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A multifactorial intervention to increase adherence to oral appliance therapy with a titratable mandibular advancement device for obstructive sleep apnea: a randomized controlled trial.
Liu, Jie; Sheets, Victoria; Maerz, Rachel; Ni, Ai; Magalang, Ulysses; Ko, Ching-Chang; Firestone, Allen.
Afiliação
  • Liu J; Division of Orthodontics, The Ohio State University College of Dentistry, Room 4088, 305 W 12th Ave., Columbus, OH, 43210, USA.
  • Sheets V; Former resident Division of Orthodontics, The Ohio State University College of Dentistry, Private practice, Lexington, KY, USA.
  • Maerz R; Former resident Division of Orthodontics, The Ohio State University College of Dentistry, Private practice, Reynoldsburg, OH, USA.
  • Ni A; Division of Biostatistics, College of Public Health, The Ohio State University, Columbus, OH, USA.
  • Magalang U; Department of Internal Medicine, Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, The Wexner Medical Center, The Ohio State University, Columbus, OH, USA.
  • Ko CC; Division of Orthodontics, The Ohio State University College of Dentistry, Room 4088, 305 W 12th Ave., Columbus, OH, 43210, USA.
  • Firestone A; Division of Orthodontics, The Ohio State University College of Dentistry, Room 4088, 305 W 12th Ave., Columbus, OH, 43210, USA. firestone.17@osu.edu.
Sleep Breath ; 26(4): 1739-1745, 2022 12.
Article em En | MEDLINE | ID: mdl-35013898
PURPOSE: Obstructive sleep apnea (OSA) is a common chronic condition, associated with several conditions that account for leading causes of mortality. Adherence to treatment of a chronic condition is, along with treatment efficacy, a major determinant of treatment outcome. The aim of this study was to test whether or not a multifactorial intervention in addition to standard care increases adherence rates in patients using a titratable oral appliance for OSA. METHODS: All subjects were 18 years old or older, had a diagnosis of OSA, and were treated with an oral appliance with an embedded sensor to measure appliance wear time objectively. The control group received routine care, while the experimental subjects received an additional multifactorial intervention. Comparison of adherence was at 30 days (Phase I) and 90 days (Phase II) after appliance delivery. RESULTS: Data are reported for 82 subjects in Phase I (control 43; experimental 39) and 66 subjects in Phase II (control 36; experimental 30). There were no significant differences for age, sex, body mass index, and apnea-hypopnea index (p > 0.05) between groups. In both Phase I and Phase II, the mean number of nights the appliance was worn 4 or more hours and the mean time the appliance was worn nightly were significantly greater in the experimental than in the control group (p < 0.05). CONCLUSIONS: Interventions were well received by subjects and can be carried out by auxiliary personnel. The experimental interventions resulted in clinically important and statistically significant improvements in patient adherence to treatment.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Avanço Mandibular / Apneia Obstrutiva do Sono Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Humans Idioma: En Revista: Sleep Breath Assunto da revista: NEUROLOGIA / OTORRINOLARINGOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Avanço Mandibular / Apneia Obstrutiva do Sono Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Humans Idioma: En Revista: Sleep Breath Assunto da revista: NEUROLOGIA / OTORRINOLARINGOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos