Frankel Bruce M, Jones Tanya, Wang Chiang
Department of Neurosurgery, Medical University of South Carolina, Charleston, South Carolina 29425, USA.
Neurosurgery. 2007 Sep;61(3):531-7; discussion 537-8. doi: 10.1227/01.NEU.0000290899.15567.68.
Instrumentation of the osteoporotic spine may result in bone failure because of pedicle screw loosening and pullout. A clinical evaluation of a novel fenestrated bone tap used in pedicle screw augmentation was performed to determine the performance and safety of this technique.
Over a 2.5-year period, the clinical and radiographic results of 119 consecutive patients who underwent instrumented arthrodesis were reviewed. Of these patients, 23 had bone softening secondary to osteoporosis and/or metastatic spinal tumor involvement. These patients underwent surgical decompression and spinal instrumentation.
Six patients (26%) had metastatic spine disease (squamous cell lung carcinoma, renal cell carcinoma, bladder carcinoma, breast, prostate, and uterine adenocarcinoma); five patients (22%) had a degenerative spondylolisthesis; and 12 patients (52%) had burst fractures, eight as a result of benign causes and four as a result of metastatic disease. Four (17%) patients underwent revision surgery of previous pedicle screw failure resulting from bone softening and pseudarthrosis. A total of 98 levels were fused using 158 polymethylmethacrylate-augmented screws. None of the patients experienced operative death, myocardial infarction, hypoxemia, intraoperative hypotension, radiculopathy, or myelopathy. Asymptomatic anterior cement extravasation was observed in nine patients (39%). There was one asymptomatic polymethylmethacrylate pulmonary embolus and one wound infection. There was no significant relationship between cement extravasation and the quantity used, levels augmented, or location (P > 0.05). There were no construct failures.
Polymethylmethacrylate-augmented pedicle screw fixation reduces the likelihood of pedicle screw loosening and pullout in patients with osteoporosis requiring instrumented arthrodesis.
由于椎弓根螺钉松动和拔出,骨质疏松性脊柱的内固定可能导致骨衰竭。对一种用于椎弓根螺钉强化的新型开窗式骨钻进行了临床评估,以确定该技术的性能和安全性。
在2.5年的时间里,回顾了119例连续接受器械辅助关节融合术患者的临床和影像学结果。在这些患者中,23例因骨质疏松和/或转移性脊柱肿瘤累及而出现骨软化。这些患者接受了手术减压和脊柱内固定。
6例(26%)患有转移性脊柱疾病(鳞状细胞肺癌、肾细胞癌、膀胱癌、乳腺癌、前列腺癌和子宫腺癌);5例(22%)患有退变性腰椎滑脱;12例(52%)患有爆裂性骨折,8例为良性原因所致,4例为转移性疾病所致。4例(17%)患者因骨软化和假关节导致先前的椎弓根螺钉失败而接受了翻修手术。总共使用158枚聚甲基丙烯酸甲酯强化螺钉融合了98个节段。所有患者均未发生手术死亡、心肌梗死、低氧血症、术中低血压、神经根病或脊髓病。9例患者(39%)观察到无症状的前路骨水泥渗漏。有1例无症状的聚甲基丙烯酸甲酯肺栓塞和1例伤口感染。骨水泥渗漏与使用量、强化节段或位置之间无显著关系(P>0.05)。没有内固定失败。
聚甲基丙烯酸甲酯强化椎弓根螺钉固定可降低需要器械辅助关节融合术的骨质疏松患者椎弓根螺钉松动和拔出的可能性。