Sathasivam Sivakumar
The Walton Centre for Neurology & Neurosurgery, Lower Lane, Liverpool, United Kingdom.
Eur J Intern Med. 2009 Jul;20(4):355-8. doi: 10.1016/j.ejim.2008.09.002. Epub 2008 Oct 11.
Amyotrophic lateral sclerosis (ALS) is the most common rapidly progressive adult-onset neurodegenerative disorder. There have been great advances in the management of patients with ALS over the past decade. It starts with the giving of the diagnosis and continues to the terminal phase of the disease. This review will examine the impact of medical and non-medical interventions on improving survival and quality of life in these patients, emphasizing the importance of a multidisciplinary approach.
肌萎缩侧索硬化症(ALS)是最常见的成人起病的快速进展性神经退行性疾病。在过去十年中,ALS患者的管理取得了巨大进展。这一过程始于诊断的给出,并持续到疾病的终末期。本综述将探讨医学和非医学干预措施对改善这些患者的生存和生活质量的影响,强调多学科方法的重要性。