Effects of verapamil and lidocaine in a canine model of sudden coronary death

The efficacy of verapamil and lidocaine for treating ischemia-induced arrhythmias was determined in a conscious canine model with a previous myocardial infarction remote from the ischemic area. Temporary (up to 5.5 minutes) occlusion of the circumflex coronary artery was made in eight conscious dogs...

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Veröffentlicht in:Journal of the American College of Cardiology 1985-09, Vol.6 (3), p.674-681
Hauptverfasser: Temesy-Armos, Peter N., Legenza, Mary, Southworth, Stephen R., Hoffman, Brian F.
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container_title Journal of the American College of Cardiology
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creator Temesy-Armos, Peter N.
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Southworth, Stephen R.
Hoffman, Brian F.
description The efficacy of verapamil and lidocaine for treating ischemia-induced arrhythmias was determined in a conscious canine model with a previous myocardial infarction remote from the ischemic area. Temporary (up to 5.5 minutes) occlusion of the circumflex coronary artery was made in eight conscious dogs that had sustained an anterior myocardial infarction 13 to 35 days previously. Each dog served as its own control. Ventricular arrhythmias were observed in 100% of control experiments but in only 25% of experiments after verapamil pretreatment at 0.4 mg/kg body weight. Repetitive ventricular complexes, defined as two or more consecutive ventricular complexes terminating spontaneously in sinus rhythm, were seen in 88% of control experiments and I3% of verapamil experiments, whereas ventricular fibrillation was seen in 6% of control experiments but in no verapamil experiment. Thus, verapamil abolished arrhythmias or reduced the grade of arrhythmias in all dogs. Six of the eight dogs were also tested with Lidocaine pretreatment at one or two doses resulting in mean plasma levels of 3.8 ± 2.0 µg/ml. Ventricular arrhythmias were seen in 92% of control experiments and 100% of lido-caine experiments. The incidence of ventricular fibrillation increased from 8% in control to 60% in Lidocaine experiments. It is concluded that verapamil may prevent severe ischemia-induced arrhythmias after a recent myocardial infarction, whereas Lidocaine may in some cases aggravate arrhythmias.
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Temporary (up to 5.5 minutes) occlusion of the circumflex coronary artery was made in eight conscious dogs that had sustained an anterior myocardial infarction 13 to 35 days previously. Each dog served as its own control. Ventricular arrhythmias were observed in 100% of control experiments but in only 25% of experiments after verapamil pretreatment at 0.4 mg/kg body weight. Repetitive ventricular complexes, defined as two or more consecutive ventricular complexes terminating spontaneously in sinus rhythm, were seen in 88% of control experiments and I3% of verapamil experiments, whereas ventricular fibrillation was seen in 6% of control experiments but in no verapamil experiment. Thus, verapamil abolished arrhythmias or reduced the grade of arrhythmias in all dogs. Six of the eight dogs were also tested with Lidocaine pretreatment at one or two doses resulting in mean plasma levels of 3.8 ± 2.0 µg/ml. Ventricular arrhythmias were seen in 92% of control experiments and 100% of lido-caine experiments. The incidence of ventricular fibrillation increased from 8% in control to 60% in Lidocaine experiments. 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Temporary (up to 5.5 minutes) occlusion of the circumflex coronary artery was made in eight conscious dogs that had sustained an anterior myocardial infarction 13 to 35 days previously. Each dog served as its own control. Ventricular arrhythmias were observed in 100% of control experiments but in only 25% of experiments after verapamil pretreatment at 0.4 mg/kg body weight. Repetitive ventricular complexes, defined as two or more consecutive ventricular complexes terminating spontaneously in sinus rhythm, were seen in 88% of control experiments and I3% of verapamil experiments, whereas ventricular fibrillation was seen in 6% of control experiments but in no verapamil experiment. Thus, verapamil abolished arrhythmias or reduced the grade of arrhythmias in all dogs. Six of the eight dogs were also tested with Lidocaine pretreatment at one or two doses resulting in mean plasma levels of 3.8 ± 2.0 µg/ml. 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Drug treatments</topic><topic>Premedication</topic><topic>Ventricular Fibrillation - etiology</topic><topic>Ventricular Fibrillation - prevention &amp; control</topic><topic>Verapamil - pharmacology</topic><topic>Verapamil - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Temesy-Armos, Peter N.</creatorcontrib><creatorcontrib>Legenza, Mary</creatorcontrib><creatorcontrib>Southworth, Stephen R.</creatorcontrib><creatorcontrib>Hoffman, Brian F.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American College of Cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Temesy-Armos, Peter N.</au><au>Legenza, Mary</au><au>Southworth, Stephen R.</au><au>Hoffman, Brian F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of verapamil and lidocaine in a canine model of sudden coronary death</atitle><jtitle>Journal of the American College of Cardiology</jtitle><addtitle>J Am Coll Cardiol</addtitle><date>1985-09</date><risdate>1985</risdate><volume>6</volume><issue>3</issue><spage>674</spage><epage>681</epage><pages>674-681</pages><issn>0735-1097</issn><eissn>1558-3597</eissn><coden>JACCDI</coden><abstract>The efficacy of verapamil and lidocaine for treating ischemia-induced arrhythmias was determined in a conscious canine model with a previous myocardial infarction remote from the ischemic area. 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subjects Animals
Antiarythmic agents
Arrhythmias, Cardiac - etiology
Arrhythmias, Cardiac - prevention & control
Biological and medical sciences
Cardiovascular system
Death, Sudden
Dogs
Female
Heart Conduction System - drug effects
Heart Rate - drug effects
Lidocaine - pharmacology
Lidocaine - therapeutic use
Male
Medical sciences
Myocardial Infarction - complications
Pharmacology. Drug treatments
Premedication
Ventricular Fibrillation - etiology
Ventricular Fibrillation - prevention & control
Verapamil - pharmacology
Verapamil - therapeutic use
title Effects of verapamil and lidocaine in a canine model of sudden coronary death
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