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Sleep and psychiatric abnormalities in Gullian Barré Syndrome

BACKGROUND: The sensori-motor manifestations of Guillain Barré Syndrome (GBS) are usually severe enough to mask the psychiatric and sleep problems which are in need for more attention for better functional outcome. METHODS: This study was performed on 20 GBS patients and 10 healthy controls. Patient...

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Autores principales: Bahnasy, Wafik Said, El-Heneedy, Yasser Abo Elfotoh, El-Shamy, Ahmed Mohamed, Badr, Marwa Yassin, Amer, Reham Ahmed, Ibrahim, Ibrahim Salah Eldeen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954782/
https://www.ncbi.nlm.nih.gov/pubmed/29780225
http://dx.doi.org/10.1186/s41983-018-0007-1
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author Bahnasy, Wafik Said
El-Heneedy, Yasser Abo Elfotoh
El-Shamy, Ahmed Mohamed
Badr, Marwa Yassin
Amer, Reham Ahmed
Ibrahim, Ibrahim Salah Eldeen
author_facet Bahnasy, Wafik Said
El-Heneedy, Yasser Abo Elfotoh
El-Shamy, Ahmed Mohamed
Badr, Marwa Yassin
Amer, Reham Ahmed
Ibrahim, Ibrahim Salah Eldeen
author_sort Bahnasy, Wafik Said
collection PubMed
description BACKGROUND: The sensori-motor manifestations of Guillain Barré Syndrome (GBS) are usually severe enough to mask the psychiatric and sleep problems which are in need for more attention for better functional outcome. METHODS: This study was performed on 20 GBS patients and 10 healthy controls. Patients were evaluated initially before immunotherapy using the Overall Disability Sum Score (ODSS), Neuropathy Pain Scale (NPS), Hamilton Anxiety Scale (HAS), Montgomery–Åsberg Depression Rating Scale (MADRS) and one-night polysomnography (PSG) followed by the multiple sleep latency test (MSLT) to evaluate the mean sleep latencies. Reevaluation was done using the same parameters 1 month after completing immunotherapy. RESULTS: The study showed significant increase in HAS in GBS patients which were positively correlated with the degree of motor disability. The mean sleep latencies of MSLT were significantly shortened and PSG showed shortening of the total sleep time, sleep efficiency, lowest O(2) saturation and pulse transit time with increased wake after sleep onset, sleep stage transition index, apnea hypopnea index, desaturation index, arousal index, snore index and periodic limb movement index. One month after immunotherapy, the anxiety symptoms and sleep abnormalities showed non-significant improvements which were not correlated with the improvements in the sensori-motor manifestations. CONCLUSIONS: GBS patients usually have sleep and psychiatric abnormalities which may take longer time to improve than the sensori-motor manifestations. So, they need more attention in the management protocol for early patients’ independence and return to usual daily activities.
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spelling pubmed-59547822018-05-18 Sleep and psychiatric abnormalities in Gullian Barré Syndrome Bahnasy, Wafik Said El-Heneedy, Yasser Abo Elfotoh El-Shamy, Ahmed Mohamed Badr, Marwa Yassin Amer, Reham Ahmed Ibrahim, Ibrahim Salah Eldeen Egypt J Neurol Psychiatr Neurosurg Research BACKGROUND: The sensori-motor manifestations of Guillain Barré Syndrome (GBS) are usually severe enough to mask the psychiatric and sleep problems which are in need for more attention for better functional outcome. METHODS: This study was performed on 20 GBS patients and 10 healthy controls. Patients were evaluated initially before immunotherapy using the Overall Disability Sum Score (ODSS), Neuropathy Pain Scale (NPS), Hamilton Anxiety Scale (HAS), Montgomery–Åsberg Depression Rating Scale (MADRS) and one-night polysomnography (PSG) followed by the multiple sleep latency test (MSLT) to evaluate the mean sleep latencies. Reevaluation was done using the same parameters 1 month after completing immunotherapy. RESULTS: The study showed significant increase in HAS in GBS patients which were positively correlated with the degree of motor disability. The mean sleep latencies of MSLT were significantly shortened and PSG showed shortening of the total sleep time, sleep efficiency, lowest O(2) saturation and pulse transit time with increased wake after sleep onset, sleep stage transition index, apnea hypopnea index, desaturation index, arousal index, snore index and periodic limb movement index. One month after immunotherapy, the anxiety symptoms and sleep abnormalities showed non-significant improvements which were not correlated with the improvements in the sensori-motor manifestations. CONCLUSIONS: GBS patients usually have sleep and psychiatric abnormalities which may take longer time to improve than the sensori-motor manifestations. So, they need more attention in the management protocol for early patients’ independence and return to usual daily activities. Springer Berlin Heidelberg 2018-04-25 2018 /pmc/articles/PMC5954782/ /pubmed/29780225 http://dx.doi.org/10.1186/s41983-018-0007-1 Text en © The Author(s) 2018 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.
spellingShingle Research
Bahnasy, Wafik Said
El-Heneedy, Yasser Abo Elfotoh
El-Shamy, Ahmed Mohamed
Badr, Marwa Yassin
Amer, Reham Ahmed
Ibrahim, Ibrahim Salah Eldeen
Sleep and psychiatric abnormalities in Gullian Barré Syndrome
title Sleep and psychiatric abnormalities in Gullian Barré Syndrome
title_full Sleep and psychiatric abnormalities in Gullian Barré Syndrome
title_fullStr Sleep and psychiatric abnormalities in Gullian Barré Syndrome
title_full_unstemmed Sleep and psychiatric abnormalities in Gullian Barré Syndrome
title_short Sleep and psychiatric abnormalities in Gullian Barré Syndrome
title_sort sleep and psychiatric abnormalities in gullian barré syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954782/
https://www.ncbi.nlm.nih.gov/pubmed/29780225
http://dx.doi.org/10.1186/s41983-018-0007-1
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