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remifentanyl (Ultiva)

Tradename: Ultiva. DEA-controlled substance: class 2 Indications: - analgesic component of monitored general anesthesia - treatment of acute pain Contraindications: (& cautions) 1) NOT for epidural/intrathecal administration due to glycine component 2) due to potency of drug, clear all IV lines which may contain drug prior to step-down care 3) concurrent use of MAO inhibitors is contraindicated 4) endotracheal intubation: inferior to neuromuscular blockers [2] Dosage: - general anesthesia: a) induction: 0.5-1 ug/kg IV over 30-60 seconds b) maintenance: 0.05-2.0 ug/kg/minute IV infusion Pharmacokinetics: 1) rapid onset of action 2) metabolized by blood & tissue esterase 3) 95% metabolized to an inactive metabolite that is cleared by the kidney 4) 1/2life is 3-10 minutes 5) recovery is 5-10 mintues Adverse effects: 1) rash 2) headache 3) shivering 4) bradycardia 5) hypotension 6) nausea/vomiting 7) respiratory depression (dose-related) 8) drowsiness 9) constipation 10) muscle rigidity (dose & rate-related) Drug interactions: 1) benzodiazepines, barbiturates, alcohol in combination increase adverse CNS effects 2) MAO inhibitors in combination is contraindicated: fatal reactions have occurred 3) naloxone is a direct opiate antagonist 4) scorpion venom in combination increases toxic effects of the venom Mechanism of action: 1) opiate agonist 2) phenylpiperidine derivative 3) 5-10 times as potent as fentanyl

General

opiate

Properties

MISC-INFO: elimination route PLASMA 1/2life 3-10 MINUTES

Database Correlations

PUBCHEM correlations

References

  1. Drug Information & Medication Formulary, Veterans Affairs, Central California Health Care System, 1st ed., Ravnan et al eds, 1998
  2. Grillot N, Lebuffe G, Huet O et al Effect of Remifentanil vs Neuromuscular Blockers During Rapid Sequence Intubation on Successful Intubation Without Major Complications Among Patients at Risk of Aspiration. A Randomized Clinical Trial. JAMA. 2023;329(1):28-38. PMID: 36594947 https://jamanetwork.com/journals/jama/fullarticle/2800025