Lumbar disc herniation is usually treated by discectomy alone. Nonfusion system such as Wallis interspinous implants have also been successfully used in disc degenerative diseases. However, the superiority of a discectomy with Wallis in comparison to a discectomy alone for primary lumbar disc herniation has yet to be determined.The aim of our study is to investigate whether lumbar discectomy combined with the Wallis device provides better radiographic and clinical short-term outcome than posterior lumbar discectomy alone.
The most commonly used therapy for lumbar disc herniation (LDH) are partial discectomy or discectomy with fusion if there was an additional mechanical disorder in the underlying functional spinal unit. However, the problems associated with discectomy are intervertebral disc height loss and the segmental instability, thought to be a risk for failed back surgery syndrome or recurrence lumbar disc herniation. Fusion has also been criticised for its side effects of adjacent segment degeneration(ASD), pseudarthrosis and bone-graft morbidity. To prevent such complications , a new family of dynamic implants have been established. Wallis interspinous implant (Abbott Laboratories, Bordeaux, France) , invented by J. Senegas, is one of them. It consisted of a interspinous blocker made out of polyetheretherketone (PEEK) to limit extension and two dacron tapes around the spinous processes in order to secure the implant and limit flexion. The aim of using this device is to unload the facet joints, to restore foraminal height and to provide sufficient stability especially in extension but still allow motion in the treated segment. Previous clinical trials and biomechanical studies are promising, however, the superiority of a discectomy with Wallis in comparison to a discectomy alone for primary lumbar disc herniation has yet to be determined. The purpose of this prospective controlled study was to evaluate the clinical effect of lumbar discectomy combined with Wallis interspinous device, comparing with posterior lumbar discectomy alone. Our hypothesis was that the use of the Wallis device would have better clinical and radiological outcomes than lumbar discectomy alone.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
All the patients were in prone positions on the operation table and received general anesthesia. A midline incision was made and paravertebral muscles were dissected unilaterally. Disc excision and nerve root decompression were initially accomplished through a unilateral transflaval approach. Then the wound was closed with a suction drain.
The Wallis interspinous implant is placed after a lumbar discectomy. Interspinal ligaments of operated segment were removed and supraspinal ligament were retained. And then the proper size of Wallis implant was mounted underneath the supraspinous ligament and secured to the spine with the attached Dacron bands,above and below the corresponding spinous processes.
Guangdong Gerneral Hospital
Guangzhou, Guangdong, China
Visual Analogue Scale (VAS) at 2 days before intervention
baseline VAS
Time frame: 2 days before intervention
Visual Analogue Scale (VAS) at 1 week after intervention
Time frame: 1 week after intervention
Visual Analogue Scale (VAS) at 12 months after intervention
Time frame: 12 months after intervention
Visual Analogue Scale (VAS) at 24 months after intervention
Time frame: 24 months after intervention
Japanese Orthopedics Association (JOA) at 2 days before intervention
baseline JOA
Time frame: 2 days before intervention
Japanese Orthopedics Association (JOA) at 1 week after intervention
Time frame: 1 week after intervention
Japanese Orthopedics Association (JOA) at 12 months after intervention
Time frame: 12 months after intervention
Japanese Orthopedics Association (JOA) at 24 months after intervention
Time frame: 24 months after intervention
Oswestry Disability Index (ODI) at 2 days before intervention
baseline ODI
Time frame: 2 days before intervention
Oswestry Disability Index (ODI) at 1 week after intervention
Time frame: 1 week after intervention
Oswestry Disability Index (ODI) at 12 months after intervention
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Masking
NONE
Enrollment
80
Time frame: 12 months after intervention
Oswestry Disability Index (ODI) at 24 months after intervention
Time frame: 24 months after intervention
Intervertebral disc height of the operated segments
Time frame: 2 days before intervention and 1 week, 12 months and 24 months after intervention
Range of motion of the operated segments
Time frame: 2 days before intervention, 12 months and 24 months after intervention
Complications
Complications: includes dural laceration, implant loose, lumbar kyphosis, spinous process fracture or recurrent lumbar disc herniation
Time frame: 1 week, 12 months and 24 months after intervention