| Literature DB >> 31607072 |
Jutty Parthiban1, Oscar L Alves2, Komal Prasad Chandrachari3, Premanand Ramani4, Mehmet Zileli5.
Abstract
Cervical spondylotic myelopathy (CSM) is a common cause of adult spinal cord dysfunction. Although the therapeutic options for moderate to severe CSM patients have been established well, the existing guidelines for therapeutic decisions in mild cases of CSM are unclear. We present a review of literature on conservative treatment and surgery for CSM and suggest general recommendations applicable in various clinical presentations and in different geographic locations across the globe, with due considerations to available resources and locally prevalent practices.Entities:
Keywords: Cervical spondylotic myelopathy; Degenerative cervical myelopathy; Recommendations; Surgical management
Year: 2019 PMID: 31607072 PMCID: PMC6790727 DOI: 10.14245/ns.1938238.119
Source DB: PubMed Journal: Neurospine ISSN: 2586-6591
Comparison of AOSpine North America and CSRS guidelines and WFNS Spine Committee Recommendations
| Grade | AOSpine North America and CSRS guidelines (2017) | WFNS Spine Committee Recommendations (2019) |
|---|---|---|
| Moderate to severe CSM (mJOA score < 15) | Recommend surgical intervention | Surgical intervention is recommended. |
| Mild CSM (mJOA score 15–17) | Suggest offering surgical intervention or a supervised trial of structured rehabilitation for patients with mild DCM. | Suggest offering surgical intervention or rehabilitation for patients with mild CSM. |
| If initial nonoperative management is pursued, we recommend operative intervention if there is neurological deterioration and suggest operative intervention if the patient fails to improve. | If at the beginning nonoperative management was followed, we recommend operative intervention when rapid progression of symptoms appear. | |
| Nonoperative management may be considered for slowly progressive disease. | ||
| Nonmyelopathic patients with evidence of cervical cord compression without signs or symptoms of radiculopathy | Suggest not offering prophylactic surgery. | Should not be offered a prophylactic surgery. |
| Suggest that these patients be counselled as to potential risks of progression, educated about relevant signs and symptoms of myelopathy, and be followed clinically. | These patients should be counselled about the potential risk of worsening, educated about the signs and symptoms of progression and followed up regularly. | |
| An informed consent should be obtained about neurological deficits that may follow trivial injury. | ||
| Nonmyelopathic patients with cord compression and clinical evidence of radiculopathy with or without electrophysiological confirmation | Patients are at a higher risk of developing myelopathy and should be counselled about this risk. | Patients are potential candidates who may deteriorate thus carrying high risk and hence need to be counselled about it. These patients are recommended to undergo surgery or close observation with rehabilitation if the patient refuses to undergo surgery. |
| Suggest offering either surgical intervention or nonoperative treatment consisting of close serial follow-up or a supervised trial of structured rehabilitation. | ||
| In the event of myelopathic development, the patient should be managed according to the recommendations above. | In the event of developing myelopathic signs they are advised to go for surgery at the earliest. | |
| An informed consent should be obtained about neurological deficits that may follow trivial injury. | ||
CSRS, Cervical Spine Research Society; WFNS, World Federation of Neurosurgical Societies; DCM, degenerative cervical myelopathy; CSM, cervical spondylotic myelopathy; mJOA, modified Japanese Orthopaedic Association.