Literature DB >> 11676997

Patients' health-related quality of life and utilities associated with different stages of amyotrophic lateral sclerosis.

G M Kiebert1, C Green, C Murphy, J D Mitchell, M O'Brien, A Burrell, P N Leigh.   

Abstract

OBJECTIVES: Amyotrophic lateral sclerosis (ALS) is a devastating disease that has serious consequences in terms of impairments and disabilities, which are expected to impact on health-related quality of life (HRQL). The aim of the present study was to assess self-reported health status and HRQL, as well as patients' own valuation of their present health state in a sample of patients with different levels of severity of ALS.
METHODS: Structured interviews were conducted with 77 patients with different levels of disease severity. Patients completed a disease-specific health status measure (ALSAQ-40), a generic health status measure (EuroQol EQ-5D), visual analogue scale (VAS) rating of current health and a standard gamble (SG) exercise to provide health state utilities for their own health state.
RESULTS: The results from the ALSAQ-40 and EQ-5D descriptive system indicate that patients' HRQL decreases systematically with increasing severity of disease. Patients' mean VAS rating of their own health ranged from 0.74 for stage 1 (early) disease severity, to 0.37 for stage 4 (late stage) disease severity. Utilities elicited via SG were systematically higher than VAS scores and ranged from a mean of 0.79 for stage 1 disease severity to a mean of 0.45 for stage 4 disease severity.

Entities:  

Mesh:

Year:  2001        PMID: 11676997     DOI: 10.1016/s0022-510x(01)00616-5

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  17 in total

1.  Administration of a soluble activin type IIB receptor promotes skeletal muscle growth independent of fiber type.

Authors:  Samuel M Cadena; Kathleen N Tomkinson; Travis E Monnell; Matthew S Spaits; Ravindra Kumar; Kathryn W Underwood; R Scott Pearsall; Jennifer L Lachey
Journal:  J Appl Physiol (1985)       Date:  2010-05-13

2.  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

3.  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

4.  Quality of life during hemodialysis and study dialysis treatment in patients referred to teaching hospitals in Urmia-Iran in 2007.

Authors:  Nader Aghakhani; Hamid Sharif Nia; Saeed Samad Zadeh; Vahid Toupchi; Saeed Toupchi; Narges Rahbar
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Review 5.  Economic Studies in Motor Neurone Disease: A Systematic Methodological Review.

Authors:  Alan Moore; Carolyn A Young; Dyfrig A Hughes
Journal:  Pharmacoeconomics       Date:  2017-04       Impact factor: 4.981

6.  Health-related quality of life in ALS, myasthenia gravis and facioscapulohumeral muscular dystrophy.

Authors:  Yaroslav Winter; Karsten Schepelmann; Annika E Spottke; Detlef Claus; Christoph Grothe; Rolf Schröder; Dieter Heuss; Stefan Vielhaber; Björn Tackenberg; Veit Mylius; Jens-Peter Reese; Reinhard Kiefer; Bertold Schrank; Wolfgang H Oertel; Richard Dodel
Journal:  J Neurol       Date:  2010-04-10       Impact factor: 4.849

7.  Health-related quality of life in amyotrophic lateral sclerosis: determining a meaningful deterioration.

Authors:  Josephine M Norquist; Ray Fitzpatrick; Crispin Jenkinson
Journal:  Qual Life Res       Date:  2004-10       Impact factor: 4.147

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.  Patient-Perceived Outcomes and Quality of Life in ALS.

Authors:  Zachary Simmons
Journal:  Neurotherapeutics       Date:  2015-04       Impact factor: 7.620

10.  Health-related quality of life and supportive care in patients with rare long-term neurological conditions.

Authors:  Melanie Calvert; Hardev Pall; Thomas Hoppitt; Benjamin Eaton; Edward Savill; Catherine Sackley
Journal:  Qual Life Res       Date:  2012-09-23       Impact factor: 4.147

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