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. 2019 Jan 3;276(4):1039–1047. doi: 10.1007/s00405-018-05270-y

Table 2.

Medium score (and interquartile range) for the Nasal Obstruction Symptom Evaluation Scale (NOSE), the Snore Outcomes Survey (SOS; selected items), the 20-Item Sino-Nasal Outcome Test, German Adapted Version (SNOT-20 GAV), the EQ-5D-5L questionnaire and parameters of disordered breathing and snoring during sleep assessed by the WatchPAT200 at study enrollment (t1) and 90 days after radiofrequency treatment (t3); sample size and significance level of the Wilcoxon signed-rank test

t 1 t 3 N p (one-tailed)
Mdn (IQR) Mdn (IQR)
Nasal Obstruction Symtom Evaluation Scale (NOSE) 65.00 (20.00) 30.00 (25.00) 31 0.000
Snore Outcomes Survey (SOS; selected items) 66.67 (31.25) 41.67 (29.17) 27 0.000
20-Item Sino-Nasal Outcome Test, German Adapted Version (SNOT-20 GAV)
 Total Score (TS) 30.00 (26.00) 19.00 (16.00) 31 0.000
 Primary Nasal Symptoms (PNS) 32.00 (28.00) 20.00 (16.00) 31 0.000
 Secondary Rhinogenic Symptoms (SRS) 20.00 (20.00) 10.00 (10.00) 31 0.000
 Generic Quality of Life (GQL) 28.89 (28.89) 20.00 (24.44) 31 0.003
EuroQoL group questionnaire for generic quality of life (EQ-5D-5L)
 Visual Analog Scale (VAS) 80.00 (22.50) 80.00 (21.00) 29 0.030
 Sum Score (SS) 95.00 (20.00) 95.00 (10.00) 31 0.033
WatchPAT200
 Apnea–Hypopnea Index (AHI) 8.21 (10.39) 8.15 (16.96) 31 0.197
 Mean snoring intensity (dB) 41.00 (1.00) 41.00 (1.00) 30 0.497
 Percent of sleeping time spent with a snoring intensity > 45 dB 2.25 (5.18) 2.45 (5.13) 30 0.237

Bold—Significance level p: probability that the difference between the data collected at the measurement time points mentioned occured randomly or by chance, but is instead attributed to the low energy radiofrequency remodeling treatment (probabilty of error α)

Statistical comparisons by Wilcoxon signed-rank test; p significance level (one-tailed) concerning the difference of scores at time points t1 and t3

Mdn median, IQR interquartile range, N number of participants