Drug Guide
Ipratropium Bromide
Classification
Therapeutic: Respiratory agent, Bronchodilator
Pharmacological: Anticholinergic (Muscarinic receptor antagonist)
FDA Approved Indications
- Chronic obstructive pulmonary disease (COPD)
- emphysema
- chronic bronchitis
Mechanism of Action
Ipratropium Bromide blocks the action of acetylcholine on muscarinic receptors in the airway smooth muscle, leading to bronchial dilation.
Dosage and Administration
Adult: Inhalation of 0.2 mg via metered-dose inhaler (MDI) 3-4 times daily. For nebulization, 0.5 mg 3-4 times daily.
Pediatric: Children 6 years or older: 0.25-0.5 mg via nebulizer 3-4 times daily. Adjust based on response.
Geriatric: Use with caution, as with all respiratory medications, and monitor for adverse effects.
Renal Impairment: Use with caution; no specific dosage adjustment has been established.
Hepatic Impairment: No specific guidance available.
Pharmacokinetics
Absorption: Minimal systemic absorption from inhalation routes.
Distribution: Widely distributed in tissues after inhalation.
Metabolism: Metabolized in the liver via ester hydrolysis.
Excretion: Excreted mainly in urine and feces.
Half Life: Approximate terminal half-life: 1.6 hours.
Contraindications
- Hypersensitivity to ipratropium or other atropine derivatives.
- Use with caution in patients with urinary retention, BPH, glaucoma.
- Avoid in patients with soy or peanut allergy (due to excipients).
Precautions
- Use cautiously in patients with cardiovascular disease, urinary retention, glaucoma. Monitor for anticholinergic side effects.
Adverse Reactions - Common
- Dry mouth (Common)
- Pharyngeal irritation (Common)
- Cough (Common)
Adverse Reactions - Serious
- Paradoxical bronchospasm (Rare)
- Allergic reactions (rash, urticaria, anaphylaxis) (Rare)
Drug-Drug Interactions
- Additional anticholinergic agents (increased anticholinergic effects)
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor respiratory status and lung sounds, baseline pulmonary function tests.
Diagnoses:
- Impaired gas exchange
- Ineffective airway clearance
Implementation: Administer via inhaler or nebulizer as prescribed. Educate patient on proper inhaler technique.
Evaluation: Assess for improvement in symptoms, lung function, and adverse effects.
Patient/Family Teaching
- Use inhaler/spacer correctly to ensure proper dosing.
- Report any signs of allergic reactions, paradoxical bronchospasm.
- Maintain regular follow-up appointments.
Special Considerations
Black Box Warnings: N/A
Genetic Factors: None specific.
Lab Test Interference: None.
Overdose Management
Signs/Symptoms: Dry mouth, blurred vision, urinary retention, tachycardia, worsening bronchospasm.
Treatment: Discontinue drug, provide symptomatic treatment, and supportive care. In case of overdose, activated charcoal may be considered if ingestion was recent.
Storage and Handling
Storage: Store at room temperature, away from light and moisture.
Stability: Stable until expiration date on package.