Guyer Richard D, Pettine Kenneth, Roh Jeffrey S, Dimmig Thomas A, Coric Domagoj, McAfee Paul C, Ohnmeiss Donna D
*Texas Back Institute, Plano, TX †Loveland Orthopedic Clinic, Loveland, CO ‡Proliance Surgeons, Seattle, WA §Triangle Orthopaedic Associates, Durham, NC ¶Carolina Neurosurgery and Spine Associates, Charlotte, NC ||Towson Orthopaedic Associates, Scoliosis and Spine Center, Towson, MD #Texas Back Institute Research Foundation, Plano, TX.
Spine (Phila Pa 1976). 2016 Jan;41(1):3-8. doi: 10.1097/BRS.0000000000001168.
This was a prospective, randomized, controlled, multicenter study.
The purpose of this study was to compare outcomes of two lumbar total disc replacements (TDRs) at 5-year follow-up and report results of serum ion level analysis in a subgroup of patients receiving a metal-on-metal implant.
Lumbar TDR has been compared with fusion in several randomized studies, finding TDR noninferior to fusion and superior on some measures. Receiving less attention has been comparing TDR devices. Additionally, there is concern about metal-on-metal implants, with little data available for spine devices.
The study included 204 patients receiving Kineflex-L (investigational) and 190 receiving CHARITÉ (control). Outcome measure included Oswestry Disability Index, visual analog pain scales (VAS), patient satisfaction, neurological status, complications, reoperations, and a composite success score. Radiographic assessment included range of motion, subsidence, and heterotrophic ossification. In 32 investigational patients, serum ion analysis was performed for cobalt and chromium. These values were compared with Medicines and Healthcare Products Regulatory Agency values to merit monitoring total hip replacement patients for potential wear problems.
Mean Oswestry and VAS scores in both groups improved significantly by 6 weeks and remained improved during 5-year follow-up (Oswestry Disability Index, scores in both groups were approximately 60 preoperatively vs. 20 at 2- and 5-year follow-up; P < 0.01; VAS scores improved >50% by 6 weeks and remained significantly improved; P < 0.05). Approximately 11% of both groups underwent reoperation. Radiographic analysis found segmental range of motion decreased at 3 month, then increased through 24 months, and was maintained thereafter. Serum ion level analysis found the greatest mean value at any follow-up point was less than 20% of Medicines and Healthcare Products Regulatory Agency recommended minimum value to merit monitoring hip replacement patients.
This prospective, randomized study comparing two TDRs found no significant differences in outcomes during 5-year follow-up. Both provided statistically significant improvements by 6 weeks that were maintained. This results support other studies. Serum ion levels in TDR patients were well below the recommended threshold levels to merit monitoring.
这是一项前瞻性、随机、对照、多中心研究。
本研究的目的是比较两种腰椎全椎间盘置换术(TDR)在5年随访时的结果,并报告接受金属对金属植入物的患者亚组的血清离子水平分析结果。
在几项随机研究中,腰椎TDR已与融合术进行了比较,发现TDR不劣于融合术,且在某些指标上更优。对TDR装置进行比较的研究较少受到关注。此外,人们对金属对金属植入物存在担忧,而脊柱装置的相关数据很少。
该研究纳入了204例接受Kineflex-L(试验性)的患者和190例接受CHARITÉ(对照)的患者。结局指标包括Oswestry功能障碍指数、视觉模拟疼痛量表(VAS)、患者满意度、神经状态、并发症、再次手术以及综合成功评分。影像学评估包括活动范围、下沉和异位骨化。对32例试验性患者进行了钴和铬的血清离子分析。将这些值与药品和医疗产品监管局的值进行比较,以评估监测全髋关节置换患者潜在磨损问题的必要性。
两组患者的平均Oswestry和VAS评分在6周时均显著改善,并在5年随访期间持续改善(Oswestry功能障碍指数,两组术前评分均约为60分,而在2年和5年随访时为20分;P<0.01;VAS评分在6周时改善>50%,并持续显著改善;P<0.05)。两组中约11%的患者接受了再次手术。影像学分析发现,节段活动范围在3个月时减小,然后在24个月内增加,并在此后保持稳定。血清离子水平分析发现,在任何随访点的最大平均值均低于药品和医疗产品监管局推荐的监测髋关节置换患者的最低值的20%。
这项比较两种TDR的前瞻性、随机研究发现,在5年随访期间,两种TDR的结果没有显著差异。两者在6周时均有统计学上的显著改善,并持续保持。这一结果支持了其他研究。TDR患者的血清离子水平远低于推荐的阈值水平,无需进行监测。