Literature DB >> 19626161

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

Dorothée Lulé1, Sonja Häcker, Albert Ludolph, Niels Birbaumer, Andrea Kübler.   

Abstract

INTRODUCTION: There is increasing debate on the issue of whether to facilitate the end-of-life decisions of severely disabled patients with diseases such as amyotrophic lateral sclerosis (ALS). Our two studies were intended to explore the emotional state and quality of life of patients with ALS.
METHODS: Two studies were performed to investigate depression and the quality of life in ALS patients: one was a longitudinal study, the other a comparison of ALS patients to normal control subjects.
RESULTS: These studies found no correlation between physical disability in ALS and either depression or the quality of life. The severity of depression was found to be inversely related to educational status. In ALS patients the quality of life was comparable with healthy controls. DISCUSSION: The rationale for not providing life-sustaining treatment to severely disabled patients is that a poor quality of life is expected after such treatment. Our studies have shown, however, that ALS patients can experience a satisfactory quality of life without depressive manifestations even if they are severely physically impaired, including in the terminal phase.

Entities:  

Keywords:  amyotrophic lateral sclerosis; assisted suicide; depression; quality of life; respiratory insufficiency

Year:  2008        PMID: 19626161      PMCID: PMC2696844          DOI: 10.3238/arztebl.2008.0397

Source DB:  PubMed          Journal:  Dtsch Arztebl Int        ISSN: 1866-0452            Impact factor:   5.594


  39 in total

1.  Subjective experience and coping in ALS.

Authors:  Martin Hecht; Thomas Hillemacher; Elmar Gräsel; Sebastian Tigges; Martin Winterholler; Dieter Heuss; Max-Josef Hilz; Bernhard Neundörfer
Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord       Date:  2002-12

2.  Correlates of suffering in amyotrophic lateral sclerosis.

Authors:  L Ganzini; W S Johnston; W F Hoffman
Journal:  Neurology       Date:  1999-04-22       Impact factor: 9.910

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

Authors:  J G Rabkin; S M Albert; M L Del Bene; I O'Sullivan; T Tider; L P Rowland; H Mitsumoto
Journal:  Neurology       Date:  2005-07-12       Impact factor: 9.910

4.  Quality-of-life measurement in advanced cancer: assessing the individual.

Authors:  D Waldron; C A O'Boyle; M Kearney; M Moriarty; D Carney
Journal:  J Clin Oncol       Date:  1999-11       Impact factor: 44.544

5.  Individual quality of life is not correlated with health-related quality of life or physical function in patients with amyotrophic lateral sclerosis.

Authors:  Christian Neudert; Maria Wasner; Gian Domenico Borasio
Journal:  J Palliat Med       Date:  2004-08       Impact factor: 2.947

6.  Discontinuation of mechanical ventilation in patients with amyotrophic lateral sclerosis.

Authors:  G D Borasio; R Voltz
Journal:  J Neurol       Date:  1998-11       Impact factor: 4.849

7.  Home ventilation for amyotrophic lateral sclerosis patients: outcomes, costs, and patient, family, and physician attitudes.

Authors:  A H Moss; P Casey; C B Stocking; R P Roos; B R Brooks; M Siegler
Journal:  Neurology       Date:  1993-02       Impact factor: 9.910

8.  Assessing the quality of life of the individual: the SEIQoL with a healthy and a gastroenterology unit population.

Authors:  H M McGee; C A O'Boyle; A Hickey; K O'Malley; C R Joyce
Journal:  Psychol Med       Date:  1991-08       Impact factor: 7.723

9.  Quality of life and dyadic adjustment in oral cancer patients and their female partners.

Authors:  J Jenewein; R A Zwahlen; D Zwahlen; N Drabe; H Moergeli; S Büchi
Journal:  Eur J Cancer Care (Engl)       Date:  2008-03       Impact factor: 2.520

10.  Individualized quality of life, standardized quality of life, and distress in patients undergoing a phase I trial of the novel therapeutic Reolysin (reovirus).

Authors:  Linda E Carlson; Barry D Bultz; Donald G Morris
Journal:  Health Qual Life Outcomes       Date:  2005-01-27       Impact factor: 3.186

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  32 in total

1.  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

2.  Association between depression and survival in Chinese amyotrophic lateral sclerosis patients.

Authors:  Qianqian Wei; Zhenzhen Zheng; Xiaoyan Guo; Ruwei Ou; Xueping Chen; Rui Huang; Jing Yang; Huifang Shang
Journal:  Neurol Sci       Date:  2016-01-13       Impact factor: 3.307

3.  Live and let die: existential decision processes in a fatal disease.

Authors:  Dorothée Lulé; Sonja Nonnenmacher; Sonja Sorg; Johanna Heimrath; Martin Hautzinger; Thomas Meyer; Andrea Kübler; Niels Birbaumer; Albert C Ludolph
Journal:  J Neurol       Date:  2014-01-12       Impact factor: 4.849

Review 4.  Review: Human Intracortical Recording and Neural Decoding for Brain-Computer Interfaces.

Authors:  David M Brandman; Sydney S Cash; Leigh R Hochberg
Journal:  IEEE Trans Neural Syst Rehabil Eng       Date:  2017-03-02       Impact factor: 3.802

5.  Emotional adjustment in amyotrophic lateral sclerosis (ALS).

Authors:  Dorothée Lulé; Sandra Pauli; Ertan Altintas; Ulrike Singer; Thomas Merk; Ingo Uttner; Niels Birbaumer; Albert C Ludolph
Journal:  J Neurol       Date:  2011-08-02       Impact factor: 4.849

6.  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

7.  Generic quality of life assessment in dementia patients: a prospective cohort study.

Authors:  Claudia Schiffczyk; Barbara Romero; Christina Jonas; Constanze Lahmeyer; Friedemann Müller; Matthias W Riepe
Journal:  BMC Neurol       Date:  2010-06-20       Impact factor: 2.474

8.  Quality of life in fatal disease: the flawed judgement of the social environment.

Authors:  Dorothée Lulé; Benedikt Ehlich; Dirk Lang; Sonja Sorg; Johanna Heimrath; Andrea Kübler; Niels Birbaumer; Albert C Ludolph
Journal:  J Neurol       Date:  2013-08-30       Impact factor: 4.849

9.  Implementation of a population-based epidemiological rare disease registry: study protocol of the amyotrophic lateral sclerosis (ALS)--registry Swabia.

Authors:  Gabriele Nagel; Hatice Unal; Angela Rosenbohm; Albert C Ludolph; Dietrich Rothenbacher
Journal:  BMC Neurol       Date:  2013-02-17       Impact factor: 2.474

10.  Independent home use of a brain-computer interface by people with amyotrophic lateral sclerosis.

Authors:  Jonathan R Wolpaw; Richard S Bedlack; Domenic J Reda; Robert J Ringer; Patricia G Banks; Theresa M Vaughan; Susan M Heckman; Lynn M McCane; Charles S Carmack; Stefan Winden; Dennis J McFarland; Eric W Sellers; Hairong Shi; Tamara Paine; Donald S Higgins; Albert C Lo; Huned S Patwa; Katherine J Hill; Grant D Huang; Robert L Ruff
Journal:  Neurology       Date:  2018-06-27       Impact factor: 11.800

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