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Comparative Study
. 2011 Aug;20(8):1289-96.
doi: 10.1007/s00586-011-1831-5. Epub 2011 May 5.

In vivo preclinical evaluation of the influence of osteoporosis on the anchorage of different pedicle screw designs

Affiliations
Comparative Study

In vivo preclinical evaluation of the influence of osteoporosis on the anchorage of different pedicle screw designs

Gianluca Giavaresi et al. Eur Spine J. 2011 Aug.

Abstract

We investigate the anchorage of pedicle screws with different surface treatments in osteoporotic bone. Eight ewes were divided into two groups of four animals each: four sheep underwent bilateral ovariectomy (OVX Group), whereas the operation was simulated in the remaining group (SHAM Group). Eighteen months after the first operation, the Dynesys(®) System was fitted to the sheep using pedicle screws with three different surface treatments: untreated, rough blasted (uncoated) and bioactive coated (bioactive). Uncoated screws showed a significantly higher bone ingrowth value compared with the untreated screws in the OVX group (9.3%, p < 0.005) and a significantly lower bone ingrowth value in the SHAM group (-11.0%, p < 0.05). Furthermore, the bioactive pedicle screws had a significant lower bone ingrowth value than the untreated screws in the SHAM group (-12.1%, p < 0.05). These results suggest that both tested surface treatments of pedicular screws may provide an advantage in terms of bone quality and osseointegration, when implanted in osteoporotic vertebrae.

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Figures

Fig. 1
Fig. 1
SEM microphotograph of the treated implant surface before (a) and after (b) soaking in SBF (30 days). Apatite crystals are observable. In the presence of body fluids, this treated surface induces apatite nucleation at the bone implant interface, resulting in a dense and homogenous calcium-phosphate layer at the surface and a graded structure down to the substrate metal with no distinct implant-coating interface
Fig. 2
Fig. 2
Anteroposterior X-rays of lumbar spines of OVX_3 (a) and SHAM_1 (b) sheep. Asterisks indicate pedicle screw loosening
Fig. 3
Fig. 3
Histologies of bioactive coated (a, b), rough blasted (c, d) and untreated (e, f) pedicle screws implanted in the vertebral pedicles (L2–L5) of OVX (a, c, e) and SHAM (b, d, f) sheep at a magnification of ×10 (Fuchsin acid and Fast green) (Scale bar 400 μm). All tested screws are in direct contact with peri-implant bone. Signs of bone rarefaction are evident in OVX sheep. The presence of coatings improves the screw–biomaterial interface even in the presence of osteopenia and no areas of biomaterial not in direct contact with bone are visible

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References

    1. Boden SD. Bone repair and enhancement of clinical trial design: spine applications. Clin Orthop. 1998;355:336–346. - PubMed
    1. Stoll TM, et al. The dynamic neutralization system for the spine: a multi-center study of a novel non-fusion system. Eur Spine J. 2002;11:S170–S178. - PMC - PubMed
    1. Mulholland RC. The myth of lumbar instability: the importance of abnormal loading as a cause of low back pain. Eur Spine J. 2008;17(5):619–625. doi: 10.1007/s00586-008-0612-2. - DOI - PMC - PubMed
    1. Beastall J, et al. The Dynesys lumbar spinal stabilization system: a preliminary report on positional magnetic resonance imaging findings. Spine. 2007;32:685–690. doi: 10.1097/01.brs.0000257578.44134.fb. - DOI - PubMed
    1. Schlegel JD, et al. Lumbar motion segment pathology adjacent to thoracolumbar, lumbar, and lumbosacral fusions. Spine. 1996;21:970–981. doi: 10.1097/00007632-199604150-00013. - DOI - PubMed