We're starting to learn more about late-life care, thanks in large measure to the Dartmouth Atlas Project.
For example, in a recent report Trends and Variation in End-of-Life Care for Medicare Beneficiaries
with Severe Chronic Illness (read here), we learned more about the final 30 days of life of a patient with cancer. More than half (54.7%) were hospitalized during that period. 5.6% received life-sustaining procedures. Half of the final month was spent in hospice (11 days) and an acute-care hospital bed (4 days). Interesting, but without context. Likely, the past 10 years has seen considerable improvement in these measures. How much more improvement should we expect? Can hospitalizations be cut in half? If so, what might be the most effective methods? A transitional care document , like POLST? A provider reimbursement structure where collaboration, rather than procedures, is more highly valued? A community palliative care officer who's accountable for late-life care across settings within a specific community or region? Any of these, or all of them?
And how much better can the health care system do to encourage earlier referral to palliative services, so that greater than 11 days out of the final 30 can be spent under hospice care? As always, your ideas and opinions are invited.
Parental Rights, Best Interests and Significant Harms: A Comparative Perspective on Medical Decision-Making on Behalf of Children - CALL FOR CONTRIBUTIONS - Parental Rights, Best Interests and Significant Harms: A Comparative Perspective on Medical Decision-Making on Behalf of Children ...
1 day ago