Literature DB >> 21294667

Psychological health in patients with ALS is maintained as physical function declines.

Julia Cupp1, Zachary Simmons, Arthur Berg, Stephanie H Felgoise, Susan M Walsh, Helen E Stephens.   

Abstract

Although quality of life (QoL) in patients with ALS has been shown to be independent of physical function and to be maintained over time, the status of psychological health over the disease course has not been studied using an ALS-specific instrument. It is also uncertain how three common interventions - antidepressants, percutaneous endoscopic gastrostomy (PEG), and non-invasive ventilatory support (NIPPV) - influence psychological health. We performed a retrospective review of the Negative Emotion subscale (NES) score, a measure of psychological health within the ALS-Specific QoL Instrument. Analysis of 72 patients over three months, and of a subset of 48 over six months, showed stability of psychological health despite a decline in the ALS Functional Rating Scale-Revised to 88.4% of baseline at three months and 82.6% at six months. NES did not change after antidepressants, PEG, or NIPPV, although there was a suggestion of improvement with antidepressants in a subgroup. In conclusion, as with overall QoL, psychological health of ALS patients as measured with an ALS-specific instrument does not decline as physical function is lost. Supports found in a multidisciplinary ALS clinic may influence expectations, facilitate response shift, and stabilize psychological health while masking the independent effects of specific interventions.

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Mesh:

Year:  2011        PMID: 21294667     DOI: 10.3109/17482968.2011.554555

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler        ISSN: 1471-180X


  12 in total

Review 1.  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

2.  Cross-cultural adaptation and validation for the Brazilian population of the instrument Amyotrophic Lateral Sclerosis-Specific Quality of Life-Short Form (ALSSQOL-SF).

Authors:  Maisa Vitória Gayoso; Flávia Seullner Domingues; Marcondes Cavalcante França Junior; Stephanie H Felgoise; Acary Souza Bulle Oliveira; Guilherme Antonio Moreira de Barros
Journal:  Qual Life Res       Date:  2019-10-29       Impact factor: 4.147

3.  Functional Decline is Associated with Hopelessness in Amyotrophic Lateral Sclerosis (ALS).

Authors:  Sabrina Paganoni; Erin McDonnell; David Schoenfeld; Hong Yu; Jing Deng; Hamza Atassi; Alexander Sherman; Padmaja Yerramilli-Rao; Merit Cudkowicz; Nazem Atassi
Journal:  J Neurol Neurophysiol       Date:  2017-04-29

Review 4.  Patient-Perceived Outcomes and Quality of Life in ALS.

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

Review 5.  Comprehensive rehabilitative care across the spectrum of amyotrophic lateral sclerosis.

Authors:  Sabrina Paganoni; Chafic Karam; Nanette Joyce; Richard Bedlack; Gregory T Carter
Journal:  NeuroRehabilitation       Date:  2015       Impact factor: 2.138

6.  Patient-reported problematic symptoms in an ALS treatment trial.

Authors:  Divisha Raheja; Helen E Stephens; Erik Lehman; Susan Walsh; Chengwu Yang; Zachary Simmons
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2016-01-29       Impact factor: 4.092

7.  Assessing social isolation in motor neurone disease: a Rasch analysis of the MND Social Withdrawal Scale.

Authors:  Chris J Gibbons; Everard W Thornton; John Ealing; Pamela J Shaw; Kevin Talbot; Alan Tennant; Carolyn A Young
Journal:  J Neurol Sci       Date:  2013-08-09       Impact factor: 3.181

Review 8.  Associations between psychological factors and health-related quality of life and global quality of life in patients with ALS: a systematic review.

Authors:  Annerieke C van Groenestijn; Esther T Kruitwagen-van Reenen; Johanna M A Visser-Meily; Leonard H van den Berg; Carin D Schröder
Journal:  Health Qual Life Outcomes       Date:  2016-07-20       Impact factor: 3.186

9.  Modelling disease course in amyotrophic lateral Sclerosis: pseudo-longitudinal insights from cross-sectional health-related quality of life data.

Authors:  Tino Prell; Nayana Gaur; Robert Steinbach; Otto W Witte; Julian Grosskreutz
Journal:  Health Qual Life Outcomes       Date:  2020-05-01       Impact factor: 3.186

10.  Psychosocial adjustment to ALS: a longitudinal study.

Authors:  Tamara Matuz; Niels Birbaumer; Martin Hautzinger; Andrea Kübler
Journal:  Front Psychol       Date:  2015-09-14
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