Sufentanil Citrate
A to Z Drug Facts
Sufentanil Citrate |
(sue-FEN-tuh-nill SIH-trate) |
Sufenta, Sufentanil Citrate |
Class: Narcotic analgesic |
Action Relieves pain by stimulating opiate receptors in CNS; causes respiratory depression, peripheral vasodilation, inhibition of intestinal peristalsis, sphincter of Oddi spasm, stimulation of chemoreceptors that cause vomiting and increased bladder tone.
Indications Adjunct for surgical analgesia; induction of primary anesthesia for major surgical procedures requiring favorable myocardial or cerebral oxygen balance or when extended postoperative ventilation is anticipated; epidural analgesia with bupivacaine during labor and vaginal delivery.
Contraindications Upper airway obstruction; acute asthma; diarrhea caused by poisoning or toxins.
General Surgery (with Nitrous Oxide/Oxygen)
ADULTS: IV 1 to 2 mcg/kg initially; 10 to 25 mcg prn for maintenance.
Major Surgical Procedures (with Nitrous Oxide/Oxygen)
ADULTS: IV 2 to 8 mcg/kg initially; 10 to 50 mcg prn for maintenance.
Major Cardiovascular Surgery/Neurosurgery (with 100% Oxygen)
ADULTS: IV 8 to 30 mcg/kg initially; 25 to 50 mcg prn for maintenance. CHILDREN < 12 YR: IV 10 to 25 mcg/kg initially; 25 to 50 mcg prn for maintenance.
Labor and Delivery
ADULTS: Epidural 10 to 15 mcg sufentanil mixed with 10 ml bupivacaine 0.125% with or without epinephrine. Can give total of 3 doses ³ 1 hr intervals until delivery.
Barbiturate anesthetics: May cause increased CNS and respiratory depression. Beta blockers: The incidence and degree of bradycardia and hypotension during induction of sufentanil may be greater in patients on chronic beta blocker therapy. Calcium channel blockers: The incidence and degree of bradycardia and hypotension during induction of sufentanil may be greater in patients on chronic calcium channel blocker therapy. Nitrous oxide: Nitrous oxide may cause cardiovascular depression with high-dose sufentanil.
Lab Test Interferences Increased amylase and lipase for up to 24 hr after dose may occur.
CV: Hypotension; orthostatic hypotension; hypertension; bradycardia; tachycardia; arrhythmias. CNS: Sedation. DERM: Pruritus. GI: Nausea; vomiting. RESP: Bronchospasm; depression of cough reflex; respiratory depression; postoperative respiratory depression; chest wall rigidity. OTHER: Chills; intraoperative muscle movement; tolerance.
Pregnancy: Category C. Lactation: Undetermined. Children: Safety and efficacy have been demonstrated in limited number of children < 2 yr undergoing cardiovascular surgery. Elderly or debilitated patients: May require dosage reduction. Special risk patients: Use drug with caution in patients with decreased respiratory reserve, head injury or increased intracranial pressure or hypoxia. Drug dependence: Has abuse potential. Hypoventilation: Naloxone and intubation equipment must be available in case hypoventilation occurs. Obese patients: If patient is > 20% above ideal weight, dose must be adjusted based on ideal body weight. Renal or hepatic impairment: Duration of action may be prolonged; dosage reduction may be required. Skeletal muscle rigidity: May cause skeletal muscle rigidity, particularly of the truncal muscles. The incidence and severity of muscle rigidity is usually dose-related.
PATIENT CARE CONSIDERATIONS |
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Copyright © 2003 Facts and Comparisons
David S. Tatro
A to Z Drug Facts