METHODS
This was a prospective observational study conducted in patients admitted at the
hospital or referred from secondary hospitals with documented CAD as proved by
non invasive test (ECG, echocardiography, treadmill exercise, myocardial
perfusion imaging or multisided CT scan coronary angiography) requiring invasive
coronary angiography. The study population was composed of patients admitted in
a 5-month period between December 2008 to April 2009.
All patients referred for coronary angiography with no absolute contraindication
aged > 18 years old were included in this study.12
The exclusion criteria included clinical situations that may result in secondary
aVL lead T wave inversion and or ST segment depression from analysis as Bundle
branch block either left or right, aortic stenosis, left ventricular hypertrophy
and strain and paced ventricular rhythms.13
ECGs were recorded in 12-lead format at a paper speed of 25 mms and
calibrated correctly. Detailed 12-lead ECG data were interpreted by senior
cardiologists who were blinded to the outcomes. Special interest was made to
record ST-T changes and pathological Qs suggestive of CAD with more focus on T
wave direction in aVL lead. T waves in aVL were categorized into one of 3
groups, upright, flat or inverted and ST segment depression as isoelectric or
depressed.
An informed consent was obtained from each patient prior to the procedure.
The angiographic view displaying the greatest degree of luminal diameter
reduction of the stenosed coronary segment was selected. The criteria for the
choice of the optimal angle of view included elimination of vessel overlapping
and minimization of segment foreshortening. Coronary angiograms were analyzed by
interventional cardiologist. Left main coronary artery (LM), LAD, left
circumflex (LCX), Ramus Intermedius (RI) and right coronary artery (RCA) with
all their branches were defined and plotted on the data sheet. The ostial lesion
was defined as lesion affecting the origin of the vessel and or within 3
millimeters (mm) from the origin. Proximal LAD was defined as segment 3 mm from
LAD origin to the first diagonal branch (D1), mid LAD from D1 to second diagonal
branch (D2) and distal LAD segment was beyond D2. Proximal LVX was defined as
segment 3 mm after the origin of LCX to first obtuse marginal branch (OM1), mid
LCX from OM1 to second obtuse marginal branch (OM2) and distal LCX was the
segment beyond OM2. Proximal RCA 3 mm from RCA origin to the right ventricular
branch, mid RCA from the right ventricular branch to RCA bifurcation and distal
RCA was the segment beyond its bifurcation.
Descriptive statistics were used to describe the data. For categorical
variables, frequencies and percentages were reported. Differences between groups
were analyzed using Pearson’s chi-squared test. For continuous variables, means
and standard deviations (±SD) were presented.
A priori two-tailed level of significance was set at the 0.05 level.
Statistical analysis was conducted using STATA version 10.1 (STATA Corporation,
College Station, TX).
RESULTS
Out of the 257 patients enrolled in this study, 66 were excluded because they
met the exclusion criteria (left bundle branch block 23, right bundle branch
block 8, aortic stenosis 18, left ventricular hypertrophy and strain caused by
hypertension 16 and paced ventricular rhythm in one patient).
The study population comprised of the remaining 191 patients.
Old myocardial infarction either STEMI or NSTEMI was
documented in 49 patients (25.7%).
In terms of demographic and clinical data, the baseline characteristics of the
patients with respect to gender, mean age, and risk factors for CAD are depicted
in Table 1. Patients enrolled in this study were predominantly males (71.2%),
with a mean age of 55.2±11.5 years with multiple risk factors for coronary
artery disease. The incidence of hypertension was very high (84 patients, 44%)
as well as diabetes mellitus (71 patients, 37.2%) reflecting high risk patients
for CAD.
Angiographic characteristics are detailed in Tables 2A and 2B. The incidence of
CAD in the studied population was 86.3%, other coronary angiograms proved
evidence of normal coronaries except 3 angiograms that demonstrated slow flow
(1.57%) and another one (0.5%) with myocardial bridge. Single, two and
multivessel CAD was found in 38.8%, 28.5% and 32.7% respectively. The prevalence
of left main, left anterior descending, left circumflex and right coronary
arteries were 4.7%, 61.2%, 29.3% and 44.5% respectively. Table 2B detailed
lesion location in all main vessels.
The baseline ECG characteristics according to ST changes suggestive of CAD are
listed in Table 3. There were 89 patients (46.8%) who had T wave inversion in
aVL and only 9 patients (4.7%) had ST depression in aVL. Overall, ECG changes
suggestive of CAD were noticed in 97 patients (50.8%) with stand alone T wave
inversion in lead aVL found in 27 ECGs (14.1%) while ischemic changes in other
leads with normal aVL were identified in 36 ECGs (18.8%).
DISCUSSION
The ECG has been established in medical literature as an
applicable and reproducible non‑invasive diagnostic tool for
assessing myocardial ischemia. 14
In the setting of acute coronary
syndrome, several ECG findings help to localize the occlusion site
of the LAD coronary artery with respect to its major branches as
ST segment elevation in lead aVR was found to be very useful in
identifying LAD occlusion proximal to first septal perforator.
15,16
Until now, it is
to the authors’ understanding that the value of lead aVL in diagnosing CAD in
patients with chronic stable angina has not yet been addressed in literature.
Wellens syndrome refers to “LAD coronary T-wave syndrome”, the criteria of which
includes history of anginal chest pain, normal or minimally elevated cardiac
enzyme levels, and finally, ECG changes without Q waves with deep inversion of
the T-wave in the precordial leads.17,18,19 In contrast to Wellens
syndrome, this study addressed patients with chronic stable angina and relevance
of lead aVL in diagnosis of CAD. Given into account the increasing frequency of
CAD and limited health resources, it is crucial to identify patients
with increased risk for cardiac events for further intervention.
In evaluating the prognostic value of lead aVL T wave inversion in patients with
chronic stable angina; after excluding secondary etiologies that may alter the T
wave polarity such bundle branch block, left ventricular out flow tract
obstruction, hypertension with strain pattern and paced ventricular rhythms, the
results from this study showed that T wave inversion in lead aVL significantly
predicts LAD lesion typically mid segment.
On ECG ischemic changes,
pathological Qs and or ST-T changes suggestive of CAD were identified in 50.8%
of all ECGs. The baseline coronary angiographic data proved evidence of
obstructive CAD in 86.7% of patients. In the presence of obstructive CAD, there
was higher prevalence of left anterior descending artery lesions (61.2%)
especially in mid segments (62.4%). Lead aVL T wave inversion was the only
abnormal finding that predicted mid LAD lesions (odds ratio 2.931955, 95%
confidence interval 1.59-5.37, p=0.001). Despite the fact that
there was a trend to predict proximal LAD lesions, it did not however reach
statistical significance (p=0.066).
In terms of the prevalence of T wave inversion in lead aVL, interestingly, T wave
inversion in lead aVL found in 46.8%, flat and upright T wave seen in 12.8% and
40.4% respectively. Neither flat nor upright T wave in such lead predicted CAD.
More interestingly, stand alone T wave inversion in lead aVL was found in 27
ECGs (14.1%) with no pathological Qs and or ST-T changes in other leads, all
these ECGs have been described as normal ECG by the referring physicians. (Fig.
1)
Other ECG ischemic changes in lead aVL: In this series, significant (more than 1
mm) ST segment depression in lead aVL denoting CAD was found in 4.7% of the
study population with no statistical correlation with the diagnosis of CAD.
The mechanism by which why only T
wave inversion in lead aVL predicts CAD, namely mid LAD lesions as opposed to ST
segment depression and or pathological Qs or even flat T wave in the same lead
is beyond the scope of this study.
The strength of the association between ECG findings and subsequent CAD
with increasing morbidity and mortality is particularly interesting when
comparing their prognostic value with that of established risk factors such as
hypertension, diabetes, smoking, hyperlipidaemia, obesity, and family history of
CAD. The observations from this study suggest that aVL lead T wave inversion
should alert the health care providers during ECG interpretation in absence of
secondary causes that might alter the polarity of T wave amplitude especially in
presence of major risk factors for CAD. It is the understanding of the authors
that this is the only report showing the high relative importance of this ECG
finding in relation to CAD.
CONCLUSION
This study confirmed the prognostic value of T wave inversion in lead aVL with
coronary artery disease typically mid left anterior descending artery lesions in
patients with chronic stable angina in absence of secondary ST-T changes. Such
undemanding findings add important information to the medical field especially
to general practitioners during routine check up or cardiac risk assessment
before non cardiac surgery.
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