Spinal Muscular Atrophy Type 1 Survival Without New Pharmacotherapies

被引:3
|
作者
Bach, John R. [1 ,2 ]
Saporito, Louis [1 ]
Weiss, William [1 ]
机构
[1] Rutgers State Univ, New Jersey Med Sch, Dept Phys Med & Rehabil, Newark, NJ USA
[2] Rutgers State Univ, Dept Phys Med & Rehabil, New Jersey Med Sch, Behav Hlth Sci Bldg,183 S Orange Ave, Newark, NJ 07103 USA
关键词
Spinal Muscular Atrophy Type 1; Cough Flows; Noninvasive Ventilatory Support; Noninvasive Ventilation; Outcomes; Survival; NONINVASIVE RESPIRATORY MANAGEMENT; VITAL CAPACITY; VENTILATION;
D O I
10.1097/PHM.0000000000002354
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
ObjectivesThe aims of the study are to present noninvasive respiratory management outcomes using continuous noninvasive ventilatory support and mechanical in-exsufflation from infancy for spinal muscular atrophy type 1 and to consider bearing on new medical therapies.DesignNoninvasive ventilatory support was begun for consecutively referred symptomatic infants with spinal muscular atrophy type 1 from 1 to 10 mos of age. Intercurrent episodes of respiratory failure were managed by intubation then extubation to continuous noninvasive ventilatory support and mechanical in-exsufflation despite failing ventilator weaning and extubation attempts. Intubations, tracheotomies, and survival were monitored.ResultsOf 153 patients with spinal muscular atrophy 1 consecutively referred since 1995, 37 became continuous noninvasive ventilatory support dependent, almost half before 10 yrs of age. Of the 37, 18 required continuous noninvasive ventilatory support for a mean 18.6 +/- 3.3 yrs to a mean 25.3 (range, 18-30) yrs of age, dependent from as young as 4 mos of age with 0 to 40 ml of vital capacity. One of the 18 died from COVID-19 acute respiratory distress syndrome at age 24 after 23 yrs of continuous noninvasive ventilatory support. Extubation success rate of 85% per attempt (150/176) resulted in only one undergoing tracheotomy.ConclusionsMedical treatments begun during the first 6 wks of age convert spinal muscular atrophy 1 into spinal muscular atrophy 2 or 3 but cough flows remain inadequate to avoid many pneumonias that, once resolved by a treatment paradigm of extubation to continuous noninvasive ventilatory support and mechanical in-exsufflation, eliminates need to resort to tracheotomies.
引用
收藏
页码:233 / 237
页数:5
相关论文
共 50 条
  • [31] Gingival hyperplasia in a child with spinal muscular atrophy type 1
    Beri, Nidhi
    Narayan, Omendra
    Mundada, Vivek
    ARCHIVES OF DISEASE IN CHILDHOOD, 2024, 109 (10) : 782 - 783
  • [32] New treatments in spinal muscular atrophy
    Gowda, Vasantha Lakshmi
    Fernandez-Garcia, Miguel A.
    Jungbluth, Heinz
    Wraige, Elizabeth
    ARCHIVES OF DISEASE IN CHILDHOOD, 2023, 108 (07) : 511 - 517
  • [33] New treatments for spinal muscular atrophy
    Wurster, C. D.
    Guenther, R.
    NERVENARZT, 2020, 91 (04): : 294 - 302
  • [34] Spinal Muscular Atrophy Type 1 With Exon 8 Deletion and Bilateral Optic Atrophy
    Behera, Bijaylaxmi
    Kumar, Ajay
    INDIAN PEDIATRICS, 2020, 57 (12) : 1191 - 1191
  • [35] Spinal Muscular Atrophy Type 1 With Exon 8 Deletion and Bilateral Optic Atrophy
    Bijaylaxmi Behera
    Ajay Kumar
    Indian Pediatrics, 2020, 57 : 1191 - 1191
  • [36] Type III Spinal Muscular Atrophy Mimicking Muscular Dystrophies
    Alsaman, Abdulaziz S.
    AlShaikh, Nahla M.
    PEDIATRIC NEUROLOGY, 2013, 48 (05) : 363 - 366
  • [37] Spinal muscular atrophy-type I
    Hardart, MKM
    Truog, RD
    ARCHIVES OF DISEASE IN CHILDHOOD, 2003, 88 (10) : 848 - 850
  • [38] Spinal muscular atrophy with respiratory distress type 1 (SMARD1)
    San Millan, Beatriz
    Fernandez, Jose M.
    Navarro, Carmen
    Reparaz, Alfredo
    Teijeira, Susana
    CLINICAL NEUROPATHOLOGY, 2016, 35 (02) : 58 - 65
  • [39] Burden of Illness of Spinal Muscular Atrophy Type 1 (SMA1)
    Droege, M.
    Dabbous, O.
    Arjunji, R.
    Seda, J.
    Gauthier-Loiselle, M.
    Cloutier, M.
    Sproule, D.
    ANNALS OF NEUROLOGY, 2019, 86 : S122 - S122
  • [40] Burden of illness of spinal muscular atrophy type 1 (SMA1)
    Droege, M.
    Dabbous, O.
    Arjunji, R.
    Seda, J.
    Gauthier-Loiselle, M.
    Cloutier, M.
    Sproule, D.
    NEUROMUSCULAR DISORDERS, 2019, 29 : S128 - S128