Literature DB >> 20028340

Well-being in patients with amyotrophic lateral sclerosis and their next of kin over time.

A G Olsson1, I Markhede, S Strang, L I Persson.   

Abstract

OBJECTIVES: The well-being and physical function among patients with ALS and their next of kin was studied over time.
MATERIALS AND METHODS: Thirty-five patients with ALS and their next of kin were studied with respect to physical, general and psychological well-being by the visual analogue scale (VAS) every 4-6 months. Physical function in patients was rated by the ALSFRS-R and the Norris scale. Patients and next of kin rated the well-being of themselves and their counterpart.
RESULTS: The well-being was stable and there was a relation between the well-being of patients and next of kin throughout the time studied. Next of kin rated the well-being of the patients worse than patients rated themselves, while patients rated the well-being of their next of kin at the same level as their counterpart.
CONCLUSIONS: The basic state of well-being as well as the interaction between patient and next of kin seem to be factors that influence the well-being of both patients and their next of kin.

Entities:  

Mesh:

Year:  2009        PMID: 20028340     DOI: 10.1111/j.1600-0404.2009.01191.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  5 in total

Review 1.  Patient-Perceived Outcomes and Quality of Life in ALS.

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

2.  A phase II open label clinical study of the safety, tolerability and efficacy of ILB® for Amyotrophic Lateral Sclerosis.

Authors:  Ann Logan; Zsuzsanna Nagy; Nicholas M Barnes; Antonio Belli; Valentina Di Pietro; Barbara Tavazzi; Giuseppe Lazzarino; Giacomo Lazzarino; Lars Bruce; Lennart I Persson
Journal:  PLoS One       Date:  2022-05-25       Impact factor: 3.752

3.  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

4.  Family caregivers' accounts of caring for a family member with motor neurone disease in Norway: a qualitative study.

Authors:  Sverre Vigeland Lerum; Kari Nyheim Solbrække; Jan C Frich
Journal:  BMC Palliat Care       Date:  2016-02-24       Impact factor: 3.234

5.  Psychosocial adjustment to ALS: a longitudinal study.

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

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