We have located links that may give you full text access.
Biomechanical evaluation of an atlantoaxial lateral mass fusion cage with C1-C2 pedicle fixation.
Spine 2010 June 16
STUDY DESIGN: A biomechanical testing protocol was used to evaluate atlantoaxial fixation techniques in a human cadaveric model.
OBJECTIVE: To compare in vitro biomechanics of atlantoaxial lateral mass fusion cage combined with C1-C2 pedicle screw technique with those of C1-C2 pedicle screw technique alone and C1-C2 transarticular screws combined with Gallie wires.
SUMMARY OF BACKGROUND DATA: An atlantoaxial lateral mass fusion cage was designed, knowing that the cage, when rigidly combined with C1-C2 pedicle screws, could offer other fusion spots for atlantoaxial stabilization in cases when the posterior arch of the atlas is absent or removed for decompression and a Gallie fixation is impossible. No comparative in vitro biomechanical test has been conducted previously to evaluate the feasibility of this method.
METHODS: Anatomic measurements of the atlantoaxial lateral masses were taken using computed tomography in normal human subjects. Six fresh-frozen human cadaveric cervical spines (C0-C4) were used in the biomechanical study. Specimens were tested in their intact condition, after destabilization via transverse-alar-apical ligament disruption, and after implantation of 3 fixation constructs: (1) transarticular screws combined with Gallie wires, (2) C1-C2 pedicle screws, and (3) atlantoaxial lateral mass fusion cage combined with C1-C2 pedicle screws. Pure moment loading up to 1.5 Nm in flexion/extension, right-left lateral bending, and right-left axial rotation was applied to the occiput, and relative intervertebral rotations were determined using stereophotogrammetry. Range of motion for the intact, destabilized, and 3 fixation scenarios were determined.
RESULTS: The anatomic data indicated that feasible cage design were in 3 sizes: 11/8, 12/9, and 13/10 mm for length/width, and 3.5, 4, and 4.5 mm for height. The biomechanical data indicated that transverse-alar-apical ligament disruption significantly increased C1-C2 motion for all directions. All the 3 fixation techniques significantly reduced motion compared with the intact and destabilized cases. There were no statistically significant differences among the 3 fixation techniques.
CONCLUSION: The biomechanical study indicated that, contrary to expectation, addition of a cage did not increase the stability compared with C1-C2 pedicle screw alone. However, the C1 + C2 + Cage technique may be a viable alternative for atlantoaxial stabilization when the posterior arch of the atlas is absent or removed for decompression and a Gallie fixation is impossible.
OBJECTIVE: To compare in vitro biomechanics of atlantoaxial lateral mass fusion cage combined with C1-C2 pedicle screw technique with those of C1-C2 pedicle screw technique alone and C1-C2 transarticular screws combined with Gallie wires.
SUMMARY OF BACKGROUND DATA: An atlantoaxial lateral mass fusion cage was designed, knowing that the cage, when rigidly combined with C1-C2 pedicle screws, could offer other fusion spots for atlantoaxial stabilization in cases when the posterior arch of the atlas is absent or removed for decompression and a Gallie fixation is impossible. No comparative in vitro biomechanical test has been conducted previously to evaluate the feasibility of this method.
METHODS: Anatomic measurements of the atlantoaxial lateral masses were taken using computed tomography in normal human subjects. Six fresh-frozen human cadaveric cervical spines (C0-C4) were used in the biomechanical study. Specimens were tested in their intact condition, after destabilization via transverse-alar-apical ligament disruption, and after implantation of 3 fixation constructs: (1) transarticular screws combined with Gallie wires, (2) C1-C2 pedicle screws, and (3) atlantoaxial lateral mass fusion cage combined with C1-C2 pedicle screws. Pure moment loading up to 1.5 Nm in flexion/extension, right-left lateral bending, and right-left axial rotation was applied to the occiput, and relative intervertebral rotations were determined using stereophotogrammetry. Range of motion for the intact, destabilized, and 3 fixation scenarios were determined.
RESULTS: The anatomic data indicated that feasible cage design were in 3 sizes: 11/8, 12/9, and 13/10 mm for length/width, and 3.5, 4, and 4.5 mm for height. The biomechanical data indicated that transverse-alar-apical ligament disruption significantly increased C1-C2 motion for all directions. All the 3 fixation techniques significantly reduced motion compared with the intact and destabilized cases. There were no statistically significant differences among the 3 fixation techniques.
CONCLUSION: The biomechanical study indicated that, contrary to expectation, addition of a cage did not increase the stability compared with C1-C2 pedicle screw alone. However, the C1 + C2 + Cage technique may be a viable alternative for atlantoaxial stabilization when the posterior arch of the atlas is absent or removed for decompression and a Gallie fixation is impossible.
Full text links
Related Resources
Trending Papers
Challenges in Septic Shock: From New Hemodynamics to Blood Purification Therapies.Journal of Personalized Medicine 2024 Februrary 4
Molecular Targets of Novel Therapeutics for Diabetic Kidney Disease: A New Era of Nephroprotection.International Journal of Molecular Sciences 2024 April 4
The 'Ten Commandments' for the 2023 European Society of Cardiology guidelines for the management of endocarditis.European Heart Journal 2024 April 18
A Guide to the Use of Vasopressors and Inotropes for Patients in Shock.Journal of Intensive Care Medicine 2024 April 14
Diagnosis and Management of Cardiac Sarcoidosis: A Scientific Statement From the American Heart Association.Circulation 2024 April 19
Essential thrombocythaemia: A contemporary approach with new drugs on the horizon.British Journal of Haematology 2024 April 9
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app
All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.
By using this service, you agree to our terms of use and privacy policy.
Your Privacy Choices
You can now claim free CME credits for this literature searchClaim now
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app