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1.
Am J Orthod Dentofacial Orthop ; 162(4): 529-537, 2022 Oct.
Article in English | MEDLINE | ID: mdl-35842358

ABSTRACT

INTRODUCTION: This study aimed to compare the early results of gingival recession in patients with Class II malocclusion treated with Class II intermaxillary elastics and the Twin Force appliance. METHODS: The sample comprised 55 patients with Class II malocclusion treated without extraction and divided into 2 groups. Group 1 consisted of 23 patients treated with fixed appliances and Class II elastics, with mean initial age of 15.41 ± 5.65 years and a mean treatment time of 3.11 ± 0.91 years. Group 2 consisted of 32 patients treated with fixed appliances and the Twin Force mandibular protraction appliance, with a mean initial age of 18.45 ± 6.63 years and a mean treatment time of 3.17 ± 1.59 years. Dolphin software measured gingival recession in initial and final intraoral photographs. Initial and final lateral cephalograms were used to measure the position of the mandibular incisors. Intragroup and intergroup comparisons were performed by dependent and independent t tests, respectively. RESULTS: In both groups, there was no significant increase in gingival recession with orthodontic treatment, and there was significant protrusion and buccal inclination of the mandibular incisors. When changes with treatment were compared between the groups, there was no statistically significant difference in gingival recession and mandibular incisor position. CONCLUSIONS: There was no significant increase in gingival recession immediately after orthodontic treatment performed with intermaxillary elastics and the Twin Force appliance.


Subject(s)
Gingival Recession , Malocclusion, Angle Class II , Cephalometry/methods , Gingival Recession/etiology , Humans , Incisor , Malocclusion, Angle Class II/therapy , Mandible
2.
Pain Manag ; 11(5): 583-593, 2021 Sep.
Article in English | MEDLINE | ID: mdl-33980033

ABSTRACT

Aim: This prospective controlled clinical study aimed to evaluate the effect of botulinum toxin Type A (BTX-A) on pain control and quality of life (QoL) in patients with chronic myofascial pain. Materials & methods: Patients with chronic myofascial pain were randomly divided into two groups (n = 20): counseling and self-care and Michigan-type occlusal splint (MOS) (CG-control group) or BTX-A injection (BTX-AG). The pain was evaluated with visual analogue scale and QoL with the oral health impact profile-14 (OHIP-14) questionnaire. Results: In both groups, the pain was reduced, and QoL improved after 30 days. The results of social disability and handicap were better for patients treated with counseling and self-care and MOS. Conclusion: Minimally invasive strategies and BTX-A application improved QoL and alleviated myofascial pain.


Subject(s)
Botulinum Toxins, Type A , Chronic Pain , Neuromuscular Agents , Botulinum Toxins, Type A/therapeutic use , Chronic Pain/drug therapy , Humans , Injections, Intramuscular , Neuromuscular Agents/therapeutic use , Prospective Studies , Quality of Life , Treatment Outcome
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