Monocentric retrospective analysis of clinical outcomes, complications, and adjacent segment disease in 507 patients undergoing ACDF for degenerative cervical myelopathy.
ACDF
Adjacent Segment Disease
Degenerative Cervical Myelopathy
Elderly Spine Surgery
Journal
World neurosurgery
ISSN: 1878-8769
Titre abrégé: World Neurosurg
Pays: United States
ID NLM: 101528275
Informations de publication
Date de publication:
15 Jul 2024
15 Jul 2024
Historique:
received:
23
02
2024
revised:
08
07
2024
accepted:
09
07
2024
medline:
18
7
2024
pubmed:
18
7
2024
entrez:
17
7
2024
Statut:
aheadofprint
Résumé
Degenerative Cervical Myelopathy (DCM) is a leading cause of non-traumatic spinal cord injury. Surgery aims to arrest neurological decline and improve conditions, but controversies surround risks and benefits in elderly patients, outcomes in mild myelopathy, and the risk of adjacent segment disease (ASD). Retrospective data of patients who underwent ACDF for DCM in our hospital were collected. Patients were stratified by preoperative mJOA (mild, moderate, severe) and age (Under 70, Over 70). Clinical outcomes, complications, and ASD rate were analyzed. We evaluated the relationship between mJOA recovery rate and the risk of complications and various preoperative parameters. 507 consecutive patients were included in the study, with a mean follow-up of 43.52 months (12-71). Improvement in all outcome variables was observed in mild, moderate and severe myelopathy categories, with elderly patients showing a lower improvement. Except for age, no other variable correlated with mJOA recovery rate. We observed 45 complications (11.1% of patients), with 14 in the U70 group and 31 in the O70 group (p-value<0.001). Age, Charlson Comorbidity index and ASA score were found to be predictors of complications. Fourteen patients (2.8% of total), mean age 54.2, developed radiological and clinical ASD. Most had cranial-level ASD with Pfirmann grade >= 2 before index surgery. Most myelopathic patients improve after ACDF. Elderly patients show a lower improvement and higher complication rates than younger counterparts. ASD rates are low, and younger patients with preexisting cranial level alterations are more susceptible.
Sections du résumé
BACKGROUND
BACKGROUND
Degenerative Cervical Myelopathy (DCM) is a leading cause of non-traumatic spinal cord injury. Surgery aims to arrest neurological decline and improve conditions, but controversies surround risks and benefits in elderly patients, outcomes in mild myelopathy, and the risk of adjacent segment disease (ASD).
METHODS
METHODS
Retrospective data of patients who underwent ACDF for DCM in our hospital were collected. Patients were stratified by preoperative mJOA (mild, moderate, severe) and age (Under 70, Over 70). Clinical outcomes, complications, and ASD rate were analyzed. We evaluated the relationship between mJOA recovery rate and the risk of complications and various preoperative parameters.
RESULTS
RESULTS
507 consecutive patients were included in the study, with a mean follow-up of 43.52 months (12-71). Improvement in all outcome variables was observed in mild, moderate and severe myelopathy categories, with elderly patients showing a lower improvement. Except for age, no other variable correlated with mJOA recovery rate. We observed 45 complications (11.1% of patients), with 14 in the U70 group and 31 in the O70 group (p-value<0.001). Age, Charlson Comorbidity index and ASA score were found to be predictors of complications. Fourteen patients (2.8% of total), mean age 54.2, developed radiological and clinical ASD. Most had cranial-level ASD with Pfirmann grade >= 2 before index surgery.
CONCLUSIONS
CONCLUSIONS
Most myelopathic patients improve after ACDF. Elderly patients show a lower improvement and higher complication rates than younger counterparts. ASD rates are low, and younger patients with preexisting cranial level alterations are more susceptible.
Identifiants
pubmed: 39019433
pii: S1878-8750(24)01219-1
doi: 10.1016/j.wneu.2024.07.079
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2024 Elsevier Inc. All rights reserved.