Evaluation of pain intensity and airway changes in non-growing patients treated by MARPE with and without micro-osteoperforation: a randomized clinical trial

Abstract Trial design Parallel. Objectives To assess the effect of mini-screw assisted rapid palatal expansion (MARPE) with/without micro-osteoperforation (MOP) on the airway and pain intensity in non-growing patients with maxillary transverse deficiency. Method Two equal groups of twenty-four indiv...

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Main Authors: Moataz Elshehaby (Author), Nehal Fouad Albelasy (Author), Mohamed A. Elbialy (Author), Ahmad Mohammed Hafez (Author), Yasser Lotfy Abdelnaby (Author)
Format: Book
Published: BMC, 2024-11-01T00:00:00Z.
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MARC

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001 doaj_ca15e41f47b5452e8bd6fb98b5720bba
042 |a dc 
100 1 0 |a Moataz Elshehaby  |e author 
700 1 0 |a Nehal Fouad Albelasy  |e author 
700 1 0 |a Mohamed A. Elbialy  |e author 
700 1 0 |a Ahmad Mohammed Hafez  |e author 
700 1 0 |a Yasser Lotfy Abdelnaby  |e author 
245 0 0 |a Evaluation of pain intensity and airway changes in non-growing patients treated by MARPE with and without micro-osteoperforation: a randomized clinical trial 
260 |b BMC,   |c 2024-11-01T00:00:00Z. 
500 |a 10.1186/s12903-024-05196-4 
500 |a 1472-6831 
520 |a Abstract Trial design Parallel. Objectives To assess the effect of mini-screw assisted rapid palatal expansion (MARPE) with/without micro-osteoperforation (MOP) on the airway and pain intensity in non-growing patients with maxillary transverse deficiency. Method Two equal groups of twenty-four individuals aged ≥ 19 years old with maxillary transverse deficit were randomly assigned. MOP-facilitated MARPE was used to treat one group (MMG), and the other group was treated with MARPE without MOP (NMG). For airway evaluation, CBCT images were obtained 2 months before starting the palatal expansion and 3 months after finishing the expansion in 28 days. The Visual Analogue Scale (VAS) was used to measure the pain level. Results Significant suture opening was observed in both groups. All linear measurements of the nasal cavity and volumetric measurements of the nasal passage and oropharyngeal airway increased significantly in both groups, with no significant difference between them. Moderate pain was experienced in the first two weeks of expansion in MMG (5.11 ± 0.30), while more significant pain was recorded in NMG (6.87 ± 0.40). Pain decreased significantly in the following two weeks in MMG (2.77 ± 0.39) and in NMG (5.11 ± 0.32), with a significant difference between the two groups throughout the entire duration of expansion. Conclusion Transverse maxillary deficit was successfully treated with both expansion methods, with and without MOP, with comparable skeletal effects at the nasal levels and airway volumetric improvement. So, MOP did not provide any further advantage in improving the airway volume after maxillary expansion. However, it significantly reduced pain intensity throughout the entire duration of expansion. Trial registration The protocol registration and results system (PRS) of ClinicalTrials.gov has this RCT registered under the number NCT06502041 on 13/07/2024. 
546 |a EN 
690 |a MARPE 
690 |a Micro-osteoperforation 
690 |a Maxillary transverse deficiency 
690 |a Pain 
690 |a Airway volume 
690 |a Randomized clinical trial 
690 |a Dentistry 
690 |a RK1-715 
655 7 |a article  |2 local 
786 0 |n BMC Oral Health, Vol 24, Iss 1, Pp 1-12 (2024) 
787 0 |n https://doi.org/10.1186/s12903-024-05196-4 
787 0 |n https://doaj.org/toc/1472-6831 
856 4 1 |u https://doaj.org/article/ca15e41f47b5452e8bd6fb98b5720bba  |z Connect to this object online.