Difference between revisions of "Electrocardiography"

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Also Known As: '''''ECG'''''
 
 
 
==Introduction==
 
==Introduction==
'''Electrocardiography''' is one of the most commonly used pieces of monitoring equipment in veterinary practices.
+
Electrocardiography is one of the most commonly found piece of monitoring equipment in modern veterinary practices. It detects the electrical activity of the heart through 3 electrodes. These electrodes are most commonly placed on the 2 forelimbs and the left hindlimb. The electrodes are attached to the patient via ECG pads (most commonly), crocodile clips (more common in horses) and transcutaneous needles (rare). Frequently, additional electrode gel or alcohol is required to improve contact between the patient and electrodes.  
 
 
The '''ECG''' can determine the '''rate, [[Arrhythmias Overview|rhythm]] and nature of cardiac depolarisation and repolarisation'''. It can also indicate changes in '''myocardial mass''', '''conductivity''' between the heart and skin and the presence of '''metabolic abnormalities''' that affect the heart.
 
 
 
==Recording an ECG==
 
The ECG detects the electrical activity of the heart through '''3 electrodes'''. In small animals these electrodes are most commonly placed on the 2 forelimbs and the left hindlimb. An additional electrode may be placed on the right hindlimb. Resting ECGs in the horse are recorded using a '''base-apex lead''' - with negative (red) electrode placed over the jugular groove, the positive electrode (yellow) placed just behind the left elbow over the apex beat of the heart (B) and the earth electrode attached at a site remote to the heart. This produces an ECG with large complexes that are not significantly affected by movement artifact.
 
 
 
The electrodes are attached to the patient via '''ECG pads''', '''crocodile clips''' (more common in horses) and '''transcutaneous needles''' (rare). Hair should be '''clipped''' to improve contact between the ECG pad and the skin. Pads should be secured with tape and additional '''electrode gel or alcohol''' should be used to improve contact between the patient and electrodes. The electrodes are connected to the ECG machine by colour-coded '''cables'''.
 
 
 
 
 
'''The colour coding system:'''
 
:<font color = "yellow">'''Yellow </font color>(positive): Left forelimb'''
 
:<font color = "red">'''Red </font color>(negative): Right forelimb'''
 
:<font color = "green">'''Green</font color>: Left hindlimb'''
 
:'''Black: Right hindlimb'''
 
  
 +
The ECG can determine the rate, rhythm and nature of cardiac depolarisation and repolarisation. It can also indicate changes in myocardial mass, conductivity between the heart and skin and the presence of metabolic abnormalities affect the heart.
 +
Indication of metabolic abnormalities affecting the myocardium
 +
Indication of alterations in conductivity between heart and skin
  
The ECG should be recorded in a '''calm and quiet environment'''. The patient should be kept as '''still and relaxed''' as possible as '''muscle tremors and movement''' can cause '''artifacts''' on the trace. In horses the ECG is recorded '''standing'''. Dogs should be placed in '''right lateral recumbency''' but positioning in a cat is less important. The cables should be positioned so that they do not drape over the animals chest as they can cause '''respiratory movement artifact'''. Electrical activity can cause interference on the ECG trace (known as '''50Hz interference'''). To prevent this it should be taken on an '''insulated surface''' away from fluorescent lighting, computers and other electrical equipment. A '''Holter''' ECG can be used in both small and large animal to record the electrical activity of the heart over 24 hours or during exercise.
+
To interpret an ECG it is necessary to understand the path of depolarisation through the heart:
 
+
The sino-atrial node depolarises spontaneously and this wave of depolarisation spreads through the atria. The impulse is then conducted through AV node slowly. Then it rapidly passes through the bundle of His and bundle branches, spreading through the ventricular myocardium. The myocardium then remains depolarised for a period before repolarising. This depolarisation and repolarisation are detected as potential differences on the skin surface - producing the classic shape of the ECG trace.  
'''Chemical restraint''' should be '''avoided''' if at all possible as this changes the ECG.
 
  
 
==Reading an ECG Trace==
 
==Reading an ECG Trace==
  
An ECG only supplies information about the '''electrical activity of the heart'''. It indicates the heart rate and rhythm and can be used to detect any arrhythmias but does not supply information about cardiac function. It is important to remember to '''treat the patient not the ECG'''!
+
An ECG supplies information about the electrical activity of the heart only. It indicates the heart rate and rhythm and can be used to detect any arrhythmias. It does not supply information about cardiac function. It is important to remember to treat the patient not the ECG!
 
 
To interpret an ECG it is necessary to understand the path of depolarisation through the [[:Category:Heart - Anatomy & Physiology|heart]]:
 
The sino-atrial node depolarises spontaneously and this wave of depolarisation spreads through the atria. The impulse is then conducted through AV node slowly. Then it rapidly passes through the bundle of His and bundle branches, spreading through the ventricular myocardium. The myocardium then remains depolarised for a period before repolarising. This '''depolarisation and repolarisation are detected as potential differences on the skin surface - producing the classic shape of the ECG trace'''.
 
  
 
[[Image:ECG.jpg|left|]]
 
[[Image:ECG.jpg|left|]]
 
 
 
 
  
 
<center>
 
<center>
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In small animals '''six limb leads''' ('''ECG traces derived from a pair of electrodes''') are produced from the reading of the '''four electrodes'''. These are named leads '''I, II, III, aVR, aLV, aVF'''.
+
 
The trace should always be read from '''left to right'''. Ideally it should be read from the start but if this is too difficult then the most recognisable portion should be identified and the trace read from this point.
+
 
 +
 
 +
 
  
  
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===An Abnormal ECG Trace===
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These 5 features should be assessed in every ECG that you interpret.
  
 
The following questions should be asked when interpreting every ECG:
 
The following questions should be asked when interpreting every ECG:
  
===='''Is E.C.G. of diagnostic quality?'''====
+
 
 +
'''Is E.C.G. of diagnostic quality?'''
  
 
It is important that no artefact is present on the trace. Interference from electrical equipment and fluorescent lighting (50Hz interference) and movement should be prevented. The ECG should be calibrated for both paper speed and vertical sensitivity, and the trace should remain within the paper edges. All leads should be demonstrated.
 
It is important that no artefact is present on the trace. Interference from electrical equipment and fluorescent lighting (50Hz interference) and movement should be prevented. The ECG should be calibrated for both paper speed and vertical sensitivity, and the trace should remain within the paper edges. All leads should be demonstrated.
  
===='''What is the heart rate?'''====
+
 
 +
'''What is the heart rate?'''
  
 
Heart rate can be calculated using one of the following two methods:
 
Heart rate can be calculated using one of the following two methods:
  
 
'''(1) Instantaneous heart rate'''
 
'''(1) Instantaneous heart rate'''
:1500/R-R interval (25 mm/sec)
+
 
:3000/R-R interval (50 mm/sec)
+
1500/R-R interval (25 mm/sec)
 +
 
 +
3000/R-R interval (50 mm/sec)
  
 
'''(2) Number of R-R intervals in 6 seconds x 10'''
 
'''(2) Number of R-R intervals in 6 seconds x 10'''
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Where multiple rhythms exist, the rate of all rhythms present should be calculated.
 
Where multiple rhythms exist, the rate of all rhythms present should be calculated.
  
A high heart rate may be due to [[Sinus Tachycardia|sinus tachycardia]], [[Supraventricular Tachycardia|supraventricular tachycardia]], [[Ventricular Tachycardia|ventricular tachycardia]] and [[Atrial Fibrillation & Atrial Flutter|atrial fibrillation]]. A slow heart rate may be caused by [[Sinus Bradycardias|sinus bradycardia]], [[Sinus Arrhythmias|sinus arrhythmia]], second or third degree [[Atrio-Ventricular Block|AV block]], [[Atrial Standstill|atrial standstill]] and [[Sinus Arrest & Sinus Block|sinus arrest]].
 
  
===='''What is the heart rhythm?'''====
+
'''What is the heart rhythm?'''
 +
 
 +
It is important to interpret whether the heart rate is regular or irregular, and if it is irregular whether it is regularly irregular or irregularly irregular.
  
It is important to interpret whether the heart rate is regular or irregular. If it is irregular you should record whether it is regularly irregular or irregularly irregular.
 
  
===='''What is the mean electrical axis?'''====
+
'''What is the mean electrical axis?'''
  
 
This figure is of limited value in small animals. It can give some indication of ventricular enlargement and the presence of intraventricular conduction defects.  
 
This figure is of limited value in small animals. It can give some indication of ventricular enlargement and the presence of intraventricular conduction defects.  
  
===='''What are the individual complex measurements?'''====
 
  
Changes in the morphology of the complexes are classed as a change in the shape, size or duration of the P wave, QRS complex or T wave. The magnitude and duration of deflections can be caused by hypertrophy of the myocardium, electrolyte abnormalities or an alterations in autonomic tone within the heart.
+
'''What are the individual complex measurements?'''
  
'''Variation in P-wave''' can be caused by a [[Sinus Arrhythmias|wandering pacemaker]] or atrial ectopy. Variation in QRS complexes may be caused by either variable conduction or electrical alternans.
+
Changes in the morphology of the complexes are classed as a change in the shape, size or duration of the P wave, QRS complex or T wave. The magnitude and duration of deflections may be altered by regional changes in myocardial mass and alterations in conduction. This can be caused by hypertrophy of the myocardium, electrolyte abnormalities or an alterations in autonomic tone within the heart.
  
'''No P to every QRS''' - this occurs when ventricular depolarisation follows an abnormal atrial depolarisation. This can be caused by [[Ventricular Premature Complexes|premature ventricular]] or [[Supraventricular Premature Complexes|junctional complexes]], [[Sinus Arrest & Sinus Block|sinus arrest]] with ventricular or junctional escape complexes, [[Atrial Standstill|atrial standstill]] and [[Atrial Fibrillation|atrial fibrillation]].
+
You should record whether all the deflections are the same, as some variations may be normal.  
  
'''No QRS to every P''' - this occurs the AV node fails to conduct impulses normally. This can be caused by second and third degree [[Atrio-Ventricular Block|AV block]]. Second degree AV block is normal in the resting horse - however it should disappear following exercise.
+
Variation in P-wave
 +
May be normal - wandering pacemaker
 +
May indicate atrial ectopy
 +
P-wave should be positive in lead II
 +
Variation in QRS complex
 +
Some variation may be normal
 +
May indicate variable conduction
 +
May indicate electrical alternans
  
The '''shape''' of a complex can be used to identify the location of the origin of a rhythm disturbance. Complexes that originate in the ventricles are produce wide and bizarre QRS complexes, whereas complexes of atrioventricular origin are narrow and upright.
+
No P to every QRS.
 +
This means that the ventricular depolarisation has not been preceded by a normal atrial depolarisation
 +
Premature complexes
 +
Ventricular premature
 +
Junctional premature
 +
Sinus arrest with escape complexes
 +
Ventricular escape
 +
Junctional escape
 +
No organised atrial depolarisation
 +
Atrial standstill
 +
Atrial fibrillation
  
====Are they consistently and reasonably related?====
+
No QRS to every P.
 +
Failure of AV conduction
 +
Second degree AV block
 +
Intermittent failure of AV conduction
 +
Mobitz type I - Prolongation of P-R interval
 +
Mobitz type II - No prolongation of P-R interval
 +
Third degree AV block
 +
Complete failure of AV conduction
 +
Complete AV dissociation
  
An '''abnormal P-R interval''' is caused by atrioventricular dissociation. This occurs secondary to junctional and [[Altered Ventricular Impulse Formations|ventricular rhythm disturbances]] and third degree [[Atrio-Ventricular Block|AV block]].
+
Consistently and reasonably related.
 +
Marked variation in P-R intervals may suggest AV dissociation
 +
Can occur with
 +
Ventricular rhythm disturbances
 +
Junctional rhythm disturbances
 +
Third degree AV block
  
To calculate this the P-P, R-R and P-R intervals should all be measured. If the P-R interval is the only variable factor this is very suggestive of AV dissociation.
+
AV dissociation:
 +
Map out P-P intervals, Map out R-R intervals, Map out P-R intervals
 +
If P-P interval is relatively consistent, R-R interval is relatively consistent but P-R interval is highly variable then you have Atrioventricular dissociation
 +
Where atrioventricular dissociation occurs the origin of the ventricular depolarisation must be within the ventricle or the AV junction
  
==Summary==
+
Alterations in intervals:
ECG is the most useful tool for assessment of '''cardiac rhythm'''. Everything possible should be done to '''minimise artifact''' and produce an ECG of good diagnostic quality. Every trace should be analysed '''consistently and methodically''' so that the results may be reliably combined with entire clinical picture. 
+
May reflect alterations in myocardial mass
 +
Increased P-wave amplitude may reflect right atrial enlargement
 +
Increased R-wave amplitude may reflect changes in ventricular myocardium
 +
Increased T-wave amplitude
 +
May occur with drugs, electrolyte and acid-base disturbances
 +
May be normal in dogs
  
{{Learning
+
Common problems:
|flashcards = [[Feline Medicine Q&A 01]]
+
Differentiation of artefact from rhythm disturbance
}}
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Determining the origin of non-sinus depolarisations
 +
Determining the significance of E.C.G. abnormalities which may be present.
  
==References==
+
Abnormalities of generation or conduction of the depolarisation can arise for various reasons
Dennis, S (2011) '''How to record and interpret ECGs''' & '''What is an ECG?''' RVC Cardiology Elective Course, ''Royal Veterinary College''
+
Intrinsic cardiac disease
 +
Hypoxia
 +
Autonomic influence
 +
Mechanical abnormalities
 +
Metabolic abnormalities
 +
Electrolyte disturbances
 +
Drugs
  
Martin, M (2002) '''ECG interpretation in small animals : 1. Understanding the electricity of the heart''' ''In Practice 2002 24: 114-12''
+
==Summary==
 
+
ECG represents electrical activity recorded at the skin surface as a consequence of depolarisation and repolarisation
Martin, M (2002) '''ECG interpretation in small animals : 3. Practical guidelines''' ''In Practice 2002 24: 250-26''
+
Unique in ability to provide information about cardiac rhythm
 
+
Able to provide clues about hypertrophy and some metabolic disturbances
Menzies-Gow, N (2001) '''ECG interpretation in the horse''' ''In Practice 2001 23: 454-45''
+
Understanding physiology and applying logical rules aids interpretation
 
 
Robinson, SA (1990) '''Practical use of ECG in the horse''' ''In Practice 1990 12: 59-6''
 
 
 
RVC staff (2009) '''Cardiovascular System''' RVC Intergrated BVetMed Course, ''Royal Veterinary College''
 
 
 
Sparks, AH & Caney, SMA (2005) '''Self-Assessment Colour Review Feline Medicine''' ''Manson''
 
  
 +
Normal organised pattern of depolarisation and repolarisation of the heart leads to regular detectable potential differences between points on skin surface
  
{{review}}
 
  
==Webinars==
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*Is there a P for every QRS?
<rss max="10" highlight="none">https://www.thewebinarvet.com/cardiology/webinars/feed</rss>
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*Is there a QRS for every P?
 +
*Are they all reasonably related?
 +
*Are they all the same?
 +
*Is rhythm regular or irregular?
 +
*Is the arrhythmia regularly irregular or irregularly irregular?
  
 
[[Category:Monitoring Anaesthesia]]
 
[[Category:Monitoring Anaesthesia]]
[[Category:Clinical Techniques]]
+
[[Category: To Do - Siobhan Brade]]
[[Category:Expert Review]]
 

Revision as of 10:36, 11 August 2011

Introduction

Electrocardiography is one of the most commonly found piece of monitoring equipment in modern veterinary practices. It detects the electrical activity of the heart through 3 electrodes. These electrodes are most commonly placed on the 2 forelimbs and the left hindlimb. The electrodes are attached to the patient via ECG pads (most commonly), crocodile clips (more common in horses) and transcutaneous needles (rare). Frequently, additional electrode gel or alcohol is required to improve contact between the patient and electrodes.

The ECG can determine the rate, rhythm and nature of cardiac depolarisation and repolarisation. It can also indicate changes in myocardial mass, conductivity between the heart and skin and the presence of metabolic abnormalities affect the heart. Indication of metabolic abnormalities affecting the myocardium Indication of alterations in conductivity between heart and skin

To interpret an ECG it is necessary to understand the path of depolarisation through the heart: The sino-atrial node depolarises spontaneously and this wave of depolarisation spreads through the atria. The impulse is then conducted through AV node slowly. Then it rapidly passes through the bundle of His and bundle branches, spreading through the ventricular myocardium. The myocardium then remains depolarised for a period before repolarising. This depolarisation and repolarisation are detected as potential differences on the skin surface - producing the classic shape of the ECG trace.

Reading an ECG Trace

An ECG supplies information about the electrical activity of the heart only. It indicates the heart rate and rhythm and can be used to detect any arrhythmias. It does not supply information about cardiac function. It is important to remember to treat the patient not the ECG!

ECG.jpg
Stage Represents
P Atrial Depolarisation
QRS Ventricular Depolarisation
T Ventricular Repolarisation








A Normal ECG Trace

Before you interpret abnormal ECG's you must know what a normal ECG looks like:

  • A P-wave precedes every QRS complex
  • A QRS complex follows every P-wave
  • P and QRS are consistently and reasonably related
  • P and QRS will all appear the same
  • They will occur at a normal rate


These 5 features should be assessed in every ECG that you interpret.

The following questions should be asked when interpreting every ECG:


Is E.C.G. of diagnostic quality?

It is important that no artefact is present on the trace. Interference from electrical equipment and fluorescent lighting (50Hz interference) and movement should be prevented. The ECG should be calibrated for both paper speed and vertical sensitivity, and the trace should remain within the paper edges. All leads should be demonstrated.


What is the heart rate?

Heart rate can be calculated using one of the following two methods:

(1) Instantaneous heart rate

1500/R-R interval (25 mm/sec)

3000/R-R interval (50 mm/sec)

(2) Number of R-R intervals in 6 seconds x 10

Where multiple rhythms exist, the rate of all rhythms present should be calculated.


What is the heart rhythm?

It is important to interpret whether the heart rate is regular or irregular, and if it is irregular whether it is regularly irregular or irregularly irregular.


What is the mean electrical axis?

This figure is of limited value in small animals. It can give some indication of ventricular enlargement and the presence of intraventricular conduction defects.


What are the individual complex measurements?

Changes in the morphology of the complexes are classed as a change in the shape, size or duration of the P wave, QRS complex or T wave. The magnitude and duration of deflections may be altered by regional changes in myocardial mass and alterations in conduction. This can be caused by hypertrophy of the myocardium, electrolyte abnormalities or an alterations in autonomic tone within the heart.

You should record whether all the deflections are the same, as some variations may be normal.

Variation in P-wave May be normal - wandering pacemaker May indicate atrial ectopy P-wave should be positive in lead II Variation in QRS complex Some variation may be normal May indicate variable conduction May indicate electrical alternans

No P to every QRS. This means that the ventricular depolarisation has not been preceded by a normal atrial depolarisation Premature complexes Ventricular premature Junctional premature Sinus arrest with escape complexes Ventricular escape Junctional escape No organised atrial depolarisation Atrial standstill Atrial fibrillation

No QRS to every P. Failure of AV conduction Second degree AV block Intermittent failure of AV conduction Mobitz type I - Prolongation of P-R interval Mobitz type II - No prolongation of P-R interval Third degree AV block Complete failure of AV conduction Complete AV dissociation

Consistently and reasonably related. Marked variation in P-R intervals may suggest AV dissociation Can occur with Ventricular rhythm disturbances Junctional rhythm disturbances Third degree AV block

AV dissociation: Map out P-P intervals, Map out R-R intervals, Map out P-R intervals If P-P interval is relatively consistent, R-R interval is relatively consistent but P-R interval is highly variable then you have Atrioventricular dissociation Where atrioventricular dissociation occurs the origin of the ventricular depolarisation must be within the ventricle or the AV junction

Alterations in intervals: May reflect alterations in myocardial mass Increased P-wave amplitude may reflect right atrial enlargement Increased R-wave amplitude may reflect changes in ventricular myocardium Increased T-wave amplitude May occur with drugs, electrolyte and acid-base disturbances May be normal in dogs

Common problems: Differentiation of artefact from rhythm disturbance Determining the origin of non-sinus depolarisations Determining the significance of E.C.G. abnormalities which may be present.

Abnormalities of generation or conduction of the depolarisation can arise for various reasons Intrinsic cardiac disease Hypoxia Autonomic influence Mechanical abnormalities Metabolic abnormalities Electrolyte disturbances Drugs

Summary

ECG represents electrical activity recorded at the skin surface as a consequence of depolarisation and repolarisation Unique in ability to provide information about cardiac rhythm Able to provide clues about hypertrophy and some metabolic disturbances Understanding physiology and applying logical rules aids interpretation

Normal organised pattern of depolarisation and repolarisation of the heart leads to regular detectable potential differences between points on skin surface


  • Is there a P for every QRS?
  • Is there a QRS for every P?
  • Are they all reasonably related?
  • Are they all the same?
  • Is rhythm regular or irregular?
  • Is the arrhythmia regularly irregular or irregularly irregular?