Drug Guide
Ivabradine
Classification
Therapeutic: Antianginal agent, Heart failure drug
Pharmacological: Selective sinus node inhibitor
FDA Approved Indications
- Chronic stable angina pectoris in patients who have a contraindication to or intolerance of beta-blockers
- Heart failure with reduced ejection fraction (HFrEF) in patients who are stable on guideline-directed medical therapy
Mechanism of Action
Ivabradine selectively inhibits the funny current (I_f) in the sinoatrial node, leading to a reduction in heart rate without affecting myocardial contractility, blood pressure, or intracardiac conduction.
Dosage and Administration
Adult: Start with 5 mg twice daily; adjust dose based on response and tolerability, range 2.5-7.5 mg twice daily.
Pediatric: Not established.
Geriatric: Use with caution; start at lower dose and titrate as needed due to potential increased sensitivity.
Renal Impairment: Adjust dose in severe renal impairment; avoid in ESRD patients on dialysis.
Hepatic Impairment: Use with caution; dose adjustments recommended.
Pharmacokinetics
Absorption: Rapidly absorbed, with peak plasma concentrations in 1 hour.
Distribution: Bound approximately 70% to plasma proteins.
Metabolism: Primarily metabolized in the liver via CYP3A4 enzyme.
Excretion: Excreted mainly in feces (70%) and urine (30%).
Half Life: Approximately 6 hours.
Contraindications
- Hypersensitivity to ivabradine or any component of the formulation.
- On concomitant strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin).
Precautions
- Use with caution in patients with severe hepatic impairment, sinoatrial block, sick sinus syndrome without pacemaker, or hypotension.
Adverse Reactions - Common
- Bradycardia (Common)
- Atrial fibrillation (Common)
- luminous phenomena (phosphenes) (Common)
- Hypertension or hypotension (Uncommon)
Adverse Reactions - Serious
- Heart block, worsening heart failure, angina (Rare)
- Severe bradycardia requiring intervention (Rare)
Drug-Drug Interactions
- Strong CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): Increase ivabradine levels, risk of bradycardia.
- Strong CYP3A4 inducers (e.g., rifampin): Decrease ivabradine levels.
- Other drugs affecting heart rate or conduction.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor heart rate prior to and during therapy; baseline and periodic blood pressure evaluation.
Diagnoses:
- Risk for decreased cardiac output related to bradycardia.
- Risk for hypotension.
Implementation: Administer with food to improve absorption; avoid sudden discontinuation; educate patient about symptoms of bradycardia and hypotension.
Evaluation: Evaluate for reduction in angina symptoms and hospitalization frequency; monitor for adverse effects.
Patient/Family Teaching
- Take medication exactly as prescribed.
- Report symptoms of unusual dizziness, fatigue, or slow heartbeat.
- Avoid grapefruit and grapefruit juice, which may increase drug levels.
- Inform about luminous phenomena; usually transient.
Special Considerations
Black Box Warnings:
- Potential for severe bradycardia, atrial fibrillation, or heart block. Patients should be monitored closely.
- Use only with concomitant stable heart failure therapy and when benefits outweigh risks.
Genetic Factors: None specified.
Lab Test Interference: None.
Overdose Management
Signs/Symptoms: Severe bradycardia, atrial fibrillation, hypotension.
Treatment: Discontinue drug; provide supportive care; monitor cardiac rhythm; administer atropine or temporary pacemaker if necessary.
Storage and Handling
Storage: Store at room temperature, 20°C to 25°C (68°F to 77°F).
Stability: Stable for the duration of use.