Suxamethonium chloride Totally Explained

Everything about Suxamethonium Chloride totally explained

Suxamethonium chloride (also known as succinylcholine, scoline, or colloquially as sux) is a medication widely used in emergency medicine and anesthesia to induce muscle relaxation, usually to make endotracheal intubation possible. Suxamethonium is sold under several trade names such as Anectine, and may be referred to as "sux" for short.
Suxamethonium acts as a depolarizing neuromuscular blocker. It imitates the action of acetylcholine at the neuromuscular junction, acting on muscle type nicotinic receptors, but it isn't degraded by acetylcholinesterase but by butyrylcholinesterase, a plasma cholinesterase. This hydrolysis by butyrylcholinesterase is much slower than that of acetylcholine by acetylcholinesterase.

Chemistry

Suxamethonium is a white crystalline substance, it's odourless; solutions have a pH of about 4, the dihydrate melts about 160 °C, the anhydrous melts at about 190 °C; it's highly soluble in water (1 gram in about 1 mL), soluble in alcohol (1 gram in about 350 mL), slightly soluble in chloroform, and practically insoluble in ether. Suxamethonium is a hygroscopic compound. The compound consists of two acetylcholine molecules that are linked by their acetyl groups.

Effects

There are two phases to the blocking effect of suxamethonium; Phase 1 block is the principal paralytic effect.

Phase 1 block

Binding of suxamethonium to the nicotinic acetylcholine receptor results in opening of the receptor's nicotinic sodium channel; sodium moves into the cell, a disorganised depolarisation of the motor end plate occurs and calcium is released from the sarcoplasmic reticulum. This results in fasciculation.
   In the normal muscle, following depolarisation, acetylcholine is rapidly hydrolysed by acetylcholinesterase and the muscle cell is able to 'reset' ready for the next signal.
   Suxamethonium has a longer duration of effect than acetylcholine and isn't hydrolysed by acetylcholinesterase. It doesn't allow the muscle cell to 'reset' and keeps the 'new' resting membrane potential below threshold. When acetylcholine binds to an already depolarised receptor it can't cause further depolarisation.
   Calcium is removed from the muscle cell cytosol independent of repolarisation (depolarisation signalling and muscle contraction are independent processes). As the calcium is taken up by the sarcoplasmic reticulum, the muscle relaxes. This explains muscle flaccidity rather than tetany following fasciculation.

Phase 2 block

Following infusion or repeated doses of suxamethonium, phase 2 block may occur. The receptor blockade takes on characteristics of a non-depolarising neuromuscular block (ie. fade in response to nerve stimulation, block can be antagonised by reversal agents and longer duration of blockade).

Medical uses

Its medical uses are limited to short-term muscle relaxation in anesthesia and intensive care, usually for facilitation of endotracheal intubation. Despite its adverse effects, including life threatening malignant hyperthermia, hyperkalaemia and anaphylaxis, it's perennially popular in emergency medicine because it arguably has the fastest onset and shortest duration of action of all muscle relaxants. The former is a major point of consideration in the context of trauma care, where endotracheal intubation may need to be completed very quickly. The latter means that, should attempts at endotracheal intubation fail and the patient can't be ventilated, there's a prospect for neuromuscular recovery and the onset of spontaneous breathing before hypoxaemia occurs.
The recent arrival of the cyclodextrin sugammadex may well render suxamethonium obsolete. Sugammadex can be used to 'instantly' reverse the effects of longer-acting muscle relaxants, particularly rocuronium. This means that rocuronium can be given in sufficiently high dose to work quickly, and then reliably reversed when necessary, all without the unwelcome side effects of suxamethonium.
Suxamethonium is quickly degraded by plasma butyrylcholinesterase and the duration of effect is usually in the range of a few minutes. When plasma levels of butyrylcholinesterase are greatly diminished or an atypical form is present (an otherwise harmless inherited disorder), paralysis may last much longer.

Side effects

Side effects include muscle pains, acute rhabdomyolysis with hyperkalemia, transient ocular hypertension, constipation and changes in cardiac rhythm including bradycardia, cardiac arrest, and ventricular dysrhythmias. In patients with neuromuscular disease or burns, a single injection of suxamethonium can lead to massive release of potassium from skeletal muscles with cardiac arrest.
Suxamethonium doesn't produce unconsciousness or anesthesia, and its effects may cause considerable psychological distress while simultaneously making it impossible for a patient to communicate. For these reasons, administration of the drug to a conscious patient is strongly contraindicated, except in necessary emergency situations.

Hyperkalemia

The side effect of hyperkalaemia is because the acetylcholine receptor is propped open, allowing continued flow of potassium ions into the extracellular fluid. A typical increase of potassium ion serum concentration on administration of suxamethonium is 0.5 mmol per litre, whereas the normal range of potassium is 3.5 to 5 mmol per litre. The increase is transient in normal patients. Hyperkalaemia doesn't generally result in adverse effects below a concentration of 6.5 to 7 mmol per litre.
Severe hyperkalemia will causes changes in cardiac electrophysiology, which, if severe, can result in asystole.

Death

This drug has occasionally been used as a paralyzing agent for executions by lethal injection, although pancuronium bromide is the preferred agent today because of its longer duration of effect and its absence of fasciculations as a side effect. It has also allegedly been used for murder. For instance, suxamethonium is the drug that's suspected to have been used to murder Nevada State Controller Kathy Augustine.

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