Cafedrine

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Cafedrine[edit | edit source]

Chemical structure of Cafedrine

Cafedrine is a sympathomimetic drug that is used primarily in the management of hypotension during anesthesia. It is a combination of caffeine and norephedrine, which work together to increase blood pressure and improve cardiac output.

Pharmacology[edit | edit source]

Cafedrine acts by stimulating the central nervous system and increasing the release of norepinephrine from sympathetic nerve endings. This leads to an increase in heart rate and myocardial contractility, resulting in elevated blood pressure. The caffeine component also contributes to the vasoconstriction and bronchodilation effects.

Clinical Use[edit | edit source]

Cafedrine is administered intravenously in a clinical setting, often during surgical procedures where anesthesia can lead to hypotension. It is particularly useful in patients who require rapid stabilization of blood pressure. The drug is typically used in combination with other vasopressors and inotropes to achieve the desired hemodynamic effect.

Side Effects[edit | edit source]

Common side effects of cafedrine include tachycardia, palpitations, and nervousness. In some cases, patients may experience headache, dizziness, or nausea. Due to its stimulant properties, cafedrine should be used with caution in patients with cardiovascular disease or hypertension.

Mechanism of Action[edit | edit source]

Cafedrine's mechanism of action involves the activation of adrenergic receptors in the heart and blood vessels. The norephedrine component primarily acts on alpha-adrenergic receptors, causing vasoconstriction and increased peripheral resistance. The caffeine component enhances the release of catecholamines and inhibits phosphodiesterase, leading to increased intracellular cyclic AMP levels and enhanced cardiac contractility.

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