Page 23 Acute Pain Management
P. 23




11.
 Non‐selective
NSAIDs
and
coxibs
are
effective
analgesics
of
similar
efficacy
for
acute
pain

(U)
(Level
I).

12.
 Preoperative
coxibs
reduce
postoperative
pain
and
opioid
consumption,
and
increase

patient
satisfaction
(N)
(Level
I).


13.
 Coxibs
given
in
addition
to
PCA
opioids
reduce
opioid
consumption
but
do
not
result
in
a

decrease
in
opioid‐related
side
effects
(N)
(Level
I).

14.
 Coxibs
and
non‐selective
NSAIDs
have
similar
adverse
effects
on
renal
function
(U)

(Level
I).

15.
 Non‐selective
NSAIDs
do
not
significantly
increase
blood
loss
after
tonsillectomy
but
do

increase
the
need
for
reoperation
due
to
bleeding
(N)
(Level
I).


16.
 Parecoxib
and/or
valdecoxib
compared
with
placebo
do
not
increase
the
risk
of
 SUMMARY

cardiovascular
adverse
events
after
non‐cardiac
surgery
(N)
(Level
I).

17.
 Coxibs
and
non‐selective
NSAIDs
are
associated
with
similar
rates
of
adverse

cardiovascular
effects,
in
particular
myocardial
infarction;
naproxen
may
be
associated

with
a
lower
risk
than
other
non‐selective
NSAIDs
and
celecoxib
may
be
associated
with
a

lower
risk
than
other
coxibs
and
non‐selective
NSAIDs
overall
(N)
(Level
I).


18.
 Perioperative
non‐selective
NSAIDs
increase
the
risk
of
severe
bleeding
after
a
variety
of

other
operations
compared
with
placebo
(N)
(Level
II).


19.
 Coxibs
do
not
impair
platelet
function;
this
leads
to
reduced
perioperative
blood
loss
in

comparison
with
non‐selective
NSAIDs
(S)
(Level
II).

20.
 Short‐term
use
of
coxibs
results
in
gastric
ulceration
rates
similar
to
placebo
(U)
(Level
II).

21.
 Use
of
parecoxib
followed
by
valdecoxib
after
coronary
artery
bypass
surgery
increases

the
incidence
of
cardiovascular
events
and
is
therefore
contraindicated
(S)
(Level
II).


 Adverse
effects
of
NSAIDs
are
significant
and
may
limit
their
use
(U).


 The
risk
of
adverse
renal
effects
of
non‐selective
NSAIDs
and
coxibs
is
increased
in
the

presence
of
factors
such
as
pre‐existing
renal
impairment,
hypovolaemia,
hypotension,

use
of
other
nephrotoxic
agents
and
ACE
inhibitors
(U).


Adjuvant
drugs

Inhalational
agents

1.
 Nitrous
oxide
has
some
analgesic
efficacy
and
is
safe
during
labour
(U)
(Level
I).

2.
 Nitrous
oxide
is
an
effective
analgesic
agent
in
a
variety
of
other
acute
pain
situations
(U)

(Level
II).

3.
 Methoxyflurane,
in
low
concentrations,
may
be
an
effective
analgesia
in
the
hospital
and

prehospital
setting
(N)
(Level
IV).

 Neuropathy
and
bone
marrow
suppression
are
rare
but
potentially
serious
complications

of
nitrous
oxide
use,
particularly
in
at‐risk
patients
(U).













 Acute
pain
management:
scientific
evidence
 xxiii

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