Literature DB >> 19482864

Neurological disability, psychological distress, and health-related quality of life in MS patients within the first three years after diagnosis.

S Kern1, W Schrempf, H Schneider, T Schultheiss, H Reichmann, T Ziemssen.   

Abstract

BACKGROUND: Psychological distress and psychiatric co-morbidity are common in multiple sclerosis (MS) and is often associated with neurological disability as well as reduced quality of life.
OBJECTIVES: This study aimed to investigate psychological distress and the possible association with quality of life as well as neurological disability in MS patients within the first 3 years after diagnosis.
METHODS: Psychological distress was measured using a standardized questionnaire (Symptom-Check-List-90-R; SCL-90-R) in 31 relapsing-remitting MS patients and 24 sex- and age-matched healthy controls.
RESULTS: Psychological distress was significantly more pronounced in MS patients when compared to healthy controls. Interpersonal sensitivity and psychoticism were positively associated with neurological disability (Expanded Disability Status Scale [EDSS]). A high EDSS group (median split EDSS; 1.5) expressed significantly more psychological distress when compared to the low EDSS group and healthy controls. MS patients with minimal to no neurological disability (low EDSS group) also expressed significantly more emotional distress when compared to healthy controls. MS-related quality of life was positively associated with neurological disability as well as SCL-90-R scores. After adjusting for neurological disability, psychological distress was still significantly associated with quality of life.
CONCLUSIONS: Early stage MS patients significantly differ in their psychological distress when compared to healthy controls. Psychological distress in these patients is associated with neurological disability, but it is also present in patients with minimal to no neurological disability. Psychological distress was identified as an independent predictor for MS-related quality of life.

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Year:  2009        PMID: 19482864     DOI: 10.1177/1352458509103300

Source DB:  PubMed          Journal:  Mult Scler        ISSN: 1352-4585            Impact factor:   6.312


  20 in total

1.  Neuropsychological and psychiatric aspects of multiple sclerosis: preliminary investigation of discrete profiles across neurological subtypes.

Authors:  Marina Katsari; Dimitrios Kasselimis; Gerasimos Gasparinatos; Roubina Antonellou; Konstantinos Voumvourakis
Journal:  Neurol Sci       Date:  2016-01-07       Impact factor: 3.307

2.  MS quality of life, depression, and fatigue improve after mindfulness training: a randomized trial.

Authors:  P Grossman; L Kappos; H Gensicke; M D'Souza; D C Mohr; I K Penner; C Steiner
Journal:  Neurology       Date:  2010-09-28       Impact factor: 9.910

3.  Longitudinal changes in quality of life and related psychosocial variables in australians with multiple sclerosis.

Authors:  Judy Ann Wollin; Nancy Spencer; Elizabeth McDonald; Gary Fulcher; Maureen Bourne; Rex D Simmons
Journal:  Int J MS Care       Date:  2013

4.  The stress-buffering effects of hope on adjustment to multiple sclerosis.

Authors:  Sindia Madan; Kenneth I Pakenham
Journal:  Int J Behav Med       Date:  2014-12

5.  Development and effectiveness of a psychoeducational wellness program for people with multiple sclerosis: description and outcomes.

Authors:  Kimberly Beckwith McGuire; Jelena Stojanovic-Radic; Lauren Strober; Nancy D Chiaravalloti; John DeLuca
Journal:  Int J MS Care       Date:  2015 Jan-Feb

Review 6.  Life issues in multiple sclerosis.

Authors:  Rex D Simmons
Journal:  Nat Rev Neurol       Date:  2010-09-21       Impact factor: 42.937

7.  Quality of life in patients with multiple sclerosis and their caregivers in Colombia: One-year follow-up.

Authors:  Elkin Beltrán; Diana Díaz; Cindy Díaz; Luis Zarco
Journal:  Biomedica       Date:  2020-03-01       Impact factor: 0.935

8.  Cognitive impairment, health-related quality of life and vocational status at early stages of multiple sclerosis: a 7-year longitudinal study.

Authors:  Aurélie Ruet; Mathilde Deloire; Delphine Hamel; Jean-Christophe Ouallet; Klaus Petry; Bruno Brochet
Journal:  J Neurol       Date:  2012-10-19       Impact factor: 4.849

9.  Improving patient-physician dialog: commentary on the results of the MS Choices survey.

Authors:  Alessandra Lugaresi; Tjalf Ziemssen; Celia Oreja-Guevara; Delyth Thomas; Elisabetta Verdun
Journal:  Patient Prefer Adherence       Date:  2012-02-17       Impact factor: 2.711

10.  Psychosocial and Medical Determinants of Health-related Quality of Life in Patients with Relapsing-Remitting Multiple Sclerosis.

Authors:  Isaac Rahimian Boogar; Siavash Talepasand; Mohammad Jabari
Journal:  Noro Psikiyatr Ars       Date:  2018-03-19       Impact factor: 1.339

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