Literature DB >> 11798482

Existential issues in palliative care: interviews of patients with amyotrophic lateral sclerosis.

I Bolmsjö1.   

Abstract

For the individual as well as for those caring for the patients, the diagnosis of amyotrophic lateral sclerosis (ALS) provides a great emotional challenge. Many factors, including existential distress, contribute to the emotional strain of patients with ALS. This study focuses on patients diagnosed with ALS and how they communicate existential issues related to meaning and guilt, relations, diagnosis and information, physical inability, and dying with dignity and respect for the person. The results of the present study indicate that (1) patients experience a number of problems, particularly in connection with physical inability, (2) the need to confide in someone is not particularly strong, (3) central for the value of life is to be respected as a person, (4) existential issues are of great importance to the patients.

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Year:  2001        PMID: 11798482     DOI: 10.1089/109662101753381647

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  7 in total

1.  Defining priorities for improving end-of-life care in Canada.

Authors:  Daren K Heyland; Deborah J Cook; Graeme M Rocker; Peter M Dodek; Demetrios J Kutsogiannis; Yoanna Skrobik; Xuran Jiang; Andrew G Day; S Robin Cohen
Journal:  CMAJ       Date:  2010-10-04       Impact factor: 8.262

2.  How Narrative Journalistic Stories Can Communicate the Individual's Challenges of Daily Living with Amyotrophic Lateral Sclerosis.

Authors:  Jørgen Jeppesen; Jes Rahbek; Ole Gredal; Helle Ploug Hansen
Journal:  Patient       Date:  2015-02       Impact factor: 3.883

3.  Emotional distress and well-being among people with motor neurone disease (MND) and their family caregivers: a qualitative interview study.

Authors:  Cathryn Pinto; Adam W A Geraghty; Lucy Yardley; Laura Dennison
Journal:  BMJ Open       Date:  2021-08-17       Impact factor: 3.006

4.  Quality of life among patients receiving palliative care in South Africa and Uganda: a multi-centred study.

Authors:  Lucy E Selman; Irene J Higginson; Godfrey Agupio; Natalya Dinat; Julia Downing; Liz Gwyther; Thandi Mashao; Keletso Mmoledi; Tony Moll; Lydia Mpanga Sebuyira; Barbara Ikin; Richard Harding
Journal:  Health Qual Life Outcomes       Date:  2011-04-08       Impact factor: 3.186

5.  Narrative meaning making and integration: Toward a better understanding of the way falling ill influences quality of life.

Authors:  Iris Hartog; Michael Scherer-Rath; Renske Kruizinga; Justine Netjes; José Henriques; Pythia Nieuwkerk; Mirjam Sprangers; Hanneke van Laarhoven
Journal:  J Health Psychol       Date:  2017-09-26

6.  Resentment, hate, and hope in amyotrophic lateral sclerosis.

Authors:  C Oster; F Pagnini
Journal:  Front Psychol       Date:  2012-11-27

7.  The experiences of, and need for, palliative care for people with motor neurone disease and their informal caregivers: A qualitative systematic review.

Authors:  Kate Flemming; Victoria Turner; Samantha Bolsher; Bill Hulme; Elizabeth McHugh; Ian Watt
Journal:  Palliat Med       Date:  2020-04-14       Impact factor: 4.762

  7 in total

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