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ECG and Arrhythmias
ECG and Arrhythmias
ECG stands for electrocardiogram; its a record of the hearts electrical activity. its a
very important tool that can provide evidences to support a specific diagnosis.
Remember that most abnormalities in the ECG are amenable to reason.
The Basics:
The quality of an ECG is determined by the presence of PATIENTS NAME,
DATE/TIME, the 12 LEADS and a RYTHEM STRIP at the bottom.
The paper moves in a speed of 25mm/s (horizontal).
?If faster (50mm/s) itll give a false impression of slow HR
Normal ECG
Positive deflection: If a wave of depolarization passing through the heart is moving
toward a surface electrode
Negative deflection: If a wave of depolarization passing through the heart is moving
away from the electrode.
Biphasic wave: If a wave of depolarization passing through the heart is moving
perpendicularly to the electrode.
6 chest leads:
V1 and V2: Parasternal at 4th intercostals space.
V3 is in between V2 and V4.
V4, V5 and V6 at the 5th intercostal space:
V4: Midclavicular line
V5: Anterior axillary line
V6: Middle axillary line.
V1, V2, V3, V4: Anteriospetal surface.
V5,V6: Lateral surface
In a normal cardiac axis (about 60 degrees):
- V1: Small R, Deep S
- V2: R increases, S decreases
- V3/V4: R=S
- V5/V6: Large R, S disappears in normal
people
If the R is poorly enlarging (poor
progression R wave sign of ischemia)
-ve Lead I
+ve Lead II
+ve Lead I
-ve Lead II
-ve Lead I, II & III
3
Patient is shivering
Remember: ECG must be individualized:
Male vs Female, Old vs Young, Chest Pain vs Normal
5
P Mitral:
Bifid in Lead II
PR Interval Abnormalities
- Wolf Parkinson White syndrome
(WPW): accessory pathway
associated with Delta wave.
- Could be normal in rapid heart
rate.
Heart block/AV block
(1st, 2nd and 3rd degrees)
Spot on Arrhythmias:
Preexcitation syndromes (WPW Syndrome):
Preexcitation is a condition characterized by an accessory pathway of conduction,
which allows the heart to depolarize in an atypical sequence.
In Wolfe-Parkinson-White (WPW) syndrome, theres a direct atrioventricular
connection allows the ventricles to begin depolarization while the standard action
potential is still traveling through the AV node.
ECG Characteristics of WPW:
1. Short PR interval 2. QRS prolongation
3. Delta Wave
4. Followed by tachycardia
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In fact, the PR interval isnt shortened, but it looks so due to the emergence of the
delta wave.
Heart Block (AV block):
1st degree Heart block:
- Prolongation of the
PR interval, which is
constant
- All P waves are
conducted
2nd degree Heart block
(Mobitz 1)/Wenckebach:
- Progressive
prolongation of the
PR interval until a P
wave is not
conducted.
- As the PR interval
prolongs, the RR
interval actually
shortens
2nd degree Heart block
(Mobitz 2):
Constant PR interval with
intermittent failure to
conduct
Third degree Heart block
(Complete):
No relationship between
P waves and QRS
complexes, Relatively
constant PP intervals and
RR intervals and Greater
number of P waves than
QRS complexes
ECG changes
RBBB
- Normal variant
- Right ventricular
hypertrophy or strain
- ASD
QRS > 3 Ssq
RSR (M shaped QRS complex)
in V1, V2 and deep S in V6.
- May present with RAD
(usually) or LAD (Atrial
septal defect, severe
conducting problem)
LBBB
- CAD
- HTN
- Aortic valve disease
- Cardiomyopathy
QRS > 3 Ssq
RSR (M shaped QRS complex)
in V5, V6, I and deep S in V1
- Usually associated with
LAD
Appearance
Mnemonic
MaRRoW:
M first letter = M in V1
WiLLiaM:
M last letter = M in V6
ST segment Abnormalities
These are usually in territories eg. anterior/lateral/inferior etc. and will be present in
contiguous leads (III,aVF or I,aVL,V5,V6 ...)
ST depression:
- Downsloping or horizontal =
abnormal
- Ischaemia (coronary stenosis):
Chest pain association
- If lateral (V4-V6), consider LVH
with strain or digoxin toxicity
ST elevation
- Infarction (coronary occlusion)
- Pericarditis (widespread)
- Prinzmetal spasm
- Post ventricular aneurysm
- Early embolization
Normal rhythm (P wave in II) and axis, ST elevation is V2-V6, and minimally in aVL, Q
wave also present: Acute MI in the proximal Left Anterior Descending Artery.
10
Sinus rhythm
ST depression Lead I, aVL, ST elevation V5, V6 Lateral MI (acute over chronic)
ST elevation in III and aVF Inferior MI
reciprocal ST depression in V1, V2 Posterior MI
InferioPosterioLateral MI
Super-dominant Right coronary artery, proximal occlusion.
ask for Right ventricular leads
Right Ventricular Infarction Cardiogenic Shock Hypotension IV fluids
T wave Abnormalities
Peaked hyperkalaemia or normal young man
What is the rate, rhythm and axis for these patients, and is there any other abnormalities?
Not sinus (ectopic) and irregular rhythm, rate = 120, right axis deviation?, LVH due to
deep S and huge R, T inversion can be seen laterally.
LVH Right atrial abnormality and fibrillation
12
QT interval Abnormalities
QT interval must be corrected because
Long QT (>450ms) can be genetic
its affected by the HR:
(long QT syndrome) or secondary
due to drugs (amiodarone, sotalol)
Associated with risk of sudden
death due to Torsades de Pointes
(check page 16)
Atrial Flutter:
Biphasic sawtooth flutter waves at a rate of >250/min
Flutter waves have constant amplitude, duration, and morphology through the
cardiac cycle.
There is usually either a 2:1 or 4:1 block at the AV node,
resulting in ventricular rates of either 150 or 75 bpm
Adenosine is used to unmask an unclear record (SVT or Flutter?) by showing
the saw-tooth appearance.
14
Atrial Fibrillation
Atrial fibrillation is caused by numerous wavelets of depolarization spreading
throughout the atria simultaneously, leading to an absence of coordinated atrial
contraction. AF is important because it can lead to: Hemodynamic compromise,
Systemic embolization and other Symptoms
On ECG:
Absent P waves, Presence of fine fibrillatory waves which vary in amplitude and
morphology, Irregularly irregular ventricular response.
15
Ectopic Beats
Abnormal early beat whether atrial or ventricular within a normal ECG
In ventricular extrasystole/ectopic beat : QRS would look broad and bizarre, not preceeded
by P and followed by opposing ST-T changes and by a compnesatory pause.
In Atrial extrasystole/ectopic beat: QRS would look normal, abnormally looking P wave and
with a compnesatory pause.
When the variations in PP interval occur in phase with respiration, this is considered
to be a normal variant, called sinus arrhythmia:
Sinus pauses
Sinus arrhythmia
Complete sinus arrest
Progressive development of atrial arrhythmias (a-flutter, a-fib, atrial
tachycardia)
Patients are usually elderly and present with lightheadedness and/or syncope,
but it can also manifest as angina, dyspnea, and palpitations.
Etiologies:
Sinus node firbosis , Atherosclerosis of the SA artery, Congenital heart disease,
Excessive vagal tone, Familial, Pericarditis, Hypothyrodism.
Multifocal Atrial Tachycardia:
Discrete P waves with at least 3 different morphologies. Atrial rate > 100 bpm.
The PP, PR, and RR intervals all vary.
Its very common with COPD and Lung fibrosis patients.
18
Hypokalemia: (U wave)
Interpret this ECG case, before checking its answer beneath it:
RBBB
19
20
Answer: AF
Note:
Arrythmias were discussed in 10 minutes out of 2 hours, this sheet provide the most
important ones according to what the doctor came through and what Davidson
emphasized on.
Make an effort to differentiate Normal from Abnormal ECG, and diagnose MI, Angina,
Bundle Branch Blocks, AV Blocks, Tachycardia, Bradycardia, Axis deviation, Atrial and
Ventricular hypertrophy, and Abnormal/ectopic/SV rhythms in general.
Good Luck.
Melad
21
Reminders
REMINDERS
WHAT TO LOOK FOR
1. The rhythm and conduction:
sinus rhythm or some early arrhythmias
evidence of first, second or third degeree
block
evidence of bundle branch block.
2. P wave abnormalities:
peaked, tall right atrial hypertrophy
notched, broad left atrial hypertrophy.
3. The cardiac axis:
right axis deviation QRS complex
predominantly downward in lead I
left axis deviation QRS complex
predominantly downward in leads II and III.
4. The QRS complex:
width:
if wide, ventricular origin, bundle branch
block or the WPW syndrome
height:
tall R waves in lead V1 in right ventricular
hypertrophy
tall R waves in lead V6 in left ventricular
hypertrophy
transition
point:
Q waves:
? septal
? infarction.
5. The ST segment:
raised in acute myocardial infarction and
in pericarditis
depressed in ischaemia and with digoxin.
6. T waves:
peaked in hyperkalaemia
flat, prolonged, in hypokalaemia
inverted:
normal in some leads
ischaemia
infarction
left or right ventricular hypertrophy
pulmonary embolism
bundle branch block.
7. U waves:
can be normal
hypokalaemia.
175
176
Reminders
REMINDERS
CAUSES OF AXIS DEVIATION
Right axis deviation
Normal variant tall thin people.
Right ventricular hypertrophy.
Lateral myocardial infarction (peri-infarction
block).
Dextrocardia or right/left arm lead switch.
The WolffParkinsonWhite (WPW) syndrome.
Left posterior fascicular block.
REMINDERS
POSSIBLE IMPLICATIONS OF ECG PATTERNS
P:QRS apparently not 1:1
If you cannot see one P wave per QRS complex,
consider the following:
atrial flutter.
If the P wave rate is 150200/min and there
are two P waves per QRS complex, the
rhythm is atrial tachycardia with block.
If the P wave rate is normal (i.e. 60100/min)
and there is 2:1 conduction, the rhythm is
sinus with second degree block.
If the PR interval appears to be different with
each beat, complete (third degree) heart
block is probably present.
continued
177
Q waves
Small (septal) Q waves are normal in leads
I, VL and V6.
A Q wave in lead III but not in VF is a normal
variant.
Q waves probably indicate infarction if
present in more than one lead, are longer
than 40 ms in duration and are deeper
than 2 mm.
Q waves in lead III but not in VF, plus right
axis deviation, may indicate pulmonary
embolism.
The leads showing Q waves indicate the site
of an infarction.
178
ST segment depression
Digoxin: ST segment slopes downwards.
Ischaemia: flat ST segment depression.
T wave inversion
Normal in leads III, VR and V1; and in V2V3
in black people.
Ventricular rhythms.
Bundle branch block.
Myocardial infarction.
Right or left ventricular hypertrophy.
The WPW syndrome.