Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Ulla Molander"'
Publikováno v:
PLoS ONE, Vol 19, Iss 4, p e0299112 (2024)
Communication about life-threatening disease and palliative care is essential but often experienced as difficult by those concerned and has mainly been studied in terms of its verbal components. Despite the fundamentality of nonverbal communication,
Externí odkaz:
https://doaj.org/article/dcf7548ec6d2440da44cf974019f219b
Publikováno v:
BMJ Open, Vol 12, Iss 5 (2022)
Objectives To investigate the experiential impact of the COVID-19 pandemic on patients with non-COVID, life-threatening disease and their family carers.Design An interpretative qualitative design informed by phenomenological hermeneutics and based on
Externí odkaz:
https://doaj.org/article/a33409c9b62b48c3a20b84e5953857a9
Publikováno v:
SAGE Open Medicine, Vol 8 (2020)
Objectives: Chronic diseases have an impact on and change patient’s lives which means that they need to find ways to cope with the new situation. The aim was to describe how the chronic disease has influenced patients’ views of their life situati
Externí odkaz:
https://doaj.org/article/07074b04d1f54e8e85ab8f0f78587f9d
Publikováno v:
Inquiry: The Journal of Health Care Organization, Provision, and Financing, Vol 54 (2017)
A prominent existential concept is that elderly parents should naturally become severely ill or die before a younger person does. If the reverse should happen, it may influence the parent’s existential view of life. The aim of this study was to inv
Externí odkaz:
https://doaj.org/article/20bf997f3abe4960ad8f2bc09d030d95
Publikováno v:
Diseases, Vol 7, Iss 3, p 53 (2019)
Background: Chronic diseases have an impact on and can change the lives of the persons affected by them. This study examines how a disease can influence patients’ daily lives, the strategies they adopt to cope, and their experiences of support. The
Externí odkaz:
https://doaj.org/article/6c4e3d6b087b42bf9efedfc632a5a5ea
Publikováno v:
SAGE Open Medicine, Vol 2 (2014)
Objective: The aim of the study was to explore the skills and strategies employed by professionals when having difficult conversations to provide information to loved ones as part of palliative care. Method: A qualitative design was chosen with in-de
Externí odkaz:
https://doaj.org/article/84ac956febd8437b909b2a82c0bdaf0a
Publikováno v:
Palliative and Supportive Care. 20:801-806
ObjectiveEnd-of-life dreams and visions (ELDVs) have been suggested to be prevalent psychic phenomena near death that can provide meaning and comfort for the dying. There is a lack of studies from the secular Nordic countries. The aim of this study w
Metaphors in End-of-Life Dreams in Patients Receiving Palliative Care: A Secondary Qualitative Study
Publikováno v:
The American journal of hospicepalliative care. 40(1)
Background: Metaphors are used by patients and professionals in the discourse of disease and can facilitate conversations about difficult topics. There is little information about metaphors present in patients’ end-of-life dreams. Objective: Identi
Publikováno v:
American Journal of Hospice and Palliative Medicine®. 38:1106-1111
Introduction:Patients with life-threatening diseases have reportedly end-of-life experiences that are perceived positively. Loved ones and healthcare personnel may mistakenly interpret the phenomena as confusion and patients can be reluctant to talk
Publikováno v:
American Journal of Hospice and Palliative Medicine®. :104990912211510
Background: Although communication is strongly emphasized in palliative care, not much research has focused on communication between patients and their loved ones. The purpose was to increase understanding of communication around severe illness betwe