CONTINUING EDUCATION

Fundamentals of Electrocardiography
Interpretation
Daniel E. Becker, DDS
Professor of Allied Health Sciences, Sinclair Community College, and Associate Director of Education, General Dental Practice
Residency, Miami Valley Hospital, Dayton, Ohio 45409

The use of dynamic electrocardiogram (ECG) monitoring is regarded as a standard

of care during general anesthesia and is strongly encouraged when providing deep
sedation. Although significant cardiovascular changes rarely if ever can be attributed
to mild or moderate sedation techniques, the American Dental Association recommends ECG monitoring for patients with significant cardiovascular disease. The purpose of this continuing education article is to review basic principals of ECG monitoring and interpretation.
Key Words: Electrocardiography; Patient monitoring; Continuing education.

ynamic electrocardiographic (ECG) monitoring is a

standard of practice when providing general anesthesia, but opinions are mixed regarding its use during
moderate (conscious) and deep sedation. The American
Dental Society of Anesthesiology included pulse oximetry for patient monitoring in its guidelines published in
1991.1 The guidelines at that time also encouraged
ECG monitoring during deep sedation, but not during
moderate (conscious) sedation. The American Dental
Association recently revised its monitoring guidelines to
include ECG monitoring for all deeply-sedated patients
and for consciously-sedated patients with compromised
cardiovascular function.2 Most publications in the medical anesthesia literature regard ECG monitoring as a
standard for both sedation and anesthesia,3 but many
experts question its actual value in preventing sedationrelated morbidity and mortality among patients without
preexisting cardiac risk. Despite this controversy, a
growing number of state dental boards are requiring
ECG monitoring for general anesthesia and all levels of
intravenous sedation.
Disregarding these legal controversies, there is an intangible reassurance provided by an ECG monitor that
adds to that provided by periodic measurement of blood
pressure and continuous pulse oximetry. This of course
presumes that the operator is comfortable witnessing

occasional benign arrhythmias and the subtle mechanical nuances all monitors present during routine use. The
purpose of this Continuing Education article is to provide fundamental concepts of ECG recognition that will
enable the dentist to feel more comfortable with the routine use of dynamic ECG monitoring.

GENERAL PRINCIPLES OF CARDIAC

FUNCTION
The output of the heart per minute (cardiac output) is
the paramount cardiovascular event required to sustain
blood flow throughout the body. In addition to blood
volume and contractile strength, the heart must sustain
a regular cycle of relaxation and contraction if it is to
fulfill its objective. This regularity is predicated on a series of complex electrophysiological events within the
cardiac tissues that can be monitored using a device
called the electrocardiogram. This device is variably referred to as an ECG or as an EKG, the latter based on
the Greek term kardia for heart. Many prefer EKG
to ECG because it is less likely to be confused verbally
with EEG, the abbreviation for electroencephalogram.
However, we will arbitrarily adopt ECG for this presentation.
The quintessential events required for a normal cardiac cycle are the rhythmic contraction and relaxation
of the atria and ventricles. The heart is composed of 2
principal cell types: working cells and specialized neural-

Received June 27, 2005; accepted for publication September 20,

2005.
Address correspondence to Dr Daniel Becker, Miami Valley Hospital, Dayton, Ohio 45409; [email protected].
Anesth Prog 53:5364 2006
2006 by the American Dental Society of Anesthesiology

ISSN 0003-3006/06/$9.50
SSDI 0003-3006(06)

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Figure 1. Specialized neural-like conductive tissues and their approximate firing rates.

like conductive cells. The working cells are the muscle

or myocardium of the atria and ventricles. Specialized
cells include the sinuatrial (SA) node, the atrioventricular
(AV) node, the bundle of His, and the Purkinje fibers
(Figure 1). These cells initiate and conduct electrical impulses throughout the myocardium, and this regulates
the rhythm of a cardiac cycle. In order to initiate impulses, specialized cells have a property called automaticity, which reflects an ability to initiate electrical
impulses spontaneously. This is independent of any
nerves or hormones, but their actual rate of firing can
be influenced by autonomic nerves, with sympathetics
increasing and parasympathetics decreasing their rate.
Each cardiac cycle commences with an impulse, spontaneously generated by the SA node, that subsequently
spreads throughout the remainder of the neural-like
conductive tissues and onto the muscle (myocardial)
cells. Abnormalities within this conduction system will

Figure 2. Depolarization and repolarization of cell membranes. A) The resting cell membrane is charged positively on
the outside and negatively on the inside. B) Following a stimulus (S), positive ions enter the cell reversing this polarity. C)
This process continues until the entire cell is depolarized. D)
Ions are returned to their normal location and the cell repolarizes to its normal resting potential.

compromise cardiac output and are called arrhythmias

or dysrhythmias synonymously.

ELECTROPHYSIOLOGICAL CONSIDERATIONS
To fully appreciate electrical impulses and the information provided by an ECG, we must first review fundamental concepts regarding electrical membrane potentials. All cardiac cell membranes are positively charged
on their outer surfaces because of the relative distribution of cations. This resting membrane potential is
maintained by an active transport mechanism called the
sodium-potassium pump. When the cell is stimulated,
ion channels open, allowing a sudden influx of sodium
and/or calcium ions and thereby reversing the resting
potential. This period of depolarization is very brief because sodium channels close abruptly, denying further
influx of sodium. Simultaneously, potassium channels
open and allow intracellular potassium to diffuse outward while sodium ions are actively pumped out. This
reestablishes a positive charge to the outside of the
membrane, a process called repolarization that returns
the membrane to its resting membrane potential. The
processes of depolarization and repolarization are referred to collectively as an action potential. This event
self-propagates as an impulse along the entire surface
of a cell and from one cell to another, provided that their
membranes are connected (Figure 2).
It is essential that one address the actual purpose of
an action potential. All human cells exhibit this phenomenon, and its purpose varies according to the cells function. The purpose of action potentials in neurons is to

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55

Figure 3. Summary of events of a cardiac cycle. Of the 8 physiologic events listed for a cardiac cycle, only 3 are actually observed
on an ECG tracing.

Figure 4. A) Einthovens triangle and B) standard limb leads I, II, and III.

initiate release of neurotransmitters that either excite or

stabilize cell membranes of the tissue innervated. In skeletal and cardiac muscle cells, action potentials release
stored calcium ions that initiate the actual contractile
process.
Cells comprising the hearts conduction system are
unique in 2 aspects. First of all, they possess automaticity. The physiological explanation for this property resides in the resting membranes partial permeability to
calcium and/or sodium ions. The gradual inward leak
of cations decreases the voltage of the resting potential
until a threshold is reached. At this point, all channels
open and rapid cation influx depolarizes the membrane.
The second unique characteristic of this specialized tis-

sue is the fact that, unlike classic neural tissue, these

cells do not release neurotransmitters. Instead, they are
in direct contact with cardiac muscle, and their action
potential initiates depolarization of the cardiac muscle
cells directly.
Cardiac muscle cells are fused to one another by special attachments called intercalated discs. This allows
them to function as a continuous sheet of cells called a
syncytium.4 The atrial syncytium is separated from that
of the ventricles by a layer of connective tissue that acts
as an insulator. The SA node initiates depolarization of
the atrial muscle, but the insulation precludes propagation into the ventricles except at 1 place, the AV node.
The AV node delays and finally relays the impulse along

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ECG Interpretation

the common bundle of His, which penetrates the connective tissue to enter the ventricles. The impulse continues along the common bundle of His and its branches
until it finally reaches the Purkinje fibers, which ignite
the ventricular muscle syncytium.
The action potential of an individual cell can be measured using microprobes inserted through its cell membrane. It is far too small an electrical event to be measured by surface electrodes. However, action potentials
that spread throughout the muscle syncytia of the heart
are great enough for surface electrodes to record and
produce a tracing known as an ECG. It is important to
appreciate that the ECG cannot record electrical events
generated by the specialized cells of the conduction system; their voltages are far too small. What you observe
in an ECG tracing is the action potentials of the atrial
and ventricular muscle cells. However, other events can
be deduced from the tracing.

THE ECG TRACING

The electrical sequence of a cardiac cycle is initiated by
the sinoatrial node, the so-called pacemaker of the
heart. This is because the SA node has a faster rate of
spontaneous firing than the remaining specialized tissues (see Figure 1). However, if this rate should decrease, other portions of this specialized system can
gain control, a phenomenon termed escape.
The baseline of an ECG tracing is called the isoelectric
line and denotes resting membrane potentials. Deflections from this point are lettered in alphabetical order,
and following each, the tracing normally returns to the
isoelectric point. The first deflection is the P wave and
represents depolarization of atrial muscle cells. It does
not represent contraction of this muscle, nor does it represent firing of the SA node. These events are deduced
based on the shape and consistency of the P waves.
One assumes that the SA node fires at the start of the
P wave, and one assumes that atrial contraction begins
at the peak of the P wave. Although atrial repolarization
follows depolarization, the ECG provides no evidence
of this event. A popular misconception is that evidence
of repolarization is obscured by the subsequent QRS
complex. Were this true, however, repolarization would
be observed in cases where the QRS complex is delayed
or absent, eg, AV blocks. The correct explanation is that
atrial repolarization is too minor in amplitude to be recorded by surface electrodes.5,6
The QRS complex represents depolarization of ventricular muscle cells. The Q portion is the initial downward deflection, the R portion is the initial upward deflection, and the S portion is the return to the baseline,
or the so-called isoelectric point. Often, the Q portion

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is not evident and the depolarization presents as only

an RS complex. In any case, the complex does not
represent ventricular contraction. One assumes that
contraction will commence at the peak of the R portion
of the complex. Unlike contraction of the atria, ventricular contraction can be confirmed clinically by palpating
a pulse or by monitoring a pulse oximeter wave form.
A patient in cardiac arrest may have normal QRS complexes on his or her ECG; ventricular muscle cells are
depolarizing, but there is no contraction. This phenomenon is called pulseless electrical activity. Following
depolarization, ventricular muscle repolarizes, and this
event is great enough in amplitude to generate the T
wave on the ECG tracing.
The PR interval is measured from the beginning of
the P wave to the beginning of the R portion of the
QRS complex. (This is conventional because the Q portion of the complex is so frequently indiscernible.) Because the PR interval commences with atrial muscle depolarization and ends with the start of ventricular depolarization, one can assume that the electrical impulse
passes through the AV node into the ventricle during
this interval. If the PR interval is prolonged, one may
deduce that AV block is present. The electrical events
of an ECG are illustrated and summarized in Figure 3.

TECHNICAL CONSIDERATIONS
In 1901 a Dutch physiologist, Willem Einthoven, developed a galvanometer that could record the electrical activity of the heart. He found that a tracing can be produced as action potentials spread between negatively
and positively charged electrodes. (A third electrode
serves to ground the current.) He found that tracings
varied according to the location of the positive and negative electrodes, and subsequently described 3 angles or
leads in the form of a triangle with the heart in the
middle. This is known today as Einthovens triangle, and
the 3 electrode arrangements are known as the primary
limb leads I, II, and III (Figure 4). As research continued
throughout the 20th century, additional arrangements
were discovered that enable physicians to analyze electrical events as they spread in many directions through
the heart, much like an apple slicer sections an apple
into various parts. Today, the cardiologist analyzes a 12lead ECG to aid in diagnosing infarctions, hypertrophy,
and complex arrhythmias. Our purpose in this article,
however, is to identify only the basic arrhythmias that
justify dynamic ECG monitoring during sedation and
general anesthesia. For this purpose, a single-lead ECG
is all that is required. Most often, lead II is selected because it generally records the largest waves.

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ECG PAPER
An ECG monitor displays a tracing that lacks any grid
as background. However, most of these monitors are
equipped with optional printers that can generate a gridded printout if desired. As the stylus of the recording
device is deflected by electrical currents, the recording
paper is moving at a speed of 25 mm/s. This creates
an ECG tracing whose components can be measured.
The vertical axis of an ECG denotes voltage and the
direction of waveforms from the baseline. These considerations are generally irrelevant during routine monitoring, but have significance for diagnosing ischemia
and infarction. The horizontal axis denotes time and sequence of events, both of which are essential for arrhythmia recognition. Standard ECG recording paper is
divided into small and large squares. The former represent 0.04-second intervals. Five small squares constitute a large square, which represents 0.20 seconds. Notice, in Figure 5, that the lines between every 5 boxes
are heavier, so that each 5-mm unit horizontally corresponds to 0.2 seconds (5 0.04 0.2). The ECG can
therefore be regarded as a moving graph with 0.04- and
0.2-second divisions.

ECG ANALYSIS
Dynamic ECG monitors display heart rate, but it can
also be ascertained from a printed tracing using either
of 2 methods:
1. When the heart rate is regular, count the number of
large (0.2-second) boxes between 2 successive QRS
complexes and divide 300 by this number. The number of large time boxes is divided into 300 because
300 0.20 60 and heart rate is calculated in
beats per minute or 60 seconds. For example, if
there are 3 large boxes between QRS complexes,
the heart rate is 100 beats/min, because 300 3
100. Similarly, if 4 large time boxes are counted
between QRS complexes, the heart rate is 75 beats/
min (Figure 6).
2. If the heart rate is irregular, the first method will not
be accurate because the intervals between QRS complexes vary from beat to beat. In most cases, ECG
graph paper is scored with marks at 3-second intervals. In such cases simply count the number of QRS
complexes every 3 or 6 seconds and multiply this
number by 20 or 10 respectively.
How one chooses to analyze an ECG rhythm strip is
arbitrary. Each clinician must adopt a sequence of analysis that accommodates personal methods of reasoning.

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57

Always keep in mind that events during the PR interval

pertain to supraventricular activity. When abnormalities
are detected, try to establish the event as ventricular or
supraventricular in origin. The following sequence represents one suggestion for analysis of an ECG tracing.
I describe it as a 5-step analysis. Refer to Figure 6 during
the following explanation.
Step 1: Is the Rhythm Regular or Irregular?
If the intervals between QRS complexes (R-R intervals)
are consistent, ventricular rhythm is regular. If intervals
between P waves (P-P intervals) are consistent, the atrial
rhythm is regular. In Figure 6 the rhythm is regular.
Step 2: Are All QRS Complexes Similar, and
Are They Narrow?
The duration of the QRS complex should not exceed
0.10 seconds (2 small squares). A widened complex
indicates ventricular enlargement (hypertrophy) or that
ventricular depolarization is being initiated by pacemaker tissue below the AV node, eg, ventricular-paced
rhythm. In this case, 1 ventricle depolarizes first and the
current must spread into the second ventricle. This takes
more time than when the current spreads down the bundle into both ventricles simultaneously. If QRS complexes are narrow, the rhythm is being initiated by a pacemaker at the AV node or higher and is described as a
supraventricular rhythm. If the complexes are wide, the
pacemaker is in the ventricles and is described as a ventricular rhythm. Should complexes vary in appearance,
more than one pacemaker is generating impulses. This
phenomenon is referred to as ectopic pacemakers, and
the rhythm described as ectopy.
Step 3: Are All P Waves Similar and Are PR
Intervals Normal?
If P waves are all similar, and normal in shape, one can
assume that the SA node is the primary pacemaker. In
this case the rhythm is sinus in character. If P waves
vary in shape or are absent, other tissue(s) are functioning as pacers.
The PR interval is normally 0.120.20 seconds (35
small squares). Longer intervals indicate that the impulse
is being delayed from entering the ventricles and the
condition is designated AV block.
Step 4: Is the Rate Normal?
If the rhythm is regular, count the number of large
squares between QRS complexes and divide this num-

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Figure 6. The normal ECG tracing.

Figure 5. Standard ECG paper.

Figure 7. Sinus bradycardia. Each cycle commences with a P wave and the PR interval is normal. Therefore, rhythms are sinuspaced and differ only in rate: normal sinus rhythm, sinus bradycardia, or sinus tachycardia. In this case, it is sinus bradycardia,
because the rate is 60.

Figure 8. Junctional rhythm. There are no P waves and a PR interval cannot be ascertained. Therefore, the sinoatrial node is
not pacing this rhythm. But the QRS complexes are narrow, so the pacemaker is above the ventricles. The logical conclusion is
that the atrioventricular node or neighboring tissue is pacing the heart. This is called junctional rhythm. Because this node has a
slower firing rate than the sinoatrial node (See Figure 1), rates of 50 and 90 are the cutoffs for bradycardic and tachycardic rates,
ie, junctional bradycardia or tachycardia.

Figure 9. Normal sinus rhythm with first-degree atrioventricular block. Each cycle commences with a P wave, but the PR interval
is prolonged. Therefore, rhythm is sinus-paced but the impulse is being delayed at the atrioventricular node. Rates can be normal,
bradycardic, or tachycardic.

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Figure 10. Supraventricular tachycardia. There are no P waves and a PR interval cannot be ascertained. Only 1 wave is discernible
between QRS complexes and one cannot determine whether a P wave is absent or occurring simultaneously with the T wave.
The rhythm is rapid, but one cannot conclude whether it is sinus-paced or paced by some other tissue. It could be sinus tachycardia
or junctional tachycardia, but we cant be sure. This dilemma surfaces when rates become greater than 150. Therefore, because
the QRS complexes are narrow, we know only that the rhythm is being paced from above the ventricle. Is it sinus or junctional
paced? We cop out and call it supraventricular.

Figure 11. Atrial flutter. Multiple waves appear between each QRS complex and we cannot ascertain whether they are P or T
waves. This pattern emerges when an ectopic pacemaker emerges in the atrial muscle and fires more rapidly than the sinuatrial
node. This generates multiple depolarizations in the atrial muscle, reflected as so-called flutter waves. Each has a slant to its anterior
portion; we can describe this as a saw-toothed pattern. Normally, the atrioventricular node allows only one of them to pass into
the ventricle each cycle, which results in a regular ventricular response.

Figure 12. Premature atrial and junctional complexes. Most cycles commence with a P wave, and most PR intervals are normal.
Therefore, the rhythm is sinus-paced, but occasionally an extra impulse is fired from an ectopic pacemaker that travels down into
the ventricle and creates an extra QRS complex. Notice that normally there is a pause, or a period of time following a T wave
until the next P wave commences. In the case of premature complexes, this pause is interrupted. At this point in your training, it
is not important to interpret the source of this premature complex; is it atrial or junctional? We know it is coming from above the
ventricle, and it is always acceptable to call it a premature atrial complex. The difference between the two has little clinical relevance.

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Figure 13. Atrial fibrillation. The waves between each QRS complex are random and indistinct; in essence, theyre a mess!
Furthermore, the R-R intervals are consistently irregular. This pattern emerges when several ectopic pacemakers emerge in the
atrial muscle and all fire more rapidly than the sinuatrial node. This generates multiple depolarizations in the atrial muscle, far
more numerous than those with atrial flutter. The atrioventricular node is so overwhelmed with impulses that it cannot allow any
to pass through on a regular basis. Therefore, we see this striking irregular ventricular response.

Figure 14. Normal sinus rhythm with second-degree (Mobitz) atrioventricular block. Each cycle commences with a P wave, but
occasionally the P wave is not followed by a QRS and another P wave appears. This is called a dropped beat and is the
fundamental defect in a second-degree or Mobitz block. First look at tracing A. (Dont be disturbed by the fact that the QRS
complexes go down instead of up. Waves are waves! Their direction depends on the particular lead used to record the tracing.)
Notice that each successive PR interval lengthens until finally 1 P wave stands alone and a beat is dropped. Also notice that after
the beat is dropped, the PR intervals commence again to progressively lengthen until another beat is dropped. This strange pattern
of PR intervals was first described by a cardiologist named Wenckebach. Therefore, this type of second-degree block is called a
Mobitz 1 or Wenckebach block. In tracing B, notice that all PR intervals are identical. They may be normal in length or delayed,
but they are all the same; even after a beat is dropped, they resume their duration. This is called a Mobitz 2 block. In this particular
example, the ratio of P waves to QRS complexes is 2 : 1. Therefore, the R-R intervals are regular. With any other ratio, eg, 3 : 1
or 4 : 1, the R-R interval would appear irregular.

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Figure 15. Ventricular tachycardia. There are no P waves and a PR interval cannot be ascertained. No waves are discernible
between QRS complexes, but the R-R intervals are regular and the QRS complexes are wide. The rhythm is rapid and is being
paced by tissue in the ventricle. This rhythm differs from supraventricular tachycardia (Figure 10) only in the fact that the QRS
complexes are wide rather than narrow.

Figure 16. Idioventricular rhythm. There are no P waves and a PR interval cannot be ascertained. No waves are discernible
between QRS complexes, but the R-R intervals are regular and the QRS complexes are wide. The rhythm is slow and is being
paced by tissue in the ventricle. This rhythm differs from ventricular tachycardia (Figure 15) only in the fact that the rate is slow;
it could just as well be called ventricular bradycardia.

Figure 17. Third-degree (complete) block. There are P waves but the PR intervals appear inconsistent; no pattern is repeated.
If impulses were being conducted into the ventricles, the R-R intervals would be irregular and the QRS complexes would be narrow.
Neither is the case, however; the R-R intervals are regular and the complexes are slightly widened. (They get wider and wider
according to the location of the ventricular pacemaker. In this case, the pacer is probably in the bundle of His, because the complex
is relatively narrow.) On closer analysis, one can detect that intervals between P waves (P-P intervals) are consistent and that R-R
intervals are consistent. The only explanation is that the SA node is pacing the atria but impulses are not reaching the ventricles.
Therefore, the ventricles have developed their own pacemaker and we have a complete (third-degree) heart block.

Figure 18. Premature ventricular complexes. Most cycles contain narrow QRS complexes and could represent any of the supraventricular rhythms described in groups A or B. But occasionally one sees a wide QRS complex interposed between the cardiac
cycles. Therefore, the primary rhythm may be sinus- or supraventricular-paced, but occasionally an extra impulse is fired from an
ectopic pacemaker within the ventricle and creates a wide QRS complex. These complexes are called premature ventricular
complexes and may accompany any of the supraventricular rhythms described thus far. If the complexes on a tracing all resemble
one another in shape, a single irritable focus is the culprit and is described as unifocal. If the premature ventricular complexes
have variable shapes, multiple foci are implicated and the rhythm is described as multifocal.

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Table Suggested System for Logical Analysis of ECG Tracings*

Narrow QRS Supraventricular Rhythm
(Sinus, Atrial, or Junctional)
Group A: Regular R-R
NSR, sinus bradycardia, sinus
tachycardia
Junctional rhythm
AV block: first-degree

Wide QRS Ventricular Rhythm

Group B: Irregular R-R

Group C: Regular R-R

Group D: Variable R-R

PAC or PJC

Ventricular tachycardia

PVC

Atrial fibrillation
AV block: Mobitz (second-degree)
1 or 2

Idioventricular rhythm
AV block: third-degree

Ventricular fibrillation
Asystole

Supraventricular tachycardia
Atrial flutter
* Possible rhythms are separated according to width of QRS complex and R to R regularity. There will always be exceptions,
but do not consider these in your initial attempts at analysis. ECG indicates electrocardiogram; NSR, normal sinus rhythm; PAC,
premature atrial complex; PJC, premature junctional complex; PVC, premature ventricular complex; and AV, atrioventricular.
The most noted exceptions: atrial flutter can present as an irregular R-R, and a second-degree Mobitz II AV block will have a
regular R-R if the conduction ratio is 2:1.

Figure 19. Ventricular fibrillation and asystole. Here we have the worst tracings of all. Tracing A is pure chaos with no consistent
waves whatsoeverventricular fibrillation. In tracing B, following a single beat, we have no further evidence of electrical activity.
This is called asystole. In either case, the patient is in cardiac arrest with no pulse.

ber into 300. However, if the rhythm is irregular, count

the number of QRS complexes in a 6-second segment
and multiply by 10. Rates below 60 indicate bradycardia; those above 100 indicate tachycardia. In Figure 6
there are approximately 4 large boxes between QRS
complexes, so the rate is approximately 75.

Step 5: Do Waves and Complexes Proceed in

Normal Sequence?
Each P wave should be followed by a QRS complex,
which is followed by a T wave. This assures a normal
sequence for each cardiac cycle.

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ARRHYTHMIA IDENTIFICATION
Most basic courses in ECG interpretation emphasize
the precise recognition of at least 1520 arrhythmias.
The primary objectives are rote memorization of a
name for each rhythm and its deviant characteristics.
However, this approach nurtures an inability to assess
the clinical significance of a particular arrhythmia. ECG
analysis must be correlated with the patients appearance and vital signs. Collectively, these will establish
the clinical significance of the electrical disturbance and
determine any indication for intervention. One method
for organizing your thoughts is presented in the Table.
By performing the first 2 steps described above, you
can organize all basic arrhythmias into 4 groups (Table).

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Rhythms in Group C
During the first 2 steps of your 5-step analysis, you find
that the R-R intervals are regular but all QRS complexes
are wide. From this, we know that the heart is being
paced from tissue below the AV node, within the ventricles. The possible rhythms in group C are illustrated
in Figures 1517. For each, apply steps 35 of your 5step analysis.
Rhythms in Group D
During the first 2 steps of your 5-step analysis, you find
that the R-R intervals are irregular and that the QRS
complexes vary in shape. The possible rhythms in group
D are illustrated in Figures 1819. For each, apply steps
35 of your 5-step analysis.

Rhythms in Group A
REFERENCES
During the first 2 steps of your 5-step analysis, you find
that the R-R intervals are regular and all QRS complexes are narrow. From this, we know that the heart
is being paced from tissue above the ventricle. The
possible rhythms in group A are illustrated in Figures
711. For each, apply steps 35 of your 5-step analysis.
Rhythms in Group B
During the first 2 steps of your 5-step analysis, you find
that the R-R intervals are irregular but all QRS complexes are narrow. From this, we know that the heart
is being paced from tissue above the ventricles. The
possible rhythms in group B are illustrated in Figures
1214. For each, apply steps 35 of your 5-step analysis.

1. Rosenberg MB, Campbell RL. Guidelines for intraoperative monitoring of dental patients undergoing conscious sedation, deep sedation, and general anesthesia. Oral Surg Oral
Med Oral Pathol. 1991;71:28.
2. American Dental Association. Guidelines for the Use of
Conscious Sedation, Deep Sedation and General Anesthesia for Dentists. Adopted by the House of Delegates, American Dental Association, October 2005.
3. Eichhorn JH, Cooper JB, Cullen DJ, et al. Standards for
patient monitoring during anesthesia at Harvard Medical
School. JAMA. 1986;256:10171020.
4. Guyton AC, Hall JE. Textbook of Medical Physiology.
10th ed. Philadelphia, Pa: WB Saunders Co; 2000.
5. Brunwald E, Zipes DP, Libby P. Heart Disease: A Textbook of Cardiovascular Medicine. 6th ed. Philadelphia, Pa:
WB Saunders Co; 2001.
6. Goldberger AL. Clinical Electrocardiography: A Simplified Approach. 6th ed. St Louis, Mo: Mosby Inc; 1999.

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ECG Interpretation

CONTINUING EDUCATION QUESTIONS

1. Which of the following events is recorded in an ECG
tracing?
A. Depolarization of the SA node.
B. Contraction of ventricular muscle.
C. Repolarization of atrial muscle.
D. Depolarization of ventricular muscle.
2. An ECG tracing reveals upright P waves preceding
each QRS complex, but they have varied shapes and
sizes. The QRS complexes are narrow but the R-R
intervals are irregular. Which of the following can be
concluded regarding this rhythm?
A. It is a sinus rhythm.
B. The heart is being paced by multiple pacemaker
sites within the atria.
C. A heart block is present.
D. The AV node or common bundle of His is pacing
the heart.
3. An ECG tracing reveals several P waves that are not
followed by QRS complexes, but all remaining cycles

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have PR intervals that measure 0.16 mm. Which of

the following can be concluded regarding this
rhythm?
A. A first-degree block is present.
B. A second-degree Mobitz I block is present.
C. A second-degree Mobitz II block is present.
D. A third-degree block is present.
4. An ECG tracing reveals mostly normal cycles, but
occasionally a single isolated QRS complex appears
following a T wave. These extra complexes have a
wide, bizarre shape but they are all similar. Which of
the following would be an accurate explanation for
these bizarre complexes?
A. They are premature complexes generated by the
same ectopic pacemaker in the ventricles.
B. They are premature complexes generated by
multiple ectopic pacemakers in the ventricles.
C. They are premature atrial complexes triggered by
the SA node.
D. They are premature atrial complexes triggered by
an irritable focus in the nodal area.