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PubMed Original Article Evidence Unclassified

Current Management of Cervical Spondylotic Myelopathy.

Clinical spine surgery | 2022 | Donnally CJ 3rd, Patel PD, Canseco JA, Vaccaro AR

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PubMed
Type
Original Article
Evidence
Unclassified

Abstract

[Indexed for MEDLINE] Conflict of interest statement: Dr Vaccaro has consulted or has done independent contracting for DePuy, Medtronic, Stryker Spine, Globus, Stout Medical, Gerson Lehrman Group, Guidepoint Global, Medacorp, Innovative Surgical Design, Orthobullets, Ellipse, and Vertex. He has also served on the scientific advisory board/board of directors/committees for Flagship Surgical, AO Spine, Innovative Surgical Design, and Association of Collaborative Spine Research. Dr Vaccaro has received royalty payments from Medtronic, Stryker Spine, Globus, Aesculap, Thieme, Jaypee, Elsevier, and Taylor Francis/Hodder and Stoughton. He has stock/stock option ownership interests in Replication Medica, Globus, Paradigm Spine, Stout Medical, Progressive Spinal Technologies, Advanced Spinal Intellectual Properties, Spine Medica, Computational Biodynamics, Spinology, In Vivo, Flagship Surgical, Cytonics, Bonovo Orthopaedics, Electrocore, Gamma Spine, Location Based Intelligence, FlowPharma, R.S.I., Rothman Institute and Related Properties, Innovative Surgical Design, and Avaz Surgical. In addition, Dr Vaccaro has also provided expert testimony. He has also served as deputy editor/editor of Clinical Spine Surgery. The remaining authors declare no conflict of interest. 5. Acta Neurochir (Wien). 2023 May;165(5):1105-1119. doi: 10.1007/s00701-023-05558-x. Epub 2023 Apr 1. Degenerative cervical myelopathy: Where have we been? Where are we now? Where are we going? Hejrati N(#)(1)(2), Pedro K(#)(2), Alvi MA(3), Quddusi A(3), Fehlings MG(4)(5)(6). Author information: (1)Division of Genetics and Development, Krembil Research Institute, Toronto Western Hospital, University Health Network, 399 Bathurst Street, Suite 4WW-449, Toronto, ON, M5T 2S8, Canada. (2)Division of Neurosurgery and Spine Program, Department of Surgery, University of Toronto, Toronto, ON, Canada. (3)Institute of Medical Science, University of Toronto, Toronto, ON, Canada. (4)Division of Genetics and Development, Krembil Research Institute, Toronto Western Hospital, University Health Network, 399 Bathurst Street, Suite 4WW-449, Toronto, ON, M5T 2S8, Canada. Michael.Fehlings@uhn.ca. (5)Division of Neurosurgery and Spine Program, Department of Surgery, University of Toronto, Toronto, ON, Canada. Michael.Fehlings@uhn.ca. (6)Institute of Medical Science, University of Toronto, Toronto, ON, Canada. Michael.Fehlings@uhn.ca. (#)Contributed equally Degenerative cervical myelopathy (DCM), a recently coined term, encompasses a group of age-related and genetically associated pathologies that affect the cervical spine, including cervical spondylotic myelopathy and ossification of the posterior longitudinal ligament (OPLL). Given the significant contribution of DCM to global disease and disability, there are worldwide efforts to promote research and innovation in this area. An AO Spine effort termed 'RECODE-DCM' was initiated to create an international multistakeholder consensus group, involving patients, caregivers, physicians and researchers, to focus on launching actionable discourse on DCM. In order to improve the management, treatment and results for DCM, the RECODE-DCM consensus group recently identified ten priority areas for translational research. The current article summarizes recent advancements in the field of DCM. We first discuss the comprehensive definition recently refined by the RECODE-DCM group, including steps taken to arrive at this definition and the supporting rationale. We then provide an overview of the recent advancements in our understanding of the pathophysiology of DCM and modalities to clinically assess and diagnose DCM. A focus will be set on advanced imaging techniques that may offer the opportunity to improve characterization and diagnosis of DCM. A summary of treatment modalities, including surgical and nonoperative options, is then provided along with future neuroprotective and neuroregenerative strategies. This review concludes with final remarks pertaining to the genetics involved in DCM and the opportunity to leverage this knowledge toward a personalized medicine approach. © 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature. DOI: 10.1007/s00701-023-05558-x

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