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SINTX

Two Level ACDF Using Silicon Nitride (Si₃N₄) Implants Review

Research by Graham Calvert, M.D. Mississippi Sports Medicine and Orthopaedic Center


Summary


A 50-year-old female with unbearable neck and arm pain, accompanied by right triceps weakness, underwent two-level anterior cervical discectomy and fusion (ACDF) using silicon nitride ceramic implants at C5-6 and C6-7 cervical vertebrae. Patient experienced fusion and full resolution of symptoms with return to normal activity after the anterior cervical decompression.

anterior cervical discectomy and fusion acdf

ACDF Diagnosis & Procedure


Patient had intractable neck and arm pain for 2 months, along with profound right triceps weakness. Severity of symptoms resulted in extreme discomfort while trying to sleep, requiring the patient to miss work. During examination, extension recreated right arm pain characterized as a sharp burning sensation. 


Patient had failed conservative treatment consisting of Percocet, Medrol, anti-inflammatories, and muscle relaxers. Radiographs indicated C5-6 and C6-7 spondylosis with a disc height collapse (collapsed disc) and arthropathy. MRI revealed severe neuroforaminal stenosis (neural foraminal narrowing) from disc osteophyte complexes (DOC) (also known as disc osteophyte bar), as well as some central stenosis.


Patient underwent a two-level ACDF at C5-6 and C6-7 using silicon nitride interbody implants (Amedica Valeo ™ II C – 14x12mm footprint, 7mm height, 6º lordosis) packed with demineralized bone matrix (DBM) putty and local autograft. Plate and screws were used for anterior fixation.


ACDF Surgery Results


At 6-week postoperative follow-up, the patient's shooting arm pain had significantly improved and only mild mechanical neck pain remained. At 3-months post-op, both arm and neck pain were completely resolved. By 6-month follow-up, the patient had completed physical therapy and returned to work and normal activities. 


Radiographic examination performed at 6-weeks, 3-months, and 6-months postoperative confirmed hardware and implants were in alignment with no sign of loosening, and demonstrated integration of bony fusion between levels. One-year follow-up confirmed successful surgery and fully fused C5-C7 vertebrae.


Conclusion


  1. Patient’s pain and weakness were quickly resolved at 6 weeks

  2. Stable and successful spinal fusion at 1 year using Amedica Valeo ™ II C interbody cages


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