Su Chen-Hsing, Tu Po-Hsun, Yang Tao-Chieh, Tseng Yuan-Yun
Department of Neurosurgery, Changhua Christian Hospital, Changhua, Taiwan, ROC.
J Spinal Disord Tech. 2013 Jun;26(4):200-6. doi: 10.1097/BSD.0b013e31823f6298.
Comparing a prospective group of 32 patients, who underwent percutaneous vertebroplasty (PVP) and who were treated with teriparatide for at least 18 months after a new-onset adjacent vertebral compression fracture (VCF), and compared it with a retrospective group of 33 patients, who received antiresorptive agents combined with repeated PVPs for post-PVP new-onset adjacent VCFs.
This comparative study aimed to assess the immediate and mid-term efficacy and safety of teriparatide for treating new adjacent VCFs after vertebroplasty.
Vertebroplasty may provoke fractures in adjacent, nonaugmented vertebrae. Subsequent VCFs can occur much sooner and more frequently after PVPs. Antiresorptive agents do not effectively prevent new-onset VCFs or prompt pain relief. Treatment with teriparatide is effective and rapid in increasing spinal bone mineral density (BMD) and in decreasing vertebral fracture risk in patients with osteoporosis.
Relevant clinical data were compared between a prospective group of patients who received teriparatide and a retrospective group of patients who received antiresorptive agents and repeated PVPs for new-onset adjacent VCFs after PVP.
Data in prospective group, including visual analogue scale scores and BMD were compared with those in a retrospective group. In group A, only 1 new-onset VCF occurred during the mean follow-up period of 22.56 months. In group B, 5 patients (6 vertebrae) developed new-onset VCFs after the second PVP, and 2 of these 5 patients had additional new VCFs after the third PVP. Teriparatide significantly reduced the risk of new VCFs after vertebroplasty (odds ratio=0.18; 95% confidence interval, 0.02-1.64). The increase of lumbar spine BMD was 26.32% after 18 months of treatment with teriparatide and 4.62% after 18 months of treatment with antiresorptive agents. In addition, at the 18-month follow-up, mean visual analogue scale scores had decreased from 8.03±1.97-1.37±0.52 in the teriparatide group and from 7.91±1.95-4.23±1.21 in the antiresorptive group.
For the treatment of new-onset adjacent VCF after PVPs, the therapeutic effects of teriparatide is better than that of the combined vertebroplasty and an antiresorptive agent in fracture prevention, BMD change, and sustained pain relief.
比较一组32例接受经皮椎体成形术(PVP)且在新发相邻椎体压缩骨折(VCF)后接受特立帕肽治疗至少18个月的前瞻性患者,并将其与一组33例接受抗吸收剂联合重复PVP治疗PVP后新发相邻VCF的回顾性患者进行比较。
本比较研究旨在评估特立帕肽治疗椎体成形术后新发相邻VCF的近期和中期疗效及安全性。
椎体成形术可能会引发相邻未强化椎体的骨折。随后的VCF在PVP后可能更快且更频繁地发生。抗吸收剂不能有效预防新发VCF或迅速缓解疼痛。特立帕肽治疗可有效且快速地增加骨质疏松症患者的脊柱骨密度(BMD)并降低椎体骨折风险。
比较一组接受特立帕肽的前瞻性患者与一组接受抗吸收剂联合重复PVP治疗PVP后新发相邻VCF的回顾性患者的相关临床数据。
将前瞻性组的数据,包括视觉模拟评分和BMD与回顾性组的数据进行比较。在A组中,在平均22.56个月的随访期内仅发生1例新发VCF。在B组中,5例患者(6个椎体)在第二次PVP后出现新发VCF,这5例患者中有2例在第三次PVP后又出现了新的VCF。特立帕肽显著降低了椎体成形术后新发VCF的风险(优势比=0.18;95%置信区间,0.02 - 1.64)。特立帕肽治疗18个月后腰椎BMD增加26.32%,抗吸收剂治疗18个月后增加4.62%。此外,在18个月随访时,特立帕肽组的平均视觉模拟评分从8.03±1.97降至1.37±0.52,抗吸收剂组从7.91±1.95降至4.23±1.21。
对于治疗PVP后新发相邻VCF,特立帕肽在预防骨折、BMD变化和持续缓解疼痛方面的治疗效果优于椎体成形术联合抗吸收剂。