MedPath

Isoprenaline

Generic Name
Isoprenaline
Brand Names
Isuprel
Drug Type
Small Molecule
Chemical Formula
C11H17NO3
CAS Number
7683-59-2
Unique Ingredient Identifier
L628TT009W
Background

Isoprenaline is a non-selective beta adrenergic receptor agonist indicated to treat heart block, Adams-Stokes attacks, bronchospasm in anesthesia, cadiac arrest, hypovolemic shocks, septic shock, hypoperfusion, congestive hear failure, and cardiogenic shock.

Isoprenaline research in the 1940s found that this isopropyl analog of epinephrine dilated the bronchi, as well as raising the heart rate and cardiac output, without vasoconstriction. The US patent from 1943 states that this compound had a wider therapeutic index and a stronger action than adrenaline.

Isoprenaline was granted FDA approval on 19 February 1948.

Indication

Isoprenaline is indicated to treat mild or transient episodes of heart block not requiring electric shock or pacemakers, serious episodes of heart block and Adams-Stokes attacks not caused by ventricular tachycardia or fibrillation, and bronchospasm during anesthesia. Isoprenaline is also indicated for cases of cardiac arrest until preferable treatments like electric shock and pacemakers are available. Isoprenaline is also indicated as an adjunct therapy to fluid and electrolyte replacement therapy in hypovolemic shock, septic shock, hypoperfusion, congestive heart failure, and cardiogenic shock.

Associated Conditions
Adams-Stokes attacks, Bradycardia, Bronchospasm, Cardiac Arrest, Cardiac electrical storm, Congestive Heart Failure (CHF), Hypoperfusion, Septic Shock, Serious Heart Block, Shock, Cardiogenic, Shock, Hypovolemic, Short QT syndrome, Syncope, Torsades de Pointes, Transient Heart Block, Ventricular Arrhythmia, Beta blocker overdose, Mild Heart Block
Associated Therapies
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Effect of heart rate control with ivabradine on hemodynamic in patients with sepsis

A prospective, multicenter, parallel-group, exploratory randomized controlled clinical study in 8 Chinese ICUs aims to evaluate the efficacy of enteral ivabradine in sepsis patients. Inclusion criteria include adult ICU patients with sepsis-3.0, sinus rhythm with heart rate ≥95 bpm, and stable hemodynamic state. Exclusion criteria cover prior ivabradine use, severe liver dysfunction, chronic renal failure, seizure disorder, and other conditions. The study involves randomization (1:1) and open-label intervention with standard treatment vs. standard treatment plus ivabradine, targeting heart rate control between 70-94 bpm. Recruitment began in June 2023 and will last 2 years.
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