New data comparing Oregon to Washington and rest of country show complexity of care near end of life.
People with serious illness or frailty in Oregon are more likely to have their end–of–life care wishes honored, and, consequently, less likely to be hospitalized and more likely to use home hospice services compared with Washington state and the rest of the country, according to data published in the New England Journal of Medicine.

“The level of care you receive near the end of life depends more on the state you live in and the systems they have in place than your actual wishes,” says author Susan Tolle, MD, director of the OHSU Center for Ethics in Health Care and co–creator of the Physician Orders for Life–Sustaining Treatment, or POLST Program.

Through a grant from the Robert Wood Johnson Foundation, co–author Joan Teno, MD, MS, of the University of Washington, looked at utilization trends for Medicare fee–for–service, including the percentage of patients who died at home, died in hospice, were admitted to the intensive care unit in the last 30 days of life, and were discharged home after hospitalization in the last 30 days of life.

The utilization patterns are strikingly different in Oregon:

• Nearly two–thirds of Oregonians die at home, compared with 39.6 percent of Americans nationwide.
• Intensive care unit use in the last 30 days of life in Oregon was 18.2 percent, compared with 23 percent in Washington state and 28.5 percent nationwide.
• Patients who were hospitalized in the last month of life were more likely to be discharged home in Oregon than in Washington state or nationwide (73.5 percent in Oregon, 63.5 percent in Washington and 54.2 percent nationwide).

According to Tolle, Oregon has integrated end–of–life care initiatives throughout all levels of the health care system, from state government to local health care systems, with the creation of the POLST Program to better elicit, record and honor patients’ wishes to have or to limit medical treatments near the end of life.

The POLST Program allows patients with advanced illness and frailty to have a meaningful conversation with their health care professional in which they can discuss goals of care and document patient preferences with the POLST form, a medical order that can be honored across settings of care and by emergency medical technicians.

“It is difficult to pinpoint exactly why there are such differences in care at the end of life in Oregon compared with other states, but we think it reflects the complexity and intensity of the initiatives developed to support not only the POLST Program but a more comprehensive plan of care to honor a person’s wishes and ensure their desired symptom management,” says Teno, a professor in the Division of Gerontology and Geriatric Medicine and the Cambia Palliative Care Center of Excellence at the University of Washington.