Walsh Kevin M, Machado Andre G, Krishnaney Ajit A
Department of Neurosurgery, Neurological Institute, Cleveland Clinic, 9500 Euclid Ave., S40, Cleveland, OH 44195, USA.
Department of Neurosurgery, Neurological Institute, Cleveland Clinic, 9500 Euclid Ave., S40, Cleveland, OH 44195, USA; Center for Neurological Restoration, Neurological Institute, Cleveland Clinic, 500 Euclid Ave., Cleveland, OH 44195, USA; Center for Spine Health, Neurological Institute, Cleveland Clinic, 500 Euclid Ave., Cleveland, OH 44195, USA.
Spine J. 2015 Aug 1;15(8):1864-9. doi: 10.1016/j.spinee.2015.04.043. Epub 2015 May 6.
There is currently no consensus on appropriate perioperative management of patients with spinal cord stimulator implants. Magnetic resonance imaging (MRI) is considered safe under strict labeling conditions. Electrocautery is generally not recommended in these patients but sometimes used despite known risks.
The aim was to discuss the perioperative evaluation and management of patients with spinal cord stimulator implants.
A literature review, summary of device labeling, and editorial were performed, regarding the safety of spinal cord stimulator devices in the perioperative setting.
A literature review was performed, and the labeling of each Food and Drug Administration (FDA)-approved spinal cord stimulation system was reviewed. The literature review was performed using PubMed and the FDA website (www.fda.gov).
Magnetic resonance imaging safety recommendations vary between the models. Certain systems allow for MRI of the brain to be performed, and only one system allows for MRI of the body to be performed, both under strict labeling conditions. Before an MRI is performed, it is imperative to ascertain that the system is intact, without any lead breaks or low impedances, as these can result in heating of the spinal cord stimulation (SCS) and injury to the patient. Monopolar electrocautery is generally not recommended for patients with SCS; however, in some circumstances, it is used when deemed required by the surgeon. When cautery is necessary, bipolar electrocautery is recommended. Modern electrocautery units are to be used with caution as there remains a risk of thermal injury to the tissue in contact with the SCS. As with MRI, electrocautery usage in patients with SCS systems with suspected breaks or abnormal impedances is unsafe and may cause injury to the patient.
Spinal cord stimulation is increasingly used in patients with pain of spinal origin, particularly to manage postlaminectomy syndrome. Knowledge of the safety concerns of SCS and appropriate perioperative evaluation and management of the SCS system can reduce risks and improve surgical planning.
目前对于脊髓刺激器植入患者的围手术期管理尚无共识。在严格的标签条件下,磁共振成像(MRI)被认为是安全的。电灼术一般不推荐用于这些患者,但尽管存在已知风险,有时仍会使用。
旨在讨论脊髓刺激器植入患者的围手术期评估与管理。
进行了一项关于脊髓刺激器设备在围手术期安全性的文献综述、设备标签总结及编辑评论。
进行了文献综述,并查阅了美国食品药品监督管理局(FDA)批准的每个脊髓刺激系统的标签。文献综述使用PubMed和FDA网站(www.fda.gov)进行。
不同型号的MRI安全建议有所不同。某些系统允许在严格的标签条件下进行脑部MRI检查,只有一个系统允许进行身体MRI检查。在进行MRI之前,必须确定系统完好无损,没有任何导线断裂或低阻抗情况,因为这些可能导致脊髓刺激(SCS)发热并对患者造成伤害。一般不建议对脊髓刺激患者使用单极电灼术;然而,在某些情况下,外科医生认为必要时会使用。当需要电灼时,建议使用双极电灼术。使用现代电灼设备时要谨慎,因为与脊髓刺激系统接触的组织仍有热损伤风险。与MRI一样,在怀疑有断裂或阻抗异常的脊髓刺激系统患者中使用电灼术是不安全的,可能会对患者造成伤害。
脊髓刺激在脊髓源性疼痛患者中越来越多地被使用,特别是用于治疗椎板切除术后综合征。了解脊髓刺激系统的安全问题以及对其进行适当的围手术期评估和管理可以降低风险并改善手术规划。