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Effects of tocainide studied with programmed electrical stimulation of the heart in patients with reentrant tachyarrhythmias

Identifieur interne : 000F62 ( Main/Corpus ); précédent : 000F61; suivant : 000F63

Effects of tocainide studied with programmed electrical stimulation of the heart in patients with reentrant tachyarrhythmias

Auteurs : André Waleffe ; Patrick Bruninx ; Luc Mary-Rabine ; Henri E. Kulbertus

Source :

RBID : ISTEX:C1DB2349E090FFFAB63418E6D6E4DC12FB563F4C

Abstract

The electrophysiologic effects of tocainide were studied with programmed electrical stimulation of the heart in two patients with atrioventricular (A-V) nodal tachycardia, five patients with reentrant tachycardia involving an accessory pathway and two patients with paroxysmal ventricular tachycardia. The measurements were made before and after a 15 minute perfusion of tocainide at a dose of 0.75 mg/kg per min in the first seven patients and of 0.5 mg/kg per min in the last two. At the end of perfusion, the drug plasma level ranged from 2.0 to 10.2 μg/ml (mean 6). During the subsequent 60 minutes, the plasma level decreased extremely slowly, its mean value remaining constantly between 3 and 4 μg/ml. Tocainide failed to achieve statistically significant effects on the functional properties of the A-V node. However, an increase of A-H time (two patients), prolongation of nodal refractory period (one patient) and lengthening of the cycle length producing a second degree A-V block (four patients) were observed in isolated cases. The H-V interval increased by 20 msec in three of the eight cases in which its measurement was not hampered by the constant presence of a preexcitation wave. No systematic effect on the refractory periods of the atrial and ventricular muscle was noted. In six patients, tocainide was perfused during sustained episodes of tachycardia (A-V nodal tachycardia, two patients; circus movement tachycardia using an accessory pathway, three patients; and paroxysmal ventricular tachycardia, one patient). Sinus rhythm was restored in all six patients. The drug prevented reinitiation of tachycardia in four of the eight patients in whom it could easily be triggered during the control period; it lengthened the tachycardia cycle length in the remaining four. No side effects were noted. These results, obtained with low plasma levels of tocainide, allow one to consider this drug a promising antiarrhythmic agent.

Url:
DOI: 10.1016/S0002-9149(79)80018-1

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ISTEX:C1DB2349E090FFFAB63418E6D6E4DC12FB563F4C

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<div type="abstract" xml:lang="en">The electrophysiologic effects of tocainide were studied with programmed electrical stimulation of the heart in two patients with atrioventricular (A-V) nodal tachycardia, five patients with reentrant tachycardia involving an accessory pathway and two patients with paroxysmal ventricular tachycardia. The measurements were made before and after a 15 minute perfusion of tocainide at a dose of 0.75 mg/kg per min in the first seven patients and of 0.5 mg/kg per min in the last two. At the end of perfusion, the drug plasma level ranged from 2.0 to 10.2 μg/ml (mean 6). During the subsequent 60 minutes, the plasma level decreased extremely slowly, its mean value remaining constantly between 3 and 4 μg/ml. Tocainide failed to achieve statistically significant effects on the functional properties of the A-V node. However, an increase of A-H time (two patients), prolongation of nodal refractory period (one patient) and lengthening of the cycle length producing a second degree A-V block (four patients) were observed in isolated cases. The H-V interval increased by 20 msec in three of the eight cases in which its measurement was not hampered by the constant presence of a preexcitation wave. No systematic effect on the refractory periods of the atrial and ventricular muscle was noted. In six patients, tocainide was perfused during sustained episodes of tachycardia (A-V nodal tachycardia, two patients; circus movement tachycardia using an accessory pathway, three patients; and paroxysmal ventricular tachycardia, one patient). Sinus rhythm was restored in all six patients. The drug prevented reinitiation of tachycardia in four of the eight patients in whom it could easily be triggered during the control period; it lengthened the tachycardia cycle length in the remaining four. No side effects were noted. These results, obtained with low plasma levels of tocainide, allow one to consider this drug a promising antiarrhythmic agent. </div>
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<ce:simple-para view="all" id="simple-para.0010">The electrophysiologic effects of tocainide were studied with programmed electrical stimulation of the heart in two patients with atrioventricular (A-V) nodal tachycardia, five patients with reentrant tachycardia involving an accessory pathway and two patients with paroxysmal ventricular tachycardia. The measurements were made before and after a 15 minute perfusion of tocainide at a dose of 0.75 mg/kg per min in the first seven patients and of 0.5 mg/kg per min in the last two. At the end of perfusion, the drug plasma level ranged from 2.0 to 10.2 μg/ml (mean 6). During the subsequent 60 minutes, the plasma level decreased extremely slowly, its mean value remaining constantly between 3 and 4 μg/ml.</ce:simple-para>
<ce:simple-para view="all" id="simple-para.0015">Tocainide failed to achieve statistically significant effects on the functional properties of the A-V node. However, an increase of A-H time (two patients), prolongation of nodal refractory period (one patient) and lengthening of the cycle length producing a second degree A-V block (four patients) were observed in isolated cases. The H-V interval increased by 20 msec in three of the eight cases in which its measurement was not hampered by the constant presence of a preexcitation wave. No systematic effect on the refractory periods of the atrial and ventricular muscle was noted.</ce:simple-para>
<ce:simple-para view="all" id="simple-para.0020">In six patients, tocainide was perfused during sustained episodes of tachycardia (A-V nodal tachycardia, two patients; circus movement tachycardia using an accessory pathway, three patients; and paroxysmal ventricular tachycardia, one patient). Sinus rhythm was restored in all six patients. The drug prevented reinitiation of tachycardia in four of the eight patients in whom it could easily be triggered during the control period; it lengthened the tachycardia cycle length in the remaining four. No side effects were noted. These results, obtained with low plasma levels of tocainide, allow one to consider this drug a promising antiarrhythmic agent.</ce:simple-para>
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<sb:author>
<ce:surname>Coltart</ce:surname>
<ce:given-name>DJ</ce:given-name>
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<sb:author>
<ce:surname>Bernd</ce:surname>
<ce:given-name>TB</ce:given-name>
</sb:author>
<sb:author>
<ce:surname>Kernoff</ce:surname>
<ce:given-name>R</ce:given-name>
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<ce:surname>Harrison</ce:surname>
<ce:given-name>DC</ce:given-name>
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<title>Effects of tocainide studied with programmed electrical stimulation of the heart in patients with reentrant tachyarrhythmias</title>
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<titleInfo type="alternative" lang="en" contentType="CDATA">
<title>Effects of tocainide studied with programmed electrical stimulation of the heart in patients with reentrant tachyarrhythmias</title>
</titleInfo>
<name type="personal">
<namePart type="given">André</namePart>
<namePart type="family">Waleffe</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>From the Laboratory of Electrocardiology, Division of Cardiology, Institute of Medicine, University of Liège School of Medicine, Liège, Belgium</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Patrick</namePart>
<namePart type="family">Bruninx</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>From the Laboratory of Electrocardiology, Division of Cardiology, Institute of Medicine, University of Liège School of Medicine, Liège, Belgium</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Luc</namePart>
<namePart type="family">Mary-Rabine</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>From the Laboratory of Electrocardiology, Division of Cardiology, Institute of Medicine, University of Liège School of Medicine, Liège, Belgium</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Henri E.</namePart>
<namePart type="family">Kulbertus</namePart>
<namePart type="termsOfAddress">MD, FACC</namePart>
<affiliation>From the Laboratory of Electrocardiology, Division of Cardiology, Institute of Medicine, University of Liège School of Medicine, Liège, Belgium</affiliation>
<description>Address for reprints: H. E. Kulbertus, MD, Division of Cardiology, Institute of Medicine, 66 Bvd de la Constitution, B 4020 Liège, Belgium.</description>
<role>
<roleTerm type="text">author</roleTerm>
</role>
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<publisher>ELSEVIER</publisher>
<dateIssued encoding="w3cdtf">1979</dateIssued>
<dateCaptured encoding="w3cdtf">1978-07-11</dateCaptured>
<dateValid encoding="w3cdtf">1978-09-20</dateValid>
<dateModified encoding="w3cdtf">1978-09-19</dateModified>
<copyrightDate encoding="w3cdtf">1979</copyrightDate>
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<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
<languageTerm type="code" authority="rfc3066">en</languageTerm>
</language>
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<abstract lang="en">The electrophysiologic effects of tocainide were studied with programmed electrical stimulation of the heart in two patients with atrioventricular (A-V) nodal tachycardia, five patients with reentrant tachycardia involving an accessory pathway and two patients with paroxysmal ventricular tachycardia. The measurements were made before and after a 15 minute perfusion of tocainide at a dose of 0.75 mg/kg per min in the first seven patients and of 0.5 mg/kg per min in the last two. At the end of perfusion, the drug plasma level ranged from 2.0 to 10.2 μg/ml (mean 6). During the subsequent 60 minutes, the plasma level decreased extremely slowly, its mean value remaining constantly between 3 and 4 μg/ml. Tocainide failed to achieve statistically significant effects on the functional properties of the A-V node. However, an increase of A-H time (two patients), prolongation of nodal refractory period (one patient) and lengthening of the cycle length producing a second degree A-V block (four patients) were observed in isolated cases. The H-V interval increased by 20 msec in three of the eight cases in which its measurement was not hampered by the constant presence of a preexcitation wave. No systematic effect on the refractory periods of the atrial and ventricular muscle was noted. In six patients, tocainide was perfused during sustained episodes of tachycardia (A-V nodal tachycardia, two patients; circus movement tachycardia using an accessory pathway, three patients; and paroxysmal ventricular tachycardia, one patient). Sinus rhythm was restored in all six patients. The drug prevented reinitiation of tachycardia in four of the eight patients in whom it could easily be triggered during the control period; it lengthened the tachycardia cycle length in the remaining four. No side effects were noted. These results, obtained with low plasma levels of tocainide, allow one to consider this drug a promising antiarrhythmic agent. </abstract>
<note type="content">Section title: Report On Therapy</note>
<relatedItem type="host">
<titleInfo>
<title>The American Journal of Cardiology</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>AJC</title>
</titleInfo>
<originInfo>
<dateIssued encoding="w3cdtf">197902</dateIssued>
</originInfo>
<identifier type="ISSN">0002-9149</identifier>
<identifier type="PII">S0002-9149(79)X8001-0</identifier>
<part>
<date>1979</date>
<detail type="volume">
<number>43</number>
<caption>vol.</caption>
</detail>
<detail type="issue">
<number>2</number>
<caption>no.</caption>
</detail>
<extent unit="issue pages">
<start>171</start>
<end>464</end>
</extent>
<extent unit="pages">
<start>292</start>
<end>299</end>
</extent>
</part>
</relatedItem>
<identifier type="istex">C1DB2349E090FFFAB63418E6D6E4DC12FB563F4C</identifier>
<identifier type="DOI">10.1016/S0002-9149(79)80018-1</identifier>
<identifier type="PII">S0002-9149(79)80018-1</identifier>
<identifier type="ArticleID">79800181</identifier>
<recordInfo>
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