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11.
The
combination
of
thoracic
epidural
analgesia
with
local
anaesthetics
and
nutritional

support
leads
to
preservation
of
total
body
protein
after
upper
abdominal
surgery
(U)

(Level
II).

12.
The
risk
of
permanent
neurological
damage
in
association
with
epidural
analgesia
is
very

low;
the
incidence
is
higher
where
there
have
been
delays
in
diagnosing
an
epidural

haematoma
or
abscess
(S)
(Level
IV).


13.
Immediate
decompression
(within
8
hours
of
the
onset
of
neurological
signs)
increases
the

likelihood
of
partial
or
good
neurological
recovery
(U)
(Level
IV).

The
following
tick
boxes

represent
conclusions
based
on
clinical
experience
and
expert

opinion.

 The
provision
of
epidural
analgesia
by
continuous
infusion
or
patient‐controlled

administration
of
local
anaesthetic‐opioid
mixtures
is
safe
on
general
hospital
wards,
as

long
as
supervised
by
an
anaesthesia‐based
pain
service
with
24‐hour
medical
staff
cover

and
monitored
by
well‐trained
nursing
staff
(U).

 Magnetic
resonance
imaging
investigation
may
be
warranted
if
patients
who
have
had
an

epidural
catheter
inserted
develop
a
fever
and
infection
at
the
catheter
insertion
site;

urgent
investigation
is
especially
indicated
if
other
signs
are
present
that
could
indicate
an

abscess,
such
as
back
pain
or
neurological
change
(N).


7.3 INTRATHECAL ANALGESIA



7.3.1 Drugs used for intrathecal analgesia
CHAPTER
7
 Local
anaesthetics
given
intrathecally
provide
only
short‐term
postoperative
analgesia.

Local anaesthetics


The
use
of
spinal
microcatheters
(<24
gauge)
for
postoperative
infusions
of
local
anaesthetics

became
controversial
when
multiple
cases
of
cauda
equina
syndrome
were
reported

(Bevacqua,
2003).
See
also
Section
5.1.3.

Opioids
Intrathecal
opioids
have
been
used
for
surgical
procedures
ranging
from
lower
limb

orthopaedic
surgery
to
CABG
because
of
their
ability
to
provide
prolonged
postoperative

analgesia
following
a
single
dose.
Clinical
experience
with
morphine,
fentanyl
and
sufentanil

has
shown
no
neurotoxicity
or
behavioural
changes
at
normal
intrathecal
doses
(Hodgson
et
al,

1999
Level
IV).


Intrathecal
morphine
produces
analgesia
lasting
12
hours
or
more.
Side
effects
include

respiratory
depression,
nausea,
vomiting
and
pruritus.
Early
clinical
studies
used
very
high

intrathecal
morphine
doses
(ie
0.5
mg
or
more),
however
adequate
postoperative
analgesia

with
fewer
adverse
effects
may
be
obtained
with
significantly
less
morphine
—
although
at

lower
doses
there
is
not
a
clear
dose‐response
relationship
for
some
side
effects
or
analgesia

(Meylan
et
al,
2009
Level
I).
A
meta‐analysis
comparing
intrathecal
morphine
doses
of
less
than

300
mcg,
equal
to
or
greater
that
300
mcg,
and
placebo
reported
a
greater
risk
of
respiratory

depression
with
the
higher
doses
of
morphine
(there
was
no
increased
risk
with
lower

morphine
doses)
and
while
the
incidence
of
pruritus
was
increased
for
all
doses,
the
risk
of

nausea
and
vomiting
was
increased
only
in
those
patients
given
less
than
300
mcg
morphine

(Gehling
&
Tryba,
2009
Level
I).



190
 Acute
Pain
Management:
Scientific
Evidence

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