Literature DB >> 20374278

Italian validation of INQoL, a quality of life questionnaire for adults with muscle diseases.

V A Sansone1, M Panzeri1, M Montanari2, G Apolone2, S Gandossini1, M R Rose3, L Politano4, C Solimene4, G Siciliano5, L Volpi5, C Angelini6, A Palmieri6, A Toscano7, O Musumeci7, T Mongini8, L Vercelli8, R Massa9, M B Panico9, M Grandi10, G Meola1.   

Abstract

BACKGROUND AND
PURPOSE: A quality of life (QoL) questionnaire for neuromuscular diseases was recently constructed and validated in the United Kingdom in a sample of adult patients with a variety of muscle disorders. Preliminary results suggested it could be a more relevant and practical measure of QoL in muscle diseases than generic health measures of QoL. The purpose of our work was: (i) To validate INQoL in Italy on a larger sample of adult patients with muscle diseases (ii) to compare INQoL to SF-36.
METHODS: We have translated into Italian and applied language adaptations to the original UK INQoL version. We studied 1092 patients with different muscle disorders and performed (i) test-retest reliability (n = 80); (ii) psychometric (n = 345), known-group (n = 1092), external criterion (n = 70), and concurrent validity with SF-36 (n = 183).
RESULTS: We have translated and formally validated the Italian version of INQoL confirming and extending results obtained in the United Kingdom. In addition to good results in terms of reliability, known-group and criterion validity, a comparison with the SF-36 scales showed a stronger association between INQoL total index and SF-36 physical (r = -0.72) than mental (r = -0.38) summary health indexes. When considering comparable domains of INQoL and SF-36 with respect to an objective measure of muscle strength assessment (MMRC), regression analysis showed a stronger correlation using INQoL rather than SF-36 scores.
CONCLUSIONS: INQoL is recommended to assess QoL in muscle diseases because of its ability to capture physical limitations that are specifically relevant to the muscle condition.

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Year:  2010        PMID: 20374278     DOI: 10.1111/j.1468-1331.2010.02992.x

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  12 in total

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Review 2.  A systematic review of quality of life in adults with muscle disease.

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7.  213th ENMC International Workshop: Outcome measures and clinical trial readiness in idiopathic inflammatory myopathies, Heemskerk, The Netherlands, 18-20 September 2015.

Authors:  Olivier Benveniste; Lisa G Rider
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Authors:  V A Sansone; C Ricci; M Montanari; G Apolone; M Rose; G Meola
Journal:  Eur J Neurol       Date:  2012-05-19       Impact factor: 6.089

9.  Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study.

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10.  Assessment of self-reported and objective daytime sleepiness in adult-onset myotonic dystrophy type 1.

Authors:  Valeria A Sansone; Paola Proserpio; Luca Mauro; Andrea Lizio Biostat; Erica Frezza; Andrea Lanza; Paola Rogliani; Gabriella Pezzuto; Elisa Falcier; Carola Ferrari Aggradi; Alice Pirola; Fabrizio Rao; Elisabetta Roma; Claudia Galluzzi; Matteo Spanetta; Federica Cattaneo; Annalisa Rubino; Elio Clemente Agostoni; Federica Amico; Alice Zanolini; Francesca Izzi; Giulia Greco; Andrea Romigi; Claudio Liguori; Lino Nobili; Fabio Placidi; Roberto Massa
Journal:  J Clin Sleep Med       Date:  2021-12-01       Impact factor: 4.062

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