Literature DB >> 7572067

Reliable disability scale for myasthenia gravis sensitive to clinical changes.

R D'Alessandro1, M Casmiro, G Benassi, R Rinaldi, G Gamberini.   

Abstract

INTRODUCTION: we developed a disability scale to monitor myasthenia gravis (MG) patients, based on degree of function impairment and daily frequency of each symptom. MATERIAL &
METHODS: the scale was based on standardized questions and clinical examination. The scale was administered to 12 patients, one or more times, for a total of 22 interviews. Each observation was recorded on videotape and reviewed by five independent observers. The ability of our scale to discriminate clinical changes was also compared with the Osserman classification.
RESULTS: our scale showed from substantial to almost perfect inter and intraobserver agreement. Our findings showed that clinically relevant changes not detected by Osserman staging were disclosed by our scale.
CONCLUSION: our scale is simple and easy to use in clinical practice. It offers an accurate means of evaluating disability in MG patients and may detect clinically relevant changes in disability. It would therefore be useful to monitor the effects of therapy.

Entities:  

Mesh:

Year:  1995        PMID: 7572067     DOI: 10.1111/j.1600-0404.1995.tb00471.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  3 in total

1.  The relationship between health, disability and quality of life in myasthenia gravis: results from an Italian study.

Authors:  Matilde Leonardi; Alberto Raggi; Carlo Antozzi; Paolo Confalonieri; Lorenzo Maggi; Ferdinando Cornelio; Renato Mantegazza
Journal:  J Neurol       Date:  2009-08-08       Impact factor: 4.849

2.  Epidemiological study of myasthenia gravis in the province of Reggio Emilia, Italy.

Authors:  D Guidetti; R Sabadini; M Bondavalli; S Cavalletti; M Lodesani; R Mantegazza; V Cosi; F Solime
Journal:  Eur J Epidemiol       Date:  1998-06       Impact factor: 8.082

3.  Clinical and electrophysiological evaluation of myasthenic features in an alpha-dystroglycanopathy cohort (FKRP-predominant).

Authors:  Paloma Gonzalez-Perez; Cheryl Smith; Wendy L Sebetka; Amber Gedlinske; Seth Perlman; Katherine D Mathews
Journal:  Neuromuscul Disord       Date:  2020-01-25       Impact factor: 4.296

  3 in total

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