Presymptomatic spondylotic cervical cord compression
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
15480138
DOI
10.1097/01.brs.0000142434.02579.84
PII: 00007632-200410150-00012
Knihovny.cz E-resources
- MeSH
- Anterior Horn Cells physiology MeSH
- Early Diagnosis MeSH
- Adult MeSH
- Electromyography MeSH
- Cohort Studies MeSH
- Spinal Cord Compression diagnostic imaging etiology physiopathology MeSH
- Cervical Vertebrae * MeSH
- Middle Aged MeSH
- Humans MeSH
- Magnetic Resonance Imaging MeSH
- Evoked Potentials, Motor MeSH
- Follow-Up Studies MeSH
- Spinal Osteophytosis complications diagnostic imaging physiopathology MeSH
- Disease Progression MeSH
- Prospective Studies MeSH
- Radiography MeSH
- Aged MeSH
- Evoked Potentials, Somatosensory MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
STUDY DESIGN: We conducted a cohort study of clinically asymptomatic spondylotic cervical cord compression cases with the primary end point of the development of clinical signs of cervical myelopathy. OBJECTIVES: To investigate whether various demographic, clinical, radiologic, and electrophysiological parameters could predict progression from clinically asymptomatic (preclinical) spondylotic cervical cord compression to symptomatic myelopathy. SUMMARY OF BACKGROUND DATA: The data available on the prediction of the outcome in surgical and conservative treatment of spondylotic cervical myelopathy are controversial. Little is known about the clinical natural history of asymptomatic magnetic resonance image-detected spondylotic cervical cord compression and/or changes of signal intensity. METHODS: A group of 66 patients (32 women, 34 men, median age 50 years) with magnetic resonance signs of spondylotic cervical cord compression but without clear clinical signs of myelopathy was followed prospectively for at least 2 years (range, 2-8 years; median, 4 years). Various demographic, clinical, imaging, and electrophysiological parameters were correlated with clinical outcome. RESULTS: Clinical signs of myelopathy during the follow-up period were detected in 13 patients (19.7%). The only variables significantly associated with the development of clinically symptomatic spondylotic cervical myelopathy (SCM) were the presence of symptomatic cervical radiculopathy, electromyographic signs of anterior horn lesion, and abnormal somatosensory-evoked potentials. A multivariate logistic regression model based on these variables correctly classified 90% of cases into 2 subgroups: a group with development of symptomatic SCM and that without clinical manifestation of subclinical cervical cord compression. CONCLUSIONS: Electrophysiological abnormalities together with clinical signs of cervical radiculopathy could predict clinical manifestation of preclinical spondylotic cervical cord compression.
References provided by Crossref.org
Quantitative MR Markers in Non-Myelopathic Spinal Cord Compression: A Narrative Review
Predictors of symptomatic myelopathy in degenerative cervical spinal cord compression
Presymptomatic spondylotic cervical myelopathy: an updated predictive model