Obstructive sleep apnea screening with a 4-item instrument, named GOAL questionnaire
Main Author: | |
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Publication Date: | 2020 |
Other Authors: | , , , , |
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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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 |
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.uri.fl_str_mv |
http://hdl.handle.net/10362/92368 |
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http://hdl.handle.net/10362/92368 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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1179-1608 PURE: 16702781 https://doi.org/10.2147/NSS.S238255 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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11 application/pdf |
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