Succinylcholine pretreatment using gallamine or mivacurium during rapid sequence induction in children: a randomized,

M C Theroux1, J B Rose, S Iyengar

  • 1Department of Anesthesiology and Critical Care Medicine, Alfred I. duPont Hospital for Children, Wilmington, DE 19899, USA. mtheroux@nemours.org

Insights

Mivacurium pretreatment effectively reduces succinylcholine-induced increases in serum potassium, myoglobin, and creatine phosphokinase (CPK) in children. This study highlights mivacurium

Area of Science:

  • Anesthesiology
  • Pediatric Pharmacology
  • Clinical Chemistry

Background:

  • Succinylcholine is commonly used for rapid sequence induction (RSI) in pediatric anesthesia.
  • RSI can lead to undesirable side effects such as fasciculations, myalgias, and elevations in serum potassium, myoglobin, and creatine phosphokinase (CPK).
  • Pretreatment with neuromuscular blocking agents is sometimes employed to mitigate these effects.

Purpose of the Study:

  • To evaluate the efficacy of gallamine or mivacurium as pretreatment agents before succinylcholine administration in pediatric patients.
  • To assess the impact of these pretreatments on reducing fasciculations, postoperative myalgias, and serum levels of potassium, CPK, and myoglobin.

Main Methods:

  • A prospective, randomized, double-blinded study was conducted in 45 pediatric patients (ASA physical status I, aged 3-15 years) undergoing emergency surgery.
  • Patients received either normal saline, mivacurium (0.03 mg/kg), or gallamine (0.04 mg/kg) 2 minutes prior to RSI with thiopental, fentanyl, and succinylcholine.
  • Serum potassium, myoglobin, and CPK levels were measured at various time points. Fasciculations and myalgias were scored.

Main Results:

  • Mivacurium pretreatment significantly reduced the increase in serum potassium at 5 minutes, myoglobin at 5 and 15 minutes, and CPK at 24 hours compared to normal saline.
  • No significant differences were observed in fasciculation or myalgia scores between the groups.
  • Gallamine was not effective in reducing the measured biochemical markers, although a lower dose was used compared to mivacurium.

Conclusions:

  • Mivacurium, when administered intravenously 2 minutes before succinylcholine in children, is effective in attenuating the acute rise in serum potassium, myoglobin, and CPK.
  • This pretreatment strategy may help minimize the adverse biochemical effects associated with succinylcholine use in pediatric anesthesia.
  • Gallamine did not demonstrate similar efficacy in this study at the tested dose.
Abstract

Related Concept Videos

Depolarizing Blockers: Pharmocokinetics01:19

Depolarizing Blockers: Pharmocokinetics

Depolarizing blockers are administered through intravenous injection. Succinylcholine is the most common choice of depolarizing blockers in emergency clinical practices. Although they have a rapid onset, they readily diffuse away from the motor end plate into the extracellular fluid. They are metabolized by enzymes such as liver butyrylcholinesterase and plasma pseudocholinesterases. This produces a short duration of action, typically 5-10 minutes long, unlike nondepolarizing blockers, which...
Depolarizing Blockers: Mechanism of Action01:28

Depolarizing Blockers: Mechanism of Action

Depolarizing blockers act on skeletal muscle fibers' membranes and induce their depolarization. Most depolarizing blockers have two quaternary N+ atoms that bind the nicotinic acetylcholine receptors and cause neuromuscular blockade within minutes.
Succinylcholine is the most commonly used depolarizing blocker. Chemically, it constitutes two molecules of acetylcholine joined together by an acetate methyl group. They act on the receptors in the same way as acetylcholine. Because succinylcholine...
Skeletal Muscle Relaxants: Therapeutic Uses01:31

Skeletal Muscle Relaxants: Therapeutic Uses

Skeletal muscle relaxants are used to relax muscle tone and alleviate painful muscle contractions. However, the choice of skeletal muscle relaxants depends on the duration of the surgical procedure in order to minimize potential side effects. Skeletal muscle relaxants like neuromuscular blocking agents [NMBAs] are commonly employed as adjuvants alongside general anesthetics in clinical settings. NMBAs are also used to maintain controlled ventilation during surgery of the larynx or pharynx as...
Skeletal Muscle Relaxants: Adverse Effects01:21

Skeletal Muscle Relaxants: Adverse Effects

Skeletal muscle relaxants are widely used for muscle paralysis and relieving pain following any muscle injury or stiffness. However, depending on the drug type, they can have adverse effects that range from mild to severe. Usually, nondepolarizing neuromuscular blockers have minimal side effects. For example, drugs like d-tubocurarine, cisatracurium, and rocuronium cause hypotension, whereas drugs like baclofen, when stopped abruptly, can lead to the recurrence of spastic conditions.
Unlike...
Nondepolarizing (Competitive) Neuromuscular Blockers: Mechanism of Action01:17

Nondepolarizing (Competitive) Neuromuscular Blockers: Mechanism of Action

Nondepolarizing neuromuscular blockers induce paralysis by competitively blocking nicotinic acetylcholine receptors at the muscle end plate. Examples include pancuronium, mivacurium, vecuronium, and rocuronium. These quaternary ammonium derivatives are administered intravenously, are poorly absorbed, and are excreted via the kidneys.
Competitive antagonists prevent acetylcholine from binding to its receptor, inhibiting membrane depolarization. Without conformational changes or intrinsic...
Anticholinesterase Agents: Poisoning and Treatment01:26

Anticholinesterase Agents: Poisoning and Treatment

Anticholinesterases, also known as cholinesterase inhibitors, work by blocking the breakdown of acetylcholine, leading to its accumulation in the synaptic cleft. This accumulation indirectly enhances both muscarinic and nicotinic actions. These agents are classified as reversible or irreversible based on their mechanism of action.     
Irreversible agents form a strong bond with the cholinesterase enzyme, making it inactive. The breakdown of the phosphorylated enzyme is slower than the...