>From: "mcglonerg" <[log in to unmask]>
>Reply-To: [log in to unmask]
>To: "Acad-ae-med" <[log in to unmask]>
>Subject: Use of anti-emetics for opiates
>Date: Mon, 17 Apr 2000 20:37:14 +0100
>
>There was an interesting study in Emergency Medicine (1999) 11,240-43 on
>"The role of prophylactic anti-emetic therapy in emergency department
>patients receiving intravenous morphine for musculoskeletal trauma".
>
>The conclusion was that the routine use of prophylactic anti-emetics was
>not indicated in trauma.
>
>Is anyone aware of any other research into this. How about the use of
>anti-emetics in M.I.'s prior to giving an opiate?
>
>Regards,
>
>Ray McGlone
>
>A&E Department
>Lancaster
>UK
A quick Medline search shows that there are trials comparing antiemetics for
postoperative nausea and vomiting after opiates, but I've not been able to
find anything comparing antiemetics with placebo in the setting of emergency
department-prescribed opiates.
Having personally experienced extrapyramidal side-effects in the form of
akathisia from both i.v. metoclopramide and i.m. prochlorperazine (given for
migraine) I'm loathe to inflict these symptoms on my patients. Most of us
are familiar with the uncommon extrapyramidal side-effect of dystonias such
as oculogyric crisis, which are more than obvious when they occur, but I
suspect we under-appreciate the frequency of this other side-effect, which
is characterised by extremely unpleasant restlessness and a feeling of 'not
knowing where to put yourself'. See below for an abstract from an
interesting study in a recent Annals of Emergency Medicine and for a fuller
definition of akathisia (lifted from the same article).
Having said all that, I still routinely give antiemetics with opiates to
trauma patients whose c.spines are immobilised, and to AMI patients who have
had oral aspirin, since vomiting could be be hazardous and interfere with
life-saving treatment in these two patient groups respectively.
Cliff Reid
SpR in EM
Abstract
Study objective: Prochlorperazine (PCZ), a commonly used antiemetic and
analgesic agent, is known to cause akathisia. The incidence of akathisia
after a single 10-mg dose of intravenous PCZ has not been prospectively
evaluated. We determined the incidence and severity of PCZ-induced akathisia
at 1 hour and the incidence of delayed akathisic symptoms at 48 hours.
Methods: This prospective controlled study evaluated a convenience sample of
140 adult patients at a 400-bed, academic, tertiary-care medical center with
an annual emergency department census of 95,000 patient visits. One hundred
patients who received intravenous PCZ for the treatment of severe headache
or vomiting constituted the PCZ group. Forty patients receiving nonakathisic
intravenous therapy (eg, saline solution or antibiotics) served as control
subjects. Patients were excluded if they had preexisting motor disorders
(eg, restless-leg syndrome or Parkinson’s disease) or if they recently had
received any medication with extrapyramidal, anticholinergic, sedative, or
antiakathisic properties. All patients underwent an akathisia assessment
before and 1 hour after receiving their respective intravenous medications.
An established scale was used to detect the presence of akathisia and grade
its severity as mild, moderate, or severe. The delayed development of
akathisic symptoms within 48 hours also was measured in the PCZ group.
Results: Akathisia developed in 44 (44%) of the patients receiving PCZ
within 1 hour (95% confidence interval, 34% to 54%). The akathisia was
graded as mild, moderate, and severe in 14, 22, and 8 subjects,
respectively. Delayed symptoms suggestive of akathisia developed in 3 other
patients within 48 hours. None of the 40 control subjects developed
akathisia.
Conclusion: Single-dose intravenous PCZ frequently induced akathisia within
1 hour of administration. Acute akathisia was not observed in patients
receiving intravenous saline solution or antibiotics. The delayed
development of akathisia symptoms 48 hours after a single dose of
intravenous PCZ was uncommon. [Drotts DL, Vinson DR: Prochlorperazine
induces akathisia in emergency patients. Ann Emerg Med October
1999;34:469-475.]
Akathisia, a peculiar state of mental and motor restlessness characterized
by an intense desire to move in order to gain respite from overwhelming
feelings of distress was first observed with the use of dopamine antagonists
in 1947.6 Akathisic patients report restlessness and inner tension or
discomfort, have an urge to constantly move their legs, and have difficulty
in maintaining a posture for several minutes, such as sitting still in a
chair or standing in one place. They display semipurposeful or purposeless
limb movements and tend to repeatedly shift their bodily position while
sitting and shift weight from foot to foot or pace while standing.7 In its
milder presentation, the disorder may resemble anxiety. Akathisia in
patients taking psychotropic or antiemetic agents may be quite
distressing,8-11 perhaps even leading to violent behavior12,13 and suicidal
ideation.14-17
Akathisia is not restricted to patients taking daily oral medication but
also occurs in those who receive a single dose of parenteral dopamine
antagonists. Agents commonly used in emergency medicine include
metoclopramide, promethazine, PCZ, haloperidol, and droperidol. The mental
and motor manifestations of akathisia are well described in a fascinating
report by an expert on drug-induced movement disorders who writes of his
experience while a medical student after receiving a single dose of
haloperidol for a research study. He explains that “the intensity of the
dysphoria was striking and the sense of a foreign influence forcing me to
move was dramatic.”18 Studies of the pharmacology of intravenous PCZ have
been short-circuited because volunteers have withdrawn themselves from
further participation because of the development of single-dose PCZ-induced
akathisia.19,20 On development of acute akathisia, patients undergoing
preoperative evaluation have suddenly refused to have surgery for which they
had previously consented. This disruption of medical care has been reported
with both single-dose intravenous droperidol21 and single-dose intravenous
metoclopramide.22 The effect of acute akathisia in emergency medicine has
not been elucidated.
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