CommentLessons from the Liverpool Care Pathway—evidence is key
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Cited by (19)
A systematic review of strategies used to increase recruitment of people with cancer or organ failure into clinical trials: Implications for palliative care research
2015, Journal of Pain and Symptom ManagementCitation Excerpt :The consenting process can be burdensome and required when mental capacity is reduced or fluctuating in a context of distress for the patient and family and increased gatekeeping among clinical staff and ethics committees.14,88–91 Symptom management interventions for dying patients commonly have low-level evidence partly because of challenges of consenting dying patients to clinical trials.5,92 The ethical challenges of recruiting palliative care patients to clinical trials of delirium have been summarized well in a recent discussion article,78 which highlighted the importance of memory and other aids to facilitate capacity (such as that used by Rubright et al.).72,93
Dying in the hospital: What happens and what matters, according to bereaved relatives
2015, Journal of Pain and Symptom ManagementCitation Excerpt :As a result, to our knowledge, this is the 1st study explaining one-third of the aspects determining QOD in the hospital. QOD appeared to be strongly affected by medical care and staff attentiveness, and these results may contribute to the debate on QOD and quality of care for the dying, in the scientific literature and in society.31–34 One limitation of the study is that it was performed in one hospital, and although it was a large hospital with 18 different participating wards, this might diminish the generalizability of our results.
Protecting seriously ill populations during pragmatic clinical trials
2023, Journal of the American Geriatrics SocietyEnd-of-life care and the use of an integrated care pathway
2020, Qualitative Report