Evidence map›Paper›PMID 42668450›Full record

ArticleEClinicalMedicine2026

Identification, validation, and prediction of longitudinal recovery phenotypes in degenerative cervical myelopathy: analysis of prospective cohorts and a randomised controlled trial.

Karlo M Pedro, Mohammed Ali Alvi, Christopher Lozano, Vishwathsen Karthikeyan, Alex B Bak, Benjamin M Davies, James S Harrop, Jetan H Badhiwala, Jefferson R Wilson, Wendy Lou and 3 more

Abstract read
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Article in EClinicalMedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Karlo M PedroDivision of Neurosurgery and Spine Program, Department of Surgery, University of Toronto, Toronto, ON, Canada.
Mohammed Ali AlviDivision of Neurosurgery and Spine Program, Department of Surgery, University of Toronto, Toronto, ON, Canada.
Christopher LozanoDivision of Neurosurgery and Spine Program, Department of Surgery, University of Toronto, Toronto, ON, Canada.
Vishwathsen KarthikeyanDivision of Neurosurgery and Spine Program, Department of Surgery, University of Toronto, Toronto, ON, Canada.
Alex B BakDepartment of Anesthesiology and Pain Medicine, University of Toronto, Toronto, ON, Canada.
Benjamin M DaviesDepartment of Neurosurgery, University of Cambridge, Cambridge, UK.
James S HarropDepartment of Neurological Surgery, Thomas Jefferson University, Philadelphia, PA, USA.
Jetan H BadhiwalaDivision of Neurosurgery and Spine Program, Department of Surgery, University of Toronto, Toronto, ON, Canada.
Jefferson R WilsonDivision of Neurosurgery and Spine Program, Department of Surgery, University of Toronto, Toronto, ON, Canada.
Wendy LouBiostatistics Division, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.
Zihang LuDepartment of Mathematics and Statistics, Department of Public Health Sciences, Queen's University, Kingston, ON, Canada.
Kevin E ThorpeBiostatistics Division, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.
Michael G FehlingsDivision of Neurosurgery and Spine Program, Department of Surgery, University of Toronto, Toronto, ON, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Symptom evolution in degenerative cervical myelopathy (DCM) is traditionally characterized by severity of neurological deficit. A recent expert consensus challenged this view, proposing that DCM fluctuates across neurological, functional and health-related quality of life measures. We examined whether joint changes across these three domains define distinct recovery patterns in a clinic-based cohort of adult patients with DCM. Methods: Cohorts analysed were the Cervical Spondylotic Myelopathy-North America (CSM-NA, 2005-2007, N = 278), CSM-International (CSM-I, 2007-2011, N = 479) and the CSM-PROTECT Trial (2012-2017, N = 290). All participants were symptomatic adult DCM patients who underwent surgical treatment and completed at least three longitudinal assessments. Bayesian consensus clustering (BCC) was used to simultaneously model one-year changes in the modified Japanese Orthopaedic Association (mJOA), Neck Disability Index (NDI), and health-related quality of life (SF-36 Score). The optimal number of trajectory clusters was selected using maximum mean adjusted adherence. Multivariable logistic regression examined association between trajectory classes and achievement of minimal clinically important difference (MCID) across outcomes with internal validation performed using 100 bootstrap resamples. Findings: The final analytical cohort consisted of 1047 patients diagnosed with DCM. The mean age was 56.8 years, and 60.7% were male. The mean symptom duration was 29.8 months, and most patients exhibited involvement of two spinal levels. Joint modelling of multiple longitudinal outcomes resulted in three distinct patient groups. Trajectory 1 (n = 177, 17%) was characterised by minimal postoperative improvement with persistently low neurological function and health-related quality-of-life scores. Trajectory 2 (n = 524, 50%) demonstrated the greatest reductions in neck pain disability. Trajectory 3 (n = 346, 33%) exhibited global recovery, with substantial improvements across neurological, functional, and quality-of-life domains. Trajectory 3 patients had markedly higher odds of achieving MCID in neurological function (odds ratio [OR] 10.90, 95% CI 6.15-19.32), physical quality of life (OR 7.32, 95% CI 3.53-15.22), and disability (OR 3.02, 95% CI 1.85-4.93) compared to patients in Trajectory 1. BCC-derived models reduced clustering uncertainty and improved model discrimination beyond conventional outcome predictors. Predictors of global recovery included an anterior surgical approach (OR 3.55, 95% CI 1.21-10.37) and higher baseline frailty (OR 1.42, 95% CI 1.14-1.76). Interpretation: We provide evidence that outcomes in DCM follow three distinct, multidimensional trajectories that are not captured by neurological severity alone. Simultaneous assessment of neurological, functional, and health-related quality-of-life outcomes is both valid and informative, enabling phenotypic stratification and improved longitudinal prognostication in DCM. External validation of these recovery phenotypes in independent DCM cohorts is warranted. Funding: None.

Indexed as

Degenerative cervical myelopathyJoint predictive modellingOutcomesPatient phenotypesTrajectory

Identifiers

PMID42668450
PMCPMC13524543

What OpenQuestion holds

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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.