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Cotrel–Dubousset instrumentation in neuromuscular scoliosis

机译:神经肌肉脊柱侧弯的Cotrel–Dubousset仪器

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The study design is retrospective. The aim is to describe our experience about the treatment of patients with neuromuscular scoliosis (NMS) using Cotrel–Dubousset instrumentation. Neuromuscular scoliosis are difficult deformities to treat. A careful assessment and an understanding of the primary disease and its prognosis are essential for planning treatment which is aimed at maximizing function. These patients may have pelvic obliquity, dislocation of the hip, limited balance or ability to sit, back pain, and, in some cases, a serious decrease in pulmonary function. Spinal deformity is difficult to control with a brace, and it may progress even after skeletal maturity has been reached. Surgery is the main stay of treatment for selected patients. The goals of surgery are to correct the deformity producing a balanced spine with a level pelvis and a solid spinal fusion to prevent or delay secondary respiratory complications. The instrumented spinal fusion (ISF) with second-generation instrumentation (e.g., Luque–Galveston and unit rod constructs), are until 1990s considered the gold standard surgical technique for neuromuscular scoliosis (NMS). Still in 2008 Tsirikos et al. said that “the Unit rod instrumentation is a common standard technique and the primary instrumentation system for the treatment of pediatric patients with cerebral palsy and neuromuscular scoliosis because it is simple to use, it is considerably less expensive than most other systems, and can achieve good deformity correction with a low loss of correction, as well as a low prevalence of associated complications and a low reoperation rate.” In spite of the Cotrel–Dubousset (CD) surgical technique, used since the beginning of the mid 1980s, being already considered the highest level achieved in correction of scoliosis by a posterior approach, Teli et al., in 2006, said that reports are lacking on the results of third-generation instrumentation for the treatment of NMS. Patients with neuromuscular disease and spinal deformity treated between 1984 and 2008 consecutively by the senior author (G.D.G.) with Cotrel–Dubousset instrumentation and minimum 36 months follow-up were reviewed, evaluating correction of coronal deformity, sagittal balance and pelvic obliquity, and rate of complications. 24 patients (Friedreich’s ataxia, 1; cerebral palsy, 14; muscular dystrophy, 2; polio, 2; syringomyelia, 3; spinal atrophy, 2) were included. According the evidence that the study period is too long (1984–2008) and that in more than 20 years many things changed in surgical strategy and techniques, all patients were divided in two groups: only hooks (8 patients) or hybrid construct (16 patients). Mean age was 18.1 years at surgery (range 11 years 7 months–max 31 years; in 17 cases the age at surgery time was between 10 and 20 years old; in 6 cases it was between 20 and 30 and only in 1 case was over 30 years old). Mean follow-up was 142 months (range 36–279). The most frequent patterns of scoliosis were thoracic (10 cases) and thoracolumbar (9 cases). In 8 cases we had hypokyphosis, in 6 normal kyphosis and in 9 hyperkyphosis. In 8 cases we had a normal lordosis, in 11 a hypolordosis and in 4 a hyperlordosis. In 1 case we had global T4–L4 kyphosis. In 8 cases there were also a thoracolumbar kyphosis (mean value 24°, min 20°–max 35°). The mean fusion area included 13 vertebrae (range 6–19); in 17 cases the upper end vertebra was over T4 and in 11 cases the lower end vertebra was over L4 or L5. In 7 cases the lower end vertebra was S1 to correct the pelvic obliquity. In 5 cases the severity of the deformity (mean Cobb’s angle 84.2°) imposed a preoperative halo traction treatment. There were 5 anteroposterior and 19 posterior-only procedures. In 10 cases, with low bone quality, the arthrodesis was performed using iliac grafting technique while in the other (14 cases) using autologous bone graft obtained in situ from vertebral arches and spinous processes (in all 7 cases with fusion extended until S1, it was augmented with calcium phosphate). The mean correction of coronal deformity and pelvic obliquity averaged, respectively, 57.2% (min 31.8%; max 84.8%) and 58.9% (mean value preoperative, 18.43°; mean value postoperative, 7.57°; mean value at last follow-up, 7.57°). The sagittal balance was always restored, reducing hypo or hyperkyphosis and hypo or hyperlordosis. Also in presence of a global kyphosis, we observed a very good restoration (preoperatory, 65°; postoperatory, 18° kyphosis and 30° lordosis, unmodified at last f.u.). The thoracolumbar kyphosis, when present (33.3% of our group) was always corrected to physiological values (mean 2°, min 0°–max 5°). The mean intraoperative blood lost were 2,100 cc (min 1,400, max 5,350). Major complications affected 8.3% of patients, and included 1 postoperative death and 1 deep infection. Minor complications affected none of patients. CD technique provides lasting correction of spinal deformity in patients with neuromuscular scoliosis, with a lower complications rate compared to reports on second-generation instrumented spinal fusion.
机译:研究设计是回顾性的。目的是描述我们使用Cotrel–Dubousset仪器治疗神经肌肉性脊柱侧凸(NMS)的经验。神经肌肉性脊柱侧弯很难治疗。对原发疾病及其预后的仔细评估和理解对于计划旨在最大化功能的治疗至关重要。这些患者可能有盆腔倾斜,髋关节脱位,平衡能力有限或坐姿,背部疼痛,在某些情况下,肺功能严重下降。用撑杆很难控制脊柱畸形,即使已经达到骨骼成熟,脊柱畸形也可能进展。外科手术是某些患者的主要治疗方法。手术的目的是纠正畸形,使脊柱平衡,骨盆水平,并进行牢固的脊柱融合术,以预防或延迟继发性呼吸系统并发症。具有第二代仪器(例如Luque–Galveston和单位棒结构)的仪器化脊柱融合术(ISF)一直被认为是1990年代神经肌肉性脊柱侧弯(NMS)的金标准手术技术。仍然在2008年,Tsirikos等人。他说:“ Unit Rod仪器是一种通用的标准技术,是治疗小儿脑瘫和神经肌肉性脊柱侧弯患者的主要仪器系统,因为它使用简单,比大多数其他系统便宜得多,并且可以取得良好的效果。畸形矫正,矫正损失少,相关并发症的患病率低,再手术率低。”尽管自1980年代中期以来一直使用的Cotrel-Dubousset(CD)外科手术技术,Teli等人在2006年已被认为是通过后路入路矫正脊柱侧弯所达到的最高水平,但据报道,缺乏用于NMS的第三代仪器的结果。回顾了1984年至2008年间由资深作者(GDG)连续使用Cotrel–Dubousset仪器治疗的神经肌肉疾病和脊柱畸形患者,并进行了至少36个月的随访,评估了冠状畸形,矢状位平衡和骨盆倾斜的矫正率以及并发症。其中包括24例患者(弗里德里希共济失调1例;脑瘫14例;肌肉营养不良2例;小儿麻痹症2例;脊髓空洞症3例;脊髓萎缩2例)。根据研究时间过长的证据(1984年至2008年),并且在20多年的时间里,手术策略和技术发生了许多变化,所有患者均分为两组:仅钩(8例)或混合结构(16例)耐心)。手术的平均年龄为18.1岁(范围11岁7个月至最大31岁;在17例中,手术时间在10至20岁之间;在6例中,在20至30岁之间,只有1例在30岁)。平均随访142个月(范围36-279)。脊柱侧弯最常见的类型是胸廓(10例)和胸腰椎(9例)。在8例我们有后凸畸形,6例正常后凸畸形和9例后凸畸形中。在8例中,我们患有正常的脊柱前凸,在11例中为垂毛病,在4例中为高囊病。在1例中,我们有全身性T4–L4后凸。在8例中,还有胸腰椎后凸畸形(平均值24°,最小20°-最大35°)。平均融合区域包括13个椎骨(范围6–19);每个椎骨的融合区域为5个。在17例中,上端椎骨超过T4,在11例中,下端椎骨超过L4或L5。在7例中,下端椎骨为S1以矫正骨盆倾斜。在5例畸形的严重程度(平均Cobb角为84.2°)下,术前进行了光晕牵引治疗。前后5例,仅后侧19例。在10例骨质量低下的患者中,采用骨移植技术进行了关节固定术,而其他14例患者则采用了从椎弓根和棘突原位获得的自体骨移植物(所有7例融合持续至S1,加入磷酸钙)。冠状畸形和骨盆倾斜度的平均矫正分别平均为57.2%(最小31.8%;最大84.8%)和58.9%(术前平均值18.43°;术后平均值7.57°;上次随访平均值) 7.57°)。矢状面平衡始终得以恢复,减少了后凸或后凸畸形以及前凸或下凸畸形。同样在存在整体性后凸畸形的情况下,我们观察到非常好的恢复(术前65°;术后18°后凸和30°前凸,最后一次未改变)。出现胸腰椎后凸畸形(占本组病例的33.3%)时,始终校正为生理值(平均2°,最小0°-最大5°)。术中平均失血量为2,100 cc(最小1,400 cc,最大5,350 cc)。主要并发症影响了8.3%的患者,包括1例术后死亡和1例深层感染。轻微并发症未影响任何患者。 CD技术可为神经肌肉性脊柱侧凸患者提供脊柱畸形的持久矫正,与第二代器械性脊柱融合术的报道相比,并发症发生率更低。

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