Zusammenfassung
Vernakalant ist ein vielversprechendes neuartiges Antiarrhythmikum
zur intravenösen Konversion von Vorhofflimmern in Sinusrhythmus.
Es hemmt mehrere Ionenströme inklusive IKr und
unterscheidet sich von herkömmlichen Antiarrhythmika durch
eine relative Vorhofselektivität. Erreicht wird dies durch
eine Hemmung des Kaliumstroms IKur , der nur im Vorhof
vorkommt, und Ito , der aufgrund der kürzeren
Aktionspotentiale eine relativ gesehen stärkere Auswirkung
auf die Refraktärzeiten im Vorhof hat. Des Weiteren hemmt
Vernakalant frequenz- und spannungsabhängig Natriumströme
(INa ). Die schnellen atrialen Aktionspotentiale bei Vorhofflimmern
reagieren daher besonders gut auf Vernakalant, was sich klinisch
in einer Konversionsrate von über 50 % bei
weniger als 7 Tage bestehendem Vorhofflimmern zeigt. Eine Dosisanpassung
von Vernakalant aufgrund von Alter, Geschlecht, Organinsuffizienzen
oder Ko-Medikation scheint nicht erforderlich zu sein. Noch sind
die Patientenzahlen in den durchgeführten Studien zu klein,
um eine Aussage über das kardiale Nebenwirkungspotential
von Vernakalant zu treffen. Die Kombination aus einem Trend zu Arrhythmogenität
und noch geringer Erfahrung mit dieser neuen Substanz gebietet allerdings
große Vorsicht auch nach Markteinführung.
Abstract
Vernakalant is a promising novel antiarrhythmic intravenous drug
for the rapid conversion of atrial fibrillation to sinus rhythm.
It blocks several ion currents important in cardiac action potential
including IKr. Its difference to traditional antiarrhythmic drugs
is a preferential effect on the atria, achieved by an inhibition
of repolarizing potassium ion currents IKur , which is
atrial-specific, and Ito , predominantly affecting atrial
repolarization, as there is little atrial plateau potential. Furthermore
vernakalant blocks frequency- and voltage-dependent sodium ion currents
(INa ). Thus rapid action potentials in atrial fibrillation
are particularly targeted by vernakalant: this leads to a conversion
rate to sinus rhythm in about 50 % of recent-onset
attacks (less than 7 days) of atrial fibrillation. Age, gender,
organ function and concomitant medication seem to have no clinically
significant influence on the pharmacokinetics of vernakalant. The
number of patients included in the studies is still too small to
provide a definitive answer on its cardiac toxicity. However, a
demonstrated tendency towards proarrhythmia and little experience
with this new drug demands precaution even after it has been officially
approved.
Schlüsselwörter
Vorhofflimmern - vorhofselektive Antiarrhythmika - ultraschneller verzögerter Gleichrichter - IKur
- Vernakalant
Keywords
atrial fibrillation - atrial selective antiarrhythmic drugs - ultrarapid delayed rectifier - IKur
- Vernakalant
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Prof. Dr. med. Thomas Eschenhagen
Universitätsklinikum Hamburg-Eppendorf, Institut
für Experimentelle und Klinische Pharmakologie und Toxikologie
Martinistraße 52
20246 Hamburg
Telefon: 040/7410-52180
Fax: 040/7410-54876
eMail: t.eschenhagen@uke.uni-hamburg.de