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Palliative care is specialized care that treats the symptoms and burdens associated with serious illness. Palliative care is delivered by an interdisciplinary team that includes physicians, nurses, social workers, and chaplains.
Palliative care is not synonymous with hospice care (see later).
Palliative care collaboratively addresses multiple domains for patients with serious illness. These domains include:
treatment of distressing physical and psychological symptoms
help outline goals and preferences for treatment decision making and end of life
support spiritual needs and beliefs
address caregiver needs
Palliative care is appropriate at any stage of serious illness. Hospice care is a Medicare benefit provided to patients with terminal illness or when prognosis is likely less than 6 months and the goals of care have shifted toward symptom management rather than life-prolonging therapies. The broad domains of palliative care are still used, but the structure of care is focused on symptom relief and bereavement needs as patients’ approach end of life.
A helpful schematic ( Fig. 80.1 ) shows the gradual shift from curative to palliative care and eventual hospice care over the illness course.
Based on data from the US Renal Data Service (USRDS), adults older than 75 years have the highest rates for dialysis initiation. This subset of patients presents an important challenge to nephrologists due to their limited prognosis, high symptom burden, and increased need for palliative care.
Nephrologists care for a medically complex population who are at risk for having untreated symptoms, medical setbacks, and limited survival. Palliative care domains that specifically address nephrology needs fall into three domains:
Symptom management
Shared decision making
Advance care planning
Studies from patients with ESKD have shown that physical symptoms such as pain, fatigue, and pruritus are present in a majority of hemodialysis patients. The severity of symptom burden correlated with decreased health-related quality of life. Dialysis patients are at increased risk for depressive symptoms, with a prevalence of approximately 20%.
The prevalence of patient-reported symptoms, quality of life, and presence of depression are not substantially different between patients with CKD and those who have started dialysis.
Fatigue, worrying, pruritus, dry skin, dry mouth, feelings of sadness, sleep disturbances, irritability, loss of libido, and muscle cramps were reported by at least 40% of patients in either the CKD or ESKD group in a study of 177 patients.
From the same study, at least 20% of patients in either the CKD or ESKD group reported having pain or soreness, shortness of breath, anxiety, constipation, edema, restless legs, diarrhea, anorexia, headache, cough, nausea, lightheadedness or dizziness, and lower extremity paresthesias.
Symptom management is a top priority for patients. Despite this, these symptoms are not commonly identified or known by their treating nephrologists. Based on a study of dialysis patients and their providers, at least 25% of providers answered “Don’t know” for the 10 most commonly reported symptoms by patients. Current evidence suggests that nephrology providers’ unawareness of symptoms is one of the main barriers to improving quality of life for patients with renal disease.
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