Objective To study differences between repetitive monomorphic ventricular tachycardia (RMVT) of right ventricular origin, and ventricular tachycardia in arrhythmogenic right ventricular dysplasia (ARVD).
Patients Consecutive groups with RMVT (n = 15) or ARVD (n = 12), comparable for age and function.
Methods Analysis of baseline, tachycardia, and signal averaged ECGs, clinical data, and right endomyocardial biopsies. Pathological findings were related to regional depolarisation (QRS width) and repolarisation (QT interval, QT dispersion).
Results There was no difference in age, ejection fraction, QRS width in leads I, V1, and V6, and QT indices. During ventricular tachycardia, more patients with ARVD had a QS wave in V1 (p < 0.05). There were significant differences for unfiltered QRS, filtered QRS, low amplitude signal duration, and the root mean square voltage content. In the absence of bundle branch block, differences became non-significant for unfiltered and filtered QRS duration. Mean (SD) percentage of biopsy surface differed between RMVT and ARVD: normal myocytes (74(3.4)% v 64.5(9.3)%; p < 0.05); fibrosis (3(1.7)% v 8.9(5.2)%; p < 0.05). When all patients were included, there were significant correlations between fibrosis and age (r = 0.6761), and fibrosis and QRS width (r = 0.5524 for lead I; r = 0.5254 for lead V1; and r = 0.6017 for lead V6).
Conclusions The ECG during tachycardia and signal averaging are helpful in discriminating between ARVD and RMVT patients. There are differences in the proportions of normal myocytes and fibrosis. The QRS duration is correlated with the amount of fibrous tissue in patients with ventricular tachycardia of right ventricular origin.
- arrhythmogenic right ventricular dysplasia
- endomyocardial biopsy
- ventricular arrhythmias
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- arrhythmogenic right ventricular dysplasia
- endomyocardial biopsy
- ventricular arrhythmias
It is not always easy to differentiate idiopathic or repetitive monomorphic ventricular tachycardia (RMVT) of right ventricular origin from tachycardia in early stages of arrhythmogenic right ventricular dysplasia (ARVD).1 From a clinical point of view, the major points helpful in the recognition of RMVT remain the absence of overt cardiomyopathy and myocardial dysfunction.2 A good tolerance of the arrhythmia (which does not exclude symptoms) is also suggestive of RMVT.3 RMVT is thought to have a good long term prognosis. Unfortunately, patients affected by ARVD in the early stages often also have a normal heart at routine examination and even after full non-invasive and invasive investigations the diagnosis is not always definite. This is embarrassing, as some patients with ARVD may experience palpitations due to minor ventricular arrhythmias, while others may die suddenly.4 Furthermore, ARVD can progress to left ventricular disease, making confusion with other pathology possible (for example, dilated cardio myopathy).5
To improve our understanding of the two diseases, we analysed clinical data, routine ECG data, ECG data during ventricular tachycardia, QT measurements, and signal averaged electrocardiograms (ECGs) in two groups of consecutive patients with RMVT and ARVD. Right ventricular biopsies were not only subjected to routine analysis but morphometric analysis was also performed and the results were correlated with the electrocardiographic data.
The study population included 27 consecutive patients, as described in table 1, with ventricular tachycardia of right ventricular origin as defined by ECG criteria, and without coronary artery disease. Patients with overt cardiomyopathy with dilatation of the left ventricle or depressed left ventricular ejection fraction or both were excluded. The patients were divided into two different groups: 12 patients had ARVD and 15 (idiopathic) RMVT. A prospective diagnosis of ARVD was made using criteria published by the task force of the working group on myocardial and pericardial disease of the ESC.6In the ARVD group, 42% had a family history of ARVD or sudden cardiac death. Six patients (50%) had echocardiographic or angiographic evidence of global or regional dysfunction of the right ventricle. T wave inversion in the right precordial leads was present in six patients (50%). Clinical ventricular tachycardia with left bundle branch block (LBBB) morphology was present in 11 patients, and in one at electrophysiological study, and positive late potentials on signal averaged ECG were present in seven (58%). Endomyocardial biopsy was performed in eight patients and was diagnostic of ARVD in six (75%).
ROUTINE ECG AND ECG DURING VENTRICULAR TACHYCARDIA
In all patients a 12 lead ECG during sinus rhythm was recorded at a paper speed of 25 mm/s when no antiarrhythmic drug treatment was given. The heart rate was calculated from the first four complexes. Specific descriptive features of the ECG during sinus rhythm were noted (T wave inversion in V2 and V3, RsR morphology in V1, presence of epsilon waves or right bundle branch block).6 The morphology of the QRS during ventricular tachycardia was analysed in leads V1 and V6.
QT AND QRS MEASUREMENTS
For QT measurements, all ECGs were enlarged to 200% and an average of three consecutive intervals was taken from all leads.7 The mean QT (QTmean) was the arithmetic mean from all 12 leads. We calculated QTc from Bazett’s formula, and also by the cube root formula [QT/(RR)1/3] from QTmean and QT in V4 (Qtcub).7 For QT dispersion, we used the difference between the maximum and the minimum QT interval (QTd), and a second, corrected parameter was calculated from the next to the longest and the next to the shortest interval (QTd′). Adjusted QT dispersion (aQTd) was calculated from QTd divided by the square root of the number of leads available for analysis. QRS duration was measured from enlarged ECGs in leads I, V1, and V6 during sinus rhythm. The intrinsic deflection (ID) of the QRS during ventricular tachycardia was measured in leads V1 and V6.
SIGNAL AVERAGED ECG
All patients were examined with the LP 2000 (Fidelity Medical, Millburn, New Jersey, USA). From X, Y, and Z leads, 200 normal beats were averaged and processed with a four pole filter between 40 and 250 Hz. A noise level of < 1 μV was required.
Ejection fraction of the left ventricle was determined during normal sinus rhythm by radionuclide angiography (Tc99).
ENDOMYOCARDIAL BIOPSY AND MORPHOMETRIC ANALYSIS
Three to five biopsy specimens were taken from the apical region of right ventricular cavity and the right ventricular septum. The biopsies were routinely processed for histology and stained with haematoxylin-eosin and by the trichrome method. Seven fields were randomly selected and studied at ×80 power to avoid any overlap. Only fields in which the entire screen was occupied by tissue were analysed. Using a Kontron Mini-Mop analyser, the percentage area of the following variables was determined: myocytes, fibrous tissue, fatty tissue, and interstitium (not including the fibrous and fatty tissue in the interstitium).8 Biopsies were performed in eight patients from the ARVD group, and nine from the RMVT group.
The SPSS package (4.0) was used for statistical analysis. Data are expressed as mean (SD). A non-parametric test was used to assess differences between the groups. The 0.05 level was used for significance.
Data for the two groups are presented in table 1. No differences were found in age and sex distribution, or in the mean values of the ejection fraction between the groups.
Complete right bundle branch block (RBBB) was not present in the group with RMVT, but was present in three patients with ARVD (p < 0.05). Most other electrocardiographic data are shown in table2. The differences remained non-significant when patients with bundle branch block were excluded (table 3). T wave inversion in leads V2 and/or V3 was noted in six of 12 patients in the ARVD group and in three of 15 patients in the RMVT group (NS).
ECG DURING VENTRICULAR TACHYCARDIA
Mean heart rate during ventricular tachycardia in the ARVD group was only slightly higher than in the RMVT group (table 2). More than one morphology was observed in one patient with RMVT. LBBB morphology was associated with left axis in four of 11 cases with ARVD (fig 1), but also in two of 15 cases with RMVT. All the other patients had an inferior axis associated with LBBB morphology (fig 2). In the ARVD group, the QRS complex in V1 showed a QS wave in nine patients and a rS pattern in two. In lead V6, the pattern of the QRS complex showed an R wave in six cases, a RS waves in two, and Rs in three. In the RMVT group, the QRS in lead V1 had a QS pattern in three patients, an rS pattern in seven, and an Rs pattern in one. These differences were significant (p < 0.05). In lead V6, the QRS morphology showed an R wave in all patients from this group (p < 0.01). No differences between groups were apparent for intrinsic deflection.
There were no significant differences between the two groups in any of the QT and QT dispersion indices (table 2), or after exclusion of bundle branch block.
SIGNAL AVERAGED ELECTROCARDIOGRAPHY
There were significant differences between the two groups for all variables (tables 2 and 3). In the absence of bundle branch block the differences persisted for low amplitude signal duration (LAS) and root mean square value of the last 40 ms (RMS). In the ARVD group, seven patients (58%) showed late potentials, versus only three patients (20%) in the RMVT group.
As shown in tables 2 and 3, the proportion of normal myocytes in the biopsies was lower in the ARVD group than in the RMVT group (p < 0.05). The amount of fibrous tissue was higher in the ARVD group (p < 0.05). No differences were found for fatty tissue and interstitium. In the absence of bundle branch block, significant differences persisted only for the myocyte area (less in the ARVD group; p < 0.05).
CORRELATION OF PATHOLOGY WITH ELECTROCARDIOGRAPHY
The percent of myocytes, interstitium, fibrous and fatty tissue was not correlated with clinical data, routine ECG features, QT indices, and signal averaging data within both groups, except for a positive correlation in the RMVT group between fibrosis and QTd′ (r = 0.6890; p < 0.01). In all patients (ARVD + RMVT), a significant correlation was detected between fibrosis and age (r = 0.6761; p < 0.01). QRS width was also associated with fibrosis: r = 0.5524 for lead I (fig 3),r = 0.5254 for lead V1, and r = 0.6017 for lead V6. All these correlations were significant (p < 0.01).
ARVD and RMVT are difficult clinical entities. They seem to constitute a continuous spectrum of disease, varying from a minor (RMVT) to a more severe expression (ARVD). It is therefore not surprising that new diagnostic techniques for ARVD are continuously being assessed, for example magnetic resonance imaging9and body surface QRST integral mapping.10 The latter was found to be abnormal in ARVD and to a lesser extend in idiopathic right ventricular tachycardia,10 in contrast to other data reporting an abnormal body surface QRST integral map in only one of six patients with ARVD.11 The discrepancy may be caused by the different severity of the disease in the two groups. These recent data prove that it is worthwhile challenging existing ideas about both diseases.
Nevertheless, some electrocardiographic criteria have been proposed for both pathologies.2 ,6 ,12 These include criteria for the morphology of the ventricular tachycardia in RMVT, and for the resting ECG in ARVD. However, our study shows that it is almost impossible to be certain from ventricular tachycardia morphology alone whether one is dealing with RMVT, since one can have exactly the same electrocardiographic pattern during ventricular tachycardia in ARVD as in RMVT.13 The fact that LBBB morphology is the only criterion for ventricular tachycardia in ARVD puts an important restriction on the ECG criteria. Some investigators assume that an axis other than the inferior axis is a marker of organic heart disease in RMVT.2 Also, multiple ventricular tachycardia patterns—logically associated with more extensive disease (and hence, more probably with ARVD)—were also present in one patient from our RMVT group, indicating that not all forms were located at a single site in the right ventricular outflow tract.14 However, one can assume that the resting ECG in ARVD is more or less specific.15 In a group of 30 patients with ventricular tachycardia of right ventricular origin (excluding ARVD), Buxtonet al found that in each patient the resting ECG was normal, and none of the characteristic abnormalities for ARVD were observed.16 Nevertheless, we were able to demonstrate T wave inversion in leads V1 to V3 in only 50% of ARVD patients, while it was present in 20% of the RMVT group.
A QRS duration of more than 110 ms in lead V1 has a sensitivity of 55% and a specificity of 100% for ARVD.15 A combination of QRS prolongation in V1 and T wave inversion in the right precordial leads improves sensitivity and specificity.17In our study, a combination of these two features had a sensitivity of 75% and a specificity of 80%, although no differences in the mean QRS duration in leads V1, V6, and I between the ARVD and the RMVT groups were observed. In the ARVD group the QRS duration was more prolonged in lead V1 than in lead V6, whereas in the RMVT group differences were not significant. This prolongation may reflect local delay in right ventricular activity due to morphological changes in the right ventricle (fatty and fibrofatty infiltration), as was recently described by Fontaine et al.17 ,18
There are no published reports about the predictive value of QT indices in ARVD. We found a QTc of ⩾ 440 ms in 50% of ARVD patients, and in 20% of the RMVT group. QT dispersion in both groups was comparable to values in a healthy control.19
The presence of late potentials is one of the other minor criteria for the diagnosis of ARVD.6 The signal averaged ECG may be abnormal in 47% to 69% of patients with ARVD with clinical ventricular tachycardia.20 ,21 In patients with ventricular tachycardia of right ventricular origin and without clinically apparent heart disease, the presence of abnormalities varies from 0% to 25%.16 ,22 We found abnormalities in 58% of ARVD patients and in 20% of patients with RMVT. In this study, only signal averaging was helpful in discriminating the ARVD and RMVT groups.
The demonstration of fibrofatty replacement of myocardium in the endomyocardial biopsy is a cornerstone of the diagnosis of ARVD.6 However, false negatives occur because of sampling errors, and it is possible that normal hearts with recurrent ventricular tachycardia show an increased amount of fibrotic tissue.22 Adipose infiltration of the myocardium, primarily the right ventricle, has also been reported in alcoholics dying suddenly, and in viral or mycoplasmal myocarditis.23 ,24 Extensive adipose or fibrous infiltration occurs usually at advanced stages of ARVD. It has been suggested that amounts of fatty tissue and fibrous tissue exceeding 3.2% and 40%, respectively, should be considered as highly suggestive of ARVD.25 Using morphometric techniques, we detected significantly more fibrous tissue in the ARVD group, but this value (9%) was less than reported in other studies.20 ,25This supports the idea that we were dealing with early stages of ARVD in the majority of the ARVD group.
It has been suggested that idiopathic ventricular tachycardia is nothing other than a concealed form of ARVD.26 However, the use of magnetic resonance imaging and signal averaged electrocardiography did not support the view that RMVT is an early or localised form of ARVD.27 In contrast, Carlson et al showed that in the vast majority of patients with RVOT tachycardia there are structural abnormalities in the infundibulum area on magnetic resonance imaging.28 While ECG data are comparable in most patients with ARVD and RMVT, differences were detected during ventricular tachycardia in the signal averaged ECG and the amount of fibrous tissue and myocytes in the right ventricular endomyocardial biopsy. This lends support to the view that there are two different entities, though it is not impossible that one is a more diffuse form, or the end stage, of the other, and that in the more advanced forms more extensive abnormalities can be detected. Therefore, it would be logical for late potentials to be correlated with the extent of fibrosis in ARVD, but this was not observed in our small series.29 However, we found a consistent relation between the amount of fibrosis and the QRS width in the group as a whole. Furthermore, there are differences between younger and older patients with ARVD, lending support to the idea that this disease is a changing continuum.20
It is evident that we shall have to refine our diagnostic techniques to gain a better understanding of what is going on. Genetic markers and familial forms have been described, at least for ARVD.30Apoptosis (programmed cell death) was proposed as a possible mechanism for the non-inflammatory loss of myocardial cells.31 If ARVD is a consequence of acquired injury (myocyte death) followed by fibrofatty replacement or patchy myocarditis, such disease could have a predilection for the right ventricular outflow tract, as the haemodynamic stress is greater there than in other parts of the right ventricle. This could explain some of the similarities between ARVD and idiopathic ventricular tachycardia arising in the outflow tract.
JK had a grant from The European Society of Cardiology for a research fellowship at The University of Ghent.