Circulation, Vol 87, 773-782, Copyright © 1993 by American Heart Association
F Kornreich, TJ Montague and PM Rautaharju
BACKGROUND. Several large, randomized clinical trials have shown that early
thrombolytic therapy substantially reduces early mortality after acute
myocardial infarction (MI). In most trials, eligibility criteria include
typical chest pain and diagnostic ST segment elevation in two or more
contiguous leads of the standard 12-lead ECG. Unfortunately, large areas of
the thoracic surface are left unexplored by the standard electrode
positions. As a consequence, acute MI patients with ST elevation in regions
not interrogated by the conventional electrodes may not receive reperfusion
therapy and its attendant benefits. METHODS AND RESULTS. The present study
compares 120-lead body surface potential map (BSPM) data from 131 patients
with acute MI and 159 normal control subjects (N). The MI population was
stratified according to the location of ventricular wall motion
abnormalities evidenced by radionuclide imaging into 76 patients with
anterior MI (AMI), 32 patients with inferior MI (IMI), and 23 patients with
posterior MI (PMI). BSPM were recorded within 24 hours of admission. Group
mean BSPM of the ST segment were obtained for N, AMI, IMI, and PMI by
sampling the time-normalized ST-T waveform at 18 equal intervals and
averaging the voltages at each electrode site over the first five of these
18 ST- T time instants. Corresponding discriminant maps were also computed
for each pairwise comparison (AMI versus N, IMI versus N, and PMI versus N)
by subtracting the normal group mean voltages from each MI group mean
voltages and by further dividing each resulting difference by the composite
standard deviation calculated from the pooled groups. Discriminant analysis
for each bigroup classification was also performed using as measurements
the ST magnitudes in 120 electrode sites from each individual. Finally, the
number of patients in each MI group with ST changes outside the 95% normal
range was calculated for each electrode position. The following results
were obtained: 1) In each MI group, ST depression departs more
significantly from normal values than ST elevation. 2) The most significant
ST changes (both ST elevation and ST depression) are observed in IMI, the
least significant in AMI. 3) For each pairwise comparison, measurements
from two lead sites are entered into the stepwise discriminant procedure:
the first measurement is ST depression, the second ST elevation.
Classification rates are 82% for AMI, 93% for PMI, and 100% for IMI at a
specificity level of 95%. 4) From the six leads selected for optimal
classification of the three MI groups, five are outside the area sampled by
the conventional precordial electrodes. 5) The use of site-dependent
thresholds for ST measurements based on 95% normal range yields the best
compromise between sensitivity and specificity. A fixed threshold of 1 mm
for ST elevation or ST depression produces increased sensitivity in AMI at
the cost of marked loss in specificity and reduces sensitivity in both IMI
and PMI with no benefit in specificity. CONCLUSIONS. Analysis of BSPM
identifies areas on the torso where the most significant ST changes most
frequently occur in acute MI. Two leads from areas with the most abnormal
ST changes achieve optimal classification in each MI class. Of these six
leads, five are outside the standard precordial lead positions. ST
depression is the most potent discriminator for each MI group and contains
information independent from ST elevation. Quantitative analysis of ST
magnitude at each electrode site allows determination of best thresholds
for ECG criteria. Appropriate selection of ECG leads may help remove
inconsistencies in current ECG selection criteria and improve comparability
of treatment results.
ARTICLES
Body surface potential mapping of ST segment changes in acute myocardial infarction. Implications for ECG enrollment criteria for thrombolytic therapy
Unit for Cardiovascular Research and Engineering, Free University Brussels, Belgium.
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