Poll Finds Wide Gap Between the Care Patients Want and Receive at End of Life


New research shows most Californians would prefer a natural death at home without becoming a burden on family. But few document their wishes, leaving their loved ones in the dark.

When it comes to how they want to spend their final days, Californians would prefer to die a natural death at home without being a burden, financially or emotionally, on their families. Yet according to a new poll released today by the California HealthCare Foundation, a disparity exists between what people say they want at the end of life and what actually occurs.

The survey, Final Chapter: Californians’ Attitudes and Experiences with Death and Dying, finds nearly 8 in 10 Californians say that if seriously ill, they would want to speak with their doctor about end-of-life care, but fewer than 1 in 10 report having had a conversation, including just 13% of those age 65 or older.

Additionally, while 82% say that it is important to put their wishes in writing, less than one quarter have actually done so. More than half say they have not talked with a loved one about the kind of care they want at the end of life.

The survey explores differences in attitudes toward death and dying among major ethnic groups in California. For example, Latinos rate “living as long as possible” much more highly than other groups.

“With end-of-life treatment, there is a clear gap between wishes and actions,” said Mark D. Smith, MD, MBA, president and CEO of the California HealthCare Foundation, which commissioned the survey. “People consistently stress they want to die comfortably and without pain. If so, the single most important thing they can do is to talk to their loved ones and physicians, and put their wishes in writing, something most Californians aren’t doing.”

Preferences Not Being Followed

The survey finds patients’ wishes regarding treatment are not always honored. Only 44% of Californians who have lost a loved one in the last 12 months say their loved one’s end-of-life preferences were completely followed and honored by medical providers. These numbers drop to 26% for those whose loved ones experienced a language barrier and 25% for those who were uninsured at the time of death.

Similarly, most Californians would prefer to die at home, but that is not typical. Seventy percent of those surveyed say their home is their preferred place of death, but only 32% passed away in their homes, according to death records data from the California Department of Public Health.

Paying for the Conversation

A major barrier to effective end-of-life planning is the lack of frank discussion between patients and health care providers. The average 15-minute office visit does not leave time to explore the natural progression of illness and the preferred treatment options for those nearing death.

As part of its original package to expand health coverage, the Obama Administration proposed requiring public and private insurance to cover voluntary conversations about end-of-life planning between patients and providers. After the issue became politicized, the idea was dropped from the final bill.

The new poll finds broad support among Californians, regardless of political affiliation, for reimbursing doctors to talk about end-of-life options. Eighty-four percent of Democrats, 72% of Republicans, and 80% of Independents say it would be a good idea to pay for the conversation.

Putting a Plan in Place

To help patients have their say if they are unable to speak, CHCF promotes the use of Physician Orders for Life-Sustaining Treatment (POLST). Developed in Oregon two decades ago, POLST is a standardized medical order form (in California it is printed on bright pink paper) that indicates the specific types of treatment a seriously ill patient does or does not want. The voluntary form is signed by the doctor and the patient and is designed to travel with a patient across medical settings.

POLST complements, but does not replace, the Advance Health Care Directive. An advance directive, which should be filled out by any adult regardless of one’s health status, provides a broad outline of a person’s wishes relating to end-of-life care, and allows an individual to appoint a “health care proxy” — the person they want to speak on their behalf. Only POLST, however, carries the power of a physician order.

According to the survey, nearly two-thirds of Californians say they would want to complete a POLST form if they became seriously ill, including 77% of those who are 65 or older. Seventy-one percent say they would want a seriously ill loved one to complete the form so they could understand their wishes.

The State of Palliative Care

In 2009, nearly 100,000 Californians with serious illness died in hospitals, according to public health records. Palliative care treats pain and other symptoms, provides psychosocial and spiritual support, and ensures that medical treatments align with patient and family wishes. Increasingly, hospitals are recognizing the enormous value of palliative care to patients who are seriously ill.

CHCF is releasing an accompanying report on palliative care: When Compassion Is the Cure: Progress and Promise in Hospital-Based Palliative Care. Produced by the National Health Foundation and the University of California, San Francisco Palliative Care Program, it profiles the state of palliative care in California’s acute care hospitals.

Among the findings:

  • Palliative care consultation services have experienced a great deal of growth in recent years: Between 2007 and 2011, pediatric services increased by 128%, while adult services increased by 24%.
  • Most palliative care services have modest budgets, with 60% operating on less than $300,000 annually.
  • Every major metropolitan area in California except Los Angeles increased the number of hospital-based palliative care programs between 2007 and 2011. The percentage of Los Angeles hospitals with such programs actually decreased.
Source: California Healthcare Foundation
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~ by Brendan Kober on February 16, 2012.

One Response to “Poll Finds Wide Gap Between the Care Patients Want and Receive at End of Life”

  1. Thank you for a great article. I am sure if this survey was done in every state, you would have similar findings. I had worked at a major teaching hospital to start their Palliative Care program so I speak from firsthand experience. Unfortunately, we have become ingrained with a value of preserving “life at all costs” due to medical and technological advances which has morphed into “we can’t let people die.” Death and dying has been so far removed from everyday life in the US, unless one personally experiences it with close friends and family, that it’s become something to avoid and fear. Conflicts also arise due to religious beliefs, fear of lawsuits, lack of education for both the public and health care providers, and many other reasons. It is a good thing Palliative Care is growing, and more funds should be allocated to it. The money spent at the end of life could be better spent providing quality of life. But, societal values need a readjustment to the fact that death and dying is just a part of life.

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