Temperature-controlled radiofrequency tissue volume reduction of the soft palate (Somnoplasty (R)) in the treatment of habitual snoring: Results of aEuropean multicenter trial

Citation
A. Boudewyns et P. Van De Heyning, Temperature-controlled radiofrequency tissue volume reduction of the soft palate (Somnoplasty (R)) in the treatment of habitual snoring: Results of aEuropean multicenter trial, ACT OTO-LAR, 120(8), 2000, pp. 981-985
Citations number
20
Categorie Soggetti
Otolaryngology,"da verificare
Journal title
ACTA OTO-LARYNGOLOGICA
ISSN journal
00016489 → ACNP
Volume
120
Issue
8
Year of publication
2000
Pages
981 - 985
Database
ISI
SICI code
0001-6489(200010)120:8<981:TRTVRO>2.0.ZU;2-V
Abstract
Temperature-controlled radiofrequency tissue volume reduction of the soft p alate has been introduced as a minimally invasive, outpatient procedure for the treatment of habitual snoring and mild obstructive sleep apnea. A pros pective. non-randomized multi-center European clinical study was conducted to investigate the efficacy of Somnopiasty(R) in reducing snoring. Each pat ient underwent a pre- and post-treatment full-night polysomnography. TCRFe of the soft pal;lte (1 midline lesion/session) was carried out under local anesthesia with a maximum of 3 consecutive treatment sessions. Forty-Ave, n onapneic snorers (RDI 5.1 +/- 4.3, BMI 26.6 +/- 3.2 kg/m(2)) completed the protocol. A mean of 692.3 (+/- 67.7) J was delivered/treatment session. The re was a significant improvement in the snoring index 7.6 (+/- 2.1) vs 4.1 (+/- 2.9), p< 0.001 and in the Epworth Sleepiness Score 8.5 (+/- 5.0) versu s 6.0 (+/-4.3), p = 0.001. No major adverse events were reported and postop erative pain was minimal. Overall, 45% of patients had a post-treatment sno ring index <3 (success) and 84%, of the patients reported an improvement in snoring. It was concluded that Somnoplasty(R), following a protocol with I midline lesion of maximal 700 J/lesion for 1-3 treatment sessions, improve s snoring in the majority of patients. Further studies are required to inve stigate whether treatment efficacy can be improved by utilizing multiple le sions/session or by increasing the amount of energy/lesion. The absence of serious adverse events and the findings of minimal postoperative pain suppo rt the use of TCRFe (Somnoylasty(R)) as a minimally invasive surgical proce dure For snoring.