Classes
DEA Class; Rx
Common Brand Names; Ultane
- General Anesthetics, Inhalation
Description
Halogenated general anesthetic; depth of anesthesia is easily adjusted; induction and recovery from anesthesia is rapid; cardiorespiratory depression is minimal; generally safe in patients with coronary artery disease; appropriate for pediatric patients
Indications
Indicated For use in general anesthesia induction during inpatient or outpatient surgery.
For general anesthesia maintenance during inpatient or outpatient surgery.
Contraindications
Known or suspected genetic susceptibility to malignant hyperthermia
Known or suspected sensitivity to sevoflurane or to other halogenated inhalational anesthetics
Adverse Effects
- Malignant hyperthermia
- Dose-dependent hypotension
- Bradycardia
- Tachycardia
- Hypotension
- Hypertension
- Nausea/vomiting
- Cough
- Agitation
- Increased salivation
- Airway obstruction
- Laryngospasm
- Apnea
- Increased BUN
- Increased ALT
- Respiratory irritation
- Nephrotoxicity
- Glycosuria
- Proteinuria
- Seizures (majority of cases in children and young adults, most had no medical history of seizures)
- Cardiac arrest
- Cases of mild, moderate and severe post-operative hepatic dysfunction or hepatitis with or without jaundice
- Malignant hyperthermia
- Allergic reactions (eg, rash, urticaria, pruritus, bronchospasm, anaphylactic or anaphylactoid reactions)
- Transient elevations in glucose, liver function tests, and WBC count
- Bradycardia in patients with Down syndrome
Warnings
Volatile liquid; use appropriate vaporizer for inhalation
Agitation/delirium may occur
Postoperative hepatitis reported
Closely monitor patients with anemia, hepatic impairment, myxedema, renal impairment
Can induce malignant hyperthermia in genetically susceptible individuals
Advise patients that performance of activities requiring mental alertness, such as driving or operating machinery, may be impaired after sevoflurane anesthesia
Reports of QT prolongation, associated with torsade de pointes (in exceptional cases, fatalities reported); exercise caution when administering to susceptible patients (eg, congenital long QT syndrome, coadministration with drugs that prolong QT interval)
Should not be used as a sole agent of induction in patients with ventricular dysfunction
Risk of perioperative hyperkalemia in pediatric patients reported (rare); some resulting in cardiac arrhythmia and death
Pregnancy and Lactation
There are no adequate and well-controlled studies in pregnant women; in animal reproduction studies, reduced fetal weights were noted following exposure to 1 MAC sevoflurane for three hours a day during organogenesis
The concentrations of sevoflurane in milk are probably of no clinical importance 24 hours after anesthesia; because of rapid washout, sevoflurane concentrations in milk are predicted to be below those found with many other volatile anesthetics
Maximum Dosage
Specific maximum dosage information is not available. Dosage must be individualized.
Specific maximum dosage information is not available. Dosage must be individualized.
Specific maximum dosage information is not available. Dosage must be individualized.
Specific maximum dosage information is not available. Dosage must be individualized.
How supplied
Sevoflurane
liquid
- 100%