4.1 Article

Pain and discomfort during the first week of maxillary expansion using two different expanders: patient-reported outcomes in a randomized controlled trial

Journal

EUROPEAN JOURNAL OF ORTHODONTICS
Volume 45, Issue 3, Pages 271-280

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ejo/cjac067

Keywords

-

Ask authors/readers for more resources

This study evaluated the perceived pain intensity, discomfort, functional jaw impairment, and analgesic consumption in patients with unilateral posterior crossbite treated with either RME or QH appliances in the early mixed dentition. The results showed that patients in the QH group experienced higher pain from the tongue and chafe from the appliance on the first day of treatment, and the chafe from the appliance was still higher on the fourth day. Speech was affected in both groups on day 1, but the impairment was significantly higher in the RME group on days 4 and 7. There was no significant difference in analgesic consumption between the groups at any time. The majority of patients reported low to moderate pain and discomfort based on the visual analogue scale values.
Background Quad Helix (QH) is the appliance most preferred by orthodontists to correct unilateral posterior crossbite in the early mixed dentition while other orthodontists suggest rapid maxillary expansion (RME) on deciduous teeth in these patients. Objectives To evaluate and compare perceived pain intensity, discomfort, functional jaw impairment, and analgesic consumption during the first week of treatment with either RME or QH appliances. Trial design Two-arm parallel group, two-centre, randomized controlled trial. Material and methods Seventy-two patients, mean age 9.5 (SD +/- 0.8) years, with unilateral posterior crossbite requiring maxillary expansion were randomly allocated to either the RME (22 boys, 14 girls) or QH (22 boys, 14 girls) group. Validated questionnaires were used to assess pain intensity, discomfort, jaw function impairment, and analgesic consumption, on the first, fourth, and seventh days after appliance insertion and activation. Blinding Due to clinical limitations, only the outcome assessors were blinded to the groups to which the patients were allocated. Results Seventy patients completed the questionnaires. Pain from the tongue and chafe from the appliance were significantly higher in the QH group on the first day of treatment (P = 0.003 and P = 0.000, respectively). On the fourth day, the chafe from the appliance was still significantly higher in the QH group (P = 0.007). Speech was affected in both groups on day 1; this impairment continued and was significantly higher in the RME group days 4 and 7. No significant difference in analgesic consumption was found between the groups at any time. The analgesic consumption was highest at day 1 of treatment. Harms No harm was observed in any patient. Limitations Double blinding was not possible due to the clinical limitations. Conclusion During the initial 4 days of treatment, pain from the tongue and chafe from the appliance caused the most reported inconvenience in the patients in the QH group. A majority of reported visual analogue scale values were in the lower mid-range, suggesting low to moderate pain and discomfort in both groups.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.1
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available