Song Kun-Peng, Zhang Bin, Ma Ju-Lei, Wang Bing, Chen Bo
Department of Orthopaedics, People's Hospital of Beilun District, the First Affiliated Hospital of Zhejiang University School of Medicine, Ningbo 315800, Zhejiang, China.
Department of Orthopaedics, People's Hospital of Beilun District, the First Affiliated Hospital of Zhejiang University School of Medicine, Ningbo 315800, Zhejiang, China;
Zhongguo Gu Shang. 2019 Nov 25;32(11):991-996. doi: 10.3969/j.issn.1003-0034.2019.11.004.
To explore mid-term clinical efficacy and effect on adjacent segment degeneration of Wallis and Coflex interspinous implants for lumbar degenerative diseases.
From January 2011 to January 2013, 55 patients with L4, 5 degenerative lumbar spine diseases treated with interspinous devices were retrospectively analyzed, including 31 males and 24 females aged from 25 to 67 years old with an average of 43.3 years old; 21 patients were lumbar spinal stenosis and 34 patients were lumbar disc herniation. All patients were divided into Wallis group (33 cases) and Coflex group (22 cases) according to the interspinous fixation system. Visual analogue scale(VAS) was used to evaluate low back pain and lower limb pain, Japanese Orthopedic Association(JOA) score and Oswestry Disability Index(ODI) score were used to evaluate lumbar function. Surgical segment and adjacent segments, range of motion(ROM), disc height and the Pfirrmann grade of upper the adjacent segments were compared before and after operation.
Fifty-five patients were followed up from 48 to 72 months with an average of 60.4 months. VAS score of low back pain and lower limb pain, JOA and ODI score of lumbar at 48 months after operation were improved than before operation between two groups(<0.01), but there was no statistical difference for group comparisons(>0.05). ROM, disc height of surgical segments were significantly lower than those before operation between two groups (<0.05), while ROM of the upper and lower adjacent segments and disc height did not change significantly (>0.05). There was no significant difference in ROM and disc height for group comparisons(>0.05). There was no change in Pfirrmann grade of the upper adjacent segment degeneration between two groups(>0.05). Four patients with primary lumbar disc herniation had a recurrence of 1 to 3 years after operation, including 3 in Wallis group and 1 in Coflex group, with an average age of 35.2 years old.
Wallis and Coflex interspinous implants have the similar mid-term efficacy for the treatment of lumbar degenerative diseases, and could delay adjacent segment degeneration, but could not prevent recurrence of disc herniation.
探讨Wallis和Coflex棘突间植入物治疗腰椎退行性疾病的中期临床疗效及对相邻节段退变的影响。
回顾性分析2011年1月至2013年1月采用棘突间装置治疗的55例L4、5节段腰椎退行性疾病患者,其中男31例,女24例,年龄25~67岁,平均43.3岁;腰椎管狭窄症21例,腰椎间盘突出症34例。根据棘突间固定系统将所有患者分为Wallis组(33例)和Coflex组(22例)。采用视觉模拟评分法(VAS)评估腰痛和下肢疼痛,采用日本骨科学会(JOA)评分和Oswestry功能障碍指数(ODI)评分评估腰椎功能。比较手术节段及相邻节段术前、术后的活动度(ROM)、椎间盘高度及相邻节段上位椎间盘的Pfirrmann分级。
55例患者随访48~72个月,平均60.4个月。两组术后48个月时腰痛和下肢疼痛的VAS评分、腰椎JOA和ODI评分均较术前改善(<0.01),但组间比较差异无统计学意义(>0.05)。两组手术节段的ROM、椎间盘高度均较术前显著降低(<0.05),而相邻节段上位和下位的ROM及椎间盘高度无明显变化(>0.05)。组间ROM和椎间盘高度比较差异无统计学意义(>0.05)。两组相邻节段上位椎间盘退变的Pfirrmann分级无变化(>0.05)。4例原发性腰椎间盘突出症患者术后1~3年复发,其中Wallis组3例,Coflex组1例,平均年龄35.2岁。
Wallis和Coflex棘突间植入物治疗腰椎退行性疾病的中期疗效相似,可延缓相邻节段退变,但不能预防椎间盘突出症复发。