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

Bibliographic Details
Main Author: Duarte, Ricardo L.M.
Publication Date: 2020
Other Authors: Magalhães-Da-silveira, Flavio J., Oliveira-E-sá, Tiago S., Silva, Joana A., Mello, Fernanda C.Q., Gozal, David
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10362/92368
Summary: 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:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-22T17:43:22Zoai:run.unl.pt:10362/92368Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T17:14:42.522529Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
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
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10362/92368
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dc.language.iso.fl_str_mv eng
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PURE: 16702781
https://doi.org/10.2147/NSS.S238255
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