Electrocardiographic Diagnosis of Evolving Acute Myocardial Infarction in the Presence of Left Bundle-Branch Block
Elena B. Sgarbossa, M.D., Sergio L. Pinski, M.D., Alejandro Barbagelata, M.D., Donald A. Underwood, M.D., Kathy B. Gates, Eric J. Topol, M.D., Robert M. Califf, M.D., Galen S. Wagner, M.D., The GUSTO-1 (Global Utilization of Streptokinase and, for Tissue Plasminogen Activator for Occluded Coronary Arteries) Investigators
Background The presence of left bundle-branch block on the electrocardiogrammay conceal the changes of acute myocardial infarction, whichcan delay both its recognition and treatment. We tested electrocardiographiccriteria for the diagnosis of acute infarction in the presenceof left bundle-branch block.
Methods The base-line electrocardiograms of patients enrolledin the GUSTO-1 (Global Utilization of Streptokinase and TissuePlasminogen Activator for Occluded Coronary Arteries) trialwho had left bundle-branch block and acute myocardial infarctionconfirmed by enzyme studies were blindly compared with the electrocardiogramsof control patients who had chronic coronary artery diseaseand left bundle-branch block. The electrocardiographic criteriafor the diagnosis of infarction were then tested in an independentsample of patients presenting with acute chest pain and leftbundle-branch block.
Results Of 26,003 North American patients, 131 (0.5 percent)with acute myocardial infarction had left bundle-branch block.The three electrocardiographic criteria with independent valuein the diagnosis of acute infarction in these patients wereST-segment elevation of 1 mm or more that was concordant with(in the same direction as) the QRS complex; ST-segment depressionof 1 mm or more in lead V1, V2, or V3; and ST-segment elevationof 5 mm or more that was discordant with (in the opposite directionfrom) the QRS complex. We used these three criteria to developa scoring system (0 to 5), which allowed a highly specific diagnosisof acute myocardial infarction to be made.
Conclusions We developed and validated a clinical predictionrule based on a set of electrocardiographic criteria for thediagnosis of acute myocardial infarction in patients with chestpain and left bundle-branch block. The use of these criteria,which are based on simple ST-segment changes, may help identifypatients with acute myocardial infarction, who can then receiveappropriate treatment.
The optimal use of coronary reperfusion therapies relies ona rapid diagnosis of evolving myocardial infarction.1,2 Formost patients presenting with cardiac chest pain, the electrocardiogramis a powerful aid in diagnosing the cause of the pain and selectingthe appropriate therapy.2 In patients who present with concomitantleft bundle-branch block, however, the electrocardiographicmanifestations of acute myocardial injury may be masked. Duringthe past five decades, several electrocardiographic signs havebeen proposed to aid in the diagnosis of infarction in suchpatients, but because of methodologic limitations,3,4,5,6,7,8,9none of these signs have gained widespread acceptance. Manyphysicians believe that acute myocardial injury cannot be detectedaccurately in patients with left bundle-branch block.10 We examinedthe value of the standard electrocardiogram for the diagnosisof acute myocardial infarction in the presence of left bundle-branchblock in a large population of patients.
Methods
Derivation Sample
Criteria for the diagnosis of acute myocardial infarction inthe presence of left bundle-branch block were developed fromtwo populations (the study and control groups), which constitutedthe derivation sample. The study group consisted of the subgroupof North American patients enrolled in the GUSTO-1 (Global Utilizationof Streptokinase and Tissue Plasminogen Activator for OccludedCoronary Arteries) trial11 who had acute myocardial infarctiondocumented by serum enzyme changes and evidence of completeleft bundle-branch block on their base-line electrocardiograms.The control group was assembled by randomly selecting from theDuke Databank for Cardiovascular Disease an equal number ofpatients with stable, angiographically documented coronary arterydisease and complete left bundle-branch block.12 The patientsin the control group did not have acute chest pain at the timeof the electrocardiographic recording.
Electrocardiograms were digitally obtained at 100 Hz with aspeed of 25 mm per second and an amplification of 10 mm permillivolt.
Definition of Left Bundle-Branch Block
The normal sequence of ventricular activation (depolarizationand repolarization) can be altered by both left bundle-branchblock and acute myocardial injury. To achieve a reasonable compromisebetween the electrocardiographic changes inherent in the twoconditions,13 we used the following definition of left bundle-branchblock: a QRS duration of at least 0.125 second in the presenceof sinus or supraventricular rhythm, a QS or rS complex in leadV1, and an R-wave peak time of at least 0.06 second in leadI, V5, or V6 associated with the absence of a Q wave in thesame lead.7,14,15,16 Patients with electrocardiograms showingintermittent left bundle-branch block were excluded from thestudy.
Interpretation of Electrocardiograms
All the electrocardiograms were analyzed for signs of myocardialinjury by one of four investigators who were unaware of boththe patient's identity and the clinical variables. The signsexamined3,4,5,6,7,8,9,16,17,18,19,20 are shown in Table 1. TheST-segment deviation was measured at the J point. To assessinterobserver variability, a random sample of 10 percent ofthe electrocardiograms were read by all four investigators.
Table 1. Electrocardiographic Criteria Analyzed in Patients with Left Bundle-Branch Block.
Statistical Analysis
Interobserver agreement, as estimated with the kappa statistic,was greater than 0.85 for both QRS-complex and T-wave polarities.For both the terminal S wave in leads V5 and V6 and notchingof at least 0.05 second of the S wave in lead V3, the agreementwas 0.77, but it was low (<0.55) for lead V4, as well asfor notching of at least 0.05 second of the R wave in lead I,aVL, V5, or V6. Measurements of ST-segment deviations were closelycorrelated among the four investigators (r>0.9 for all comparisons,by Pearson's correlation coefficient).
All electrocardiographic criteria were screened by univariateanalysis (chi-square tests) to identify those associated withacute myocardial infarction. For ST-segment elevations, thereceiver-operating-characteristic curves were constructed toevaluate the diagnostic performance of different combinationsof the degree of elevation and number of leads exhibiting suchelevation. Because a high specificity is desirable for the diagnosisof acute myocardial infarction,21,22 we determined prospectivelythat the optimal cutoff point would correspond to the most sensitivedegree of ST-segment elevation that had a specificity of atleast 90 percent. Criteria for which the interobserver agreementwas at least 0.7 and the univariate analysis showed statisticalsignificance (P<0.1) were included in a stepwise logistic-regressionmodel to identify independent criteria that were significantpredictors of acute infarction (P<0.05). A scoring systemfor the diagnosis of infarction was developed from the coefficientsassigned by the logistic model for each independent criterion,on a scale of 0 to 5. Receiver-operating-characteristic curves,kappa statistics, and correlation coefficients were estimatedwith True Epistat software.23 Chi-square tests and logistic-regressionanalyses were performed with Egret software.24
The diagnostic performance of the model was then tested in anindependent population of 45 patients with left bundle-branchblock, acute chest pain, and a high likelihood of coronary arterydisease (the validation sample). Included in this sample werepatients in the GUSTO-1 registry and the GUSTO-2A (Global Useof Strategies to Open Occluded Coronary Arteries) study andthe patients from GUSTO-1 subsequently found to have normalcreatine kinase MB values.
Results
Of the base-line electrocardiograms from the 26,003 North Americanpatients, 145 met the criteria for left bundle-branch block.The diagnosis of acute myocardial infarction was confirmed bystudies showing elevated creatine kinase MB levels in 131 ofthe patients. The electrocardiograms from these 131 patientswere analyzed for the presence of the aforementioned diagnosticcriteria. Selected base-line characteristics of the patientswith acute myocardial infarction and the control patients areshown in Table 2.
Table 2. Selected Characteristics of Patients with Left Bundle-Branch Block.
Univariate Analysis
On the basis of the receiver-operating-characteristic curves,the maximal sensitivity with the target specificity (>90percent) was achieved when at least one lead exhibited ST-segmentelevation of at least 1 mm that was concordant with (in thesame direction as) the QRS complex or at least 5 mm that wasdiscordant with (in the opposite direction from) the QRS complex.
Electrocardiographic criteria with statistical significancefor the diagnosis of acute myocardial infarction and their sensitivities,specificities, and likelihood ratios are listed in Table 3.The likelihood ratios indicate to what extent a particular criterionwill increase or decrease the probability of infarction. Theelectrocardiographic criterion with the highest likelihood ratiowas ST-segment elevation of at least 1 mm in leads with a QRScomplex in the same direction. Similarly, the absence of thiscriterion was associated with the lowest likelihood ratio.
Table 3. Results of the Univariate Analysis of Electrocardiographic Criteria.
Multivariate Analysis and Index Scores for the Independent Electrocardiographic Criteria
All five electrocardiographic criteria associated with acuteinfarction in the presence of left bundle-branch block wereincluded in a stepwise multiple logistic-regression model alongwith the variable "previous myocardial infarction." The modelidentified three independent predictors of acute myocardialinfarction (Table 4 and Figure 1). Figure 2 shows the predictedprobability of infarction for each combination of criteria.A more accurate estimate of the probability of infarction canbe obtained when the weight of each criterion, as determinedby the logistic model, is used to develop a simple index score(Table 4).
Figure 1. Electrocardiogram Meeting All Three Independent Criteria for the Diagnosis of Acute Myocardial Infarction in a Patient from the GUSTO Trial with left bundle-Branch Block.The electrocardiogram shows ST-segment elevation of at least 1 mm that is concordant with the QRS complex (lead II), ST-segment depression of at least 1 mm in leads V2 and V3, and ST-segment elevation of at least 5 mm that is discordant with the QRS complex (leads III and aVF).
Figure 2. Flow Chart for the Prediction of Acute Myocardial Infarction in the Presence of Left Bundle-Branch Block, with the Use of All Possible Combinations of the Three Independent Electrocardiographic Criteria.
The discriminatory power of each combination of criteria for the diagnosis of acute myocardial infarction is indicated by the total score at the bottom, with higher scores indicating better discriminatory power. LBBB denotes left bundle-branch block, and MI myocardial infarction.
The operating characteristics of the scoring system for theindependent criteria provide a high discriminative power forthe diagnosis of infarction (area under the curve, 0.874) (Figure 3).for an accurate diagnosis, a specificity of 90 percent requiresa minimal total score of 3. Patients presenting with ST-segmentelevation of at least 5 mm in leads with a QRS complex in theopposite direction (score, 2) should therefore probably undergofurther testing.
Figure 3. Receiver-Operating-Characteristic Curve for the Combined Score for the Three Independent Electrocardiographic Criteria.
The zone to the left of the broken line indicates a high probability of acute myocardial infarction. The numbers along the curve are scores.
Testing of the Electrocardiographic Criteria in the Validation Sample
The criteria derived from the model and their index scores weretested in the validation sample, which included 22 patientswith enzymatic evidence of acute necrosis and 23 with only unstableangina (the control group). As compared with the results inthe derivation sample, the operating characteristics of thescoring system for the three criteria combined had a lower discriminativepower for the diagnosis of infarction (area under the curve,0.7). The sensitivities, specificities, likelihood ratios, andpredictive values of the criteria (for an index score >3)in both samples are shown in Table 5.
Table 5. Predictive Value of Criteria with an Index Score of at Least 3 in the Derivation and Validation Samples.
Discussion
With the advent of effective reperfusion therapies, a rapidand accurate diagnosis of acute myocardial infarction has becomeessential.22,25 Thrombolytic agents are most beneficial whenadministered promptly, and their erroneous use in patients withunstable angina or noncardiac chest pain is potentially dangerous.11,26,27Algorithms and predictive models developed to identify patientswith ongoing myocardial ischemia or infarction28,29,30,31,32,33,34do not apply to patients with left bundle-branch block. Thenew appearance of bundle-branch block in a patient with acutechest pain is highly suggestive of infarction, and ischemicchanges superimposed on a pattern of chronic left bundle-branchblock are easy to recognize when a previous electrocardiogramis available for comparison. The timely availability of a previouselectrocardiogram, however, is the exception rather than therule. Physicians usually must decide to administer appropriatetreatment or perform further testing on the basis of only themost recent electrocardiographic information. Our study suggeststhat in patients with left bundle-branch block, an examinationof the electrocardiogram obtained at the time of presentationallows a diagnosis of acute myocardial infarction to be madewith a high degree of confidence.
We found that ST-segment deviation was the only electrocardiographicfinding that was useful in the diagnosis of acute myocardialinfarction in the presence of left bundle-branch block. Previouslyproposed electrocardiographic signs involving the QRS complexwere not useful. These discrepancies may be due to the factthat we analyzed electrocardiograms obtained on admission, thusdetecting changes in the ST-segment (an early manifestationof acute coronary occlusion) rather than changes in the QRScomplex (which indicate necrosis). Furthermore, the GUSTO-1trial included patients with acute myocardial infarction, whereasprevious studies of patients with left bundle-branch block havenot always differentiated between acute and chronic infarction.6,7,8
Uncomplicated left bundle-branch block is characterized by secondaryrepolarization changes in a direction opposite that of the mainQRS deflection.9 In leads with a predominantly negative QRScomplex, the result is an electrocardiographic pattern of ST-segmentelevation with positive T waves, which is similar to the currentof injury observed during acute coronary occlusion. Studiesof patients with left bundle-branch block that examined serialelectrocardiographic changes during either acute myocardialinfarction35,36,37 or occlusion of a coronary artery by an angioplastyballoon38,39 have shown that further ST-segment elevation occursin those leads.
Our challenge was to determine the cutoff point for the ST-segmentelevation that would most effectively discriminate between patientswith acute myocardial infarction and those without infarction,in the absence of information from previous or serial electrocardiographictracings. We found that for leads with a predominantly negativeQRS complex, ST-segment elevation of at least 5 mm identifiedpatients with evolving infarction. On the other hand, ST-segmentelevation in the same direction as that of the QRS complex isnot expected in patients with uncomplicated left bundle-branchblock. We found that any degree of ST-segment elevation in alead with a positive QRS complex was a highly specific signof acute myocardial infarction. Likewise, ST-segment depressionin lead V1, V2, or V3 should not be present in patients withuncomplicated left bundle-branch block, since the QRS complexis predominantly negative in those leads. In our study, ST-segmentdepression in lead V1, V2, or V3 was also an independent markerof acute myocardial infarction. The mechanism for this findingis unclear; it could be a manifestation of true posterior-wallinfarcts (i.e., due to occlusion of the left circumflex artery)40or infarcts associated with ST-segment depression (subendocardialinfarcts).41
The presence of left bundle-branch block in patients with acutemyocardial infarction is associated with an increased risk ofcomplications and death.42 When it is new, left bundle-branchblock is correlated with the occlusion of the proximal leftanterior descending artery and a large amount of jeopardizedmyocardium.43 On the other hand, a prior left bundle-branchblock is a powerful marker of depressed left ventricular systolicfunction,44,45 and any additional loss of myocardium is likelyto result in cardiogenic shock. It is therefore not surprisingthat subgroup analyses in trials of thrombolytic therapy showa benefit of treatment in patients with bundle-branch block.46The Fibrinolytic Therapy Trialists' Collaborative Group analyzedthe results of nine randomized studies and reported a dramatic25 percent decrease in mortality at 35 days among 2032 patientswith right or left bundle-branch block treated with thrombolysis.26
The relatively small number of patients with left bundle-branchblock enrolled in these trials, however, attests to the prevailingdiagnostic uncertainty. The National Registry of MyocardialInfarction has reported that patients with nondiagnostic electrocardiograms(a category that presumably included those with left bundle-branchblock) were less likely to receive thrombolytic therapy thanpatients with diagnostic electrocardiograms.47 In the comprehensiveGUSTO-1 registry of 637 patients hospitalized for acute myocardialinfarction, 219 (34 percent) did not receive thrombolytic therapybecause their electrocardiograms were considered nondiagnostic.Left bundle-branch block was present in 20 of these patientsand was thus responsible for 9 percent of the electrocardiogram-basedexclusions (unpublished observations). In a study that did notinvolve thrombolytic therapy, the prevalence of left bundle-branchblock among patients with acute chest pain was approximately10 percent,48 which is similar to the prevalence before thrombolytictherapy was available.8
ST-segment elevation of at least 1 mm that is concordant withthe QRS complex or ST-segment depression of at least 1 mm inlead V1, V2, or V3 is a specific marker of infarction, evenwhen no other electrocardiographic change is observed. On theother hand, the sole presence of ST-segment elevation of atleast 5 mm that is discordant with the QRS complex (with a scoreof 2) indicates a moderate-to-high probability of myocardialinfarction, and further procedures should be undertaken to confirmthe diagnosis.
The index score correctly classified 84 percent of the patientsin the derivation sample but only 67 percent of the patientsin the validation sample. A poorer performance of diagnosticcriteria in the validation sample is not unexpected49 and inour study is related to the relatively low sensitivity of thecriteria. One reason for the decreased sensitivity is the differencein the two patient populations. Analysis of data from the GUSTO-1sample (the source of the derivation sample) yielded inflatedsensitivities, because the study included only patients withelectrocardiographic signs of acute myocardial infarction, whereasthe GUSTO-2A sample and the GUSTO-1 registry (the sources ofmost of the patients in the validation sample) included patientswith other ischemic syndromes as well.13
It should be noted that the sensitivity of each individual electrocardiographiccriterion in our study is also low but is similar to the sensitivityof ST-segment changes in patients with normal intraventricularconduction.25,39 Our purpose was to improve the identificationof patients with acute infarction, because they may benefitfrom thrombolytic therapy; to this end, a high specificity (ratherthan a high sensitivity) is required.21 The high specificityof our index score in the validation sample (96 percent) mayhave a medicolegal benefit.50 Electrocardiograms that are misreador considered nondiagnostic may result in a failure to diagnoseinfarction,51,52 and claims of a missed infarction account fora substantial proportion of malpractice claims involving emergencydepartments.51 Highly specific criteria may help physiciansrapidly diagnose and treat acute infarction in patients withleft bundle-branch block.
There are several potential limitations of our study. We didnot attempt to distinguish between previous and newly developedleft bundle-branch block, since this information was not availablein the GUSTO-1 study. The absence of such a distinction is probablytypical of clinical practice, since patients rarely presentto the emergency department with their previous electrocardiograms.It should nonetheless be noted that the effects of the conductiondefect on repolarization are not expected to vary over time;our proposed ST-segment criteria probably apply to both oldand new left bundle-branch block.40,41
Because the GUSTO-1 sample did not include a large group ofpatients with chest pain, left bundle-branch block, and normalcreatine kinase MB values, we used controls without evidenceof acute coronary events. This could have resulted in an increasedspecificity of the electrocardiographic signs of infarction.13
The high interobserver agreement with respect to our ST-segmentmeasurements may be due to the fact that all the investigatorswho evaluated the electrocardiograms are cardiologists. Theinterpretive accuracy may be poorer among general practitioners,emergency department physicians, or paramedics.25 Our criteria,however, rely on the identification of signs that can be interpretedby computerized electrocardiographic algorithms,31 and it shouldbe feasible to incorporate the signs into these algorithms,ensuring an accurate interpretation even in the nonhospitalsetting.
Although the diagnostic criteria were tested in patients presentingto the emergency room with both left bundle-branch block andchest pain, our validation sample may not have been sufficientlylarge. The criteria derived from our model should be validatedprospectively in a larger cohort, and the effect of the criteriaon patient care should also be examined. Meanwhile, the systematicuse of these highly specific electrocardiographic signs of acutemyocardial infarction in patients with chest pain and left bundle-branchblock should facilitate timely intervention, particularly withthrombolytic therapy.
Supported by grants from Bayer, Genentech, CIBACorning,ICI Pharmaceuticals, and Sanofi Pharmaceuticals.
Source Information
From the Cleveland Clinic Foundation, Cleveland (E.B.S., S.L.P., D.A.U., E.J.T.); the Fundación Favaloro, Buenos Aires, Argentina (A.B.); and Duke University Medical Center, Durham, N.C. (K.B.G., R.M.C., G.S.W.).
Address reprint requests to Dr. Sgarbossa at the Department of Cardiology, Desk M-24, Cleveland Clinic Foundation, Cleveland, OH 44195.
References
Kleiman NS, White HD, Ohman EM, et al. Mortality within 24 hours of thrombolysis for myocardial infarction: the importance of early reperfusion. Circulation 1994;90:2658-2665. [Free Full Text]
Muller DW, Topol EJ. Selection of patients with acute myocardial infarction for thrombolytic therapy. Ann Intern Med 1990;113:949-960.
Cabrera E, Friedland C. La onda de activación ventricular en el bloqueo de rama izquierda con infarto: un nuevo signo electrocardiográfico. Arch Inst Cardiol Mex 1953;23:441-460. [Medline]
Besoaín-Santander M, Gómez-Ebensperguer G. Electrocardiographic diagnosis of myocardial infarction in cases of complete left bundle branch block. Am Heart J 1960;60:886-897. [CrossRef]
Doucet P, Walsh TJ, Massie E. A vectorcardiographic and electrocardiographic study of left bundle branch block with myocardial infarction. Am J Cardiol 1966;17:171-179. [CrossRef][Medline]
Weiner R, Makam S, Gooch AS. Identification of myocardial infarction in the presence of left bundle-branch block: correlation of electrocardiography, vectorcardiography, and angiography. J Am Osteopath Assoc 1983;83:119-124. [Medline]
Wackers FJ. The diagnosis of myocardial infarction in the presence of left bundle branch block. Cardiol Clin 1987;5:393-401. [Medline]
Hands ME, Cook EF, Stone PH, et al. Electrocardiographic diagnosis of myocardial infarction in the presence of complete left bundle branch block. Am Heart J 1988;116:23-31. [CrossRef][Medline]
Schamroth L. Myocardial infarction associated with left bundle branch block. In: Schamroth L, ed. The 12 lead electrocardiogram. I. Cambridge, Mass.: Blackwell Scientific, 1989:193-201.
Schweitzer P. The electrocardiographic diagnosis of acute myocardial infarction in the thrombolytic era. Am Heart J 1990;119:642-654. [CrossRef][Medline]
The GUSTO Investigators. An international randomized trial comparing four thrombolytic strategies for acute myocardial infarction. N Engl J Med 1993;329:673-682. [Free Full Text]
Pryor DB, Califf RM, Harrell FE Jr, et al. Clinical data bases: accomplishments and unrealized potential. Med Care 1985;23:623-647. [CrossRef][Medline]
Ransohoff DF, Feinstein AR. Problems of spectrum and bias in evaluating the efficacy of diagnostic tests. N Engl J Med 1978;299:926-930. [Abstract]
Willems JL, de Medina EOR, Bernard R, et al. Criteria for intraventricular conduction disturbances and pre-excitation. J Am Coll Cardiol 1985;5:1261-1275. [Abstract]
Hindman NB, Schocken DD, Widmann M, et al. Evaluation of a QRS scoring system for estimating myocardial infarct size. V. Specificity and method of application of the complete system. Am J Cardiol 1985;55:1485-1490. [CrossRef][Medline]
Moia B, Acevedo HJ. El diagnóstico electrocardiográfico del infarto de miocardio complicado por bloqueo de rama. Rev Argent Cardiol 1945;11:341-58.
Pantridge JF. Observations on the electrocardiogram and ventricular gradient in complete left bundle branch block. Circulation 1951;3:589-599. [Abstract]
Flowers NC. Left bundle branch block: a continuously evolving concept. J Am Coll Cardiol 1987;9:684-697. [Abstract]
Chapman MG, Pearce ML. Electrocardiographic diagnosis of myocardial infarction in the presence of left bundle-branch block. Circulation 1957;16:558-571. [Medline]
Califf RM, Ohman EM. The diagnosis of acute myocardial infarction. Chest 1992;101:Suppl:106S-115S. [Free Full Text]
Lee TH, Weisberg MC, Brand DA, Rouan GW, Goldman L. Candidates for thrombolysis among emergency room patients with acute chest pain: potential true- and false-positive rates. Ann Intern Med 1989;110:957-962.
Gustafson T. True Epistat reference manual, version 5.0. Richardson, Tex.: Epistat Services, 1994.
EGRET reference manual. Seattle: Statistics and Epidemiological Research Corporation, 1990.
Bren GB, Wasserman AG, Ross AM. The electrocardiogram in patients undergoing thrombolysis for myocardial infarction. Circulation 1987;76:Suppl II:II-18.
Fibrinolytic Therapy Trialists' (FTT) Collaborative Group. Indications for fibrinolytic therapy in suspected acute myocardial infarction: collaborative overview of early mortality and major morbidity results from all randomised trials of more than 1000 patients. Lancet 1994;343:311-322. [Erratum, Lancet 1994;343:742.] [CrossRef][Medline]
Ohman EM, Sigmon KN, Califf RM. Is diagnostic certainty essential for the use of thrombolytic therapy during myocardial infarction in the 1990s? Circulation 1990;82:1073-1075. [Free Full Text]
Schor S, Behar S, Modan B, Barell V, Drory J, Kariv I. Disposition of presumed coronary patients from an emergency room: a follow-up study. JAMA 1976;236:941-943. [Abstract]
Pozen MW, D'Agostino RB, Selker HP, Sytkowski PA, Hood WB Jr. A predictive instrument to improve coronary-care-unit admission practices in acute ischemic heart disease: a prospective multicenter clinical trial. N Engl J Med 1984;310:1273-1278. [Abstract]
Kudenchuk PJ, Ho MT, Weaver WD, et al. Accuracy of computer-interpreted electrocardiography in selecting patients for thrombolytic therapy. J Am Coll Cardiol 1991;17:1486-1491. [Abstract]
Tierney WM, Roth BJ, Psaty B, et al. Predictors of myocardial infarction in emergency room patients. Crit Care Med 1985;13:526-531. [Medline]
Lee TH, Juarez G, Cook EF. Ruling out acute myocardial infarction: a prospective multicenter validation of a 12-hour strategy for patients at low risk. N Engl J Med 1991;324:1239-1246. [Abstract]
Puleo PR, Meyer D, Wathen C, et al. Use of a rapid assay of subforms of creatine kinase MB to diagnose or rule out acute myocardial infarction. N Engl J Med 1994;331:561-566. [Free Full Text]
Rude RE, Poole WK, Muller JE, et al. Electrocardiographic and clinical criteria for recognition of acute myocardial infarction based on analysis of 3,697 patients. Am J Cardiol 1983;52:936-942. [CrossRef][Medline]
Kennamer R, Prinzmetal M. Myocardial infarction complicated by left bundle branch block. Am Heart J 1956;51:78-90. [Medline]
Wackers FJ. Complete left bundle branch block: is the diagnosis of myocardial infarction possible? Int J Cardiol 1983;2:521-529. [CrossRef][Medline]
Sclarovsky S, Sagie A, Strasberg B, et al. Ischemic blocks during early phase of anterior myocardial infarction: correlation with ST-segment shift. Clin Cardiol 1988;11:757-762. [Medline]
Cannon A, Freedman SB, Bailey BP, Bernstein L. ST-segment changes during transmural myocardial ischemia in chronic left bundle branch block. Am J Cardiol 1989;64:1216-1217. [CrossRef][Medline]
Stark KS, Krucoff MW, Schryver B, Kent KM. Quantification of ST-segment changes during coronary angioplasty in patients with left bundle branch block. Am J Cardiol 1991;67:1219-1222. [CrossRef][Medline]
Boden WE, Kleiger RE, Gibson RS, et al. Electrocardiographic evolution of posterior acute myocardial infarction: importance of early precordial ST-segment depression. Am J Cardiol 1987;59:782-787. [CrossRef][Medline]
Cook RW, Edwards JE, Pruitt RD. Electrocardiographic changes in acute subendocardial infarction. I. Large subendocardial and large nontransmural infarcts. Circulation 1958;18:603-612. [Medline]
Hindman MC, Wagner GS, JaRo M, et al. The clinical significance of bundle branch block complicating acute myocardial infarction. 1. Clinical characteristics, hospital mortality, and one-year follow-up. Circulation 1978;58:679-688. [Free Full Text]
Opolski G, Kraska T, Ostrzycki A, Zielinski T, Korewicki J. The effect of infarct size on atrioventricular and intraventricular conduction disturbances in acute myocardial infarction. Int J Cardiol 1986;10:141-147. [CrossRef][Medline]
Freedman RA, Alderman EL, Sheffield LT, Saporito M, Fisher LD. Bundle branch block in patients with chronic coronary artery disease: angiographic correlates and prognostic significance. J Am Coll Cardiol 1987;10:73-80. [Abstract]
Hamby RI, Weissman RH, Prakash MN, Hoffman I. Left bundle branch block: a predictor of poor left ventricular function in coronary heart disease. Am Heart J 1983;106:471-477. [CrossRef][Medline]
ISIS-2 (Second International Study of Infarct Survival) Collaborative Group. Randomised trial of intravenous streptokinase, oral aspirin, both, or neither among 17 187 cases of suspected acute myocardial infarction: ISIS-2. Lancet 1988;2:349-360. [Medline]
Rogers WJ, Bowlby LJ, Chandra NC, et al. Treatment of myocardial infarction in the United States (1990 to 1993): observations from the National Registry of Myocardial Infarction. Circulation 1994;90:2103-2114. [Free Full Text]
Sabia P, Afrookteh A, Touchstone DA, Keller MW, Esquivel L, Kaul S. Value of regional wall motion abnormality in the emergency room diagnosis of acute myocardial infarction: a prospective study using two-dimensional echocardiography. Circulation 1991;84:Suppl I:I-85.
Wasson JH, Sox HC, Neff RK, Goldman L. Clinical prediction rules: applications and methodological standards. N Engl J Med 1985;313:799-799.
Pelberg AL. Missed myocardial infarction in the emergency room. Qual Assur Util Rev 1989;4:39-42. [Medline]
Rusnak RA, Stair TO, Hansen K, Fastow JS. Litigation against the emergency physician: common features in cases of missed myocardial infarction. Ann Emerg Med 1989;18:1029-1034. [CrossRef][Medline]
McCarthy BD, Beshansky JR, D'Agostino RB, Selker HP. Missed diagnoses of acute myocardial infarction in the emergency department: results from a multicenter study. Ann Emerg Med 1993;22:579-582. [CrossRef][Medline]
Goodman, S. G., Menon, V., Cannon, C. P., Steg, G., Ohman, E. M., Harrington, R. A.
(2008). Acute ST-Segment Elevation Myocardial Infarction: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (8th Edition). Chest
133: 708S-775S
[Abstract][Full Text]
Eagle, K. A., Nallamothu, B. K., Mehta, R. H., Granger, C. B., Steg, P. G., Van de Werf, F., Lopez-Sendon, J., Goodman, S. G., Quill, A., Fox, K. A.A., for the Global Registry of Acute Coronary Events (,
(2008). Trends in acute reperfusion therapy for ST-segment elevation myocardial infarction from 1999 to 2006: we are getting better but we have got a long way to go. Eur Heart J
29: 609-617
[Abstract][Full Text]
Jolobe, O. M.
(2008). Guidelines for the diagnosis and treatment of non-ST segment elevation acute coronary syndromes. Eur Heart J
29: 277-277
[Full Text]
Thygesen, K., Alpert, J. S., White, H. D., on behalf of the Joint ESC/ACCF/AHA/WHF Task Force,
(2007). Universal Definition of Myocardial Infarction. J Am Coll Cardiol
50: 2173-2195
[Full Text]
Thygesen, K., Alpert, J. S., White, H. D., on behalf of the Joint ESC/ACCF/AHA/WHF Task Force, , TASK FORCE MEMBERS: Chairpersons: Kristian Thygese, , Biomarker Group: Allan S. Jaffe, Coordinator (USA), , ECG Group: Bernard Chaitman, Co-ordinator (USA), P, , Imaging Group: Richard Underwood, Coordinator (UK), , Intervention Group: Jean-Pierre Bassand, Co-ordina, , Clinical Investigation Group: Paul W. Armstrong, C, , Global Perspective Group: Philip A. Poole-Wilson,, , Implementation Group: Lars C. Wallentin Coordinato, , ESC COMMITTEE FOR PRACTICE GUIDELINES, , Alec Vahanian, Chair (France), A. John Camm (UK),, , DOCUMENT REVIEWERS, , Joao Morais, Review Coordinator (Portugal), Sorin,
(2007). Universal Definition of Myocardial Infarction. Circulation
116: 2634-2653
[Full Text]
Task Force Members, , Thygesen, K., Alpert, J. S., White, H. D., Biomarker Group, , Jaffe, A. S., Apple, F. S., Galvani, M., Katus, H. A., Newby, L. K., Ravkilde, J., ECG Group, , Chaitman, B., Clemmensen, P. M., Dellborg, M., Hod, H., Porela, P., Imaging Group, , Underwood, R., Bax, J. J., Beller, G. A., Bonow, R., Van Der Wall, E. E., Intervention Group, , Bassand, J.-P., Wijns, W., Ferguson, T. B., Steg, P. G., Uretsky, B. F., Williams, D. O., Clinical Investigation Group, , Armstrong, P. W., Antman, E. M., Fox, K. A., Hamm, C. W., Ohman, E. M., Simoons, M. L., Global Perspective Group, , Poole-Wilson, P. A., Gurfinkel, E. P., Lopez-Sendon, J.-L., Pais, P., Mendis, S., Zhu, J.-R., Implementation Group, , Wallentin, L. C., Fernandez-Aviles, F., Fox, K. M., Parkhomenko, A. N., Priori, S. G., Tendera, M., Voipio-Pulkki, L.-M., ESC Committee for Practice Guidelines, , Vahanian, A., Camm, A. J., De Caterina, R., Dean, V., Dickstein, K., Filippatos, G., Funck-Brentano, C., Hellemans, I., Kristensen, S. D., McGregor, K., Sechtem, U., Silber, S., Tendera, M., Widimsky, P., Zamorano, J. L., Document Reviewers, , Morais, J., Brener, S., Harrington, R., Morrow, D., Sechtem, U., Lim, M., Martinez-Rios, M. A., Steinhubl, S., Levine, G. N., Gibler, W. B., Goff, D., Tubaro, M., Dudek, D., Al-Attar, N.
(2007). Universal definition of myocardial infarction: Kristian Thygesen, Joseph S. Alpert and Harvey D. White on behalf of the Joint ESC/ACCF/AHA/WHF Task Force for the Redefinition of Myocardial Infarction. Eur Heart J
28: 2525-2538
[Full Text]
Iskandrian, A. E.
(2006). Detecting Coronary Artery Disease in Left Bundle Branch Block. J Am Coll Cardiol
48: 1935-1937
[Full Text]
Masoudi, F. A., Magid, D. J., Vinson, D. R., Tricomi, A. J., Lyons, E. E., Crounse, L., Ho, P. M., Peterson, P. N., Rumsfeld, J. S., for the Emergency Department Quality in Myocardial,
(2006). Implications of the Failure to Identify High-Risk Electrocardiogram Findings for the Quality of Care of Patients With Acute Myocardial Infarction: Results of the Emergency Department Quality in Myocardial Infarction (EDQMI) Study. Circulation
114: 1565-1571
[Abstract][Full Text]
Bauer, A., Watanabe, M. A., Barthel, P., Schneider, R., Ulm, K., Schmidt, G.
(2006). QRS duration and late mortality in unselected post-infarction patients of the revascularization era. Eur Heart J
27: 427-433
[Abstract][Full Text]
Wong, C.-K., Stewart, R. A.H., Gao, W., French, J. K., Raffel, C., White, H. D., for the Hirulog and Early Reperfusion or Occlusion,
(2006). Prognostic differences between different types of bundle branch block during the early phase of acute myocardial infarction: insights from the Hirulog and Early Reperfusion or Occlusion (HERO)-2 trial. Eur Heart J
27: 21-28
[Abstract][Full Text]
Reuben, A D, Mann, C J
(2005). Simplifying thrombolysis decisions in patients with left bundle branch block. Emerg. Med. J.
22: 617-620
[Abstract][Full Text]
Wong, C.-K., French, J. K., Aylward, P. E.G., Stewart, R. A.H., Gao, W., Armstrong, P. W., Van De Werf, F. J.J., Simes, R. J., Raffel, O. C., Granger, C. B., Califf, R. M., White, H. D., for the HERO-2 Trial Investigators,
(2005). Patients With Prolonged Ischemic Chest Pain and Presumed-New Left Bundle Branch Block Have Heterogeneous Outcomes Depending on the Presence of ST-Segment Changes. J Am Coll Cardiol
46: 29-38
[Abstract][Full Text]
Haywood, L. J.
(2005). Left Bundle Branch Block in Acute Myocardial Infarction: Benign or Malignant?. J Am Coll Cardiol
46: 39-41
[Full Text]
(2005). Inside This Issue of JACC. J Am Coll Cardiol
46: A39-A40
Wang, K., Asinger, R. W., Marriott, H. J.L.
(2003). ST-Segment Elevation in Conditions Other Than Acute Myocardial Infarction. NEJM
349: 2128-2135
[Full Text]
Maynard, S J, Menown, I B A, Manoharan, G, Allen, J, McC Anderson, J, Adgey, A A J
(2003). Body surface mapping improves early diagnosis of acute myocardial infarction in patients with chest pain and left bundle branch block. Heart
89: 998-1002
[Abstract][Full Text]
Madias, J. E., Zimetbaum, P., Josephson, M. E.
(2003). The Electrocardiogram in Acute Myocardial Infarction. NEJM
348: 2362-2362
[Full Text]
Zimetbaum, P. J., Josephson, M. E.
(2003). Use of the Electrocardiogram in Acute Myocardial Infarction. NEJM
348: 933-940
[Full Text]
Adams-Hamoda, M. G., Caldwell, M. A., Stotts, N. A., Drew, B. J.
(2003). Factors to Consider When Analyzing 12-Lead Electrocardiograms for Evidence of Acute Myocardial Ischemia. Am J Crit Care
12: 9-16
[Abstract][Full Text]
Pollehn, T, Brady, W J, Perron, A D, Morris, F
(2002). The electrocardiographic differential diagnosis of ST segment depression. Emerg. Med. J.
19: 129-135
[Abstract][Full Text]
Shlipak, M. G., Go, A. S., Frederick, P. D., Malmgren, J., Barron, H. V., Canto, J. G., for the National Registry of Myocardial Infarction,
(2000). Treatment and outcomes of left bundle-branch block patients with myocardial infarction who present without chest pain. J Am Coll Cardiol
36: 706-712
[Abstract][Full Text]
Friesinger, G. C. II, Smith, R. F.
(2000). Old age, left bundle branch block and acute myocardial infarction: a vexing and lethal combination. J Am Coll Cardiol
36: 713-716
[Full Text]
Satchithananda, D K, Stone, D L, Chauhan, A, Ritchie, A J
(2000). Lesson of the week: Unrecognised accidental overdose with diltiazem. BMJ
321: 160-161
[Full Text]
Mohammed, A., Hassan, T., Hamer, W., Edhouse, J., Morris, F P
(2000). Pedestrian injuries sustained in negotiating traffic calming measures.. Emerg. Med. J.
17: 233-234
[Full Text]
Shepherd, M., Hardern, R.
(2000). Confirmation of correct endotracheal tube placement.. Emerg. Med. J.
17: 74-75
[Full Text]
Sgarbossa, E. B., Pinski, S. L., Wagner, G. S., Shlipak, M. G., Go, A. S., Browner, W. S.
(1999). Left Bundle-Branch Block and the ECG in Diagnosis of Acute Myocardial Infarction. JAMA
282: 1224-1225
[Full Text]
Shlipak, M. G., Lyons, W. L., Go, A. S., Chou, T. M., Evans, G. T., Browner, W. S.
(1999). Should the Electrocardiogram Be Used to Guide Therapy for Patients With Left Bundle-Branch Block and Suspected Myocardial Infarction?. JAMA
281: 714-719
[Abstract][Full Text]
Estes III, N. A. M., Salem, D. N.
(1999). Predictive Value of the Electrocardiogram in Acute Coronary Syndromes. JAMA
281: 753-754
[Full Text]
Panju, A. A., Hemmelgarn, B. R., Guyatt, G. H., Simel, D. L.
(1998). Is This Patient Having a Myocardial Infarction?. JAMA
280: 1256-1263
[Abstract][Full Text]
Endres, M., Laufs, U., Huang, Z., Nakamura, T., Huang, P., Moskowitz, M. A., Liao, J. K.
(1998). Stroke protection by 3-hydroxy-3-methylglutaryl (HMG)-CoA reductase inhibitors mediated by endothelial nitric oxide synthase. Proc. Natl. Acad. Sci. USA
95: 8880-8885
[Abstract][Full Text]
Brandt, R. R., Hammill, S. C., Higano, S. T.
(1998). Electrocardiographic Diagnosis of Acute Myocardial Infarction During Ventricular Pacing. Circulation
97: 2274-2275
[Full Text]
White, H. D., Van de Werf, F. J. J.
(1998). Thrombolysis for Acute Myocardial Infarction. Circulation
97: 1632-1646
[Abstract][Full Text]
Ackermann, R. J., Vogel, R. L., Levenson, J., Byrne, J., Liron, M., Sgarbossa, E. B., Pinski, S. L., Wagner, G. S.
(1996). Electrocardiographic Diagnosis of Acute Myocardial Infarction in the Presence of Left Bundle-Branch Block. NEJM
335: 131-133
[Full Text]
(1996). DIAGNOSING MI IN PATIENTS WITH LEFT BUNDLE BRANCH BLOCK. JWatch General
1996: 3-3
[Full Text]
Wellens, H. J.J.
(1996). Acute Myocardial Infarction and Left Bundle-Branch Block -- Can We Lift the Veil?. NEJM
334: 528-529
[Full Text]