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Should Dialysis Be Offered to All Patients?
Christy Price Rabetoy, Department Editor
Some Patients Should Not Be Given the Option of Dialysis
Jennifer Payton, MHCA, BSN, RN, CNN
Home Training Coordinator
Dialysis Clinic, Inc
Goose Creek, SC
Southeast Region Health Policy Advisor
Member, ANNA’s Palmetto Chapter
Dialysis should only be offered to a patient or family if it
will increase the quality as well as the quantity of a patient’s life.
I think we forget that the quality of our life is more important than
the quantity of our life. Many times, families want to keep their loved
ones alive at all costs. This is when skilled physicians and nurse
practitioners should come into the picture. Instead of dangling the
“dialysis carrot” in front of these people, they should be laying out
the facts. If dialysis will have no hope of improving the quality of a
patient’s life, it should not be used solely to increase the quantity
of life. Just as we individualize our care based on each patient’s
specific needs, we need to individualize our decision to offer dialysis
as an option to all patients.
In the transplant community, it is well known that not all patients are
offered transplants. Patients who are morbidly obese, have drug
addictions, or have multiple co-morbid conditions are not offered the
option of transplant. Giving transplants to these patients could be
seen as a “waste” of organs. Why then do we “waste” resources in the
dialysis community by dialyzing very ill patients? I have personally
seen patients in the outpatient hemodialysis unit who should not have
been started on dialysis. I had one patient who would come to dialysis
via a stretcher from a local nursing home. This patient did not know
where he was or why he was there. The patient was incontinent,
contracted, and had to be fed through a feeding tube. This patient, who
was unable to communicate and virtually unresponsive, was started on
dialysis in this grave condition. In my opinion, the patient’s family
should not have been offered the option of dialysis.
My opinion is both professional and very personal as my family went
through this trauma several years ago. One of my family members
injected cocaine into her portacath. She had the port due to her
multiple health problems and frequent hospitalizations. She ended up on
a ventilator in the ICU with multi-system organ failure. As her
situation deteriorated, her kidneys began to fail as well. My family
member was not able to make the decision regarding dialysis because of
her condition. After encouragement from the nephrologist, my family was
willing to try anything and therefore agreed to dialysis. A week later,
my family stopped the ventilator and she died. In my opinion, the use
of dialysis in this case just prolonged her suffering, my family’s
suffering, and the dying process. This is clearly a case of where
dialysis was used to increase the quantity and not the quality of
someone’s life.
Years ago, patients with kidney disease had to go through a screening
process to be started on dialysis. It now seems as if dialysis is
offered to everyone. Dialysis is even offered to the chronically ill
patients who have little quality of life. People forget that dialysis
and transplant are not the only options. The choice of not initiating
dialysis is also an option. In our technologically advanced society, we
sometimes keep patients alive just because the technology exists, and I
believe this is wrong.
The Issue May Not Be Whether, But How You Offer Dialysis
Christine Ceccarelli, MS, MBA, RN Staff Nurse
Hartford Hospital
Hartford, CT
and Central Connecticut Dialysis Unit
Meriden, CT
Member, ANNA’s Ethics Committee & ANNA’s Colonial Chapter
Every
day, nephrology nurses care for patients with life-threatening
illnesses and poor prognoses for recovery. The patient may be in an
intensive care environment with multi-system organ failure or may be an
outpatient compromised by age, limited function, or other end-stage
medical problems. The effort can seem futile, even inhumane and cruel,
as it prolongs a life destined to end due to physiological failure.
Sometimes, we know the patient and family well; sometimes, we don’t.
But we all make judgments about the appropriateness of the situation,
based on our own values, preferences, and experiences. “Why is this
person on dialysis?” is a question often discussed in lunchrooms and at
nurses’ stations.
The question of appropriateness of life-extending therapies has been
discussed as their use has outstripped our society’s ability to deal
with this issue. It became a societal norm to often initiate therapy
and then wonder whether it should have been started in the first place.
However, things are changing. Discussions about when to use therapies
and how to approach patients and families in making these decisions can
readily be found in professional literature. Our competency in dealing
with this issue is increasing, but many feel it is taking too long. As
use of dollars for essential health care is scrutinized and
professional caregiver resources dwindle, the problem seems more
urgent. How can we reverse the transgressions of offering therapies to
everyone when we know the outcome will be poor? Perhaps the answer lies
in our behavioral competence more than in our clinical knowledge.
Patients and their families facing these tough decisions have often not
thought about or discussed their possibility in advance, despite our
best efforts. Although preparation of advance directives are
encouraged, they are not yet widely used. Death, as a natural end to
life, is a private and feared experience in our society, usually viewed
for its negative effects on those left behind. The positive impact of
palliative care in providing peace and comfort to patients and families
is not part of common knowledge. Therefore, the option of foregoing
life-sustaining treatment is often poorly received despite a rational
description of its futility. When the life of a loved one is
threatened, thoughts first turn to anticipation of personal loss, and
the emotions that accompany this terrifying possibility. In addition,
cultural and religious beliefs feed into a personal interpretation of
what is “right” in terms of extending life, and efforts to withhold any
treatment can be interpreted as passive euthanasia.
In many of these cases, offering dialysis to extend life is
inappropriate according to the judgment of caring healthcare
professionals. In an effort to avoid initiating dialysis treatment,
should the patient and/or family be apprised of this decision? Is it
ethical to withhold information about declining renal function? If this
information is shared but the option of dialysis is not, is this
ethical practice? Is the amount of information discussed dependent on
the educational or socioeconomic level of the patient and/or family? Is
this a discriminatory practice? All of these questions are important to
answer and must be discussed by the healthcare team.
As difficult decisions need to be made, particularly by families when
the patient is no longer competent, a careful assessment of factors
influencing their decision-making can be a good first step. Involving
the whole team in discussion of each family’s dynamics, preferably at a
time before critical decisions are needed, will assist to create a
unified plan of communication and support. Some families need time to
process the realities of their loved one’s condition. Guilt and
perception of abandonment can lead to insistence on continued
therapies. Anticipatory grief is often experienced at these times with
family members caught in the “shock and denial mode” when the
suggestion of foregoing dialysis occurs. In other cases, family members
may differ in their attitudes and opinions, requiring ongoing
facilitation of decision-making. If the family is told that dialysis
may not be appropriate and this decision is initially rejected, a
dialysis trial may be helpful in providing the time needed for a more
permanent decision. As the professionals providing direct care of their
loved one, nurses can be the critical link to families who may feel
judged and abandoned if they reject a medical recommendation not to
initiate therapy.
In all cases, remembering that we have been through this scenario more
than once, and the patient or family has not, will assist us to
continue supporting them despite our frustration and angst. Whatever
the circumstances, patients and families deserve complete information
when this is desired, and must be part of the decision-making process,
even though the outcome may not be what we ourselves would choose.
The Controversies in Nephrology Nursing
department focuses on exploring ethical and clinical issues within the
nephrology clinic practice in a point/counterpoint format. Address
correspondence to: Christy Price Rabetoy, Department Editor, through
the ANNA National Office; East Holly Avenue/Box 56; Pitman, NJ
08071-0056; (856) 256-2320; or by emailing her at
christycpr@comcast.net. You may also log onto this column at
www.nephrologynursingjournal.net (clink on Department link) and email
your comments to the Editor (see Discussion Area). The opinions and
assertions contained herein are the private views of the contributors
and do not necessarily reflect the views of the American Nephrology
Nurses' Association.
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Copyright 2006, American Nephrology Nurses' Association. Anthony J. Jannetti, Inc., publisher. An iNurse Web site.
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