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Enhancements to the multiple sleep latency test
INTRODUCTION: The utility of multiple sleep latency tests (MSLTs) is limited to determining sleep onset latency (SOL) and rapid eye movement sleep latency. The odds ratio product (ORP) is a continuous index of sleep depth with values of 0, 1.0, and 2.5 reflecting very deep sleep, light sleep, and fu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869791/ https://www.ncbi.nlm.nih.gov/pubmed/27274327 http://dx.doi.org/10.2147/NSS.S103596 |
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author | Meza-Vargas, Sonia Giannouli, Eleni Younes, Magdy |
author_facet | Meza-Vargas, Sonia Giannouli, Eleni Younes, Magdy |
author_sort | Meza-Vargas, Sonia |
collection | PubMed |
description | INTRODUCTION: The utility of multiple sleep latency tests (MSLTs) is limited to determining sleep onset latency (SOL) and rapid eye movement sleep latency. The odds ratio product (ORP) is a continuous index of sleep depth with values of 0, 1.0, and 2.5 reflecting very deep sleep, light sleep, and full wakefulness, respectively. We determined the time course of sleep depth during MSLT naps expecting that this would enhance the test’s clinical utility. METHODS: Thirty MSLTs (150 naps) were performed for excessive somnolence. Patients indicated whether they slept (yes/no) after each nap. SOL was scored by two experienced technologists. Time course of ORP was determined with a commercial system. We determined ORP at SOL (ORP(SOL)), times ORP decreased <2.0, <1.5, <1.0 and <0.5 during the entire nap duration, and the integral of decrease in ORP over nap duration (ΔORP(INT)). RESULTS: SOL occurred almost invariably when ORP was between 1.0 and 2.0. Of 47 naps (21 patients) with SOL <5 minutes, ORP decreased <1.0 (light sleep) in <5 minutes in only 13 naps (nine patients) and <0.5 (deep sleep) in only two naps in one patient. The relation between ORP(INT) and frequency of sleep perception was well defined, allowing determination of a threshold for sleep perception. This threshold ranged widely (5–50 ΔORP*epoch). CONCLUSION: As currently identified, SOL reflects transition into a highly unstable state between wakefulness and sleep. Reporting the times of attaining different sleep depths may help better identify patients at high risk of vigilance loss. Furthermore, an ORP(SOL) outside the range 1.0–2.0 can help identify scoring errors. |
format | Online Article Text |
id | pubmed-4869791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48697912016-06-07 Enhancements to the multiple sleep latency test Meza-Vargas, Sonia Giannouli, Eleni Younes, Magdy Nat Sci Sleep Original Research INTRODUCTION: The utility of multiple sleep latency tests (MSLTs) is limited to determining sleep onset latency (SOL) and rapid eye movement sleep latency. The odds ratio product (ORP) is a continuous index of sleep depth with values of 0, 1.0, and 2.5 reflecting very deep sleep, light sleep, and full wakefulness, respectively. We determined the time course of sleep depth during MSLT naps expecting that this would enhance the test’s clinical utility. METHODS: Thirty MSLTs (150 naps) were performed for excessive somnolence. Patients indicated whether they slept (yes/no) after each nap. SOL was scored by two experienced technologists. Time course of ORP was determined with a commercial system. We determined ORP at SOL (ORP(SOL)), times ORP decreased <2.0, <1.5, <1.0 and <0.5 during the entire nap duration, and the integral of decrease in ORP over nap duration (ΔORP(INT)). RESULTS: SOL occurred almost invariably when ORP was between 1.0 and 2.0. Of 47 naps (21 patients) with SOL <5 minutes, ORP decreased <1.0 (light sleep) in <5 minutes in only 13 naps (nine patients) and <0.5 (deep sleep) in only two naps in one patient. The relation between ORP(INT) and frequency of sleep perception was well defined, allowing determination of a threshold for sleep perception. This threshold ranged widely (5–50 ΔORP*epoch). CONCLUSION: As currently identified, SOL reflects transition into a highly unstable state between wakefulness and sleep. Reporting the times of attaining different sleep depths may help better identify patients at high risk of vigilance loss. Furthermore, an ORP(SOL) outside the range 1.0–2.0 can help identify scoring errors. Dove Medical Press 2016-05-11 /pmc/articles/PMC4869791/ /pubmed/27274327 http://dx.doi.org/10.2147/NSS.S103596 Text en © 2016 Meza-Vargas et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Meza-Vargas, Sonia Giannouli, Eleni Younes, Magdy Enhancements to the multiple sleep latency test |
title | Enhancements to the multiple sleep latency test |
title_full | Enhancements to the multiple sleep latency test |
title_fullStr | Enhancements to the multiple sleep latency test |
title_full_unstemmed | Enhancements to the multiple sleep latency test |
title_short | Enhancements to the multiple sleep latency test |
title_sort | enhancements to the multiple sleep latency test |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869791/ https://www.ncbi.nlm.nih.gov/pubmed/27274327 http://dx.doi.org/10.2147/NSS.S103596 |
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