End-of-life care preferences and needs: perceptions of patients with chronic kidney disease
- PMID: 20089488
- PMCID: PMC2827591
- DOI: 10.2215/CJN.05960809
End-of-life care preferences and needs: perceptions of patients with chronic kidney disease
Abstract
Background and objectives: Despite high mortality rates, surprisingly little research has been done to study chronic kidney disease (CKD) patients' preferences for end-of-life care. The objective of this study was to evaluate end-of-life care preferences of CKD patients to help identify gaps between current end-of-life care practice and patients' preferences and to help prioritize and guide future innovation in end-of-life care policy.
Design, setting, participants, & measurements: A total of 584 stage 4 and stage 5 CKD patients were surveyed as they presented to dialysis, transplantation, or predialysis clinics in a Canadian, university-based renal program between January and April 2008.
Results: Participants reported relying on the nephrology staff for extensive end-of- life care needs not currently systematically integrated into their renal care, such as pain and symptom management, advance care planning, and psychosocial and spiritual support. Participants also had poor self-reported knowledge of palliative care options and of their illness trajectory. A total of 61% of patients regretted their decision to start dialysis. More patients wanted to die at home (36.1%) or in an inpatient hospice (28.8%) compared with in a hospital (27.4%). Less than 10% of patients reported having had a discussion about end-of-life care issues with their nephrologist in the past 12 months.
Conclusions: Current end-of-life clinical practices do not meet the needs of patients with advanced CKD.
Comment in
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Education and end of life in chronic kidney disease: disparities in black and white.Clin J Am Soc Nephrol. 2010 Feb;5(2):163-6. doi: 10.2215/CJN.09271209. Epub 2010 Jan 14. Clin J Am Soc Nephrol. 2010. PMID: 20089490 No abstract available.
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