On this blog, Professor Thaddeus Pope tracks judicial, legislative, policy, and academic developments concerning medical futility and the limits on individual autonomy at the end of life.

Friday, April 3, 2009

The Price of Denial

The New York Times' New Old Age Blog summarizes a recent study in the Archives of Internal Medicine.
Patients with advanced cancer who reported having EOL conversations with physicians generally opted for comfort, or palliative, care at home or in a hospice.  This had several significant benefits:
  • Less physican distress and a better quality of death;
  • Significantly lower health care costs in their final week of life; and
  • As much (and sometimes more) time at the end-of-life as those never talked about their end-of-life (and were likely to be resuscitated, intubated or put in intensive care)

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