Long-Term Oral Appliance Therapy Improves Daytime Function and Mood in Upper Airway Resistance Syndrome Patients

Detalhes bibliográficos
Autor(a) principal: Godoy, Luciana B. M. [UNIFESP]
Data de Publicação: 2017
Outros Autores: Palombini, Luciana [UNIFESP], Poyares, Dalva [UNIFESP], Dal-Fabbro, Cibele [UNIFESP], Guimaraes, Thais Moura [UNIFESP], Klichouvicz, Priscila Calixto [UNIFESP], Tufik, Sergio [UNIFESP], Togeiro, Sonia Maria [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://repositorio.unifesp.br/handle/11600/58068
http://dx.doi.org/10.1093/sleep/zsx175
Resumo: Objectives: To evaluate the long-term effects of an oral appliance on clinical symptoms, respiratory sleep parameters, sleep quality, and sustained attention in patients with upper airway resistance syndrome (UARS) were compared with placebo. Methods: This study was a randomized placebo-controlled clinical trial. Thirty UARS patients were randomized in two groups: placebo and mandibular advancement device (MAD) groups. UARS criteria were presence of sleepiness (Epworth Sleepiness Scale >= 10) and/or fatigue (Modified Fatigue Impact Scale >= 38) associated with an apnea/hypopnea index <= 5 and a respiratory disturbance index (RDI) > 5 events/hour of sleep, and/or flow limitation in more than 30% of total sleep time. All patients completed the Pittsburgh Sleep Quality Index (PSQI), the Functional Outcomes of Sleep Questionnaire, the Beck Anxiety and Depression Inventories, underwent full-night polysomnography, multiple sleep latency test, and Psychomotor Vigilance Test (PVT). Evaluations were performed before and after 1.5 years of treatment. Results: RDI, number of respiratory effort-related arousal, percentage of total sleep time with flow limitation, and arousal index significantly decreased after 1.5 years of MAD treatment. PSQI total score improved, severity of depression symptoms decreased, and mean reaction time in the PVT, based on the first measurement taken at 8: 00 am, significantly decreased (p=.03) at the end of the protocol. Conclusions: The MAD was effective in decreasing respiratory events in UARS patients. For UARS, 1.5 years of oral appliance therapy also improved sleep quality and sustained attention, and decreased the severity of depression symptoms.
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spelling Godoy, Luciana B. M. [UNIFESP]Palombini, Luciana [UNIFESP]Poyares, Dalva [UNIFESP]Dal-Fabbro, Cibele [UNIFESP]Guimaraes, Thais Moura [UNIFESP]Klichouvicz, Priscila Calixto [UNIFESP]Tufik, Sergio [UNIFESP]Togeiro, Sonia Maria [UNIFESP]2020-09-01T13:21:03Z2020-09-01T13:21:03Z2017Sleep. Cary, v. 40, n. 12, p. -, 2017.1550-9109https://repositorio.unifesp.br/handle/11600/58068http://dx.doi.org/10.1093/sleep/zsx17510.1093/sleep/zsx175WOS:000419000600014Objectives: To evaluate the long-term effects of an oral appliance on clinical symptoms, respiratory sleep parameters, sleep quality, and sustained attention in patients with upper airway resistance syndrome (UARS) were compared with placebo. Methods: This study was a randomized placebo-controlled clinical trial. Thirty UARS patients were randomized in two groups: placebo and mandibular advancement device (MAD) groups. UARS criteria were presence of sleepiness (Epworth Sleepiness Scale >= 10) and/or fatigue (Modified Fatigue Impact Scale >= 38) associated with an apnea/hypopnea index <= 5 and a respiratory disturbance index (RDI) > 5 events/hour of sleep, and/or flow limitation in more than 30% of total sleep time. All patients completed the Pittsburgh Sleep Quality Index (PSQI), the Functional Outcomes of Sleep Questionnaire, the Beck Anxiety and Depression Inventories, underwent full-night polysomnography, multiple sleep latency test, and Psychomotor Vigilance Test (PVT). Evaluations were performed before and after 1.5 years of treatment. Results: RDI, number of respiratory effort-related arousal, percentage of total sleep time with flow limitation, and arousal index significantly decreased after 1.5 years of MAD treatment. PSQI total score improved, severity of depression symptoms decreased, and mean reaction time in the PVT, based on the first measurement taken at 8: 00 am, significantly decreased (p=.03) at the end of the protocol. Conclusions: The MAD was effective in decreasing respiratory events in UARS patients. For UARS, 1.5 years of oral appliance therapy also improved sleep quality and sustained attention, and decreased the severity of depression symptoms.Associacao Fundo de Incentivo a Pesquisa (AFIP)Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)CAPESUniv Fed Sao Paulo, Disciplina Med & Biol Sono, Dept Psicobiol, Sao Paulo, BrazilUniv Fed Sao Paulo, Disciplina Med & Biol Sono, Dept Psicobiol, Sao Paulo, BrazilWeb of Science-engOxford Univ Press IncSleepUpper airway resistance syndromefatigueexcessive daytime sleepinessmandibular advancement devicesleep disordered breathingoral appliance therapyLong-Term Oral Appliance Therapy Improves Daytime Function and Mood in Upper Airway Resistance Syndrome Patientsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleCary4012info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/580682021-10-05 21:31:28.619metadata only accessoai:repositorio.unifesp.br:11600/58068Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-05-25T12:08:38.014776Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Long-Term Oral Appliance Therapy Improves Daytime Function and Mood in Upper Airway Resistance Syndrome Patients
title Long-Term Oral Appliance Therapy Improves Daytime Function and Mood in Upper Airway Resistance Syndrome Patients
spellingShingle Long-Term Oral Appliance Therapy Improves Daytime Function and Mood in Upper Airway Resistance Syndrome Patients
Godoy, Luciana B. M. [UNIFESP]
Upper airway resistance syndrome
fatigue
excessive daytime sleepiness
mandibular advancement device
sleep disordered breathing
oral appliance therapy
title_short Long-Term Oral Appliance Therapy Improves Daytime Function and Mood in Upper Airway Resistance Syndrome Patients
title_full Long-Term Oral Appliance Therapy Improves Daytime Function and Mood in Upper Airway Resistance Syndrome Patients
title_fullStr Long-Term Oral Appliance Therapy Improves Daytime Function and Mood in Upper Airway Resistance Syndrome Patients
title_full_unstemmed Long-Term Oral Appliance Therapy Improves Daytime Function and Mood in Upper Airway Resistance Syndrome Patients
title_sort Long-Term Oral Appliance Therapy Improves Daytime Function and Mood in Upper Airway Resistance Syndrome Patients
author Godoy, Luciana B. M. [UNIFESP]
author_facet Godoy, Luciana B. M. [UNIFESP]
Palombini, Luciana [UNIFESP]
Poyares, Dalva [UNIFESP]
Dal-Fabbro, Cibele [UNIFESP]
Guimaraes, Thais Moura [UNIFESP]
Klichouvicz, Priscila Calixto [UNIFESP]
Tufik, Sergio [UNIFESP]
Togeiro, Sonia Maria [UNIFESP]
author_role author
author2 Palombini, Luciana [UNIFESP]
Poyares, Dalva [UNIFESP]
Dal-Fabbro, Cibele [UNIFESP]
Guimaraes, Thais Moura [UNIFESP]
Klichouvicz, Priscila Calixto [UNIFESP]
Tufik, Sergio [UNIFESP]
Togeiro, Sonia Maria [UNIFESP]
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Godoy, Luciana B. M. [UNIFESP]
Palombini, Luciana [UNIFESP]
Poyares, Dalva [UNIFESP]
Dal-Fabbro, Cibele [UNIFESP]
Guimaraes, Thais Moura [UNIFESP]
Klichouvicz, Priscila Calixto [UNIFESP]
Tufik, Sergio [UNIFESP]
Togeiro, Sonia Maria [UNIFESP]
dc.subject.eng.fl_str_mv Upper airway resistance syndrome
fatigue
excessive daytime sleepiness
mandibular advancement device
sleep disordered breathing
oral appliance therapy
topic Upper airway resistance syndrome
fatigue
excessive daytime sleepiness
mandibular advancement device
sleep disordered breathing
oral appliance therapy
description Objectives: To evaluate the long-term effects of an oral appliance on clinical symptoms, respiratory sleep parameters, sleep quality, and sustained attention in patients with upper airway resistance syndrome (UARS) were compared with placebo. Methods: This study was a randomized placebo-controlled clinical trial. Thirty UARS patients were randomized in two groups: placebo and mandibular advancement device (MAD) groups. UARS criteria were presence of sleepiness (Epworth Sleepiness Scale >= 10) and/or fatigue (Modified Fatigue Impact Scale >= 38) associated with an apnea/hypopnea index <= 5 and a respiratory disturbance index (RDI) > 5 events/hour of sleep, and/or flow limitation in more than 30% of total sleep time. All patients completed the Pittsburgh Sleep Quality Index (PSQI), the Functional Outcomes of Sleep Questionnaire, the Beck Anxiety and Depression Inventories, underwent full-night polysomnography, multiple sleep latency test, and Psychomotor Vigilance Test (PVT). Evaluations were performed before and after 1.5 years of treatment. Results: RDI, number of respiratory effort-related arousal, percentage of total sleep time with flow limitation, and arousal index significantly decreased after 1.5 years of MAD treatment. PSQI total score improved, severity of depression symptoms decreased, and mean reaction time in the PVT, based on the first measurement taken at 8: 00 am, significantly decreased (p=.03) at the end of the protocol. Conclusions: The MAD was effective in decreasing respiratory events in UARS patients. For UARS, 1.5 years of oral appliance therapy also improved sleep quality and sustained attention, and decreased the severity of depression symptoms.
publishDate 2017
dc.date.issued.fl_str_mv 2017
dc.date.accessioned.fl_str_mv 2020-09-01T13:21:03Z
dc.date.available.fl_str_mv 2020-09-01T13:21:03Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Sleep. Cary, v. 40, n. 12, p. -, 2017.
dc.identifier.uri.fl_str_mv https://repositorio.unifesp.br/handle/11600/58068
http://dx.doi.org/10.1093/sleep/zsx175
dc.identifier.issn.none.fl_str_mv 1550-9109
dc.identifier.doi.none.fl_str_mv 10.1093/sleep/zsx175
dc.identifier.wos.none.fl_str_mv WOS:000419000600014
identifier_str_mv Sleep. Cary, v. 40, n. 12, p. -, 2017.
1550-9109
10.1093/sleep/zsx175
WOS:000419000600014
url https://repositorio.unifesp.br/handle/11600/58068
http://dx.doi.org/10.1093/sleep/zsx175
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Sleep
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv -
dc.coverage.none.fl_str_mv Cary
dc.publisher.none.fl_str_mv Oxford Univ Press Inc
publisher.none.fl_str_mv Oxford Univ Press Inc
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
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