[Influence of disc prosthesis position on segmental motion in the lumbar spine].

AIM OF THE STUDY Total disc arthroplasty is reported to maintain segmental motion. From finite element studies a rather posterior and central implantation of the prosthesis is recommended. However, there is yet no in vitro study with cadaveric specimens investigating the topic of implant positioning. METHODS Ten human lumbar spines were subjected to biomechanical testing. Flexion/extension and side-bending moments were applied from 2.5-7.5 Nm on a spine load simulator. First, the intact specimens were tested in 3 load cycles while motion was monitored with regard to the facet joints under different loads by an ultrasound-based system. An unconstrained total disc prosthesis was then implanted in a central position and the different load cycles were repeated. Finally the implant was positioned in a decentral position with an average offset of 6.2 mm for repetitive data acquisition. RESULTS Comparison of the facet joint motion in central and eccentric prosthesis positions resulted in the following averaged differences. During flexion of the lumbar spine an average difference of the reference point excursions of 0.38 mm was recorded on the ipsilateral facet joint with reference to the decentral position. For extension, the difference was 0.33 mm on average, for right side bending a difference of 0.63 mm was recorded while left side bending resulted in an average difference of 0.24 mm. The deviation of the reference markers on the contralateral facet joint showed the following average differences: for flexion 0.23 mm and for extension 0.54 mm, respectively. For side bending right/left the differences amounted to 0.18 mm and 0.39 mm. With regard to segmental motion there was no statistically significant difference for both the ipsilateral (p = 0.0564) and the contralateral (p = 0.2593) reference marker. CONCLUSIONS The comparison of the segmental motion after central and decentral implantation of a lumbar total disc prosthesis reveals differences that have, nevertheless, no statistical significance. However, for clinical use it is recommended to strive for a central position of the implant.

[1]  M. Weißkopf,et al.  Einfluss der Inlaygröße einer lumbalen Bandscheibenprothese auf das Bewegungsverhalten , 2008 .

[2]  G. Bergmann,et al.  Effect of position and height of a mobile core type artificial disc on the biomechanical behaviour of the lumbar spine , 2008, Proceedings of the Institution of Mechanical Engineers. Part H, Journal of engineering in medicine.

[3]  Edward Teng,et al.  Hybrid Testing of Lumbar CHARITÉ Discs Versus Fusions , 2007, Spine.

[4]  J. Katz,et al.  A Review of the 2001 Volvo Award Winner in Clinical Studies: Lumbar Fusion Versus Nonsurgical Treatment for Chronic Low Back Pain: A Multicenter Randomized Controlled Trial From the Swedish Lumbar Spine Study Group , 2006, Spine.

[5]  F. Geisler,et al.  Neurological complications of lumbar artificial disc replacement and comparison of clinical results with those related to lumbar arthrodesis in the literature: results of a multicenter, prospective, randomized investigational device exemption study of Charité intervertebral disc. Invited submission , 2004, Journal of neurosurgery. Spine.

[6]  Hyun Bae,et al.  ProDisc Artificial Total Lumbar Disc Replacement: Introduction and Early Results From the United States Clinical Trial , 2003, Spine.

[7]  B. Cunningham,et al.  Experimental Design of Total Disk Replacement—Experience with a Prospective Randomized Study of the SB Charitè , 2003, Spine.

[8]  D. Ohnmeiss,et al.  Lumbar Spine Arthroplasty: Early Results Using the ProDisc II: A Prospective Randomized Trial of Arthroplasty Versus Fusion , 2003, Journal of spinal disorders & techniques.

[9]  R. Bertagnoli,et al.  Indications for full prosthetic disc arthroplasty: a correlation of clinical outcome against a variety of indications , 2002, European Spine Journal.

[10]  K. Büttner-Janz,et al.  [Basic principles of successful implantation of the SB Charité model LINK intervertebral disk endoprosthesis]. , 2002, Der Orthopade.

[11]  J M Huyghe,et al.  Requirements for an artificial intervertebral disc , 2001, The International journal of artificial organs.

[12]  V. Goel,et al.  Load-Sharing Between Anterior and Posterior Elements in a Lumbar Motion Segment Implanted With an Artificial Disc , 2001, Spine.

[13]  A. Nachemson,et al.  Lumbar disc disease with discogenic pain. What surgical treatment is most effective , 1996 .

[14]  M M Panjabi,et al.  Biomechanical Evaluation of Spinal Fixation Devices: I. A Conceptual Framework , 1988, Spine.

[15]  Antonius Rohlmann,et al.  Effect of an artificial disc on lumbar spine biomechanics: a probabilistic finite element study , 2008, European Spine Journal.

[16]  W. S. Zeegers,et al.  Artificial disc replacement with the modular type SB Charité III: 2-year results in 50 prospectively studied patients , 1999, European Spine Journal.

[17]  L. Claes,et al.  Testing criteria for spinal implants: recommendations for the standardization of in vitro stability testing of spinal implants , 1998, European Spine Journal.

[18]  K. Büttner-Janz,et al.  [An alternative treatment strategy in lumbar intervertebral disk damage using an SB Charité modular type intervertebral disk endoprosthesis]. , 1987, Zeitschrift fur Orthopadie und ihre Grenzgebiete.

[19]  M. Panjabi,et al.  Biomechanical time‐tolerance of fresh cadaveric human spine specimens , 1985, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[20]  G. Duvel The study group. , 1980 .