首页> 外文期刊>European Spine Journal >Stand-alone cage for posterior lumbar interbody fusion in the treatment of high-degree degenerative disc disease: design of a new device for an “old” technique. A prospective study on a series of 116 patients
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Stand-alone cage for posterior lumbar interbody fusion in the treatment of high-degree degenerative disc disease: design of a new device for an “old” technique. A prospective study on a series of 116 patients

机译:后腰椎椎间融合术的独立笼治疗高度退行性椎间盘疾病:一种针对“旧”技术的新设备的设计。一系列116例患者的前瞻性研究

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摘要

Chronic lumbar pain due to degenerative disc disease affects a large number of people, including those of fully active age. The usual self-repair system observed in nature is a spontaneous attempt at arthrodesis, which in most cases leads to pseudoarthrosis. In recent years, many possible surgical fusion techniques have been introduced; PLIF is one of these. Because of the growing interest in minimally invasive surgery and the unsatisfactory results reported in the literature (mainly due to the high incidence of morbidity and complications), a new titanium lumbar interbody cage (I-FLY) has been developed to achieve solid bone fusion by means of a stand-alone posterior device. The head of the cage is blunt and tapered so that it can be used as a blunt spreader, and the core is small, which facilitates self-positioning. From 2003 to 2007, 119 patients were treated for chronic lumbar discopathy (Modic grade III and Pfirrmann grade V) with I-FLY cages used as stand-alone devices. All patients were clinically evaluated preoperatively and after 1 and 2 years by means of a neurological examination, visual analogue score (VAS) and Prolo Economic and Functional Scale. Radiological results were evaluated by polyaxial computed tomography (CT) scan and flexion–extension radiography. Fusion was defined as the absence of segmental instability on flexion–extension radiography and Bridwell grade I or II on CT scan. Patients were considered clinical “responders” if VAS evaluation showed any improvement over baseline values and a Prolo value >7 was recorded. At the last follow-up examination, clinical success was deemed to have been achieved in 90.5% of patients; the rate of bone fusion was 99.1%, as evaluated by flexion–extension radiography, and 92.2%, as evaluated by CT scan. Morbidity (nerve root injury, dural lesions) and complications (subsidence and pseudoarthrosis) were minimal. PLIF by means of the stand-alone I-FLY cage can be regarded as a possible surgical treatment for chronic low-back pain due to high-degree DDD. This technique is not demanding and can be considered safe and effective, as shown by the excellent clinical and radiological success rates.
机译:退行性椎间盘疾病引起的慢性腰痛影响着很多人,包括那些完全活跃年龄的人。自然界观察到的通常的自我修复系统是自发性的关节固定尝试,在大多数情况下会导致假性关节炎。近年来,已经引入了许多可能的手术融合技术。 PLIF是其中之一。由于对微创外科手术的兴趣不断增长,并且文献报道的结果不尽人意(主要是由于发病率和并发症的发生率很高),因此开发了一种新型的钛腰椎椎间融合器(I-FLY)以通过一种独立的后部装置。保持架的头部是钝的并且是锥形的,因此可以用作钝器,并且芯子很小,便于自我定位。从2003年到2007年,使用I-FLY笼作为独立装置治疗了119例慢性腰椎间盘疾病(Modic III级和Pfirrmann V级)。术前以及术后1年和2年,通过神经系统检查,视觉模拟评分(VAS)和Prolo经济与功能量表对所有患者进行临床评估。放射学结果通过多轴计算机断层扫描(CT)扫描和屈伸X线摄影进行评估。融合定义为在屈伸影像学上不存在节段性不稳定性,而在CT扫描中不存在Bridwell I级或II级。如果VAS评估显示基线值有任何改善,且记录的Prolo值> 7,则将患者视为临床“反应者”。在最后一次随访检查中,认为90.5%的患者已取得临床成功;通过屈伸X线照相评估,骨融合率为99.1%,通过CT扫描评估为92.2%。发病率(神经根损伤,硬脑膜病变)和并发症(下陷和假性关节炎)极少。通过独立的I-FLY笼进行PLIF可以被认为是由于高度DDD而引起的慢性腰背痛的一种可能的手术治疗方法。如出色的临床和放射学成功率所示,这种技术并不苛刻,可以被认为是安全有效的。

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