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Ultra low dose 2D/3D digital Xray system

EOS is an ultra low dose 2D/3D digital Xray system developed by Biospace Med and a team of France - Quebec engineers and clinicians. EOS is based on the Nobel Prize for Physics winner Georges Charpak’s detector technology that has been adapted for clinical Xray imaging. It allows for the simultaneous acquisition of two perpendicular digital images of patient in a weight-bearing standing position. Using a stereoradiographic reconstruction scheme based on a priori geometrical and statistical information about the 3D bones, dedicated software allows for the reconstruction and dynamic visualization of the 3D bone surface of the spine, the pelvis, the femur, the tibia, etc. Once the 3D models are obtained, it is then possible to obtain automatically over 100 true 3D angle and length measurements (cobb angles, vertebral rotations, wedging, kyphosis, lordosis, pelvic parameters, pangonogram data). Software also allows making any 3D desired measurements, using a set of simple interactive tools. A dosimetric study done in our laboratories has shown a 6 to 9 fold decrease in dose received by the patients compared to a normal full-length spinal exam. Furthermore, applications are being developed to evaluate the 3D deformity pre-operatively and post-operatively. A recent retrospective study identified several 3D parameters distinguishing patients with significant curve progression when compared to a group of patients with no progression of their initial scoliotic curve at maturity. These findings are currently evaluated in a prospective study.

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Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution 2.0 International License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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de Guise, J.A., Parent, S. Ultra low dose 2D/3D digital Xray system. Scoliosis 5 (Suppl 1), O2 (2010). https://doi.org/10.1186/1748-7161-5-S1-O2

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  • DOI: https://doi.org/10.1186/1748-7161-5-S1-O2

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