Iwata Akira, Kanayama Masahiro, Oha Fumihiro, Shimamura Yukitoshi, Hashimoto Tomoyuki, Takahata Masahiko, Iwasaki Norimasa
Spine Center, Hakodate Central General Hospital, Hokkaido, Japan.
Department of Preventive and Therapeutic Research for Metastatic Bone Tumor, Faculty of Medicine and Graduate School of Medicine, Hokkaido University.
Spine (Phila Pa 1976). 2020 Jul 1;45(13):E760-E767. doi: 10.1097/BRS.0000000000003422.
Cohort study (level 3).
The aim of this study was to identify independent risk factors for residual low back pain (LBP) following osteoporotic vertebral fracture (OVF).
Nonunion has been proposed as the primary cause of residual LBP following OVF. However, LBP can occur even when union is maintained. Other reported causes of LBP after OVF include vertebral deformities and spinopelvic malalignment.
Sixty-seven patients with single-level thoracolumbar OVF who had not received previous osteoporotic treatment were enrolled. Conservative treatment was conducted using a soft lumbosacral orthosis plus osteoporosis drugs, either weekly alendronate (bisphosphonate) or daily teriparatide. Pain scores, kyphosis angle of fractured vertebra (VKA), and spinopelvic alignment, including pelvic incidence minus lumbar lordosis (PI-LL), were assessed periodically during treatment. Radiographic union was evaluated independently by three specialists at 24 weeks post-admission. Patients were divided by pain scores >40% at 24 weeks into the LBP (n = 36) and non-LBP (n = 31) groups. Temporal changes and statistical associations were examined to identify risk factors for LBP at 24 weeks.
At 24 weeks, 25% of OVFs failed to achieve union. The LBP group consisted of 71% of nonunion and 48% of union cases. Stepwise multinomial regression analysis showed VKA at 24 weeks >25° was significant risk factor for the LBP group (odds ratio: 6.24, 95% confidence interval: 1.77-22.02, P = 0.004). Significant differences in VKA emerged during treatment in the LBP group, but PI-LL showed the tendency not to change throughout the treatment period. Non-union was correlated with VKA (area under the curve: 0.864).
Although spinopelvic malalignment is considered as a preexisting factor for LBP, VKA exacerbated by nonunion predominantly led to LBP after a new OVF. Each incidence of OVF should be treated to limit further morphological changes to the fractured vertebra.
队列研究(3级)。
本研究旨在确定骨质疏松性椎体骨折(OVF)后残留下腰痛(LBP)的独立危险因素。
骨不连被认为是OVF后残留LBP的主要原因。然而,即使保持骨愈合,LBP仍可能发生。OVF后其他报道的LBP原因包括椎体畸形和脊柱骨盆失准。
纳入67例未接受过骨质疏松治疗的单节段胸腰椎OVF患者。采用软式腰骶矫形器加骨质疏松药物进行保守治疗,药物为每周一次的阿仑膦酸盐(双膦酸盐)或每日一次的特立帕肽。在治疗期间定期评估疼痛评分、骨折椎体的后凸角(VKA)以及脊柱骨盆对线情况,包括骨盆入射角减去腰椎前凸角(PI-LL)。入院24周后由三位专家独立评估影像学骨愈合情况。根据24周时疼痛评分>40%将患者分为LBP组(n = 36)和非LBP组(n = 31)。研究时间变化和统计关联以确定24周时LBP的危险因素。
24周时,25%的OVF未实现骨愈合。LBP组中骨不连病例占71%,骨愈合病例占48%。逐步多项回归分析显示,24周时VKA>25°是LBP组的显著危险因素(比值比:6.24,95%置信区间:1.77 - 22.02,P = 0.004)。LBP组在治疗期间VKA出现显著差异,但PI-LL在整个治疗期间显示出无变化趋势。骨不连与VKA相关(曲线下面积:0.864)。
虽然脊柱骨盆失准被认为是LBP的一个既往存在的因素,但骨不连加剧的VKA在新的OVF后主要导致LBP。应治疗每一例OVF以限制骨折椎体进一步的形态学改变。
3级。