Consentfor RA2015
Consentfor RA2015
Consentfor RA2015
1
RAUK
Consent
for
peripheral
nerve
blocks
2015
2
RAUK
Consent
for
peripheral
nerve
blocks
2015
Section 1 Introduction
Section 4 References
3
RAUK
Consent
for
peripheral
nerve
blocks
2015
Peripheral
nerve
blocks
are
routinely
performed
by
anaesthetists
to
provide
anaesthesia
and
analgesia
for
patients
undergoing
limb
surgery.
Like
all
procedures
in
anaesthesia,
nerve
blocks
are
associated
with
certain
inherent
risks
and
complications.
A
properly
taken
consent
can
help
patients
make
an
informed
decision
about
undergoing
nerve
blocks
and
will
also
protect
an
anaesthetist
from
subsequent
criticism
and
litigation.
In
2006,
The
Association
of
Anaesthetists
of
Great
Britain
and
Ireland
(AAGBI)
published
“Consent
for
Anaesthesia”
1.
According
to
this
document,
information
about
anaesthesia
should
be
provided
to
patients
undergoing
elective
surgery
before
they
meet
their
anaesthetist.
This
is
preferably
in
the
form
of
a
patient
friendly
leaflet
(patient
information
leaflet).
Consent
should
be
obtained
prior
to
a
patient
coming
to
the
anaesthetic
room,
except
under
exceptional
circumstances.
The
amount
and
the
nature
of
information
provided
to
the
patient
should
be
aimed
at
helping
the
patient
to
make
an
informed
decision
about
choosing
one
of
the
available
options.
Patients
should
also
be
given
an
opportunity
to
ask
questions.
The
discussion
between
patient
and
anaesthetist
should
be
documented
in
the
notes;
this
documentation
should
cover
what
risks,
benefits
and
alternatives
were
explained
to
the
patient.
RAUK
(Regional
Anaesthesia
United
Kingdom)
advise
that
all
the
recommendations
made
in
the
AAGBI
guideline
apply
to
patients
having
a
nerve
block.
This
RAUK
guideline
contains
additional
advice
that
is
specific
to
Regional
Anaesthesia.
4
RAUK
Consent
for
peripheral
nerve
blocks
2015
Section 2: Information and the process of consent for nerve block
2.1.
Information
about
nerve
blocks
can
be
provided
preoperatively
by
an
anaesthetist
and/or
other
health
care
professionals,
including
surgeons
and
pre-‐assessment
nurses.
However,
ultimate
responsibility
for
ensuring
the
adequacy
of
information
provided
to
the
patient
lies
with
the
person
performing
the
block.
2.2.1
For
elective
surgery,
information
should
ideally
be
given
prior
to
the
day
of
surgery.
This
could
be
in
the
form
of
a
‘Patient
information
leaflet’.
This
can
be
given
to
the
patient
by
the
surgeon
at
the
time
of
booking
or
by
a
nurse
in
the
pre-‐assessment
clinic.
However
this
may
not
be
always
possible.
Information
about
the
nerve
block
can
be
given
on
the
day
of
surgery,
provided
adequate
time
has
been
given
for
the
patient
to
understand
the
information
and
to
ask
questions.
Consent
for
peripheral
nerve
blocks
should
not
be
obtained
in
the
anaesthetic
room.
2.2.2.
For
emergency
surgery
it
will
not
always
be
possible
to
provide
a
patient
information
leaflet
prior
to
surgery.
The
consent
should
be
obtained
prior
to
the
patient
coming
to
the
anaesthetic
room.
Under
exceptional
circumstances
it
may
be
necessary
to
obtain
consent
in
the
anaesthetic
room.
2.3.1.
Although
information
for
nerve
block
can
be
provided
by
other
health
care
professionals,
consent
should
ideally
be
obtained
by
the
person
performing
the
block.
2.3.2.
Consent
for
the
procedure
may
be
obtained
by
a
person
who
is
not
performing
the
block,
provided
that
he/she
understands
the
processes,
the
risks
involved,
possible
complications,
the
benefits
of
the
block
to
the
patient
and
any
alternatives
(e.g.
patient
controlled
analgesia).
However,
the
person
performing
the
block
is
still
responsible
for
ensuring
that
adequate
consent
has
been
obtained
and
specifically,
that
the
patient
has
consented
for
him/her
to
perform
the
block.
2.3.3.
If
a
trainee
is
working
under
the
direct
supervision
of
a
Consultant,
then
it
is
the
responsibility
of
that
consultant
to
ensure
adequate
consent
has
been
obtained
for
the
trainee
to
perform
the
block,
and
that
risks
are
minimised.
If
a
trainee
is
not
working
under
the
direct
supervision
of
a
Consultant,
then
it
is
the
responsibility
of
trainee
to
ensure
adequate
consent
has
been
obtained
and
that
the
indirectly
supervising
consultant
has
been
informed,
if
appropriate.
Trainees
can
function
autonomously
within
their
level
of
expertise,
as
defined
by
the
General
Medical
Council2.
If
discussion
has
occurred
with
the
supervising
consultant,
this
should
be
recorded
and
the
consultant
identified
by
name.
5
RAUK
Consent
for
peripheral
nerve
blocks
2015
2.4.1.
Patient
information
leaflets
are
a
useful
source
of
information.
However
they
may
not
help
the
patient
remember
all
the
details
of
the
nerve
block3.
They
are
not
a
substitute
for
talking
to
the
patient
directly
about
the
nerve
block.
2.4.2.
Patient
information
leaflets
should
be
available
in
the
language
understood
by
the
patient.
If
this
is
not
possible,
a
translator
should
be
provided.
2.4.3.
Patient
information
leaflets
can
be
given
to
the
patient
by
any
healthcare
professional,
but
the
anaesthetist
performing
the
block
should
make
sure
that
the
patient
has
read
and
understood
the
contents.
2.4.4.
Whenever
possible,
nationally
approved
patient
information
leaflets
should
be
used.
They
may
be
modified
to
reflect
local
circumstances.
2.4.5.
Preoperative
multimedia
information
has
been
shown
to
reduce
the
anxiety
of
patients
undergoing
surgery
under
regional
anaesthesia
and
improve
patient
experience4.
If
possible,
the
patient
should
be
shown
a
professionally
approved
video
which
explains
the
block
procedure.
The
patient
should
be
given
the
opportunity
to
ask
any
questions
relating
to
the
video.
2.4.6.
Patient
information
leaflets
should
provide
a
prompt
to
the
patient
to
ask
questions
or
express
any
concerns.
Contact
details
and
“frequently
asked
questions”
and
answers
should
be
provided.
2.4.7.
Regular
audit
and
updating
of
the
information
provided
to
the
patient
should
be
carried
out.
The
audit
may
include
the
quality
of
information
provided
and
usefulness
of
the
information
provided
to
the
patient.
2.5.1.
Patients
need
to
know
what
they
are
consenting
for.
They
should
be
told
about
the
benefits
(e.g.
opioid
sparing,
early
mobilisation,
less
risk
of
nausea
and
vomiting)
to
them
of
undergoing
nerve
block.
They
also
need
to
be
told
the
alternative
options
to
a
nerve
block
(e.g.
having
a
general
anaesthetic
for
surgery
or
using
patient
controlled
analgesia
for
pain
relief).
2.5.2.
The
Patient
should
be
told
about
the
process
of
nerve
blockade,
i.e.,
what
he/she
will
feel
and
see.
This
includes
use
of
a
nerve
stimulator
(muscle
twitches)
and/or
ultrasound.
If
they
are
going
to
be
sedated
for
the
block
then
they
should
be
told
about
this.
Patients
should
be
offered
additional
sedation
or
general
anaesthesia,
together
with
a
clear
explanation
of
the
risks
and
benefits.
2.5.3.
The
risk
of
failure
and
alternative
plans
for
anaesthesia
and
analgesia
should
be
explained
to
the
patient.
2.5.4.
Patients
should
be
told
about
any
risk
associated
with
the
nerve
block
or
any
immediate
side
effect
(e.g.
Horner’s
syndrome
with
interscalene
block)
which
has
an
incidence
of
>1:100
6
RAUK
Consent
for
peripheral
nerve
blocks
2015
2.5.5.
Any
risk
that
can
have
either
short
term
(pneumothorax
following
supraclavicular
block)
or
long
term
serious
consequences
(permanent
nerve
damage)
should
be
discussed.
2.5.6.
The
exact
incidence
of
nerve
damage
is
not
known5-‐8.
The
risk
of
complications
is
influenced
by
numerous
factors,
including
patient
co-‐morbidity,
the
experience
of
the
anaesthetist,
the
method
of
nerve
location
and
the
block
selected.
It
should
be
made
clear
to
the
patient
that
the
exact
incidence
of
nerve
damage
is
not
known.
In
the
absence
of
clear
figures
we
can
rely
only
on
the
incidences
quoted
in
the
scientific
literature
and
summarised
in
leaflets
published
by
the
Royal
College
of
Anaesthetists9,
which
quote
an
incidence
of
approximately
1:10
for
temporary
nerve
damage
and
a
range
from
1:2000
to
1:5000
for
permanent
nerve
damage.
2.5.7
If
a
unit
or
an
anaesthetist
has
audit
data
which
indicates
their
local
incidence
of
complications,
they
may
quote
these
figures.
However,
care
should
be
taken
in
interpretation,
application
and
explanation
of
uncontrolled
audit
data,
noting
that
statistical
significance
can
only
be
achieved
with
a
considerable
sample
size
when
assessing
rare
occurrences.
2.5.8.
For
all
blocks,
patients
should
be
made
aware
of
the
risk
of
thermal
damage
to
the
insensate
blocked
limb.
They
should
also
be
told
that
they
should
avoid
driving,
using
any
machinery
or
cooking
while
their
limb
is
insensate.
2.5.9.
For
lower
limb
blocks
the
patient
should
be
made
aware
of
the
specific
risk
of
falling
and
heel
pressure
sores.
2.5.10.
There
are
certain
risks
which
are
block
specific
(e.g.
Horner’s
syndrome
following
Interscalene
block,
risk
of
pneumothorax
following
periclavicular
blockade).
These
should
be
discussed
with
the
patient.
2.5.11.
If
surgery
is
performed
under
block
alone,
then
patients
should
be
made
aware
that
they
may
have
tourniquet
pain
or
operative
discomfort
even
with
a
fully
functioning
block.
They
should
also
be
informed
that
they
may
feel
surgical
pain,
but
that
if
this
happens,
the
anaesthetist
or
surgeon
will
immediately
administer
alternative
effective
analgesia.
2.5.12.
Patients
should
be
repeatedly
told
to
take
postoperative
pain
relief
well
in
advance
of
block
resolution.
7
RAUK
Consent
for
peripheral
nerve
blocks
2015
3.1.
It
is
not
necessary
to
obtain
specific
written
consent
for
RA
to
facilitate
a
surgical
procedure,
as
long
as
written,
signed
consent
has
been
obtained
for
the
surgery.
However,
when
RA
is
proposed
as
the
sole
therapeutic
procedure
(e.g.
rib
fractures,
chronic
pain
therapy),
specific
signed
consent
should
be
obtained,
using
the
local
formal
consent
process.
3.2.
All
the
risks/benefits/alternatives
to
nerve
block
that
have
been
discussed
with
the
patient
should
be
documented
in
the
patient’s
notes.
If
the
patient
asks
any
questions
related
to
nerve
blockade,
then
this
discussion
should
also
be
documented.
3.3.
If
the
patient
has
received
a
patient
information
leaflet,
this
should
be
documented,
as
well
as
any
discussion
relating
to
it.
3.4
If
the
patient
has
a
high
risk
of
a
complication
(e.g.,
nerve
damage
in
diabetics),
or
is
at
higher
risk
than
usual
from
the
effects
of
the
complication
(e.g.,
their
occupation),
care
should
be
taken
to
specifically
address
these
issues
and
record
the
discussion
in
the
notes.
3.5.
It
should
be
made
clear
in
the
notes
that
• The
patient
was
given
the
opportunity
to
ask
questions
and
all
their
questions
were
answered.
8
RAUK
Consent
for
peripheral
nerve
blocks
2015
1. http://www.aagbi.org/sites/default/files/consent06.pdf
2. http://www.gmc-‐uk.org/The_Trainee_Doctor_1114.pdf_56439508.pdf
3. Turner
P.
and
Williams
C.
(2002)
Informed
consent:
patients
listen
and
read,
but
what
information
do
they
retain?
The
New
Zealand
Medical
Journal
Vol
115
No.1164
4. Jlala
HA,
French
JL,
Foxall
GL,
Hardman
JG,
Bedforth
NM.
Effect
of
preoperative
multimedia
information
on
perioperative
anxiety
in
patients
undergoing
procedures
under
regional
anaesthesia.
Br
J
Anaesth.
2010;104:369-‐374
5. Liguori
GA.
Complications
of
regional
anesthesia:
nerve
injury
and
peripheral
neural
blockade.
J
Neurosurg
Anesthesiol
2004;16:84-‐6.
6. Auroy
Y,
Benhamou
D,
Bargues
L,
et
al.
Major
complications
of
regional
anesthesia
in
France:
the
SOS
Regional
Anesthesia
Hotline
Service.
Anesthesiology
2002;97:1274-‐80.
7. Liu
SS,
Zayas
VM,
Gordon
MA,
et
al.
A
prospective,
randomized,
controlled
trial
comparing
ultrasound
versus
nerve
stimulator
guidance
for
interscalene
block
for
ambulatory
should
surgery
for
postoperative
neurological
symptoms.
Anesth
Analg
2009;109:265-‐71.
8. Fredrickson
MJ,
Kilfoyle
DH.
Neurological
complication
analysis
of
1000
ultrasound
guided
peripheral
nerve
blocks
for
elective
orthopaedic
surgery:
a
prospective
study.
Anaesthesia
2009;64:836-‐44.
9. http://www.rcoa.ac.uk/system/files/PI-‐RISK12-‐NERVEBLOCK-‐2013.pdf
Royal College of Anaesthetist document on risk associated with anaesthetic, section 12.
9
RAUK
Consent
for
peripheral
nerve
blocks
2015