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Kathy Hochul has signed a bill designed to expand awareness of advance care planning, hospice, and palliativecare. The new law requires the New York State Department of Health to develop a public awareness campaign to promote advance care planning. That must change.”.
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-life caregiving, disproportionately impact their emotional well-being.”
So we’re going to have a link to the article that you published in JAMA IM titled The Hospital Culture and Intensity of End-of-LifeCare at Three Academic Hospitals. And I was interested in intensity of end-of-lifecare and differences in intensity of end-of-lifecare. Liz: Right.
Asking clinicians whether they had offered the option of withdrawal of life support and comfort-focused care also did not change length of stay, but did increase the discharges to hospice, odds greater than two-fold, whether it was done alone or in combination with the prognostication nudge. Was this the same? Corita: Okay.
We did not want them to already have seen home palliativecare. Eric 20:26 And that includes home hospicecare. And then we also didn’t give them access to palliativecare social work on the stepdarmouse. Because quality of life was non inferior. Pallavi 20:28 Yes, definitely. That is correct.
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