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Cervical Spondylotic Myelopathy (CMS) | Diagnosis & Treatment

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Cervical Spondylotic Myelopathy (CMS) | Diagnosis & Treatment

Introduction & Epidemiology

Cervical spondylotic myelopathy site image

Cervical spondylotic myelopathy (CSM) is a neurological condition that is the leading cause of spinal cord injury in adults. In simple terms, it involves the compression or damage of the spinal cord in the neck, primarily due to the natural aging process that affects the cervical vertebrae. The term ‘myelopathy’ stems from the Greek words ‘myelon,’ which means ‘spinal cord’ and ‘pathos,’ signifying ‘disease’.

Epidemiological studies have provided valuable insights into CSM. Northover et al. (2012) conducted an observational study involving 41 patients, and their findings revealed a male-to-female ratio of 2.7:1, with the average age at diagnosis being 63.8 years. It was observed that CSM typically affects multiple segments of the cervical spine, with the C5/C6 level being the most commonly affected.

Additionally, Aizawa et al. (2016) conducted a study on spinal surgeries performed between 1998 and 2012. They found that 19.8% of these surgeries were related to cervical myelopathy, highlighting the prevalence of this condition in the broader context of spinal health. Other spinal issues, such as lumbar spinal canal stenosis (35.9%) and lumbar disc herniation (27.7%), also featured prominently in their research.

CSM is a complex medical condition with a multifactorial pathophysiology that includes structural changes in the cervical spine. Several key factors contribute to its development and progression:

Risk Factors:

  1. Trauma: Traumatic events, such as accidents or injuries, can accelerate the degeneration of cervical spinal discs and increase the risk of CSM.
  2. Axial Weight Bearing on Neck/Head: Activities that involve bearing excessive axial weight on the neck or head can lead to increased mechanical stress on the cervical spine, exacerbating disc degeneration and other structural changes.
  3. Genetic Predisposition of Vertebrae: Some individuals may have a genetic disposition that makes their cervical vertebrae more susceptible to degenerative changes, which can contribute to CSM.
  4. Smoking: Smoking is known to have detrimental effects on vascular health and tissue oxygenation, which may exacerbate the progression of CSM and its associated symptoms.

 

Pathophysiology

  1. Disc Degeneration (Bulging Disc): CSM often begins with the degeneration of intervertebral discs in the cervical spine, causing them to bulge or protrude into the spinal canal.
  2. Subperiosteal Bone Formation (Ventral to Spinal Canal): In response to increased mechanical stress, the body forms new bone tissue on the front (ventral) side of the spinal canal, potentially narrowing the space for the spinal cord.
  3. Ossification of Posterior Longitudinal Ligament: The posterior longitudinal ligament may undergo ossification, hardening, and calcifying, contributing to spinal canal narrowing.
  4. Hypertrophy of Ligamentum Flavum: Hypertrophy of the Ligamentum Flavum causes it to thicken and become less flexible, further encroaching on the space within the spinal canal and compressing the spinal cord.

These structural changes collectively lead to the compression and narrowing of the spinal canal, resulting in the hallmark symptoms and complications associated with CSM. Recognizing these risk factors and understanding the pathophysiological mechanisms involved is essential for both prevention and management. Early diagnosis and appropriate interventions are crucial to mitigate the effects of these structural alterations on the spinal cord.

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Clinical Presentation & Examination

Cervical Spondylotic Myelopathy (CSM) is characterized by a variety of clinical signs and symptoms, although there are no specific features that exclusively define the condition. Patients with CSM may experience the following:

1. Abnormalities in Gait: Patients often exhibit changes in their walking pattern, which can include an unsteady gait, stumbling, and difficulty maintaining balance.

2. Stiffness in the Cervical Spine: CSM can lead to stiffness and reduced range of motion in the neck, making it challenging for individuals to move their heads comfortably.

3. Sharp Pain in the Arms: Patients may report sharp, shooting pain and discomfort in their arms. These symptoms are often associated with nerve compression in the cervical spine.

4. Motor Dysfunction: Motor problems are common and can manifest as muscle weakness, coordination difficulties, and a decrease in fine motor skills, such as manipulating objects.

5. Changes in Sensation: Sensory alterations are common and may involve tingling, numbness, or a “pins and needles” sensation in the arms and hands.

6. Loss of Strength: Patients may experience a loss of strength in the upper limbs, leading to difficulty with everyday tasks and activities.

7. Reduced Proprioception: Proprioception, which is the sense of body position and movement, may be impaired, making it challenging for individuals to coordinate their movements.

8. Toileting Issues: Some patients may experience difficulties with bladder or bowel control due to the involvement of the spinal cord.

9. L’Hermitte’s Sign: This is a distinctive symptom characterized by an electric shock-like sensation that radiates down the spine and into the limbs when the neck is flexed. It is a classic indicator of cervical cord involvement in CSM.

These diverse signs and symptoms can vary in severity from person to person, making the clinical presentation of CSM unique for each patient. Recognizing these manifestations is crucial for diagnosis and early intervention to prevent further spinal cord damage and improve the patient’s quality of life.

 

Examination

If CSM is suspected, the therapist can use the following test cluster (Cook et al. 2010) in order to help his decision-making:

Cook et al. (2010) produced a cluster of predictive clinical test findings for a sample of patients using a clinical diagnosis as the reference standard for the condition. The goal of the cluster is to detect the disease in early stages to rule out the condition during screening.

The five tests or patient characteristics included in the rule are the following:

  1. Gate deviation which shows as abnormally wide-based gait, ataxia, or spastic gate.
  2. A positive Hoffman’s test or Hoffman’s sign which is characterized by a reflex contraction of the thumb and index finger when flipping the distal part of the middle finger.
  3. Inverted supinator sign which is elicited by quick tapping near the styloid process of the radius which is the attachment of the brachioradialis tendon and it shows in finger flexion or slight elbow extension.
  4. Positive Babinski sign which shows as an extension of the big toe and fanning of the other four toes when stroking the lateral aspect of the foot sole from the heel forward towards the great toe.
  5. Age greater than 45 years.

So if 3+/5  of the five aforementioned characteristics are positive the positive likelihood ratio for a  cervical spondylosis myelopathy is at 30.9. If only one is positive though the negative likely ratio is at 0.18

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Treatment

Once a diagnosis of Cervical Spondylotic Myelopathy (CSM) is confirmed, the primary decision to be addressed is whether to pursue operative or nonoperative management. CSM is typically regarded as a surgical condition, as studies have shown that nonoperative treatments result in significant impairments in daily life activities over time. Specifically, at the end of one year, nonoperative treatment leads to a 6% rate of impairment, which increases to 21% at two years, 28% at three years, and a substantial 56% at the ten-year mark. (Fehlings et al. 2017)

To date, there is a lack of high-level studies directly comparing the outcomes of operative versus nonoperative management in cases of Cervical Spondylotic Myelopathy (CSM). Nonetheless, significant insights have been gained from various research efforts. Sampath et al. (2000) conducted a prospective, multicenter, nonrandomized trial aimed at comparing surgical and nonoperative treatments for CSM. Their findings indicated that surgical patients tend to experience better outcomes, encompassing functional status, overall pain, and relief from neurologic symptoms, despite a higher burden of disease before the operation.

In 2013, Rhee et al. published a systematic review on CSM management, recommending against nonoperative treatment as the primary approach for patients with moderate-to-severe myelopathy. They suggested that individuals with mild myelopathy might initially opt for nonoperative management but should be closely monitored for any signs of deterioration.

In 2017, AOSpine North America and the Cervical Spine Research Society (CSRS) jointly released guidelines for CSM management based on its severity. For patients with mild CSM, the options of surgical intervention or a supervised trial of structured rehabilitation should be presented. If nonoperative management does not yield improvement or the patient’s condition worsens, surgical intervention is recommended. In cases of moderate-to-severe CSM, the guidelines strongly advocate for surgical intervention. Patients with cervical cord compression but lacking clear signs of myelopathy or root compression should receive counseling on the risks of disease progression, education about symptoms to watch for, and regular clinical follow-up.

Finally, for patients exhibiting cervical cord compression along with evidence of radiculopathy, the authors propose considering either surgical treatment or structured rehabilitation with close follow-up. The 2017 practice guidelines for CSM management, stratified by severity, are summarized in the table below:

Csm table
McCormick et al. (2020)

 

Do you want to learn more about the cervical area and cervical radiculopathy in particular? Then check out our blog articles and research reviews:

 

References

Aizawa, T., Hashimoto, K., Kanno, H., Handa, K., Takahashi, K., Onoki, T., … & Ozawa, H. (2022). Retrospective comparison of the surgical results for patients with thoracic myelopathy caused by ossification of the posterior longitudinal ligament: Posterior decompression with instrumented spinal fusion versus modified anterior decompression through a posterior approach. Journal of Orthopaedic Science, 27(2), 323-329.

Cook, C., Brown, C., Isaacs, R., Roman, M., Davis, S., & Richardson, W. (2010). Clustered clinical findings for diagnosis of cervical spine myelopathy. Journal of Manual & Manipulative Therapy18(4), 175-180.

Fehlings, M. G., Tetreault, L. A., Riew, K. D., Middleton, J. W., & Wang, J. C. (2017). A clinical practice guideline for the management of degenerative cervical myelopathy: introduction, rationale, and scope. Global Spine Journal, 7(3_suppl), 21S-27S.

Fehlings, M. G., Tetreault, L. A., Riew, K. D., Middleton, J. W., Aarabi, B., Arnold, P. M., … & Wang, J. C. (2017). A clinical practice guideline for the management of patients with degenerative cervical myelopathy: recommendations for patients with mild, moderate, and severe disease and nonmyelopathic patients with evidence of cord compression. Global spine journal, 7(3_suppl), 70S-83S.

McCormick, J. R., Sama, A. J., Schiller, N. C., Butler, A. J., & Donnally, C. J. (2020). Cervical spondylotic myelopathy: a guide to diagnosis and management. The Journal of the American Board of Family Medicine33(2), 303-313.

Rhee, J. M., Shamji, M. F., Erwin, W. M., Bransford, R. J., Yoon, S. T., Smith, J. S., … & Kalsi-Ryan, S. (2013). Nonoperative management of cervical myelopathy: a systematic review. Spine, 38(22S), S55-S67.

Sampath, P., Bendebba, M., Davis, J. D., & Ducker, T. B. (2000). Outcome of patients treated for cervical myelopathy: a prospective, multicenter study with independent clinical review. Spine, 25(6), 670-676.

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