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. 2021 Jan 28;11:2568. doi: 10.1038/s41598-021-82041-6

Table 2.

Headache characteristics according to headache responder group.

Variables Headache responder (n = 8) Headache non-responder (n = 5)
Pre-OA Post-OA Pre-OA Post-OA
Frequency (days/3 month)a 6.00 (4.25–11.50)** 1.50 (0.00–2.75)** 1.00 (0.50–75.00) 3.00 (0.50–75.00)
Type (migraine, tension-type)b,d 5/8 (63%) 1/8 (13%) 3/5 (60%) 1/5 (20%)
Intensity (average)c,e 4.75 (1.75) 4.13 (3.14) 4.40 (1.52) 4.60 (2.88)
Intensity (current)c,e 2.13 (2.85) 0.38 (1.06) 3.20 (2.17) 2.40 (3.36)
Intensity (when severest)c,e 7.88 (1.64)** 4.43 (3.74)** 5.60 (1.82) 5.40 (3.13)
Duration of episode (mins)c 158.57 (110.52) 192.86 (254.47) 97.50 (51.23) 120.00 (81.24)
Morning headacheb,d 6/8 (75%) 4/8 (50%) 5/5 (100%) 3/5 (60%)
MIDAS scorea 1.00 (0.00–12.00) 1.00 (0.00–4.25) 0 (0.00–35.00) 0 (0.00–75.00)
MIDAS gradeb,d 6/8 (75%) 8/8 (100%) 3/5 (60%) 3/5 (60%)
Localization (unilateral, bilateral)b,d 8/8 (100%)* 0/8 (0%) 2/5 (40%)* 2/5 (40%)
Nausea/Vomitingb,d 3/8 (38%) 1/8 (13%) 2/5 (40%) 1/5 (20%)
Sensitivity (light, sound, smell)b,d 6/8 (75%) 3/8 (38%) 4/5 (80%) 3/5 (60%)
Autonomic symptomsb,d 4/8 (50%) 3/8 (38%) 2/5 (40%) 3/5 (60%)

Grouping was based on ≥ 30% reduction in headache frequency.

OA oral appliance.

*Significant difference: P < 0.05, comparison between headache responder and non-responder.

**Significant difference: P < 0.05, comparison between pre- and post-oral appliance treatment.

aDifferences between groups were tested with Mann–Whitney test and pre- and post-OA data were tested with Wilcoxon Rank-sum test: Median (lower quartile-upper quartile).

bDifferences between groups were tested with Chi-square test and pre- and post-OA data were tested with McNemar’s test.

cDifferences between groups were tested with t-test and pre- and post-OA data were tested with paired t-test: Mean (SD).

dResults given as number of patients with migraine, morning headaches, low disability, bilateral headache, nausea (vomiting), sensitivity, autonomic symptoms/total number of patients (percentage of patients with each characteristic).

eBased on a visual analog scale, 0 (no pain) − 10 (worst pain imaginable).