Page 212 Acute Pain Management
P. 212

 




5.
 Rectal
administration
of
single
doses
of
paracetamol
results
in
highly
variable
plasma

concentrations
that
often
remain
subtherapeutic
(N)
(Level
II).

6.
 Intermittent
subcutaneous
morphine
injections
are
as
effective
as
intramuscular
injections

and
have
better
patient
acceptance
(U)
(Level
II).


7.
 Intranasal
opioids,
in
particular
the
more
lipid‐soluble
drugs
such
as
fentanyl,
are
effective

for
the
management
of
acute
pain
(N)
(Level
II).

8.
 Continuous
intravenous
infusion
of
opioids
in
the
general
ward
setting
is
associated
with

an
increased
risk
of
respiratory
depression
compared
with
other
methods
of
parenteral

opioid
administration
(U)
(Level
IV).


9.
 Transdermal
fentanyl
should
not
be
used
in
the
management
of
acute
pain
because
of

safety
concerns
and
difficulties
in
short‐term
dose
adjustments
needed
for
titration;

furthermore,
in
most
countries,
it
lacks
regulatory
approval
for
use
in
other
than
opioid‐
tolerant
patients
(S)
(Level
IV).

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

opinion.

 Other
than
in
the
treatment
of
severe
acute
pain,
and
providing
there
are
no

contraindications
to
its
use,
the
oral
route
is
the
route
of
choice
for
the
administration
of

most
analgesic
drugs
(U).


 Titration
of
opioids
for
severe
acute
pain
is
best
achieved
using
intermittent
intravenous

bolus
doses
as
it
allows
more
rapid
titration
of
effect
and
avoids
the
uncertainty
of
drug

absorption
by
other
routes
(U).

CHAPTER
6
  Controlled‐release
opioid
preparations
should
only
be
given
at
set
time
intervals
(U).


 Immediate‐release
opioids
should
be
used
for
breakthrough
pain
and
for
titration
of

controlled‐release
opioids
(U).

 The
use
of
controlled‐release
opioid
preparations
as
the
sole
agents
for
the
early

management
of
acute
pain
is
discouraged
because
of
difficulties
in
short‐term
dose

adjustments
needed
for
titration
(U).

 Neither
oral
transmucosal
fentanyl
citrate
nor
fentanyl
buccal
tablets
should
be
used
in
the

management
of
acute
pain
because
of
safety
concerns
and,
in
most
countries,
lack
of

regulatory
approval
for
use
in
other
than
opioid‐tolerant
patients
(N).



REFERENCES


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TK,
Zhu
J,
Gangolly
J
et
al
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Transnasal
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Scand
35(1):
14–8.


Anderson
B,
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G
(1996)
Analgesic
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BJ,
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Ashburn
MA,
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164
 Acute
Pain
Management:
Scientific
Evidence

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