Long-term outcomes following impedance-controlled radiofrequency ablation for the treatment of chronic rhinitis

IF 1.6 4区 医学 Q2 OTORHINOLARYNGOLOGY Laryngoscope Investigative Otolaryngology Pub Date : 2024-06-04 DOI:10.1002/lio2.1286
Douglas D. Reh MD, Kristopher Lay MD, Greg Davis MD, Marc G. Dubin MD, David M. Yen MD, Ellen M. O'Malley MS, Michael Sillers MD
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Abstract

Objective

To assess long-term safety and effectiveness of a multipoint, impedance-controlled, RF ablation device for treatment of chronic rhinitis through 12-month follow-up.

Methods

A prospective, multicenter study. Bilateral posterior nasal nerve (PNN) ablation was performed on all participants. Assessments at 6-, 9-, and 12-month visits included Visual Analog Scale Nasal Symptom Score (VAS NSS), reflective Total Nasal Symptom Score (rTNSS), mini-Rhinoconjunctivitis Quality of Life Questionnaire (mini RQLQ), and adverse events.

Results

Thirty-six participants were enrolled and 35 completed the 12-month follow-up. All 5 VAS NSS items demonstrated statistically significant improvement (p < .0001) over baseline at all 3 time points. The total rTNSS improved from 7.9 ± 1.8 at baseline to 4.3 ± 2.1 at 6-months, 3.8 ± 2.4 at 9-months, and 4.0 ± 2.1 at 12-months (all p < .0001). At 12-months, 91% (31/35) of participants had achieved the minimum clinically important difference (MCID) of a reduction from baseline of ≥1 point and 80% (28/35) of the participants met the responder criteria of ≥30% reduction from baseline. The total mean mini RQLQ was reduced from 3.0 ± 1.0 at baseline to 1.4 ± 0.8 at 6-months, 1.4 ± 1.0 at 9-months, and 1.3 ± 0.8 at 12-months (all p < .0001). At 12-months, 86% (30/35) of participants achieved the MCID of a reduction from baseline of ≥0.4 points for the mini RQLQ. No related serious adverse events occurred during the study.

Conclusions

Impedance-controlled RF ablation of the PNN is safe and resulted in durable, significant improvement in rhinitis symptoms and quality of life through 12-month follow-up.

Trial Registration

The study is registered at www.clinicaltrials.gov with the unique identifier of NCT05324397.

Level of Evidence

4.

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阻抗控制射频消融治疗慢性鼻炎后的长期疗效。
目的:评估多点阻抗控制射频消融装置治疗慢性鼻炎的长期安全性和有效性:通过 12 个月的随访,评估多点阻抗控制射频消融设备治疗慢性鼻炎的长期安全性和有效性:方法:前瞻性多中心研究。所有参与者均接受了双侧后鼻神经(PNN)消融术。6个月、9个月和12个月的随访评估包括视觉模拟量表鼻症状评分(VAS NSS)、反映性鼻症状总评分(rTNSS)、迷你鼻结膜炎生活质量问卷(mini RQLQ)和不良事件:共有 36 人参加,其中 35 人完成了为期 12 个月的随访。所有 5 个 VAS NSS 项目在统计学上都有显著改善(p p p p 结论):阻抗控制的射频消融 PNN 是安全的,在 12 个月的随访中,鼻炎症状和生活质量得到了持久、显著的改善:该研究注册于 www.clinicaltrials.gov,唯一标识符为 NCT05324397。证据级别:4:4.
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CiteScore
3.00
自引率
0.00%
发文量
245
审稿时长
11 weeks
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