Living Wills Don't Work
Time to abandon a failed policy! Living wills don't work -- and can't work -- for their intended purpose of allowing people to plan in advance how they'd want to be treated in end-of-life situations. According to a University of Michigan study, the very documents designed to help people choose the care they want at the end of their life fails to meet five key criteria for success.
The U of M report takes on a document that has become ingrained in American medical culture and is recognized by every state. It is a document that many experts recommend to avoid the kind of problems raised by the Terry Schiavo case in Florida; A case in which a patient's husband and parents have fought a long legal battle over whether she should be kept alive. The U of M team can imagine circumstances where the living wills may be useful for patients who are imminently facing death, who know their medical circumstances and who have strong and specific beliefs about them. The best patients can do, argue the researchers, is to use a "durable power of attorney for health care issues (DPA)" to appoint someone to make decisions for them when they can no longer make their own choices.
A review shows that living wills fail all five tests that would have to be passed for them to work. First, most people don't even have living wills. Second, those who do rarely know what care they would truly want in some hypothetical future. Third, it's surprisingly hard for people to state their wishes accurately and understandably. Fourth, the document is often unavailable when decisions need to be made. Fifth, even when it is available, surrogate decision makers usually cannot reliably apply its instructions to the patient's current health condition.
The living will was designed by bioethicists who wanted to give patients a chance to spell out what treatment they would want and what treatment they would reject if they became unconscious or unable to make their own decisions The idea of the living will is to allow people to maintain control even at the end of their life. Often, the living will starts as a blank form for patients to fill out in writing, stating their individual preferences. The instructions might suggest that patients write down whether they'd want to be kept on life-support machines if they had a catastrophic accident or were terminally ill.
For instance, according to the instructions for the form on the U of M Health System Web site, a patient could write, "Do whatever is necessary for my comfort, but nothing further," or, "I authorize all measures be taken to prolong my life." Patients can also write about their wishes regarding specific medical interventions, such as respirators, cardiopulmonary resuscitation (CPR), surgery and blood transfusions. And they could say how they feel about receiving food and water administered through "feeding tubes." The functional illiteracy of many Americans, and the difficulty even for skilled writers of expressing their wishes well, add to the problem, the articles authors suggest. And, people's preferences often change as their situations or medical technology changes.
For most people, the article’s authors say, a durable power of attorney for health care may be adequate. DPA's allow people to name someone whom they would want to make decisions about their care. That person is usually the patient's spouse or child, but it can be any trusted individual.
DPA's only require a few simple choices, and they don't differ significantly from the existing system of allowing family members to make medical decisions about incompetent patients. They also allow the decision-maker to use the information about the patient's condition that's available at the time a decision is needed, rather than asking the patient to guess about something far in the future. And they're inexpensive. If living wills were free, perhaps their failure wouldn't matter. But living wills cost money. Patients must take time to write them, and doctors and lawyers must be paid for their help in writing them. What is more, the federal Patient Self-Determination Act, which requires hospitals to tell patients about living wills and other "advance directives," cost an estimated $101.5 million to startup nationwide and demands additional untold time and effort from hospital administrators and clinicians each year. In addition, the authors find, here is no convincing evidence that living wills save money by reducing the cost of end-of-life care.
So the bottom line is pretty clear; Talk to your attorney about Durable Powers of Attorney for Health Care Issues"
Author: Craig Carnick, a Member of the Paladin Registry





