Cement-augmented pedicle screws (CPS) and hybrid construct (HC) consisting of pedicle screws and additional hooks are common methods in osteoporotic fracture of the thoracic and lumbar spine. No study has compared the surgical results between CPS and HC techniques for treatment of the osteoporotic thoracic and lumbar spine fracture. The aim of the retrospective study was to compare surgical results using CPS or HC for osteoporotic fractures in the thoracic or lumbar spine. Patients who received surgical treatment with CPS or HC for osteoporotic fractures in the thoracic or lumbar spine.
Osteoporosis, the most common metabolic bone disease, leads to alteration of bone density that has been shown to compromise the strength of spinal instrumentation. With elderly populations growing, rates of spine surgery performed on osteoporotic patients have increased to treat a variety of conditions. Vertebral fracture is the most common osteoporotic fracture in the elderly, and surgical intervention is sometimes needed for patients who are diagnosed as nonunion, failure of vertebroplasty, and neurologic deficits. Therefore, spine surgeons will increasingly face the challenge of achieving rigid fixation of osteoporotic spines. Cement-augmented pedicle screws are the most common strategy to maximize pullout strength for fixation of osteoporotic spines. Hybrid constructs, a combination of pedicle screws and hooks, offer an alternative approach to avoid implant failure and increasing construct stability when placing instrumentation in the osteoporotic spine. Biomechanical studies of either cement-augmented pedicle screws or combined pedicle screws and hooks for osteoporotic spine have demonstrated superior results compared to pedicle screws only in terms of improving implant pullout strength. However, few clinical investigation to date has focused on comparing surgical results of the cement-augmented pedicle screws (CPS) and hybrid construct (HC) techniques. The goal of the retrospective cohort study was to compare the surgical outcomes and surgery-, patient- and implant-related complications between the CPS and HC techniques for osteoporotic vertebral fractures in the thoracic or lumbar spine.
Study Type
OBSERVATIONAL
Enrollment
200
Patients who received surgical treatment with CPS for osteoporotic fractures in the thoracic or lumbar spine
Patients who received surgical treatment with HC consisting of pedicle screws and additional hooks for osteoporotic fractures in the thoracic or lumbar spine
Dep. of Orthopedics and Traumatology, Taipei Veterans General Hospital
Taipei, Taiwan
RECRUITINGImplant Failure
Implant failure was defined as pull-out or breakage of the implants on plain X-ray film.
Time frame: Postoperative 1 year
Kyphotic Angle
Cobb's method was used to measure the regional kyphotic angle
Time frame: Preoperative
Kyphotic Angle
Cobb's method was used to measure the regional kyphotic angle
Time frame: Postoperative 1 month.
Kyphotic Angle
Cobb's method was used to measure the regional kyphotic angle
Time frame: Postoperative 2 months.
Kyphotic Angle
Cobb's method was used to measure the regional kyphotic angle
Time frame: Postoperative 3 months.
Kyphotic Angle
Cobb's method was used to measure the regional kyphotic angle
Time frame: Postoperative 6 months.
Kyphotic Angle
Cobb's method was used to measure the regional kyphotic angle
Time frame: Postoperative 12 months.
Visual Analogue Scale (VAS)
Functional outcomes, Back pain evaluated
Time frame: Preoperative
Visual Analogue Scale (VAS)
Functional outcomes, Back pain evaluated
Time frame: Postoperative 1 month.
Visual Analogue Scale (VAS)
Functional outcomes, Back pain evaluated
Time frame: Postoperative 2 months.
Visual Analogue Scale (VAS)
Functional outcomes, Back pain evaluated
Time frame: Postoperative 3 months.
Visual Analogue Scale (VAS)
Functional outcomes, Back pain evaluated
Time frame: Postoperative 6 months.
Visual Analogue Scale (VAS)
Functional outcomes, Back pain evaluated
Time frame: Postoperative 12 months.
Oswestry Disability Index (ODI)
Functional outcomes, Disability evaluated
Time frame: Preoperative
Oswestry Disability Index (ODI)
Functional outcomes, Disability evaluated
Time frame: Postoperative 1 month.
Oswestry Disability Index (ODI)
Functional outcomes, Disability evaluated
Time frame: Postoperative 2 months.
Oswestry Disability Index (ODI)
Functional outcomes, Disability evaluated
Time frame: Postoperative 3 months.
Oswestry Disability Index (ODI)
Functional outcomes, Disability evaluated
Time frame: Postoperative 6 months.
Oswestry Disability Index (ODI)
Functional outcomes, Disability evaluated
Time frame: Postoperative 12 months.
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