Literature DB >> 11884906

Neural space integrity of the lower cervical spine: effect of normal range of motion.

David J Nuckley1, Mark A Konodi, Geoffrey C Raynak, Randal P Ching, Sohail K Mirza.   

Abstract

STUDY
DESIGN: An experimental investigation of intervertebral foramen and spinal canal neural space integrity was performed throughout physiologic range of motion of the lower cervical spine in intact human cadaver specimens.
OBJECTIVE: To investigate cervical positions that might place the neural tissues of the spine in heightened risk of injury. To meet this objective the following hypotheses were tested: 1) spinal canal integrity varies with specific normal range of motion positions of the lower cervical spine, and 2) intervertebral foramen integrity is dependent on and unique for different physiologic positions of the lower cervical spine. SUMMARY OF BACKGROUND DATA: Cervical spine injuries are frequently associated with compressive damage to neurologic tissues and consequently poor clinical outcomes. Neurologic injury typically occurs from disc, ligamentous, or bony occlusion of the spinal canal and intervertebral foraminal spaces dynamically during an injury event or with abnormal alignment and position after the injury event. Prior studies have shown pressure and geometric changes in cervical spine neural spaces in certain cervical spine positions. However, to the authors' knowledge, this is the first research effort aimed at elucidating the integrity of the cervical spine neural spaces throughout the normal physiologic range of motion.
METHODS: The authors instrumented 17 fresh-frozen unembalmed cadaveric human cervical spines (C3-C7) with specially designed intervertebral foramen occlusion transducers and a spinal canal occlusion transducer. The specimens were loaded with pure bending moments to produce simulated physiologic motions of the lower cervical spine. The resulting occlusion profiles for the intervertebral foramen and spinal canal were recorded along with the 6-degree of freedom position of the cervical spine. Because these occlusion measurements describe the ability of the spine to preserve the space for the neural structures, the authors define this neuroprotective role of the vertebral column as neural space integrity.
RESULTS: The range of motion developed experimentally in this study compared well with published reports of normal cervical motion. Thus, subsequent changes in neural space integrity may be regarded as resulting from normal human cervical spine motion. No significant change in the spinal canal space was detected for any physiologic motion; however, intervertebral foramen integrity was significantly altered in extension, ipsilateral bending, combined ipsilateral bending and extension, and combined contralateral bending with extension when compared with intact upright neutral position.
CONCLUSIONS: This study defines the range of neural space integrity associated with simulated physiologic motion of the lower cervical spine in an experimental setting. This information may be useful in comparing neural space changes in pathologic conditions and may enhance refinement of neurologic injury prevention strategies.

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Mesh:

Year:  2002        PMID: 11884906     DOI: 10.1097/00007632-200203150-00006

Source DB:  PubMed          Journal:  Spine (Phila Pa 1976)        ISSN: 0362-2436            Impact factor:   3.468


  13 in total

1.  Cervical neural space narrowing during simulated rear crashes with anti-whiplash systems.

Authors:  Paul C Ivancic
Journal:  Eur Spine J       Date:  2012-01-24       Impact factor: 3.134

2.  Spinal canal narrowing during simulated frontal impact.

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3.  Measurement of volume-occupying rate of cervical spinal canal and its role in cervical spondylotic myelopathy.

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4.  Dimensional changes of the neuroforamina in subaxial cervical spine during in vivo dynamic flexion-extension.

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Review 5.  The role of tissue damage in whiplash-associated disorders: discussion paper 1.

Authors:  Michele Curatolo; Nikolai Bogduk; Paul C Ivancic; Samuel A McLean; Gunter P Siegmund; Beth A Winkelstein
Journal:  Spine (Phila Pa 1976)       Date:  2011-12-01       Impact factor: 3.468

6.  Dorsal root compression produces myelinated axonal degeneration near the biomechanical thresholds for mechanical behavioral hypersensitivity.

Authors:  Raymond D Hubbard; Beth A Winkelstein
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7.  Transient cervical nerve root compression modulates pain: load thresholds for allodynia and sustained changes in spinal neuropeptide expression.

Authors:  Raymond D Hubbard; Zhen Chen; Beth A Winkelstein
Journal:  J Biomech       Date:  2007-10-31       Impact factor: 2.712

8.  Controlled release of GDNF reduces nerve root-mediated behavioral hypersensitivity.

Authors:  Raymond D Hubbard; Joan J Martínez; Jason A Burdick; Beth A Winkelstein
Journal:  J Orthop Res       Date:  2009-01       Impact factor: 3.494

9.  Dimensions of the cervical neural foramen in conditions of spinal deformity: an ex vivo biomechanical investigation using specimen-specific CT imaging.

Authors:  Zachary A Smith; Saeed Khayatzadeh; Joshua Bakhsheshian; Michael Harvey; Robert M Havey; Leonard I Voronov; Muturi G Muriuki; Avinash G Patwardhan
Journal:  Eur Spine J       Date:  2016-02-01       Impact factor: 3.134

10.  Cervical radiculopathy: study protocol of a randomised clinical trial evaluating the effect of mobilisations and exercises targeting the opening of intervertebral foramen [NCT01500044].

Authors:  Pierre Langevin; Jean-Sébastien Roy; François Desmeules
Journal:  BMC Musculoskelet Disord       Date:  2012-01-31       Impact factor: 2.362

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