Literature DB >> 12495573

Correlates of Quality of Life in people with motor neuron disease (MND).

L H Goldstein1, L Atkins, P N Leigh.   

Abstract

OBJECTIVES: Previous work has not found correlations between standardized questionnaire measures of quality of life (QoL) and physical strength/functional ability in people with motor neuron disease (MND). Little is known about the relationship between ratings on an abbreviated self-generated measure of QoL, the Schedule for Evaluation of Individual Quality of Life-Direct Weighting (SEIQoL-DW), and measures of functional status such as the Sickness Impact Profile (SIP), although the former has been rated by people with MND as providing a more valid measure of their own QoL than the latter. The aim of this study was to examine whether self-generated ratings of QoL correlated with measures of physical impairment and self-reported functional status, psychological wellbeing and self-reported cognitive functioning, and with factors such as social support, which elsewhere has been reported to be a determinant of QoL in MND.
DESIGN: The present cross-sectional study investigated between SEIQoL-DW ratings and SIP and the relationship ALS Severity Scale (ALSSS) scores, as well as with self-reported anxiety, depression, social support and everyday cognitive functioning in 31 people with MND.
RESULTS: Overall QoL ratings on the SEIQoL-DW failed to correlate with any of the ALSSS or SIP subscale scores. This was despite the fact that health was nominated as an important QoL-related category by 64.5% of the sample. QoL scores were, however, found to correlate positively with the existence of confiding and emotional support; they also correlated negatively with the presence of self-rated everyday cognitive difficulties but not with affective state.
CONCLUSIONS: Current findings support recent observations that individuals' ratings of their QoL cannot simply be equated with their physical impairment and functional limitations, and that support systems may be important. Cognitive functioning, known to be impaired in some people with MND, should also be considered when evaluating QoL.

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Mesh:

Year:  2002        PMID: 12495573     DOI: 10.1080/146608202760834120

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord        ISSN: 1466-0822


  32 in total

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

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Journal:  Neurol Sci       Date:  2010-06-03       Impact factor: 3.307

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

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Review 3.  The use, feasibility and psychometric properties of an individualised quality-of-life instrument: a systematic review of the SEIQoL-DW.

Authors:  L Wettergren; A Kettis-Lindblad; M Sprangers; L Ring
Journal:  Qual Life Res       Date:  2009-06-03       Impact factor: 4.147

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

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Journal:  J Neurol       Date:  2011-04-02       Impact factor: 4.849

5.  Prevalence of depressive disorders and change over time in late-stage ALS.

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6.  Cognitive impairment across ALS clinical stages in a population-based cohort.

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Review 7.  The neuropathological signature of bulbar-onset ALS: A systematic review.

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8.  Depression and QOL in patients with ALS: how do self-ratings and ratings by relatives differ?

Authors:  Torsten Grehl; Mirjam Rupp; Paula Budde; Martin Tegenthoff; Heiner Fangerau
Journal:  Qual Life Res       Date:  2010-11-18       Impact factor: 4.147

Review 9.  Evaluation of quality of life in individuals with severe chronic motor disability: A major challenge.

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Journal:  Intractable Rare Dis Res       Date:  2016-05

10.  Speech Movement Measures as Markers of Bulbar Disease in Amyotrophic Lateral Sclerosis.

Authors:  Sanjana Shellikeri; Jordan R Green; Madhura Kulkarni; Panying Rong; Rosemary Martino; Lorne Zinman; Yana Yunusova
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