Sleep disorders and respiratory function in amyotrophic lateral sclerosis

Rebekah M. Ahmed; Rowena E. A. Newcombe; Amanda J. Piper; Simon J. Lewis; Brendon J. Yee; Matthew C. Kiernan; Ron R. Grunstein

doi:10.1016/j.smrv.2015.05.007

Sleep disorders and respiratory function in amyotrophic lateral sclerosis

Rebekah M. Ahmed^*, Rowena E. A. Newcombe, Amanda J. Piper, Simon J. Lewis, Brendon J. Yee, Matthew C. Kiernan, Ron R. Grunstein

^*Corresponding author for this work

Research output: Contribution to journal › Review article › peer-review

57 Citations (Scopus)

Abstract

Sleep disorders in amyotrophic lateral sclerosis (ALS) present a significant challenge to the management of patients. Issues include the maintenance of adequate ventilatory status through techniques such as non-invasive ventilation, which has the ability to modulate survival and improve patient quality of life. Here, a multidisciplinary approach to the management of these disorders is reviewed, from concepts about the underlying neurobiological basis, through to current management approaches and future directions for research.

Original language	English
Pages (from-to)	33-42
Number of pages	10
Journal	Sleep Medicine Reviews
Volume	26
DOIs	https://doi.org/10.1016/j.smrv.2015.05.007
Publication status	Published - Apr 2016
Externally published	Yes

Keywords

Amyotrophic lateral sclerosis
Respiratory
Sleep
Ventilation

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10.1016/j.smrv.2015.05.007

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title = "Sleep disorders and respiratory function in amyotrophic lateral sclerosis",

abstract = "Sleep disorders in amyotrophic lateral sclerosis (ALS) present a significant challenge to the management of patients. Issues include the maintenance of adequate ventilatory status through techniques such as non-invasive ventilation, which has the ability to modulate survival and improve patient quality of life. Here, a multidisciplinary approach to the management of these disorders is reviewed, from concepts about the underlying neurobiological basis, through to current management approaches and future directions for research.",

keywords = "Amyotrophic lateral sclerosis, Respiratory, Sleep, Ventilation",

author = "Ahmed, {Rebekah M.} and Newcombe, {Rowena E. A.} and Piper, {Amanda J.} and Lewis, {Simon J.} and Yee, {Brendon J.} and Kiernan, {Matthew C.} and Grunstein, {Ron R.}",

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doi = "10.1016/j.smrv.2015.05.007",

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AU - Ahmed, Rebekah M.

AU - Newcombe, Rowena E. A.

AU - Piper, Amanda J.

AU - Lewis, Simon J.

AU - Yee, Brendon J.

AU - Kiernan, Matthew C.

AU - Grunstein, Ron R.

PY - 2016/4

Y1 - 2016/4

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AB - Sleep disorders in amyotrophic lateral sclerosis (ALS) present a significant challenge to the management of patients. Issues include the maintenance of adequate ventilatory status through techniques such as non-invasive ventilation, which has the ability to modulate survival and improve patient quality of life. Here, a multidisciplinary approach to the management of these disorders is reviewed, from concepts about the underlying neurobiological basis, through to current management approaches and future directions for research.

KW - Amyotrophic lateral sclerosis

KW - Respiratory

KW - Sleep

KW - Ventilation

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DO - 10.1016/j.smrv.2015.05.007

M3 - Review article

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SN - 1087-0792

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EP - 42

JO - Sleep Medicine Reviews

JF - Sleep Medicine Reviews

ER -

Sleep disorders and respiratory function in amyotrophic lateral sclerosis

Abstract

Keywords

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