Wang Biao, Guo Hua, Yuan Li, Huang Dageng, Zhang Haiping, Hao Dingjun
Department of Spine Surgery, Honghui Hospital, Xi'an Jiaotong University College of Medicine, No. 76 Nanguo Road, Xi'an, 710054, Shanxi, China.
Eur Spine J. 2016 Nov;25(11):3486-3494. doi: 10.1007/s00586-016-4425-4. Epub 2016 Feb 5.
To compare the clinical and radiological outcomes of patients undergoing percutaneous vertebroplasty (PVP) versus those undergoing facet blocking (FB) for severe pain due to osteoporotic vertebral compression fractures (OVCFs).
Two hundred and six patients who had OVCFs on spine radiography and intractable back pain for ≤8 weeks were recruited between January 2009 and January 2013 (165 females and 41 males, age ≥55 years). Patients were randomly assigned to the PVP group (100 patients) or the FB group (106 patients). VAS, ODI, Roland Morris disability (RMD) scores, scores on the Standardized Physical Component of the SF-36 form (SPC) and scores on the Standardized Mental Component of the SF-36 form (SMC) were determined preoperatively and at each follow-up time (1 day, 1 week, 1, 3, 6, and 12 months). In addition, plain radiographs were obtained at 3, 6, and 12 months postoperatively to detect new fractures.
Significantly lower VAS, ODI, and RMD scores for patients in the PVP group compared to those in the FB group were observed at follow-up of 1 day and 1 week (p < 0.05). However, differences in the VAS, ODI, RMD and SPC/MCS (SF-36) scores between the two groups at follow-ups of more than 1 month were statistically insignificant (p > 0.05). Difference in numbers of new fractures in the two groups at the follow-up of 12 months was also statistically insignificant.
PVP produced better pain relief than FB in the short term (≤1 week). However, the difference in pain-relief between these two techniques was insignificant in the long term (follow-up between 1 month and 12 months).
比较经皮椎体成形术(PVP)与小关节阻滞术(FB)治疗骨质疏松性椎体压缩骨折(OVCFs)所致严重疼痛患者的临床和影像学结果。
2009年1月至2013年1月招募了206例脊柱X线片显示有OVCFs且顽固性背痛≤8周的患者(165例女性和41例男性,年龄≥55岁)。患者被随机分配到PVP组(100例患者)或FB组(106例患者)。术前及每次随访时(1天、1周、1、3、6和12个月)测定视觉模拟评分(VAS)、Oswestry功能障碍指数(ODI)、罗兰·莫里斯残疾评分(RMD)、SF-36量表标准生理成分评分(SPC)和SF-36量表标准心理成分评分(SMC)。此外,术后3、6和12个月拍摄X线平片以检测新发骨折。
在1天和1周的随访中,观察到PVP组患者的VAS、ODI和RMD评分显著低于FB组(p<0.05)。然而,两组在随访超过1个月时,VAS、ODI、RMD和SPC/MCS(SF-36)评分的差异无统计学意义(p>0.05)。两组在12个月随访时新发骨折数量的差异也无统计学意义。
短期内(≤1周),PVP比FB能更好地缓解疼痛。然而,从长期来看(随访1个月至12个月),这两种技术在缓解疼痛方面的差异不显著。