Lee Sang-Ho, Ahn Yong, Choi Won-Chul, Bhanot Arun, Shin Song-Woo
Department of Neurosurgery, Wooridul Spine Hospital, Seoul, Korea.
Photomed Laser Surg. 2006 Aug;24(4):508-13. doi: 10.1089/pho.2006.24.508.
The purpose of this study was to evaluate the long-term clinical outcome of percutaneous laser disc decompression (PLDD) for cervical disc herniation and to identify factors affecting long-term favorable outcome.
PLDD using the Ho:YAG laser has been regarded as an effective alternative for soft disc herniation. However, little is known about long-term favorable outcome parameters.
We retrospectively reviewed the clinical and radiological data of 60 patients who underwent PLDD with laser-assisted spinal endoscopy (LASE) for contained cervical soft disc herniation from January 1998 to January 2000. The clinical outcome was measured using the Macnab criteria. Statistical analysis was performed using Fisher's exact test. Sex, age, operated level and location of disc herniation, amount of laser energy, and time for symptom improvement were selected as parameters.
The mean follow-up period was 71.0 months (range, 59-83 months). The mean age was 45.7 years (range, 26-68 years), and the mean symptom duration was 13.0 months (range, 2-60 months). The Visual Analogue Scale (VAS) score was significantly improved from 7.9 preoperatively to 2.6 at the final follow-up (p < 0.001). At the final follow-up, 51 (85.0%) patients achieved a favorable outcome. Immediate (within 24 h) pain relief was achieved in 19 patients, and it was strongly related to long-term success (p = 0.006).
The long-term clinical outcome of PLDD with LASE was fairly good, with a success rate of 85%. Immediate pain relief is a useful prognostic factor predicting favorable outcome following the procedure.
本研究旨在评估经皮激光椎间盘减压术(PLDD)治疗颈椎间盘突出症的长期临床疗效,并确定影响长期良好疗效的因素。
使用钬激光的PLDD已被视为治疗软性椎间盘突出症的有效替代方法。然而,关于长期良好疗效参数的了解甚少。
我们回顾性分析了1998年1月至2000年1月期间60例行激光辅助脊柱内镜(LASE)下PLDD治疗包容性颈椎软性椎间盘突出症患者的临床和放射学资料。采用Macnab标准评估临床疗效。使用Fisher精确检验进行统计学分析。选择性别、年龄、手术节段和椎间盘突出位置、激光能量、症状改善时间作为参数。
平均随访期为71.0个月(范围59 - 83个月)。平均年龄为45.7岁(范围26 - 68岁),平均症状持续时间为13.0个月(范围2 - 60个月)。视觉模拟评分(VAS)从术前的7.9显著改善至末次随访时的2.6(p < 0.001)。在末次随访时,51例(85.0%)患者取得了良好疗效。19例患者在24小时内实现了即刻疼痛缓解,且与长期成功密切相关(p = 0.006)。
LASE辅助下PLDD的长期临床疗效相当好,成功率为85%。即刻疼痛缓解是预测该手术后良好疗效的有用预后因素。