Bipolar radiofrequency volumetric tissue reduction of the inferior turbinates: evaluation of short-term efficacy in a prospective, randomized, single-blinded, placebo-controlled crossover trial
The objective of the study was to assess the short-term efficacy of radiofrequency volumetric tissue reduction (RFVTR) of the inferior turbinates in patients with nasal obstruction caused by turbinate hypertrophy. The study is a prospective, randomized, single-blinded, placebo-controlled, crossover...
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| Main Authors: | , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
2013
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| In: |
European archives of oto-rhino-laryngology and head & neck
Year: 2013, Volume: 270, Issue: 2, Pages: 595-601 |
| ISSN: | 1434-4726 |
| DOI: | 10.1007/s00405-012-2088-2 |
| Online Access: | Verlag, Volltext: http://dx.doi.org/10.1007/s00405-012-2088-2 Verlag, Volltext: https://link.springer.com/article/10.1007/s00405-012-2088-2 
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| Author Notes: | Gregor M. Bran, Sophia Hünnebeck, Raphael M. Herr, Karl Hörmann, Boris A. Stuck |
MARC
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| 245 | 1 | 0 | |a Bipolar radiofrequency volumetric tissue reduction of the inferior turbinates |b evaluation of short-term efficacy in a prospective, randomized, single-blinded, placebo-controlled crossover trial |c Gregor M. Bran, Sophia Hünnebeck, Raphael M. Herr, Karl Hörmann, Boris A. Stuck |
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| 520 | |a The objective of the study was to assess the short-term efficacy of radiofrequency volumetric tissue reduction (RFVTR) of the inferior turbinates in patients with nasal obstruction caused by turbinate hypertrophy. The study is a prospective, randomized, single-blinded, placebo-controlled, crossover trial. A total of 22 patients (age range 21-72 years; median age 41 years) were randomized into two treatment arms. Using a bipolar radiofrequency system, the first group (VP-group) received RFVTR (verum = V) first (at t1) followed by a placebo treatment (P) 6-8 weeks later (at t2). The PV-group was treated with placebo first at t1 and received RFVTR at t2. Subjects in both groups underwent identical procedures in an office-based setting. Delivery of radiofrequency energy was the only difference between the two groups. The outcome measures assessed were rhinomanometry, physician’s evaluation of the degree of hypertrophy of the inferior turbinates and patients’ estimation of nasal obstruction. Physician and patient evaluations were documented using a score ranging from 0 = none to 4 = severe. Evaluation was performed 6-8 weeks after every intervention. No intraoperative or postoperative complications occurred. Inferior turbinate hypertrophy improved significantly in both groups after RFVTR was performed (VP-group: p < 0.001; PV-group: p = 0.002). Nasal obstruction also decreased only after RFVTR (VP-group: p = 0.004, PV-group: p = 0.002). This study confirmed the safety of bipolar RFVTR as an office-based treatment of nasal obstruction due to inferior turbinate hypertrophy. We could prove that RFVTR is superior to placebo for reduction in turbinate hypertrophy and subjective improvement in nasal obstruction. To our knowledge, this is the first level I study proving the short-term efficacy of a bipolar radiofrequency system. Level of evidence 1b. | ||
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