Palliative care of the cancer patient

1968 ◽  
Vol 115 (5) ◽  
pp. 743
Author(s):  
R.Robinson Baker
2009 ◽  
Vol 21 (2) ◽  
pp. 131-139 ◽  
Author(s):  
B.J.A. Laird ◽  
M.T. Fallon

2020 ◽  
Vol 30 (Supplement_5) ◽  
Author(s):  
E Faggian ◽  
S Favero ◽  
D Gregori ◽  
M Martinato

Abstract Background caregivers of home-cared cancer patient during palliative phase are often under psychological and physical pressure. This can lead to a low level quality of life (QoL). This study assesses the QoL of this type of caregiver, more specifically it aims to outline which factors (age, type of palliative care, amount of time spent daily with the patient) affect positively or negatively the QoL score. Methods The AC-QoL questionnaire has been completed by 25 caregivers of oncological patients in home care in north-eastern Italy. The questionnaire is made of 40 items divided into 8 subjects: support in care, choice of care, stress, economic issues, personal growth, sense of value, care skills and personal satisfaction. It has been administered during a home visit or during a follow-up phone call. Results The average score obtained is 71/120, which means a medium level of QoL. The factors which worsen the QoL are the psychological and physical stress (average score 5/15) and restrictions on caregivers' private life (average score 6/15). No significant differences in the QoL of the caregivers are related to social and personal variables (such as age, working condition, relationship with the patient, type of palliative care, amount of time spent daily with the patient). Conclusions These caregivers play a fundamental role in the management of an appropriate continuity of care and their health and QoL are important. Stress and restrictions on private life are the factors which worsen QoL, that's why nurses should evaluate the caregivers' wellbeing during home-visits. Caregivers usually feel able to offer adequate assistance if they have been adequately trained to by healthcare professionals: nurses should provide every useful tool to aloud the caregiver to feel able of and comfortable providing assistance to his/her relative trough an “empowerment process”. Key messages Caregiver of cancer patient in charge of home palliative care is fundamental for an appropriate continuity of care and his health and quality of life (QoL) are important to provide good assistance. Psycho-physical stress and restrictions on private life worsen QoL. Caregiver’s wellbeing should be assessed and useful tools should be provided by home care nurses to ease caregivers’ job.


1988 ◽  
Vol 36 (10) ◽  
pp. 961-961
Author(s):  
Francisco Fernandez ◽  
Monica Shotwell

2007 ◽  
Vol 15 (2) ◽  
pp. 350-354
Author(s):  
Míria Conceição Lavinas Santos ◽  
Lorita Marlena Freitag Pagliuca ◽  
Ana Fátima Carvalho Fernandes

This reflective study presents the approach of the Nursing Palliative Care to the cancer patient without therapeutic possibility according to the Paterson and Zderad's Humanistic Nursing Theory. The palliative care aims to provide the patient without therapeutic possibility and his family better quality of life. When the nurse, in addition to delivering palliative care to the cancer patient, uses the Humanistic Theory, (s)he starts to recognize each person as a singular existence. This recognition permits one to understand the person's meaning in the process of his(er) disease.


2020 ◽  
pp. 146879412097691
Author(s):  
Lisa Lindén ◽  
Vicky Singleton

This article explores the potential of describing things at the periphery of our attention. It discusses how our practices of ‘describing collaboratively’ shifted what we attended to in observations of participants in a Swedish gynaecological cancer patient organisation. We show how the care the organisation aims to promote is troubled and seemingly undermined by attending to palliative care. Our aim is to explore the ethico-political potential of describing things that ‘unsettle’ care practices. Building on Feminist Technoscience Studies, arguing that researchers should attend to ‘neglected things’ in order to care for them, we focus on affects, atmospheres and fleeting moments that are overlooked, or threaten to undermine, participants’ practices of care. We show how our descriptions that zoom in on things at the periphery and attend to the elusive, restage what gets to count as care and could support care practices that are more liveable for those concerned.


2020 ◽  
Vol 7 (1) ◽  
pp. 1-8
Author(s):  
Eme Stepani Sitepu ◽  
◽  
Atika Wahyu Puspitasari ◽  
Nuriza Ulul Azmi, ◽  
Lila Nilam Sari ◽  
...  

2016 ◽  
Vol 6 (4) ◽  
pp. 362-366
Author(s):  
In-Sung Kim ◽  
Eun-Jung Kim ◽  
Seung-Kyu Kwon ◽  
Dong-Hyuk Park ◽  
Der-Lih Wang

Sign in / Sign up

Export Citation Format

Share Document