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Understanding Anesthesiology - The Global Regional Anesthesia ...

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Contraindications<br />

Opioids must not be given to those with a known allergy.<br />

Intravenous opioids must not be given in settings<br />

where one is not able to support ventilation.<br />

Caution should be used when administering opioids to<br />

patients with hypovolemic or cardiogenic shock, where<br />

the blunting of sympathetic tone may exacerbate hypotension.<br />

Non-Depolarizing Muscle Relaxants<br />

<strong>The</strong> decision to use non-depolarizing muscle relaxants<br />

during maintenance of anesthesia depends on both the<br />

type of surgical procedure and the type of anesthetic.<br />

Some procedures require muscle relaxation to facilitate<br />

exposure (e.g. intra-abdominal surgery). In other cases,<br />

muscle relaxation is required because patient movement<br />

would be detrimental (e.g. neurosurgery, ophthalmic<br />

surgery). In a balanced technique, the use of muscle<br />

relaxants decreases the requirements of the other<br />

agents and facilitates mechanical ventilation.<br />

Historically, the choice of succinylcholine versus a nondepolarizing<br />

muscle relaxant (NDMR) for use during<br />

induction of anesthesia was a decision which balanced<br />

the need for rapid airway control against the side effects<br />

of succinylcholine. With the introduction of the<br />

rapidly acting non-depolarizing agent, rocuronium, the<br />

use of succinylcholine has steadily declined. In the rare<br />

circumstance where succinylcholine is used to facilitate<br />

intubation, a NDMR is given after the effects of succinylcholine<br />

have worn off. However, in the vast majority<br />

of cases NDMR is given at induction to provide relaxation<br />

for both intubation and surgery.<br />

Mechanism of action<br />

In order to appreciate how NDMR cause muscular paralysis,<br />

one must have a basic understanding of how<br />

neuromuscular transmission occurs (Figure 20). Normally<br />

a nerve impulse travels the length of the nerve to<br />

arrive at the motor nerve terminal where it causes release<br />

of acetylcholine (Ach) into the synaptic cleft. <strong>The</strong><br />

Ach then binds to post-synaptic nicotinic Ach receptors<br />

causing a conformational change in those receptors.<br />

This conformational change leads to a change in membrane<br />

permeability of sodium and potassium causing<br />

depolarization of the post-junctional membrane. <strong>The</strong><br />

propagation of this action potential leads directly to<br />

muscular contraction. NDMR interfere with this process<br />

by binding to the post-synaptic Ach receptors<br />

thereby acting as a competitive inhibitor to Ach.<br />

Dose, onset, duration, elimination and effects<br />

<strong>The</strong> choice of which muscle relaxant to use is influenced<br />

by the speed of onset, duration of action, method<br />

of elimination and side effect profile of the various<br />

agents. Except in the case of very brief procedures,<br />

NDMR are used for relaxation during maintenance of<br />

anesthesia. Commonly-used NDMR are rocuronium<br />

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