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P084 Is there a clinical role for repeating the Multiple Sleep Latency Test across childhood?

INTRODUCTION: The gold standard investigation for central disorders of hypersomnolence in children is the Multiple Sleep Latency Test (MSLT). MSLT diagnostic cut-offs are extrapolated from adult data. Currently there are no guidelines available regards the utility and timing of repeating paediatric...

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Autores principales: Nisbet, L, Nixon, G, Anantharajah, A, Davey, M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10109250/
http://dx.doi.org/10.1093/sleepadvances/zpac029.154
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author Nisbet, L
Nixon, G
Anantharajah, A
Davey, M
author_facet Nisbet, L
Nixon, G
Anantharajah, A
Davey, M
author_sort Nisbet, L
collection PubMed
description INTRODUCTION: The gold standard investigation for central disorders of hypersomnolence in children is the Multiple Sleep Latency Test (MSLT). MSLT diagnostic cut-offs are extrapolated from adult data. Currently there are no guidelines available regards the utility and timing of repeating paediatric MSLTs. METHODS: Retrospective review of children with ≥2MSLTs at our tertiary centre between 2005–2022. Narcolepsy defined as mean sleep latency (MSL) <8min with ≥2 sleep onset REM (SOREM); idiopathic hypersomnolence (IH) defined as MSL <8min with <2 SOREM. MSLTs not meeting these criteria were labelled non-diagnostic. PROGRESS: 19 children (9F) with initial non-diagnostic MSLT underwent repeat MSLT with 5 proceeding to a 3rd MSLT following 2 non-diagnostic MSLTs. Repeat MSLT resulted in diagnosis in 6/19 (32%) (3 narcolepsy, 3 IH); whereas only 1/5 3rd repeat MSLT was diagnostic (IH). Median age at initial MSLT was 7.5y (range 3.4-17.8y), with repeat after 2.9y (range 0.9-8.2y), and 3rd after 2.1 years (range 1.2-4.2y). Mean change in MSL on repeat testing was -2min (range -15.5min to +4.9min, p=0.18). MSL reduced to <10 minutes in one child, allowing access to PBS subsidised treatment. Of the 7 diagnostic repeat MSLTs, 2 had ≥2 SOREM and reduced MSL, 1 had reduced MSL (with 3 SOREM on initial and subsequent test), 4 had reduced MSL without SOREM. OUTCOME: A third of repeat MSLTs became diagnostic, suggesting repeat MSLT in childhood should be considered if clinical suspicion persists. Further work needs to address the repeat interval between MSLTs and current diagnostic cut-points in the paediatric population.
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spelling pubmed-101092502023-05-15 P084 Is there a clinical role for repeating the Multiple Sleep Latency Test across childhood? Nisbet, L Nixon, G Anantharajah, A Davey, M Sleep Adv Poster Presentations INTRODUCTION: The gold standard investigation for central disorders of hypersomnolence in children is the Multiple Sleep Latency Test (MSLT). MSLT diagnostic cut-offs are extrapolated from adult data. Currently there are no guidelines available regards the utility and timing of repeating paediatric MSLTs. METHODS: Retrospective review of children with ≥2MSLTs at our tertiary centre between 2005–2022. Narcolepsy defined as mean sleep latency (MSL) <8min with ≥2 sleep onset REM (SOREM); idiopathic hypersomnolence (IH) defined as MSL <8min with <2 SOREM. MSLTs not meeting these criteria were labelled non-diagnostic. PROGRESS: 19 children (9F) with initial non-diagnostic MSLT underwent repeat MSLT with 5 proceeding to a 3rd MSLT following 2 non-diagnostic MSLTs. Repeat MSLT resulted in diagnosis in 6/19 (32%) (3 narcolepsy, 3 IH); whereas only 1/5 3rd repeat MSLT was diagnostic (IH). Median age at initial MSLT was 7.5y (range 3.4-17.8y), with repeat after 2.9y (range 0.9-8.2y), and 3rd after 2.1 years (range 1.2-4.2y). Mean change in MSL on repeat testing was -2min (range -15.5min to +4.9min, p=0.18). MSL reduced to <10 minutes in one child, allowing access to PBS subsidised treatment. Of the 7 diagnostic repeat MSLTs, 2 had ≥2 SOREM and reduced MSL, 1 had reduced MSL (with 3 SOREM on initial and subsequent test), 4 had reduced MSL without SOREM. OUTCOME: A third of repeat MSLTs became diagnostic, suggesting repeat MSLT in childhood should be considered if clinical suspicion persists. Further work needs to address the repeat interval between MSLTs and current diagnostic cut-points in the paediatric population. Oxford University Press 2022-11-09 /pmc/articles/PMC10109250/ http://dx.doi.org/10.1093/sleepadvances/zpac029.154 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Sleep Research Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Poster Presentations
Nisbet, L
Nixon, G
Anantharajah, A
Davey, M
P084 Is there a clinical role for repeating the Multiple Sleep Latency Test across childhood?
title P084 Is there a clinical role for repeating the Multiple Sleep Latency Test across childhood?
title_full P084 Is there a clinical role for repeating the Multiple Sleep Latency Test across childhood?
title_fullStr P084 Is there a clinical role for repeating the Multiple Sleep Latency Test across childhood?
title_full_unstemmed P084 Is there a clinical role for repeating the Multiple Sleep Latency Test across childhood?
title_short P084 Is there a clinical role for repeating the Multiple Sleep Latency Test across childhood?
title_sort p084 is there a clinical role for repeating the multiple sleep latency test across childhood?
topic Poster Presentations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10109250/
http://dx.doi.org/10.1093/sleepadvances/zpac029.154
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