SYMPOSIUM  
Niger J Paed 2012;39 (2):84 - 89  
Afolabi JK  
Oloko GYA  
Paediatrics Electrocardiography  
DOI:http://dx.doi.org/10.4314/njp.v39i2.10  
These waves' produce two impor-  
tant intervals (PR and QT) and two  
segments (PQ and ST)., After the  
recording has been made, each strip  
of the electrocardiogram should be  
analyzed systematically for the fol-  
lowing: Rate, rhythm, P waves, PR  
interval, QRS Axis, QRS morphol-  
ogy, QT interval, T wave, U wave  
and RS progression.Paediatric ECG  
is unique and difficult to interpret,  
but can be used within certain limits  
to identify anatomical, metabolic,  
ionic and hemodynamic abnormali-  
ties. Used alone as the basis of a  
clinical diagnosis the error margin  
could be quite wide. On the other  
hand, when used in the proper con-  
text, it is a very useful adjunct to  
cardiac diagnosis.  
Received: 28th November 2011  
Accepted: 28th November 2011  
Abstract Electrocardiogram (ECG)  
is a graphic recording of the electri-  
cal potential generated in the heart  
on the body surface using a device  
called electrocardiograph which  
was invented more than 100years  
ago by Eithoven. The cardiac mus-  
cle possesses intrinsic properties of  
automaticity, excitability and con-  
ductivity. Sinoatria (SA) node is the  
dominant pace maker. Therefore the  
electrical activity generated here  
spreads through the conduction  
tissue pathways, (i.e. atria, then to  
atrioventricular (AV) node, bundle  
of His and its branches, the purkinje  
system and ultimately to the ventri-  
cles resulting in an electrocardio-  
graphic complex consisting of P-  
QRS-T during a cardiac cycle. One  
cardiac cycle is represented by suc-  
cessive wave forms on an electro-  
cardiographic tracing, the P wave,  
QRS complex, and the T wave.  
(
)
Afolabi JK  
Oloko GYA  
Department of Paediatrics and  
Child Health  
University of Ilorin Teaching Hos-  
pital, Ilorin - Nigeria  
Keyword: Sinoatria node, Electro-  
cardiogram, Paediatric ECG,  
Unique.  
than systole.  
Introduction  
Stroke volume (SV): this is the amount of blood  
ejected from either ventricle in a single contraction.  
Starling's law of the heart states that degree of car-  
diac muscle stretch can increase force of ejected  
blood. More blood filling the ventricles increase the  
stroke volume.  
Properties of Cardiac Cells/ Mechanics of Heart Func-  
tion  
Automaticity: generates electrical impulse inde-  
pendently, without involving the nervous system.  
Excitability: responds to electrical stimulation.  
Conductivity: passes or propagates electrical im-  
pulses from cell to cell.  
Cardiac output (CO): the amount of blood pumped  
through the cardiovascular system per minute.  
CO = SV × heart rate (HR)  
Contractility: shortens in response to electrical  
stimulation.  
Cardiac cycle: sequence of events in one heartbeat.  
Blood is pumped through the entire cardiovascular  
system.  
Sinoatrial (SA) node: dominant pacemaker of the  
heart located in the upper portion of the right  
atrium. Intrinsic rate is 60-100 beats/min.  
Atrioventricular (AV) node: part of AV junctional  
tissue. The AV node slows conduction, creating a  
slight delay before impulses reach ventricles. Intrin-  
sic rate is 40-60 beats/min  
Systole: contraction phase and usually refers to ven-  
tricular contraction.  
Diastole: relaxation phase during which the atria  
and ventricles are filling. This phase lasts longer  
Intermodal pathways: directs electrical impulses  
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between SA and AV nodes.  
V5, V6  
-
L ventricular activity  
Bundle of His: transmits impulses to bundle  
branches. It is located below the AV node.  
Left bundle branch: conducts impulses that lead to  
the left ventricle.  
Right bundle branch: conducts impulses that lead to  
the right ventricle.  
Purkinje system: network of fibres that spread im-  
pulses rapidly throughout the ventricular walls. This  
is located at terminals of bundle branches and has  
an intrinsic rate of 20-40 beats/min.  
Axis Calculation  
Definition and Historical Perspective  
An electrocardiogram (ECG) is the recording (“gram”)  
of the electrical activity (“electro”) generated by the  
cells of the heart (“cardio”) that reaches the body sur-  
face. Material used is the electrocardiograph.  
Electrodes are electrical sensor connected to monitor  
and record. Each ECG recording electrode provides the  
view of this electrical activity that it “sees” from its par-  
ticular position on the body surface.  
Components of the Standard ECG  
Electrocardiograph is the devise used, electrocardiogram  
is the recording, and electrocardiography is the proce-  
dure.  
Electrocardiography was first introduced about 100yrs  
ago by Eithoven. Lead I, II and III form Eithoven trian-  
gle of 60 0. Golberger added aVR, aVL and aVF to pro-  
duce hexaxial refrence system of 300. Lead V1- V6  
were later added for horizontal view.  
Leads in ECG Recording  
The standard limb leads (leads I, II, III) are bipolar leads  
which consist of two electrodes of opposite polarity  
(
positive and negative). The third (ground) electrode  
minimizes electrical activity from other sources.  
Augmented limb leads (aVR, aVL, and aVF) are unipo-  
lar leads which consist of a single positive electrode and  
a reference point (with zero electrical Potential) that lies  
in the center of the heart's electrical field. The precordial  
leads (leads V1-V6) are unipolar leads and consist of a  
single positive electrode with a negative reference point  
found at the electrical center of the heart.  
A segment is a straight line connecting two waves,  
whereas an interval encompasses at least one wave plus  
the connecting straight line.  
P wave: This is the first wave seen. It is a small  
rounded upright (positive) wave indicating atrial  
depolarization (and contraction).  
PR interval: This is the distance between the begin-  
ning of P wav e and beginning of QRS complex. It  
measures the time which a depolarization wave  
travels from the atria to the ventricles.  
Voltage changes are amplified and visually displayed on  
an oscilloscope and graph paper.  
Placement of Precordial Leads  
V1  
V2  
V3  
V4  
V5  
V6  
:
:
:
:
:
:
4th R intercostal space, parasternal  
4th L intercostal space, parasternal  
exactly mid way between V2 and V4  
5th L intercostal space, MCL  
same transverse level as V4, AAL  
same transverse level as V4, MAL  
QRS interval: Includes three deflections following  
the P wave and indicates ventricular depolarization  
and contraction. The Q wave is the first negative  
deflection, R wave is the first positive deflection  
and S wave is the first negative deflection after the  
R wave.  
V3R : corresponds to V3 on the Right side  
V4R : corresponds to V4 on the Right side  
V1, V2, V3R and V4R - R ventricular activity  
ST segment is the distance between S wave and the be-  
ginning of T wave. It measures the time between ven-  
V3, V4 (transitional)  
-
septal activity  
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tricular depolarization and the beginning of repolariza-  
tion.  
Rate: This is age dependent faster at 1/12 than at birth,  
gradually slowing with increasing age thereafter.  
In calculating the rate, either:  
T wave is a rounded upright (positive) wave following  
QRS, and represents ventricular repolarization.  
QT interval is measured from the beginning of QRS to  
the end of the T wave. It represents total ventricular ac-  
tivity.  
Divide 300 by the number of large squares in be-  
tween R waves of successive beats OR  
Divide 1500 by the number of small squares in be-  
tween R waves of successive beats OR  
Multiply the number of R-R cycles in 6 large  
squares (1.2 sec.) by 50. OR  
Multiply the number of R-R cycles between 2 mark-  
ers on a rhythm strip (3 sec.) by 20.  
U wave is a small rounded, upright wave following T  
wave. It is most easily seen with a slow heart rate and  
represents repolarization of purkinje fibres.  
Rhythm: (the pace maker)  
Paediatric ECG  
Sinus: normal, tachycardia, bradycardia, arrhyth-  
mia.  
Proper interpretation of ECG relies on comparisons with  
standards derived from normal population. While ECG  
standards for normal adults have been firmly estab-  
lished, few studies are available for children. Many au-  
thors have demonstrated that these ECG standards could  
be influenced by age, sex, nutrition and race. Paediatric  
ECG is unique and also difficult to interpret in the neo-  
natal period because of the rapid perinatal hemodynamic  
changes and the wide overlap of normal and abnormal  
values. Adequate analysis of the tracing requires a well-  
standardized recording technique (size and position of  
electrode and calibration). Information is particularly  
scarce for some of the leads frequently used in the new  
born infants and young children (V4R, V3R and V7). In  
addition, data are often grouped together over relatively  
wide period of time. Most of the age related changes in  
paediatric ECG are related to the changes in the ratio of  
left ventricular (LV) to right ventricular (RV) weight. At  
birth, the right ventricle is thicker than the left ventricle,  
thus making a right axis deviation (LAD) a normal find-  
ing in the ECG of a term new born. As the child grows,  
the normal RV dominance of the new born period is  
gradually replaced by the LV dominance of the latter  
childhood and adult. There is a tremendous variation of  
the normal ECG at each age group. The ECG can diag-  
nose many conditions and these can be inferred from  
measurement of various intervals or specific patterns.  
However, ECG could be normal in a child with a cardiac  
disease and abnormal in a perfectly normal heart. There-  
fore, electrocardiogram should be correlated with his-  
tory, physical examination, radiographs and echocardio-  
graph of the heart and should only be rarely used to di-  
agnose cardiac disease outside this context.  
Junctional: accelerated, tachycardia, PJC.  
Atrial: flutter, fibrillation, paroxysmal supraven-  
tricular tachycardia (PSVT), Parox-A-T, Wolff-  
Parkinson-White syndrome  
Ventricular: tachycardia, fibrillation, torsade de  
pointes, premature ventricular contraction (PVC).  
Pace maker rhythm: Atrial or ventricular.  
P waves  
Normal P wave: < 2.5mm in height (at normal  
standardisation) ie 0.25mv. < 0.10 sec in duration.  
Right atrial hypertrophy: P waves tall and peaked  
(
>2.5mm high)  
Left atrial hypertrophy: P waves broad (>0.10  
sec in duration), broad and flat topped, broad and  
notched (M-shaped) = P mitrale, broad and bi-  
phasic.  
COMBINE hypertrophy: there is tall and wide p  
wave.  
PR interval  
The normal interval is age and heart rate dependent.  
Usually  
0.07 - 0.12 sec in children under 1 year of age  
0.08 - 0.16 sec in children over 1 year of  
0.10 - 0.18 sec in adolescents  
age  
0.10 - 0.20 sec in adults Shortened in pre  
excitation syndromes, for example WPW  
syndrome (short PR interval, widened QRS  
interval, delta wave preceding the QRS com-  
plex)  
Prolonged in heart block  
In the standard ECG recording:  
1st degree heart block prolonged PR interval  
2nd degree heart block  
-Mobitz type I (Wenckebach).  
-Mobitz type II  
Paper speed  
= 25mm/sec  
small square (horizontal) = 0.04 sec  
large square (horizontal) = 0.2 sec  
0mm (vertical) = 1 mV  
1
1
1
3rd degree (complete) heart block  
(
Avdissociation  
Variable in - wandering atrial pacemaker  
-multi-focal atrial tachycardia  
After the recording has been made, each strip of the  
electrocardiograph should be analyzed for each of the  
following: Rate, rhythm, P waves, PR Interval, QRS  
Axis, QRS morphology, QT interval, T wave, U wave,  
ST Segment, and RS progression  
Electrical axis of the heart  
The electrical axis is the sum total of all electrical cur-  
rents generated by the ventricular myocardium during  
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depolarization and its direction. It helps to determine the  
location and extent of cardiac injury, such as ventricular  
hypertrophy, bundle branch block, or changes in the  
position of the heart in the chest such as ascites. The  
direction of the QRS complex in leads I and aVF deter-  
mines the axis quadrant in relation to the heart.  
Q waves normally absent in RPLs.  
Deep Q in LPLs in ventricular hypertrophy of vol-  
ume overload type  
Deep and wide Q in myocardial infarction and myo-  
cardial fibrosis  
Q waves in V1 in severe right ventricular hypertro-  
phy (RVH), ventricular inversion (L-TGA) single  
ventricle, occasionally in newborns.  
Absent Q in V6 may be seen in LBBB & ventricular  
inversion.  
Calculation using Leads I and aVF  
Determine the value of R minus S in lead I -  
horizontal (x)  
Determine R minus S in lead aVF - vertical (y)  
Determine point of intersection (p) of perpen-  
dicular line drawn through x and y  
QRS Morphology  
Join P to centre and determine the value of the  
angle on standard graph paper.  
Leads V  
Leads V  
Leads V  
1
3
5
, V  
, V  
, V  
2
4
6
, V4R - right ventricle activity  
(transitional) - septal activity  
- left ventricle activity  
Calculation using successive approximation  
method  
Q wave  
Use leads I and aVF to locate the quadrant of  
the axis.  
Represent septal depolarization wave from left to right.  
It normally presents in LV leads as a negative wave, and  
absent in RV leads. The normal duration is 0.08sec.  
Normal depth should not exceed 5mm in LV leads.  
I
aVF  
Axis  
Dominant R(+ve) Dominant R (+ve) 00 to + 900  
Dominant S (-ve) Dominant R (+ve) +900 to + 1800  
Dominant S (-ve) Dominant S (-ve) +1800 to +2700  
Dominant R (+ve) Dominant S (-ve) +2700 to + 3600  
Q wave presence in RV leads can be due to: Left bundle  
branch block, ischemia, severe RVH, right sided endo-  
myocardial fibrosis (EMF), congenitally corrected TGA  
in which Q is absent in LV leads, premature ventricular  
contraction, ventricular tachycardia and ischemia.  
Determine lead with the most equiphasic RS wave or  
least voltage.  
Criteria for RVH  
Axis is perpendicular to this lead within the quadrant  
located in leads I and aVF.  
S in lead I, 12mm - R in aVR, 8mm  
Pure R (no S) in V1 > 10mm - R in V1 25mm  
A qR pattern in V1 - Upright T in V1 > 3days +  
upright T in V6 RAD > 1800  
NB;  
Lead I is perpendicular to Lead aVF  
Lead II is perpendicular to Lead aVL  
Lead III is perpendicular to Lead aVR.  
OR  
Voltage criteria:  
Determine the lead with the greatest R or S deflection in  
the quadrant located in (i). The mean QRS axis is close  
to the +ve or ve limb (respectively) of that lead.  
RVH = R in V4R >15mm in children aged <3 months  
>10mm in children aged >3 months  
Abnormalities in electrical axis may give an indication  
as to the presence of structural defects for example:  
Criteria for LVH  
LAD for patient's age - R in 1, II & III,  
aVL,aVF,V5 or V6 > normal  
S in V1 or V2 > upper limit for age.  
R/S in favour of LV  
Q in V5 & V6 > 5mm with tall symmetric T wave  
Wide QRS-T angle in the presence of LVH inverted  
T in lead I or aVF.  
Right axis deviation- Tetralogy of Fallot, pulmonary  
atresia, transposition of the great arteries (TGA).  
Superior axis deviation- Atrioventricular septal defect,  
tricuspid atresia.  
- Abnormal  
QRS Complex  
The QRS complex represents ventricular depolarization  
and the normal duration 0.10 seconds or less. It is meas-  
ured from the beginning of the Q to the end of the S  
deflection.  
Voltage criteria:  
LVH = R in V6 >20mm in children <3 month  
>
25mm in children >3 months  
Combine Ventricular Hypertrophy  
General considerations:  
R/S ratio large in right precordial leads (RPLs) and  
small in the left precordial leads (LPLs) in normal  
infants and small children (tall R in RPLs and deep  
S in LPLs).  
Voltage criteria for RVH and LVH in absence of  
BBB or WPW syndrome  
Positive voltage criteria for RVH or LVH  
BVH = R + S in V3 or V4 >70mm  
Normal Q waves are narrow < 5mm in LPLs & aVF  
(
may be up to 8mm in lead III in children aged  
<
3yrs).  
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RS progression pattern  
Prolonged in- hypocalcaemia, myocarditis, myocardial  
disease, head injury; CVA, quinidine, procainamide or  
amiodorone therapy, Long QT  
syndrome such as Jervell and Lange-Nielsen Syndrome  
and Romano-Ward Syndrome.  
RV leads LV leads  
Neonatal pattern (up to 6/52) Dom R Dom S  
Infant pattern (6/52 - 18/12) Dom R Dom R  
Adult pattern (> 18/12) Dom S Dom R  
Shortened in - hypercalcaemia, digitalis effect.0  
An 'adult' pattern found in a neonate would suggest  
LVH, whereas an 'infant' pattern found in a child of five  
years would suggest RVH.  
Digitalis effect include shortening of QTc, sagging of  
ST segment, and slowing of heart rate while digoxin  
toxicity causes prolongation of PR interval, sinus bra-  
dycardia/ SA block, 2nd degree heart block, supraven-  
tricular arrhythmia, ventricular bigeminy/ trigeminy  
QRS amplitude may be reduced in - pericardial effusion,  
endomyocardial fibrosis (EMF), hypothyroidism  
(
rare in children), premature ventricular contractions,  
and ventricular tachycardia.  
ECG Strips For Practice  
Normal sinus rhythm  
T Waves  
In LV leads, it is normally upright in all ages, but  
may be flattened in the neonatal period.  
In RV lead, it is upright at birth up to one week of  
life, become inverted till puberty, then upright for  
the rest of life.  
Presence of upright T waves in RV leads in a prepu-  
bertal patient over the age of one week suggests  
RVH.  
Normal height of T Waves  
V5  
V6  
<
>
1yr: <11mm  
1yr: <14mm  
<7mm  
<9mm  
Sinus arrhythmia  
Tall, tented T waves - Causes include hyperkalaemia,  
LVH, early myocardial infarction, cerebrovascular acci-  
dent (CVA).  
Flattened/inverted T waves - Causes include myocardial  
disease, pericardial disease, LVH with myocardial  
strain, hypokalaemia, digitalis effect, hypothyroidism,  
and neonatal period  
Left atrial hypertrophy  
ST Segment  
It is not more than 1-2mm above the isoelectric line.  
ST segment depression: can be caused by myocardial  
ischemia, left ventricular hypertrophy, intraventricular  
conduction defect, medications such as digitalis.  
ST segment elevation: an elevation of 1 mm in the limb  
leads and 2 mm in the chest leads indicates an evolving  
acute myocardial infarction until proven otherwise.  
Other primary causes of ST segment elevation are early  
repolarization (normal variant in young adults), pericar-  
ditis, ventricular aneurysm, pulmonary embolism, and  
intracranial hemorrhage.  
QT Interval  
The QT interval varies with heart rate, but not with age  
(
(
except in infancy) and must therefore be corrected for  
QTc) using either a table, on Bazett's formula:  
QTc  
= Measured QT  
RR interval  
QTc should not exceed 0.44 sec. except in infants. Up  
to 0.49 sec. may be normal in the first 6 months of life.  
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The electrical axis of the heart  
ST depression  
Prolonged QT interval  
Right axis deviation  
Conflict of interest: none  
Funding : none  
Right ventricular hypertrophy  
Acknowledgement  
Reproduced with kind permission of the department of  
Paediatrics and Child Health of the University of Ilorin  
Teaching Hospital, Ilorin Nigeria owners of the Ilorin  
Paediatric Digest 2010.  
References  
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The Alan E. Lindsay ECG  
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Yanowitz FG. http://  
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Shinebourne, EA. Investiga-  
tions: The Electrocardiogram.  
In: Shinebourne EA, Anderson  
RH, eds. Current Paediatric  
Cardiology. Oxford: Oxford  
4. Paediatric Cardiology for  
Medical Professionals. Http://  
pediatriccardiol-  
ogy.uchicago.edu/MP/  
pcmedprof.htm  
5. Chugh SN. Physiological  
Mechanisms Governing Elec-  
trocardiographic Deflections in  
textbook of clinical electrocar-  
diography; 2nd edition; Jaypee  
Brothers, new Delhi 2006; 1-  
40.  
2
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1
980: 49-56.  
3
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Park MK and Guntheroth WG  
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1
992; 1-55.