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Well-being in patients with amyotrophic lateral sclerosis and their next of kin over time
Acta neurologica Scandinavica, 2010-04, Vol.121 (4), p.244-250
Olsson, A. G.
Markhede, I.
Strang, S.
Persson, L. I.
2010
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Olsson, A. G.
Markhede, I.
Strang, S.
Persson, L. I.
Titel
Well-being in patients with amyotrophic lateral sclerosis and their next of kin over time
Ist Teil von
Acta neurologica Scandinavica, 2010-04, Vol.121 (4), p.244-250
Ort / Verlag
Oxford, UK: Blackwell Publishing Ltd
Erscheinungsjahr
2010
Quelle
Psychology & Behavioral Sciences Collection
Beschreibungen/Notizen
Olsson AG, Markhede I, Strang S, Persson LI. Well‐being in patients with amyotrophic lateral sclerosis and their next of kin over time. Acta Neurol Scand: 2010: 121: 244–250. © 2009 The Authors Journal compilation © 2009 Blackwell Munksgaard. 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.
Sprache
Englisch
Identifikatoren
ISSN: 0001-6314, 1600-0404
eISSN: 1600-0404
DOI: 10.1111/j.1600-0404.2009.01191.x
Titel-ID: cdi_swepub_primary_oai_gup_ub_gu_se_109323
Format
–
Schlagworte
Adult
,
Aged
,
Aged, 80 and over
,
amyotrophic lateral sclerosis
,
Amyotrophic Lateral Sclerosis - physiopathology
,
Amyotrophic Lateral Sclerosis - psychology
,
Biological and medical sciences
,
caregiver
,
Caregivers - psychology
,
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
,
Family - psychology
,
Female
,
gender
,
Humans
,
Interpersonal Relations
,
Male
,
MEDICAL AND HEALTH SCIENCES
,
Medical sciences
,
MEDICIN OCH HÄLSOVETENSKAP
,
Middle Aged
,
Neurology
,
next of kin
,
Physical Fitness - physiology
,
Physical Fitness - psychology
,
physical function
,
quality of life
,
Quality of Life - psychology
,
Severity of Illness Index
,
Surveys and Questionnaires
,
Time Factors
,
well-being
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