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Management of amyotrophic lateral sclerosis.

机译:肌萎缩性侧索硬化的处理。

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摘要

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease affecting the motor neurons, in both the spinal cord and medulla (lower motor neurons) and cerebral cortex (upper motor neurons). Even though ALS remains fatal, several advances have been made during the last decade in improving the consequences of motor dysfunction, quality of life and survival time of patients. Treatment of ALS cannot be restricted to riluzole, the only molecule that has been proved to modify the evolution of the disease. Symptomatic treatments have an important role in controlling the major consequences of the disease, such as pain, sleep disorders, spasticity, hypersialhorroea, emotional lability, depression and digestive disorders (constipation and reflux). All these symptoms need to be recognized and their possible causes identified in order to provide the most appropriate management of patients with ALS. However, an advance in the daily care of patients is the identification of two important phenomena that occur during the evolution of the disease: swallowing difficulties and the occurrence of diaphragmatic dysfunction. For both, specific medical interventions have been developed to allow correction of the consequences (i.e. weight loss and respiratory insufficiency). Although no controlled trials have been performed, observational studies suggest that gastrostomy and non-invasive ventilation may improve at least quality of life and survival. All of these various approaches, pharmaceutical and non-pharmaceutical therapies, are prescribed according to individual symptoms and require the involvement of a large range of health professionals. This multidisciplinary approach in ALS clinics is considered to be one of the more important factors impacting on survival rate and appears to be the gold standard of medical care of ALS patients. Important findings have been made in understanding the nature of the degenerative process that affects the motor neurons. All these data have allowed new therapeutic molecules to be testedalone or in combination with riluzole. Despite the negative results obtained until now, we hope to demonstrate very soon a greater improvement in therapy.
机译:肌萎缩性侧索硬化症(ALS)是一种神经退行性疾病,会影响脊髓和髓质(下运动神经元)和大脑皮层(上运动神经元)中的运动神经元。尽管ALS仍然具有致命性,但在过去十年中,在改善运动功能障碍,生活质量和患者生存时间方面已取得了一些进展。 ALS的治疗不能仅限于利鲁唑(利鲁唑),利鲁唑是已被证实可改变疾病发展进程的唯一分子。对症治疗在控制疾病的主要后果方面具有重要作用,例如疼痛,睡眠障碍,痉挛,唾液分泌过多,情绪不稳,抑郁和消化系统疾病(便秘和反流)。所有这些症状都需要得到认识,并找出其可能的原因,以便为ALS患者提供最适当的管理。然而,患者日常护理的进步是确定了疾病发展过程中发生的两个重要现象:吞咽困难和diaphragm肌功能障碍的发生。对于这两种情况,已经开发出具体的医疗干预措施,以纠正后果(即体重减轻和呼吸功能不全)。尽管尚未进行任何对照试验,但观察性研究表明,胃造口术和无创通气至少可以改善生活质量和生存。所有这些不同的方法,包括药物和非药物疗法,都是根据个体症状开出的处方,需要大量医疗专业人员的参与。 ALS诊所中的这种多学科方法被认为是影响生存率的更重要因素之一,并且似乎是ALS患者医疗服务的金标准。在了解影响运动神经元的退化过程的性质方面已取得重要发现。所有这些数据使新的治疗分子可以单独或与利鲁唑组合进行测试。尽管到目前为止取得的负面结果,我们希望很快能证明治疗有更大的改善。

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