Analysis of short-term efficacy of radiofrequency thermocoagulation in the treatment of classic trigeminal neuralgia.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Qi Wang, Wen-Jie Du
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引用次数: 1

Abstract

The objectives of the study were to explore the short-term efficacy of radiofrequency thermocoagulation for the treatment of classic trigeminal neuralgia (TGN). A retrospective analysis of 58 patients with classical TGN treated with radiofrequency thermocoagulation at our institution between 2016 and 2019, including 23 men and 35 women. The mean age of all patients was 62.1±10.9 years, the duration of the disease ranged from 2 months to 360 months, and the mean duration of the disease was 80.1±77.9 months. Patients were divided into three groups, V2, V3, and V2+V3, according to the site of symptom presenta-tion. Treatment effectiveness was evaluated by observing patients' before surgery, after surgery, and 1-year after surgery visual pain simulation (VAS) scores. The clinical efficacy was evaluated by calculating the percentage of patients whose net improve-ment in VAS scores of the three groups of patients V2, V3, and V2+V3 reached the minimal clinically important differences MCID value of TGN. Patients' after surgery VAS scores and 1-year after surgery VAS scores all showed meaningful improvement (p<0.001) compared with pre-operative VAS scores, and after surgery VAS scores showed meaningful change (p<0.05) com-pared with 1-year after surgery VAS scores. About 84.62%, 95.45%, and 86.96% of patients in V2, V3, and V2+V3 groups showed net improvement in after surgery VAS scores to MCID values, and 69.2%, 86.4%, and 74.0% of patients in 1-year after surgery VAS scores showed net improvement to MCID values, respectively. The early efficacy of radiofrequency thermocoagulation for classic TGN is significant, but patients have a tendency to have recurrence of pain symptoms 1 year after surgery.

射频热凝治疗经典三叉神经痛的近期疗效分析。
本研究旨在探讨射频热凝治疗经典三叉神经痛(TGN)的短期疗效。回顾性分析2016年至2019年我院58例经射频热凝治疗的经典TGN患者,其中男性23例,女性35例。患者平均年龄62.1±10.9岁,病程2个月~ 360个月,平均病程80.1±77.9个月。根据症状表现部位分为V2、V3、V2+V3三组。通过观察患者术前、术后及术后1年视觉疼痛模拟(VAS)评分来评价治疗效果。通过计算三组患者V2、V3、V2+V3 VAS评分净改善达到TGN临床重要差异最小值的患者百分比来评价临床疗效。患者术后VAS评分及术后1年VAS评分均有显著性改善(p
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.00
自引率
16.70%
发文量
22
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