Normative Measurements of L1-S1 Neuroforaminal Dimensions derived from Plain Film Radiography, Computed Tomography, and Magnetic Resonance Imaging.


Journal

Spine
ISSN: 1528-1159
Titre abrégé: Spine (Phila Pa 1976)
Pays: United States
ID NLM: 7610646

Informations de publication

Date de publication:
08 Nov 2023
Historique:
received: 01 08 2023
accepted: 17 10 2023
medline: 8 11 2023
pubmed: 8 11 2023
entrez: 8 11 2023
Statut: aheadofprint

Résumé

retrospective cohort. To report normative measurements of L1-S1 lumbar neuroforamina on plain film radiography (PFR), computed tomography (CT), and magnetic resonance imaging (MRI), accounting for patient sex and ethnicity. Quantitative criteria for diagnosis of neuroforaminal stenosis (NFS) remains unknown. Acquiring a thorough understanding of normative foraminal dimensions is a key step in formulating objective parameters for NFS. We measured 988 images from 494 patients between 18 and 35 years-old without spinal pathology who received PFR, CT, or MRI within one year of each other. Neuroforaminal measurements were defined as the height, area, and sagittal and axial widths. Statistical analyses were performed to assess relationships among PFR-, CT-, and MRI-derived neuroforaminal measurements as well as the influence of patient sex and ethnicity. 330 PFR, 377 CT, and 281 MRI were measured. Of these, 213 PFR and CT, 117 PFR and MRI, and 164 MRI and CT intrapatient images were compared. Statistically significant differences were observed among PFR, CT, and MRI measurements across all levels L1-S1. PFR measurements were larger compared to those derived from CT and MRI. Weak-to-moderate correlations were observed between PFR and CT, PFR and MRI, and CT and MRI, with the magnitude of correlation decreasing caudally from L1-S1. Variations in neuroforaminal anatomy were observed based on sex and ethnicity. This study reports 25,951 measurements of normal L1-S1 neuroforaminal anatomy assessed by PFR, CT, and MRI. The values reported in this study may be used as normative reference measurements of the lumbar neuroforamina. PFR measurements of the neuroforamina are larger compared to those derived from CT and MRI across all levels from L1-S1. There is poor correlation among PFR, CT and MRI when measuring the lumbar neuroforamina. Differences in neuroforaminal anatomy are evident based on patient sex and ethnicity.

Sections du résumé

STUDY DESIGN METHODS
retrospective cohort.
OBJECTIVE OBJECTIVE
To report normative measurements of L1-S1 lumbar neuroforamina on plain film radiography (PFR), computed tomography (CT), and magnetic resonance imaging (MRI), accounting for patient sex and ethnicity.
SUMMARY OF BACKGROUND DATA BACKGROUND
Quantitative criteria for diagnosis of neuroforaminal stenosis (NFS) remains unknown. Acquiring a thorough understanding of normative foraminal dimensions is a key step in formulating objective parameters for NFS.
METHODS METHODS
We measured 988 images from 494 patients between 18 and 35 years-old without spinal pathology who received PFR, CT, or MRI within one year of each other. Neuroforaminal measurements were defined as the height, area, and sagittal and axial widths. Statistical analyses were performed to assess relationships among PFR-, CT-, and MRI-derived neuroforaminal measurements as well as the influence of patient sex and ethnicity.
RESULTS RESULTS
330 PFR, 377 CT, and 281 MRI were measured. Of these, 213 PFR and CT, 117 PFR and MRI, and 164 MRI and CT intrapatient images were compared. Statistically significant differences were observed among PFR, CT, and MRI measurements across all levels L1-S1. PFR measurements were larger compared to those derived from CT and MRI. Weak-to-moderate correlations were observed between PFR and CT, PFR and MRI, and CT and MRI, with the magnitude of correlation decreasing caudally from L1-S1. Variations in neuroforaminal anatomy were observed based on sex and ethnicity.
CONCLUSION CONCLUSIONS
This study reports 25,951 measurements of normal L1-S1 neuroforaminal anatomy assessed by PFR, CT, and MRI. The values reported in this study may be used as normative reference measurements of the lumbar neuroforamina. PFR measurements of the neuroforamina are larger compared to those derived from CT and MRI across all levels from L1-S1. There is poor correlation among PFR, CT and MRI when measuring the lumbar neuroforamina. Differences in neuroforaminal anatomy are evident based on patient sex and ethnicity.

Identifiants

pubmed: 37937514
doi: 10.1097/BRS.0000000000004857
pii: 00007632-990000000-00507
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest and Source of Funding: Dr. Wayne Cheng reports consulting for Medtronic and Orthofix, a research grant from DePuy Synthes, and speaking and consultation for Radius. Dr. Olumide Danisa declares royalties from Globus Medical, consultation for Stryker, reimbursement for travel and expenses for services as an oral examiner for the American Board of Orthopaedic Surgery (ABOS), and reimbursement for travel to the annual meeting of the Musculoskeletal Transplant Foundation as a medical board member. Uncompensated disclosures for Dr. Danisa include his service on the patient safety committee for the North American Spine Society, the spine education committee for Orthopaedic Research Society and American Academy of Orthopaedic Surgeons (AAOS), and associate editor for SpineLine and NASSJ. For all remaining authors no conflicts of interest are declared. The author(s) received no financial or material support for the research, authorship, and/or publication of this article. The authors report no conflicts of interest specific to the research, authorship, and/or publication of this article.

Auteurs

Jacob Razzouk (J)

School of Medicine, Loma Linda University, Loma Linda, CA, USA.

Ethan Vyhmeister (E)

School of Medicine, Loma Linda University, Loma Linda, CA, USA.

Davis Carter (D)

School of Medicine, Loma Linda University, Loma Linda, CA, USA.

Grant Sajdak (G)

School of Medicine, Loma Linda University, Loma Linda, CA, USA.

Kai Nguyen (K)

School of Medicine, Loma Linda University, Loma Linda, CA, USA.

Mei Carter (M)

School of Medicine, Loma Linda University, Loma Linda, CA, USA.

Whitney Kagabo (W)

Department of Orthopaedic Surgery, Johns Hopkins University, Baltimore, MD, USA.

Omar Ramos (O)

Twin Cities Spine Center, Minneapolis, MN, USA.

Wayne Cheng (W)

Division of Orthopaedic Surgery, Jerry L. Pettis VA Medical Center, Loma Linda, CA, USA.

Olumide Danisa (O)

Department of Orthopaedic Surgery, Loma Linda University Health, Loma Linda, CA, USA.

Classifications MeSH