Informed Consent, Patient Autonomy and Causation: Competing Perspectives - The United States, Ireland and Germany

AuthorDavid Vos
PositionJunior Sophister LLB Candidate, Trinity College Dublin
Pages147-167
INFORMED
CONSENT,
PATIENT
AUTONOMY
AND
CAUSATION:
COMPETING
PERSPECTIVES
THE
UNITED
STATES,
IRELAND
AND
GERMANY
DAVID
VOS*
Introduction
Historically,
medical practice
has
been based
on
the
Hippocratic
Oath,
governed
primarily
by
principles
of
paternalism
and
beneficence.
Under
such
an
approach,
the
patient
is
subject
to
whatever
treatment
a
physician
deems
to
be
in
his
best
interests,
with
little
or
no
regard
to
his
personal
autonomy.
In
the
past
century,
however,
there
has
been
an
increasing
recognition
of
the value
of
personal
autonomy
in
the
decision-making
process.
This
has
led
to
the
development
in
all
common
law and
civil
jurisdictions
that,
at
the very least,
health
care
must
not
be
administered
without
the
patient's
consent.
Recognition
of
patient
autonomy
has
been
fuelled by
changes
in
societal
values.
An evolving view
of
the
relationship
between doctor
and
patient,
increased
recognition
of
the
importance
accorded
to
individual
freedom
of
action, increased
recognition
of
the
application
and
importance
of
basic
human
rights, advances
in
medical
techniques,
increasingly educated
populations,
access to
information
over
the
internet
and
greater
patient
choice
are
all
responsible
for
the increased
weight
afforded
to
patient
autonomy
today.'
The
principles
of
patient
autonomy
dictate
that
an
adult
of
"sound"
mind
can
determine
absolutely
what
is
done
to
his
or
her
body.
2
True
patient
autonomy
is
thus based
on the
right
of
the
patient
to
knowingly
make
decisions
regarding
medical
treatment,
no
matter
how
unwise
others
may
consider them,
or
how
disastrous
their
effects
on the
patient
may
be.
3
The
doctrine
of
informed consent
to
medical
treatment,
inherently
linked
to
this
concept,
has
played
a
central
role
in
the emergence
of
patient
autonomy
as
a
key
tenet
of
medical practice.
"Informed
consent"
is
commonly
used
as
shorthand
for
two
distinct
but
nonetheless
interrelated
duties: the
duty to
obtain
a
patient's
consent
before
treatment,
and
the
duty
*
Junior
Sophister
LLB
Candidate, Trinity College
Dublin.
1Meg
Wallace,
Health
Care
and
the
Law
(2
nd
ed.,
Law Lawbook
Co,
1995),
at
63.
2
bid.,
at
64.
3
Ibid.
©
2010
David
Vos and
Dublin
University Law
Society
Trinity
College
Law
Review
to
ensure
that
a
patient
has
been
given enough
information
to enable
him
to
make
an
"informed"
choice.
4
The
concepts
of
patient
autonomy
and
informed
consent
are
not, however,
the
sole
concern
of
the
courts.
All
jurisdictions
have
found
it
necessary
to
resolve conflicts
between
patient
autonomy
on
the
one
hand,
and
concerns
over
remaining
interests
in
medical
paternalism,
deference to
the
medical
profession,
limitations
on
the
scope
of
medical liability,
and
practicalities
in
court
proceedings
on
the
other.
Different
jurisdictions
have
afforded
varying
weights
to
each
of
these
considerations,
resulting
in
different
relative
strengths
being accorded
to
the
principle
of
patient
autonomy.
This
article deals
with
the balance
struck
in
three
jurisdictions:
the
United
States,
Ireland
and
Germany.
Jurisprudence
in
the
United
States seems
on
its
face
to
accord
significant
weight
to
patients'
"rights"
of
autonomy
and
self-determination, but
the
adoption
of
a
negligence-based framework
and
an
objective
stance
to
causation
ultimately
negates
much
of
the
practical
strength
of
these
"rights."
In
Ireland,
a
significant
traditional
deference to
the
medical
profession
is
still
manifest
in
relation
to
the
standard
of
care
owed
by
practitioners
in
a
medical malpractice
context. However,
an
emerging
body
of
case
law
in
the
courts
advocates increased
respect
for
patient
autonomy
and
a
mitigation
of
the
harshness
of
both
the
negligence
framework
and
principles
of
causation
to
give
practical
effect
to
autonomy
values. The
German
courts
have
had
the
highest
regard
for
patient
autonomy,
fuelled
by
express
recognition
of
rights
of
self-determination
and
autonomy
in
the
German
Constitution
(Grundgesetz)
5
and
a
legal
framework
that
is
far
more
favourable
to
the
patient than
standard
common
law
negligence.
The
Position
in
the United
States
In
the
United
States,
the
original
justification
for
consent
and
disclosure
requirements
in
a
medical
context
was
derived
from
a
beneficence model
of
health
care,
in
which
the
principal obligation
of
the
physician
was
to
provide medical assistance.
6
Thus,
non-disclosure
of
medical information
was
often
justified
on the basis
of
a
paternal
desire
to
avoid causing
undue
4
Emily
Jackson,
"'Informed
Consent'
to
Medical
Treatment
and the
Importance
of
Tort"
in
Sheila AM McLean
ed.,
First
Do
No
Harm:
Law,
Ethics
and
Healthcare
(Ashgate,
2006),
at
273.
5
See
Article
2
1
of
the
German
Constitution.
6
Leanna
Darvall,
Medicine
Law
and
Social
Change:
The
Impacts
of
Bioethics, Feminism
and
Rights
Movements
on
Medical
Decision-Making
(Aldershot,
1993),
at
34.
[Vol. 13

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