A narrative review of the published ethical debates in palliative care research and an assessment of their adequacy to inform research governance

被引:35
作者
Duke, Sue [1 ]
Bennett, Helen [2 ]
机构
[1] Univ Southampton, Southampton, Hants, England
[2] Naomi House Hosp Children, Winchester, Hants, England
关键词
narrative review; palliative care; research ethics; systematic review; QUALITATIVE RESEARCH; MAXIMIZING BENEFITS; CONDUCTING RESEARCH; MINIMIZING RISKS; CLINICAL-TRIALS; EVIDENCE BASE; END; ISSUES; EDUCATION; BARRIERS;
D O I
10.1177/0269216309352714
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
The quality of research, and the resulting quality of evidence available to guide palliative care, is dependent on the ethical decisions underpinning its design, conduct and report. Whilst much has been published debating the ethics of palliative care research, an assessment of the quality and synthesis of the central debates is not available. Such a review is timely to inform research governance. The methodology of this study is based on the principles of systematic reviews. Fifty-seven papers were reviewed following a thorough search, and were critically appraised for their literary quality, the knowledge on which they drew and the research standards they addressed. The debates identified address vulnerability, moral appropriateness, consent, gate-keeping and inclusion and research culture. The quality of debate and the sources of knowledge varied. The debate was rich in quality and knowledge with respect to the protection of the dignity, rights and safety of research participants, but less developed in relation to those of researchers and other staff. There is also little debate about the ethics of reporting of research and the ethics underpinning research leadership. A framework is offered that reconciles the ethical issues raised with potential methodological strategies identified from the review.
引用
收藏
页码:111 / 126
页数:16
相关论文
共 69 条
[1]   Research sensitivities to palliative care patients [J].
Addington-Hall, J .
EUROPEAN JOURNAL OF CANCER CARE, 2002, 11 (03) :220-224
[2]  
Addington-Hall J, 2005, CAN J NURS RES, V37, P85
[3]   Voluntariness in clinical research at the end of life [J].
Agrawal, M .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2003, 25 (04) :S25-S32
[4]  
Agrawal Manish, 2002, J Palliat Med, V5, P729, DOI 10.1089/109662102320880552
[5]  
[Anonymous], PRINCIPLES MED ETHIC
[6]  
[Anonymous], 2005, Research Governance Framework for Health and Social Care
[7]  
Aranda Sanchia, 1995, Int J Palliat Nurs, V1, P41, DOI 10.12968/ijpn.1995.1.1.41
[8]   Using the Canadian code of ethics for registered nurses to explore ethics in palliative care research [J].
Arraf, K ;
Cox, G ;
Oberle, K .
NURSING ETHICS, 2004, 11 (06) :600-609
[9]  
Badger D., 2000, EVALUATION RES ED, V14, P220, DOI [DOI 10.1080/09500790008666974, 10.1080/09500790008666974]
[10]   Interviewing terminally ill people: is it fair to take their time? [J].
Barnett, M .
PALLIATIVE MEDICINE, 2001, 15 (02) :157-158