Literature DB >> 19965950

Review: a narrative review of the published ethical debates in palliative care research and an assessment of their adequacy to inform research governance.

Sue Duke1, Helen Bennett.   

Abstract

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.

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Mesh:

Year:  2009        PMID: 19965950     DOI: 10.1177/0269216309352714

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  14 in total

Review 1.  Ethical challenges and solutions regarding delirium studies in palliative care.

Authors:  Lisa Sweet; Dimitrios Adamis; David J Meagher; Daniel Davis; David C Currow; Shirley H Bush; Christopher Barnes; Michael Hartwick; Meera Agar; Jessica Simon; William Breitbart; Neil MacDonald; Peter G Lawlor
Journal:  J Pain Symptom Manage       Date:  2013-12-31       Impact factor: 3.612

Review 2.  Experiences in recruiting volunteers through community based initiatives in phase-1 vaccine trials in India.

Authors:  Seema Sahay; Makesh Kumar; Aylur K Srikrishnan; Vadakkuppatu Ramanathan; Sanjay Mehendale
Journal:  Hum Vaccin Immunother       Date:  2013-10-18       Impact factor: 3.452

3.  Conducting research interviews with bereaved family carers: when do we ask?

Authors:  Brenda Bentley; Moira O'Connor
Journal:  J Palliat Med       Date:  2014-12-17       Impact factor: 2.947

4.  The Benefits and Burdens of Pediatric Palliative Care and End-of-Life Research: A Systematic Review.

Authors:  Meaghann S Weaver; Kim Mooney-Doyle; Katherine Patterson Kelly; Kathleen Montgomery; Amy R Newman; Christine A Fortney; Cynthia J Bell; Jessica L Spruit; Melissa Kurtz Uveges; Lori Wiener; Cynthia M Schmidt; Vanessa N Madrigal; Pamela S Hinds
Journal:  J Palliat Med       Date:  2019-03-05       Impact factor: 2.947

Review 5.  Borrowed beauty? Understanding identity in Asian facial cosmetic surgery.

Authors:  Yves Saint James Aquino; Norbert Steinkamp
Journal:  Med Health Care Philos       Date:  2016-09

6.  Lessons from the field: challenges in accruing hospice heart failure patients to intervention research.

Authors:  Cheryl H Zambroski; Harleah Buck; Christopher M Garrison; Susan C McMillan
Journal:  J Cardiovasc Nurs       Date:  2014 Jan-Feb       Impact factor: 2.083

7.  Inviting parents to take part in paediatric palliative care research: a mixed-methods examination of selection bias.

Authors:  Joanna C Crocker; Emma Beecham; Paula Kelly; Andrew P Dinsdale; June Hemsley; Louise Jones; Myra Bluebond-Langner
Journal:  Palliat Med       Date:  2014-12-17       Impact factor: 4.762

8.  Is the patient satisfaction questionnaire an acceptable tool for use in a hospice inpatient setting? A pilot study.

Authors:  Kate Me Henriksen; Naomi Heller; Anne M Finucane; David Oxenham
Journal:  BMC Palliat Care       Date:  2014-06-02       Impact factor: 3.234

9.  Participant recruitment in sensitive surveys: a comparative trial of 'opt in' versus 'opt out' approaches.

Authors:  Katherine J Hunt; Natalie Shlomo; Julia Addington-Hall
Journal:  BMC Med Res Methodol       Date:  2013-01-11       Impact factor: 4.615

10.  Patient, caregiver, health professional and researcher views and experiences of participating in research at the end of life: a critical interpretive synthesis of the literature.

Authors:  Marjolein H Gysels; Catherine Evans; Irene J Higginson
Journal:  BMC Med Res Methodol       Date:  2012-08-17       Impact factor: 4.615

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