Neurology and Therapy (Oct 2022)

Validation of a Set of Instruments to Assess Patient- and Caregiver-Oriented Measurements in Spinal Muscular Atrophy: Results of the SMA-TOOL Study

  • Juan F. Vázquez-Costa,
  • María Branas-Pampillón,
  • Julita Medina-Cantillo,
  • Mónica Povedano,
  • Inmaculada Pitarch-Castellano,
  • Mercedes López-Lobato,
  • Joaquín A. Fernández-Ramos,
  • Miguel Lafuente-Hidalgo,
  • Ricard Rojas-García,
  • José M. Caballero-Caballero,
  • Ignacio Málaga,
  • Jesús Eirís-Puñal,
  • Mencía De Lemus,
  • María G. Cattinari,
  • Rosana Cabello-Moruno,
  • Paola Díaz-Abós,
  • Victoria Sánchez-Menéndez,
  • Pablo Rebollo,
  • Jorge Maurino,
  • Marcos Madruga-Garrido

DOI
https://doi.org/10.1007/s40120-022-00411-2
Journal volume & issue
Vol. 12, no. 1
pp. 89 – 105

Abstract

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Abstract Introduction Outcome measures traditionally used in spinal muscular atrophy (SMA) clinical trials are inadequate to assess the full range of disease severity. The aim of this study was to assess the psychometric properties of a set of existing questionnaires and new items, gathering information on the impact of SMA from the patient and caregiver perspectives. Methods This was a multicenter, prospective, noninterventional study including patients with a confirmed diagnosis of 5q-autosomal-recessive SMA aged 8 years and above, or their parents (if aged between 2 and 8 years). The set of outcome measurements included the SMA Independence Scale (SMAIS) patient and caregiver versions, the Neuro-QoL Fatigue Computer Adaptive Test (CAT), the Neuro-QoL Pain Short Form—Pediatric Pain, the PROMIS adult Pain Interference CAT, and new items developed by Fundación Atrofia Muscular España: perceived fatigability, breathing and voice, sleep and rest, and vulnerability. Reliability, construct validity, discriminant validity, and sensitivity to change (4 months from baseline) were measured. Results A total of 113 patients were included (59.3% 2–17 years old, 59.3% male, and 50.4% with SMA type II). Patients required moderate assistance [mean patient and caregiver SMAIS (SD) scores were 31.1 (12.8) and 7.6 (11.1), respectively]. Perceived fatigability was the most impacted domain, followed by vulnerability. Cronbach’s alpha coefficient for perceived fatigability, breathing and voice, and vulnerability total scores were 0.92, 0.88, and 0.85, respectively. The exploratory factor analysis identified the main factors considered in the design, except in the sleep and rest domain. All questionnaires were able to discriminate between the Clinical Global Impression—Severity scores and SMA types. Sensitivity to change was only found for the SMAIS caregiver version and vulnerability items. Conclusions This set of outcome measures showed adequate reliability, construct validity, and discriminant validity and may constitute a valuable option to measure symptom severity in patients with SMA.

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