Drug Guide
Atropine
Classification
Therapeutic: Anticholinergic agent
Pharmacological: Muscarinic receptor antagonist
FDA Approved Indications
- Bradycardia (to increase heart rate)
- Organophosphate poisoning reversal
- Preoperative reduction of salivary and respiratory secretions
Mechanism of Action
Atropine blocks muscarinic acetylcholine receptors, inhibiting parasympathetic nerve impulses, thereby increasing heart rate and reducing secretions.
Dosage and Administration
Adult: 0.5 mg IV every 3-5 minutes as needed; maximum dose 3 mg.
Pediatric: 0.02 mg/kg IV; typically administered every 3-5 minutes as needed, not exceeding 0.5 mg per dose or 3 mg total.
Geriatric: Same as adult, but monitor closely for anticholinergic side effects; adjust dose as necessary.
Renal Impairment: Use with caution; no specific dose adjustment established.
Hepatic Impairment: Use with caution; no specific dose adjustment established.
Pharmacokinetics
Absorption: Well absorbed via IV, IM, SC, and topical routes.
Distribution: Widely distributed including CNS, crosses the blood-brain barrier.
Metabolism: Primarily hepatic.
Excretion: Renally excreted as unchanged drug and metabolites.
Half Life: About 2-4 hours.
Contraindications
- Obstructive disease of the gastrointestinal or urinary tracts
- Myasthenia gravis (except in cholinergic crisis)
- Tachyarrhythmias (except during bradycardia)
- Allergy to atropine or belladonna alkaloids
Precautions
- Use with caution in patients with glaucoma, cardiovascular disease, hypertension, or in the elderly. Caution in pregnancy and lactation; use only if clearly needed. Monitor for signs of anticholinergic toxicity.
Adverse Reactions - Common
- Dry mouth (Common)
- Blurred vision (Common)
- Photophobia (Common)
- Urinary retention (Uncommon)
- Constipation (Uncommon)
Adverse Reactions - Serious
- Tachycardia or arrhythmias (Uncommon)
- Anaphylactic reactions (Rare)
- Central nervous system disturbances (e.g., hallucinations, delirium) (Uncommon)
Drug-Drug Interactions
- Other anticholinergic drugs, antihistamines, tricyclic antidepressants, phenothiazines, quinidine
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor heart rate, blood pressure, signs of anticholinergic toxicity (dry mouth, blurred vision, urinary retention). Watch for changes in mental status.
Diagnoses:
- Risk for decreased cardiac output due to tachyarrhythmia
- Risk for urinary retention
- Risk for CNS disturbances
Implementation: Administer IV doses slowly; monitor patient response.
Evaluation: Assess effectiveness by restoring or maintaining adequate heart rate; monitor for adverse effects.
Patient/Family Teaching
- Report any signs of dry mouth, blurred vision, dizziness, or difficulty urinating.
- Use caution when operating machinery or driving.
- Follow instructions carefully regarding dosage and timing.
Special Considerations
Black Box Warnings:
- None.
Genetic Factors: Pharmacogenomic variations are not well characterized for atropine.
Lab Test Interference: May affect certain laboratory tests (e.g., urinary catecholamines) due to anticholinergic effects.
Overdose Management
Signs/Symptoms: Dry mouth, fever, blurred vision, hallucinations, seizures, coma, tachycardia, urinary retention, hot, dry skin.
Treatment: Supportive care; administer activated charcoal if ingestion was recent; physostigmine may be used under specialist guidance for severe toxicity.
Storage and Handling
Storage: Store at room temperature (20-25°C), protect from light.
Stability: Stable under recommended storage conditions.