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胸椎疾病的微创治疗:完全经皮和混合入路

Minimally invasive treatment of the thoracic spine disease: completely percutaneous and hybrid approaches.

作者信息

Tamburrelli Francesco Ciro, Scaramuzzo Laura, Genitiempo Maurizio, Proietti Luca

机构信息

Department of Spinal Surgery, Catholic University of Rome, lg A. Gemelli 8, 00135 Rome, Italy.

出版信息

Minim Invasive Surg. 2013;2013:508920. doi: 10.1155/2013/508920. Epub 2013 Dec 16.

Abstract

The aim of the study was to evaluate the feasibility of a limited invasive approach for the treatment of upper thoracic spine disease. Seven patients with type-A thoracic fractures and three with tumors underwent long thoracic stabilization through a minimally invasive approach. Four patients underwent a completely percutaneous approach while the other three underwent a modified hybrid technique, a combination of percutaneous and open approach. The hybrid constructs were realized using a percutaneous approach to the spine distally to the spinal lesion and by open approach proximally. In two patients, the stabilization was extended proximally up to the cervical spine. Clinical and radiographic assessment was performed during the first year after the operation at 3, 6, and 12 months. No technically related complications were seen. The postoperative recovery was rapid even in the tumor patients with neurologic impairment. Blood loss was irrelevant. At one-year follow-up there was no loosening or breakage of the screws or failure of the implants. When technically feasible a completely percutaneous approach has to be taken in consideration; otherwise, a combined open-percutaneous approach could be planned to minimize the invasivity of a completely open approach to the thoracic spine.

摘要

本研究的目的是评估有限侵入性方法治疗上胸椎疾病的可行性。7例A型胸椎骨折患者和3例肿瘤患者通过微创方法进行了长节段胸椎固定。4例患者采用完全经皮入路,另外3例采用改良混合技术,即经皮与开放入路相结合。混合固定结构是通过对脊柱病变远端采用经皮入路,近端采用开放入路实现的。2例患者的固定范围近端延伸至颈椎。术后第1年的3、6和12个月进行了临床和影像学评估。未发现与技术相关的并发症。即使是有神经功能障碍的肿瘤患者,术后恢复也很快。失血量可忽略不计。在1年随访时,未发现螺钉松动或断裂或植入物失败。在技术可行的情况下,应考虑采用完全经皮入路;否则,可以计划采用开放-经皮联合入路,以尽量减少对胸椎完全开放入路的侵入性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/286e/3876877/a84ce52d3895/MIS2013-508920.001.jpg

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