Literature DB >> 15489393

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

A Chiò1, A Gauthier, A Montuschi, A Calvo, N Di Vito, P Ghiglione, R Mutani.   

Abstract

BACKGROUND: Understanding the determinants of quality of life (QoL) in amyotrophic lateral sclerosis (ALS) has become increasingly important with the recent emphasis on the comprehensive management of patients.
OBJECTIVE: To evaluate the determinants of QoL in ALS using two scales with different theoretical constructs: the Schedule for the Evaluation of QoL-Direct Weighting (SEIQoL-DW), which evaluates subjective aspects of QoL, and the McGill QoL Questionnaire (MQOL), which evaluates both health related and non-health related factors of QoL.
METHODS: Eighty consecutive patients with ALS underwent a battery of tests evaluating QoL and a series of physical, emotional, psychological, and socioeconomic predictor variables. A stepwise linear regression model was used to compare QoL scores and explicatory variables.
RESULTS: SEIQoL-DW score was related to social support, depression, religiosity, and socioeconomic status. Total MQOL score was related to social support, socioeconomic status, and clinical status. MQOL single item score (MQOL-SIS) was related to social support, depression, social withdrawal, and socioeconomic status. SEIQoL-DW score was not related to total MQOL score. Conversely, a significant correlation was found between SEIQoL-DW and MQOL-SIS.
CONCLUSIONS: With both QoL scales, the most important explicatory variable of QoL was the self perceived quality of social support. Physical status was not relevant in determining QoL. This study indicates that health related QoL measures are not adequate to assess QoL in patients with ALS, because their appreciation of QoL mainly relies on psychological, supportive, and spiritual factors. Therapeutic interventions should consider the psychological needs of patients and pay greater attention to caregivers' issues.

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Year:  2004        PMID: 15489393      PMCID: PMC1738825          DOI: 10.1136/jnnp.2003.033100

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  32 in total

1.  Spiritual well-being of the individual with amyotrophic lateral sclerosis.

Authors:  V Dal Bello-Haas; D Andrews-Hinders; J Bocian; E Mascha; T Wheeler; H Mitsumoto
Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord       Date:  2000-12

2.  Quality of life in ALS depends on factors other than strength and physical function.

Authors:  Z Simmons; B A Bremer; R A Robbins; S M Walsh; S Fischer
Journal:  Neurology       Date:  2000-08-08       Impact factor: 9.910

3.  Impact of spirituality and religiousness on outcomes in patients with ALS.

Authors:  P L Murphy; S M Albert; C M Weber; M L Del Bene; L P Rowland
Journal:  Neurology       Date:  2000-11-28       Impact factor: 9.910

4.  A neuropsychological investigation of dementia in motor neurone disease (MND).

Authors:  F P Barson; G J Kinsella; B Ong; S E Mathers
Journal:  J Neurol Sci       Date:  2000-11-01       Impact factor: 3.181

5.  A SELF-RATING DEPRESSION SCALE.

Authors:  W W ZUNG
Journal:  Arch Gen Psychiatry       Date:  1965-01

6.  Assessing individual quality of life in amyotrophic lateral sclerosis.

Authors:  S Clarke; A Hickey; C O'Boyle; O Hardiman
Journal:  Qual Life Res       Date:  2001       Impact factor: 4.147

7.  Quality of life assessment in MND: development of a social withdrawal scale.

Authors:  S A Rigby; E W Thornton; S Tedman; F Burchardt; C A Young; C Dougan
Journal:  J Neurol Sci       Date:  1999-10-31       Impact factor: 3.181

8.  Agreement among three quality of life measures in patients with ALS.

Authors:  P S Smith; B Crossley; J Greenberg; C Wilder; B Carroll
Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord       Date:  2000-09

Review 9.  Improving the quality of life for people with ALS: the challenge ahead.

Authors:  H Mitsumoto; M Del Bene
Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord       Date:  2000-12

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

Authors:  R A Robbins; Z Simmons; B A Bremer; S M Walsh; S Fischer
Journal:  Neurology       Date:  2001-02-27       Impact factor: 9.910

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  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.  Depression in amyotrophic lateral sclerosis.

Authors:  Nazem Atassi; Amanda Cook; Cristiana M E Pineda; Padmaja Yerramilli-Rao; Darlene Pulley; Merit Cudkowicz
Journal:  Amyotroph Lateral Scler       Date:  2010-11-24

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.  Caregiver burden in amyotrophic lateral sclerosis: a cross-sectional investigation of predictors.

Authors:  Tom Burke; Marwa Elamin; Miriam Galvin; Orla Hardiman; Niall Pender
Journal:  J Neurol       Date:  2015-04-23       Impact factor: 4.849

5.  Ethical challenges in tracheostomy-assisted ventilation in amyotrophic lateral sclerosis.

Authors:  Morten Magelssen; Trygve Holmøy; Morten Andreas Horn; Ove Arne Fondenæs; Knut Dybwik; Reidun Førde
Journal:  J Neurol       Date:  2018-09-14       Impact factor: 4.849

6.  Apathy and its impact on patient outcome in amyotrophic lateral sclerosis.

Authors:  J Caga; S Hsieh; E Highton-Williamson; M C Zoing; E Ramsey; E Devenney; R M Ahmed; M C Kiernan
Journal:  J Neurol       Date:  2017-11-30       Impact factor: 4.849

7.  Depression, pain and quality of life in patients with amyotrophic lateral sclerosis: a cross-sectional study.

Authors:  A Pizzimenti; M Aragona; E Onesti; M Inghilleri
Journal:  Funct Neurol       Date:  2013 Apr-May

Review 8.  The role of palliative care in patients with neurological diseases.

Authors:  Gian Domenico Borasio
Journal:  Nat Rev Neurol       Date:  2013-04-02       Impact factor: 42.937

9.  Longitudinal predictors of caregiver burden in amyotrophic lateral sclerosis: a population-based cohort of patient-caregiver dyads.

Authors:  Tom Burke; Orla Hardiman; Marta Pinto-Grau; Katie Lonergan; Mark Heverin; Katy Tobin; Anthony Staines; Miriam Galvin; Niall Pender
Journal:  J Neurol       Date:  2018-02-02       Impact factor: 4.849

Review 10.  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
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