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Lumbar subtotal corpectomy non-fusion model produced using a novel prosthesis.
Jiantao Liu1, Feng Zhang2, Zhengchao Gao1
1Department of Orthopedics, Second Affiliated Hospital of Xi'an Jiaotong University, No. 157, The West Fifth Road, Xincheng District, Xi'an, Shaanxi, People's Republic of China.
Archives of Orthopaedic and Trauma Surgery
|September 11, 2017
Summary
This study introduces a movable artificial lumbar complex (MALC) prosthesis for lumbar reconstruction. The MALC prosthesis provides stability and preserves segment movement without affecting adjacent spinal segments.
Area of Science:
- Spinal biomechanics
- Orthopedic surgery
- Biomaterials engineering
Background:
- Lumbar subtotal corpectomy often necessitates spinal reconstruction.
- Non-fusion techniques aim to preserve spinal segment mobility.
- Evaluating novel prostheses requires robust biomechanical models.
Purpose of the Study:
- To design and evaluate a movable artificial lumbar complex (MALC) prosthesis.
- To establish an in vitro model for assessing non-fusion lumbar reconstruction.
- To determine the biomechanical stability and segmental movement preservation of the MALC prosthesis.
Main Methods:
- A movable artificial lumbar complex (MALC) prosthesis was designed.
- An in vitro anterolateral lumbar corpectomy non-fusion model was established using 26 goat lumbar spine specimens.
- Biomechanical testing assessed range of motion (ROM) in flexion-extension, lateral bending, and axial rotation.
Main Results:
- The MALC prosthesis demonstrated comparable stability to intact spines in flexion, extension, lateral bending, and axial torsion.
- Non-fusion reconstruction with MALC significantly preserved L2-3 ROM while allowing controlled increases in L3-4 and L4-5 ROM.
- No significant difference in Bone Mineral Density (BMD) was observed among groups.
Conclusions:
- The MALC prosthesis offers immediate stability and preserves functional segment movement after lumbar subtotal corpectomy.
- The prosthesis effectively maintains mobility without abnormal adjacent segment hypermobility.
- Further in vivo and human specimen studies are recommended to validate findings.

