Abstract | OBJECTIVE: METHODS:
Cancer patients consulting a university hospital (N=620) filled out a questionnaire. Their cancer related data were collected through the treating oncologist. This study is performed in Belgium, where " palliative care for all" is a patient's right embedded in the law and euthanasia is possible under certain conditions. RESULTS: Around 80% received information about their illness course and treatments. Ten percent received information about palliative care and euthanasia. Most information about palliative care and euthanasia was given when the patient had a life expectancy of less than six months. However, a quarter of those in earlier phases in their illness trajectory, particularly those who experienced high pain, fatigue or nausea requested more information on these topics. CONCLUSION: Many patients want more information about palliative care and euthanasia than what is currently provided, also those in an earlier than terminal phase of their disease. PRACTICE IMPLICATIONS: Healthcare professionals should be more responsive, already from diagnosis, to the information needs about palliative care and possible end-of-life decisions. This should be patient-tailored, as some patients want more and some patients want less information.
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Authors | Kim Beernaert, Chloë Haverbeke, Simon Van Belle, Luc Deliens, Joachim Cohen |
Journal | Patient education and counseling
(Patient Educ Couns)
Vol. 101
Issue 1
Pg. 132-138
(Jan 2018)
ISSN: 1873-5134 [Electronic] Ireland |
PMID | 28729130
(Publication Type: Journal Article)
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Copyright | Copyright © 2017 Elsevier B.V. All rights reserved. |
Topics |
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Belgium
- Cross-Sectional Studies
- Delivery of Health Care
- Euthanasia
- Female
- Health Services Needs and Demand
- Humans
- Male
- Middle Aged
- Needs Assessment
- Neoplasms
(psychology, therapy)
- Palliative Care
- Surveys and Questionnaires
- Terminal Care
- Young Adult
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