CONSIDERATIONS ON THE SCIENTIFIC AND ETHICAL
PROBLEMS
RELATED TO VEGETATIVE STATE
1) Vegetative State (VS) is a state of unresponsiveness,
currently defined as a condition marked by:
- a state of vigilance;
- some alternation of sleep/wake cycles;
- absence of signs of awareness of self and of surroundings;
- lack of behavioural responses to stimuli from the environment;
- maintenance of autonomic and other brain functions.
2) VS must be clearly distinguished from:
- encephalic death;
- coma;
- “Locked-in” syndrome;
- minimally conscious state.
VS cannot be simply equalled to cortical death either, considering
that in VS patients islands of cortical tissue which may even
be quite large can keep functioning.
3) In general, VS patients do not require any technological support
in order to maintain their vital functions.
4) VS patients cannot in any way be considered terminal patients,
since their condition can be stable and enduring.
5) VS diagnosis is still clinical in nature and requires careful
and prolonged observation, carried out by specialized and experienced
personnel, using specific assessment standardized for VS patients
in an optimum controlled environment. Medical literature, in fact,
shows diagnostic errors in a substantially high proportion of
cases. For this reason, when needed, all available modern technologies
should be used to substantiate the diagnosis.
6) Modern neuroimaging techniques demonstrated the persistence
of cortical activity and response to certain kinds of stimuli,
including painful stimuli, in VS patients. Although it is not
possible to determine the subjective quality of such perceptions,
some elementary discriminatory processes between meaningful and
neutral stimuli seem to be nevertheless possible.
7) No single investigation method available today allows us to
predict, in individual cases, who will recover and who will not
among VS patients.
8) Until today, statistical prognostic indexes regarding VS have
been obtained from studies quite limited as to number of cases
considered and duration of observation. Therefore, the use of
adjectives like “permanent” referred to VS should
be discouraged, by indicating only the cause and duration of VS.
9) We acknowledge that every human being has the dignity of a
human person, without any discrimination based on race, culture,
religion, health conditions, or socio-econimic conditions. Such
a dignity, based on human nature itself, is a permanent and intangible
value, that cannot depend on specific circumstances of life and
cannot be subordinated to anybody’s judgement. We recognize
the search for the best possible quality of life for every human
being as an intrinsic duty of medicine and society, but we believe
that it cannot and must not be the ultimate criterion used to
judge the value of a human being’s life.
We acknowledge that the dignity of every person can also be expressed
in the practice of autonomous choices; however, personal autonomy
can never justify decisions or actions against one’s own
life or that of others: in fact, the exercise of freedom is impossible
outside of life.
10) Based on these premises, we feel the duty to state that VS
patients are human persons, and, as such, they need to be fully
respected in their fundamental rights. The first of these rights
is the right to live and to the safeguard of health. In particular,
VS patients have the right to:
- correct and thorough diagnostic evaluation, in order to avoid
possible mistakes and to orient rehabilitation in the best way;
- basic care, including hydration, nutrition, warming and personal
hygiene;
- prevention of possible complications and monitoring for any
possible signs of recovery;
- adequate rehabilitative processes, prolonged in time, favouring
the recovery and maintenance of all progress achieved;
- be treated as any other patients with reference to general assistance
and affective relationships.
This requires that any decision based on a probability judgement
be discouraged, considering the insufficiency and unreliability
of prognostic criteria available to date.
The possible decision of withdrawing nutrition and hydration,
necessarily administered to VS patients in an assisted way, is
followed inevitably by the patients’ death as a direct consequence.
Therefore, it has to be considered a genuine act of euthanasia
by omission, which is morally unacceptable.
At the same time, we refuse any form of therapeutic obstinacy
in the context of resuscitation, which can be a substantial cause
of post-anoxic VS.
11) To the rights of VS patients corresponds the duty of health
workers, institutions and societies in general to guarantee what
is needed for their safeguard, and the allocation of sufficient
financial resources and the promotion of scientific research aimed
to the understanding of cerebral physiopathology and of the mechanisms
on which the plasticity of the Central Nervous System is based.
12) Particular attention has to be paid to families having one
of their members affected by VS. We are sincerely close to their
daily suffering, and we reaffirm their right to obtain help from
all health workers and a full human, psychological and financial
support, which enables them to overcome isolation and feel part
of a network of human solidarity.
13) In addition, it is necessary for institutions to organize
models of assistance, specialized with reference to the care of
these patients (awakening centres and specialized rehabilitation
centres), sufficiently spread over the territory. Institutions
should also promote the training of competent personnel.
14) VS patients cannot be considered as “burdens”
for society; rather, they should be viewed as a “challenge”
to implement new and more effective models of health care and
of social solidarity.