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   <subfield code="a">Lidocaine has a narrow antiarrhythmic dose range against ventricular arrhythmias induced by programmed electrical stimulation in conscious postinfarction dogs</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Kurt Krejcy, Gunther Krumpl, Hannes Todt, Gerhard Raberger]</subfield>
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   <subfield code="a">Summary: The aim of the present study was to investigate the dose-dependent antiarrhythmic efficacy of lidocaine against electrically induced tachycardias in conscious, chronically instrumented postinfarction dogs. Programmed electrical stimulation (PES) was performed in 16 dogs 8 to 21 days after a 4 h occlusion of the left anterior descending coronary artery (LAD). Infusion of saline in 8 control animals with sustained ventricular tachycardia (SVT) inducible at baseline did not affect subsequent inducibility. In the treatment group 7 of 8 animals responded with SVT and one exhibited ventricular fibrillation at baseline. After an initial bolus of 1 mg/kg lidocaine intravenously (i.v.), the drug was infused at infusion rates of 40, 80 and 120 μg/kg/min (i.v.). During 80 μg/kg/min lidocaine (mean plasma level 3.5 μg/ml) 7 out of 8 animals displayed an antiarrhythmic response; both the lower and the higher infusion rate were associated with a smaller antiarrhythmic efficacy (3 of 8 animals responded to 40 μg/kg/min and 4 of 8 to 120 μg/kg/min). Licocaine did not affect ventricular refractory periods, but induced an increase in intraventricular conduction time at all infusion rates, from 66.2 ms at baseline to 67.7 ms (p&lt;0.05), 67.7 ms (p&lt;0.05), 70.0 ms (p&lt;0.01) respectively. In conclusion the present study demonstrates that lidocaine is of considerable value in the management of PES-induced ventricular arrhythmias in the postinfarction phase. However there is only a small optimal therapeutic plasma level range, where lidocaine exhibits its antiarrhythmic efficacy against this type of arrhythmia; this makes a carefully titration of the drug necessary both in the experimental and in the clinical setting.</subfield>
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   <subfield code="a">Springer-Verlag, 1992</subfield>
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   <subfield code="a">Lidocaine</subfield>
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   <subfield code="a">Programmed electrical stimulation</subfield>
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   <subfield code="a">Postinfarction phase</subfield>
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   <subfield code="a">Conscious dogs</subfield>
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   <subfield code="a">Krejcy</subfield>
   <subfield code="D">Kurt</subfield>
   <subfield code="u">Department of Cardiovascular Pharmacology, Institute of Pharmacology, University of Vienna, Wahringerstrasse 13A, A-1090, Vienna, Austria</subfield>
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   <subfield code="a">Krumpl</subfield>
   <subfield code="D">Gunther</subfield>
   <subfield code="u">Department of Cardiovascular Pharmacology, Institute of Pharmacology, University of Vienna, Wahringerstrasse 13A, A-1090, Vienna, Austria</subfield>
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   <subfield code="a">Todt</subfield>
   <subfield code="D">Hannes</subfield>
   <subfield code="u">Department of Cardiovascular Pharmacology, Institute of Pharmacology, University of Vienna, Wahringerstrasse 13A, A-1090, Vienna, Austria</subfield>
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   <subfield code="a">Raberger</subfield>
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   <subfield code="u">Department of Cardiovascular Pharmacology, Institute of Pharmacology, University of Vienna, Wahringerstrasse 13A, A-1090, Vienna, Austria</subfield>
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   <subfield code="t">Naunyn-Schmiedeberg's Archives of Pharmacology</subfield>
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   <subfield code="g">346/2(1992-08-01), 213-218</subfield>
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