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Lagging supportive services around social determinants of health and limited access to hospice and palliativecare are driving disparities among rural family caregivers. These determinants, along with the natural stressors of palliative and end-of-lifecaregiving, disproportionately impact their emotional well-being.”
In this PONDER-ICU trial, we didn’t rely on palliativecare specialists; we engaged bedside clinicians to have ICU communication and adhere to guidelines. There is a lot of literature suggesting that standard transplant care doesn’t really meet the needs of these patients and their caregivers. Eric: Okay.
And if they have symptoms, you address symptoms, and at some point, you might elicit goals and values, and at some point, you might talk about end of lifecare. Because quality of life was non inferior. And this is where I think qualitative data from caregiver bereaved caregivers would be super useful.
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