Post on 02-Jul-2015
When confronted with an ECG, always use a systematic approach, following all steps to come to the correct conclusion.In this course we use the 7+2 step plan
7+2 Step Plan
1.Rhythm– Rate– Conduction– Heart axis– P wave morphology– QRS morphology– ST morphology
1. Compare with previous ECG2. Conclusion
Step 1: What is the Rhythm?
Normal (conducted) sinus rhythm• A P wave (atrial contraction) precedes
every QRS complex.• A QRS complex follows every P wave. • The rhythm is regular, but varies slightly
during respirations. • The rate ranges between 60 and 100
beats per minute. • The P waves maximum height is 2.5 mm
in II and/or III. • The P wave is positive in I and II, and
biphasic in V1. • The PQ time is between 0,12 and 0,2
seconds.
I
II
AVF
V1
P wave
An example of normal sinus rhythm
Not sinus rhythm?
• If the rhythm is not sinus rhythm you proceed with the arrhythmia algorithm (which you will learn with the next topics) after determining the heart rate, heart axis and conduction intervals.
• (A purist definition of sinus rhythm is that sinus rhythm is present in the atria and not by definition in the ventricles, e.g. there may be sinus rhythm in the atria, complete AV block and a nodal escape rhythm in the ventricles).
Step 2: What is the heart rate?
Knowing the ECG paperspeed (usually 25 mm/sec) allows us to calculate the heart rate from the ECG using any of these methods:• Use the "square counting"
method• Use a calculator• Use a separate ECG ruler
The square counting method
The square counting method is ideal for regular heart rates. Use the sequence:
300-150-100-75-60-50-43-37.
Count from the first QRS complex (preferably occuring on a thick line). If the next QRS complex would occur on the next thick line, the heart rate would be 300, 150 if at the second thick line, 100 if at the third thick line and so on. When the second QRS complex is between two lines, take the mean of the two numbers from the sequence.
The count method to determine the heart frequency. The second QRS complex is between 75 and 60 beats per minute. This heartbeat is between that, around 65 beats per minute.
Step 3: Conduction
The speed of conduction of the signal through the heart results in conduction intervals:• PQ interval• QRS duration• QT interval
PQ interval
• Normal between 0.12 and 0.2 seconds.• Starts at the beginning of the atrial complex and ends at
the beginning of the ventricular complex.
May be shortened if there is pre-excitation of the ventricles through abnormal conduction between the atria and ventricles (accessory pathway).If the PQ interval is prolonged there is a degree of AV block (which will be discussed later).
QRS duration
• Normal < 0.10 - 0.12 seconds• Indicates how fast the ventricles depolarize
• QRS longer than 120 milliseconds may result from:o Left bundle branch blocko Right bundle branch blocko Electrolyte disorderso Idioventricular rhythm or paced rhythm
QT interval
• Indicates how fast the ventricles are repolarized, becoming ready for a new cycle.
• The normal value for QTc is: below 450ms for men and below 460ms for women
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Correct assessment of the QTc interval
The QT interval is comprised of the QRS-complex, the ST-segment, and the T-wave. One difficultly of QT interpretation is that the QT interval gets shorter as the heart rate increases. This problem can be solved by correcting the QT time for heart rate using the Bazett formula:
Correct QT measurements are important because QT prolongation may make the patient prone to arrhythmias, especially when combined with QT-prolonging drugs.
Stepwise approach to correct measurement of the QT interval
1. Use lead II. Use lead V5 alternatively if lead II cannot be read. – Draw a line through the baseline (PR segment, or TP alternatively) – Draw a tangent against the steepest part of the end of the T wave. If the T
wave has two positive deflections, the taller deflection should be chosen. If the T wave is biphasic, the end of the taller deflection should be chosen.
– The QT interval starts at the beginning of the QRS interval and ends where the tangent and baseline cross.
– If the QRS duration exceeds 120ms, the amount surpassing 120ms should be deducted from the QT interval (i.e. QT=QT-(QRS width-120ms) )
– Calculate QTc according to Bazett. You can use the QTc calculator for this.
Causes of QT prolongation
• Congenital long QT syndrome.
But QT prolongation can also occur as a consequence of (a.o.):• Medication (anti-arrhythmics, tricyclic antidepressants,
phenothiazides). See torsades.org for a full list.• Electrolyte imbalances.• Ischemia.
Step 4: Heart axis
The heart axis points in the direction of the average electrical vector of all the depolarizing heart cells.
A change of the heart axis or an extreme deviation can be an indication of pathology.
A positive QRS complex (more above than below the baseline) in a certain lead means that the heart axis is going (at least slightly) in that lead's direction.
The heart axis is normal between -30 and +90 degrees.
Therefore, if QRS is positive in both leads I and II, the heart axis is normal.
Interpretation
There are four areas where the QRS vector can point: • Left axis deviation (between
-30º and -90º) • Normal axis between -30º and
90º• Right lower quadrant --> right
axis deviation (between 90º and -180º)
• Right upper quadrant --> extreme right axis deviation(between -90º and -180º)
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Abnormal heart axis
Heart axis deviation to the left in case of an inferior infarct. Left anterior hemiblock is another common cause. A left axis is present between -30 and -90 degrees.
Heart axis deviation to the right can result from right ventricular overload as in COPD or pulmonary embolism. A right axis is between +90 and +180 degrees.A left - right arm lead exchange is the most common cause of right axis deviation!
Step 5: P Wave morphology
The P wave morphology can reveal right or left atrial dilatation or atrial arrhythmias and is best determined in leads II and V1 during sinus rhythm.
Normal P wave morphology :• The maximal height of the P wave is 2.5 mm
in leads II and / or III. • The P wave is positive in II and AVF,
and biphasic in V1.• The P wave duration is shorter than 0.12
seconds.
I
II
AVF
V1
Left atrial dilatation
Terminal part of V1 > 1mm2 and/or P > 0.12 seconds in I and/ or II
Right atrial dilatation
P > 2.5 mm in II and/ or III and/ or aVFand/ or P > 1.5 mm in V1
Condition P Wave Morphology
Normal Sinus Rhythm
Right atrial enlargement(= P Pulmonale)
Left Atrial Enlargement(= P Mitrale)
Step 6: QRS Morphology
Check presence or absence of any of the following abnormalities:• Pathological Q waves• LVH / RVH• Microvoltages (QRS < 5 mm)• Conduction problems (normal or prolonged)• Abnormal R wave propagation
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Pathological Q wave
• Q waves point at electrically silent areas and can be a sign of previous myocardial infarction
• Definition of a pathologic Q wave:o Any Q wave in leads V2–V3 o Q wave ≥ 0.03 s and > 0.1 mV
deep in other leads.o To be defined as pathologic, Q
waves need to be present in two contiguous leads (e.g. II and AVF or I and AVL or V1 and V2)
Left ventricular hypertrophy
Hypertrophic myocardium has more electrical activity, resulting in larger peaks.
Definition of LVH: R in V5 or V6 + S in VI > 35mm (Sokolow-Lyon criteria)Often a "strain pattern" is seen in V5 and V6.
Right ventricular hypertrophy
Right ventricular hypertrophy is probably present when R is larger than S in VI
V1
Microvoltages
Microvoltages:QRS < 5 mm in limb leadsQRS < 10 mm in chest leads
Occurs in infiltrative disease (e.g. amylodosis), and COPD
Conduction disordersIf the QRS duration is more than 0.12 seconds there may be a block in the conductive tissue. Most often it will be either right or left bundle branch block.
Rule of thumb: when distinguishing left and right bundle branch block--look at V1 only!
Does the signal end negative (below the baseline) in V1? (away from V1) >> the ventricle farther from V1 is depolarized later>> it must be a left bundle branch block
Does the signal end positive in V1? (towards V1) >> the ventricle closer to V1 is depolarized later >> it must be a right bundle branch block
Conduction disorders: right bundle branch block
• QRS > 0.12 seconds• RSR'-pattern in V1 where
R' > R• Slurred S wave in lead I
and V6
V1
Conduction disorders: left bundle branch block
• QRS > 0.12 seconds• Broad monomorphic S waves in V1, may have a small
initial R wave • Broad monomorphic R waves in I and V6 with no Q
waves
Normal R wave progression
Normally R waves become larger from V1-V5. At V5 it should be maximal. If the R wave in V2 is larger than in V3, this could be a sign of a (previous) posterior myocardial infarction.
Step 7ST morphology
• The ST segment represents ventricular repolarization. During repolarization the cardiomyocytes elongate and prepare for the next heartbeat. On the ECG, the repolarization phase starts at the junctional, or J point, and continues until the T wave. The ST segment is normally at or near the baseline.
• The T wave is usually concordant with the QRS complex. Thus if the QRS complex is positive in a certain lead (the area under the curve above the baseline is greater than the area under the curve below the baseline) then the T wave usually is positive too in that lead. Accordingly the T wave is normally upright or positive in leads I, II, AVL, AVF and V3-V6. The T wave is negative in V1 and AVR. The T wave flips around V2, but there is likely some genetic influence in this as in Blacks the T wave usually flips around V3.
• The T wave angle is the result of small differences in the duration of the repolarization between the endocardial and epicardial layers of the left ventricle. The endocardial myocytes need a little more time to repolarize (about 22 ms). This difference causes an electrical current from the endocardium to the epicardium, which reads as a positive signal on the ECG.
Step 7ST morphology
• ST segment elevation• Ischemia• Pericarditis• Aneurysma cordis• Normal variant
• ST depression• Ischemia• LVH• Digitalis• Low potassium/ low magnesium• Neurologic
• T wave changes• Ischemia• Pericarditis• Myocarditis• LVH / RVH• Electrolyte changes (especially potassium)
Common causes of ST shift
ST elevationnormal
90% of healthy (young) men and women to a lesser extent have ST elevation in precordial leads.
Normal variants of ST segment elevation are:• 1: normal• 2: ‘early repolarization’• 3: normal 'variant'
Abnormal ST segment elevation
1: LVH2: LBBB3: Pericarditis4: High pottasium 5: Acute AS infarct6: Acute AS infarct + RBBB7: Brugada syndrome
ST segment elevation (upper ECG) due to pericarditis. The lower ECG shows PTa depression, which is typically seen in pericarditis.
Diffuse ST elevation in pericarditis
ST depression
The most important cause of ST segment depression is ischemia. Causes of ST segment depression include: Reciprocal ST segment depression during ischemia. If one lead shows
ST segment elevation then usually the lead "on the other side" shows ST segment depression.
Left ventricular hypertophy with "strain" or depolarization abnormality Digoxin effect Low potassium/low magnesium Heart rate-induced changes (post tachycardia), 'cardiac memory' During acute neurologic events
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ST segment elevation due to high potassium levels
T wave• The T wave is quite labile and long lists of possible causes of T wave
changes exist. A changing T wave can be a sign that something is abnormal, but it doesn't say much about the severity. T waves can be peaked, normal, flat, or negative. Flat and negative T waves are defined as:
• flat T wave:
< 0.5 mm negative or positive T wave in leads I, II, V3, V4, V5 or V6 • negative T wave:
> 0.5 mm negative T wave in leads I, II, V3, V4, V5 or V6
Possible causes of T wave changeso Ischemia and myocardial infarctiono Pericarditis, myocarditiso Cardiac contusiono Acute neurologic events, such as subarachnoid bleeding (SAB)o Digoxin effecto Right and left ventricular hypertrophy with strain
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Prominent U waveSometimes a U wave is present: an extra wave following the T wave. During hypokalemia (and hypocalcemia) the U wave can become more prominent:
Step 7+1Compare with previous ECG
• New LBBB?• Change in heart axis?• New pathologic Q?• Decreased R wave height?
All of these can exist as chronic abnormalities, but when the are new it can be a sign of acute ischemia or another condition.
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Step 7+2Conclusion
Try to formulate one sentence that summarizes your finding with a clinical useful conclusion.Examples: "Sinus tachycardia with ST elevation in V2-V5, likely
caused by acute anterior myocardial infarction" "Supraventricular tachycardia of 200 beats per minute
caused by an AV nodal re-entry" "Previous infarction combined with an acute lateral
myocardial infarction with widening of the QRS complexes"
"Normal ECG"