Article Contents ::
- 1 Details About Generic Salt :: Ibutilid
- 2 Main Medicine Class:: Antiarrhythmic
- 3 (ih-BYOO-tih-lide FEW-muh-rate) Corvert Class: Antiarrhythmic
- 4 Drugs Class ::
- 5 Disclaimer ::
- 6 The Information available on this site is for only Informational Purpose , before any use of this information please consult your Doctor .Price of the drugs indicated above may not match to real price due to many possible reasons may , including local taxes etc.. These are only approximate indicative prices of the drug.
Details About Generic Salt :: Ibutilid
Main Medicine Class:: Antiarrhythmic
(ih-BYOO-tih-lide FEW-muh-rate)
Corvert
Class: Antiarrhythmic
Drugs Class ::
Action Prolongs atrial and ventricular action potential duration and refractoriness by activation of a slow inward current (predominantly sodium).
Indications for Drugs ::
Indications Rapid conversion of recent onset atrial fibrillation or atrial flutter to sinus rhythm.
Drug Dose ::
Route/Dosage
ADULTS: IV Initial infusion: ³ 60 kg (³ 132 lbs) 1 mg (1 vial) infused over 10 min; < 60 kg (< 132 lbs) 0.01 mg/kg (0.1 ml/kg) infused over 10 min. If the arrhythmia does not terminate within 10 min after the end of the initial infusion, a second 10 min infusion of equal strength may be administered 10 min after completion of the first infusion.
Contraindication ::
Contraindications Standard considerations.
Drug Precautions ::
Precautions
Pregnancy: Category C. Lactation: Undetermined. Children: Safety and efficacy not established. Elderly patients: No age-related differences in safety and efficacy have been observed. Proarrhythmia: Potentially fatal ventricular arrhythmias may be induced or worsened. Ibutilide must be administered in a setting on continuous ECG monitoring by personnel trained in identification and treatment of acute ventricular arrhythmias, particularly polymorphic ventricular tachycardia. Hypokalemia/Hypomagnesemia: Should be corrected to reduce potential for proarrhythmia. Anticoagulation: Patients with atrial fibrillation > 2 to 3 days must be adequately anticoagulated, generally for ³ 2 weeks before attempted conversion.
PATIENT CARE CONSIDERATIONS |
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Drug Side Effects ::
Adverse Reactions
CV: Nonsustained monomorphic ventricular extrasystoles and ventricular tachycardia (VT); sinus; supraventricular sustained and nonsustained polymorphic VT; hypotension; postural hypotension; hypertension; bundle branch block; sustained polymorphic VT; AV block; sinus bradycardia; QT segment prolongation; palpitations. CNS: Headache. GI: Nausea.
Drug Mode of Action ::
Action Prolongs atrial and ventricular action potential duration and refractoriness by activation of a slow inward current (predominantly sodium).
Drug Interactions ::
Interactions Concomitant Class Ia and III antiarrhythmic agents (eg, amiodarone, disopyramide, procainamide, quinidine, sotalol): Do not give concurrently. Withhold for 5 half-lives prior to and for 4 hr after ibutilide infusion. Medications that prolong the QT interval (eg, phenothiazines, tricyclic and tetracyclic antidepressants): Potential for proarrhythmia may be increased. Digoxin: Cardiotoxicity (supraventricular arrhythmia) due to excessive digoxin concentrations may be masked.
Drug Assesment ::
Assessment/Interventions
- Obtain patient history, including drug history and any known allergies. Note use of antiarrhythmics (eg, Class Ia or III) or other agents (eg, phenothiazines, tricyclic antidepressants) which may increase arrhythmia risk.
- Obtain baseline 12-lead ECG, electrolytes, and liver function tests prior to treatment.
- Ensure that potassium and magnesium serum levels are within normal levels.
- Ensure that any Class Ia or III antiarrhythmics have been discontinued for ³ 5 half-lives.
- Observe patient with continuous ECG monitoring for ³ 4 hours following infusion or until QTc has returned to baseline. Longer monitoring is required if any arrhythmic activity is noted or if patient has abnormal liver function tests.
- Monitor blood pressure and pulse closely during administration.
- Have appropriate resuscitation equipment at bedside (eg, cardioverter/defibrillator, medications) during therapy.
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Drug Storage/Management ::
Administration/Storage
- Available for IV administration only.
- Store unopened vials at room temperature (59° to 77° F).
- May be administered undiluted or further diluted in 50 ml of either Normal Saline (NS) or D5W.
- Diluted medication may be stored for up to 24 hr at room temperature (59° to 86° F), or for 48 hr refrigerated (36° to 46° F), following which any unused solution should be discarded.
Drug Notes ::
Patient/Family Education
- Advise patient that this is a short-term treatment for their arrhythmia and long-term oral medications will likely be required for control if this therapy is successful.
- Teach patient and family how to take blood pressure and pulse for home management with medications.
- Advise patient to report any chest pain, shortness of breath, palpitations, fluttering in the chest, headache, or faintness immediately to the nurse while the medication is infusing.