Cervical Disk Replacement
 
 
       
 

Cervical Disk Replacement at a Glance

  • Instead of fusing and eliminating movement in the joint space, the joint is replaced allowing for continued movement
  • Eliminates pseudoarthrosis (failure to obtain a bony fusion)
  • Intended to reduce progression of adjacent level disease
  • FDA investigational study in progress
  • Drs. Lewis and Pollina are co-investigators in the study
  • Patients who would be candidates for single level anterior cervical diskectomy with fusion and meet other criteria are eligible to be a part of the study
 

Fig. 1: The Prestige LP Artificial Cervical Disk is implanted between the vertebral bodies.

     
 
 
Fig. 2: Implanted cervical disk at C5-6. Note the normal function at replaced joint. (Click on images for enlarged view)

Why Perform Disk Replacement When Fusion is so Successful?

Anterior cervical diskectomy and fusion (ACDF) remains the gold standard procedure for the surgical treatment of cervical disk herniation and cervical spondylosis that produce intractable neck and or radicular arm pain that is unresponsive to conservative methods of treatment. It is also used in cases of cervical disk herniations and cervical spondylosis causing nerve root and spinal cord compression that result in radiculopathies and myelopathies with motor and sensory deficits. The use of the operating microscope has resulted in a safer and more complete decompression of the spinal canal and exiting nerve roots. High speed pneumatic drills and the development of fine microsurgical drilling technique, for example, skull base egg shell drilling, have advanced the art of removing the offending anterior compressive osteophytes and herniated disk from the dura and nerve roots. In the majority of cases, osteophytes must first be drilled out and removed before the disk herniation can be adequately identified and removed. The decompression has become wider and more complete with the development of this microsurgical technique. We attribute a large part of the success of this procedure to the proper decompression of the dura and nerve roots. The reported success rate for relief of pain is around 78% for ACDF (1). The procedure takes 1-1.5 hrs to perform for a single level and in the majority of cases, patients go home the same day.

Given the high rate of success for this procedure, why is there interest in a revolutionary change from fusion to artificial disk replacement? The answer lies in the “fusion” aspect of the procedure. Pseudoarthrosis, or the failure of the bone to fuse with the adjacent vertebral body, can occur following the ACDF procedure. This can cause foraminal stenosis and recurrence of symptoms. (Fig. 3) Another reason for interest in artificial disk replacement is something called adjacent segment disk disease. Following ACDF, once fusion takes place there is no movement in the joint. The joint can no longer do what it was originally intended to do, that is, to perform its share of work as a member of the array of joints that allow a full range of motion in the neck. The fusion of one level is felt to create greater stress on the remaining “movable” joints leading to their early failure. (Fig. 3) Both of these problems can result in the need for another operation.

Reference: 1. Silvers HR, Lewis PJ, Suddaby LS, Asch HL, Clabeaux DE, Blumenson, LE: Day Surgery For Cervical Microdiscectomy: Is It Safe And Effective? J Of Spinal Disorders 9:287-293, 1996.

           
       
     

For more detailed information on cervical disk replacement, click here to download a PDF file

       
Fig. 3: CT sagital reconstruction image. Good bony fusion is present at C4-5 and C5-6. At C6-7 a pseudoarthrosis (failed bone fusion) is present. Adjacent level disease is also present at C3-4 with cervical subluxation.
Performing the Implant Procedure
     
      Fig. 4: The Prestige LP Artificial Cervical Disk    
             
  Fig. 5: Sagital MRI showing a huge C6-7 disk herniation with spinal cord compression where the artificial disk will be implanted. The level above, C5-6 has disk degeneration and spondylosis. This level does not require surgery at this time, however, a fusion at the level below it could accelerate its degeneration.      
                   
   

Fig. 6: Intra-operative photo showing the disk space after removal of the herniated disk (left) and the implanted Prestige Cervical Disk (right).

 

Preserving motion while still achieving the necessary important decompression of the offending disk, theoretically can greatly reduce healing time (especially in smokers) and reduce the need for re-operation by avoiding pseudoarthrosis and reducing the effect of adjacent segment disk disease. Preserving motion of the operated disk segment may also improve the success of pain relief by restoring the segment to it’s more natural function of motion and reduce the excess strain on the other segments of the cervical spine.

Patients interested in being evaluated to determine if this procedure would help them should contact our offices at 716-677-6000. Information can be provided about current FDA status as well.

   
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