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Proposal of a new clinical protocol for evaluating fatigability in adult SMA patients.
Ricci, Giulia; Torri, Francesca; Govoni, Alessandra; Chiappini, Roberto; Manca, Laura; Vadi, Gabriele; Roccella, Stefano; Magri, Francesca; Meneri, Megi; Fassini, Federica; Vacchiano, Veria; Tomassini, Silvia; Gironella, Noemi; Coccia, Michela; Comi, Giacomo; Liguori, Rocco; Siciliano, Gabriele.
Afiliação
  • Ricci G; Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
  • Torri F; Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
  • Govoni A; Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
  • Chiappini R; Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
  • Manca L; Department of Mathematics, University of Pisa, Pisa, Italy.
  • Vadi G; Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
  • Roccella S; The Biorobotics Institute, Sant'Anna Superior Studies School, Pisa, Italy.
  • Magri F; Ospedale Maggiore Policlinico; University of Milan, Dpt Neurological Sciences, Milano, Italy.
  • Meneri M; Ospedale Maggiore Policlinico; University of Milan, Dpt Neurological Sciences, Milano, Italy.
  • Fassini F; Ospedale Maggiore Policlinico; University of Milan, Dpt Neurological Sciences, Milano, Italy.
  • Vacchiano V; IRCCS Istituto Delle Scienze Neurologiche di Bologna, Bologna, Italy.
  • Tomassini S; Centro NeMO Ancona, Ancona, Italy.
  • Gironella N; Centro NeMO Ancona, Ancona, Italy.
  • Coccia M; Centro NeMO Ancona, Ancona, Italy.
  • Comi G; Ospedale Maggiore Policlinico; University of Milan, Dpt Neurological Sciences, Milano, Italy.
  • Liguori R; IRCCS Istituto Delle Scienze Neurologiche di Bologna, Bologna, Italy.
  • Siciliano G; Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Acta Myol ; 42(2-3): 65-70, 2023.
Article em En | MEDLINE | ID: mdl-38090548
ABSTRACT

Objective:

Spinal Muscular Atrophy (SMA) is a genetic neuromuscular disease affecting the lower motor neuron, carrying a significant burden on patients' general motor skills and quality of life, characterized by a great variability in phenotypic expression. As new therapeutic options make their appearance on the scene, sensitive clinical tools and outcome measures are needed, especially in adult patients undergoing treatment, in which the expected clinical response is a mild improvement or stabilization of disease progression.

Methods:

Here, we describe a new functional motor scale specifically designed for evaluating the endurance dimension for the upper and lower limbs in adult SMA patients.

Results:

The scale was first tested in eight control healthy subjects and then validated in ten adult SMA patients, proving intra- and inter-observer reliability. We also set up an evaluation protocol by using wearable devices including surface EMG and accelerometer.

Conclusions:

The endurance evaluation should integrate the standard clinical monitoring in the management and follow-up of SMA adult patients.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Atrofia Muscular Espinal Limite: Adult / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Atrofia Muscular Espinal Limite: Adult / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article