Drug Guide
Esmolol Hydrochloride
Classification
Therapeutic: Beta-adrenergic blocker, antiarrhythmic
Pharmacological: Selective beta-1 adrenergic receptor antagonist
FDA Approved Indications
- Short-term treatment of supraventricular tachycardia (SVT)
- Atrial fibrillation/flutter with rapid ventricular response
- Ventricular tachycardia
Mechanism of Action
Esmolol selectively blocks beta-1 adrenergic receptors in the heart, resulting in decreased heart rate, myocardial contractility, and cardiac output, thereby exerting antiarrhythmic effects.
Dosage and Administration
Adult: Initial dose of `500 mcg/kg` IV over 1 minute, followed by continuous infusion of 50-150 mcg/kg/min, titrated based on response.
Pediatric: For pediatric use, doses are titrated based on weight and clinical response; consult specific protocols.
Geriatric: Start at lower doses; monitor closely due to increased sensitivity.
Renal Impairment: Adjustments not typically required, but monitoring is advised.
Hepatic Impairment: No specific adjustments recommended.
Pharmacokinetics
Absorption: Administered intravenously; bioavailability not applicable.
Distribution: Widely distributed; volume of distribution approximately 0.2-0.3 L/kg.
Metabolism: Rapidly metabolized in the plasma by esterases to inactive metabolites.
Excretion: Excreted primarily in urine.
Half Life: Approximately 9 minutes.
Contraindications
- Known hypersensitivity to esmolol or other beta-blockers.
- Severe obstructive airway disease (e.g., asthma).
- Second- or third-degree AV block without pacemaker.
Precautions
- Use with caution in patients with heart failure, severe hypertension, or cooking asthmatic conditions.
- Monitor blood pressure and heart rate closely.
Adverse Reactions - Common
- Hypotension (Common)
- Bradycardia (Common)
- Nausea (Uncommon)
- Dizziness (Uncommon)
Adverse Reactions - Serious
- Severe bradycardia or AV block requiring intervention (Rare)
- Anaphylactic reactions (Rare)
Drug-Drug Interactions
- Other antiarrhythmics, especially calcium channel blockers and other beta-blockers.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor heart rate, blood pressure, and ECG continuously during administration.
Diagnoses:
- Risk for decreased cardiac output
Implementation: Administer via infusion pump; titrate dose based on clinical response.
Evaluation: Assess for effectiveness in controlling arrhythmias and monitor for adverse effects.
Patient/Family Teaching
- Notify healthcare provider if you experience chest pain, dizziness, or slow heartbeat.
- Do not halt medication abruptly without medical advice.
Special Considerations
Black Box Warnings:
- Use with caution in patients with heart failure; may worsen symptoms.
- Avoid abrupt discontinuation to prevent exacerbation of angina or arrhythmias.
Genetic Factors: N/A
Lab Test Interference: N/A
Overdose Management
Signs/Symptoms: Severe bradycardia, hypotension, bronchospasm.
Treatment: Discontinue drug immediately; supportive care, atropine for bradycardia, vasopressors for hypotension, and advanced cardiac life support if needed.
Storage and Handling
Storage: Store at controlled room temperature, 20-25°C (68-77°F).
Stability: Stable when stored properly; check expiration date.