Sleep Apnea, Obstructive
Conditions
Interventions
The aim of this study is to evaluate changes in quality of life and sleep parameters in patients undergoing orthognathic surgery.This prospective study was submitted (CAAE: 63755922.4.0000.0104) and a
sleep
Patients with craniofacial syndromes
Patients with clinical conditions of chronic obstructive pulmonary disease, hypothermia, vasoconstriction, hypovolemia, peripheral vascular disease and anemia
Patients with a previous history of orthognathic surgery or any other type of airway surgery
of additional treatment for OSAHS between the evaluated periods.Patients who made continuous use of medications such as: sleep inducers, sedatives, muscle relaxants and anxiolytics. Measurements: Data
V03.175.500
Sponsors
Universidade Estadual de Maringá
Universidade Estadual de Maringá
Eligibility
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Patients from the Orthognathic Surgery Outpatient Clinic of the State University of Maringá (UEM) who underwent orthognathic surgery of the jaws between 2022 and 2023 (patients who were already going to undergo the surgery, regardless of our research) that we were able to follow up with at least , 3 months postoperatively; patients of both sexes; aged between 18 and 60 years; with or without a previous diagnosis of Obstructive Sleep Apnea and Hypopnea Syndrome (OSAS)
Exclusion criteria
Exclusion criteria: Patients using continuous positive airway pressure (CPAP); patients using an intraoral appliance for obstructive sleep apnea; patients with craniofacial syndromes; patients with clinical conditions of chronic obstructive pulmonary disease, hypothermia, vasoconstriction, hypovolemia, peripheral vascular disease and anemia; patients with a previous history of orthognathic surgery or any other type of airway surgery; patients who underwent some type of additional treatment for Obstructive Sleep Apnea and Hypopnea Syndrome (OSAS) between the evaluated periods; patients who made continuous use of medications such as: sleep inducers, sedatives, muscle relaxants and anxiolytics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find an improvement in the objective parameters of sleep quality after orthognathic surgery, which will be evaluated by type IV ultrasonography, through the IDO (oxygen desaturation index). Data will be collected before (maximum 30 days) and 3-6 months after orthognathic surgery.;It is expected to find improvement in the subjective parameters of quality of sleep and quality of life through the scores of the STOP-BANG, EPWORTH and Quality of Life of Ortho-surgical Patients questionnaires, all performed before (up to 30 days) and after (3 -6 months) orthognathic surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected. | — |
Countries
Brazil
Contacts
Public ContactWillian Jacomacci
Universidade Estadual de Maringá
Outcome results
None listed