Terminally Ill Elderly Patient's Experiences, Attitudes, and Needs
A Qualitative Study
Dados Bibliográficos
| ID | 13629348 |
|---|---|
| Autores | Marja‐Liisa Laakkonen (0000-0001-6528-8242, Herttoniemi Hospital, autor correspondente), M L Laakkonen (Helsinki City Hospital Koskela), Kaisu Pitkälä (0000-0001-9659-6985, Herttoniemi Hospital), K H Pitkälä (Helsinki City Hospital Koskela), Timo Strandberg (0000-0001-6299-925X), T E Strandberg (Helsinki University Hospital) |
| Ano | 2004 |
| Volume | 49 |
| Fascículo | 2 |
| Páginas | 117-129 |
| Data de publicação | 2004-10-01 |
| Peer Reviewed | Sim |
| Open Access | Sim |
| Tipo | ARTICLE |
| Periódico | OMEGA - Journal of Death and Dying (JOURNAL) |
| Identificadores do periódico | ISSN: 0030-2228 • E-ISSN: 1541-3764 |
| Editora | SAGE Publishing (PUBLISHER • US) |
| DOI | 10.2190/kvm3-ulm7-0ruh-kvqh |
| OpenAlex | W2115381542 |
| Idioma | EN |
| Citações recebidas | 1 |
| Referências citadas | 27 |
The aim of this qualitative study was to clarify how terminally ill elderly patients in acute wards perceive the end of life and what are their needs and wishes regarding care. The patients, despite their advanced illness, wished to be treated actively and hoped for more conversations with doctors about active care. They were content with their daily care but evaluated the care in light of the great workload of the nurses, forgiving them for not having time to talk to individual patients. They had specific modest wishes, but were reluctant to express even these because of concern about troubling their caregivers. We conclude that death remained a distant abstraction for these patients with a terminal prognosis. The challenge is to create an intimate caring atmosphere, where the issues related to dying may be elaborated in interaction and the last wishes expressed in a safe atmosphere
End-of-life care · Palliative care · Qualitative research · Sociology · Terminal care · Terminally ill · Workload · Medicine · Nursing · Palliative Care and End-of-Life Issues · Patient Dignity and Privacy · Patient-Provider Communication in Healthcare · Psychology
Measuring patients’ desire for autonomy
Who should measure quality of life, the doctor or the patient?
Qualitative Research in Health Care
American oncology and the discourse on hope
Embodying illness, embodying cancer
Patient Preferences for Medical Decision Making
How reliable are relatives' retrospective reports of terminal illness? Patients' and relatives' accounts compared
Awareness of dying
Are bereaved family members a valid proxy for a patient's assessment of dying
| Obras citantes distintas | 1 |
|---|---|
| Citações por ano | 0,06 |
| Intervalo de citações | 2010 - 2010 (1) |
| Velocidade de citação | historical |
| Altamente citado | Não |
| Tipos de citação | Neutras: 1 |