Shim Chan Shik, Lee Sang-Ho, Shin Ho-Dong, Kang Han Sug, Choi Won-Chul, Jung Byungjoo, Choi Gun, Ahn Yong, Lee Seungcheol, Lee Ho Yeon
Department of Neurosurgery, Wooridul Spine Hospital, Seoul, Korea.
Spine (Phila Pa 1976). 2007 Apr 20;32(9):1012-8. doi: 10.1097/01.brs.0000260795.57798.a0.
A retrospective study.
To evaluate and compare clinical and radiologic outcomes of the CHARITE and ProDisc.
There is no clinical report comparing CHARITE and ProDisc.
Among a total of 61 patients who underwent total disc replacement, 57 patients followed more than 3 years were enrolled. The CHARITE was used in 33 patients and ProDisc in 24. MRI follow-up was possible in 52 patients. Clinical and radiologic data including range of motion (ROM) and facet degeneration of the replaced segment, and degeneration of the disc at the adjacent level were evaluated.
Mean percentage improvement of Oswestry Disability Index (ODI) score was 78.9% in the CHARITE group and 75.8% in ProDisc group. The mean improvement of the Visual Analogue Scale (VAS) pain score was 72% in the CHARITE and 74.2% in ProDisc. There was no statistical difference between 2 groups in improvement rates either of the ODI scores and VAS scores. Degradation of the facets was seen in 36.4% of the CHARITE and 32% of the ProDisc. Degradation of disc degeneration at the adjacent level above the index level was seen in 19.4% in the CHARITE and 28.6% in the ProDisc. The degradation rates of facet joints and disc at adjacent segment between the 2 groups were not significantly different. Segmental ROM of the replaced segments was well preserved, but ROM of L5-S1 of the ProDisc was significantly less than that of the CHARITE.
While clinical outcomes of both CHARITE and ProDisc groups were fairly good, the facet joint of the index level and the disc at the adjacent level showed an aggravation of the degenerative process in a significant number of patients, regardless of the device used, raising concerns of possible late consequences of total disc replacement, especially regarding facet arthrosis and adjacent segment disease.
一项回顾性研究。
评估并比较CHARITE人工椎间盘和ProDisc人工椎间盘的临床及影像学结果。
尚无比较CHARITE和ProDisc的临床报告。
在总共61例行全椎间盘置换术的患者中,纳入57例随访超过3年的患者。其中33例患者使用CHARITE人工椎间盘,24例使用ProDisc人工椎间盘。52例患者可行MRI随访。评估临床和影像学数据,包括置换节段的活动度(ROM)、小关节退变情况以及相邻节段椎间盘退变情况。
CHARITE组Oswestry功能障碍指数(ODI)评分的平均改善百分比为78.9%,ProDisc组为75.8%。视觉模拟评分法(VAS)疼痛评分的平均改善率在CHARITE组为72%,在ProDisc组为74.2%。两组在ODI评分和VAS评分的改善率方面无统计学差异。CHARITE组36.4%的患者出现小关节退变,ProDisc组为32%。在CHARITE组,指数节段上方相邻节段椎间盘退变的发生率为19.4%,ProDisc组为28.6%。两组相邻节段小关节和椎间盘的退变率无显著差异。置换节段的节段性ROM保存良好,但ProDisc的L5-S1节段ROM明显低于CHARITE。
虽然CHARITE组和ProDisc组的临床结果都相当不错,但无论使用哪种器械,相当一部分患者的指数节段小关节和相邻节段椎间盘都出现了退变过程的加重,这引发了对全椎间盘置换术可能产生的晚期后果的担忧,尤其是关于小关节病和相邻节段疾病。