Literature DB >> 11222784

Quality of life in ALS is maintained as physical function declines.

R A Robbins1, Z Simmons, B A Bremer, S M Walsh, S Fischer.   

Abstract

OBJECTIVES: To study patients with ALS to determine how physical function, quality of life (QOL), and spirituality or religiousness change over time, and what relationship these changes have to one another.
METHODS: Sixty patients with ALS were studied prospectively. They were assessed at baseline, 3 months, and 6 months, using questionnaires designed to measure general quality of life (McGill Quality of Life questionnaire), religiosity (Idler Index of Religiosity), ALS-specific health-related quality of life (SIP/ALS-19), and ALS-specific function (ALS functional rating scale).
RESULTS: A two-way repeated measures multivariate analysis of variance revealed that both the passage of time and the specific QOL scales used were factors in predicting patient quality of life (F[1, 59]= 9.87, p < 0.003 and F[3, 177]= 16.90, p < 0.001) Despite a progressive decline in physical function as measured by the ALS-specific function score, the general QOL and religiosity scores changed little. In contrast, the ALS-specific health-related QOL score declined in parallel with the ALS-specific function score.
CONCLUSIONS: QOL in patients with ALS appears to be independent of physical function, which agrees with a previous cross-sectional study. The ALS-specific health-related QOL score is primarily a measure of physical function. QOL instruments that assess spiritual, religious, and psychological factors produce different results than those obtained using measures of physical function alone.

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Year:  2001        PMID: 11222784     DOI: 10.1212/wnl.56.4.442

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  43 in total

1.  Psychopathological features and suicidal ideation in amyotrophic lateral sclerosis patients.

Authors:  Arianna Palmieri; Gianni Sorarù; Elisa Albertini; Carlo Semenza; Francesca Vottero-Ris; Carla D'Ascenzo; Giorgia Querin; Alessandro Zennaro; Elena Pegoraro; Corrado Angelini
Journal:  Neurol Sci       Date:  2010-06-03       Impact factor: 3.307

2.  A cross sectional study on determinants of quality of life in ALS.

Authors:  A Chiò; A Gauthier; A Montuschi; A Calvo; N Di Vito; P Ghiglione; R Mutani
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-11       Impact factor: 10.154

3.  ALS multidisciplinary clinic and survival. Results from a population-based study in Southern Italy.

Authors:  Stefano Zoccolella; Ettore Beghi; Guerrino Palagano; Angela Fraddosio; Vito Guerra; Vito Lepore; Isabella Laura Simone; Paolo Lamberti; Luigi Serlenga; Giancarlo Logroscino
Journal:  J Neurol       Date:  2007-04-13       Impact factor: 4.849

4.  The multidisciplinary clinic, quality of life and survival in motor neuron disease.

Authors:  Ammar Al-Chalabi
Journal:  J Neurol       Date:  2007-08-11       Impact factor: 4.849

5.  Phase II screening trial of lithium carbonate in amyotrophic lateral sclerosis: examining a more efficient trial design.

Authors:  R G Miller; D H Moore; D A Forshew; J S Katz; R J Barohn; M Valan; M B Bromberg; K L Goslin; M C Graves; L F McCluskey; A L McVey; T Mozaffar; J M Florence; A Pestronk; M Ross; E P Simpson; S H Appel
Journal:  Neurology       Date:  2011-08-03       Impact factor: 9.910

6.  Quality of life of ALS and LIS patients with and without invasive mechanical ventilation.

Authors:  Marie-Christine Rousseau; Stéphane Pietra; José Blaya; Anne Catala
Journal:  J Neurol       Date:  2011-04-02       Impact factor: 4.849

Review 7.  Clinical diagnosis and management of amyotrophic lateral sclerosis.

Authors:  Orla Hardiman; Leonard H van den Berg; Matthew C Kiernan
Journal:  Nat Rev Neurol       Date:  2011-10-11       Impact factor: 42.937

Review 8.  Evaluation of quality of life in individuals with severe chronic motor disability: A major challenge.

Authors:  Marie-Christine Rousseau; Karine Baumstarck; Thierry Billette de Villemeur; Pascal Auquier
Journal:  Intractable Rare Dis Res       Date:  2016-05

9.  The influence of psychological state and motivation on brain-computer interface performance in patients with amyotrophic lateral sclerosis - a longitudinal study.

Authors:  Femke Nijboer; Niels Birbaumer; Andrea Kübler
Journal:  Front Neurosci       Date:  2010-07-21       Impact factor: 4.677

10.  Depression and quality of life in patients with amyotrophic lateral sclerosis.

Authors:  Dorothée Lulé; Sonja Häcker; Albert Ludolph; Niels Birbaumer; Andrea Kübler
Journal:  Dtsch Arztebl Int       Date:  2008-06-06       Impact factor: 5.594

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