Eg. Vester et al., IMMUNOSUPPRESSIVE THERAPY FOR THE CONTROL OF LIFE-THREATENING VENTRICULAR ARRHYTHMIAS IN CHRONIC MYOCARDITIS, Zeitschrift fur Kardiologie, 86(4), 1997, pp. 298-308
Chronic myocarditis predisposes to the occurrence of spontaneous ventr
icular arrhythmias. It is not known if an immunosuppressive treatment
- as a causal therapy - leads to arrhythmia suppression. In the presen
t study, 12 patients (four female, eight male, mean age 53 +/- 15 year
s) with a mean left-ventricular ejection fraction of 52 +/- 19 % were
included. After exclusion of coronary macroangiopathy, the presence of
chronic myocarditis was demonstrated by immunohistological evaluation
of right-ventricular biopsies taking the number of specific lymphocyt
es (CD 2-8), of activated macrophages and the degree of HLA-expression
on interstitial and endothelial cells as a basis. Seven patients had
a successful resuscitation due to ventricular fibrillation in their ca
se history, three patients presented sustained monomorphic ventricular
tachycardia and two syncopes with inducible tachyarrhythmias. As a ''
conventional'' therapy ten patients received antiarrhythmic drugs and
four patients an implantable cardioverter/defibrillator. After confirm
ation of the diagnosis by a second biopsy after 3 months, all patients
underwent an immunosuppressive therapy with methylprednisolone. The i
nitial dose of 1 mg/kg body weight was reduced by 20 mg each every 2 w
eeks, until a maintenance dosage of 8-12 mg/day was achieved. If the c
ontrol study after 6 months still gave a positive result, a combined t
herapy with azathioprine, 100-150 mg/day, was carried out for a furthe
r 6 months. In nine patients (75 %), the control biopsy became negativ
e, in three patients (25 %), the biopsy remained to be positive. In th
e group presenting negative bioposies no tachyarrhythmia relapse occur
red within a follow-up period of 49 +/- 13 months, while in the group
with positive biopsies, relapses occurred in two of three patients. Co
mplete suppression during EPS after therapy was achieved in 50 % of th
e patients who were inducible before therapy. In addition to lymphocyt
e infiltration, particularly HLA expression on endothelial and interst
itial cells was significantly reduced; left-ventricular ejection fract
ion was improved only in tendency, while left-ventricular filling pres
sure decreased significantly. In summary, in patients with chronic myo
carditis and malignant ventricular arrhythmias, a high-dose immunosupp
ressive long-term therapy results in the significant reduction of infl
ammatory infiltrations in about 75 % of the cases and, at the same tim
e, in the effective suppression of arrhythmias.