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pubmed-article:12736484pubmed:abstractTextThe aims of this study were to evaluate the changes in the electrophysiological characteristics of the right atrium after the administration of flecainide and to clarify whether flecainide has a selective effect on human atrial tissue. Electrophysiological measurements were made in 38 patients, before and after intravenous administration of flecainide (2 mg/kg per 10 min). The effective refractory period of the right atrium (ERP-A), maximum conduction delay (Max.CD), repetitive atrial firing zone (RAFZ), fragmented atrial activity zone (FAAZ), and conduction delay zone (CDZ) were studied in the patients who were divided into 2 groups based on whether repetitive atrial firing (RAF) was induced in the baseline study. Flecainide significantly prolonged the ERP-A (202+/-22 to 238+/-33 ms, p<0.001) and shortened Max.CD (77+/-17 to 63+/-32 ms, p<0.05) in the patients with RAF, but not in those without RAF in the baseline study. After flecainide administration, there were significant reductions in the RAFZ (43+/-22 to 13+/-19 ms, p<0.0001), FAAZ (51+/-22 to 28+/-26 ms, p<0.001) and CDZ (70+/-21 to 48+/-30 ms, p<0.01) in the patients with RAF. However, atrial fibrillation (AF) was induced by stimulation after flecainide in 2 patients without RAF in the baseline study. There was a significant negative correlation between the ERP-A in the baseline study and the change in the ERP-A upon flecainide administration (r=0.45, p<0.01). Flecainide may preferentially activate the substrate for AF and RAF, but that action is mainly based on the electrophysiological characteristics found in the baseline study.lld:pubmed
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pubmed-article:12736484pubmed:authorpubmed-author:MatsuzakiMasu...lld:pubmed
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pubmed-article:12736484pubmed:authorpubmed-author:OhmuraMasatoMlld:pubmed
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pubmed-article:12736484pubmed:pagination437-42lld:pubmed
pubmed-article:12736484pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:12736484pubmed:year2003lld:pubmed
pubmed-article:12736484pubmed:articleTitleEffects of flecainide on the electrophysiological properties of atrial vulnerability in humans.lld:pubmed
pubmed-article:12736484pubmed:affiliationThe Department of Medical Bioregulation, Faculty of Science, Yamaguchi University School of Medicine, Ube, Japan.lld:pubmed
pubmed-article:12736484pubmed:publicationTypeJournal Articlelld:pubmed