Patient-reported symptom relief from percutaneous benign thyroid nodule radiofrequency ablation in routine clinical care.

Michelle Mai, Vincent M Levesque, Ellen Marqusee, Matthew I Kim, Jeffrey P Guenette
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Abstract

Background and purpose: We investigated patient-reported symptom relief from percutaneous ultrasound-guided radiofrequency ablation of benign thyroid nodules in routine clinical care, given that prior studies have reported efficacy based on size reduction and specific symptom scores but not patient-reported effectiveness.

Materials and methods: This retrospective cohort study included all consecutive adults treated 5/12/2021-8/7/2024 with ultrasound-guided radiofrequency ablation for symptomatic benign thyroid nodules at a quaternary care hospital. Procedures were performed by a single board certified neuroradiologist utilizing a trans-isthmus moving shot technique. Patient-reported symptom relief (symptoms resolved yes/no) was assessed at 6-month routine clinical follow-up. Descriptive statistics were performed. Pre-ablation nodule size associations with symptom resolution were assessed with Wilcoxon tests.

Results: 49 patients (mean age 56.6±13.1 years; 45 females) had average pre-ablation nodule volume of 30.6±31.0 mL, higher than 20.1±22.4 mL reported in a recent meta-analysis of efficacy studies. Common pre-ablation symptoms were cosmetic deformity (37/49, 77.1%), dysphagia (28/49, 58.3%), and dysphonia (15/49, 30.6%). Thirty-six patients (73.0%) completed at least one follow-up visit. Post-ablation symptom resolution was 78.0% (28/36, 95%CI 61.9%-88.3%) among those with follow-up, higher than the 64.4% reported in the single study included in the meta-analysis that assessed subjective symptom relief. Relative mean volume reduction was 52.3±27.4% in those with follow-up and was associated with symptom resolution (59% reduction with symptom resolution vs. 30% without, p=0.035). One patient experienced a minor bleeding complication.

Conclusions: Patient-reported symptom relief from percutaneous ultrasound-guided thermal ablation of benign thyroid nodules in our clinic has resulted in approximately 80% clinically-relevant effectiveness based on patient-reported symptom relief, with a slightly lower volume reduction rate compared to those reported in efficacy studies. Our clinic patients had larger nodule volumes than typical in published studies and many patients opted to forgo post-treatment follow-up. This likely led to underestimation of our effectiveness and volume reduction measurements.

Abbreviations: RFA= radiofrequency ablation; BTN= benign thyroid nodule; VAS= visual analog scale; VRR= volume reduction ratio; TSH = thyroid stimulating hormone; LA= laser ablation; MWA= microwave ablation.

常规临床护理中经皮良性甲状腺结节射频消融后患者报告的症状缓解。
背景和目的:我们调查了常规临床护理中经皮超声引导的良性甲状腺结节射频消融的患者报告的症状缓解情况,考虑到先前的研究报告的疗效是基于体积缩小和特定症状评分,而不是患者报告的有效性。材料和方法:本回顾性队列研究纳入了所有连续的成年人,于2021年5月12日至2024年8月7日在一家第四护理医院接受超声引导射频消融治疗症状性良性甲状腺结节。手术由一名经过认证的神经放射学家使用峡部移动射击技术进行。在6个月的常规临床随访中评估患者报告的症状缓解(症状缓解是/否)。进行描述性统计。使用Wilcoxon试验评估消融前结节大小与症状缓解的关系。结果:49例患者(平均年龄56.6±13.1岁,女性45例)消融前平均结节体积为30.6±31.0 mL,高于近期疗效研究荟萃分析报告的20.1±22.4 mL。消融前常见的症状为外观畸形(37/49,77.1%)、吞咽困难(28/49,58.3%)和发音困难(15/49,30.6%)。36例患者(73.0%)完成了至少一次随访。在随访患者中,消融后症状缓解率为78.0% (28/36,95%CI 61.9%-88.3%),高于meta分析中评估主观症状缓解的单一研究报告的64.4%。随访患者的相对平均体积减少为52.3±27.4%,与症状缓解相关(症状缓解组减少59%,未随访组减少30%,p=0.035)。一名患者出现了轻微的出血并发症。结论:在我们的临床中,患者报告的经皮超声引导下良性甲状腺结节热消融的症状缓解,基于患者报告的症状缓解,产生了大约80%的临床相关有效性,与疗效研究报告的体积缩小率相比,体积缩小率略低。我们的临床患者比发表的研究中典型的结节体积更大,许多患者选择放弃治疗后随访。这可能导致低估我们的有效性和体积减少测量。缩写词:RFA=射频消融;BTN=良性甲状腺结节;视觉模拟量表;VRR=体积缩小比;促甲状腺激素;LA=激光消融;微波消融。
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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