Pharm
Ibutilide
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Ibutilide
, Corvert
See Also
Antiarrhythmic
Indications
Atrial Fibrillation Chemical Cardioversion
Consider in combination with
Electrical Synchronized Cardioversion of Atrial Fibrillation
Contraindications
QTc Prolongation
(or QT >500 msec)
Severe
Left Ventricular Dysfunction
Combination with Class 1a or Class III
Antiarrhythmic
s
Mechanism
Class III
Antiarrhythmic
Precautions
Cardiac monitoring on starting Ibutilide
Monitor for a minimum of 4 hours after drug administration
Continue monitoring until
QTc Interval
normalizes
Correct
Electrolyte
abnormalities before starting Ibutilide (and continue to monitor
Electrolyte
levels)
Serum Potassium
Serum Magnesium
Dosing
Initial
Weight <60 kg: 0.01 mg/kg IV over 10 min
Weight >60 kg: 1 mg IV over 10 min
Subsequent
May repeat once after 10 min if not converted to sinus rhythm with first dose
Stop infusion on conversion to sinus rhythm
Adverse Effects
Significantly proarrhythmic
Ventricular Tachycardia
or fibrillation risk: 1-2%
Requires EKG monitoring for 4 hours after dose
Prolonged QT
c
Risk of
Torsades de Pointes
Observe in monitored setting
Efficacy
Atrial Fibrillation Cardioversion
Time to Cardioversion: 1 hour
Conversion Rate: 33-45% (60% in
Atrial Flutter
)
Safety
Unknown safety in
Lactation
Pregnancy Category C
Resources
Ibutilide Injection Solution (DailyMed)
https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2428969a-7431-4e94-9503-ad5c680e2ea4
Ibutilide (Stat Pearls)
https://www.ncbi.nlm.nih.gov/books/NBK526021/
References
Viktorsdottir (2006) Emerg Med J 23(2):133-4 +PMID: 16439743 [PubMed]
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