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ROHHAD syndrome and evolution of sleep disordered breathing
BACKGROUND: Rapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulation (ROHHAD) is a rare disease with a high mortality rate. Although nocturnal hypoventilation (NH) is central to ROHHAD, the evolution of sleep disordered breathing (SDB) is not well studied. The a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967322/ https://www.ncbi.nlm.nih.gov/pubmed/27473663 http://dx.doi.org/10.1186/s13023-016-0484-1 |
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author | Reppucci, Diana Hamilton, Jill Yeh, E Ann Katz, Sherri Al-Saleh, Suhail Narang, Indra |
author_facet | Reppucci, Diana Hamilton, Jill Yeh, E Ann Katz, Sherri Al-Saleh, Suhail Narang, Indra |
author_sort | Reppucci, Diana |
collection | PubMed |
description | BACKGROUND: Rapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulation (ROHHAD) is a rare disease with a high mortality rate. Although nocturnal hypoventilation (NH) is central to ROHHAD, the evolution of sleep disordered breathing (SDB) is not well studied. The aim of the study was to assess early manifestations of SDB and their evolution in ROHHAD syndrome. METHODS: Retrospective study of children with ROHHAD at two Canadian centers. All children with suspected ROHHAD at presentation underwent polysomnography (PSG) to screen for nocturnal hypoventilation. PSG findings at baseline and follow-up were collected. Interventions and diagnostic test results were recorded. RESULTS: Six children were included. The median age of rapid onset obesity and nocturnal hypoventilation (NH) was 3.5 and 7.2 years respectively. On initial screening for ROHHAD 4/6 (66.7 %) children had obstructive sleep apnea (OSA), 1/6 (16.7 %) had NH and 1/6 (16.7 %) had both OSA and NH. Follow up PSGs were performed in 5/6 children as one child died following a cardiorespiratory arrest. All children at follow up had NH and required non-invasive positive pressure ventilation. Additionally, 3/6 (50 %) children demonstrated irregular breathing patterns during wakefulness. CONCLUSIONS: Children with ROHHAD may initially present with OSA and only develop NH later as well as dysregulation of breathing during wakefulness. The recognition of the spectrum of respiratory abnormalities at presentation and over time may be important in raising the index of suspicion of ROHHAD. Early recognition and targeted therapeutic interventions may limit morbidity and mortality associated with ROHHAD. |
format | Online Article Text |
id | pubmed-4967322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49673222016-07-31 ROHHAD syndrome and evolution of sleep disordered breathing Reppucci, Diana Hamilton, Jill Yeh, E Ann Katz, Sherri Al-Saleh, Suhail Narang, Indra Orphanet J Rare Dis Research BACKGROUND: Rapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulation (ROHHAD) is a rare disease with a high mortality rate. Although nocturnal hypoventilation (NH) is central to ROHHAD, the evolution of sleep disordered breathing (SDB) is not well studied. The aim of the study was to assess early manifestations of SDB and their evolution in ROHHAD syndrome. METHODS: Retrospective study of children with ROHHAD at two Canadian centers. All children with suspected ROHHAD at presentation underwent polysomnography (PSG) to screen for nocturnal hypoventilation. PSG findings at baseline and follow-up were collected. Interventions and diagnostic test results were recorded. RESULTS: Six children were included. The median age of rapid onset obesity and nocturnal hypoventilation (NH) was 3.5 and 7.2 years respectively. On initial screening for ROHHAD 4/6 (66.7 %) children had obstructive sleep apnea (OSA), 1/6 (16.7 %) had NH and 1/6 (16.7 %) had both OSA and NH. Follow up PSGs were performed in 5/6 children as one child died following a cardiorespiratory arrest. All children at follow up had NH and required non-invasive positive pressure ventilation. Additionally, 3/6 (50 %) children demonstrated irregular breathing patterns during wakefulness. CONCLUSIONS: Children with ROHHAD may initially present with OSA and only develop NH later as well as dysregulation of breathing during wakefulness. The recognition of the spectrum of respiratory abnormalities at presentation and over time may be important in raising the index of suspicion of ROHHAD. Early recognition and targeted therapeutic interventions may limit morbidity and mortality associated with ROHHAD. BioMed Central 2016-07-30 /pmc/articles/PMC4967322/ /pubmed/27473663 http://dx.doi.org/10.1186/s13023-016-0484-1 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Reppucci, Diana Hamilton, Jill Yeh, E Ann Katz, Sherri Al-Saleh, Suhail Narang, Indra ROHHAD syndrome and evolution of sleep disordered breathing |
title | ROHHAD syndrome and evolution of sleep disordered breathing |
title_full | ROHHAD syndrome and evolution of sleep disordered breathing |
title_fullStr | ROHHAD syndrome and evolution of sleep disordered breathing |
title_full_unstemmed | ROHHAD syndrome and evolution of sleep disordered breathing |
title_short | ROHHAD syndrome and evolution of sleep disordered breathing |
title_sort | rohhad syndrome and evolution of sleep disordered breathing |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967322/ https://www.ncbi.nlm.nih.gov/pubmed/27473663 http://dx.doi.org/10.1186/s13023-016-0484-1 |
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