Movement Disorders (revue)

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Assessment of Quality of Life with the Multiple System Atrophy Health-Related Quality of Life Scale

Identifieur interne : 000279 ( PascalFrancis/Checkpoint ); précédent : 000278; suivant : 000280

Assessment of Quality of Life with the Multiple System Atrophy Health-Related Quality of Life Scale

Auteurs : Wassilios G. Meissner [France] ; Alexandra Foubert-Samier [France] ; Sandrine Dupouy [France] ; Angélique Gerdelat-Mas [France] ; Rachel Debs [France] ; Fabienne Marquant [France] ; Valérie Cochen De Cock [France] ; Olivier Rascol [France] ; François Tison [France] ; Anne Pavy-Le Traon [France]

Source :

RBID : Pascal:12-0423950

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English descriptors

Abstract

Background: Multiple system atrophy (MSA) has considerable effect on health-related quality of life (Hr-QoL). The aim of this study was to prospectively evaluate Hr-QoL by using the MSA health-related Quality of Life (MSA-QoL) scale. Methods: Evaluation of 100 patients at baseline and after a mean follow-up of 11.5 months was performed. Assessment was made of potential associations with established markers of disease progression. Calculation was performed of sample-size estimates for various effect sizes. Results: MSA-QoL scale scores were less responsive to change than Unified MSA Rating Scale (UMSARS) scores. Responsiveness was largely improved and reasonable sample-size estimates were obtained when limiting the analysis to items with significant change over time. Conclusions: The UMSARS remains the "gold standard" for disease-modifying/neuroprotection trials. An MSA-QoL Change Scale, based on the most responsive items, may become a valuable tool.


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Pascal:12-0423950

Le document en format XML

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<term>Multiple system atrophy</term>
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<div type="abstract" xml:lang="en">Background: Multiple system atrophy (MSA) has considerable effect on health-related quality of life (Hr-QoL). The aim of this study was to prospectively evaluate Hr-QoL by using the MSA health-related Quality of Life (MSA-QoL) scale. Methods: Evaluation of 100 patients at baseline and after a mean follow-up of 11.5 months was performed. Assessment was made of potential associations with established markers of disease progression. Calculation was performed of sample-size estimates for various effect sizes. Results: MSA-QoL scale scores were less responsive to change than Unified MSA Rating Scale (UMSARS) scores. Responsiveness was largely improved and reasonable sample-size estimates were obtained when limiting the analysis to items with significant change over time. Conclusions: The UMSARS remains the "gold standard" for disease-modifying/neuroprotection trials. An MSA-QoL Change Scale, based on the most responsive items, may become a valuable tool.</div>
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