Kidney Clinicians' Perceptions of Challenges and Aspirations to Improve End-Of-Life Care Provision

Kathryn Ducharlet; Jennifer Weil; Hilton Gock; Jennifer Philip

doi:10.1016/j.ekir.2023.04.031

Kidney Clinicians' Perceptions of Challenges and Aspirations to Improve End-Of-Life Care Provision

Kidney Int Rep. 2023 Jun 8;8(8):1627-1637. doi: 10.1016/j.ekir.2023.04.031. eCollection 2023 Aug.

Authors

Kathryn Ducharlet^{1

2

3

4}, Jennifer Weil^{1

3}, Hilton Gock^{2

3}, Jennifer Philip^{1

3}

Affiliations

¹ Department of Palliative Medicine, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.
² Department of Nephrology, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.
³ Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia.
⁴ Eastern Health Clinical School, Monash University, Melbourne, Victoria, Australia.

Abstract

Introduction: End-of-life care is an essential part of integrated kidney care. However, renal clinicians' experiences of care provision and perceptions of end-of-life care needs are limited. This study explored renal clinicians' experiences of providing end-of-life care and developed recommendations to improve experiences.

Methods: An exploratory qualitative study using semistructured focus groups and 1 interview was undertaken at 5 kidney services in Victoria, Australia. The transcripts were analyzed thematically.

Results: Between February and December 2017, 54 renal clinicians (21 doctors and 33 nurses) participated in the study. Clinicians reported multiple challenges of end-of-life care experiences resulting in compromised treatment planning and decision making and highlighted priorities to guide better care experiences. Challenges of providing end-of-life care were underpinned by mismatches in illness and treatment expectations, limited engagement in advance care planning, medical complexity, and differences between clinicians and patients in what constituted quality of life. These challenges were associated with compromised end-of-life care planning, which resulted in care experiences that were rushed with a prolonged treatment focus, risking limited preparation for death and moral distress. Clinicians aspired for positive end-of-life care experiences, including patient control and consensus in decision making, and a coordinated and collaborative approach across healthcare providers.

Conclusions: Renal clinicians highlighted multiple factors and circumstances which resulted in experiences of compromised end-of-life care for patients with kidney disease. To improve care experiences, clinician-directed priorities included more training and support to facilitate systematic and earlier discussions about illness expectations and end-of-life care planning and greater communication and collaboration across healthcare providers is required.

Keywords: end-of-life care; experiences of care; kidney disease; palliative care; qualitative.