Oral and Swallowing Abilities Tool (OrSAT) for Type 1 SMA Patients: Development of a New Module

J Neuromuscul Dis. 2021;8(4):589-601. doi: 10.3233/JND-200614.

Abstract

We describe the development of a new tool specifically designed to record oral abilities, swallowing and, more generally, feeding in young type 1 SMA patients, to be used during the first 24 months of life.The tool is composed by a checklist and a separate section summarizing the functional abilities into levels of feeding/swallowing impairment. The checklist includes 12 questions assessing aspects thought to be clinically meaningful for a type 1 SMA population and developmentally appropriate for infants during the first months of life. Each item is graded with a score of 0 or 1, depending on the child's ability to perform the activity. As some items are age-dependent, the number of items to be used, and therefore the maximum score, changes with increasing age. The levels of feeding/swallowing impairment include four levels that can be identified using easily identifiable clinical criteria.In an attempt to validate the tool in an untreated population we applied it to 24 type 1 SMA patients (age range: 2.3-24.1 months, mean: 10.8) in whom the same information collected by the new tool had been previously recorded using a less-structured format.When patients were classified in three groups according to the Dubowitz decimal classification, there was a significant difference both at baseline and at follow-up (p < 0.001). The items assessing fatigue during the nursing sessions were the most frequently impaired even in infants who did not have any other obvious clinical sign of swallowing difficulties.

Keywords: Spinal muscular atrophy; dysphagia; oral motor function; swallowing; type 1 SMA infants.

Publication types

  • Validation Study

MeSH terms

  • Activities of Daily Living
  • Deglutition
  • Deglutition Disorders / complications
  • Deglutition Disorders / diagnosis*
  • Fatigue / diagnosis
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Spinal Muscular Atrophies of Childhood / complications*
  • Surveys and Questionnaires