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

被引:7
|
作者
Sansone, Valeria A. [1 ,2 ]
Pirola, Alice [1 ]
Lizio, Andrea [1 ]
Greco, Lucia Catherine [1 ]
Coratti, Giorgia [3 ]
Casiraghi, Jacopo [1 ]
Pane, Marika [3 ,4 ]
Pera, Maria Carmela [3 ]
Italiano, Cristina [1 ]
Messina, Sonia [5 ,6 ]
Pozzi, Susanna [1 ]
Sframeli, Maria [6 ]
D'Amico, Adele [7 ]
Bertini, Enrico [7 ]
Bruno, Claudio [8 ]
Mauro, Luca [1 ]
Salmin, Francesca [1 ]
Stancanelli, Claudia [6 ]
Pedemonte, Marina [8 ]
Albamonte, Emilio [1 ]
Zizzi, Christine [9 ,10 ]
Heatwole, Chad [9 ,10 ]
Mercuri, Eugenio [3 ]
机构
[1] NEMO Clin Ctr Milan, Milan, Italy
[2] Univ Milan, Neurorehabil Unit, Milan, Italy
[3] Univ Cattolica Sacro Cuore, Pediat Neurol, Rome, Italy
[4] Fdn Policlin Univ Agostino Gemelli IRCCS, Ctr Clin Nemo, Rome, Italy
[5] Univ Messina, Dept Clin & Expt Med, Messina, Italy
[6] Univ Hosp G Martino, Nemo SUD Clin Ctr, Messina, Italy
[7] Bambino Gesu Pediat Hosp, Dept Neurosci, Unit Neuromuscular & Neurodegenerat Disorders, IRCCS, Rome, Italy
[8] IRCCS Ist Giannina Gaslini, Ctr Translat & Expt Myol, Genoa, Italy
[9] Univ Rochester, Rochester, NY 14627 USA
[10] Ctr Hlth & Technol, Outcomes Div, Rochester, NY USA
关键词
Spinal muscular atrophy; Spinal muscular atrophy health index; Patient-reported outcomes; Test-retest reliability; Internal validity; QUALITY-OF-LIFE; QUESTIONNAIRE; PATIENT; ADULTS;
D O I
10.1016/j.nmd.2021.02.006
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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. (C) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页码:409 / 418
页数:10
相关论文
共 50 条
  • [31] The development and validation of a disease-specific quality of life measure in hyperhidrosis: the Hyperhidrosis Quality of Life Index (HidroQOL©)
    Kamudoni, P.
    Mueller, B.
    Salek, M. S.
    QUALITY OF LIFE RESEARCH, 2015, 24 (04) : 1017 - 1027
  • [32] The development and validation of a disease-specific quality of life measure in hyperhidrosis: the Hyperhidrosis Quality of Life Index (HidroQOL©)
    P. Kamudoni
    B. Mueller
    M. S. Salek
    Quality of Life Research, 2015, 24 : 1017 - 1027
  • [33] VALIDATION OF A DISEASE-SPECIFIC PATIENT-REPORTED OUTCOME MEASURE FOR ARABIC PATIENTS WITH SYSTEMIC LUPUS ERYTHEMATOSUS
    El Miedany, Y.
    El Gaafary, M.
    Sayed, S.
    Ahmed, I.
    ANNALS OF THE RHEUMATIC DISEASES, 2014, 73 : 189 - 189
  • [34] The Liver Disease Symptom Index 2.0; Validation of a Disease-Specific Questionnaire
    Simone M. van der Plas
    Bettina E. Hansen
    Josien B. de Boer
    Theo Stijnen
    Jan Passchier
    Rob A. de Man
    Solko W. Schalm
    Quality of Life Research, 2004, 13 : 1469 - 1481
  • [35] The Liver Disease Symptom Index 2.0; Validation of a disease-specific questionnaire
    van der Plas, SM
    Hansen, BE
    de Boer, JB
    Stijnen, T
    Passchier, J
    de Man, RA
    Schalm, SW
    QUALITY OF LIFE RESEARCH, 2004, 13 (08) : 1469 - 1481
  • [36] Cross-cultural validation of a disease-specific patient-reported outcome measure for lupus in Philippines
    Navarra, S. V.
    Tanangunan, R. M. D. V.
    Mikolaitis-Preuss, R. A.
    Kosinski, M.
    Block, J. A.
    Jolly, M.
    LUPUS, 2013, 22 (03) : 262 - 267
  • [37] Outcome measures for pediatric spinal muscular atrophy
    Iannaccone, ST
    NEUROMUSCULAR DISORDERS, 2001, 11 (6-7) : 646 - 647
  • [38] Internal Construct Validity of the Swiss Spinal Stenosis Questionnaire Rasch Analysis of a Disease-Specific Outcome Measure for Lumbar Spinal Stenosis
    Comer, Christine M.
    Conaghan, Philip G.
    Tennant, Alan
    SPINE, 2011, 36 (23) : 1969 - 1976
  • [39] Clinical Outcome Measures in Spinal Muscular Atrophy
    Montes, Jacqueline
    Gordon, Andrew M.
    Pandya, Shree
    De Vivo, Darryl C.
    Kaufmann, Petra
    JOURNAL OF CHILD NEUROLOGY, 2009, 24 (08) : 968 - 978
  • [40] Outcome measures for pediatric spinal muscular atrophy
    Iannaccone, ST
    ANNALS OF NEUROLOGY, 2001, 50 (03) : S127 - S127