When tracheal intubation is
required for a short procedure, can one avoid the myalgias associated with
succinylcholine?
Until the development of mivacurium, a
short-acting nondepolarizing agent, patients who required tracheal intubation
for surgical procedures less than 20 minutes in duration could be managed only
by the administration of a bolus dose of succinylcholine to facilitate
intubation followed by a continuous infusion for maintenance of neuromuscular
blockade. Alternatively, after administering succinylcholine for intubation
high concentrations of isoflurane could be administered to provide a
satisfactory degree of muscle relaxation. Isoflurane could also be used to
facilitate the action of small doses of a short-acting nondepolarizing muscle
relaxant. However, the use of high concentrations of a volatile anesthetic can
result in delayed awakening, an undesirable consequence in the setting of
ambulatory surgery.
Disadvantages of succinylcholine include
postoperative myalgias and the potential triggering of malignant hyperther-mia.
At times, myalgias, which occur 5 times more commonly after ambulatory surgery
than in the inpatient population, may far outlast the discomforts associated
with the surgical procedure itself. These muscle pains may vary in intensity
from mild to incapacitating in nature and often develop on the first
postoperative day.
Mivacurium, like succinylcholine, is degraded
by plasma cholinesterase. In the patient with atypical pseudo-cholinesterase,
the effective duration of action is markedly prolonged. However, it may still
be possible to antagonize the drug. Ordinarily, the majority of the mivacurium
is rapidly hydrolyzed to inactive metabolites. The recom-mended intubating dose
is 0.2–0.25 mg/kg in adults. When employing the 0.25 mg/kg dose, an initial
dose of 0.15 mg/ kg should be followed 30 seconds later by 0.10 mg/kg. In
children, a dose of 0.2–0.3 mg/kg is often used. Satisfactory intubating
conditions are usually achieved in approximately 1.5–2.5 minutes. The duration
of neuromus-cular blockade is 15–20 minutes in adults but only 9–11 minutes in
children. Unfortunately, mivacurium is not free of side-effects. The drug may
cause histamine release, which may cause cutaneous flushing and even bronchospasm
and hypotension in some patients. Hypotension has not been a problem when
dosage guidelines are not exceeded and the drug is administered slowly.
Antagonism can be easily accomplished by conventional dosages of edrophonium or
neostigmine administered in conjunction with the appro-priate anticholinergic
agent. Twenty minutes after a single bolus dose, it may be unnecessary to
antagonize the block when the train-of-four has returned to normal and fade is
not present to a tetanic stimulus.
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