The European College of Veterinary Internal Medicine – Companion Animals.
17 th
ECVIM-CA Congress & 9 th ESVCP Congress.
13 th
– 15 th September 2007 – Budapest –
Hungary.
Cited in: Ettinger S.J., Feldman E.C., 2010 –
Textbook of Veterinary Internal
Medicine. Saunders – Elsevier.
USE OF
MEXILETIN AT DOGS WITH
VENTRICULAR ARRYTHMIAS
Brăslaşu Corneliu Mihail, Brăslaşu E. Daniela, Brădăţan Cătălina,
Budai Mihai.
Faculty of Veterinary Medicine Bucharest . Romania .
Mexiletin
is an antiarrhythmic from I b class (Vaughan-Williams) indicated in multiple
and multifocal premature ventricular beats and ventricular tachycardia.
A number
of 27 dogs from mid and large breed were diagnosed with ventricular arrhythmia:
multifocal premature beats and
ventricular tachycardia.
Ventricular
tachycardia with a high frequency caused syncope and this case we used first,
lidocaina in dose of 2-4 mg/kg in continue rate infusion; then we used
Mexiletin in dose of 5-8 mg/kg p.o. bid-tid to prevent ventricular arrhythmias.
After
administration of doses 2-5 mg there weren’t
stopped the ventricular arrhythmia. High doses of 8 or 10 mg/kg p.o.
bid determined a total disappearance of
ventricular arrhythmias.
Biochemical
blood exams didn’t show an increase of blood values, creatinine and
transaminase levels. There weren’t observed decrease either cardiac frequency or blood pressure. Also a adverse reaction wasn’t observed.
In
conclusion, Mexiletin administration in dog determined the end of ventricular
arrhythmias, the drug being well tolerate by animal.
Mexiletine
is used to suppress frequent ventricular ectopy and to reduce the frequency and
duration of abrupt self-limiting ventricular tachycardia.
Class IB
antiarrhythmics are used only to treat ventricular arrhythmias. These drugs
slightly depress depolarization in myocardial cells. Class IB antiarrhythmics
are cell membrane stabilizers, but do not affect the automatist of the
sinoatrial node or conductivity through the atrioventricular node.
As their
major action, class IB antiarrhythmics decrease the action potential duration
and to a lesser extent the effective refractory period. The drugs especially
affect the Purkinje fibers and myocardial cells in the ventricles. By
shortening the effective refractory period, class IB antiarrhythmics eliminate
unidirectional block, which can trigger a reentry arrhythmia. The drugs also
decrease ventricular ectopy by blocking the slow influx of sodium during
plateau (phase 2) and by decreasing the slope of phase 4 depolarization. Class
IB antiarrhythmics neither block nor mimic autonomic control of the heart.
(Richard K. Gibson and Douglas R. Geraets, 1996).
Usual
dosage: 5 – 8 mg/kg PO
BID-TID.
Table 1. Clinical
cases with Mexiletin administration
Nr. crt.
|
Breed,
age, sex
|
Clinical
diagnosis
|
1.
|
Schnauzer, male,
9.6 years old
|
Dilated
cardiomyopathy
|
2.
|
Boxer, male, 11
years old
|
Dilated
cardiomyopathy
|
3.
|
Great dane, male, 6
years old
|
Dilated
cardiomyopathy
|
4.
|
Boxer, female, 9.6
years old
|
Multiple
ventricular premature beats, Ventricular parasystolie
|
5.
|
German shepard,
male, 5.6 years old
|
Myocarditis
|
6.
|
Boxer, male, 8.6
years old
|
Multiple,
multifocal ventricular premature beats
|
7.
|
German shepard,
male, 6 years old
|
Tumoral
pericarditis
|
8.
|
German shepard,
male,14 months old
|
Congenital heart
disease (Dilated cardiomyopathy ?)
|
9.
|
German shepard, female, 13 years old
|
Dilated
cardiomyopathy
|
10.
|
Great dane, female,
10 years old
|
Pyometra
|
11.
|
Boxer, male, 10
years old
|
Dilated
cardiomyopathy
|
12.
|
Dog, medium size,
male, 10 years old
|
Cardiac failure,
Ventricular tachycardia
|
13.
|
Cocker, mascul, 14
ani
Cocker, male, 14
years old
|
Right ventricular
hypertrophy-Dirophilariosis
|
14.
|
Boxer, female, 11.6
years old
|
Ventricular
tachycardia
|
15.
|
Boxer, female, 12
years old
|
Dilated
cardiomyopathy
|
16.
|
Basset Hound, male,
9 years old
|
Dilated
cardiomyopathy
|
17.
|
Saint Bernard,
female, 2.5 years old
|
Dilated
cardiomyopathy
|
18.
|
Vijla, female, 3.6
years old
|
Congenital
ventricular arrhythmia
|
19.
|
Russian greyhound,
female, 12 years old
|
Tumoral
pericarditis and pleuresia
|
20.
|
Schnauzer, male, 9
yeras old
|
Myocardial
infarction
|
21.
|
Doberman, male, 8.6
years old
|
Dilated
cardiomyopathy + Gastric torsion
|
22.
|
Doberman, male, 7
years old
|
Dilated
cardiomyopathy
|
23.
|
Great dane, male, 5
years old
|
Dilated
cardiomyopathy
|
24.
|
Greyhound, mascul,
9 ani
|
Multiple
ventricular premature beats
Pleurisy
|
The conclusions of table 1 are:
-
ventricular premature beats which required specific therapy were
diagnosed in large breed dogs;
-
a higher incidence of these ventricular premature beats are recorded in
males (70.9%)
-
the diseases with ventricular premature beats in their evolution are:
dilated cardiomyopathy (in most of the cases), idiopathic ventricular premature
beats and rarely congenital heart disease, myocardial infarction,
dirophilariosis (Heartworm disease), malignant congenital ventricular premature beats
Table 2. ECG changes after Mexiletin
administration (a)
A. Initial
ECG
B. ECG
after. Mexiletin
Patient
|
1.
|
2.
|
3.
|
4.
|
5.
|
|
P – T interval
|
A.
|
0.32
|
0.30
|
0.28
|
0.34
|
0.28
|
B
|
0.30
|
0.30
|
0.26
|
0.34
|
0.28
|
|
Q – T interval
|
A.
|
0.20
|
0.20
|
0.18
|
0.20
|
0.20
|
B.
|
0.18
|
0.20
|
0.16
|
0.20
|
0.20
|
|
Heart rate beats/min
|
A.
|
150
|
148.8
|
176.5
|
166.6
|
166.6
|
B.
|
100
|
125
|
166.6
|
150
|
150
|
Patient
|
6.
|
7.
|
8.
|
9.
|
10.
|
|
P – T interval
|
A.
|
0.32
|
0.30
|
0.32
|
0.30
|
0.28
|
B
|
0.34
|
0.26
|
0.32
|
0.30
|
0.28
|
|
Q – T interval
|
A.
|
0.16
|
0.20
|
0.20
|
0.16
|
0.16
|
B.
|
0.18
|
0.20
|
0.20
|
0.16
|
0.16
|
|
Heart rate beats/min
|
A.
|
150
|
166.6
|
176.4
|
187.5
|
|
B.
|
187.5
|
166.6
|
150
|
120
|
136.36
|
Observations regarding Mexiletin
therapy in dog
-
Mexiletin was administered in multiple ventricular premature beats with
different origins (multifocal).
-
Lidocain i.v. (2-4mg/kg) was used until remission of ventricular
premature beats in cases with diagnosed multiple ventricular premature beats or
ventricular tachycardia, with clinical signs of syncope or heart failure (III
Class – ISACHC, 1992).
-
At low doses of Mexiletin, 3-4mg/kg, no clinical signs were observed
(persistence of ventricular premature beats).
-
At high doses of Mexiletin (6-8mg/kg), the ventricular premature beats
and ventricular tachycardia disappeared and there was an improvement of
clinical status (remission of pulmonary edema).
-
Animals receiving Mexiletin were ECG monitored (from 1-2 to 7 days,
depending on the diagnosis and clinical status). Mexiletin doses were decreased
when the ventricular premature beats were remised and the clinical status was
improved. In many cases, after using Mexiletin for 3-4 weeks (together with the
therapy for the the principal disease), the interruption in Mexiletin
administration wasn’t follow by reappearance of ventricular premature beats.
-
By monitoring hepatic, renal function and glycemia, no increase in
creatinine, BUN, SGPT, SGOT were observed. In some cases (Boxer, 10 years, male
– Dilatative cardiomyopathy) a decrease in the value of these parameters was
observed (creatinine decreased from 1mg/dl to 0.85mg/dl; BUN decreased from
59,15mg/dl to 40.8mg/dl).
-
Except one case, in which during Mexiletin therapy a sinusal bradicardia
was diagnosed (Mexiletin administration was interrupted), no other adverse
reactions were observed.
Clinical cases
Ventricular tachycardia – paroxysmic
attack. Greyhound, male, 9 years
Ventricular tachycardia - paroxysmic attack.
Greyhound, male, 9 years
Remission of ventricular premature beats
after
Mexiletin administration – 7 mg/kg BID (day 4 of treatment)
The case discussed above.
ECG aspect one month after administration of
Mexiletin
Ventricular tachycardia - paroxysmic attack,
Boxer, female. 11.6 years old
Ventricular tachycardia - paroxysmic attack.
The case discussed above
Control of ventricular tachycardia by i.v.
Lidocaine (80 mg)
ECG aspect after the administration of
Mexiletin
6 mg/kg P.O. (second day of treatment)
CONCLUSIONS
- Mexiletin is an IB class anti-arrhythmic
used in the treatment of ventricular arrhythmia (ventricular premature
beats and ventricular tachycardia). The dosage in dog is 5-8mg/kg BID-TID.
- After the administration of low doses of
Mexiletin there was no improvement of ventricular premature beats, on the
contrary, high doses (6-8mg/kg) determined the remission of ventricular
premature beats/ventricular tachycardia.
3. No adverse reactions were observed during Mexiletin administration.
The creatinine, BUN and glycemia were in normal limits when the biochemical
blood exam was performed. In the situations when these parameters were
improved, the explanation was due to the decrease of hemostasis, consecutive to the ventricular
arrhythmia.
4. No significant changes in the
length of ventricular and general electric systole were observed on the ECG;
instead, a decrease of heart frequency has been shown.
5. The examination of cases in which Mexiletin was administered has
shown: most of the clinical cases were large size males (70,90%). Ventricular
arrhythmia were diagnosed in most of the cases in dilated cardiomyopathy; other
cases were represented by myocardial infarction, congenital ventricular
arrhythmia, congenital heart disease, etc. Mexiletin can be called, because of
its rapid clinical effects and its low adverse reactions, the oral Lidocaine,
which can be given P.O.
Bibliography
1. Bonaduce D., Ferrara N., Abete P., Longobardi G., Leosco D., Canonico
V., Morgano G., Rengo F., 1986 - Effect
of mexiletine on reperfusion-induced ventricular arrhythmias: comparison with lidocaine.
Arch. Int. Pharmacodyn.
Ther., 284, 1, 19 - 29.
2. Chinushi M., Tagawa M., Sugiura H., Komura S., Hosaka Y., Washizuka
T., Aizawa Y., 2003 - Ventricular tachyarrhythmias in a canine model of LQT3:
arrhythmogenic effects of sympathetic
activity and therapeutic effects
of mexiletine. Circ.
J., 67, 3, 263 - 268.
3. Duff H.J., 1989 -
Mexiletine-quinidine combination: enhanced antiarrhythmic and
electrophysiologic activity in the dog. J. Pharmacol. Exp. Ther., 249, 2, 617 -
622.
4. Meurs K.M., Spier A.W., Wright N.A., Atkins C.E., DeFrancesco T.C.,
Gordon S.G., Hamlin R.L., Keene B.W., Miller M.W., Moise N.S., 2002 -
Comparison of the effects of four antiarrhythmic treatments for familial
ventricular arrhythmias in Boxer. JAVMA, 221, 4, 522 - 527.
5. Takahara A., Sugiyama A., Satoh Y., Hashimoto K., 2003 - Effects of
mexiletine on the canine model of
sparfloxacin-induced long QT syndrome. Eur. J. Pharmacol., 22, 476, 1-2, 115 -
122.
6. Tilley L.P., Goodwin J.K., 2001 - Manual of Canine and Feline
Cardiology. Third ed. Saunders. An
Imprint of Elsevier Science.
7. Yoshida H., Sugiyama A., Satoh Y., Ishida Y., Kugiyama K., Hashimoto
K., 2002 - Effects of disopyramide and
mexiletine on the terminal repolarization process of the in situ heart assessed
using the halothane-anesthetized in vivo
canine model. Circ. J., 66, 9, 857 - 862.
Currently, Mexiletin no longer used
in Europe .
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