(Circulation. 1995;91:2541-2548.)
© 1995 American Heart Association, Inc.
Articles |
From St Louis University Health Sciences Center (F.V.A., L.T.Y., B.R.C., M.J.K.), St Louis, Mo; Maryland Medical Research Institute (R.P.M., G.K.), Baltimore, Md; Mayo Clinic (P.B.B.), Rochester, Minn; University of Alabama (W.J.R.) (Birmingham); George Washington University (A.M.R.), Washington, DC; National Heart, Lung, and Blood Institute (G.S.), Bethesda, Md; Duke University (L.S.), Durham, NC, and Harvard Medical School (E.B.), Boston, Mass.
Correspondence to Frank V. Aguirre, MD, St Louis University Health Sciences Center, Division of Cardiology, 3635 Vista Ave at Grand Blvd, St Louis, MO 63110.
| Abstract |
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Methods and Results A secondary analysis of 2634 patients enrolled in the TIMI II trial with a first myocardial infarction was performed to determine 6-week and 1-year cardiac event rates and identify clinical and angiographic differences between the 1867 patients (70.9%) who evolved a Q-wave infarct and the 767 patients (29.1%) who sustained a nonQ-wave infarct after treatment with intravenous thrombolytic therapy. Male sex (85.3% versus 75.6%; P<.001) and anterior wall infarcts (53.8% versus 43.7%; P<.001) were more frequent in the Q-wave versus the nonQ-wave group. During recombinant tissue-type plasminogen activator (rTPA) infusion, a greater percentage of nonQ-wave patients (37.3% versus 23.5%; P=.001) had normalization of initial ST-segment elevation. Infarct-related artery patency (TIMI flow grade 2 or 3) (P=.02), complete infarct-related artery reperfusion (TIMI 3 flow grade) (P<.001), and the percentage of patients with a predischarge resting left ventricular ejection fraction >55% (P<.001) were greater in the nonQ-wave group. New congestive heart failure during hospitalization developed more frequently in Q-wave patients (18.9% versus 11.6%; P<.001). After 42 days, the occurrences of reinfarction (P=.76), death (P=.76), and combined death or reinfarction (P=.43) were similar in patients assigned to the invasive or conservative postlytic management strategy, regardless of infarct type. One-year mortality was 3.4% versus 4.4% for nonQ-wave versus Q-wave infarct type, respectively (P=.25).
Conclusions Angiographic and clinical differences were observed between patients who present with initial ST-segment elevation and evolve early nonQ-wave versus Q-wave myocardial infarcts after treatment with rTPA, heparin, and aspirin. Early mortality and adverse clinical cardiac events in these patients are not significantly different after a conservative compared with an invasive treatment strategy, regardless of whether the infarct type is nonQ wave or Q wave.
Key Words: myocardial infarction thrombolysis nonQW infarcts clinical trials
| Introduction |
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In the past decade, thrombolytic therapy has evolved as the standard treatment for appropriately selected patients with acute myocardial infarction presenting with ECG ST-segment elevation.9 10 Results of placebo-controlled trials of intravenous thrombolytic therapy have indicated that pharmacological reperfusion limits infarct size and reduces in-hospital and 1-year mortality rates, producing clinical outcomes similar to those observed in patients with nonQ-wave infarction in the prethrombolytic era.10 11 The majority of patients with acute infarction who present with ST-segment elevation evolve Q-wave infarcts even though thrombolytic therapy reduces infarct size and enhances infarct artery reperfusion.12
Patients receiving thrombolytic therapy are a selected population compared with nonselected consecutive patients with myocardial infarction. However, there are few data comparing the clinical features of patients with nonQ-wave and Q-wave infarcts after thrombolytic therapy. The aims of the present study were to determine the prevalence of nonQ-wave and Q-wave infarctions in patients treated with thrombolytic therapy who present with initial ST-segment elevation; compare 21-day, 42-day, and 1-year clinical outcomes of both patient groups; and determine whether an invasive strategy applied to patients evolving a nonQ-wave myocardial infarction after thrombolysis results in fewer adverse cardiac events than a conservative strategy.
| Study Design and Study Population |
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0.1 mV
in two or more contiguous ECG leads and no contraindication to
thrombolytic therapy. Patients received intravenous recombinant
tissue-type plasminogen activator (rTPA) and concomitant intravenous
heparin and oral aspirin as previously described.13 To avoid misclassification of the qualifying event as nonQ-wave versus Q-wave infarction due to the presence of old Q waves on ECGs or Q waves resulting from reinfarction after the initial event, this analysis was restricted to TIMI II patients who met the following criteria: enzymatically and electrocardiographically confirmed first myocardial infarction, an interpretable day-2 ECG, and freedom from reinfarction before the day-2 ECG.
The magnitude and extent of ST-segment elevation of abnormal leads were
measured from the qualifying ECG in the TIMI II Central ECG Laboratory.
Normalization of ST-segment elevation was assessed and defined as
return of ST segments to or close to baseline during infusion of rTPA.
Infarct site was classified from the qualifying ECG as either
anterior (ST-segment elevation of
0.1 mV in two or more
adjacent V1 to V6 leads)or
nonanterior.
The determination of nonQ-wave and Q-wave infarct ECG patterns was assessed in the TIMI II Central Exercise ECG Laboratory at St Louis University by analysis of the day-2 ECG. Measurements included Q-wave depth and duration, R-wave amplitude, S-wave depth, and degree of ST-segment displacement determined using a three-powercalibrated magnifying loupe. Averaged measurements were determined. Standard Minnesota Q-wave codes were generated using Q-wave width, depth, and Q-to-R ratio for the anterior (V1 to V5), inferior (II, III, and aVF), and lateral (I, aVL, and V6) lead groups, respectively ("Appendix").14
Patients were classified as having a Q-wave infarct if new Q-wave criteria were present on the day-2 ECG. The remaining patients were classified as having a nonQ-wave infarct. The day-2 ECG was obtained at a mean±1 SD of 24.5±49.6 hours and 24.2±33.0 hours after study entry for the Q-wave and nonQ-wave groups, respectively (P=.83).
At study entry, patients were defined as being "not low risk"
if
any of the following criteria were present: age
70 years,
anterior infarct location, rales involving
one third of the lung
fields, systemic hypotension with sinus tachycardia, atrial
fibrillation or flutter, pulmonary edema, or cardiogenic shock.
| Invasive Versus Conservative Postlytic Management Strategies |
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Before hospital discharge, radionuclide ventriculography (RVG) was performed at rest and during supine exercise to a heart rate of 120 beats per minute or to a maximum workload of 400 kilopound meter. The RVGs were analyzed at a central radionuclide core laboratory.13
| Cardiac Catheterization Analysis |
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60% of the
luminal diameter as assessed by visual and caliper-assisted methods. An
occluded infarct artery was defined by either TIMI 0 (no perfusion) or
TIMI 1 (penetration without perfusion) grade flow. A patent infarct
artery was defined by either TIMI 2 (partial perfusion) or TIMI 3
(complete perfusion) grade flow.15 | Clinical End Points |
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| Statistical Analysis |
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2 tests or Fisher's exact test for differences
in proportions of categorical variables and Student's t
test for differences in mean values of continuous variables. The
cumulative probability of events (eg, death, death or myocardial
infarction, fatal and nonfatal recurrent myocardial infarction) was
determined by the Kaplan-Meier method,16 and differences
in the distribution of events during the first year after study entry
were evaluated with the log-rank test.17 The effects of
treatment strategy on 42-day outcomes were compared between patients
with nonQ-wave versus Q-wave myocardial infarction using the
Breslow-Day test for the homogeneity of the odds ratio.18
To account for potential biases due to nonrandomly missing data,
outcomes on the hospital discharge resting RVGs were compared between
patient subgroups using a composite unfavorable end point of death by
14 days, failure to complete a study, or a study with abnormal findings
(ie, rest ejection fraction <55%). To account for the multiple
statistical hypothesis tested in this analysis, P values
<.01 were required to show evidence of a difference, and P
values <.001 showed strong evidence. | Results |
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Baseline Characteristics of Postlytic Q-Wave Versus NonQ-Wave
Infarction Groups
A greater percentage of the Q-wave patients were
male (85.3%
versus 75.6%; P<.001) and presented with ST-segment
elevation in the anterior leads (53.8% versus 43.7%,
P<.001, Table 1
). Atrial fibrillation or
flutter and the use of nitrates during the week before study entry were
more common among the nonQ-wave group (each P<.01). The
baseline mean diastolic blood pressure was slightly greater (2 mm Hg)
in the nonQ-wave group (P<.01). The mean±SD time
from
symptom onset to treatment with rTPA was 2.7±0.8 and 2.6±0.8
hours
for Q-wave and nonQ-wave patients, respectively
(P=.09).
Infusion of rTPA began less than 2 hours after symptom onset in 27.1%
of patients with nonQ-wave myocardial infarction and in 24.4% of
patients with Q-wave myocardial infarction (P=.14) (Table
1
).
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Qualifying ECG Findings
ECG indicators of infarct severity
were fewer and of less
magnitude in nonQ-wave patients compared with those who developed Q
waves: the mean number of leads with ST-segment elevation of
0.l mV
was 3.6 versus 4.2 leads (P<.001); the mean of the maximal
ST-segment elevation in any ECG lead was 0.33±0.22 versus
0.43±0.28
mV (P<.001); and the percentage of patients with
0.3 mV
of ST-segment elevation in any individual ECG lead was 41% versus
65%, respectively (P<.001). NonQ-wave patients were more
likely to have normalization of ST-segment elevation during the rTPA
infusion than the Q-wave group (37.3% versus 23.5%;
P<.001).
Cardiac Catheterization Findings
Among invasive strategy
patients receiving protocol
catheterization, the percentage of patients with two or more coronary
arteries with
60% diameter stenosis (27.5% versus 29.2%,
respectively, P=.27), the percentage of patients with
collateral blood flow to the infarct-related artery, and the mean
percent residual stenosis of the infarct-related artery were similar in
the nonQ-wave and Q-wave groups (Table 2
). TIMI grade
3 flow was more frequent in nonQ-wave patients
(P<.001).
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The circumflex coronary artery was more commonly
classified as the
infarct-related vessel in patients who evolved a nonQ-wave infarction
(20.6% versus 9.9%, P<.001; Table 2
). In a
multivariate
logistic model, both occlusion of the infarct artery (TIMI grade 0 or
I) and location of the infarct artery were significant
(P=.01) predictors of Q-wave versus nonQ-wave
myocardial
infarction. The odds ratio for Q-wave myocardial infarction was 1.6 for
an occluded versus a patent infarct artery; the odds ratio for Q-wave
myocardial infarction was 2.3 for an infarct in the right coronary
artery compared with the left circumflex artery, 2.5 for the left
anterior descending coronary artery compared with the left circumflex
artery, and 1.1 for the left anterior descending versus the right
coronary artery (P=NS).
Predischarge Rest and Exercise ECG and RVG
The mean resting
left ventricular ejection fraction was 56.4% and
48.6% for the nonQ-wave and Q-wave groups, respectively. A greater
percentage of patients evolving a nonQ-wave infarct had a left
ventricular ejection fraction >55% (43.4% versus 24.1%;
P=.001); severe left ventricular dysfunction (ie, ejection
fraction
35%) was approximately threefold higher (11.1% versus
3.0%) in Q-wave infarction patients (Table 3
).
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The
percentages of patients with an increase in exercise ejection
fraction
5% and without exercise-induced ST-segment depression were
similar in the two groups (Table 3
).
Clinical Outcome
The development of new congestive heart
failure by hospital
discharge occurred in a greater percentage of the Q-wave patients,
whereas in-hospital recurrent cardiac ischemic pain occurred in a
similar percentage of patients (Table 4
). A trend toward
more frequent reinfarction by 21 days (5.9% versus 4.0%), 42 days
(6.0% versus 4.6%), and 1 year (9.4% versus 7.4%) after study entry
was observed in the nonQ-wave compared with the Q-wave group
(P=.07). The odds ratio for reinfarction by 1 year was 1.3
(99% confidence interval [CI], 0.9 to 1.9). Fatal reinfarctions
occurred in 1.0% of both the nonQ-wave and Q-wave groups,
respectively.
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The cumulative 1-year mortality was 3.4% among
nonQ-wave
and 4.4% among Q-wave patients (P=.25). The 1-year
combined end point of death or reinfarction was also similar for the
two groups (P=.24; Figure
). The odds
ratio for 1-year mortality was 0.8 (99% CI, 0.4 to 1.4).
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To assess whether lack of sensitivity of ECGs for detection of posterior infarction could lead to bias in comparison of prognosis of nonQ-wave versus Q-wave infarction, we compared 1-year prevalence of events according to infarction type among invasive strategy patients after excluding patients with circumflex artery infarctions. One-year mortality (3.1% versus 3.8%), reinfarction (7.6% versus 7.3%), and death or reinfarction (9.3% versus 9.8%) for nonQ-wave versus Q-wave patients, respectively, were not significantly different.
Treatment Strategy
Approximately half of the patients in each
infarct group were
randomly assigned to either the invasive or conservative strategy
(Table 5
). Of the 1867 Q-wave patients, 929 and 938 were
randomly assigned to the invasive and conservative strategies,
respectively. Of the 767 nonQ-wave patients, 395 and 372 were
assigned to the invasive and conservative postlytic strategies.
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Invasive Strategy
By 42 days after study entry, a similar
percentage of Q-wave and
nonQ-wave infarct patients assigned to the invasive strategy
underwent revascularization (Table 5
). Protocol PTCA was
performed on
248 (62.8%) and 523 (56.3%) of nonQ-wave and Q-wave patients,
respectively. The protocol PTCA was considered partially or fully
successful in 237 (95.6%) and 473 (90.4%) of patients in whom it was
attempted, respectively. The occurrence of clinical complications
related to the protocol catheterization was similar for the two infarct
groups (P=.80).
Conservative Strategy
Among patients randomly assigned to the conservative strategy,
cardiac catheterization and revascularization were performed,
respectively, in 47.5% and 27.6% of nonQ-wave patients and in
51.8% and 24.3% of Q-wave patients by 42 days after study entry.
Among the 143 (38.4%) nonQ-wave and 373 (39.8%) Q-wave patients
undergoing cardiac catheterization before discharge, recurrent ischemic
pain (46.2% versus 42.6%), suspected reinfarction (5.6% versus
4.6%), and an abnormal exercise test (2.1% versus 2.9%) accounted
for the majority of reasons for cardiac catheterization.
Among conservative strategy patients not receiving catheterization during the initial hospitalization who completed a hospital discharge exercise test, 74 of 140 patients (52.8%) with a positive exercise test, 169 of 621 patients (27.2%) with a negative test, and 58 of 167 patients (37.7%) with an equivocal test had received cardiac catheterization by 42 days after study entry. The percentage of patients with a clearly positive or negative test receiving cardiac catheterization by 42 days was nearly identical for nonQ-wave and Q-wave patients; among patients with an equivocal test, a slightly higher percentage of Q-wave patients (38.8%) than nonQ-wave patients (23.9%) received cardiac catheterization.
Clinical Outcome
Within 42 days of study entry, the
occurrence of death
(P=.76), fatal or nonfatal reinfarction
(P=.81),
or death or reinfarction (P=.43) was similar in the
invasively and conservatively treated patients regardless of Q-wave or
nonQ-wave infarct type (Table 5
). Subgroup analyses did
not indicate
evidence for differences in the effect of treatment strategy in
Q-wave versus nonQ-wave patients in either the low-risk or
not-low-risk patient groups.
| Discussion |
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In TIMI II, 29.1% of the 2632 patients with a first myocardial infarction who were eligible for this analysis and presented with ST-segment elevation were classified as evolving a nonQ-wave infarct pattern within 24 hours of treatment with intravenous rTPA. Similar findings have recently been observed in another large thrombolytic trial enrolling patients with ST-segment elevation.19 In TIMI II, nonQ-wave infarction was more frequently associated with circumflex artery occlusions, more brisk perfusion of the infarct-related vessel, enhanced predischarge left ventricular function, and a lower frequency of developing new congestive heart failure during the index hospitalization.
Clinical Outcome of Q-Wave and NonQ-Wave Infarct Types After
Thrombolysis: Infarct Size
In the TIMI II study, nonQ-wave
infarct patients were more
frequently observed to have resolution of ST-segment elevation during
rTPA infusion, suggesting successful infarct artery
reperfusion.20 The greater percentage of nonQ-wave
patients observed to have TIMI grade 3 flow of the infarct-related
vessel may have in part contributed to the observed differences in left
ventricular function and the lower prevalence of new congestive heart
failure occurring during hospitalization in postlytic nonQ-wave
infarct patients, supporting earlier studies.21 22
Alternatively, the greater preservation of postinfarct left ventricular
function among nonQ-wave patients may be in part attributable to a
smaller initial ischemic myocardial burden, as reflected by the finding
of fewer ECG leads with ST-segment elevation and more frequent
circumflex artery infarcts.
Reinfarction and Mortality
A trend was present
(P=.07) toward slightly more
frequent recurrent myocardial infarctions in nonQ-wave compared with
Q-wave patients during the year after study entry. Mortality rates were
low at both 21 days and 1 year after study entry and were similar for
the two infarct groups. These findings are in contrast to
prethrombolytic studies23 24 25 and a
recent report from the
TPA/SK Mortality investigators.19 The latter study group
have made a preliminary report of a significantly higher 6-month
frequency of postdischarge reinfarction (6.2% versus 3.6%; odds ratio
[95% CI], 1.8 [1.22 to 2.66]) and mortality (4.6% versus
3.5%)
among patients evolving a postlytic nonQ-wave compared with Q-wave
myocardial infarction. The higher event rate in TIMI II compared with
the TPA/SK report for Q-wave and nonQ-wave patients may be accounted
for by (1) differences in reporting (ie, this report includes all
events after the day-2 ECG, whereas the TPA/SK report includes only the
lower-risk period after hospital discharge); (2) exclusion of patients
with prior myocardial infarction, enhancing the ability to detect new
Q-wave versus nonQ-wave items on the surface ECG; and (3) differences
in postlytic treatment strategies (ie, greater use of coronary
revascularization and the use of adjunctive intravenous heparin) in the
TIMI II study. The TIMI II study had limited power to detect modest
differences in mortality and reinfarction rates according to infarct
type, and the odds ratios in this report do not exclude risks for death
or reinfarction similar to those in the TPA/SK study among the
nonQ-wave patients.
Comparison of Postlytic Management Strategies Among the Q-Wave and
NonQ-Wave Infarct Groups
In TIMI II, approximately half of the
patients who evolved a
postlytic nonQ-wave and Q-wave infarction were randomly assigned to
an invasive or a conservative postinfarct strategy. Within 42 days of
study entry, the occurrence of fatal and nonfatal reinfarction, death,
and combined death and reinfarction were similar for patients assigned
to the invasive or conservative strategy, regardless of the
infarct type (ie, Q wave or nonQ wave).
The nonQ-wave and
Q-wave patients in the conservative strategy group
who experienced spontaneous or exercise-induced ischemia received
coronary angiography and underwent coronary revascularization if
technically feasible by study design, potentially reducing event rates
in these TIMI II patients. The findings from this secondary
analysis are consistent with the overall results of the TIMI II
trial13 and demonstrate that patients with a first acute
myocardial infarction who evolve either a nonQ-wave or a Q-wave
myocardial infarction after early (ie,
4 hours) intravenous
thrombolysis experience a comparable clinical outcome and suggest
satisfactory clinical outcomes whether managed by either an invasive or
a conservative postlytic strategy.
The TIMI II data are further supported by the recently completed TIMI IIIB study,26 which reported similar 42-day rates of reinfarction and combined death and reinfarction in patients with unstable angina or nonQ-wave myocardial infarction regardless of whether an invasive or a conservative strategy was used. In TIMI IIIB, most patients presented with ST-segment depression or T-wave inversion; in TIMI II, all enrolled patients were required to exhibit ST-segment elevation on the qualifying ECG. Additional studies that assess postlytic revascularization strategies in larger series of nonQ-wave patients who present with ST-segment elevation would be important to confirm our observations.
Study Limitations
The exclusion of very elderly patients
(>76 years), patients with
prior myocardial infarction, and patients dying or developing
reinfarction within the initial 24 hours after thrombolysis limits this
secondary analysis to a relatively low-risk patient population. In
the overall TIMI II study of 3339 patients, the mortality rate was
1.9% within the initial 18 hours of study enrollment.27
Thus, high-risk patients who died before the acquisition of the day-2
ECG were not included for comparison in this analysis.
The ECG criteria for diagnosis of nonQ-wave and Q-wave myocardial infarction are not standardized. The prognostically established Minnesota code criteria were used in TIMI II, in contrast to some of the earlier studies of nonQ-wave and Q-wave infarction.3 19 23 24 25 28 The time of ECG classification of nonQ-wave and Q-wave myocardial infarction has also varied in previous studies, with most classifications performed at hospital discharge.29 In the present report, categorization of infarct type was based on the day-2 ECG since this is the time frame physicians use most frequently to make clinical decisions concerning cardiac catheterization in stable patients. Eisenberg et al30 report progression of nonQ-wave to Q-wave infarction in only 1.5% of patients treated with thrombolytic therapy from 24 hours to hospital discharge. Thus, the potential for overestimating the percentage of nonQ-wave myocardial infarctions in the present study is small.
Conclusions
The findings from this secondary TIMI II analysis
indicate ECG, angiographic, and clinical outcome differences among
patients with a first acute myocardial infarction evolving early
nonQ-wave or Q-wave myocardial infarction. However, early (ie,
21-day) and 1-year mortality and reinfarction rates were similar for
the two infarct groups. The occurrence of combined death and
reinfarction by 42 days was similar in both infarct groups
receiving an invasive or a conservative postlytic treatment
strategy as used in the TIMI II trial. A longer-term follow-up will be
necessary to confirm these early observations between the two infarct
groups given the differences in left ventricular function and
congestive heart failure.
| Acknowledgments |
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| Footnotes |
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Guest editor for this article was J. David Bristow, MD, Oregon Health Sciences University, Portland.
1 Investigators and participating centers are listed in
N Engl J Med. 1989;320:618-627. ![]()
Minnesota Q-Wave Code Criteria
Anterolateral Site
(Leads I, aVL, and V6)
1-1-1 Q/R amplitude ratio
1/3,
plus Q duration
0.03
second in lead I or V6.
1-1-2 Q duration
0.04 second in
lead I or V6.
1-1-3 Q duration
0.04 second, plus R
amplitude
3 mm in lead
aVL.
1-2-1 Q/R amplitude ratio
1/3, plus Q-wave duration
0.02
second and <0.03 second in lead I or V6.
1-2-2 Q duration
0.03 second and <0.04 second in lead
I or V6.
1-2-3 QS pattern in lead I.
1-2-8 Initial R amplitude decreasing to 2 mm or less in every beat between V5 and V6. (All beats in lead V5 must have an initial R >2 mm.)
1-3-1 Q/R amplitude
ratio
1/5 and <1/3, plus Q duration
0.02 second and <0.03 second in lead I or V6.
1-3-3 Q
duration
0.03 second and <0.04 second, plus R
amplitude
3 mm in lead aVL.
Inferior Site (Leads II,
III, and aVF)
1-1-1 Q/R amplitude ratio
1/3, plus Q duration
0.03
second in lead II.
1-1-2 Q duration
0.04 second in lead II.
1-1-4 Q duration
0.05 second in lead III, plus a Q-wave
amplitude
1.0 mm in the majority of beats in lead aVF.
1-1-5 Q
duration
0.05 second in lead aVF.
1-2-1 Q/R amplitude ratio
1/3, plus Q duration
0.02 second
and <0.03 second in lead II.
1-2-2 Q duration
0.03 second and
<0.04 second in lead
II.
1-2-3 QS pattern in lead II.
1-2-4 Q duration
0.04
second and <0.05 second in lead III,
plus a Q-wave
1.0 mm amplitude in the majority of beats in aVF.
1-2-5 Q duration
0.04 second and <0.03 second in lead
aVF.
1-2-6 Q amplitude
5.0 mm in lead III or aVF.
1-3-1 Q/R
amplitude ratio
1/5 and <1/3, plus Q duration
0.02 second and <0.03 second in lead II.
1-3-4 Q duration
0.03 second and <0.04 second in lead III,
plus a Q-wave
1.0 mm amplitude in the majority of beats in lead
aVF.
1-3-5 Q duration
0.03 second and <0.04 second in lead
aVF.
1-3-6 QS pattern in each of leads III and aVF.
Anterior Site (Leads V1, V2,
V3, V4, and V5)
1-1-1 Q/R amplitude
ratio
1/3 plus Q duration
0.03 second
in any of leads V2, V3,
V4, V5.
1-1-2 Q duration
0.04 second in any
of leads
V1, V2, V3,
V4, V5.
1-1-6 QS pattern when initial R-wave is present in adjacent lead to the right on the chest, in any of leads V2, V3, V4, V5, V6.
1-1-7 QS pattern in all of leads V1-V4 or V1-V5.
1-2-1 Q/R amplitude ratio
1/3, plus
Q duration
0.02 second
and <0.03 second, in any of leads V2,
V3, V4, V5.
1-2-2 Q duration
0.03
second and <0.04 second in any of
leads V2, V3,
V4, V5.
1-2-7 QS pattern in all of leads V1, V2, and V3.
1-2-8 Initial R amplitude decreasing to 2.0 mm or less in every beat between any of leads V2 and V3, V3 and V4, or V4 and V5. (All beats in the lead immediately to the right on the chest must have an initial R >2 mm.)
1-3-1 Q/R amplitude ratio
1/5 and <1/3 plus Q duration
0.02 second and <0.03 second in any of leads V2,
V3, V4, V5.
1-3-2 QS pattern in lead V1 and V2.
Received June 13, 1994; revision received November 22, 1994; accepted December 3, 1994.
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