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Pregnancy Category C
Drug class
Antiarrhythmic (predominately class III)
Therapeutic actions
Prolongs cardiac action potential, increases atrial and ventricular refractoriness; produces
mild slowing of sinus rate and AV conduction.
Indications
• Rapid conversion of atrial fibrillation or flutter of recent onset to sinus rhythm;
most effective in arrhythmias of < 90 days' duration
Available forms
Solution—0.1 mg/mL
Dosages
ADULTS
< 60 kg: 0.1 mL/kg (0.01 mg/kg) infused over 10 min; may be repeated after 10 min if
arrhythmia is not terminated.
> 60 kg (132 lb): 1 vial (1 mg) infused over 10 min; may be repeated after 10 min if
arrhythmia is not terminated.
PEDIATRIC PATIENTS
Not recommended.
Pharmacokinetics
Route Onset Peak
IV Immediate 10 min
IV facts
Preparation: May be diluted in 50 mL of diluent, 0.9% sodium chloride, or 5% dextrose
injection; one 10-mL vial added to 50 mL of diluent yields a concentration of
0.017 mg/mL; may also be infused undiluted; diluted solution is stable for 24 hr at room
temperature or for 48 hr refrigerated.
Infusion: Infuse slowly over 10 min.
Compatibilities: Compatible with 5% dextrose injection, 0.9% sodium chloride
injection.
Incompatibilities: Do not mix in solution with any other drugs.
Adverse effects
• CNS: Headache, light-headedness, dizziness, tingling in arms, numbness
• CV: Ventricular arrhythmias, hypotension, hypertension
• GI: Nausea
Interactions
Drug-drug
• Increased risk of serious to life-threatening arrhythmias with disopyramide,
quinidine, procainamide, amiodarone, sotalol; do not give together
• Increased risk of proarrhythmias with phenothiazines, TCAs, antihistamines
• Use cautiously with digoxin because ibutilide may mask digoxin cardiotoxicity
Nursing considerations
Assessment
• History: Hypersensitivity to ibutilide; second- or third-degree AV heart block,
time of onset of atrial arrhythmia; prolonged QTc intervals; pregnancy, lactation;
ventricular arrhythmias
• Physical: Orientation; BP, P, auscultation, ECG; R, adventitious sounds
Interventions
• Determine time of onset of arrhythmia and potential benefit before beginning
therapy. Conversion is more likely in patients with arrhythmias of short (< 90
days') duration.
• Ensure that patient is adequately anticoagulated, generally for at least 2 wk, if
atrial fibrillation lasts > 2–3 days.
• Monitor ECG continually during and for at least 4 hr after administration. Be alert
for possible arrhythmias, including PVCs, sinus tachycardia, sinus bradycardia,
varying degrees of block at time of conversion.
• Keep emergency equipment readily available during and for at least 4 hr after
administration.
• Provide appointments for continued follow-up, including ECG monitoring;
tendency to revert to atrial arrhythmia after conversion increases with length of
time patient was in abnormal rhythm.
Teaching points
• This drug can only be given by IV infusion. You will need ECG monitoring
during and for 4 hours after administration.
• Arrange for follow-up medical evaluation, including ECG, which is important to
monitor the effect of the drug on your heart.
• These side effects may occur: Rapid or irregular heartbeat (usually passes
shortly), headache.
• Report chest pain, difficulty breathing, numbness or tingling.
Adverse effects in Italic are most common; those in Bold are life-threatening.