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Volume 08

Clinical Pharmacology & Biopharmaceutics

ISSN: 2167-065X

Pharmacology 2019

World Heart Congress 2019

August 19-20, 2019

JOINT EVENT

conferenceseries

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August 19-20, 2019 Vienna, Austria

&

7

th

World Heart Congress

24

th

World Congress on

Pharmacology

Effectiveness of combine therapyusingAllapininandcardiac glycosides for suppressionof supraventricular

paroxysmal tachyarrhythmias in patients with ischemic heart disease

Kapustnyk Yurii

Ukrainian Medical Stomatological Academy, Ukraine

P

aroxysmal atrial fibrillation and paroxysmal supraventricular tachycardia can be treated using several

preparations. Author of this abstract has developed the newmethod of treatment for paroxysmal supraventricular

tachyarrhythmia’s including such disorder of cardiac rhythm in patients with severe heart failure. In accordance with

this method combination of preparations with antiarrhythmic action (allapinin + cardiac glycosides) is used.

Allapinin is the alkaloid of bromhydrate lappaconitine. This alkaloid was extracted from the perennial plant. It can

be extracted from the wild plant of the aconite, which belongs to the group of buttercup plants. It is produced in

tablets at 50 mg and in solution for intravenous or intramuscular administration: 1% solution in ampoules at 2 ml.

Allapinin occupies the special place among antiarrhythmic agents of the 1st class according to Vaughan-Williams

classification. It differs from agents of IA and IB subclass. Being different from quinidine, procainamide, gilurytmal

and others agents of the 1st class of antiarrhythmic drugs allapinin in effective antiarrhythmic doses has small

influence on the width of ventricular QRS complex, P-Q interval and Q-T interval. Allapinin in doses, which provide

denominated antiarrhythmic effect, unlike the other antiarrhythmic drugs, does not lead to reduction of the system

arterial pressure and to negative inotropic action in myocardium fibers.

In accordance with the new method of treatment of paroxysmal supraventricular tachyarrhythmias a cardiac

glycoside – digoxin (lanoxin) in dose 0,25 mg or strophantin in dose 0,25 mg is administered intravenously. Then in

20-30 minutes after administration of cardiac glycoside allapinin is used intravenously in dose 30-40 mg

In case of suppression of paroxysmal tachyarrhythmia prophylactic treatment must be administered using the

above preparations. Allapinin is administered orally in daily dose 75 mg (25 mg 3 times daily). In combination with

allapinin digoxin is used orally in dose 0,25 mg (1 tab) 1-2 times daily. In case of positive result of therapy the daily

dose of allapinin can be reduced to 50 mg (1 tablet 2 times a day) and digoxin - to the minimum effective one, which

is 0,25 mg (1 tablet) once a day.

The criterion of such positive result of therapy is occurrence of the periods without paroxysms of tachyarrhythmia,

which are greater than 1,5-2 periods. Such periods occurred earlier between paroxysms of tachyarrhythmia. Thus,

this therapy provides prophylactic effect in respect to occurrence of tachyarrhythmia attack.

The significant advantage of this method is the possibility of using it for the patients with severe heart failure. Unlike

the majority of other antiarrhythmic drugs of synthetic origin allapinin does not have any negative inotropic action

in effective antiarrhythmic doses. For the patients with cardiac failure this cardiac glycoside leads to improving of

metabolism in myocardial cells. Such improvement of myocardium metabolism contributes to the elimination of

paroxysmal tachyarrhythmias.

The most expressive effect of combined therapy is observed in case of intravenous administration of allapinin in

single dose 30-40 mg and cardiac glycoside in 20-30 minutes after using allapinin. Such combination of these agents

is conditioned by their pharmacodynamics. The beginning of antiarrhythmic effect occurred only in 10-15 minutes

after its intravenous administration. The maximal effect of allapinin is achieved in 20-40 minutes after using this

antiarrhythmic drug. This property of allapinin is conditioned by the time of intravenous administration of cardiac

Kapustnyk Yurii, Clin Pharmacol Biopharm, Volume 08