Obstructive sleep apnea screening with a 4-item instrument, named GOAL questionnaire

Detalhes bibliográficos
Autor(a) principal: Duarte, Ricardo L.M.
Data de Publicação: 2020
Outros Autores: Magalhães-Da-silveira, Flavio J., Oliveira-E-sá, Tiago S., Silva, Joana A., Mello, Fernanda C.Q., Gozal, David
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10362/92368
Resumo: Background: Obstructive sleep apnea (OSA) is a very prevalent disorder. Here, we aimed to develop and validate a practical questionnaire with yes-or-no answers, and to compare its performance with other well-validated instruments: No-Apnea, STOP-Bang, and NoSAS. Methods: A cross-sectional study containing consecutively selected sleep-lab subjects underwent full polysomnography. A 4-item model, named GOAL questionnaire (gender, obesity, age, and loud snoring), was developed and subsequently validated, with item-scoring of 0–4 points (≥2 points indicating high risk for OSA). Discrimination was assessed by area under the curve (AUC), while predictive parameters were calculated using contingency tables. OSA severity was classified based on conventionally accepted apnea/hypopnea index thresholds: ≥5.0/h (OSA≥5), ≥15.0/h (OSA≥15), and ≥30.0/h (OSA≥30). Results: Overall, 7377 adults were grouped into two large and independent cohorts: derivation (n = 3771) and validation (n = 3606). In the derivation cohort, screening of OSA≥5, OSA≥15, and OSA≥30 revealed that GOAL questionnaire achieved sensitivity ranging from 83.3% to 94.0% and specificity ranging from 62.4% to 38.5%. In the validation cohort, screening of OSA≥5, OSA≥15, and OSA≥30, corroborated validation steps with sensitivity ranging from 83.7% to 94.2% and specificity from 63.4% to 37.7%. In both cohorts, discriminatory ability of GOAL questionnaire for screening of OSA≥5, OSA≥15, and OSA≥30 was similar to No-Apnea, STOP-Bang or NoSAS. Conclusion: All four instruments had similar performance, leading to a possible greater practical implementation of the GOAL questionnaire, a simple instrument with only four parameters easily obtained during clinical evaluation.
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spelling Obstructive sleep apnea screening with a 4-item instrument, named GOAL questionnaireDevelopment, validation and comparative study with no-apnea, STOP-bang, and NoSASDiagnosisObstructive sleep apneaPolysomnographyQuestionnaireScreeningApplied PsychologyBehavioral NeuroscienceSDG 3 - Good Health and Well-beingBackground: Obstructive sleep apnea (OSA) is a very prevalent disorder. Here, we aimed to develop and validate a practical questionnaire with yes-or-no answers, and to compare its performance with other well-validated instruments: No-Apnea, STOP-Bang, and NoSAS. Methods: A cross-sectional study containing consecutively selected sleep-lab subjects underwent full polysomnography. A 4-item model, named GOAL questionnaire (gender, obesity, age, and loud snoring), was developed and subsequently validated, with item-scoring of 0–4 points (≥2 points indicating high risk for OSA). Discrimination was assessed by area under the curve (AUC), while predictive parameters were calculated using contingency tables. OSA severity was classified based on conventionally accepted apnea/hypopnea index thresholds: ≥5.0/h (OSA≥5), ≥15.0/h (OSA≥15), and ≥30.0/h (OSA≥30). Results: Overall, 7377 adults were grouped into two large and independent cohorts: derivation (n = 3771) and validation (n = 3606). In the derivation cohort, screening of OSA≥5, OSA≥15, and OSA≥30 revealed that GOAL questionnaire achieved sensitivity ranging from 83.3% to 94.0% and specificity ranging from 62.4% to 38.5%. In the validation cohort, screening of OSA≥5, OSA≥15, and OSA≥30, corroborated validation steps with sensitivity ranging from 83.7% to 94.2% and specificity from 63.4% to 37.7%. In both cohorts, discriminatory ability of GOAL questionnaire for screening of OSA≥5, OSA≥15, and OSA≥30 was similar to No-Apnea, STOP-Bang or NoSAS. Conclusion: All four instruments had similar performance, leading to a possible greater practical implementation of the GOAL questionnaire, a simple instrument with only four parameters easily obtained during clinical evaluation.NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)RUNDuarte, Ricardo L.M.Magalhães-Da-silveira, Flavio J.Oliveira-E-sá, Tiago S.Silva, Joana A.Mello, Fernanda C.Q.Gozal, David2020-02-06T23:45:10Z20202020-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article11application/pdfhttp://hdl.handle.net/10362/92368eng1179-1608PURE: 16702781https://doi.org/10.2147/NSS.S238255info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T04:41:11Zoai:run.unl.pt:10362/92368Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:37:31.676759Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Obstructive sleep apnea screening with a 4-item instrument, named GOAL questionnaire
Development, validation and comparative study with no-apnea, STOP-bang, and NoSAS
title Obstructive sleep apnea screening with a 4-item instrument, named GOAL questionnaire
spellingShingle Obstructive sleep apnea screening with a 4-item instrument, named GOAL questionnaire
Duarte, Ricardo L.M.
Diagnosis
Obstructive sleep apnea
Polysomnography
Questionnaire
Screening
Applied Psychology
Behavioral Neuroscience
SDG 3 - Good Health and Well-being
title_short Obstructive sleep apnea screening with a 4-item instrument, named GOAL questionnaire
title_full Obstructive sleep apnea screening with a 4-item instrument, named GOAL questionnaire
title_fullStr Obstructive sleep apnea screening with a 4-item instrument, named GOAL questionnaire
title_full_unstemmed Obstructive sleep apnea screening with a 4-item instrument, named GOAL questionnaire
title_sort Obstructive sleep apnea screening with a 4-item instrument, named GOAL questionnaire
author Duarte, Ricardo L.M.
author_facet Duarte, Ricardo L.M.
Magalhães-Da-silveira, Flavio J.
Oliveira-E-sá, Tiago S.
Silva, Joana A.
Mello, Fernanda C.Q.
Gozal, David
author_role author
author2 Magalhães-Da-silveira, Flavio J.
Oliveira-E-sá, Tiago S.
Silva, Joana A.
Mello, Fernanda C.Q.
Gozal, David
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)
RUN
dc.contributor.author.fl_str_mv Duarte, Ricardo L.M.
Magalhães-Da-silveira, Flavio J.
Oliveira-E-sá, Tiago S.
Silva, Joana A.
Mello, Fernanda C.Q.
Gozal, David
dc.subject.por.fl_str_mv Diagnosis
Obstructive sleep apnea
Polysomnography
Questionnaire
Screening
Applied Psychology
Behavioral Neuroscience
SDG 3 - Good Health and Well-being
topic Diagnosis
Obstructive sleep apnea
Polysomnography
Questionnaire
Screening
Applied Psychology
Behavioral Neuroscience
SDG 3 - Good Health and Well-being
description Background: Obstructive sleep apnea (OSA) is a very prevalent disorder. Here, we aimed to develop and validate a practical questionnaire with yes-or-no answers, and to compare its performance with other well-validated instruments: No-Apnea, STOP-Bang, and NoSAS. Methods: A cross-sectional study containing consecutively selected sleep-lab subjects underwent full polysomnography. A 4-item model, named GOAL questionnaire (gender, obesity, age, and loud snoring), was developed and subsequently validated, with item-scoring of 0–4 points (≥2 points indicating high risk for OSA). Discrimination was assessed by area under the curve (AUC), while predictive parameters were calculated using contingency tables. OSA severity was classified based on conventionally accepted apnea/hypopnea index thresholds: ≥5.0/h (OSA≥5), ≥15.0/h (OSA≥15), and ≥30.0/h (OSA≥30). Results: Overall, 7377 adults were grouped into two large and independent cohorts: derivation (n = 3771) and validation (n = 3606). In the derivation cohort, screening of OSA≥5, OSA≥15, and OSA≥30 revealed that GOAL questionnaire achieved sensitivity ranging from 83.3% to 94.0% and specificity ranging from 62.4% to 38.5%. In the validation cohort, screening of OSA≥5, OSA≥15, and OSA≥30, corroborated validation steps with sensitivity ranging from 83.7% to 94.2% and specificity from 63.4% to 37.7%. In both cohorts, discriminatory ability of GOAL questionnaire for screening of OSA≥5, OSA≥15, and OSA≥30 was similar to No-Apnea, STOP-Bang or NoSAS. Conclusion: All four instruments had similar performance, leading to a possible greater practical implementation of the GOAL questionnaire, a simple instrument with only four parameters easily obtained during clinical evaluation.
publishDate 2020
dc.date.none.fl_str_mv 2020-02-06T23:45:10Z
2020
2020-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10362/92368
url http://hdl.handle.net/10362/92368
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1179-1608
PURE: 16702781
https://doi.org/10.2147/NSS.S238255
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 11
application/pdf
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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