Page 138 Acute Pain Management
P. 138




with
placebo
was
3.7
(CI
2.4
to
7.8);
the
NNH
for
a
major
adverse
event
was
insignificant

(Wiffen,
McQuay
&
Moore,
2005
Level
I).

Phenytoin

A
review
of
phenytoin
for
the
treatment
of
chronic
neuropathic
pain
calculated
a
NNT
of
2.1

(CI
1.5
to
3.6)
for
painful
diabetic
neuropathy.
The
NNH
for
a
minor
adverse
effect
compared

with
placebo
was
3.2
(CI
2.1
to
6.3);
the
NNH
for
a
major
adverse
event
was
not
significant

(Wiffen,
Collins
et
al,
2005
Level
I).

Gabapentin

A
review
of
gabapentin
for
the
treatment
of
chronic
neuropathic
pain
calculated
a
NNT
of
4.3

(CI
3.5
to
5.7)
overall;
the
NNTs
for
painful
diabetic
neuropathy
and
postherpetic
neuralgia

were
2.9
(CI
2.2
to
4.3)
and
3.9
(CI
3
to
5.7)
respectively
(Wiffen,
McQuay,
Edwards
et
al,
2005

Level
I).
The
NNH
for
a
minor
adverse
effects
compared
with
a
placebo
was
3.7
(CI
2.4
to
5.4);

the
NNH
for
a
major
adverse
event
was
not
significant.
Gabapentin
was
effective
in
the

treatment
of
phantom
limb
pain
(Bone
et
al,
2002
Level
I)
and
smaller
later
trials
support
the

effectiveness
of
gabapentin
in
the
treatment
of
central
pain
after
spinal
cord
injury
(Levendoglu

et
al,
2004
Level
II;
Tai
et
al,
2002
Level
II).

Pregabalin

CHAPTER
4
 al,
2008
Level
I;
Gutierrez‐Alvarez
et
al,
2007
Level
I)
with
an
NNT
of
3.24
(Gutierrez‐Alvarez
et
al,
2007

Pregabalin
was
effective
for
the
management
of
pain
related
to
diabetic
neuropathy
(Hurley
et


Level
I)
and
an
increased
risk
of
sedation
and
dizziness
(Hurley
et
al,
2008
Level
I).
Pregabalin
was

effective
for
persistent
neuropathic
spinal
cord
injury
pain
(Siddall
et
al,
2006
Level
II).

Sodium
valproate

Sodium
valproate
was
effective
for
the
prevention
of
migraine
(Mulleners
&
Chronicle,
2008

Level
I)
but
ineffective
in
the
treatment
of
spinal
cord
injury
pain
(Drewes
et
al,
1994
Level
II).

Lamotrigine

A
review
of
lamotrigine
concluded
that
it
was
unlikely
to
be
of
benefit
for
the
treatment
of

neuropathic
pain
(Wiffen
&
Rees,
2007
Level
I).


Key
messages


1.
 Gabapentin
is
effective
in
the
treatment
of
chronic
neuropathic
pain
(Q);
lamotrigine
is

most
likely
ineffective
(N)
(Level
I
[Cochrane
Review]).



2.
 Carbamazepine
is
effective
in
the
treatment
of
trigeminal
neuralgia
(N)
(Level
I
[Cochrane

Review]).

3.
 Pregabalin
is
effective
in
the
treatment
of
chronic
neuropathic
pain
related
to
diabetic

neuropathy
(N)
(Level
I).


4.
 Perioperative
gabapentinoids
(gabapentin/
pregabalin)
reduce
postoperative
pain
and

opioid
requirements
(U)
and
reduce
the
incidence
of
vomiting,
pruritus
and
urinary

retention,
but
increase
the
risk
of
sedation
(N)
(Level
I).

The
following
tick
box

represents
conclusions
based
on
clinical
experience
and
expert

opinion.

 Based
on
the
experience
in
chronic
neuropathic
pain
states,
it
would
seem
reasonable
to

use
anticonvulsants
in
the
management
of
acute
neuropathic
pain
(U).





90
 Acute
Pain
Management:
Scientific
Evidence

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