Drug Guide
Succinylcholine Chloride
Classification
Therapeutic: Neuromuscular blocker
Pharmacological: Depolarizing neuromuscular blocker
FDA Approved Indications
- Facilitation of endotracheal intubation during anesthesia
- Adjunct to general anesthesia to relax skeletal muscles during surgery, mechanical ventilation, and endoscopy
Mechanism of Action
Succinylcholine acts as an agonist at the nicotinic acetylcholine receptors at the neuromuscular junction, causing persistent depolarization of the motor endplate and reduced muscle contraction, leading to paralysis.
Dosage and Administration
Adult: 0.6 to 1.1 mg/kg IV for intubation; repeat doses as needed, based on clinical response
Pediatric: 1 to 1.5 mg/kg IV for intubation; doses may vary depending on age and weight
Geriatric: Dose adjustments are generally not necessary but should be based on clinical condition and response
Renal Impairment: Monitor closely; dose adjustments may be necessary due to altered drug clearance
Hepatic Impairment: Use with caution; no specific adjustments but monitor for prolonged paralysis
Pharmacokinetics
Absorption: Not applicable (administered IV)
Distribution: Distributed rapidly to neuromuscular junctions and tissues
Metabolism: Minimal hepatic metabolism; primarily hydrolyzed by plasma pseudocholinesterase
Excretion: Primarily excreted unchanged in urine via plasma pseudocholinesterase activity
Half Life: Approx. 1 to 10 minutes
Contraindications
- History of malignant hyperthermia
- Known hypersensitivity to succinylcholine or other neuromuscular blockers
- Prior history of hyperkalemia or risk factors for hyperkalemia
Precautions
- Risk of hyperkalemia, especially in burns, crush injuries, severe infections, or neuromuscular diseases; or in children with undiagnosed muscular dystrophy
- Can cause increased intraocular pressure, increased intracranial pressure, or severe bradycardia
Adverse Reactions - Common
- Muscle fasciculations (Common)
- Malignant hyperthermia (Rare but serious)
- Hyperkalemia (Potential in certain populations)
- Prolonged paralysis (Rare)
- Myalgia after recovery (Common)
Adverse Reactions - Serious
- Anaphylaxis (Rare)
- Cardiac arrhythmias (Rare)
- Increased intraocular or intracranial pressure (Rare)
Drug-Drug Interactions
- Inhalational anesthetics (risk of malignant hyperthermia)
- Agents that increase plasma pseudocholinesterase activity (can decrease effectiveness)
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Assess airway and breathing; monitor for signs of hyperkalemia, malignant hyperthermia, or bradycardia
Diagnoses:
- Impaired gas exchange
- Risk for hyperkalemia
- Altered LOC due to anesthesia
Implementation: Administer IV as ordered; premedicate as needed; have resuscitative equipment available
Evaluation: Observe for adequate paralysis; monitor vital signs and oxygenation; monitor for adverse reactions
Patient/Family Teaching
- Inform about the temporary paralysis and that it will resolve after the drug wears off
- Advise on the importance of informing healthcare providers about succinylcholine use in case of anesthesia or surgery
- Report any muscle pain, difficulty breathing, or unusual signs immediately
Special Considerations
Black Box Warnings:
- Potential for hyperkalemia leading to cardiac arrest, especially in children and certain neurological conditions
Genetic Factors: Pseudocholinesterase deficiency can prolong paralysis
Lab Test Interference: May interfere with cholinesterase activity assays
Overdose Management
Signs/Symptoms: Prolonged paralysis, hyperkalemia, arrhythmias, malignant hyperthermia
Treatment: Supportive care; administer anti-hyperkalemic agents if needed; treat hyperthermia aggressively; use dantrolene for malignant hyperthermia; long-term paralysis may require mechanical ventilation
Storage and Handling
Storage: Store at room temperature away from light and moisture
Stability: Stable until expiration date when stored properly