Subscribe to our newsletter to receive information on new and updated content

 

ST Elevation without Infarction

Author: Leilah J Dare / Editor: Jason Kendall / Codes: CAP7, HAP8 / Published: 22/11/2010 / Review Date: 22/11/2013

Jump to: Top | Introduction | MedicoLegal and other considerations | References

Introduction

The need to establish the correct diagnosis in patients who have ST segment elevation on their ECG is paramount when considering that the most important differential is ST elevation Myocardial Infarction (STEMI). There are 2 main issues when trying to diagnose STEMI: (i) the speed with which we need to make the diagnosis because of the time critical nature of treatment and (ii) the potential consequences of inappropriate urgent reperfusion therapy (i.e. thrombolysis or angioplasty).

The interpretation of the ECG is usually made under time pressure and without the luxury of added investigations to help clarify the diagnosis. Consequently we need to rely on our clinical assessment (ie history and examination) of the patient in conjunction with our interpretation of the ECG in order to make the correct diagnosis.

There are a large number of causes of ST segment elevation without infarction. The aim of this learning module is to review the conditions which are likely to mimic STEMI. Many are primarily cardiac in origin (e.g. benign early repolarisation (BER), Brugada Syndrome, or pericarditis) but many are not (e.g. hyperkalaemia or pulmonary embolism).

There is evidence available which demonstrates that ECG interpretation is not perfect. One study evaluating the pre-hospital recognition of ST elevation meeting criteria for thrombolysis showed that 51% did not have myocardial infarction as their final diagnosis1. A further study reported that correct differentiation of BER from STEMI by a group of emergency physicians and cardiologists occurred in 81% and 90% of cases respectively2. The authors concluded that the cardiologists had significantly more years of experience and that this was why they were more accurate in making the correct diagnosis.

Learning bite

The ability to recognize BER from STEMI is not always straightforward and is in part related to clinician experience and clinical context

The causes of ST segment elevation (see Table 1)

This learning module discusses the cardiac causes of ST segment elevation unrelated to acute myocardial infarction (MI) and the non-cardiac causes which might present similarly to MI (i.e. with collapse or chest pain: subarachnoid haemorrhage or pulmonary embolism) or which might complicate MI (e.g. hyperkalaemia).

Table 1: Pathological Causes of ST elevation

ST Table 1

Learning bite

There are many causes of ST segment elevation which are not related to acute myocardial infarction

Recognition of ST segment elevation

The ST segment represents completed ventricular myocardial depolarization. This segment can be FLAT (see Figure 1), or can be sloping (see Figure 3).

The European Society of Cardiology4 defines the height of ST elevation in AMI as being measured at the J point (see Figures 1-4). One study demonstrated how measuring the height of the ST segment is highly variable between Junior Doctors,sup>5 with the point of measurement varying by up to 5 mm beyond the J point (see Figure 4).

Learning bite

Measuring ST segment elevation needs to occur at the J point

Figure 1: components of the ECG – identification of the J point

ST 1_1

Three questions are important in evaluating the ST segment:

  1. Where is the baseline?
  2. What is the J point?
  3. Where along the ST segment do we measure?

Where is the baseline?

ST segment elevation is defined as deviation of the ST segment by greater than 0.1mV above a line joining 2 successive TP segments3; if the TP segment is not clearly identifiable then the PR segment can be used (see Figure 2).

Figure 2: Demonstrating the baseline

ST2_0

What is the J point?

This is be defined as the junction between the QRS complex and the ST segment (see Figure 3)

ST3

Where along the ST segment do we measure elevation?

This is not so clear-cut: measuring the height of a flat ST segment (eg. in Figure 1) will be straightforward but the same cannot be said for a sloping ST segment (eg. in Figure 2).

Figure 4: Demonstrating variability in measuring the J point

ST4

Recognition of ST segment elevation without infarction

(i) ST segment morphology (i.e. shape – see Figure 5):

BER has elevated upward sloping concave ST segements3. This concave nature cannot be used as a discriminator on its own but when seen in conjunction with the other features of BER it may be of help. Pericarditis is also associated with a concave ST morphology; in pericarditis, this “saddle shape” is characteristically seen globally throughout the ECG.

Figure 5: ST segment morphology

ST5

It has been reported that a non-concave (i.e. convex) morphology has a sensitivity of 77% and a specificity of 97% for a diagnosis of STEMI. This means that a convex or flat morphology can be used as a “rule in” feature for AMI but that morphology alone is a poor feature to use to “rule out” AMI6.

Learning bite

A convex ST segment shape is more likely to be associated with AMI than a concave shape

Pitfall

However,do not assume that because ST segment elevation is not convex that it cannot be a STEMI

(ii) Distribution of ST segment elevation:

ST segment elevation due to STEMI follows a coronary artery “territorial” distribution which is not typically seen in other conditions. It may also be accompanied by reciprocal changes: seen in 70% of inferior and 30% of anterior STEMI6 (see Figure 6).

ST segment elevation due to BER is typically evident in the precordial leads: 74% in V1-V2, 73% in V3-V4 and 37% in inferior leads8.

ST segment elevation is more diffuse in pericarditis (see Table 2).

Figure 6: ST segment changes of STEMI (with reciprocal changes)
in a distribution clearly reflecting coronary artery territory

ST6_1

Table 2: Distribution of ST segment changes and association with cause

ST Table 2

Learning bite

Territorial ST segment elevation make AMI more likely; more diffuse ST segment changes are typical of pericarditis

(iii) Magnitude of ST segment elevation:

The magnitude of ST segment elevation can help to differentiate BER from STEMI: one study reported that 57% of ECGs showing ST elevation due to BER was of 1mV amplitude or less; where the amplitude was 5mV or greater it was due to BER in only 2% of cases.3

(iv) “Notch” or “Slur” at the end of the QRS (at the J point):

One of the features seen in BER is an upward sloping notch at the end of the QRS segment. This is seen more in the precordial leads in BER and is not a feature of pericarditis3 (see Figure 7).

Learning bite

a notch at the end of the QRS segment is often seen in BER

Figure 7: Representation of notch at the end of the QRS complex

ST7_0-1

(v) ST segment elevation to T wave height ratio (see Figure 8):

Both BER and pericarditis can have ST segments and T waves that look morphologically similar making distinguishing between them difficult. Comparing the height of the ST segment to that of the T wave can aid in this process. This can be expressed as a ratio. The most useful place to measure this is in V6. When this ratio is greater than 0.25 it indicates the diagnosis of pericarditis is more likely with a positive predictive value of 90%9. It can be done in other leads but with less accuracy.

Learning bite

The ST:T wave ratio in V6 of > 0.25 makes Pericarditis more likely

Figure 8: Demonstration of ST/T wave ratio measurement

ST8

Important causes of ST elevation without infarction

Cardiac Causes

(i) Normal variant / Benign Early Repolarisation (BER):

Hiss et al in 1960 studied the ECGs of 6014 healthy men in the US Air force. They found that 91% had ST segment elevation of 1mm to 3 mm in one or more precordial leads. This demonstrates the common nature of BER. The incidence of this finding decreases with age. Women demonstrate ST elevation of > 1mm in only 20% of cases and this does not appear to change with increasing age3. It is equally common in all races11. ST segment elevation due to BER reduces in amplitude during exercise – however, exercising people with ST elevation in order to confirm BER may be hazardous!

Learning bite

BER is common especially at younger ages

(ii) Pericarditis:

5% of ED admissions with chest pain are due to acute pericarditis12. 90% of cases are classified as idiopathic or viral in aetiology. Table 3 lists the causes of pericarditis.

Table 3: Causes of pericarditis

ST Table 3

85% of patients have an audible friction rub during the course of their diease. 15% of patients with idiopathic pericarditis and up to 60% of patients with neoplastic, TB or purulent pericarditis have clinical evidence of tamponade.

Learning bite

85% of patients with pericarditis have a pericardial friction rub at some point during their illness

ECG findings include widespread concave ST elevation, ST depression in lead aVR and widespread PR depression. The ST segment to T wave height ratio in lead V6 is normally > 0.259.

Troponin levels are elevated in 35-50% of patients with pericarditis. Other blood tests (eg. full blood count, viral serology) are of little help in finding a cause. Echocardiography should be performed to aid diagnosis, evaluate the size of any associated effusion and to look for other poor prognostic indicators (Table 4).

Table 4: Poor prognostic indicators associated with pericarditis

ST Table 4

The treatment for uncomplicated pericarditis is non-steroidal anti-inflammatory medication (NSAIDs) to relieve discomfort. Steroids are not to be used in the first instance for idiopathic pericarditis as they may increase the risk of recurrence. They may be used in pericarditis associated with systemic inflammatory disorders. Colchicine can be considered in conjunction with the NSAIDs.

Learning bite

Avoid steroids as first line treatment in idiopathic uncomplicated pericarditis

Pitfall

Discharging someone from ED without an echocardiogram means that not all poor prognostic indicators have been excluded and that an incomplete assessment has been made. Following a normal echocardiogram a patient may be discharged with NSAIDs if otherwise well.

(iii) Brugada Syndrome:

This is a rare but serious cause of ST segment elevation without AMI. It is an autosomal dominant condition with incomplete penetrance that has an incidence ranging from 5 to 66 per 10 000. It is endemic in Southeast Asia13.

Clinical features include: episodes of arrhythmia (usually rapid polymorphic VT), collapse or sudden death. The episodes are more common in the night or the early hours of the morning. There may be a family history of sudden death. It has a male predominance (ratio 8:1).

There are 3 types, each with specific ECG appearances (see Figure 9). These ECG findings can be dynamic and can be unmasked or exaggerated by sodium channel blockers such as flecainide. Brugada Syndrome is not associated with identifiable structural cardiac abnormalities.

ST segment elevation occurs in the right precordial leads V1 to V3. The exact morphology of the ST segment gives rise to the 3 types (see Table 5).

Table 5: Morphology of Brugada Syndrome types

ST Table 5

Figure 9: ECG characteristics of Brugada Syndrome:

ST9

If Type 1 ECG morphology is demonstrated there is no need for drug testing but this is not the case in Types 2 and 3 where sodium channel blockers are used to confirm the diagnosis. In view of the potentially catastrophic nature of this disease inpatient referral is mandatory if Brugada syndrome is suspected to be the cause of ST elevation.

Learning bite

Consider Brugada Syndrome in anyone with downward sloping ST segment elevation in the right precordial chest leads

Pitfall

Be cautious of ruling out Brugada Syndrome in someone who gives you a good history just because they do not have the characteristic Type 1 ECG changes. Remember the use of drug testing.

(iv) Ventricular aneurysm:

The majority of ventricular aneurysms are seen after large anterior myocardial infarctions14. This diagnosis may be indicated by the clinical history and the presence of previously recorded discharge ECGs. The commonest site of ST segment elevation is in the anterior leads reflecting the most likely site of the original STEMI. Clinical and ECG features will be static unlike those of a patient presenting with an acute STEMI. The other ECG characteristics can be seen Table 6.

Table 6: ECG characteristics associated with ventricular aneurysm

ST Table 6

(v) Left Bundle Branch Block (LBBB):

The appearance of LBBB on an ECG makes any further interpretation of the ECG difficult. There are various features that allow you to “read through” LBBB to identify an acute STEMI: Sgarbossa15 described 3 independent ECG signs suggestive of AMI in a patient with LBBB on their ECG (see Table 6). These are highly specific but not sensitive for AMI and so have limited use in everyday clinical practice. Much more importance is attached to a good history for AMI.

Table 7: Sgarbossa Criteria for AMI in LBBB

ST Table 7

Learning bite

A patient presenting with a good history of AMI and with LBBB on their ECG should be treated as an AMI even in the absence of the Sgarbossa criteria

Non Cardiac Causes

Extra emphasis has been placed on those conditions which may have STEMI as a differential diagnosis.

(i) Pulmonary Embolism (PE):

ECG changes associated with significant PE reflect right ventricular strain (due to outflow obstruction) and are mainly in the inferior and anteroseptal leads. In addition to ST segment elevation (which is an unusual finding in PE), there are other ECG findings that are associated with PE (see Table 8).

Table 8: ECG features associated with PE16

ST Table 8

The presence of right ventricular dysfunction indicates a poorer prognosis and it has been suggested that these specific ECG findings can be used as an independent predictor of outcome17.

(ii) Hyperkalaemia:

Tenting of the T waves is the classic appearance associated with hyperkalaemia; however ST segment elevation may also be seen. This is characteristically downward sloping10. Other features of hyperkalaemia include widening of the QRS complex and low amplitude or absent P waves. These changes resolve as hyperkalaemia is treated.

(iii) Subarachnoid Haemorrhage:

25% of people with SAH have ECG findings consistent with MI or ischaemia18. T wave inversion is the most common abnormality found, followed by ST segment depression, ST segment elevation and Q waves. Changes are commonly in an anterior distribution or may be diffuse.

Learning bite

Non-specific ST segment changes are associated with SAH in 25% of cases

Summary Table: ECG changes associated with conditions causing ST segment elevation

ST Shape Site P wave
PR depression
Reciprocal
Changes
Q waves T waves

STEMI
(Dynamic)
Convex Territorial Common Will develop Hyperacute
Large Amplitude

Pericarditis
(Dynamic Slower)
Concave/
Saddle Shape
Global PR depression aVR not aVL No ST:T wave ratio > 0.25

BER
Concave
Notch at J point
Mostly Chest Leads aVR in 50% No May have large amplitude

Ventricular Aneurysm
(Static)
Mainly Anterior May be present Anterior Small amplitude

Brugada Syndrome
Downward Sloping V1 and V2 No No Normal

LBBB
Anterior &
Inferior
Discordant to QRS normally
Present As part of the LBB pattern May have large amplitude

Pulmonary Embolism
Changes normally Antero septal & inferior Inverted in Inferior or anteroseptal leads

Hyperkalaemia
Downward sloping Low amplitude or Absent Tall tented T waves

SAH
Anterior or Diffuse Maybe present May have T wave inversion

Jump to: Top | Introduction | MedicoLegal and other considerations | References

MedicoLegal and other considerations

Key Learning Points

  • There are many causes of ST segment elevation which are unrelated to myocardial infarction.
  • ST segment elevation is measured from the TP baseline to the J point.
  • ST segment elevation is defined as >0.1 mV above the baseline and is measured at the J point.
  • There are features on the ECG (eg. morphology, distribution and amplitude of ST segment elevation) that can help to establish the underlying diagnosis.
  • BER is a normal finding in young males (Level of evidence Grade 2b).
  • Convex shaped ST segment elevation is more likely to indicate STEMI (Level of evidence Grade 2b).
  • Ventricular aneurysm, like STEMI, manifests as ST segment elevation that is territorial in distribution; however, unlike STEMI, it is static.
  • An ST:T wave height ratio in lead V6 >0.25 is typically associated with pericarditis (Level of evidence Grade 3b).
  • Brugada Syndrome has 3 types; in Type 1 the ECG findings are diagnostic; Types 2 and 3 need to have further evaluation to unmask the ECG findings.
  • The presence of Sgarbossa criteria with LBBB makes STEMI likely but the absence of the Sgarbossa criteria does not rule out STEMI (Level of evidence Grade 2a).

Jump to: Top | Introduction | MedicoLegal and other considerations | References

References

  1. Otto LA, Aufderhaide TP. Evaluation of ST segment criteria for the prehospital electrocardiographic diagnosis of myocardial infarction. Annals of Emergency Medicine 1994; 23 17-24.
  2. Turnipseed SD, Bair AE, Douglas Kirk J, Dierks DB et al: Electrocardiogram Differentiation of Benign Early Repolarisation Versus Acute Myocardial Infarction by Emergency Physicians and Cardiologists. Academic Emergency Medicine 2006; 13; 961-967.
  3. Mehta M , Jain AC. Early Repolarization on scalar electrocardiogram. American Journal of Medical Sciences 1995 ; 309: 305-311.
  4. Thygesen K, Alpert JS, White HD et al. Universal definition of Myocardial Infarction. European Heart Journal 2007; 28; 2525-2538.
  5. Carley SD, Gamon R, Driscoll PA, Brown G, Wallman P: Whats the point of ST elevation? Emergency Medicine Journal 2002; 19; 126-128.
  6. Brady WJ, et al. Electrocardiographic ST segment Elevation: The Diagnosis of Acute Myocardial Infarction by Morphologic Analysis of the ST segment. Academic Emergency Medicine 2001; 8 :961-967.
  7. Morris F, Edhouse J, Brady WJ, Camm J: ABC of Clinical Electrocardiography BMJ Books 2003.
  8. Hiss RG, Lamb LE, Allen MF. Electrocardiographic findings in 67, 375 asymptomatic subjects. American Journal of Cardiology 1960; 6: 200-31.
  9. Ginzton LE Laks MM. The differential diagnosis of acute pericarditis from the normal variant: new electrocardiographic criteria. Circulation 1982; 65: 1004-9.
  10. Wang K, Asinger RW, Marriott HJL. ST segment elevation in conditions other than Acute Myocardial Infarction. New England Journal of Medicine 2003; 349:2128-35.
  11. Mehta M, Jain AC, Mehta A. Early Repolarization. Clinical Cardiology 1999; 22: 59-65.
  12. Lange RA, Hills L: Acute Pericarditis. New England Journal of Medicine 2004; 351:2195-2202.
  13. Wilde AM, et al . Proposed Diagnostic Criteria for the Brugada Syndrome: Consensus report. Circulation 2002; 106; 2514-2519.
  14. Brady W, Harrigan RA, Chan T: Diagnosis: Left Ventricular Aneurysm. Emergency Medicine News 2006; 28: 38.
  15. Sgarbossa EB et al: Electrocardiographic Diagnosis of Evolving Acute Myocardial Infarction in the Presence of Left Bundle-Branch Block. New England Journal Of Medicine 1996; 334:481-487.
  16. Sreeram N, Cheriex EC, Smeets JL, Gorgels AP, Wellens HJ. Value of the 12 lead electrocardiogram in hospital admission in the diagnosis of pulmonary embolism. American Journal of Cardiology 1994; 73(4) 298-303.
  17. Geibel A, Zehender M, Kasper w, Olschewski M, Klima C, Konstantinides SV. Prognostic value of the ECG on admission in patients with acute major pulmonary embolism. European Respiratory Journal 2005; 25: 843-848.
  18. Zaroff JG, Rordorf GA, Newell JB, Ogilvy CS, Levinson JR: Cardiac outcome in patients with SAH and ECG abnormalities. Neurosurgery 1999 44(1) 34-39.

Leave a Reply