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脊髓刺激器植入术后出现的不适性感觉异常和感觉障碍

Uncomfortable Paresthesia and Dysesthesia Following Tonic Spinal Cord Stimulator Implantation.

作者信息

Sethi Zubin, Aijaz Tabish, Ortega-Camacho Alvaro, Nasr Ned F, Knezevic Nebojsa Nick

机构信息

Department of Anesthesiology, Advocate Illinois Masonic Medical Center, Chicago, IL 60657, USA.

Department of Anesthesiology, University of Illinois, Chicago, IL 60607, USA.

出版信息

Brain Sci. 2025 Jun 7;15(6):616. doi: 10.3390/brainsci15060616.

Abstract

: To determine the incidence of and risk factors for uncomfortable paresthesia and/or dysesthesia after tonic percutaneous spinal cord stimulator implantation. : A retrospective analysis was conducted on the prospectively collected data of patients that had permanent percutaneous tonic spinal cord stimulators implanted. Our primary objective was to assess the prevalence of complications over a period of 24 months after the implantation of this device. : The mean post-implantation follow-up time was 27.3 months. The mean pain score before spinal cord stimulator implantation was 8.05, which was reduced to 3.6 after 24 months. The most common complications in our study sample were the need for revision and the development of unpleasant paresthesia, which were reported by 34.95% and 27.86% of patients, respectively. There was no association between paresthesia and age, sex, or body mass index (BMI). The only risk factor of statistical significance was current tobacco use ( = 0.001). : The development of uncomfortable paresthesia after SCS is associated with considerable morbidity, particularly the explantation of SCS, despite adequate pain relief. Focusing on strategies, such as appropriate waveform selection, might reduce the incidence of uncomfortable paresthesia requiring revision or explantation. Current tobacco use appears to be a significant risk factor for the development of unpleasant paresthesia/dysesthesia when compared with non-tobacco and former tobacco users after tonic percutaneous spinal cord stimulator implantation.

摘要

确定强直性经皮脊髓刺激器植入后不适性感觉异常和/或感觉障碍的发生率及危险因素。

对前瞻性收集的植入永久性经皮强直性脊髓刺激器患者的数据进行回顾性分析。我们的主要目标是评估该设备植入后24个月内并发症的发生率。

植入后的平均随访时间为27.3个月。脊髓刺激器植入前的平均疼痛评分为8.05,24个月后降至3.6。我们研究样本中最常见的并发症是需要进行翻修以及出现令人不适的感觉异常,分别有34.95%和27.86%的患者报告了这两种情况。感觉异常与年龄、性别或体重指数(BMI)之间无关联。唯一具有统计学意义的危险因素是当前吸烟(P = 0.001)。

脊髓刺激术后出现不适性感觉异常与相当高的发病率相关,尤其是脊髓刺激器的取出,尽管疼痛得到了充分缓解。关注诸如选择合适波形等策略可能会降低需要翻修或取出的不适性感觉异常的发生率。与非吸烟和既往吸烟的使用者相比,当前吸烟似乎是强直性经皮脊髓刺激器植入后出现令人不适的感觉异常/感觉障碍的一个重要危险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3225/12190327/e3040be28b51/brainsci-15-00616-g001.jpg

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