Literature DB >> 28890289

The Myotonic Dystrophy Health Index: Italian validation of a disease-specific outcome measure.

Valeria A Sansone1, Andrea Lizio2, Lucia Greco2, Gaia Gragnano2, Alice Zanolini2, Marco Gualandris2, Marino Iatomasi2, Chad Heatwole3.   

Abstract

The Myotonic Dystrophy Health Index (MDHI) is a disease-specific, self-reported outcome measure that assesses total disease burden and 17 areas of Myotonic Dystrophy type 1 (DM1) specific health. This study translated the MDHI into Italian and validated the instrument using a cohort of Italian DM1 patients. Italian DM1 patients were interviewed regarding the form and content of the instrument. Thirty-eight DM1 patients were subsequently recruited to test the reliability and concurrent validity of the instrument by serially completing the MDHI and a battery of clinical tests. Lastly, we determined the internal consistency of the Italian MDHI and each of its subscales. The internal consistency was excellent in the total Italian MDHI score and acceptable in all of its subscales; the test-retest reliability was high (intraclass correlation coefficient = 0.95); Italian MDHI total scores and subscales were associated with neuromuscular function, cognitive and social health, respiratory function, and quality of life. Overall, the Italian MDHI is valid and well suited to measure the multi-dimensional aspects of disease burden in Myotonic Dystrophy clinical trials.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Italian validation; MDHI; Muscular Dystrophy; Myotonic Dystrophy Health Index; Myotonic Dystrophy type 1; Patient-reported outcome measure

Mesh:

Year:  2017        PMID: 28890289     DOI: 10.1016/j.nmd.2017.07.004

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  2 in total

1.  The Charcot-Marie-Tooth Health Index: Evaluation of a Patient-Reported Outcome.

Authors:  Nicholas E Johnson; Chad Heatwole; Peter Creigh; Michael P McDermott; Nuran Dilek; Man Hung; Jerry Bounsanga; Wan Tang; Michael E Shy; David N Herrmann
Journal:  Ann Neurol       Date:  2018-08-29       Impact factor: 10.422

2.  Quality of life and subjective symptom impact in Japanese patients with myotonic dystrophy type 1.

Authors:  Haruo Fujino; Toshio Saito; Masanori P Takahashi; Hiroto Takada; Takahiro Nakayama; Osamu Imura; Tsuyoshi Matsumura
Journal:  BMC Neurol       Date:  2022-02-14       Impact factor: 2.474

  2 in total

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