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Low lordosis is a common finding in young lumbar disc herniation patients

Joel Beck, Helena Brisby, Adad Baranto, Olof Westin

2020Journal of Experimental Orthopaedics15 citationsDOIOpen Access PDF

Abstract

PURPOSE: The sagittal alignment of the lumbar spine and pelvis can be classified into several subtypes. It has been suggested that the risk of developing certain pathologies, such as a lumbar disc herniation (LDH) is affected by spinal sagittal profiles. The main aim of this study was to investigate the sagittal profile in young patients surgically treated for a lumbar disc herniation and if a discectomy would alter the sagittal parameters. METHODS: Sixteen active young patients (mean age 18.3 ± 3.2 SD) with a lumbar disc herniation having a discectomy were included. A classification according to Roussouly of the sagittal parameters was made by two senior spinal surgeons, both pre-operatively and post-operatively on radiographs. The distribution of sagittal parameters and spinopelvic profiles were analysed and compared to a previous established healthy normal population. RESULTS: This series of active young patients with LDH exhibited a low lumbar lordosis dominance, with Roussouly sagittal profiles type 1 and type 2 accounting for more than 75% of the examined patients. An analysis of the erect radiographs revealed no significant changes in the post-operative sagittal profile. CONCLUSIONS: This study showed that sagittal spinal alignment according to Roussouly in a young population with LDH is skewed compared with a normal population cohort. Furthermore, the lack of post-operative correction is suggestive of a non-ephemeral response to a LDH. Roussouly type 2 spinal sagittal profile may be a risk factor in young individuals suffering a disc herniation.

Topics & Concepts

Sagittal planeMedicineLumbarPopulationLordosisRadiographyOrthopedic surgeryOrthodonticsDiscectomyLumbar vertebraeSurgeryRadiologyEnvironmental healthSpine and Intervertebral Disc PathologyScoliosis diagnosis and treatmentCervical and Thoracic Myelopathy