
Advance Directives
- Pt. II by Stan Seagraves, M.D.Scenario One:
Your 74 year dad, hardworking guy, now retired from the
mill, is in poor health. He started smoking at age 15, and
has been weakened by heart disease since shortly after his
retirement. A year and a half ago he was diagnosed with lung
cancer. After some initial response to treatments, his
cancer seems to be growing faster, and he's decided not to
pursue any further therapy. He filled out an advanced
directive (AD) back when his cancer was diagnosed. His wife
is his durable power of attorney, and she's been getting a
tad forgetful of late.
One fall day, while you are visiting your daughter who is
away at college, dad takes a rapid turn for the worse. He
can't seem to get his breath. Your mom calls 911, and by the
time the paramedics arrive, he is really struggling to
breathe, and can scarcely speak. Your mother is in a panic
as they bundle dad off to the emergency room. In route, his
situation deteriorates to the point that a breathing tube is
inserted into his windpipe. When the dust settles at the
hospital, dad is in the intensive care unit on a ventilator
to support his breathing. He has a terrible case of
pneumonia. You race back to town, get a bead on the
situation. You meet with the doctors and discuss the poor
prognosis, especially given his background health. Even
before you think of it, one of the docs asks if your dad had
an AD. “Yes, its somewhere at home.” You are next asked
whether your dad had made a declaration about life support.
“Well, I'm pretty sure he did not want to be on any machines
or anything...”
Now you are in over your head. Rather than the “easier”
decision NOT to start the life support, you have the
wrenching issue of withdrawing it. Turns out dads AD is a
little vague on life support – but seems to indicate that
he'd not want it if he had little or no chance of a
meaningful recovery. On his third day in hospital, dad has a
heart attack, and deteriorates further. With a tube in his
throat he cannot talk, and he is sedated all the time in
order tolerate the breathing tube. Your mom cannot bring
herself to a decision regarding how long to continue the
ventilator. Your older sister is adamant that this “is not
what dad would want”, while your baby brother is hinging his
hopes on a TV show he just saw in which a guy survived after
months on life support. Impasse. On his sixth day in the
hospital, your dads heart becomes unstable, his blood
pressure drops in spite of all measures, and because no
decision has yet been reached on cardiopulmonary
resuscitation, chest compressions are begun. The family is
rushed in for an urgent conference, and a decision made to
stop CPR. Your father passes away shortly thereafter. He
sustained multiple rib fractures during the chest
compressions and never regained consciousness.
Scenario Two: Starts out like number one, except that
when you father found out his cancer was worsening, he
completed a POLST form. He made it clear to his wife and
family that he did not want any life sustaining treatments
outside of a trial of antibiotics if he got an infection. He
was OK with the idea of going to the hospital. He wanted no
mechanical ventilation nor CPR. When he got sick with
pneumonia and the paramedics called, his POLST wishes were
readily available, so a breathing tube was not inserted.
Some “non-invasive” measures to support his breathing were
tried, and antibiotics started. He was not taken to the
intensive care unit – rather, he was admitted to a less
chaotic part of the hospital, and a nurse with skills in end
of life care was assigned to him. His comfort was the
priority. He responded to the antibiotics, at least for a
time. Without the stress of the ventilator, his heart
condition did not deteriorate as seriously. He was
surrounded by family and friends. On his fourth hospital
day, he decided he wanted to go home with hospice nursing
care, and passed away two weeks later. In that time, his
grandchildren had time to visit, and he relayed and recorded
many previously untold childhood stories.
So what is this POLST thing, anyhow? It is your typically
clumsy medical acronym, and stands for a Physicians Orders
for Life - Sustaining Treatment. This long-overdue program –
which has really taken off of late – started in Oregon in
1991. The purpose was to create a standardized, portable
physician/ medical order that legally documented ones
treatment wishes. Here is what Montana's and most forms look
like:
http://www.dphhs.mt.gov/sltc/services/vethome/MVHForms/POLST.pdf
A POLST declaration does not in an of itself limit care.
What it does do is legally document ones care desires, and
quite specifically so for critical issues like resuscitation
and hospitalization. It allows - in fact, requires - ones
desires for care to be respected by paramedical personnel,
emergency room providers, hospitals, and other care givers.
In the past, absent a visible, officially recognized and
legal “medical order”, ones wishes, even in the too-rare
instance that they were documented and found, were often
ignored. Medico legal concerns, shifting family preferences,
caregiver biases and myriad other circumstances led to their
violation. The POLST goal is to eliminate scenario one.
Who should have a POLST form? Anyone with a life-limiting
or terminal illness should consider this. Most long term
nursing home residents are candidates. A rule of thumb for
providers which POLST organizers in Oregon suggested is the
following: “would I be surprised if this patient died within
the next year?” If the answer is no, this individual should
be considered for a POLST.
These forms are completed only after a lengthy –
generally 45 minutes to one hour – consultation with
providers trained in the process. Both the patient and their
legal representative/DPOA should be present for this
conference. The purpose of that visit it to be clear about
the forms purpose and significance, and to answer the many
questions that this crucial discussion brings forth. In some
instances, the discussion may be led by the patients primary
care provider, though time constraints in the typical office
practice are likely to make the completion of the POLST a
separate process, perhaps performed by a panel of trained
providers.
A POLST form is meant to compliment rather than replace
the AD. The living will section of the AD can add
significant further detail in terms of care wishes and
philosophy, but it cannot function as a recognized, enforced
medical “order.” The living well is the background for the
POLST.
The state of Montana is currently in the development
stages of the “POLST Paradigm.” There are numerous hurdles
to overcome to roll this out on a statewide basis. However,
the forms are already available, and a great number of
patients, including many nursing home residents in the state
of Montana, have had POLST forms completed.
So....if you or a loved one suffers from a life-limiting
illness and you want to both clarify and legally document
your care preferences, go to the following link, educate
yourself on POLST, and strongly consider filing an official
form.
An excellent place to start in terms of educating
yourself on this excellent program is the following:
http://www.ohsu.edu/polst/
Stan Seagraves M.D., an internist who has practiced in
Missoula for over 20 years. He is currently practicing
hospital medicine at St. Patrick Hospital, and is medical
director of their hospitalist program.
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