Patient report outcome measures in Spinal Muscular Atrophy (SMA) represent a potential complement to observer rated scales which can be used to better understand treatment response. We developed, translated and validated an Italian version of the Spinal Muscular Atrophy Health Index (SMAHI), a disease-specific, patient reported outcome measure questionnaire, designed to estimate the patients' perception of disease burden. Test-retest reliability was assessed in 37 patients (16 children aged 12-17 and 21 adults) and was excellent in both cohorts. Internal consistency in an additional 98 patients (24 children, 74 adults) was also excellent (Cronbach's alpha = 0.93 and 0.91 respectively). In children the highest level of disease burden was generated from lower limb dysfunction and fatigue as well as their perception of decreased performance in social situations. Most patients in the adult cohort were sitters and complained of problems with upper limb functions as well as of fatigue. The SMAHI-IT was also able to differentiate between SMA types according to diseases severity. The results of our study demonstrate that the SMAHI can be considered a marker of disease-specific burden in patients with SMA with a high test-retest reliability and internal validity in Italian patients aged 12 and older.

The Spinal Muscular Atrophy Health Index: Italian validation of a disease-specific outcome measure / V. Sansone, A. Pirola, A. Lizio, L. Greco, G. Coratti, J. Casiraghi, M. Pane, M. Pera, C. Italiano, S. Messina, S. Pozzi, M. Sframeli, A. D'Amico, E. Bertini, C. Bruno, L. Mauro, F. Salmin, C. Stancanelli, M. Pedemonte, E. Albamonte, C. Zizzi, C. Heatwole, E. Mercuri. - In: NEUROMUSCULAR DISORDERS. - ISSN 0960-8966. - 31:5(2021 May), pp. 409-418. [10.1016/j.nmd.2021.02.006]

The Spinal Muscular Atrophy Health Index: Italian validation of a disease-specific outcome measure.

V. Sansone
Primo
;
2021

Abstract

Patient report outcome measures in Spinal Muscular Atrophy (SMA) represent a potential complement to observer rated scales which can be used to better understand treatment response. We developed, translated and validated an Italian version of the Spinal Muscular Atrophy Health Index (SMAHI), a disease-specific, patient reported outcome measure questionnaire, designed to estimate the patients' perception of disease burden. Test-retest reliability was assessed in 37 patients (16 children aged 12-17 and 21 adults) and was excellent in both cohorts. Internal consistency in an additional 98 patients (24 children, 74 adults) was also excellent (Cronbach's alpha = 0.93 and 0.91 respectively). In children the highest level of disease burden was generated from lower limb dysfunction and fatigue as well as their perception of decreased performance in social situations. Most patients in the adult cohort were sitters and complained of problems with upper limb functions as well as of fatigue. The SMAHI-IT was also able to differentiate between SMA types according to diseases severity. The results of our study demonstrate that the SMAHI can be considered a marker of disease-specific burden in patients with SMA with a high test-retest reliability and internal validity in Italian patients aged 12 and older.
Spinal muscular atrophy; Spinal muscular atrophy health index; Patient-reported outcomes; Test-retest reliability; Internal validity;
Settore MED/26 - Neurologia
mag-2021
Article (author)
File in questo prodotto:
File Dimensione Formato  
Sansone et al Neuromusc Dis 2021.pdf

accesso riservato

Tipologia: Publisher's version/PDF
Dimensione 683.89 kB
Formato Adobe PDF
683.89 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/853333
Citazioni
  • ???jsp.display-item.citation.pmc??? 1
  • Scopus 6
  • ???jsp.display-item.citation.isi??? 6
social impact