Improvements in the medical care of spinal muscular atrophy have increased survival across all SMA types1
Important advances in the treatment of spinal muscular atrophy over the last decade since 2007 include:1
- Expansion of the use of non-invasive ventilation and cough machine support
- Introduction of early spinal surgery
- Greater emphasis on a multidisciplinary approach to care
- Advent of clinical trials and new drug approvals in spinal muscular atrophy
Survival in infantile-onset (Type I) spinal muscular atrophy has improved substantially3
TIME PERIOD |
% OF PATIENTS |
MEDIAN SURVIVAL |
1980-1994 |
37% |
7.5 |
1995-2006 |
79% |
24 |
Adoption of comprehensive supportive care in infantile-onset (Type I) spinal muscular atrophy has increased3,8
SUPPORTIVE CARE |
1980-1994 |
1995-2006 |
Noninvasive positive pressure ventilation (NIPPV) |
31% |
82% |
Mechanical insufflation/exsufflation (MI-E) |
8% |
63% |
Supplementary feeding |
40% |
78% |
Spinal muscular atrophy is a neuromuscular disease that requires multidisciplinary medical care, and in some instances, a palliative approach1
PROACTIVE CARE1,3An approach to intensively manage the symptoms of the disease. For children with SMA, a proactive approach may include earlier placement of a feeding tube, intensive respiratory support (e.g. non-invasive ventilation and cough assist machines), early spinal surgery and regular sessions of physical therapy. |
PALLIATIVE CARE1,4,5An approach that aims to improve quality of life and relieve stress and discomfort. For children with SMA, the use of non-invasive ventilation may help avoid hospitalisation and the need for tracheostomy. |
Adopting a proactive approach to care can influence the trajectory of disease progression and improve the natural history of spinal muscular atrophy.1 |
While some children receive multidisciplinary care from physicians in their community, others go to a neuromuscular disease centre specialising in SMA
Assembling a multidisciplinary care team in the community
While spinal muscular atrophy has a single genetic cause, its presentation, progression, and needs can vary widely.6,7
Clinical specialties involved in a child’s care team may vary based on individual needs, but can include1: |
For more information on the roles and responsibilities of those caring for children with SMA, click here. |
At some centres, centralised (shared) appointments allow families to see all necessary physicians on a single day at one facility
These centres provide care for the entire family, which may include genetic counselling and education
These centres may provide assistance (e.g. parking, meals, lodging) for families travelling to the centre
REFERENCES
1. Mercuri E, et al. Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care. Neuromuscl Disord. 2018;28(2):103-115. 2. Finkel RS, et al. Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethics. Neuromuscul Disord. 2018;28(3):197-207. 3. Oskoui M, Levy G, Garland CJ, et al. The changing natural history of spinal muscular atrophy type 1. Neurology. 2007;69(20):1931-1936. 4. World Health Organization. WHO definition of palliative care. http://www.who.int/cancer/palliative/definition/en/. Accessed April 25, 2016. 5. The World Federation of Right to Die Societies. Comfort and palliative care. http://www.worldrtd.net/comfort-palliative-care. Accessed April 25, 2016. 6. Darras BT, Royden Jones H Jr, Ryan MM, De Vivo DC, eds. Neuromuscular Disorders of Infancy, Childhood, and Adolescence: A Clinician’s Approach. 2nd ed. London, UK: Elsevier; 2015. 7. Markowitz JA, Singh P, Darras BT. Spinal muscular atrophy: a clinical and research update. Pediatr Neurol. 2012;46(1):1-12. 8. Chatwin M, Bush A, Simonds AK. Outcome of goal-directed non-invasive ventilation and mechanical insufflation/exsufflation in spinal muscular atrophy type I. Arch Dis Child. 2011;96:426-432.
The updated 2017 Consensus Statement for Standard of Care in Spinal Muscular Atrophy reflects new data and important advances in the management of SMA.1,2