Percutaneous endoscopic laser annuloplasty for discogenic low back pain.

BACKGROUND: Laser-assisted spinal endoscopy (LASE) kit has been used for percutaneous intradiscal decompression to evaporate and shrink the posterior and central nucleus for improvement of leg and radicular pain due to contained disc herniation. Percutaneous endoscopic laser annuloplasty (PELA), a new minimally invasive technique, uses LASE to directly coagulate the inflamed disc granulation tissue associated with annular tears. The small diameter of the endoscope including Ho:YAG laser, irrigation, and light, plus the extreme posterolateral approach into the posterior annulus, enables one to minimize damage to normal nuclear tissue. The authors sought to demonstrate the safety and efficacy of PELA for controlling discogenic low back pain (DLBP) due to abnormal disc tissues, new vessels, and nerves in the central torn posterior annulus. METHODS: Clinical outcomes of PELA were investigated in patients having DLBP with an annulus-torn degenerative disc or contained disc herniation. Thirty patients treated at a single level and achieving a mean follow-up of 9.7 months were analyzed. Outcomes were assessed using the visual analog scale (VAS) for back pain, the Korean Oswestry Disability Index (KODI), and the modified Macnab's criteria. RESULTS: The mean back pain VAS score improved from 8.0 to 2.4, and the mean KODI score improved from 79.0 to 22.4 (P < .001). Results by the modified Macnab's criteria also showed a good outcome, with a success rate of 90.0%. There were no serious complications observed during follow-up. CONCLUSIONS: Percutaneous endoscopic laser annuloplasty using the Ho:YAG laser provides favorable outcomes for carefully selected groups of patients with DLBP.

Foraminoplastic ventral epidural approach for removal of extruded herniated fragment at the L5-S1 level.

The 'foraminoplastic' ventral epidural approach and its advantages in the treatment of extruded disk herniation at the L5-S1 level are described. Percutaneous endoscopic lumbar discectomy is a minimally invasive procedure applicable to various types of lumbar disk herniation, but the L5-S1 disk space is still challenging to access due to anatomic limitations such as high iliac crest or severely narrowed foramen. The 'foraminoplastic' ventral epidural approach was performed in 25 patients with herniated disk radiculopathy at L5-S1 from March 2003 to May 2004. Their mean age was 39.2 years (range 20-67 years) and the mean follow-up duration was 32.5 months (range 28-42 months). During the procedure, 'foraminoplasty' was performed by undercutting the hypertrophic superior facet with the endoscopic bone cutter under C-arm guidance. The clinical result was assessed according to the visual analogue scale (VAS) and Oswestry disability index (ODI). Preoperative mean VAS score of 7.4 for leg pain fell to 1.6 postoperatively and mean preoperative ODI of 55.5% improved to 16.9% postoperatively, both showing significant improvements (p < 0.001). Mean hospital stay was 14.2 hours. Twenty-two patients had the favorable outcomes. Two patients required conversion to open microdiscectomy due to incomplete decompression and recurrent disk herniation. The 'foraminoplastic' approach is a safe and efficient surgical option for L5-S1 disk herniation even in patients with high iliac crest and narrow foramen.

CHARITE versus ProDisc: a comparative study of a minimum 3-year follow-up.

STUDY DESIGN: A retrospective study. OBJECTIVES: To evaluate and compare clinical and radiologic outcomes of the CHARITE and ProDisc. SUMMARY OF BACKGROUND DATA: There is no clinical report comparing CHARITE and ProDisc. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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.

Early clinical and radiologic outcomes of cervical arthroplasty with Bryan Cervical Disc prosthesis.

Among 61 patients underwent disc replacement with the Bryan prosthesis, 47 patients were followed more than 3 months and their clinical and radiologic data were retrospectively analyzed to clarify very early clinical and radiologic outcomes and complications of disc arthroplasty with the Bryan Cervical Disc prosthesis during the learning period. Mean follow-up period was 6 months. Mean age was 45.6 years. Single-level procedure was done in 39 patients and 2-level in 8; a total of 55 levels replaced. Neck disability index improved from 59.8% to 22.9%. Visual analog pain score (VAS) of the neck improved from 8.4 to 1.6. VAS of shoulder/arm pain improved from 8.8 to 2.4. Mean patients' subjective improvement rate of symptoms was 71.1%. According to improvement in the neck disability index and VAS (over 50% improvement rate in each parameter), patients' subjective improvement rate (over 50%), and patients' satisfaction, the surgical success was achieved in 39 patients (83%). Eight patients (17%) showed failure. Mean segmental angle became more kyphotic after surgery from -0.7 degree of kyphosis (-11 to 7.7 degrees) to -1.3 degrees (-32 to 20.9 degrees) without statistical significance (P=0.55). Among 24 segments that showed preoperative kyphosis, 13 (54.2%) showed aggravated kyphosis, 7 (29.1%) showed decreased kyphosis and 4 (16.7%) recovered to lordosis. Among 31 segments that showed preoperative lordosis, 19 (61.3%) showed loss of lordosis and 12 (38.7%) showed increased lordosis. Mean range of motion increased significantly after surgery (6.7 to 8.5 degrees, P=0.04). Preoperative and postoperative segmental kyphosis was not related to clinical success. Cervical arthroplasty with the Bryan Cervical Disc prosthesis failed to restore segmental lordotic angle. A concern arises because it is well known that the fusion in kyphotic curvature causes more frequent problems on adjacent levels in anterior cervical discectomy and fusion. For the present, it seems preferable to exclude the patient who already has significant segmental kyphosis from disc arthroplasty with Bryan Cervical Disc prosthesis.