GenESA
GenESA - General Information
GenESA, administered through a closed-loop, computer-controlled drug-delivery system, is indicated to elicit acute cardiovascular responses, similar to those produced by exercise, in order to aid in diagnosing the presence or absence of coronary artery disease in patients who cannot exercise adequately .
Pharmacology of GenESA
Not Available
GenESA for patients
GenESA Interactions
Beta-adrenergic blocking agents: concurrent use may blunt the response to arbutamine. Beta-adrenergic blocking agents should be withdrawn at least 48 hours before conducting an arbutamine-mediated stress test. Antiarrhythmic agents, class I (such as flecainide, lidocaine, or quinidine): concurrent use with arbutamine may have a proarrhythmic effect. Antidepressants (tricyclic), atropine or other anticholinergic agents, or digitalis glycosides: concurrent use with arbutamine may produce additive inotropic and/or chronotropic effects.
GenESA Contraindications
Additional information about GenESA
GenESA Indication: Used to elicit acute cardiovascular responses, similar to those produced by exercise, in order to aid in diagnosing the presence or absence of coronary artery disease (CAD) in patients who cannot exercise adequately.
Mechanism Of Action: GenESA is a synthetic catecholamine with positive chronotropic and inotropic properties. The chronotropic (increase in heart rate) and inotropic (increase in force of contraction) effects of arbutamine serve to mimic exercise by increasing cardiac work (producing stress) and provoke myocardial ischemia in patients with compromised coronary arteries. The increase in heart rate caused by arbutamine is thought to limit regional subendocardial perfusion, thereby limiting tissue oxygenation. In functional assays, arbutamine is more selective for beta-adrenergic receptors than for alpha-adrenergic receptors. The beta-agonist activity of arbutamine provides cardiac stress by increasing heart rate, cardiac contractility, and systolic blood pressure. The degree of hypotension that occurs for a given chronotropic activity is less with arbutamine than, for example, with isoproterenol because alpha receptor activity is retained.
Drug Interactions: Not Available
Food Interactions: Not Available
Generic Name: Arbutamine
Synonyms: Not Available
Drug Category: Cardiotonic Agents; Adrenergic beta-Agonists
Drug Type: Small Molecule; Approved
Other Brand Names containing Arbutamine: GenESA;
Absorption: Not Available
Toxicity (Overdose): Not Available
Protein Binding: 58%
Biotransformation: Primarily metabolized to methoxyarbutamine. Another possible metabolite is ketoarbutamine. The metabolites of arbutamine appear to have less pharmacological activity and a longer half-life and than the parental drug.
Half Life: Elimination half-life is approximately 8 minutes.
Dosage Forms of GenESA: Not Available
Chemical IUPAC Name: 4-[(1R)-1-hydroxy-2-[4-(4-hydroxyphenyl)butylamino]ethyl]benzene-1,2-diol
Chemical Formula: C18H23NO4
Arbutamine on Wikipedia: Not Available
Organisms Affected: Humans and other mammals