Breathing new life into treatment advances for respiratory failure in amyotrophic lateral sclerosis patients. (February 2014)

• Record Type: Journal Article
• Authors: Pinto, Susana; Carvalho, Mamede de
• Is Part Of: Neurodegenerative disease management. Volume 4:Number 1(2014)
• Page Start: 83
• Page End: 102
• Publication Date: 2014-02
• Subjects: Nervous system -- Degeneration -- Periodicals; 616.8
• DOI: 10.2217/nmt.13.74
• Languages: English
• ISSNs: 1758-2024

Abstract

SUMMARY In the last three decades, improvements in respiratory management are responsible for increasing survival and improving quality of life for amyotrophic lateral sclerosis (ALS) patients. Nowadays, ALS patients with respiratory involvement are offered a support treatment other than the traditional respiratory palliative care. Knowledge about available respiratory support potentialities is essential for appropriate, customized and effective treatment of ALS, which should probably be started sooner than the conventional approach. There is evidence supporting that respiratory support has a larger impact than riluzole on survival. Noninvasive ventilation is essential in the treatment of ALS patients with respiratory involvement. In this article methods to determine respiratory failure in ALS, mechanical invasive and noninvasive ventilation, telemetry, diaphragm pacing, cough aids and respiratory exercise are reviewed, after a brief overlook of respiratory insufficiency in ALS.