Biomechanical and histologic assessment of a novel screw retention technology in an ovine lumbar fusion model. Academic Article uri icon

Overview

abstract

  • BACKGROUND CONTEXT: Screw loosening is a prevalent failure mode in orthopedic hardware, particularly in osteoporotic bone or revision procedures where the screw-bone engagement is limited. PURPOSE: The objective of this study was to evaluate the efficacy of a novel screw retention technology (SRT) in an ovine lumbar fusion model. STUDY DESIGN/SETTING: This was a biomechanical, radiographic, and histologic study utilizing an ovine lumbar spine model. METHODS: In total, 54 (n=54) sheep lumbar spines (L2-L3) underwent posterior lumbar fusion (PLF) via pedicle screw fixation, connecting rod, and bone graft. Following three experimental variants were investigated: positive control (ideal clinical scenario), negative control (simulation of compromised screw holes), and SRT treatments. Biomechanical and histologic analyses of the functional spinal unit (FSU) were determined as a function of healing time (0, 3, and 12 months postoperative). RESULTS: Screw pull-out, screw break-out, and FSU stability of the SRT treatments were generally equivalent to the positive control group and considerably better than the negative control group. Histomorphology of the SRT treatment screw region of interest (ROI) observed an increase in bone percentage and decrease in void space during healing, consistent with ingrowth at the implant interface. The PLF ROI observed similar bone percentage throughout healing between the SRT treatment and positive control. Less bone formation was observed for the negative control. CONCLUSIONS: The results of this study demonstrate that the SRT improved screw retention and afforded effective FSU stabilization to achieve solid fusion in an otherwise compromised fixation scenario in a large animal model.

publication date

  • July 31, 2018

Research

keywords

  • Bone Transplantation
  • Lumbar Vertebrae
  • Pedicle Screws
  • Spinal Fusion

Identity

Scopus Document Identifier

  • 85053306562

Digital Object Identifier (DOI)

  • 10.1016/j.spinee.2018.07.021

PubMed ID

  • 30075298

Additional Document Info

volume

  • 18

issue

  • 12