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Ethical principles in patient-centered medical care to support quality of life in amyotrophic lateral sclerosis

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-196239
  • It is one of the primary goals of medical care to secure good quality of life (QoL) while prolonging survival. This is a major challenge in severe medical conditions with a prognosis such as amyotrophic lateral sclerosis (ALS). Further, the definition of QoL and the question whether survival in this severe condition is compatible with a good QoL is a matter of subjective and culture-specific debate. Some people without neurodegenerative conditions believe that physical decline is incompatible with satisfactory QoL. Current data provideIt is one of the primary goals of medical care to secure good quality of life (QoL) while prolonging survival. This is a major challenge in severe medical conditions with a prognosis such as amyotrophic lateral sclerosis (ALS). Further, the definition of QoL and the question whether survival in this severe condition is compatible with a good QoL is a matter of subjective and culture-specific debate. Some people without neurodegenerative conditions believe that physical decline is incompatible with satisfactory QoL. Current data provide extensive evidence that psychosocial adaptation in ALS is possible, indicated by a satisfactory QoL. Thus, there is no fatalistic link of loss of QoL when physical health declines. There are intrinsic and extrinsic factors that have been shown to successfully facilitate and secure QoL in ALS which will be reviewed in the following article following the four ethical principles (1) Beneficence, (2) Non-maleficence, (3) Autonomy and (4) Justice, which are regarded as key elements of patient centered medical care according to Beauchamp and Childress. This is a JPND-funded work to summarize findings of the project NEEDSinALS (www.NEEDSinALS.com) which highlights subjective perspectives and preferences in medical decision making in ALS.zeige mehrzeige weniger

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Metadaten
Autor(en): Dorothée Lulé, Andrea Kübler, Albert C. Ludolph
URN:urn:nbn:de:bvb:20-opus-196239
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Fakultät für Humanwissenschaften (Philos., Psycho., Erziehungs- u. Gesell.-Wissensch.) / Institut für Psychologie
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):Frontiers in Neurology
ISSN:1664-2295
Erscheinungsjahr:2019
Band / Jahrgang:10
Aufsatznummer:259
Originalveröffentlichung / Quelle:Frontiers in Neurology 2019, 10:259. doi: 10.3389/fneur.2019.00259
DOI:https://doi.org/10.3389/fneur.2019.00259
Allgemeine fachliche Zuordnung (DDC-Klassifikation):1 Philosophie und Psychologie / 15 Psychologie / 150 Psychologie
Freie Schlagwort(e):amyotrophic lateral sclerosis (ALS); care; coping; depression; ethics; psychosocial adaptation; quality of life (QoL); well-being
Datum der Freischaltung:02.12.2020
Datum der Erstveröffentlichung:22.03.2019
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International