Drug Guide
Metipranolol Hydrochloride
Classification
Therapeutic: Antihypertensive, Anti-anginal
Pharmacological: Beta-adrenergic blocker (beta-blocker)
FDA Approved Indications
- Chronic stable angina pectoris
- Hypertension (off-label or under additional approval)
Mechanism of Action
Metipranolol is a non-selective beta-adrenergic blocker that reduces myocardial oxygen demand by decreasing heart rate, myocardial contractility, and cardiac output, resulting in its anti-anginal and antihypertensive effects.
Dosage and Administration
Adult: Typically, 20 mg twice daily, titrated up to 40 mg twice daily as needed. Doses should be individualized based on patient response.
Pediatric: Not generally recommended for pediatric patients due to lack of sufficient data.
Geriatric: Start at lower doses due to increased sensitivity and potential comorbidities; monitor closely.
Renal Impairment: Use with caution; dose adjustments may be necessary.
Hepatic Impairment: Use with caution; no specific dosage adjustments established.
Pharmacokinetics
Absorption: Well absorbed orally.
Distribution: Widely distributed in body tissues.
Metabolism: Extensively metabolized in the liver.
Excretion: Primarily excreted in the urine.
Half Life: Approximately 6-10 hours.
Contraindications
- Severe bradycardia
- Heart block greater than first degree (without pacemaker)
- Cardiogenic shock
- Uncompensated heart failure
Precautions
- Use with caution in patients with asthma or other obstructive airway diseases, diabetes mellitus, and peripheral vascular disease.
Adverse Reactions - Common
- Fatigue (Common)
- Dizziness (Common)
- Bradycardia (Less common)
Adverse Reactions - Serious
- Severe hypotension (Rare)
- Bronchospasm (in asthmatics) (Rare)
- Heart block (Rare)
Drug-Drug Interactions
- Other antihypertensives, calcium channel blockers, antiarrhythmics, cocaine, and clonidine — may enhance hypotensive effects.
- May increase serum levels of concomitant drugs metabolized by hepatic enzymes.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor blood pressure, heart rate, and respiratory status regularly. Assess for signs of worsening heart failure and bronchospasm.
Diagnoses:
- Risk for falls due to hypotension or dizziness.
- Ineffective tissue perfusion related to bradycardia or hypotension.
Implementation: Administer with food if GI upset occurs, monitor for adverse effects, and educate patient about signs of hypotension and bradycardia.
Evaluation: Assess effectiveness by reduction in anginal attacks and blood pressure control.
Patient/Family Teaching
- Take medication exactly as prescribed.
- Do not suddenly stop medication to avoid rebound hypertension or angina.
- Notify provider if symptoms worsen or if experiencing side effects like dizziness or slow heart rate.
- Caution in activities requiring alertness until response to medication is known.
Special Considerations
Black Box Warnings:
- None currently.
Genetic Factors: None established.
Lab Test Interference: May alter glucose and triglyceride levels.
Overdose Management
Signs/Symptoms: Severe bradycardia, hypotension, bronchospasm, loss of consciousness.
Treatment: Supportive measures including atropine for bradycardia, vasopressors for hypotension, and advanced cardiac life support as needed.
Storage and Handling
Storage: Store at room temperature away from light and moisture.
Stability: Stable under recommended storage conditions.