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Related Concept Videos

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: Pharmacological Actions01:27

Nondepolarizing (Competitive) Neuromuscular Blockers: Pharmacological Actions

Nondepolarizing neuromuscular blockers prevent the membrane depolarization of muscle cells and inhibit muscle contraction. These are usually administered with anesthetics to achieve complete muscle relaxation. Upon administration, these drugs first block the small, rapidly contracting muscles of the face and hands, followed by the larger muscles of the trunk and the intercostal muscles. The diaphragm is the last muscle to be affected.
Although all competitive neuromuscular blockers are designed...
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...
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...
Directly Acting Muscle Relaxants: Dantrolene and Botulinum Toxin01:26

Directly Acting Muscle Relaxants: Dantrolene and Botulinum Toxin

Directly acting muscle relaxants like dantrolene and botulinum toxin (BoNT) have distinct mechanisms and applications. Dantrolene, a hydantoin derivative, acts on the ryanodine receptor (RYR1) in skeletal muscle cells. RYR1 are calcium channels present at the sarcoplasmic reticulum membrane. In response to excitation, they release calcium ions from the sarcoplasmic reticulum to the cytosol. Calcium promotes actin-myosin-mediated contraction of muscles.
The binding of dantrolene to the RYR1...

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Updated: May 21, 2026

Magnetic Resonance-Guided High Intensity Focused Ultrasound Generated Hyperthermia: A Feasible Treatment Method in a Murine Rhabdomyosarcoma Model
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Delayed-onset malignant hyperthermia in association with rocuronium use.

Ashton E Beggs1, Jennifer Quinn McCann, Jan M Powers

  • 1St. Vincent Indianapolis Hospital, 2001 West 86th Street, Indianapolis, IN 46260, USA.

American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists
|June 23, 2012
PubMed
Summary

Rocuronium, a nondepolarizing neuromuscular blocker, may trigger malignant hyperthermia in susceptible patients. Discontinuation of rocuronium led to fever resolution in two reported cases, suggesting a potential link.

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Area of Science:

  • Anesthesiology
  • Pharmacology
  • Clinical Medicine

Background:

  • Malignant hyperthermia (MH) is a rare pharmacogenetic disorder often linked to anesthetic gases and depolarizing neuromuscular blockers.
  • Nondepolarizing neuromuscular blockers are generally considered safe for MH-susceptible patients, with limited reports suggesting a potential association.

Observation:

  • Two cases of delayed-onset malignant hyperthermia are presented in patients who received rocuronium, a nondepolarizing neuromuscular blocker.
  • One patient, a 27-year-old male, developed a fever 4 days after rocuronium infusion, reaching 105.2°F.
  • A 63-year-old male developed a fever of 107.1°F approximately 4 days after receiving rocuronium boluses and infusion.

Findings:

  • Rocuronium was suspected as the trigger for malignant hyperthermia in both patients, who had no prior history of the disorder.
  • Discontinuation of rocuronium therapy resulted in rapid fever reduction within 12-36 hours in both cases.
  • After evaluating other potential causes, rocuronium was identified as the most probable cause of the severe febrile response.

Implications:

  • These cases suggest a potential, albeit rare, association between rocuronium use and malignant hyperthermia.
  • Clinicians should consider malignant hyperthermia when unexplained fever occurs post-rocuronium administration, especially in critically ill patients.
  • Further investigation into the safety profile of nondepolarizing neuromuscular blockers in MH-susceptible individuals may be warranted.