Ha. Rajasinghe et al., ARRHYTHMOGENIC VENTRICULAR ANEURYSMS UNRELATED TO CORONARY-ARTERY DISEASE, The Annals of thoracic surgery, 59(5), 1995, pp. 1079-1084
Malignant ventricular tachycardia occurs most frequently in patients w
ith coronary artery disease who have had a previous myocardial infarct
ion and in whom a ventricular aneurysm subsequently develops in the sc
arred section of myocardium. Ventricular tachycardia in the presence o
f normal coronary arteries and a left ventricular aneurysm is unusual
and can be refractory to medical therapy. We retrospectively reviewed
our experience of 10 patients treated at our institution from 1983 to
1993. Age ranged from 22 to 76 years, and all patients presented with
sustained ventricular tachycardia. All patients underwent complete ele
ctrophysiologic testing. Cardiac catheterization was performed in 9 pa
tients, and each had normal coronary artery anatomy without evidence o
f significant fixed lesions. A left ventricular aneurysm, diagnosed by
either echocardiography, thoracic cine computed tomography or magneti
c resonance imaging, or ventricular angiography was present in all pat
ients. Ventricular tachycardia could not be suppressed pharmacological
ly in 7 of 10 patients using multiple agents including procainamide, q
uinidine, flecanide, tocainide, propaferone, and amiodarone. Six patie
nts were treated surgically by intraoperative electrophysiologic mappi
ng, endocardial resection of foci, and left ventricular aneurysmectomy
. An implantable cardiac defibrillator device was implanted in 2 patie
nts. One patient died on the second postoperative day after simultaneo
us mapping-guided aneurysmectomy and implantable cardioverter defibril
lator placement. There was one late postoperative death. All other sur
gically treated patients had postoperative electrophysiologic studies
demonstrating no inducible ventricular tachycardia, and these patients
remain without antiarrhythmic therapy in follow-up extending from 29
to 86 months (mean, 56 months). Surgical pathologic examination showed
nonspecific myocardial scarring and fibrosis in the aneurysm walls, w
hich ranged in size from small apical to large broad-based basilar ane
urysms with a cavity volume equal to that of the left ventricle. Our e
xperience supports surgical therapy for medically refractory arrhythmo
genic left ventricular aneurysms unrelated to coronary artery disease.