Concentration-dependent pharmacologic properties of sotalol
Autor: | Ted Wang, Katherine A. Thompson, Dan M. Roden, Robert H Bergstrand, Lyle A. Siddoway, Henry J. Duff, Raymond L. Woosley |
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Rok vydání: | 1986 |
Předmět: |
medicine.medical_specialty
Dose Dose-Response Relationship Drug business.industry Refractory period Sotalol Antagonist Torsades de pointes Arrhythmias Cardiac medicine.disease QT interval Blockade Placebos Kinetics Internal medicine Anesthesia Heart rate Cardiology Exercise Test Medicine Humans Cardiology and Cardiovascular Medicine business medicine.drug |
Zdroj: | The American journal of cardiology. 57(13) |
ISSN: | 0002-9149 |
Popis: | Sotalol is a nonselective β-receptor antagonist that prolongs action potential duration and refractoriness in vitro at higher concentrations than those associated with heart rate slowing. To determine if this additional action can be expressed in humans, 17 patients with chronic stable ventricular premature complexes were studied. Each patient was hospitalized and arrhythmia frequency was quantified during a 48-hour drug-free baseline and during every third day of therapy with increasing incremental sotalol dosages. The dosages were 160, 320, 640 and 960 mg/day, administered in 1 or 2 doses. An index of action potential duration, the rate-corrected QT (QTc), was measured using serial 12-lead electrocardiograms on the third day of each dosage at presumed steady state and the degree of β-receptor blockade was assessed by the reduction of the maximal exercise-induced heart rate. Of the 17 patients, 11 had an antiarrhythmic response (70 to 100% reduction in VPCs), at a wide range of plasma concentrations (340 to 3,440 ng/ml). the responders to sotalol included 8 patients in whom therapy with conventional β-receptor antagonists had failed. In the group as a whole, the concentration associated with significant QTc prolongation (2,550 ng/ml) was greater than that associated with 50% reduction of the maximal slowing in heart rate (804 ng/ml). Sotalol was generally well tolerated, but in 1 nonresponder torsades de pointes developed 3 hours after the first 640-mg dose at a plasma sotalol concentration well within the concentration range measured in other patients. Sotalol's repolarization-prolonging actions are seen at higher concentrations than those associated with heart rate slowing and may contribute to its clinical effects. |
Databáze: | OpenAIRE |
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