scholarly journals Doctors’ learning experiences in end-of-life care – a focus group study from nursing homes

2017 ◽  
Vol 17 (1) ◽  
Author(s):  
Anette Fosse ◽  
Sabine Ruths ◽  
Kirsti Malterud ◽  
Margrethe Aase Schaufel
2017 ◽  
Vol 16 (1) ◽  
Author(s):  
Lucy Ellen Selman ◽  
Lisa Jane Brighton ◽  
Vicky Robinson ◽  
Rob George ◽  
Shaheen A. Khan ◽  
...  

2016 ◽  
Vol 99 (12) ◽  
pp. 2043-2048 ◽  
Author(s):  
Kristian Jansen ◽  
Sabine Ruths ◽  
Kirsti Malterud ◽  
Margrethe Aase Schaufel

2016 ◽  
Vol 37 (6) ◽  
pp. 440-445 ◽  
Author(s):  
Johannes Bükki ◽  
Petra M. Neuhaus ◽  
Piret Paal

2021 ◽  
Vol 20 (1) ◽  
Author(s):  
Emilio Mota-Romero ◽  
Ana Alejandra Esteban-Burgos ◽  
Daniel Puente-Fernández ◽  
María Paz García-Caro ◽  
Cesar Hueso-Montoro ◽  
...  

Abstract Background Nursing homes are likely to become increasingly important as end-of-life care facilities. Previous studies indicate that individuals residing in these facilities have a high prevalence of end-of-life symptoms and a significant need for palliative care. The aim of this study was to develop an end-of-life care program for nursing homes in Spain based on previous models yet adapted to the specific context and the needs of staff in nursing homes in the country. Methods A descriptive study of a complex intervention procedure was developed. The study consisted of three phases. The first phase was a prospective study assessing self-efficacy in palliative care (using the SEPC scale) and attitudes towards end-of-life care (using the FATCOD-B scale) among nursing home staff before and after the completion of a basic palliative care training program. In the second phase, objectives were selected using the Delphi consensus technique, where nursing home and primary care professionals assessed the relevance, feasibility, and level of attainment of 42 quality standards. In phase 3, interventions were selected for these objectives through two focus group sessions involving nursing home, primary care, and palliative care professionals. Results As a result of the training, an improvement in self-efficacy and attitudes towards end-of-life care was observed. In phase 2, 14 standards were selected and grouped into 5 objectives: to conduct a comprehensive assessment and develop a personalized care plan adapted to the palliative needs detected; to provide information in a clear and accessible way; to request and record advance care directives; to provide early care with respect to loss and grief; to refer patients to a specialized palliative care unit if appropriate, depending on the complexity of the palliative care required. Based on these objectives, the participants in the focus group sessions designed the 22 interventions that make up the program. Conclusions The objectives and interventions of the NUHELP program constitute an end-of-life care program which can be implemented in nursing homes to improve the quality of end-of-life care in these facilities by modifying their clinical practice, organization, and relationship with the health system as well as serving as an example of an effective health intervention program.


2012 ◽  
Vol 44 (2) ◽  
pp. 206-214 ◽  
Author(s):  
Clare Gardiner ◽  
Merryn Gott ◽  
Christine Ingleton ◽  
Philippa Hughes ◽  
Michelle Winslow ◽  
...  

Author(s):  
Mirinae Kim ◽  
Minju Kim

We qualitatively investigated end-of-life care needs. Data were collected via focus-group interviews with three groups: young adults, middle-aged adults, and older adults. The key question was, “What kind of care would you like to receive at the end of life?” Interview data were transcribed and analyzed using content analysis. End-of-life care needs were classified into six categories: life-sustaining treatment needs, physical care needs, emotional care needs, environmental needs, needs for respect, and needs for preparation for death. Because the Korean culture is family-oriented and talking about death is taboo, Korean patients at the end of their life do not make decisions about life-sustaining treatment or actively prepare for death. Therefore, to provide proper end-of-life care, conversations and shared decision-making among patients and their families are crucial. Further, we must respect patients’ dignity and help them achieve a good death by understanding patients’ basic care preferences. Future research should continue examining end-of-life care needs that reflect the social and cultural context of Korea to inform instrument development.


2019 ◽  
Vol 57 (1) ◽  
pp. 93-99 ◽  
Author(s):  
Paola Di Giulio ◽  
Silvia Finetti ◽  
Fabrizio Giunco ◽  
Ines Basso ◽  
Debora Rosa ◽  
...  

2014 ◽  
Vol 29 (1) ◽  
pp. 60-70 ◽  
Author(s):  
Eleanor Wilson ◽  
Hazel Morbey ◽  
Jayne Brown ◽  
Sheila Payne ◽  
Clive Seale ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document