STUDY DESIGN: A retrospective study. PURPOSE: The aim of this study is to compare the efficacy and outcome of vertebroplasty compared with unipedicular and bipedicular kyphoplasty for the treatment of osteoporotic vertebral compression fractures in terms of pain, functional capacity and height restoration rates. OVERVIEW OF LITERATURE: The vertebroplasty procedure was first performed in 1984 for the treatment of a hemangioma at the C2 vertebra. Kyphoplasty was first performed in 1998 and includes vertebral height restoration in addition to using inflation balloons and high-viscosity cement. Both are efficacious, safe and long-lasting procedures. However, controversy still exists about pain relief, improvement in functional capacity, quality of life and height restoration the superiority of these procedures and assessment of appropriate and specific indications of one over the other remains undefined. METHODS: Between 2004 and 2011, 296 patients suffering from osteoporotic vertebral compression fracture underwent 433 vertebroplasty and kyphoplasty procedures. Visual analogue scale (VAS), the Oswestry Disability Index (ODI) and height restoration rates were used to evaluate the results. RESULTS: Mean height restoration rate was 24.16%+/-1.27% in the vertebroplasty group, 24.25%+/-1.28% in the unipedicular kyphoplasty group and 37.05%+/-1.21% in the bipedicular kyphoplasty group. VAS and ODI scores improved all of the groups. CONCLUSIONS: Vertebroplasty and kyphoplasty are both effective in providing pain relief and improvement in functional capacity and quality of life after the procedure, but the bipedicular kyphoplasty procedure has a further advantage in terms of height restoration when compared to unipedicular kyphoplasty and vertebroplasty procedures.
Fractures, Compression* ; Hemangioma ; Humans ; Inflation, Economic ; Kyphoplasty* ; Osteoporosis ; Quality of Life ; Retrospective Studies ; Spine ; Vertebroplasty*

No abstract available.
Amniotic Fluid* ; Animals ; Female ; Fibrosis* ; Humans ; Hyaluronic Acid* ; Laminectomy* ; Mitomycin* ; Rats*

No abstract available.
Amniotic Fluid* ; Animals ; Female ; Fibrosis* ; Humans ; Hyaluronic Acid* ; Laminectomy* ; Mitomycin* ; Rats*

STUDY DESIGN: A retrospective study. PURPOSE: The aim of this study was to evalute the effects of mitomycin-C, sodium hyaluronate and human amniotic fluid on preventing spinal epidural fibrosis. OVERVIEW OF LITERATURE: The role of scar tissue in pain formation is not exactly known, but it is reported that scar tissue causes adhesions between anatomic structures. Intensive fibrotic tissue compresses on anatomic structures and increases the sensitivity of the nerve root for recurrent herniation and lateral spinal stenosis via limiting movements of the root. Also, neuronal atrophy and axonal degeneration occur under scar tissue. METHODS: The study design included 4 groups of rats: group 1 was the control group, groups 2, 3, and 4 receieved antifibrotic agents, mitomycin-C (group 2), sodium hyaluronate (group 3), and human amniotic fluid (group 4). Midline incision for all animals were done on L5 for total laminectomy. Four weeks after the surgery, the rats were sacrificed and specimens were stained with hematoxylin-eosin and photos of the slides were taken for quantitive assesment of the scar tissue. RESULTS: There was no significant scar tissue in the experimental animals of groups 2, 3, and 4. It was found that there was no significant difference between drug groups, but there was a statistically significant difference between the drug groups and the control group. CONCLUSIONS: This experimental study shows that implantation of mitomycin-C, sodium hyaluronate and human amniotic fluid reduces epidural fibrosis and adhesions after spinal laminectomy in rat models. Further studies in humans are needed to determine the complications of the agents researched.
Amniotic Fluid* ; Animals ; Atrophy ; Axons ; Cicatrix ; Equidae ; Female ; Fibrosis* ; Humans* ; Hyaluronic Acid* ; Laminectomy* ; Mitomycin* ; Models, Animal ; Neurons ; Rats* ; Retrospective Studies ; Sodium* ; Spinal Stenosis