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"Vex not his ghost. Oh, let
him pass! He hates him, that would upon the rack of this tough world
stretch him out longer."
The
Tragedy of King Lear, Act V, Scene III
From time
immemorial it has been taken for granted that a doctor's primary
occupation is to treat his patient - "to cure sometimes, to relieve
often, to comfort always". Till a few decades ago, there was no real
conflict of interests - a doctor did his best to preserve life, the
sanctity of his patient's life being considered paramount. The increasing
availability of sophisticated medical technology, life support systems
and critical care units changed the entire picture. Today the
question is, how long to continue treatment and the purpose of such
treatment. It is possible, to keep a person biologically alive -
heart, lungs, kidney and other organs functioning - but in coma,
"living" in a critical care unit setting.
The
"quality of life" of the patient being treated, is the critical
issue. Langfitt in a thought provoking article "Critical care, when is
enough enough?" discusses the several issues involved. What is "quality
of life"? Who decides this and whose life is it any way?
Social
Utility is a recent concept - the concept that a person can be
biologically alive but socially dead. The same respirator that helps a
patient with Gillian Barre syndrome to recover completely senselessly
prolongs the life of a young individual, in irreversible coma. The
mature physician should realize, that healing the sick, at some point
fails.
Life can
be revered not only in its preservation, but also in the manner in
which we allow a given life to reach its end.
Death
with dignity is as important as life with dignity.
To keep a
person biologically alive in a critical care setting would mean an
expenditure of Rs 5000 to 7500 a day in India. Can we afford this, when
there are thousands dying of malnutrition and diarrhea every day.
Even in the USA where 12% of the gross national product is pumped into the
health industry cost containment is the talk of the day. At the same
time is it not morally repugnant to deny useful treatment purely on
economic grounds.
Today,
with the legal recognition of brain death it is necessary for the
critical care specialist to view his/her brain dead patient also as a
potential organ donor. To whom does the doctor owe a greater
responsibility - to his brain dead unsalvageable patient or to a kidney
failure patient desperately waiting for a functioning kidney. Would
providing eyesight to two blind people, by switching of the
respirator, be termed a conflict of interests? Again from the
patient's point of view what can be a nobler way to die than to save five
dying persons? As one mother of a head trauma victim, who consented for
multiple organ donation put it "My son never died. He is traveling in
different people".
Several
ethical issues have to be considered in the diagnosis of brain
death especially when organ transplantation is the primary aim.
They
include the following:
Waiving
of intensive care bills normally payable, when the relatives agree
for organ donation. Sometimes this bill is settled by the recipient.
Is this not a form of compensation ?
Providing free medical care to the relatives of the brain dead
individual. Is this not a form of inducement ?
The
death certifying team should be different from the transplant
team.
Terms like
"heart beating cadaver" have come to stay. Unfortunately, in India there
are hardly any formal courses in medical ethics either at the
undergraduate or postgraduate level. Hospital ethical committees are
few and far between. Serious discussions on the definitions of death, o~
the personal, moral, legal and economic issues involved in death
related decisions are totally absent in the training of a doctor. How
does the physician of today, dealing with critically ill patients,
face these complex challenges.
Managing a
critically ill patient is not a purely technical affair. It is much
more than correcting the serum sodium or monitoring arterial blood gas
levels. The attitude to death, both of the physician and the patient
(or his near and dear) play a vital part. What happens after death -
the fear of the unknown - is a very real fear. A student once asked
a Zen master as to what happens after death. The master replied "I do
not know". "But you are a Zen master" said the student. "Not a dead one"
replied the master.
Seldom
does one accept death with equanimity. The fear of leaving behind loved
ones and to cope with loneliness is a very real fear. "I have not lived
enough" applies to the centurion as well as the teenager.
When is
enough enough? When does the physician treating a critically ill
patient say "This far and no farther". Unfortunately, not withstanding
all the rhetoric, there are no unambiguous rules. Medicine is never
black or white. It is always various shades of gray. Neither patients
nor the organs in their bodies read the latest journals, monographs or
the Supreme Court judgments. The science of medicine can never do away
with the art of medicine. It is this very element of uncertainty
whether it be in life or death, which makes managing a critically ill
patient a challenging affair.
The
fundamental ethical guidelines in the management of a patient
probably revolve around the following:
Beneficence - to do good by restoring health and relieving
suffering.
"Primum
non nocere" - to do no harm or non-malificence, a concept which
the doctor treating the critically ill patient has to always remember.
Administration of morphine may relieve pain. It may also cause
respiratory depression. The dividing line is often a very thin one.
Justice
- when medical resources are limited, treatment should be
administered to the patient who is most likely to benefit. However
the primary obligation is to the patient at hand.
To
follow the directions of a "living will" if one exists - that is a
written document or a reliable testimony, that the patient had prior
to his illness, expressed a desire for a par-ticular mode of treatment
in a particular condition.
Autonomy
- a legally competent informed adult, has the right to refuse or
accept medical treatment, including life support measures. The right
to self determination does not however include the right to commit
suicide with or without physician assistance.
Easier
said than done. In a situation where the brain is primarily
involved, either in head injury or other neurological problems, due to
organic brain damage, the patient may not be able to take part in the
decision making process. Who then is empowered to take the role of a
surrogate decision maker? Even if the attending doctor gives the full
information to the patient's relatives, is it reasonable to expect them
to take a calm, unruffled calculated decision after weighing the pros
and cons, all in a critical care setting. Any decision making process
involving life and death, is influenced by the cultural and socio economic
milieu.
By the
same token is it fair to ask the attending doctor to play God. Combining
the role of a "devils advocate" and "amicus curae" he has to justify the
blind faith reposed in him by the patient's grief stricken relatives.
Quality of life may mean different things to different people at
different times. In a developing country, where there is seldom a third
party payor, the socio economic burden for caring for a chronically
comatose patient, is so enormous that it reflects on the health and
wealth of the family.
As in
any discussion on ethical issues, this article asks more questions
rather than providing answers. It is essential that medical ethics be
introduced in the curriculum so that the delivery of critical care will
truly be need based. |