Evidence map›Paper›PMID 38955515›Full record

ArticleNeurospine2024

Pharmacological Treatment of Degenerative Cervical Myelopathy: A Critical Review of Current Evidence.

Jordan J Levett, Miltiadis Georgiopoulos, Simon Martel, Wissam Al Mugheiry, Nikolaos A Stavropoulos, Miguel Vega-Arroyo, Carlo Santaguida, Michael H Weber, Jeff D Golan, Peter Jarzem and 3 more

Abstract read
In one paragraph

Article in Neurospine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Revisiting Secondary Dilative Cardiomyopathy.International journal of molecular sciences · 2025
    Pooled it
  2. Article
  3. Article
  4. Conservative and newer drug treatment for degenerative cervical myelopathy.Journal of clinical orthopaedics and trauma · 2025
    Article
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Jordan J LevettFaculty of Medicine, University of Montreal, Montreal, QC, Canada.
Miltiadis GeorgiopoulosDepartment of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada.
Simon MartelDivision of Orthopaedic Surgery, McGill University, Montreal, QC, Canada.
Wissam Al MugheiryDepartment of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada.
Nikolaos A StavropoulosFirst Department of Orthopaedic Surgery NKUA, "ATTIKON" University General Hospital, Athens, Greece.
Miguel Vega-ArroyoWinnipeg Spine Program, University of Manitoba, Winnipeg, MB, Canada.
Carlo SantaguidaDepartment of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada.
Michael H WeberDivision of Orthopaedic Surgery, McGill University, Montreal, QC, Canada.
Jeff D GolanDepartment of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada.
Peter JarzemDivision of Orthopaedic Surgery, McGill University, Montreal, QC, Canada.
Jean A OuelletDivision of Orthopaedic Surgery, McGill University, Montreal, QC, Canada.
Georgios KlironomosDepartment of Neurosurgery, Zucker School of Medicine at Hofstra/Northwell, Bay Shore, NY, USA.
Andreas K DemetriadesEdinburgh Spinal Surgery Outcomes Study Group, Department of Neurosurgery, Royal Infirmary, Edinburgh, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Degenerative cervical myelopathy (DCM) is the leading cause of spinal cord dysfunction in adults, representing substantial morbidity and significant financial and resource burdens. Typically, patients with progressive DCM will eventually receive surgical treatment. Nonetheless, despite advancements in pharmacotherapeutics, evidence for pharmacological therapy remains limited. Health professionals from various fields would find interest in pharmacological agents that could benefit patients with mild DCM or enhance surgical outcomes. This review aims to consolidate all clinical and experimental evidence on the pharmacological treatment of DCM. We conducted a comprehensive narrative review that presents all pharmacological agents that have been investigated for DCM treatment in both humans and animal models. Riluzole exhibits effectiveness solely in rat models, but not in treating mild DCM in humans. Cerebrolysin emerges as a potential neuroprotective agent for myelopathy in animals but had contradictory results in clinical trials. Limaprost alfadex demonstrates motor function improvement in animal models and exhibits promising outcomes in a small clinical trial. Glucocorticoids not only fail to provide clinical benefits but may also lead to adverse events. Cilostazol, anti-Fas ligand antibody, and Jingshu Keli display promise in animal studies, while erythropoietin, granulocyte colony-stimulating factor and limaprost alfadex exhibit potential in both animal and human research. Existing evidence mainly rests on weak clinical data and animal experimentation. Current pharmacological efforts target ion channels, stem cell differentiation, inflammatory, vascular, and apoptotic pathways. The inherent nature and pathogenesis of DCM offer substantial prospects for developing neurodegenerative or neuroprotective therapies capable of altering disease progression, potentially delaying surgical intervention, and optimizing outcomes for those undergoing surgical decompression.

Indexed as

Cervical cordErythropoietinGlucocorticoidsIntervertebral disc degenerationlimaprost-alfadexRiluzole

Identifiers

PMID38955515
PMCPMC11224758

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.