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Electrophysiology and long-term efficacy of pentisomide in patients with supraventricular tachycardia

Identifieur interne : 001223 ( Main/Corpus ); précédent : 001222; suivant : 001224

Electrophysiology and long-term efficacy of pentisomide in patients with supraventricular tachycardia

Auteurs : Volker Kühlkamp ; Christian Mewis ; Ludger Seipel

Source :

RBID : ISTEX:04D7D7F767F9F3104FAC178805B6E200C1604262

Abstract

The electrophysiologic effects of pentisomide were investigated after intravenous (5 mg/kg) and oral (900–1200 mg three times a day) application in 9 patients with drug refractory atrioventricular nodal tachycardia and 6 patients with orthodromic atrioventricular re-entrant tachycardia. Pentisomide did not change sinus cycle length, effective refractory period of the right ventricle and the atrioventricular node. AH, HV interval, effective refractory period of the right atrium, QRS duration and QTc duration were (p ≤ 0.01) increased. Tachycardia cycle length was only increased after intravenous application of pentisomide, antegrade effective refractory periods of the accessory pathways and shortest fully pre-excited R-R intervals during atrial fibrillation were increased after the oral treatment phase (p = 0.054). Intravenous pentisomide prevented tachycardia in 69 patients with atrioventricular nodal tachycardia and in 26 patients with atrioventricular re-entrant tachycardia. If intravenous pentisomide did not prevent induction of the tachycardia, oral pentisomide was not effective either. During long-term follow-up 27 patients with atrioventricular nodal tachycardia and 14 patient with atrioventricular re-entrant tachycardia had a recurrence. Long-term treatment with pentisomide had to be discontinued because of possible side effects in 2 patients. It is concluded, that the electrophysiological effects of pentisomide are similar to those of flecainide and propafenone.

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DOI: 10.1016/0167-5273(92)90110-O

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ISTEX:04D7D7F767F9F3104FAC178805B6E200C1604262

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<abstract lang="en">The electrophysiologic effects of pentisomide were investigated after intravenous (5 mg/kg) and oral (900–1200 mg three times a day) application in 9 patients with drug refractory atrioventricular nodal tachycardia and 6 patients with orthodromic atrioventricular re-entrant tachycardia. Pentisomide did not change sinus cycle length, effective refractory period of the right ventricle and the atrioventricular node. AH, HV interval, effective refractory period of the right atrium, QRS duration and QTc duration were (p ≤ 0.01) increased. Tachycardia cycle length was only increased after intravenous application of pentisomide, antegrade effective refractory periods of the accessory pathways and shortest fully pre-excited R-R intervals during atrial fibrillation were increased after the oral treatment phase (p = 0.054). Intravenous pentisomide prevented tachycardia in 69 patients with atrioventricular nodal tachycardia and in 26 patients with atrioventricular re-entrant tachycardia. If intravenous pentisomide did not prevent induction of the tachycardia, oral pentisomide was not effective either. During long-term follow-up 27 patients with atrioventricular nodal tachycardia and 14 patient with atrioventricular re-entrant tachycardia had a recurrence. Long-term treatment with pentisomide had to be discontinued because of possible side effects in 2 patients. It is concluded, that the electrophysiological effects of pentisomide are similar to those of flecainide and propafenone.</abstract>
<note type="content">Section title: Original study</note>
<subject>
<genre>Article category</genre>
<topic>Electrophysiology</topic>
</subject>
<subject>
<genre>Keywords</genre>
<topic>Pentisomide</topic>
<topic>Supraventricular tachycardia</topic>
<topic>Medical treatment of arrhythmia</topic>
</subject>
<relatedItem type="host">
<titleInfo>
<title>International Journal of Cardiology</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>IJCA</title>
</titleInfo>
<genre type="Journal">journal</genre>
<originInfo>
<dateIssued encoding="w3cdtf">199207</dateIssued>
</originInfo>
<identifier type="ISSN">0167-5273</identifier>
<identifier type="PII">S0167-5273(00)X0177-5</identifier>
<part>
<date>199207</date>
<detail type="volume">
<number>36</number>
<caption>vol.</caption>
</detail>
<detail type="issue">
<number>1</number>
<caption>no.</caption>
</detail>
<extent unit="issue pages">
<start>1</start>
<end>134</end>
</extent>
<extent unit="pages">
<start>69</start>
<end>79</end>
</extent>
</part>
</relatedItem>
<identifier type="istex">04D7D7F767F9F3104FAC178805B6E200C1604262</identifier>
<identifier type="DOI">10.1016/0167-5273(92)90110-O</identifier>
<identifier type="PII">0167-5273(92)90110-O</identifier>
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