AI Article Synopsis

  • A new elastic screw spacer technique was created to help maintain movement in patients with lumbar degenerative diseases.
  • A biomechanical comparison was conducted using different models (ISES-1/2, ISES-1/3, unilateral and bilateral fixation, and a Coflex-F model) to find the best entry point for the screws and evaluate the effectiveness of unilateral fixation.
  • The results showed that the ISES technique offers lower pressure and stress on spinal components, improved mobility, and is particularly beneficial for patients with osteoporosis.

Article Abstract

A novel interlaminar elastic screw spacer technique was designed to maintain lumbar mobility in treating lumbar degenerative diseases. A validated finite element model of L4/5 was used to establish an ISES-1/2 model and an ISES-1/3 model based on different insertion points, a unilateral fixation model and a bilateral fixed model based on different fixation methods, and a Coflex-F model based on different implants. The elastic rods were used to fix screws. Under the same mechanical conditions, we compared the biomechanical characteristics to investigate the optimal entry point for ISES technology, demonstrate the effectiveness of unilateral fixation, and validate the feasibility of the ISES technique. Compared to ISES-1/3, the ISES-1/2 model had lower intradiscal pressure, facet cartilage stress, and posterior structural stress. Compared to the ISES-BF model, the ISES-UF model had lower intervertebral pressure, larger mobility, and smaller stress on the posterior structures. The ISES model had a similar intervertebral pressure and limitation of extension as the Coflex-F model. The ISES model retained greater mobility and reduced the stress on the facet cartilage and posterior structure compared with the Coflex-F model. Our study suggests that the ISES technique is a promising treatment of lumbar degenerative diseases, especially those with osteoporosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10604319PMC
http://dx.doi.org/10.3390/bioengineering10101204DOI Listing

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