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Caregivers’ divergent perspectives on patients’ well-being and attitudes towards hastened death in Germany, Poland and Sweden

Andersen, Peter M., 1962- (författare)
Umeå universitet,Neurovetenskaper
Kuźma-Kozakiewicz, Magdalena (författare)
Department of Neurology, Medical University of Warsaw, Warsaw, Poland; Neurodegenerative Diseases Research Group, Medical University of Warsaw, Warsaw, Poland
Keller, Jürgen (författare)
Department of Neurology, University of Ulm, Ulm, Germany
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Maksymowicz-Śliwińska, Anna (författare)
Department of Neurology, Medical University of Warsaw, Warsaw, Poland
Barć, Krzysztof (författare)
Department of Neurology, Medical University of Warsaw, Warsaw, Poland
Nieporęcki, Krzysztof (författare)
Department of Neurology, Medical University of Warsaw, Warsaw, Poland
Finsel, Julia (författare)
Department of Neurology, University of Ulm, Ulm, Germany
Vazquez, Cynthia (författare)
Department of Neurology, University of Ulm, Ulm, Germany
Helczyk, Olga (författare)
Department of Neurology, University of Ulm, Ulm, Germany
Linse, Katharina (författare)
Department of Neurology, Technische Universität Dresden, and German Center for Neurodegenerative Diseases (DZNE), Dresden, Germany
Häggström, Ann-Cristin E. (författare)
Umeå universitet,Neurovetenskaper
Stenberg, Erica (författare)
Umeå universitet,Neurovetenskaper
Semb, Olof, 1968- (författare)
Umeå universitet,Professionell utveckling
Ciećwierska, Katarzyna (författare)
Department of Neurology, Medical University of Warsaw, Warsaw, Poland
Szejko, Natalia (författare)
Department of Neurology, Medical University of Warsaw, Warsaw, Poland
Uttner, Ingo (författare)
Department of Neurology, University of Ulm, Ulm, Germany
Herrmann, Andreas (författare)
Department of Neurology, Technische Universität Dresden, and German Center for Neurodegenerative Diseases (DZNE), Dresden, Germany
Petri, Susanne (författare)
Department of Neurology, Hannover Medical School, Hannover, Germany
Meyer, Thomas (författare)
Department of Neurology, Charité CVK, Berlin, Germany
Ludolph, Albert C. (författare)
Department of Neurology, University of Ulm, Ulm, Germany; German Center for Neurodegenerative Diseases (DZNE), Ulm, Germany
Lulé, Dorothée (författare)
Department of Neurology, University of Ulm, Ulm, Germany
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 (creator_code:org_t)
2021-06-30
2022
Engelska.
Ingår i: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. - : Taylor & Francis. - 2167-8421 .- 2167-9223. ; 23:3-4, s. 252-262
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background: During the course of amyotrophic lateral sclerosis (ALS), patients and their families are faced with existential decisions concerning life-prolonging and -shortening measures. Correct anticipation of patient’s well-being and preferences is a prerequisite for patient-centered surrogate decision making.Methods: In Germany (N = 84), Poland (N = 77) and Sweden (N = 73) patient-caregiver dyads were interviewed. Standardized questionnaires on well-being (ADI-12 for depressiveness; ACSA for global quality of life) and wish for hastened death (SAHD) were used in ALS patients. Additionally, caregivers were asked to fill out the same questionnaires by anticipating patients’ perspective (surrogate perspective).Results: Caregivers significantly underestimated patients’ well-being in Germany and Poland. For Swedish caregivers, there were just as many who underestimated and overestimated well-being. The same was true for wish for hastened death in all three countries. For Swedish and Polish patients, caregivers’ estimation of well-being was not even associated with patients’ responses and the same was true for estimation of wish for hastened death in all three countries. Older caregivers and those with the most frequent encounter with the patient were the closest in their rating of well-being and wish for hastened death to the patients’ actual state, while caregivers with chronic disease him/herself were more likely to underestimate patient’s well-being.Discussion: Despite distinct cultural differences, there was a clear discrepancy between patients’ and caregivers’ perspective on patients’ well-being and preferences towards life in all three countries. This possible bias in caregivers’ judgment needs to be taken into account in surrogate decision making.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Omvårdnad (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Nursing (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

amyotrophic lateral sclerosis
caregivers
Decision making
palliative care
quality of life

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