ECG Abnormalities
ECG Abnormalities
This summary of ECG abnormalities is part of the almostadoctor ECG series. For a more in depth explanation of ECG
abnormalities, see ECG abnormalities. To learn about the basic principle of an ECG, see Understanding ECGs
Sinus Tachycardia Same as above, except All leads Does not represent
>100bpm (best to look cardiac patholoy. May be
at the a sign of anxiety,
rhythm strip) dehydration, recent
exercise, or general illness
(e.g. sepsis, pneumonia,
respiratory pathology,
other illness)
Sinus bradycardia Same as above except All leads This is normal in young fit
<60bpm (best to look people
at the
rhythm strip)
Right ventricular hypertrophy Negative QRS Lead I Because the cardiac axis
has shifted from 11-5
o’clock to 1-7 o’clock, thus
lead I which measures
laterally from right to left
now gets a negative
signal because the signal
is going from left to right.
This axis shift is called
right axis deviation.
Right ventricular hypertrophy Taller QRS Lead III – Because lead III measures
becomes vertically but also slightly
taller than left to right, and this is
lead II pretty much the exact
direction of the new shifted
axis. Lead II, measuring
from right arm to left leg is
no longer lined up as well.
This axis shift is called
right axis deviation.
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Atrial fibrillation Absent P waves – just an some? As well as no p waves,
irregular baseline. the rhythm will be
irregularly irregular. There
Irregularly Irregular, irregular Rhythm will be a fibrillating
QRS (but QRS is normal strip baseline due to
shape) uncoordinated activity.
The causes of
Might look messy! E.g. Generally atrial fibrillation
are:
1. Ischaemic
heart disease
2. Thyrotoxicosis
(hyperthyroidism)
3. Sepsis
4. Valvular
heart disease
5. Alcohol excess
6. PE
1st degree heart block PR interval >0.2s (one Allover – This is an AV node block
big square) best in I or Can be caused by CAD,
V1 acute rheumatic carditis,
digoxin toxicity, or
electrolyte disturbance
It is NOT an
medical
1st Degree Heart Block emergency
2/8
2nd degree heart block Progressive lengthening Anywhere This can be an AV node
Mobitz type 1 – Wencebach of the PR interval followed block (nearly always), or
by absent QRS, then cycle an SA node block.
repeats. Cycles are usually benign and
variable in length. R-R generally doesn’t require
Mobitz type 2 interval shortens with specific treatment. can be
lengthening of PR interval caused by CHD or acute
MI.
It is usually symptomless,
but can present with:
2:1 and 3:1 conduction –Dizziness / light-
headedness / syncope
Absent QRS every now and Anywhere This can be an SA node
again block, or far more
commonly infra-Hisian
block (distal block). It
can progress to
complete heart block,
from which there is
often no escape
rhythm; and thus this
needs treatment! the
definitive treatment is an
implanted pacemaker.
Can be caused by CHD
or MI
This is the ratio of P:QRS Anywhere May require a pacemaker,
particularly if the rate is
slow
Complete (third degree) heart block 90 P waves/min, only about Best in II This is an AV node
38 QRS/min, and not and V1 block.
relationship between the P Atrial activity will be
waves and the QRS completely normal, but
complexes. QRS will often this conductivity does not
have an abnormal shape, pass into the ventricles.
and be broad (>120ms). This always indicates
However, the P-P intervals underlying disease – the
will be regular, as will the R-R disease is often fibrosis
intervals – they are just not rather than ischaemia, but
in time with each other. The it can occur in MI.
rhythm of the ventricles is the
escape rhythm.
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RBBB – right bundle branch block ECG may appear normal. These are infra-Hisian
In some people there may blocks. In bundle branch
be 2 R waves. This creates blockages, the wave of
a distinctive pattern: depolarisation can still
V1 – there is an M reach the IV septum,
shaped QRS – this is then the PR interval will
sometimes called an RSR be normal – and it is.
pattern However, the time
V6 – there is a W taken for the
shaped QRS depolarisation to
Wide QRS (120ms) spread throughout the
ventricles is longer –
LBBB – left bundle branch block V1 – there is an W
thus QRS complex
shaped QRS
duration is
V6 – there is a M
lengthened.
shaped QRS
In the acute setting it may
Wide QRS (>120ms)
be caused by MI
The axis can be deviated
RBBB – may indicate right
either way in BBB’s, but it is
sided disease. The two R
most commonly normal
waves indicate the
depolarisation of the right
and left sides of the heart
at different times (the
right depolarises after the
left).
You can remember the
pattern with the word
MarroW – there is M in
V1, and W in v6, and the
‘rr’ tells you it is on the
right!
There is NOT specific
treatment, and it is often
caused by an atrial septal
defect.
In the acute setting it may
be caused by MI
LBBB – often indicates
left sided heart
disease. Remember
the pattern with
WillaM.
Causes:
Aortic stenosis, dilated
cardiomyopathy, acute
MI, CAD
Symptoms:
Syncope, and in more
severe cases; heart
failure. Those with
syncope and / or
heart failure will
usually be treated
with a pacemaker.
4/8
Ventricular Wide QRS complexes Anywhere
rhythms (aka escape
rhythms) Atrial Abnormal p wave (e.g. Anywhere This occurs when the SA
escape Junctional inverted) node fails to
escape Ventricular Normal depolarise. Instead,
escape QRS some other part of the
Accelerated idioventricular rhythm Some normal beats after the atrium depolarises and
abnormal one sends the signal to the
ventricles.
No p The escape occurs
waves somewhere at the AV
Normal junction. It occurs when
QRS the rate of depolarisation
Slightly slow rate (max of the SA node falls below
75bpm) the rate of the AV node,
thus the AV node starts
the beat instead. The
resulting bradycardia
reduces cardiac output
and can cause
symptoms similar to
other bradycardias
such as:
–Dizziness
–Light-headedness
–Syncope
–Hypotension
Usually the bradycardia
can be tolerated as long
as it is above 50bpm
5/8
Posterior MI ST depression, tall R V1-V3 Posterior MI is
waves unusual! The changes
that occur are opposite
to the changes of
other type of MI. thus
the tall R waves are the
opposite of Q waves
(remember Q waves are
negative), and ST
depression occurs in
place of ST elevation
ST elevation ST elevation >2mm in 2+ T wave Both factors, if they occur,
MI (STEMI) chest leads OR >1mm in inversion are usually permanent. In
2+ limb leads, occurs a full thickness
T-wave inversion (after within a few infarction then there are
several hours) hours of MI, pathological Q waves,
Pathological Q waves (24 pathological and T wave inversion,
hours +) Q waves but in a non-full
occur thickness MI then there is
several days only T wave inversion.
after initial The differentiation
MI between full /thickness
and non full thickness is
pretty much the same as
NSTEMI Pathological Q waves only ST elevation / non-ST
elevation
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The digoxin effect Depression of ST, inverted T widesprea This causes a sloping ST
waves d segment that has a
‘reversed tick’ look. This
occurs because digoxin
blocks the na/K pump,
which increases
intracellular Ca2+
concentrations. (similarly,
ischaemia causes
reduced production of
ATP, and thus reduced
pump activity)
Axis deviation
7/8
Lead I Lead II Axis
+ + Normal
+ – LAD
– Either RAD
Applying the pressure reduces the frequency of QRS complexes, and allows the underlying atrial arrhythmia to
become more visible.
8/8