PAlliative Care in chronic Kidney diSease: the PACKS study--quality of life, decision making, costs and impact on carers in people managed without dialysis

• Published in: BMC nephrology 2015-07, Vol.16 (1), p.104-104, Article 104
• Main Authors: Noble, Helen Rose, Agus, Ashley, Brazil, Kevin, Burns, Aine, Goodfellow, Nicola A, Guiney, Mary, McCourt, Fiona, McDowell, Cliona, Normand, Charles, Roderick, Paul, Thompson, Colin, Maxwell, A P, Yaqoob, M M
• Format: Article
• Language: English
• Subjects: Care and treatment; Caregivers - psychology; Chronic kidney failure; Cognition Disorders - psychology; Complications and side effects; Cost of Illness; Decision Making; Economic aspects; Health aspects; Health Care Costs; Humans; Kidney Failure, Chronic - economics; Kidney Failure, Chronic - nursing; Kidney Failure, Chronic - psychology; Kidney Failure, Chronic - therapy; Longitudinal Studies; Medical research; Medicine, Experimental; Nephrology; Palliative Care; Palliative treatment; Prospective Studies; Qualitative Research; Quality of Life; Renal Insufficiency, Chronic - economics; Renal Insufficiency, Chronic - nursing; Renal Insufficiency, Chronic - psychology; Renal Insufficiency, Chronic - therapy; Study Protocol; United Kingdom
• ISSN: 1471-2369; 1471-2369
• DOI: 10.1186/s12882-015-0084-7

The number of patients with advanced chronic kidney disease opting for conservative management rather than dialysis is unknown but likely to be growing as increasingly frail patients with advanced renal disease present to renal services. Conservative kidney management includes ongoing medical input and support from a multidisciplinary team. There is limited evidence concerning patient and carer experience of this choice. This study will explore quality of life, symptoms, cognition, frailty, performance decision making, costs and impact on carers in people with advanced chronic kidney disease managed without dialysis and is funded by the National Institute of Health Research in the UK. In this prospective, multicentre, longitudinal study, patients will be recruited in the UK, by renal research nurses, once they have made the decision not to embark on dialysis. Carers will be asked to 'opt-in' with consent from patients. The approach includes longitudinal quantitative surveys of quality of life, symptoms, decision making and costs for patients and quality of life and costs for carers, with questionnaires administered quarterly over 12 months. Additionally, the decision making process will be explored via qualitative interviews with renal physicians/clinical nurse specialists. The study is designed to capture patient and carer profiles when conservative kidney management is implemented, and understand trajectories of care-receiving and care-giving with the aim of optimising palliative care for this population. It will explore the interactions that lead to clinical care decisions and the impact of these decisions on informal carers with the intention of improving clinical outcomes for patients and the experiences of care givers.