Department of Ultrasound, First Medical Center, Chinese PLA General Hospital, Beijing, China.
Health Management Center, The Second Hospital of Dalian Medical University, Dalian, China.
Int J Hyperthermia. 2020;37(1):777-785. doi: 10.1080/02656736.2020.1778197.
To compare results in patients treated with additional radiofrequency ablation (RFA) after clinical evaluation or vital volume (Va) increase. Forty patients with 42 benign thyroid nodules who underwent additional RFA were evaluated in this retrospective study. According to the different indication for additional RFA, 18 patients were divided into Vv increase group (V group) and 22 into clinical evaluation group (C group). Patients were followed up at 1, 3, 6, 12 months and every 12 months thereafter by conventional ultrasound (US), contrast-enhancement ultrasound (CEUS) and clinical evaluation. Volume, volume reduction rate (VRR), symptom score and cosmetic score were evaluated before treatment and each ablation. After the first RFA, there were no statistically differences between two groups in volume, VRR, cosmetic and symptom scores. Compared with the first RFA, volume of all the patients after additional RFA decreased significantly ( < 0.001). In additional RFA, during a mean follow-up time of 10.15 ± 9.17 months, volume in V group was significantly smaller than in C group (2.84 ± 5.43 ml Vs 7.39 ± 13.01 ml, = 0.046). VRR in V group was significantly larger than in C group (90.18 ± 12.74% Vs 75.66 ± 26.47%, = 0.007) with significant improvement of cosmetic and symptom scores ( = 0.047; = 0.030). No complications occurred after each session ablation. Vv increase was a more reliable indicator for additional RFA than clinical evaluation. Additional RFA performed after Vv increase was more effective with respect to volume reduction and improvement of clinical outcomes. Therefore, Vv increase should be set as an indication for additional RFA.
为了比较临床评估或体积(Va)增加后接受附加射频消融(RFA)治疗的患者的结果。这项回顾性研究评估了 42 名良性甲状腺结节患者的 40 名接受附加 RFA 的患者。根据附加 RFA 的不同指征,18 名患者分为 Va 增加组(V 组)和 22 名临床评估组(C 组)。患者通过常规超声(US)、对比增强超声(CEUS)和临床评估在 1、3、6、12 个月及此后每 12 个月进行随访。在治疗前和每次消融前评估体积、体积减少率(VRR)、症状评分和美容评分。第一次 RFA 后,两组间体积、VRR、美容和症状评分无统计学差异。与第一次 RFA 相比,所有患者在附加 RFA 后体积明显减少( < 0.001)。在附加 RFA 中,在平均 10.15±9.17 个月的随访期间,V 组的体积明显小于 C 组(2.84±5.43ml Vs 7.39±13.01ml, = 0.046)。V 组的 VRR 明显大于 C 组(90.18±12.74% Vs 75.66±26.47%, = 0.007),美容和症状评分显著改善( = 0.047; = 0.030)。每次消融后均未发生并发症。Va 增加是附加 RFA 的更可靠指标,而临床评估则不是。与临床评估相比,在 Va 增加后进行的附加 RFA 对体积减少和临床结局改善更有效。因此,Va 增加应作为附加 RFA 的指征。