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Small canal diameters have been associated with increased neurologic dysfunction. Some patients with radiographic stenosis may be asymptomatic. A canal diameter of 10 to 13 mm is considered to be relatively stenotic.
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2007. Incidence of Cervical Stenosis, Radiographic and Anatomic
Small canal diameters have been associated with increased neurologic dysfunction. Some patients with radiographic stenosis may be asymptomatic. A canal diameter of 10 to 13 mm is considered to be relatively stenotic.
Small canal diameters have been associated with increased neurologic dysfunction. Some patients with radiographic stenosis may be asymptomatic. A canal diameter of 10 to 13 mm is considered to be relatively stenotic.
Cervical canal size and shape can play a role in the development of myelopathy and/or radiculopathy. Small canal diameters have been associated with increased neurologic dysfunction for a variety of conditions. Various radiographic criteria have been used to better dene sagittal canal dimensions, with variable degrees of accuracy. In addition, some patients with radiographic stenosis may be asymptomatic, thus making the signi- cance of radiographic stenosis less clear. Semin Spine Surg 19:12-17 2007 Elsevier Inc. All rights reserved. KEYWORDS cervical spine anatomy, stenosis, vertebrae T he important role that the size and shape of the cervical spinal canal plays in the development of symptoms of myelopathy or radiculopathy has been recognized for some time. A small sagittal cervical canal diameter has been asso- ciated with increased risk of neurological injury in traumatic, degenerative, and inammatory conditions. Lindgren is credited with rst pointing out the importance of the sagittal diameter of the cervical canal. 1 Two decades later, additional investigators corroborated the association of a small canal in symptomatic cervical spondylosis. 2,3 The average sagittal diameter of the cervical spinal cord ranges from 5 to 11.5 mm (mean 10 mm) as demonstrated on computed tomography (CT) and myelography. 4 The average sagittal diameter of the canal fromC3toC7ranges from15to25 mm(mean, 17 mm). Debate exists regarding the absolute canal diameter that constitutes cervical stenosis. Absolute stenosis has been dened as a cervical sagittal canal diameter of less than 10 mm, as seen on a lateral cervical spine radiograph. A canal di- ameter of 10 to 13 mm is considered to be relatively stenotic. 5 Radiographic Incidence Plain Radiography The sagittal distance, as measured from the middle of the posterior surface of the vertebral body to the closest point on the spinolaminar line, is known as the developmental seg- mental sagittal diameter (DSSD). 6 Early attempts to identify cervical stenosis based on plain radiographs focused on mea- suring the average sagittal diameter of the spinal canal on lateral radiography taken at a standardized distance. Countee and Vijayanathan reported that the normal sagittal diameter of the spinal canal was between 18.3 and 18.5 mm at C3 and 17.8 mm between C4 and C7 using this method. 7 They re- ported that males with a canal diameter less than 14 mm had a higher risk of quadriplegia following cervical trauma. This denition may be somewhat misleading and an underestima- tion, however, since the stenosis was measured at the level of the posterior mid-body, rather than at the superior or inferior aspect of the posterior body, which is the point of maximum stenosis in cervical spondylosis. Edwards and LaRocca described the spondylosis index (SI) as the difference between the DSSD and the spondylotic seg- mental sagittal diameter (SSSD). It represents the amount of canal narrowing due to the spondylotic process 6 (Fig. 1). Based on their ndings, they predicted that patients with canal sizes of less than 10 mm were likely to be myelopathic; those with a 10- to 13-mm canal were premyelopathic; those with a 13- to 17-mmcanal were less prone to myelopathy but prone to symptomatic cervical spondylosis, and those with a canal greater than 17 mm were asymptomatic. Kang and coworkers analyzed factors involved in fractures and dislocations of the cervical spine and their relation to the degree of spinal cord. 8 In reviewing preinjury cervical spine lms, they found that the mean space available for the cord at the level of traumatic injury was 10.5 mm in patients who had a complete injury, 13.1 mmfor those who had an incom- plete injury, 15.9 mm for those with an isolated nerve root *Department of Orthopaedic Surgery, Case Medical Center, Cleveland, Ohio. Department of Orthopaedic Surgery, Rush University Medical Center, Chi- cago, Illinois. Address reprint requests to Ezequiel H. Cassinelli, MD, Department of Or- thopaedic Surgery, Case Medical Center, 11100 Euclid Avenue, Cleve- land, OH 44106. E-mail: zekedr@hotmail.com 12 1040-7383/07/$-see front matter 2007 Elsevier Inc. All rights reserved. doi:10.1053/j.semss.2007.01.003 injury, and 16.7 mmfor those who had no neurologic decit. Their ndings showed a clear correlation between the space available for the cord, the sagittal diameter of the spinal canal, and the severity of spinal cord injury. They concluded that patients who had a large sagittal canal diameter were less likely to have severe spinal cord injury following a fracture or dislocation compared with patients who had a narrow canal. In this respect, a large spinal canal was considered to be protective against future spinal cord injury. In a similar study, Eismont and colleagues investigated the relationship between cervical spine sagittal canal diameter and neurologic injury in cases of cervical spine fracture-dis- location. 9 Their ndings were comparable to those reported by Kang and coworkers 8 in that small diameter canals were correlated signicantly with neurologic injury, while large diameter canals allowed protection fromneurologic injury in cervical fracture-dislocation. PavlovTorg Ratio Pavlov and coworkers introduced a ratio method to identify levels of stenosis. 10 In their ratio method, the sagittal diame- ter of the spinal canal is divided by the sagittal diameter of the corresponding vertebral body (canal diameter/vertebral body diameter) (Fig. 2). They felt that this method was more reli- able and reproducible for determining cervical spinal steno- sis and was independent of technical and magnication vari- ables. Using this method, a ratio less than 0.82 was thought Figure 2 Lateral radiograph depicting the Torg ratio, which is the sagittal diameter of the spinal canal (A) divided by the sagittal di- ameter of the corresponding vertebral body (B). Figure 1 Lateral radiograph depicting the spondylosis index (SI), which is the difference between the developmental segmental sag- ittal diameter (A) and the spondylotic segmental sagittal diameter (B) and represents the amount of narrowing due to the disease process. Incidence of cervical stenosis 13 to indicate absolute stenosis. Torg and colleagues later eval- uated the relationship of developmental narrowing of the cervical canal to reversible and irreversible injury of the cer- vical spinal cord in football players. 11 He found that a ratio of 0.80 or less had a high sensitivity (93%) for transient cervical neurapraxia. However, its low positive-predictive value (0.2%) precluded its use as a screening tool for deter- mining the susceptibility of an athlete to neurapraxia and therefore for future safe participation in contact sports. The reliability of the canal/vertebral body ratio for detect- ing the incidence of cervical stenosis has been studied exten- sively. Lim and Wong evaluated the variation of this ratio with gender and ethnicity. 12 They found that the ratio dif- fered widely not only between different ethnic groups but also between genders within the same ethnic population. The sagittal canal diameter was narrowest at C4 in both males and females, although females had smaller sagittal diameters at all levels than males. Based on these ndings, they concluded that the canal/body ratio was not an accurate indicator of the sagittal canal diameter and therefore could not be used to reliably identify the presence of cervical canal stenosis. Hukuda and Kojima also attempted to evaluate the gender variation in the canal/body ratio method. 13 They found that the canal/body ratio was signicantly larger in women than in men and that this difference may help explain the male prev- alence of cervical myelopathy. Some studies have also shown that the canal/body ratio is smaller in patients with cervical spondylotic myelopathy compared with a nonmyelopathic population. Yue and co- workers showed that the ratio is signicantly smaller in my- elopathic patients (mean, 0.72) compared with a group of control patients (0.95). 14 The authors felt that the ratio method could be used to predict the likelihood of developing cervical spondylotic myelopathy. Emery and coworkers, on the other hand, analyzed the relationship of the canal/body ratio to cervical myelopathy in a study of 108 patients. 15 Neither the canal/body ratio nor the sagittal diameter of the canal at its narrowest point were associated with the severity of preoperative or postoperative myelopathy according to the Nurick grade. The study by Kang and coworkers analyzed the relation between the canal/body ratio and the severity of spinal cord injury. 8 The mean ratio at the uninjured levels was 0.82 for the patients who had a complete injury, 0.84 for those with an incomplete injury, 0.96 for those who had an isolated nerve root injury, and 0.96 for those who had no neurologic decit. These ndings supported the predictive value of the ratio method in determining the possibility and severity of spinal cord injury. As mentioned previously, these ndings were further supported by Eismont and colleagues in their investigation of the relationship between cervical spine sag- ittal canal diameter and neurologic injury in cases of cervical fracture-dislocation. 9 Although numerous studies have both supported and re- futed the validity of using the canal/body ratio in predicting the likelihood of subsequent spinal cord injury, few have quantied the actual incidence of cervical spinal stenosis based on this method. Odor and colleagues studied the inci- dence of cervical spinal stenosis in professional and rookie football players. 16 They found that 32% of professional foot- ball players and 34% of rookies had a canal/body ratio of less than 0.80 at one or more levels from C3 to C6. This nding implied that nearly one-third of this cohort of athletes had cervical spinal stenosis as determined by the ratio method. This nding suggests that other factors and other imaging studies must be considered in the evaluation of a patient with cervical spinal stenosis. Computed Tomography The addition of CT, particularly when combined with my- elography, has several advantages over plain radiography in the evaluation of cervical spinal stenosis. Bone anatomy is visualized extremely well, as is intradural and extradural pa- thology. This is of particular importance in patients with spondylosis, since the neural foramina, lateral recess, and spinal canal are often compressed by osteophytes. CT my- elography helps distinguish soft-tissue neural compression from bony compression, which may strongly inuence sur- gical planning. CT enables measurement of both anteropos- terior (AP) and transverse canal dimensions as well as the space available for the spinal cord at each spinal level. The ability of CT to measure the sagittal dimension of the cervical spinal canal has been evaluated. Blackley and co- workers correlated lateral radiographs and corresponding CT scans of 76 patients sustaining trauma to the cervical spine, whose radiographic examinations were deemed normal. 17 They utilized CT scans to determine the true diameter of the cervical canal at each level and then compared the canal/body ratio with the CT canal diameter. They found that the canal/ body ratio was linearly related to the true diameter of the canal at each vertebral level. However, the correlation coef- cient for the canal/body ratio compared with the true diam- eter was found to be relatively low at each level. Based on these ndings, they felt that the canal/body ratio is of limited value in the assessment of the true diameter of the cervical spinal canal. In their study of 108 patients with cervical spondylotic myelopathy, Emery and coworkers utilized CT myelography in 103 of the patients. 15 The cross-sectional area of the spinal canal at the level of maximum compression was analyzed with respect to preoperative and postoperative Nurick grade of myelopathy to determine if it had any predictive value. They found that the average cross-sectional area of the spinal canal was 34.6 mm 2 . The cross-sectional area of the spinal cord was not found to be associated with the preoperative or postoperative severity of myelopathy. At this time, we are not aware of any studies to determine the exact incidence of cervical stenosis based on CT ndings alone. Signicance of Cervical Spinal Canal Shape While numerous authors have demonstrated the importance of the size of the cervical spinal canal on the development of myelopathy, few have focused on the importance of the shape of the canal and the effect that this may have on neu- rologic compromise. 14 C.L. Dean, M.J. Lee, and E.H. Cassinelli Ogino and coworkers performed a detailed clinicopatho- logic study of nine patients with cervical spondylotic myelop- athy. 18 They found a good correlation between the degree of spinal cord compression and the ratio of the AP (sagittal) canal diameter to the transverse canal diameter. They desig- nated this as the AP compression ratio. Their ndings sug- gested that as the AP compression ratio decreased, the canal assumed a more elliptical shape and the risk of neurologic compression and myelopathy increased. In other words, an elliptical-shaped canal portended a poorer prognosis with regard to the development of cervical spondylotic myelopa- thy than did a round canal. They found that developmental narrowing of the cervical spinal canal was the most signi- cant factor responsible for a decrease in the AP compression ratio, with multilevel spondylotic protrusions being less im- portant. Pathologically, they found that developmental nar- rowing resulted in extensive demyelination of the posterolat- eral funiculus and infarction of the gray matter. Matsuura and colleagues also demonstrated the impor- tance of the shape of the cervical spinal canal in spinal cord injured patients. 19 They measured the cross-sectional area and the sagittal and transverse diameters of the cervical canal in patients who had a traumatic spinal cord injury and com- pared these ndings to 100 control subjects. Interestingly, they observed no difference in the two groups with regard to cross-sectional area of the spinal canal. However, the sagittal diameter of the spinal canal of the control group was found to be signicantly larger than those of the spinal cord injured group. Conversely, the transverse diameter of the spinal ca- nal of the spinal cord injured group was signicantly larger than those of the control group. The difference between their two groups, based on the ratio of sagittal to transverse diam- eter, was highly signicant. Because this measure was a ratio, they concluded that there was no need to evaluate an indi- vidual on the basis of absolute values alone. These ndings suggested that certain patients may be predisposed to spinal Figure 3 Sagittal (A) and axial (B and C) T2-weighted images of a 43-year-old male with a history of mild neck pain which resolved. MRI reveals multilevel stenosis with myelomalacia and abnormal cord signal. The lack of CSF space around the spinal cord is indicative of lack of a functional reserve. The patient exhibited no signs or symptoms of myelopathy despite the degree of stenosis. Incidence of cervical stenosis 15 cord injury following sufcient trauma and that it may not be the total volume of space in the spinal canal that was the critical factor, but rather the shape of the canal. Magnetic Resonance Imaging (MRI) MRI has signicantly impacted the diagnosis and treatment of cervical spondylosis and symptomatic cervical canal ste- nosis. MRI demonstrates the high contrast between cerebro- spinal uid and disk/osteophyte material (Fig. 3). It is also capable of providing multiplanar images and reconstructions in numerous planes. This imaging modality has become the standard to evaluate patients with cervical spinal stenosis. Boden and coworkers prospectively investigated the prev- alence of abnormal MRI scans of the cervical spine in asymp- tomatic subjects. 20 They evaluated the MRI scans of asymp- tomatic volunteers and compared themto scans of a group of symptomatic patients. The scans demonstrated an abnormal- ity in 19% of the asymptomatic subjects, including 14% of those less than 40 years old and 28% of those older than 40. Of those less than 40, 10% had a herniated disc and 4% had foraminal stenosis. Of the subjects who were older than 40, 5% had a herniated disc, 3% had bulging of one or more discs, and 20% had foraminal stenosis. In addition, disc de- generation or disc narrowing at one or more level was present in 25% of subjects less than 40 and in nearly 60% of those older than 40. The authors concluded that the high incidence of abnormal ndings in asymptomatic subjects was part of the normal aging process of spinal degeneration. Teresi and coworkers also studied the incidence of abnormal MRI scans in 100 asymptomatic subjects. 21 They found spinal cord im- pingement by MRI in 16% of patients younger than 64 years and in 26% of patients older than 64 years. These and other studies emphasize the danger of making operative decisions based only on diagnostic imaging tests without correlating such ndings with clinical signs and symptoms (Fig. 3). Prasad and colleagues correlated cervical MRI measure- ments with canal/vertebral body ratios. 22 They found that the correlation between this ratio and the additional space avail- able for the spinal cord, as shown by the cerebrospinal uid (CSF) column surrounding the cord, was only moderate, with the best correlation being at C5. Their study demon- strated a poor correlation between the canal/body ratio and the space available for the cord, and they therefore felt that this ratio alone could not be used to infer conclusions about actual spinal cord compression. Other studies have used alternative methods of dening cervical stenosis based on MRI ndings. Cantu dened cer- vical canal stenosis as the absence of a functional reserve (Fig. 3) around the spinal cord. 23 The absence of such a functional reserve was felt to be a contraindication to further participation in contact sports following an episode of tran- sient neurapraxia. Cantu and Mueller reported a 270% re- duction in permanent spinal cord injury since 1971, from a peak of 20 per year to only 7.2 per year. 24 Although there are several possible explanations for this reduction, increased awareness of preexisting cervical canal stenosis was thought to be a major factor. Anatomic Incidence One method of assessing the cervical spine canal diameter is by direct measurement of cadaveric spinal canal specimens. This provides perhaps the most accurate assessment of bony canal diameter. However, there are several limitations to this method. Because of variation in radiographic magnication, anatomic measurements may not directly reect radio- graphic measurements, which is the most common way to assess canal diameter. Second, the presence and signicance of soft-tissue pathology cannot be accounted for by evaluat- ing only bony cadaveric specimens. Third, measurements of cadaveric specimens offer no information regarding the pres- ence or absence of symptoms. Lee and coworkers reported on the largest series of direct anatomic measurements to determine the incidence of ana- tomic cervical stenosis. 25 They analyzed 469 adult cadaveric cervical spines and correlated these measurements with plain radiographs. Based on these direct measurements, they found that the average AP canal diameter for all specimens at all levels was 14.1 mm. Males had signicantly larger cervical spinal canals than females at all levels. The C4 level was found to be the most frequently stenotic level (10.6%). In this study, stenosis was dened as a sagittal canal diameter of less than 12 mm. Overall, 21.5% of the population had at least one stenotic level. Of the specimens older than 50 years of age, 29.1% had at least one level of stenosis. In specimens greater than 70 years old, 33.3% were found to have at least one level of stenosis. After adjusting for body size and radiographic magnica- tion, they determined that cervical stenosis would have been present in 4.9% of the overall adult population, 6.8% of the population over age 50, and 9.2% of the population over 70 years of age. Allowing for potential errors associated with the correction for both body size and radiographic magnica- tion, the authors stated that the true incidence of cervical stenosis was likely between 4.9 and 21.5% of the general population. Based on these ndings, an increased incidence of cervical stenosis occurs with increasing age. Because of the frequency of cervical spine stenosis, the authors emphasized that treatment decisions should not be based on radiographic studies alone, but must be correlated with clinical signs and symptoms. Summary Various methods have been described to determine the inci- dence of cervical spinal stenosis. Based on MRI studies, up to 19% of asymptomatic individuals may demonstrate radio- graphic abnormalities. 20 This incidence increases with age, suggesting that such changes are part of the normal aging process of spinal degeneration. Similarly, cadaveric studies using direct canal measurements have suggested that cervical stenosis is common, affecting approximately 4.9 to 21.5% of the population. Neither the incidence and prevalence of asymptomatic nor the symptomatic cervical stenosis has been accurately determined. Furthermore, the natural history of asymptomatic stenosis has not been well dened. Future in- 16 C.L. Dean, M.J. Lee, and E.H. Cassinelli vestigations of these conditions will allow us to better under- stand the disease process. References 1. Lindgren E: The importance of the sagittal diameter of the spinal canal in the cervical region. Nevenartz 10:240, 1937 2. Pallis C, Jones AM, Spillane JD: Cervical spondylosis; incidence and implications. Brain 77(2):274-289, 1954 3. Payne EE, Spillane JD: The cervical spine. An anatomic pathologic study of seventy patients. Brain 70:38, 1957 4. Herzog RJ, Weins JJ, Dillingham MF, et al: Normal cervical spine mor- phometry and cervical spine stenosis in asymptomatic professional football players. Spine 16:178-186, 1991 5. Murone I: The importance of the sagittal diameters of the cervical canal in relation to spondylosis and myelopathy. J Bone Joint Surg Br 56:30- 36, 1974 6. Edwards WC, LaRocca H: The developmental segmental sagittal diam- eter of the cervical spinal canal in patients with cervical spondylosis. Spine 8(1):20-27, 1983 7. Countee RW, Vijayanathan T: Congenital stenosis of the cervical spine: diagnosis and management. J Natl Med Assoc 71:257-264, 1979 8. Kang JD, Figgie MP, Bohlman HH: Sagittal measurements of the cervi- cal spine in subaxial fractures and dislocations. An analysis of two hundred and eighty-eight patients with and without neurologic de- cits. J Bone Joint Surg Am 76(11):1617-1628, 1994 9. Eismont FJ, Clifford S, Goldberg M, et al: Cervical sagittal spinal canal size in spine injury. Spine 9(7):663-666, 1984 10. Pavlov H, Torg JS, Robie B, et al: Cervical spinal stenosis: determination with vertebral body ratio method. Radiology 164(3):771-775, 1987 11. Torg JS, Naranja RJ Jr, Pavlov H, et al: The relationship of developmen- tal narrowing of the cervical spinal canal to reversible and irreversible injury of the cervical spinal cord in football players. J Bone Joint Surg Am 78(9):1308-1314, 1996 12. Lim JK, Wong HK: Variation of the cervical spinal Torg ratio with gender and ethnicity. Spine J 4(4):396-401, 2004 13. Hukuda S, Kojima Y: Sex discrepancy in the canal/body ratio of the cervical spine implicating the prevalence of cervical myelopathy in men. Spine 27(3):250-253, 2002 14. Yue WM, Tan SB, Tan MH, et al: The Torg-Pavlov ratio in cervical spondylotic myelopathy. A comparative study between patients with cervical spondylotic myelopathy and a nonspondylotic, nonmyelo- pathic population. Spine 26(16):1760-1764, 2001 15. Emery SE, Bohlman HH, Bolesta MJ, et al: Anterior cervical decompres- sion and arthrodesis for the treatment of cervical spondylotic myelop- athy. Two to seventeen-year follow-up. J Bone Joint Surg Am 80(7): 941-951, 1998 16. Odor JM, Watkins RG, Dillin WH, et al: Incidence of cervical spinal stenosis in professional and rookie football players. Am J Sports Med 18(5):507-509, 1990 17. Blackley HR, Plank LD, Robertson PA: Determining the sagittal dimen- sions of the canal of the cervical spine. The reliability of ratios of anatomical measurements. J Bone Joint Surg Br 81(1):110-112, 1999 18. Ogino H, Tada K, Okada K, et al: Canal diameter, anteroposterior compression ratio, and spondylotic myelopathy of the cervical spine. Spine 8(1):1-15, 1983 19. Matsuura P, Waters RL, Adkins RH, et al: Comparison of computerized tomography parameters of the cervical spine in normal control subjects and spinal cord-injured patients. J Bone Joint Surg Am 71(2):183-188, 1989 20. Boden SD, McCowin PR, Davis DO, et al: Abnormal magnetic reso- nance scans of the cervical spine in asymptomatic subjects. A prospec- tive investigation. J Bone Joint Surg Am 72(8):1178-1184, 1990 21. Teresi LM, Lufkin RB, Reicher MA, et al: Asymptomatic degenerative disk disease and spondylosis of the cervical spine. Radiology 164(1): 83-88, 1987 22. Prasad SS, OMalley M, Caplan M, et al: MRI measurements of the cervical spine and their correlation to Pavlovs ratio. Spine 28(12): 1263-1268, 2003 23. Cantu RC: Functional cervical spinal stenosis: a contraindication to participation in contact sports. Med Sci Sports Exerc 25(3):316-317, 1993 24. Cantu RC, Mueller FO: Catastrophic spine injuries in American foot- ball, 1977-2001. Neurosurgery 53(2):362-363, 2003 25. Lee MJ, Cassinelli EH, Riew KD: The prevalence of cervical spine ste- nosis: an anatomic study of 469 cadaveric specimens. J Bone Joint Surg Am 2006 (in press) Incidence of cervical stenosis 17
Final - Spinal Stenosis L4, L5 Secondary To Spondylolisthesis L4, L5 Grade II With Hypertrophized Ligament Um and Radiculopathy With Myelopathy Right Sided