Respiratory care in spinal muscular atrophy in the new therapeutic era

被引:0
作者
Angelica Palomino, Maria [1 ,2 ,4 ]
Castiglioni, Claudia [1 ,3 ,5 ]
机构
[1] Clin Las Condes, Programa Trastornos Motores & Enfermedades Neurom, Las Condes, Chile
[2] Clin Las Condes, Dept Pediat, Las Condes, Chile
[3] Clin Las Condes, Dept Neurol Pediat, Las Condes, Chile
[4] Univ Chile, Dept Pediat Norte, Santiago, Chile
[5] Univ Chile, Dept Pediat Sur, Santiago, Chile
来源
REVISTA CHILENA DE PEDIATRIA-CHILE | 2018年 / 89卷 / 06期
关键词
Spinal Muscular Atrophy; Neuromuscular disease; Werdnig Hoffmann's Disease; Airway clearance; Mechanical cough assistance; Pneumonia; Respiratory failure; Restrictive lung disease; Non-invasive ventilation; Invasive ventilation; Nusinersen;
D O I
暂无
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Spinal muscular atrophy (SMA) is the first inherited cause of mortality in infants, with four subtypes: SMA0 prenatal onset, SMA1 babies less than 3 months non sitters, SMA2 sitters and SMA3 walkers. Pneumonia and respiratory insufficiency are the most severe complications. Informed parental decisions are relevant. Respiratory management includes cough assistance, prevention of lung underdevelopment due to chest deformity, prompt treatment of respiratory infections, hypoventilation, swallow problems, gastro esophageal reflux and malnutrition. In view of the FDA and EMA approval of the nonsense oligonucleotides nusinersen, the first specific treatment for SMA and the future with gene therapy and others under development, we need to optimize preventive respiratory management with the new standard of care.
引用
收藏
页码:685 / 693
页数:9
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