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 |
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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. |
doi_str_mv | 10.1016/S0735-1097(85)80130-3 |
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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.</description><identifier>ISSN: 0735-1097</identifier><identifier>EISSN: 1558-3597</identifier><identifier>DOI: 10.1016/S0735-1097(85)80130-3</identifier><identifier>PMID: 4031280</identifier><identifier>CODEN: JACCDI</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>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</subject><ispartof>Journal of the American College of Cardiology, 1985-09, Vol.6 (3), p.674-681</ispartof><rights>1985 American College of Cardiology Foundation</rights><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-2d72acbad64e0e7691fd7c2c7460a5deb9ab6577bc21ed3e008a87af0ed01d5b3</citedby><cites>FETCH-LOGICAL-c469t-2d72acbad64e0e7691fd7c2c7460a5deb9ab6577bc21ed3e008a87af0ed01d5b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0735-1097(85)80130-3$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9267267$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/4031280$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Temesy-Armos, Peter N.</creatorcontrib><creatorcontrib>Legenza, Mary</creatorcontrib><creatorcontrib>Southworth, Stephen R.</creatorcontrib><creatorcontrib>Hoffman, Brian F.</creatorcontrib><title>Effects of verapamil and lidocaine in a canine model of sudden coronary death</title><title>Journal of the American College of Cardiology</title><addtitle>J Am Coll Cardiol</addtitle><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.</description><subject>Animals</subject><subject>Antiarythmic agents</subject><subject>Arrhythmias, Cardiac - etiology</subject><subject>Arrhythmias, Cardiac - prevention & control</subject><subject>Biological and medical sciences</subject><subject>Cardiovascular system</subject><subject>Death, Sudden</subject><subject>Dogs</subject><subject>Female</subject><subject>Heart Conduction System - drug effects</subject><subject>Heart Rate - drug effects</subject><subject>Lidocaine - pharmacology</subject><subject>Lidocaine - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Myocardial Infarction - complications</subject><subject>Pharmacology. Drug treatments</subject><subject>Premedication</subject><subject>Ventricular Fibrillation - etiology</subject><subject>Ventricular Fibrillation - prevention & control</subject><subject>Verapamil - pharmacology</subject><subject>Verapamil - therapeutic use</subject><issn>0735-1097</issn><issn>1558-3597</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtrHDEMgE1o2W42-QkBH0pJDtPIM-vHnEoJSVpIyCHJ2WhsDXWZsbf2biD_vrMP9hoQSKBPsvwxdiHguwChrp9BN7IS0OpLI68MiAaq5oTNhZSmamSrP7H5EfnCTkv5CwDKiHbGZktoRG1gzh5v-57cuvDU8zfKuMIxDByj50PwyWGIxEPkyB3GbT0mT8MWLhvvKXKXcoqY37knXP85Y597HAqdH_KCvd7dvtz8qh6e7n_f_Hyo3FK166r2ukbXoVdLAtKqFb3XrnZ6qQClp67FTkmtO1cL8g0BGDQaeyAPwsuuWbBv-72rnP5tqKztGIqjYcBIaVOsVrU2Zvrkgsk96HIqJVNvVzmM071WgN1qtDuNduvIGml3Gm0zzV0cHth0I_nj1MHb1P966GNxOPQZowvliLW10lNM2I89RpOMt0DZFhcoOvIhT9atT-GDQ_4DATqO0w</recordid><startdate>198509</startdate><enddate>198509</enddate><creator>Temesy-Armos, Peter N.</creator><creator>Legenza, Mary</creator><creator>Southworth, Stephen R.</creator><creator>Hoffman, Brian F.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>198509</creationdate><title>Effects of verapamil and lidocaine in a canine model of sudden coronary death</title><author>Temesy-Armos, Peter N. ; Legenza, Mary ; Southworth, Stephen R. ; Hoffman, Brian F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c469t-2d72acbad64e0e7691fd7c2c7460a5deb9ab6577bc21ed3e008a87af0ed01d5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Animals</topic><topic>Antiarythmic agents</topic><topic>Arrhythmias, Cardiac - etiology</topic><topic>Arrhythmias, Cardiac - prevention & control</topic><topic>Biological and medical sciences</topic><topic>Cardiovascular system</topic><topic>Death, Sudden</topic><topic>Dogs</topic><topic>Female</topic><topic>Heart Conduction System - drug effects</topic><topic>Heart Rate - drug effects</topic><topic>Lidocaine - pharmacology</topic><topic>Lidocaine - therapeutic use</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Myocardial Infarction - complications</topic><topic>Pharmacology. Drug treatments</topic><topic>Premedication</topic><topic>Ventricular Fibrillation - etiology</topic><topic>Ventricular Fibrillation - prevention & 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. 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.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>4031280</pmid><doi>10.1016/S0735-1097(85)80130-3</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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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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