Showing 1 - 12 of 13 reports matching: International Society for the Advancement of Spine Surgery
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Synopsis: 209 patients experiencing single-level symptomatic cervical degenerative disc disease amid C3 and C7 were randomized to undergo either cervical artificial disc replacement (C-ADR) or anterior cervical discectomy and fusion (ACDF), in order to compare clinical outcomes of the two surgical procedures. Following assessments over Read More »
Conference Report
Synopsis: Three randomized controlled trials (RCTs; Jadad score 1-2) were included in this review and analysis which compared the efficacy of unilateral and bilateral balloon kyphoplasty for the treatment of vertebral compression fractures in osteoporotic patients. Safety, radiological outcome, and clinical outcome were compared between procedures. The results indicated Read More »
Conference Report
Synopsis: 52 patients with lumbar spinal stenosis (LSS) were randomized to be treated with either modified Marmot operation (MM) or spinous process transverse cutting laminectomy through a unilateral approach (control). The study aimed to investigate whether preventing the exposure of paravertebral muscles (PVM) though MM technique affected clinical outcomes. After a year Read More »
Conference Report
Synopsis: 291 patients with symptomatic cervical degenerative disc disease were randomized to undergo treatment with either the SECURE-C Cervical Artificial Disc or anterior cervical discectomy and fusion (ACDF)> This trial was undertaken as a means to determine whether SECURE-C Cervical Artificial Disc was a safe and efficacious treatment option. After a 5 Read More »
Conference Report
Synopsis: 345 single-level symptomatic cervical disc disease patients were distributed into either a randomized or non-randomized group. The 209 patients in the randomized group were randomized to receive cervical artificial disc replacement (C-ADR) with ProDisc-C or anterior cervical discectomy and fusion (ACDF), in order to compare the radiographic rates of progressive adjacent level degeneration between the methods. The 136 patients Read More »
Conference Report
Synopsis: 40 patients undergoing posterior lumbar interbody fusion (PLIF) were randomized to receive polyetheretherketone (PEEK) cages filled with either recombinant human bone morphogenic protein (rhBMP-2) or autologous bone to compare their clinical and radiological effects. At 24 months, Read More »
Conference Report
Synopsis: 34 patients were randomized to compare the clinical and radiographic outcomes of two different procedures for the treatment of low-grade spondylolisthesis. Patients received either lateral lumbar interbody fusion (XLIF) or transforaminal lumbar interbody fusion (TLIF) and were assessed after 3 months. Results indicated that Read More »
Conference Report
Synopsis: 39 patients treated with Freedom Disc (20) vs. ProDisc-L (19) artificial disc replacement devices (ADR) were evaluated for clinical patient self-reported outcomes after single-level lumbar disc disease L3 to S1 treatment. 2 year results concluded that both groups had similar self-reported improvements that were maintained up to 24 months. The Freedom device Read More »
Conference Report
Synopsis: 42 patients with symptomatic cervical disc degeneration were randomized to either the Prestige or Nunec cervical disc prosthesis to compare their functional outcomes. After a mean follow up of 7.88 months, both groups demonstrated in significant improvements from baseline in all outcome measures. Comparison between groups Read More »
Conference Report
Synopsis: 394 patients undergoing total disc replacement were randomized to receive either the Kineflex-L or Charite artificial lumbar disc in order to determine if there were any differences in outcomes attained by either device. Patients were followed-up for 5 years assessing clinical outcomes, disability, pain, and rate of re-operation or revision surgery. Also, a subsample Read More »
Conference Report
Synopsis: 345 patients experiencing single-level symptomatic cervical degenerative disc disease were divided into randomized and non-randomized groups. The 209 patients in the randomized group were randomized to undergo either cervical artificial disc replacement (C-ADR) or anterior cervical discectomy and fusion (ACDF), in order to compare the reoperation rates of the two surgical procedures. Following evaluations over Read More »
Conference Report
Synopsis: 416 patients were randomized to receive either the Superion or X-STOP interspinous systems in minimally invasive surgery for symptomatic treatment of lumbar spinal stenosis. The objective of the study was to determine if there was a difference in clinical outcomes of the two devices at 12 months of a 5 year trial. The results at Read More »
Conference Report