Zeman J, Matĕjka J, Belatka J, Vodicka J
Klinika ortopedie a traumatologie pohybového Ustrojí LF UK a FN Plzen.
Rozhl Chir. 2007 May;86(5):263-7.
The authors assessed options for vertebral body replacements with the Synex telescopic expansion cage. Autologic or homologic bone grafts, a titanium "Harm's" cage or a polymethylmetacrylate filling reinforced by Kirschner wires, may be used for vertebral body replacements. The cement filling is indicated in oncological patients, the Harm's cage requires filling with a quantity of bone grafts and, with massive bone grafts, the collection place or the graft availability may be a problem. The telescopic expansion implant is fairly easy to implant, is stable and requires to be filled with a minimum of spongious grafts.
From May 2001 to November 2005, 20 telescopic Synex cages were implanted in 18 patients. Vertebral body replacements were performed 14x for acute fractures, 4x for posttraumatic kyphosis and 2x for metastatic skeletal disorder in breast and prostate tumors.
Vertebral body replacement was completed with posterior transpedicular stabilization in 14 subjects, in 5 subjects, additional anterior Ventrofix stabilization was performed. Vertebral body replacements down to the L1 level were conducted through thoracotomy or video-assissted minithoracotomy, L2-L4 replacements from lumbotomy or anterior retroperitoneal approach.
The most requently affected and operated vertebrae included the L1 (4 patients), Th12 (4 patients), Th6 (3 patients). The minimal interval between the procedure and a follow- up was 12 months. No fatal outcome has been recorded. In one patient with a vertebral body metastasis, the disorder has generalized and in a second one, no further metastatic spread has been reported. In one subject, the left-sided L4 root injury was recorded postoperatively, a cauda equina syndrome, diagnosed after the injury, persits in one subject. No signs of deep infection have been recorded. There are no records of the Synex release or displacement. Correction loss (kyphotisation) of up to 2 degrees was recorded in patients with transpedicular stabilization, in Ventrofix patients the loss was up to 5 degrees, except one case, where the loss reached 10 degrees.
One of the commonest indications for the anterior approach surgical stabilization of the spine, is the vertebral body destruction in burst fractures or posstraumatic kyphotizations of the spinal column. Unhealed or poorly healed type A and B (AO classification) pincer vertebral body fractures are other common indications for partial corpectomy and vertebral body replacements. Such fractures can be managed using posterior transpedicular stabilization. However, provided the procedure results in insufficient fracture repositioning, the anterior procedure and the anterior column reconstruction must be performed. A vertebral body can be replaced by a bone graft, a cement filling with Kirschner wiring, a traditional Harm's cage or an expansion implant. The bone graft may be autologic, which involves a disadvantage of the "donor site pain", or homologic, although a potential for reconstruction is not fully evidenced here. Implant migration into the vertebral body has been recorded in the classical titanium Harm's cage with a sharp edge without an additional endplate. Furthermore, it is a rather complicated implantation, requiring an exact implant size, which is considered another disadvantage. The expansion implant may be expanded telescopically in the very place, which is considered its biggest advantage. Furthermore, it need not be filled with bone grafts, but is applied only ventrally or laterally to the cage.
The Synex titanium expansion implant has been designed for vertebral body implantations in any indication. It requires additional stabilization, either by an anterior fixator or a cast, or a posterior transpedicular fixation. It is primarily indicated in traumatic vertebral body destructions or in reconstructions of maltreated fractures. Considering its higher price and the expected shorter patient survival period in oncological patients, its use in oncological indications is controversial.
作者评估了使用Synex伸缩式撑开融合器进行椎体置换的多种选择。自体或同种异体骨移植、钛制“哈姆斯”融合器或克氏针加固的聚甲基丙烯酸甲酯填充物,均可用于椎体置换。骨水泥填充适用于肿瘤患者,哈姆斯融合器需要填充一定量的骨移植材料,而对于大量骨移植,取材部位或移植材料的可得性可能是个问题。伸缩式撑开植入物植入相对容易,稳定性好,且只需填充少量松质骨移植材料。
2001年5月至2005年11月,18例患者植入了20个Synex伸缩式融合器。进行椎体置换的原因包括急性骨折14例、创伤后脊柱后凸4例、乳腺癌和前列腺癌转移导致的骨骼疾病2例。
14例患者通过后路经椎弓根内固定完成椎体置换,5例患者还进行了前路Ventrofix内固定。L1及以下椎体置换通过开胸手术或电视辅助小切口开胸手术进行,L2 - L4椎体置换通过腰椎切开术或前路腹膜后入路进行。
最常受累及接受手术的椎体包括L1(4例患者)、T12(4例患者)、T6(3例患者)。手术与随访的最短间隔为12个月。未记录到致命结局。1例椎体转移患者病情已扩散,另1例未报告有进一步的转移扩散。1例患者术后记录有左侧L4神经根损伤,1例患者损伤后诊断为马尾神经综合征,症状持续存在。未记录到深部感染迹象。未记录到Synex融合器松动或移位情况。经椎弓根内固定患者的矫正丢失(后凸畸形)可达2度,Ventrofix内固定患者的矫正丢失可达5度,1例患者矫正丢失达10度。
脊柱前路手术稳定的最常见适应证之一,是爆裂骨折或创伤后脊柱后凸导致的椎体破坏。未愈合或愈合不良的A型和B型(AO分类)钳夹型椎体骨折是椎体次全切除和椎体置换的其他常见适应证。此类骨折可通过后路经椎弓根内固定治疗。然而,如果该手术导致骨折复位不足,则必须进行前路手术和前柱重建。椎体可通过骨移植、克氏针加固的骨水泥填充、传统哈姆斯融合器或撑开植入物进行置换。骨移植可以是自体的,但存在“供区疼痛”的缺点,也可以是同种异体的,不过在此处其重建潜力尚未得到充分证实。在没有额外终板且边缘锋利的经典钛制哈姆斯融合器中,已记录到植入物向椎体内迁移的情况。此外,其植入过程相当复杂,需要精确的植入物尺寸匹配,这被认为是另一个缺点。撑开植入物可在原位进行伸缩撑开,这被认为是其最大优势。此外,它无需填充骨移植材料,仅在融合器腹侧或外侧使用。
Synex钛制撑开植入物设计用于各种适应证的椎体植入。它需要额外的稳定措施,可通过前路固定器或石膏,或后路经椎弓根固定。它主要适用于创伤性椎体破坏或处理不当骨折的重建。考虑到其价格较高,且肿瘤患者预期生存期较短,其在肿瘤适应证中的应用存在争议。