhary
RBRoy D. Bloebaum
Roy D. Bloebaum

28 November 2011 in Journal of Biomedical Materials Research Part B: Applied Biomaterials
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Journal Article
Closed access
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DWDustin Williams
Dustin Williams
JCJ. William Costerton
J. William Costerton

25 March 2011 in Current Microbiology
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Journal Article
Closed access
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DWDustin Williams
Dustin Williams
KWKassie L. Woodbury
Kassie L. Woodbury
BHBryan S. Haymond
Bryan S. Haymond
APAlbert E. Parker
Albert E. Parker
RBRoy D. Bloebaum
Roy D. Bloebaum

10 April 2012 in Journal of Biomedical Materials Research Part A
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Journal Article
Closed access
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DWDustin Williams
Dustin Williams
BHBryan S. Haymond
Bryan S. Haymond
KWKassie L. Woodbury
Kassie L. Woodbury
JBJ. Peter Beck
J. Peter Beck
DMDavid E. Moore
David E. Moore
RBRoy D. Bloebaum
Roy D. Bloebaum

29 December 2022 in Antibiotics
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Journal Article
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ACAlexa A. Ciarolla
Alexa A. Ciarolla
NLNorman Lapin
Norman Lapin
DWDustin Williams
Dustin Williams
RCRajiv Chopra
Rajiv Chopra
DGDavid E. Greenberg
David E. Greenberg
Prosthetic joint infection (PJI) presents several clinical challenges. This is in large part due to the formation of biofilm which can make infection eradication exceedingly difficult. Following an extensive literature search, this review surveys a variety of non-pharmacological methods of preventing and/or treating biofilm within the body and how they could be utilized in the treatment of PJI. Special attention has been paid to physical strategies such as heat, light, sound, and electromagnetic energy, and their uses in biofilm treatment. Though these methods are still under study, they offer a potential means to reduce the morbidity and financial burden related to multiple stage revisions and prolonged systemic antibiotic courses that make up the current gold standard in PJI treatment. Given that these options are still in the early stages of development and offer their own strengths and weaknesses, this review offers an assessment of each method, the progress made on each, and allows for comparison of methods with discussion of future challenges to their implementation in a clinical setting.