Literature DB >> 19639395

A comparison of mood and quality of life among people with progressive neurological illnesses and their caregivers.

Marita P McCabe1, Lucy Firth, Elodie O'Connor.   

Abstract

The current study was designed to investigate differences in mood and a range of QOL domains among 423 patients and 335 caregivers of people with motor neurone disease (MND), Huntington's disease (HD), Parkinson's, and multiple sclerosis (MS). Patients and caregivers completed an anonymous questionnaire that evaluated their mood (anxiety, depression, fatigue, confusion) and QOL (physical, psychological, social, environment). The results demonstrated that caregivers of people with MND and HD experienced most problems with their mood and QOL compared to caregivers of people in the other illness groups. There were few differences in mood or QOL between patients and caregivers. Patients generally showed greater confusion, physical impairment, and psychological maladjustment. The findings suggest that educational and intervention programs need to be developed to help both patients and their caregivers to adjust and cope with these illnesses, particularly caregivers of people with MND and HD.

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Year:  2009        PMID: 19639395     DOI: 10.1007/s10880-009-9168-5

Source DB:  PubMed          Journal:  J Clin Psychol Med Settings        ISSN: 1068-9583


  23 in total

1.  Development of the World Health Organization WHOQOL-BREF quality of life assessment. The WHOQOL Group.

Authors: 
Journal:  Psychol Med       Date:  1998-05       Impact factor: 7.723

2.  The effects of caring for a spouse with Parkinson's disease on social, psychological and physical well-being.

Authors:  F O'Reilly; F Finnan; S Allwright; G D Smith; Y Ben-Shlomo
Journal:  Br J Gen Pract       Date:  1996-09       Impact factor: 5.386

3.  Severity of depressive symptoms and quality of life in patients with amyotrophic lateral sclerosis.

Authors:  Andrea Kübler; Susanne Winter; Albert C Ludolph; Martin Hautzinger; Niels Birbaumer
Journal:  Neurorehabil Neural Repair       Date:  2005-09       Impact factor: 3.919

4.  Predictors of depressive symptoms among spouse caregivers in Parkinson's disease.

Authors:  H H Fernandez; R E Tabamo; R R David; J H Friedman
Journal:  Mov Disord       Date:  2001-11       Impact factor: 10.338

Review 5.  Caring for the carers: quality of life in Huntington's disease.

Authors:  Aimee Aubeeluck
Journal:  Br J Nurs       Date:  2005 Apr 28-May 11

6.  Mood and self-esteem of persons with multiple sclerosis following an exacerbation.

Authors:  Marita P McCabe
Journal:  J Psychosom Res       Date:  2005-09       Impact factor: 3.006

7.  Quality of life among persons with multiple sclerosis and their caregivers.

Authors:  K J Aronson
Journal:  Neurology       Date:  1997-01       Impact factor: 9.910

8.  Major stressors facing patients with amyotrophic lateral sclerosis (ALS): a survey to identify their concerns and to compare with those of their caregivers.

Authors:  Marilyn Trail; Naomi Nelson; John N Van; Stanley H Appel; Eugene C Lai
Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord       Date:  2004-03

9.  Living with Huntington's disease: illness perceptions, coping mechanisms, and spouses' quality of life.

Authors:  D I Helder; A A Kaptein; G M J Van Kempen; J Weinman; J C Van Houwelingen; R A C Roos
Journal:  Int J Behav Med       Date:  2002

10.  Quality of life and psychosocial issues in ventilated patients with amyotrophic lateral sclerosis and their caregivers.

Authors:  Dagmar Kaub-Wittemer; Nicole von Steinbüchel; Maria Wasner; Gerhard Laier-Groeneveld; Gian Domenico Borasio
Journal:  J Pain Symptom Manage       Date:  2003-10       Impact factor: 3.612

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  30 in total

1.  Predictors of quality of life in carers for people with a progressive neurological illness: a longitudinal study.

Authors:  Elodie J O'Connor; Marita P McCabe
Journal:  Qual Life Res       Date:  2010-12-02       Impact factor: 4.147

2.  Increased irritability, anxiety, and immune reactivity in transgenic Huntington's disease monkeys.

Authors:  Jessica Raper; Steven Bosinger; Zachary Johnson; Gregory Tharp; Sean P Moran; Anthony W S Chan
Journal:  Brain Behav Immun       Date:  2016-07-07       Impact factor: 7.217

3.  Improving the quality of life of multiple sclerosis patients through coping strategies in routine medical practice.

Authors:  Richard Devy; Philippe Lehert; Etienne Varlan; Marc Genty; Gilles Edan
Journal:  Neurol Sci       Date:  2014-07-27       Impact factor: 3.307

Review 4.  Palliative Care for Movement Disorders.

Authors:  Christina L Vaughan; Benzi M Kluger
Journal:  Curr Treat Options Neurol       Date:  2018-02-21       Impact factor: 3.598

5.  'All the burden on all the carers': exploring quality of life with family caregivers of Huntington's disease patients.

Authors:  Aimee Victoria Aubeeluck; Heather Buchanan; Edward J N Stupple
Journal:  Qual Life Res       Date:  2011-11-13       Impact factor: 4.147

6.  Religiosity and its relation to quality of life in primary caregivers of patients with multiple sclerosis: a case study in Greece.

Authors:  Andreas A Argyriou; Gregoris Iconomou; Amalia A Ifanti; Panagiotis Karanasios; Konstantinos Assimakopoulos; Alexandra Makridou; Foteini Giannakopoulou; Nicolaos Makris
Journal:  J Neurol       Date:  2011-01-07       Impact factor: 4.849

7.  Quality of life and emotional burden of primary caregivers: a case-control study of multiple sclerosis patients in Greece.

Authors:  Andreas A Argyriou; Panagiotis Karanasios; Amalia A Ifanti; Gregoris Iconomou; Konstantinos Assimakopoulos; Alexandra Makridou; Fotini Giannakopoulou; Nicolaos Makris
Journal:  Qual Life Res       Date:  2011-04-05       Impact factor: 4.147

8.  Effect of Aerobic Exercise Training on Mood in People With Traumatic Brain Injury: A Pilot Study.

Authors:  Ali A Weinstein; Lisa M K Chin; John Collins; Divya Goel; Randall E Keyser; Leighton Chan
Journal:  J Head Trauma Rehabil       Date:  2017 May/Jun       Impact factor: 2.710

9.  Quality of life of people who inject drugs: characteristics and comparisons with other population samples.

Authors:  Jane A Fischer; Sue Conrad; Alexandra M Clavarino; Robert Kemp; Jackob M Najman
Journal:  Qual Life Res       Date:  2013-01-23       Impact factor: 4.147

10.  Caregiver Burden in Fragile X Families.

Authors:  Ana-Maria Iosif; Andres F Sciolla; Khyati Brahmbhatt; Andreea L Seritan
Journal:  Curr Psychiatry Rev       Date:  2013-02-01
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