Symptom Management and End-of-Life Care in Amyotrophic Lateral Sclerosis

被引:34
作者
Jackson, Carlayne E. [1 ]
McVey, April L. [2 ]
Rudnicki, Stacy [3 ]
Dimachkie, Mazen M. [2 ]
Barohn, Richard J. [2 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Dept Neurol, San Antonio, TX 78229 USA
[2] Univ Kansas, Med Ctr, Dept Neurol, Kansas City, KS 66160 USA
[3] Univ Arkansas Med Sci, Dept Neurol, Little Rock, AR 72205 USA
关键词
Sialorrhea; Pseudobulbar affect; Noninvasive ventilation; Secretion management; Laryngospasm; Edema; Urinary urgency; Constipation; QUALITY STANDARDS SUBCOMMITTEE; MOTOR-NEURON DISEASE; BODY-MASS INDEX; PERCUTANEOUS ENDOSCOPIC GASTROSTOMY; POSITIVE-PRESSURE VENTILATION; PRACTICE PARAMETER UPDATE; ALS PATIENTS; BOTULINUM-TOXIN; NONINVASIVE VENTILATION; AMERICAN ACADEMY;
D O I
10.1016/j.ncl.2015.07.010
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The number of available symptomatic treatments has markedly enhanced the care of patients with amyotrophic lateral sclerosis (ALS). Once thought to be untreatable, patients with ALS today clearly benefit from multidisciplinary care. The impact of such care on the disease course, including rate of progression and mortality, has surpassed the treatment effects commonly sought in clinical drug trials. Unfortunately, there are few randomized controlled trials of medications or interventions addressing symptom management. In this review, the authors provide the level of evidence, when available, for each intervention that is currently considered standard of care by consensus opinion.
引用
收藏
页码:889 / +
页数:21
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