| Literature DB >> 28872909 |
Robert G Miller1, Stanley H Appel2.
Abstract
ALS is a lethal neurodegenerative disease wherein the diagnosis is often delayed. Our understanding of the pathobiology is slowly expanding, and the number of new genes is rapidly increasing. The development of potential treatments targeting specific mechanisms is beginning to offer hope. Evidence-based treatments and the development of quality measures have raised the standard of care. The current status of treatment for ALS includes one drug riluzole that slows progression modestly, and another drug edaravone that was recently approved by FDA to slow ALS progression. Multidisciplinary clinics and symptomatic treatments ease the burden of ALS and prolong life. An overview of these treatments is provided here.Entities:
Keywords: Treatment; amyotrohpic lateral sclerosis; clinical trials; multidisciplinary clinics; practice parameters; quality measures
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Year: 2017 PMID: 28872909 DOI: 10.1080/21678421.2017.1361447
Source DB: PubMed Journal: Amyotroph Lateral Scler Frontotemporal Degener ISSN: 2167-8421 Impact factor: 4.092