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Evaluating the impact of various predictors on rapid maxillary expansion (RME) success
Mahmoud Mousa Aleesh1, Nada A Rajeh2, Ahmad Mousa Aleesh3
1Department of Orthodontics, University of Damascus Dental School, Al Mazzeh Street, Damascus, Syria. mahmoodalesh97@gmail.com.
Objectives:
To evaluate indicators that predict the success of rapid maxillary expansion (RME) in late adolescents using pretreatment cone-beam computed tomography (CBCT).
Materials And Methods:
A prospective clinical trial was conducted to integrate radiological and clinical evaluations with blinded outcome assessment. A total of 46 patients (18 males and 28 females) with a mean age of 15.7 ± 1.4 years were enrolled. All patients were diagnosed with posterior skeletal crossbite and underwent CBCT scans prior to rapid maxillary expansion (RME) using a bonded hyrax expander. Patients were divided into Successful (S-RME) or Failed (F-RME) groups based on midpalatal suture response four days after expansion initiation. Expansion was performed twice daily and continued until molar overcorrection, followed by a four-month fixation. Four CBCT variables (midpalatal suture maturation [MSM], Cervical vertebral maturation [CVM], midpalatal suture density [MSD], and the length and thickness of the palate), age, and sex were analyzed using t-tests, Mann-Whitney U, and chi-square. ICC evaluated random errors.
Results:
Age, maturation stage (MSM), CVM stage, MSD, and the length of the palate were all variables with a statistically significant correlation (P <.05). Sex, as well as the thickness and area of the palate, did not show significant differences between the groups (P >. 05).
Conclusions:
Patients with a higher stage of MSM and CVM had a greater risk of RME failure. Additionally, patients with a lower density ratio and shorter palate length had a better prognosis for conventional RME.
Clinical Relevance:
Choosing between traditional and surgically assisted rapid maxillary expansion (RME) is challenging, especially in late adolescents. Orthodontists should consider additional indicators to guide clinical decisions.
Clinical Trial Registration Number:
ISRCTN31077190.
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