Atropine for Bradycardia
Atropine given intravenously blocks vagal slowing of the sinoatrial and atrioventricular nodes, raising the heart rate in bradycardia from raised vagal tone, inferior myocardial infarction, drugs and some poisonings. It is cheap, available in all emergency stores, and is also the key drug in organophosphate poisoning.
It does not work well when the block is distal to the atrioventricular node (Mobitz type 2 or third degree block with a wide QRS), in a transplanted heart, or in most overdoses of beta blockers and calcium channel blockers.
Classification. Antimuscarinic; anticholinergic belladonna alkaloid.
Mechanism. Competitively blocks muscarinic M2 receptors in the heart, removing vagal tone, which speeds sinoatrial discharge and atrioventricular conduction.
Pharmacodynamics. IV onset within 1 to 2 minutes, peak at 2 to 4 minutes, duration 30 to 60 minutes. Doses under 500 micrograms in adults can cause paradoxical slowing from central vagal stimulation.
Pharmacokinetics. Half life 2 to 4 hours in adults (up to 10 hours in children under 2 and older adults). About 50% metabolised in the liver; 30 to 50% excreted unchanged in urine. Crosses the blood brain barrier and the placenta.













