Abstract

Degenerative cervical myelopathy (DCM) is a prevalent condition in which spinal degeneration causes cord compression and neurological dysfunction. The spinal cord is anatomically complex and operates in conjunction with the brain, the musculoskeletal system, and numerous organs to control numerous functions, including simple and coordinated movement, sensation, and autonomic functions. As a result, accurate and comprehensive measurement of spinal cord function in patients with DCM and other spinal pathologies is challenging. This project aimed to summarize the neurological, functional, and quality of life (QoL) outcome measures currently in use to quantify impairment in DCM. A systematic review of the literature was performed to identify prospective studies with at least 100 DCM subjects that utilized one or more quantitative neurological, functional, or QoL outcome measures. A total of 148 studies were identified. The most commonly used instruments were subjective functional scales including the Japanese Orthopedic Association (JOA) (71 studies), modified JOA (mJOA) (66 studies), Neck Disability Index (NDI) (54 studies), and Nurick (39 studies), in addition to the QoL measure Short-Form-36 (SF-36, 52 studies). A total of 92% (320/349) of all outcome measures were questionnaires, whereas objective physical testing of neurological function (strength, gait, balance, dexterity, or sensation) made up 8% (29/349). Studies utilized an average of 2.36 outcomes measures, while 58 studies (39%) utilized only a single outcome measure. No studies were identified that specifically assessed the dorsal column sensory pathway or respiratory, bowel, or sexual function. In the past five years, there were no significant differences in the number of total, functional, or QoL outcome measures used, but physical testing of neurological function has increased (p = 0.005). Prior to 2017, cervical spondylotic myelopathy (CSM) was the most frequently used term to describe the study population, whereas in the last five years, DCM has become the preferred terminology. In conclusion, clinical studies of DCM typically utilize limited data to characterize impairment, often relying on subjective, simplistic, and non-specific measures that do not reflect the complexity of the spinal cord. Although accurate measurement of impairment in DCM is challenging, it is necessary for early diagnosis, monitoring for deterioration, and quantifying recovery after therapeutic interventions. Clinical decision-making and future clinical studies in DCM should employ a combination of subjective and objective assessments to capture the multitude of spinal cord functions to improve clinical management and inform practice guidelines.

Highlights

  • The most common cause of spinal cord dysfunction is age-related degeneration of the discs, ligaments, and vertebrae of the cervical spine causing spinal cord compression and neurological impairment, collectively known as degenerative cervical myelopathy (DCM) [1]

  • This study provides a comprehensive review of how spinal cord function is quantified in large prospective studies of degenerative cervical myelopathy and assesses the recent trends in chosen outcome measures

  • Versions of the modified JOA (mJOA) and Japanese Orthopedic Association (JOA) scores were used in a total of 91% (135/148) of studies, suggesting that the DCM research community has reached a consensus on the use of these measures as the primary outcomes of interest

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Summary

Introduction

The most common cause of spinal cord dysfunction is age-related degeneration of the discs, ligaments, and vertebrae of the cervical spine causing spinal cord compression and neurological impairment, collectively known as degenerative cervical myelopathy (DCM) [1]. The use of the mJOA has subsequently increased, including several clinical trials and as the basis of the categorization of DCM into mild (mJOA ≥ 15), moderate (mJOA 12–14), and severe (mJOA < 12) [3]. The reliance on these outcome measures has increased to the point that clinical practice guidelines (CPGs) published by AOSpine are based on the mJOA alone, recommending surgery for moderate-severe cases and mild cases that show progressive deterioration [4]. Reliance on the mJOA is problematic in several ways, as scores can be affected by other medical conditions, interobserver reliability is limited [5,6], and it remains unclear how to best assess patients for neurological deterioration, comprehensive clinical assessments and quantitative microstructural MRI have been proposed [7,8]

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