2001
DOI: 10.1093/brain/124.10.2000
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Respiratory muscle strength and ventilatory failure in amyotrophic lateral sclerosis

Abstract: Although ventilatory failure is the most common cause of death in amyotrophic lateral sclerosis (ALS) and measurement of respiratory muscle strength (RMS) has been shown to have prognostic value, no single test of strength can predict the presence of hypercapnia reliably. RMS was measured in 81 ALS patients to evaluate the relationship between tests of RMS and the presence of ventilatory failure, defined as a carbon dioxide tension > or = 6 kPa. We studied the predictive value of vital capacity (VC), static in… Show more

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Cited by 335 publications
(262 citation statements)
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“…However, patients with neuromuscular diseases characterised by facial or bulbar muscle weakness, e.g. amyotrophic lateral sclerosis, myasthenia gravis, myotonic dystrophy and facioscapulohumeral muscular dystrophy, often cannot effectively seal the lips around the mouthpiece, especially during forced manoeuvres such as spirometric and maximal respiratory pressure measurements [9,10]. In these cases, the conventional equipment with a tube or flanged type of mouthpiece is not adequate to evaluate respiratory muscle function.…”
mentioning
confidence: 99%
“…However, patients with neuromuscular diseases characterised by facial or bulbar muscle weakness, e.g. amyotrophic lateral sclerosis, myasthenia gravis, myotonic dystrophy and facioscapulohumeral muscular dystrophy, often cannot effectively seal the lips around the mouthpiece, especially during forced manoeuvres such as spirometric and maximal respiratory pressure measurements [9,10]. In these cases, the conventional equipment with a tube or flanged type of mouthpiece is not adequate to evaluate respiratory muscle function.…”
mentioning
confidence: 99%
“…This finding is of great clinical significance given the rapidly degenerating nature of ALS. Maintaining MEP, maximum inspiratory pressure, and FVC have been shown to be highly predictive of 1‐year survival and are associated with tracheostomy‐free survival in ALS 18. Additionally, expiratory muscle weakness has been indicated as a causative factor in the inability to generate adequate cough flow rates and has been associated with concomitant inspiratory muscle weakness in ALS 19.…”
Section: Discussionmentioning
confidence: 99%
“…During an effective cough, the expiratory flow rate increases and secretions in the airway are moved towards the buccal cavity 13,18,21) . Alone, isometric training of the pelvis elevator muscles is unlikely to improve cough force, since in addition to expiratory muscle strength, factors that determine cough effectiveness include: the ability to instantaneously increase intrathoracic pressure 22) ; contraction of the expiratory muscles to increase this pressure 13) ; timing of glottis opening 23) ; and bulbar function 6,20,24) .…”
Section: Discussionmentioning
confidence: 99%