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Dive into the research topics where Wingerter S is active.

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Featured researches published by Wingerter S.


Journal of Investigative Surgery | 2007

Characterization of a Femoral Segmental Nonunion Model in Laboratory Rats: Report of a Novel Surgical Technique

George V. Russell; Tucci M; Conflitti J; Matthew L. Graves; Wingerter S; Woodall J; Ragab A; Hamed Benghuzzi

The literature is lacking conclusive results regarding the exact mechanism of maximizing the fracture healing stages with minimal traumatic side effects. This observation mandates the development of a novel surgical procedure using small animals as a model to study fracture healing in the presence of osteoinductive agents. Previously, stabilization of osteotomies in small animal models has mainly been accomplished using Kirschner wires, but the rats tremendous ability to heal an osteotomy stabilized by this method has masked the effects of osteoinductive agents. Thus, this study proposes using a modified 20-hole, 1.5-mm stainless-steel plate to stabilize a 5-mm segmental defect. Thirty of 32 adult male rats were fully weight-bearing within 2 days and were followed over a 15-week period. Two animals showed evidence of fixation failure due to technical error, and the animals were humanely sacrificed. At the end of the study, the fractures were stable with significantly less bone formation evident when compared to controls (p <. 001). Therefore, this technique can effectively be used to evaluate compounds that will enhance bone formation and allows for stable fixation of the control with minimal callus formation or bony ingrowth. The goal of this article is to allow other investigators to reproduce this technique as well as outline the advantages and disadvantages of this novel plating technique versus the former Kirschner wire technique for the study of osteoinductive agents using small animals as a model.


Journal of Investigative Surgery | 2007

Comparison of Two Different Fixation Techniques for a Segmental Defect in a Rat Femur Model

Wingerter S; Graham Calvert; Tucci M; Tsao A; George V. Russell; Ham Benghuzzi

Studies have attempted to identify the osteogenic effects of bone morphogenetic proteins using a rat femur model, which commonly involves the creation of a critical size defect followed by internal fixation of the femur. Among the most familiar fixation methods are either plating or intramedullary placement of a Kirschner wire (K-wire). There are advantages and disadvantages to each method; however, this study attempts to identify the best method by exploring the histological effects of each technique. The experiment involved two groups with no added treatment: Group P (plate fixation method) and Group K (K-wire fixation method). The animals were allowed a 4-week interval for the femurs to heal, and proximal, distal, and two midshaft cuts were examined under high-power microscopy after the fixation apparatus was removed. Group K exhibited a peculiar fibrotic healing pattern that followed the shaft of the then vacated K-wire and there was minimal new viable bone formation. Group P, however, exhibited a more natural ingrowth of newly formed bone that began at the proximal and distal cuts and proceeded centrally into the core of the defect. Due to the fibrotic tissue in Group K, this study shows that the model is insufficient due to the micromotion created and thus supports plating of critical defects as the fixation method of choice due to the creation of a stable healing environment.


Orthopedic Clinics of North America | 2011

Hip Disease and Hip Arthroplasty

Wingerter S; Robert K. Mehrle

There has been a significant increase in the prevalence of obesity in the United States over the last 20 years, with the highest percentage in Mississippi. The percentage of obese patients undergoing total hip arthroplasty (THA) appears to be increasing at an even faster rate. Orthopedic surgeons performing hip arthroplasty need to be aware of potential issues to minimize complications associated with this population. This article outlines preoperative and postoperative care and describes current techniques and tools used by surgeons in obese patients to facilitate soft tissue dissection, exposure, implant placement, and closure.


Journal of Spinal Disorders & Techniques | 2009

A preliminary report on the effects of sustained administration of corticosteroid on traumatized disc using the adult male rat model.

Ragab A; James W. Woodall; Michelle Tucci; Wingerter S; Adam W. Fosnaugh; Laura N. Franklin; Hamed Benghuzzi

Study Design A novel degenerative disc disease model and sustained delivery method for corticosteroid in male Sprague-Dawley albino rats. Objectives To develop a model of degenerative disc disease and to determine the effect of continuous sustained release of corticosteroid on the process of degeneration within the traumatized disc. Summary of Background Data The current modalities of treating symptomatic degenerative disc disease are either conservative or surgical. However, there is no cure for the degenerative process and prevention, therefore, is the ideal treatment. An understanding of the mechanisms involved in disc degeneration is crucial to develop new methods for prevention and treatment, including appropriate delivery systems and dosages of repair factors. Methods The L5-L6 intervertebral disc was pierced with a 23-gauge needle in 18 rats. The animals received either sham or corticosterone-charged tricalcium phosphate ceramic capsules. The rats were euthanized at 4 weeks. Chondrocytes in the transition zone areas were counted and compared statistically. Results The surgical technique induced degeneration of the nucleus without evidence of inflammation at adjacent levels when compared with nontraumatized controls. The number of chondrocytes per area was significantly less in the sham group than in the control group. Corticosteroid treatment showed chondrocyte numbers similar to control in 4 of 5 different views of the disc. The anterior region of the disc had 50% less chondrocytes per area than the control; however, the chondrocyte numbers were 50% greater than in the same site from discs of sham animals. Conlcusions The results show the development of a degenerative disc animal model that can be used to test the effects of growth enhancing factors in disc repair. Administration of continuous sustained release of corticosterone can slow the process of degeneration within the traumatized disc in the rat model.


Biomedical sciences instrumentation | 2006

Mechanical strength repercussions of various fixative storage methods on bone.

Wingerter S; Calvert G; Tucci M; Hamed Benghuzzi; George V. Russell; Puckett A


Biomedical sciences instrumentation | 2007

Evaluation of short-term healing following sustained delivery of osteoinductive agents in a rat femur drill defect model.

Wingerter S; Tucci M; Bumgardner J; Benghuzzi H


Biomedical sciences instrumentation | 2008

Analysis of tobramycin release from beta tricalcium phosphate drug delivery system.

Aneja A; Woodall J; Wingerter S; Tucci M; Benghuzzi H


Biomedical sciences instrumentation | 2007

Histological and radiographic comparison of allograft substitutes using a continuous delivery model in segmental defects.

Marks T; Wingerter S; Franklin L; Woodall J; Tucci M; George V. Russell; Patel R; Benghuzzi H


Biomedical sciences instrumentation | 2011

Cellular effects of catabolic inflammatory cytokines on chondrocytes - biomed 2011.

Lawyer T; Wingerter S; Tucci M; Benghuzzi H


Biomedical sciences instrumentation | 2007

Comparison of osteoconductive materials on MG63 osteoblast cell function.

Barron M; Franklin L; Woodall J; Wingerter S; Benghuzzi H; Tucci M

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Tucci M

University of Mississippi Medical Center

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Woodall J

University of Mississippi Medical Center

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Benghuzzi H

University of Mississippi

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George V. Russell

University of Mississippi Medical Center

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Ragab A

University of Mississippi Medical Center

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Hamed Benghuzzi

University of Mississippi Medical Center

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Ham Benghuzzi

University of Mississippi Medical Center

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Conflitti J

University of Mississippi Medical Center

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Graham Calvert

University of Mississippi Medical Center

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Matthew L. Graves

University of Mississippi Medical Center

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