Drug Guide
Carteolol Hydrochloride
Classification
Therapeutic: Antihypertensive, Glaucoma agent
Pharmacological: Beta-adrenergic blocker
FDA Approved Indications
- Primary open-angle glaucoma
- Ocular hypertension
Mechanism of Action
Carteolol is a non-selective beta-adrenergic blocker that reduces intraocular pressure by decreasing aqueous humor production and possibly increasing outflow.
Dosage and Administration
Adult: Typically one drop in the affected eye once or twice daily.
Pediatric: Use not established; consult ophthalmologist.
Geriatric: Adjust as needed; greater sensitivity may increase risk of systemic side effects.
Renal Impairment: Use with caution; monitor closely, as drug clearance may be affected.
Hepatic Impairment: Use with caution; pharmacokinetics may be altered.
Pharmacokinetics
Absorption: Well absorbed following topical administration.
Distribution: Widely distributed; minimal CNS penetration.
Metabolism: Partially metabolized in the liver.
Excretion: Excreted primarily in urine.
Half Life: Approximately 3-4 hours.
Contraindications
- Bronchial asthma, bronchospastic lung disease
- Sinus bradycardia, greater than first-degree heart block, cardiogenic shock
Precautions
- Use with caution in patients with diabetes mellitus, thyrotoxicosis, or a history of severe allergies; may mask signs of hypoglycemia; systemic absorption can cause cardiovascular and respiratory effects.
Adverse Reactions - Common
- Local eye irritation (Common)
- Blepharitis (Less common)
Adverse Reactions - Serious
- Systemic beta-blocker effects such as bradycardia, hypotension, bronchospasm (Less common, especially with improper use or overuse)
Drug-Drug Interactions
- Other beta-blockers, calcium channel blockers, clonidine
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor intraocular pressure, vision, and systemic cardiovascular status.
Diagnoses:
- Risk for systemic effects related to topical eye medication
Implementation: Administer as prescribed; instruct patient not to touch dropper to eye; wash hands before and after application.
Evaluation: Assess reduction in intraocular pressure and monitor for adverse systemic effects.
Patient/Family Teaching
- Use exactly as prescribed; do not touch dropper to eye or other surfaces.
- Report signs of systemic beta-blocker effects like unusual fatigue, dizziness, or slow heartbeat.
- Do not discontinue abruptly.
Special Considerations
Black Box Warnings:
- Systemic absorption can cause systemic beta-blockade effects especially in predisposed individuals.
- Potential to mask hypoglycemia symptoms in diabetics.
Genetic Factors: Not specifically documented.
Lab Test Interference: May interfere with blood glucose and thyroid function tests.
Overdose Management
Signs/Symptoms: Bradycardia, hypotension, bronchospasm, hypoglycemia.
Treatment: Supportive care; atropine for bradycardia; oxygen and vasopressors for hypotension; assist with ventilation if needed.
Storage and Handling
Storage: Store at room temperature, away from light and moisture.
Stability: Stable until expiration date on packaging.