Electrocardiography

Not to be confused with echocardiogram, electromyogram, electroencephalogram, or EEG.
Electrocardiography
Intervention

Image showing a patient connected to the 10 electrodes necessary for a 12-lead ECG
ICD-9-CM 89.52
MeSH D004562

Electrocardiography (ECG or EKG from the German Elektrokardiogramm) is a transthoracic (across the thorax or chest) interpretation of the electrical activity of the heart over a period of time, as detected by electrodes attached to the outer surface of the skin and recorded by a device external to the body.[1] The recording produced by this noninvasive procedure is termed as electrocardiogram (also ECG or EKG). An electrocardiogram (ECG) is a test that records the electrical activity of the heart.

ECG is used to measure the rate and regularity of heartbeats as well as the size and position of the chambers, the presence of any damage to the heart, and the effects of drugs or devices used to regulate the heart (such as a pacemaker). See also stress test and Holter monitor (24h).

The etymology of the word is derived from the Greek electro, because it is related to electrical activity, kardio, Greek for heart, and graph, a Greek root meaning "to write". In English speaking countries, medical professionals often use "EKG" (the abbreviation for the German word Elektrokardiogramm) in order to avoid confusion with EEG in emergency situations where background noise is high.

Most EKGs are performed for diagnostic or research purposes on human hearts, but may also be performed on animals, usually for research.

Contents

Function

The ECG device detects and amplifies the tiny electrical changes on the skin that are caused when the heart muscle depolarizes during each heartbeat. At rest, each heart muscle cell has a negative charge (membrane potential) across its outer wall (or cell membrane). Increasing this negative charge towards zero (via the influx of the positive ions, Na+ and Ca++) is called depolarization, which activates the mechanisms in the cell that cause it to contract. During each heartbeat a healthy heart will have an orderly progression of a wave of depolarisation that is triggered by the cells in the sinoatrial node, spreads out through the atrium, passes through "intrinsic conduction pathways" and then spreads all over the ventricles. This is detected as tiny rises and falls in the voltage between two electrodes placed either side of the heart which is displayed as a wavy line either on a screen or on paper. This display indicates the overall rhythm of the heart and weaknesses in different parts of the heart muscle.

Usually more than 2 electrodes are used and they can be combined into a number of pairs (For example: Left arm (LA), right arm (RA) and left leg (LL) electrodes form the three pairs LA+RA, LA+LL, and RA+LL). The output from each pair is known as a lead. Each lead is said to look at the heart from a different angle. Different types of EKGs can be referred to by the number of leads that are recorded, for example 3-lead, 5-lead or 12-lead EKGs (sometimes simply "a 12-lead"). A 12-lead EKG is one in which 12 different electrical signals are recorded at approximately the same time and will often be used as a one-off recording of an EKG, traditionally printed out as a paper copy. 3- and 5-lead EKGs tend to be monitored continuously and viewed only on the screen of an appropriate monitoring device, for example during an operation or whilst being transported in an ambulance. There may or may not be any permanent record of a 3- or 5-lead EKG, depending on the equipment used.

It is the best way to measure and diagnose abnormal rhythms of the heart,[2] particularly abnormal rhythms caused by damage to the conductive tissue that carries electrical signals, or abnormal rhythms caused by electrolyte imbalances.[3] In a myocardial infarction (MI), the EKG can identify if the heart muscle has been damaged in specific areas, though not all areas of the heart are covered.[4] The EKG cannot reliably measure the pumping ability of the heart, for which ultrasound-based (echocardiography) or nuclear medicine tests are used. It is possible for a human or other animal to be in cardiac arrest but still have a normal EKG signal (a condition known as pulseless electrical activity).

History

Alexander Muirhead is reported to have attached wires to a feverish patient's wrist to obtain a record of the patient's heartbeat while studying for his Doctor of Science (in electricity) in 1872 at St Bartholomew's Hospital.[5] This activity was directly recorded and visualized using a Lippmann capillary electrometer by the British physiologist John Burdon Sanderson.[6] The first to systematically approach the heart from an electrical point-of-view was Augustus Waller, working in St Mary's Hospital in Paddington, London.[7] His electrocardiograph machine consisted of a Lippmann capillary electrometer fixed to a projector. The trace from the heartbeat was projected onto a photographic plate which was itself fixed to a toy train. This allowed a heartbeat to be recorded in real time. In 1911 he still saw little clinical application for his work.

An initial breakthrough came when Willem Einthoven, working in Leiden, Netherlands, used the string galvanometer that he invented in 1903.[8] This device was much more sensitive than both the capillary electrometer that Waller used and the string galvanometer that had been invented separately in 1897 by the French engineer Clément Ader.[9] Rather than using today's self-adhesive electrodes Einthoven's subjects would immerse each of their limbs into containers of salt solutions from which the EKG was recorded.

Einthoven assigned the letters P, Q, R, S and T to the various deflections, Naming of the Waves in the ECG and described the electrocardiographic features of a number of cardiovascular disorders. In 1924, he was awarded the Nobel Prize in Medicine for his discovery.[10]

Though the basic principles of that era are still in use today, there have been many advances in electrocardiography over the years. The instrumentation, for example, has evolved from a cumbersome laboratory apparatus to compact electronic systems that often include computerized interpretation of the electrocardiogram.[11]

EKG graph paper

The output of an ECG recorder is a graph (or sometimes several graphs, representing each of the leads) with time represented on the x-axis and voltage represented on the y-axis. A dedicated ECG machine would usually print onto graph paper which has a background pattern of 1mm squares (often in red or green), with bold divisions every 5 mm in both vertical and horizontal directions.

It is possible to change the output of most ECG devices but it is standard to represent each mV on the y axis as 1 cm and each second as 25 mm on the x-axis (that is a paper speed of 25 mm/s). Faster paper speeds can be used, for example, to resolve finer detail in the ECG. At a paper speed of 25 mm/s, one small block of ECG paper translates into 40 ms. Five small blocks make up one large block, which translates into 200 ms. Hence, there are five large blocks per second. A calibration signal may be included with a record. A standard signal of 1 mV must move the stylus vertically 1 cm, that is, two large squares on ECG paper.

Layout

By definition, a 12-lead ECG will show a short segment of the recording of each of the 12-leads. This is often arranged in a grid of 4 columns by three rows, the first columns being the limb leads (I,II and III), the second column the augmented limb leads (aVR, aVL and aVF) and the last two columns being the chest leads (V1-V6). It is usually possible to change this layout so it is vital to check the labels to see which lead is represented. Each column will usually record the same moment in time for the three leads and then the recording will switch to the next column which will record the heart beats after that point. It is possible for the heart rhythm to change between the columns of leads.

Each of these segments is short, perhaps 1g-3 heart beats only, depending on the heart rate and it can be difficult to analyse any heart rhythm that shows changes between heart beats. To help with the analysis it is common to print one or two "rhythm strips" as well. This will usually be lead II (which shows the electrical signal from the atrium, the P-wave, well) and shows the rhythm for the whole time the ECG was recorded (usually 5–6 seconds). Some ECG machines will print a second lead II along the very bottom of the paper in addition to the output described above. This printing of Lead II is continuous from start to finish of the process.

The term "rhythm strip" may also refer to the whole printout from a continuous monitoring system which may show only one lead and is either initiated by a clinician or in response to an alarm or event.

Leads

The term "lead" in electrocardiography causes much confusion because it is used to refer to two different things. In accordance with common parlance the word lead may be used to refer to the electrical cable attaching the electrodes to the ECG recorder. As such it may be acceptable to refer to the "left arm lead" as the electrode (and its cable) that should be attached at or near the left arm. There are usually ten of these electrodes in a standard "12-lead" ECG.

Alternatively (and some would say properly, in the context of electrocardiography) the word lead may refer to the tracing of the voltage difference between two of the electrodes and is what is actually produced by the ECG recorder. Each will have a specific name. For example "Lead I" (lead one) is the voltage between the right arm electrode and the left arm electrode, whereas "Lead II" (lead two) is the voltage between the right limb and the feet. (This rapidly becomes more complex as one of the "electrodes" may in fact be a composite of the electrical signal from a combination of the other electrodes (see later). Twelve of this type of lead form a "12-lead" ECG

To cause additional confusion the term "limb leads" usually refers to the tracings from leads I, II and III rather than the electrodes attached to the limbs.

Placement of electrodes

Ten electrodes are used for a 12-lead ECG. The electrodes usually consist of a conducting gel, embedded in the middle of a self-adhesive pad onto which cables clip. Sometimes the gel also forms the adhesive.[12] They are labeled and placed on the patient's body as follows:[13][14]

. * Note that when exercise stress tests are performed, limb leads may be placed on the trunk to avoid artifacts while ambulatory (arm leads moved sub-clavicularly and leg leads medial to and above the iliac crest).

Electrode label (in the USA) Electrode placement
RA On the right arm, avoiding thick muscle.
LA In the same location that RA was placed, but on the left arm.
RL On the right leg, lateral calf muscle
LL In the same location that RL was placed, but on the left leg.
V1 In the fourth intercostal space (between ribs 4 & 5) just to the right of the sternum (breastbone).
V2 In the fourth intercostal space (between ribs 4 & 5) just to the left of the sternum.
V3 Between leads V2 and V4.
V4 In the fifth intercostal space (between ribs 5 & 6) in the mid-clavicular line (the imaginary line that extends down from the midpoint of the clavicle (collarbone)).
V5 Horizontally even with V4, but in the anterior axillary line. (The anterior axillary line is the imaginary line that runs down from the point midway between the middle of the clavicle and the lateral end of the clavicle; the lateral end of the collarbone is the end closer to the arm.)
V6 Horizontally even with V4 and V5 in the midaxillary line. (The midaxillary line is the imaginary line that extends down from the middle of the patient's armpit.)

Additional electrodes

The classical 12-lead ECG can be extended in a number of ways in an attempt to improve its sensitivity in detecting myocardial infarction involving territories not normally "seen" well. This includes an rV4 lead which uses the equivalent landmarks to the V4 but on the right side of the chest wall and extending the chest leads onto the back with a V7, V8 and V9.

Limb leads

In both the 5- and 12-lead configuration, leads I, II and III are called limb leads. The electrodes that form these signals are located on the limbs—one on each arm and one on the left leg.[16][17][18] The limb leads form the points of what is known as Einthoven's triangle.[19]

I = LA - RA.
II = LL - RA.
III = LL - LA.

Simplified electrocardiograph sensors designed for teaching purposes at e.g. high school level are generally limited to three arm electrodes serving similar purposes.[20]

Unipolar vs. bipolar leads

There are two types of leads: unipolar and bipolar. Bipolar leads have one positive and one negative pole.[21] In a 12-lead ECG, the limb leads (I, II and III) are bipolar leads. Unipolar leads also have two poles, as a voltage is measured; however, the negative pole is a composite pole (Wilson's central terminal, or WCT) made up of signals from lots of other electrodes.[22] In a 12-lead ECG, all leads besides the limb leads are unipolar (aVR, aVL, aVF, V1, V2, V3, V4, V5, and V6).

Wilson's central terminal VW is produced by connecting the electrodes, RA; LA; and LL, together, via a simple resistive network, to give an average potential across the body, which approximates the potential at infinity (i.e. zero):

V_W = \frac{1}{3}(RA%2BLA%2BLL).

Augmented limb leads

Leads aVR, aVL, and aVF are augmented limb leads (after their inventor Dr. Emanuel Goldberger known collectively as the Goldberger's leads). They are derived from the same three electrodes as leads I, II, and III. However, they view the heart from different angles (or vectors) because the negative electrode for these leads is a modification of Wilson's central terminal. This zeroes out the negative electrode and allows the positive electrode to become the "exploring electrode". This is possible because Einthoven's Law states that I + (−II) + III = 0. The equation can also be written I + III = II. It is written this way (instead of I − II + III = 0) because Einthoven reversed the polarity of lead II in Einthoven's triangle, possibly because he liked to view upright QRS complexes. Wilson's central terminal paved the way for the development of the augmented limb leads aVR, aVL, aVF and the precordial leads V1, V2, V3, V4, V5 and V6.

aVR = RA - \frac{1}{2} (LA %2B LL).
aVL = LA - \frac{1}{2} (RA %2B LL).
aVF = LL - \frac{1}{2} (RA %2B LA).

The augmented limb leads aVR, aVL, and aVF are amplified in this way because the signal is too small to be useful when the negative electrode is Wilson's central terminal. Together with leads I, II, and III, augmented limb leads aVR, aVL, and aVF form the basis of the hexaxial reference system, which is used to calculate the heart's electrical axis in the frontal plane. The aVR, aVL, and aVF leads can also be represented using the I and II limb leads:

\begin{align} aVR &= -\frac{I %2B II}{2}\\ aVL &= I - \frac{II}{2}\\ aVF &= II - \frac{I}{2} \end{align}

Precordial leads

The electrodes for the precordial leads (V1, V2, V3, V4, V5 and V6) are placed directly on the chest. Because of their close proximity to the heart, they do not require augmentation. Wilson's central terminal is used for the negative electrode, and these leads are considered to be unipolar (recall that Wilson's central terminal is the average of the three limb leads. This approximates common, or average, potential over the body). The precordial leads view the heart's electrical activity in the so-called horizontal plane. The heart's electrical axis in the horizontal plane is referred to as the Z axis.

Waves and intervals

A typical ECG tracing of the cardiac cycle (heartbeat) consists of a P wave, a QRS complex, a T wave, and a U wave which is normally visible in 50 to 75% of ECGs.[23] The baseline voltage of the electrocardiogram is known as the isoelectric line. Typically the isoelectric line is measured as the portion of the tracing following the T wave and preceding the next P wave.

Feature Description Duration
RR interval The interval between an R wave and the next R wave . Normal resting heart rate is between 60 and 100 bpm 0.6 to 1.2s
P wave During normal atrial depolarization, the main electrical vector is directed from the SA node towards the AV node, and spreads from the right atrium to the left atrium. This turns into the P wave on the ECG. 80ms
PR interval The PR interval is measured from the beginning of the P wave to the beginning of the QRS complex. The PR interval reflects the time the electrical impulse takes to travel from the sinus node through the AV node and entering the ventricles. The PR interval is therefore a good estimate of AV node function. 120 to 200ms
PR segment The PR segment connects the P wave and the QRS complex. This coincides with the electrical conduction from the AV node to the bundle of His to the bundle branches and then to the Purkinje Fibers. This electrical activity does not produce a contraction directly and is merely traveling down towards the ventricles and this shows up flat on the ECG. The PR interval is more clinically relevant. 50 to 120ms
QRS complex The QRS complex reflects the rapid depolarization of the right and left ventricles. They have a large muscle mass compared to the atria and so the QRS complex usually has a much larger amplitude than the P-wave. 80 to 120ms
J-point The point at which the QRS complex finishes and the ST segment begins. Used to measure the degree of ST elevation or depression present. N/A
ST segment The ST segment connects the QRS complex and the T wave. The ST segment represents the period when the ventricles are depolarized. It is isoelectric. 80 to 120ms
T wave The T wave represents the repolarization (or recovery) of the ventricles. The interval from the beginning of the QRS complex to the apex of the T wave is referred to as the absolute refractory period. The last half of the T wave is referred to as the relative refractory period (or vulnerable period). 160ms
ST interval The ST interval is measured from the J point to the end of the T wave. 320ms
QT interval The QT interval is measured from the beginning of the QRS complex to the end of the T wave. A prolonged QT interval is a risk factor for ventricular tachyarrhythmias and sudden death. It varies with heart rate and for clinical relevance requires a correction for this, giving the QTc. 300 to 430ms
U wave The U wave is hypothesized to be caused by the repolarization of the interventricular septum. They normally have a low amplitude, and even more often completely absent. They always follow the T wave and also follow the same direction in amplitude. If they are too prominent we suspect hypokalemia, hypercalcemia or hyperthyroidism usually.[24]
J wave The J wave, elevated J-Point or Osborn Wave appears as a late delta wave following the QRS or as a small secondary R wave . It is considered pathognomonic of hypothermia or hypocalcemia.[25]

There were originally four deflections, but after the mathematical correction for artifacts introduced by early amplifiers, five deflections were discovered. Einthoven chose the letters P, Q, R, S, and T to identify the tracing which was superimposed over the uncorrected labeled A, B, C, and D.[26]

In intracardiac electrocardiograms, such as can be acquired from pacemaker sensors, an additional wave that can be seen is the H deflection, which reflects the depolarization of the bundle of His.[27] The H-V interval, in turn, is the duration from the beginning of the H deflection to the earliest onset of ventricular depolarization recorded in any lead.[28]

Vectors and views

Interpretation of the ECG relies on the idea that different leads (by which we mean the ECG leads I, II ,III, aVR, aVL, aVF and the chest leads) "view" the heart from different angles. This has two benefits. Firstly, leads which are showing problems (for example ST segment elevation) can be used to infer which region of the heart is affected. Secondly, the overall direction of travel of the wave of depolarisation can also be inferred which can reveal other problems. This is termed the cardiac axis . Determination of the cardiac axis relies on the concept of a vector which describes the motion of the depolarisation wave. This vector can then be described in terms of its components in relation to the direction of the lead considered. One component will be in the direction of the lead and this will be revealed in the behaviour of the QRS complex and one component will be at 90 degrees to this (which will not). Any net positive deflection of the QRS complex (i.e. height of the R-wave minus depth of the S-wave) suggests that the wave of depolarisation is spreading through the heart in a direction that has some component (of the vector) in the same direction as the lead in question.

Axis

The heart's electrical axis refers to the general direction of the heart's depolarization wavefront (or mean electrical vector) in the frontal plane. With a healthy conducting system the cardiac axis is related to where the major muscle bulk of the heart lies. Normally this is the left ventricle with some contribution from the right ventricle. It is usually oriented in a right shoulder to left leg direction, which corresponds to the left inferior quadrant of the hexaxial reference system, although −30° to +90° is considered to be normal. If the left ventricle increases its activity or bulk then there is said to be "left axis deviation" as the axis swings round to the left beyond -30°, alternatively in conditions where the right ventricle is strained or hypertrophied then the axis swings round beyond +90° and "right axis deviation" is said to exist. Disorders of the conduction system of the heart can disturb the electrical axis without necessarily reflecting changes in muscle bulk.

Normal −30° to 90° Normal Normal
Left axis deviation −30° to −90° May indicate left anterior fascicular block or Q waves from inferior MI. Left axis deviation is considered normal in pregnant women and those with emphysema.
Right axis deviation +90° to +180° May indicate left posterior fascicular block, Q waves from high lateral MI, or a right ventricular strain pattern. Right deviation is considered normal in children and is a standard effect of dextrocardia.
Extreme right axis deviation +180° to −90° Is rare, and considered an 'electrical no-man's land'.

In the setting of right bundle branch block, right or left axis deviation may indicate bifascicular block.

Clinical lead groups

There are twelve leads in total, each recording the electrical activity of the heart from a different perspective, which also correlate to different anatomical areas of the heart for the purpose of identifying acute coronary ischemia or injury. Two leads that look at neighbouring anatomical areas of the heart are said to be contiguous (see color coded chart). The relevance of this is in determining whether an abnormality on the ECG is likely to represent true disease or a spurious finding.

Category Color on chart Leads Activity
Inferior leads Yellow Leads II, III and aVF Look at electrical activity from the vantage point of the inferior surface (diaphragmatic surface of heart).
Lateral leads Green I, aVL, V5 and V6 Look at the electrical activity from the vantage point of the lateral wall of left ventricle.
  • The positive electrode for leads I and aVL should be located distally on the left arm and because of which, leads I and aVL are sometimes referred to as the high lateral leads.
  • Because the positive electrodes for leads V5 and V6 are on the patient's chest, they are sometimes referred to as the low lateral leads.
Septal leads Orange V1 and V2 Look at electrical activity from the vantage point of the septal wall of the ventricles (interventricular septum).
Anterior leads Blue V3 and V4 Look at electrical activity from the vantage point of the anterior surface of the heart (sternocostal surface of heart).

In addition, any two precordial leads that are next to one another are considered to be contiguous. For example, even though V4 is an anterior lead and V5 is a lateral lead, they are contiguous because they are next to one another.

Lead aVR offers no specific view of the left ventricle. Rather, it views the inside of the endocardial wall to the surface of the right atrium, from its perspective on the right shoulder.

Filter selection

Modern ECG monitors offer multiple filters for signal processing. The most common settings are monitor mode and diagnostic mode. In monitor mode, the low frequency filter (also called the high-pass filter because signals above the threshold are allowed to pass) is set at either 0.5 Hz or 1 Hz and the high frequency filter (also called the low-pass filter because signals below the threshold are allowed to pass) is set at 40 Hz. This limits artifact for routine cardiac rhythm monitoring. The high-pass filter helps reduce wandering baseline and the low-pass filter helps reduce 50 or 60 Hz power line noise (the power line network frequency differs between 50 and 60 Hz in different countries). In diagnostic mode, the high-pass filter is set at 0.05 Hz, which allows accurate ST segments to be recorded. The low-pass filter is set to 40, 100, or 150 Hz. Consequently, the monitor mode ECG display is more filtered than diagnostic mode, because its passband is narrower.[29]

Indications

Symptoms generally indicating use of electrocardiography include:

It is also used to assess patients with systemic disease as well as monitoring during anesthesia and critically ill patients.[30]

Some pathological entities which can be seen on the ECG

Shortened QT interval Hypercalcemia, some drugs, certain genetic abnormalities.
Prolonged QT interval Hypocalcemia, some drugs, certain genetic abnormalities.
Flattened or inverted T waves Coronary ischemia, hypokalemia, left ventricular hypertrophy, digoxin effect, some drugs.
Hyperacute T waves Possibly the first manifestation of acute myocardial infarction, where T waves become more prominent, symmetrical, and pointed.
Prominent U waves Hypokalemia.

Electrocardiogram heterogeneity

Electrocardiogram (ECG) heterogeneity is a measurement of the amount of variance between one ECG waveform and the next. This heterogeneity can be measured by placing multiple ECG electrodes on the chest and by then computing the variance in waveform morphology across the signals obtained from these electrodes. Recent research suggests that ECG heterogeneity often precedes dangerous cardiac arrhythmias.

In the future, implantable devices may be programmed to measure and track heterogeneity. These devices could potentially help ward off arrhythmias by stimulating nerves such as the vagus nerve, by delivering drugs such as beta-blockers, and if necessary, by defibrillating the heart.[31]

See also

References

  1. ^ "ECG- simplified. Aswini Kumar M.D". LifeHugger. http://www.lifehugger.com/doc/120/ecg-100-steps. Retrieved 2010-02-11. 
  2. ^ Braunwald E. (Editor), Heart Disease: A Textbook of Cardiovascular Medicine, Fifth Edition, p. 108, Philadelphia, W.B. Saunders Co., 1997. ISBN 0-7216-5666-8.
  3. ^ Van Mieghem, C; Sabbe, M; Knockaert, D (2004). "The clinical value of the EKG in noncardiac conditions". Chest 125 (4): 1561–76. doi:10.1378/chest.125.4.1561. PMID 15078775. 
  4. ^ "2005 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care - Part 8: Stabilization of the Patient With Acute Coronary Syndromes." Circulation 2005; 112: IV-89 - IV-110.
  5. ^ Ronald M. Birse, rev. Patricia E. Knowlden [1] Oxford Dictionary of National Biography 2004 (Subscription required) - (original source is his biography written by his wife - Elizabeth Muirhead. Alexandernn Muirhead 1848 - 1920. Oxford, Blackwell: privately printed 1926.)
  6. ^ Burdon Sanderson J; Page, F. J. M. (1878). "Experimental results relating to the rhythmical and excitatory motions of the ventricle of the frog heart". Proc Roy Soc Lond 27 (185–189): 410–14. doi:10.1098/rspl.1878.0068. 
  7. ^ Waller AD (1887). "A demonstration on man of electromotive changes accompanying the heart's beat". J Physiol (Lond) 8: 229–34. 
  8. ^ Rivera-Ruiz, M; Cajavilca, C; Varon, J (1927-09-29). "Einthoven's String Galvanometer: The First Electrocardiograph". Texas Heart Institute journal / from the Texas Heart Institute of St. Luke's Episcopal Hospital, Texas Children's Hospital (Pubmedcentral.nih.gov) 35 (2): 174–8. PMC 2435435. PMID 18612490. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2435435. 
  9. ^ Interwoven W. Un nouveau galvanometre. Arch Neerl Sc Ex Nat 1901; 6:625
  10. ^ Cooper J (1986). "Electrocardiography 100 years ago. Origins, pioneers, and contributors". N Engl J Med 315 (7): 461–4. doi:10.1056/NEJM198608143150721. PMID 3526152. 
  11. ^ Mark, Jonathan B. (1998). Atlas of cardiovascular monitoring. New York: Churchill Livingstone. ISBN 0443088918. 
  12. ^ See images of ECG electrodes here: http://www.superboverseas.com/show_product.asp?id=104 or here: http://images.google.com/images?q=ecg+electrode&oe=UTF-8&rls=org.mozilla:en-US:official&client=firefox-a&um=1&ie=UTF-8&sa=N&tab=wi&ei=IOEHSqCELp3ItgeY8_2HBw&oi=property_suggestions&resnum=0&ct=property-revision&cd=1)
  13. ^ "lead_dia". Library.med.utah.edu. http://library.med.utah.edu/kw/ecg/ecg_outline/Lesson1/lead_dia.html. Retrieved 2009-08-15. 
  14. ^ http://www.welchallyn.com/documents/Cardiopulmonary/Electrocardiographs/PC-Based%20Exercise%20Stress%20ECG/poster_110807_pcexerecg.pdf
  15. ^ [2]
  16. ^ "Univ. of Maryland School of Medicine Emergency Medicine Interest Group". Davidge2.umaryland.edu. http://davidge2.umaryland.edu/~emig/ekgtu03.html. Retrieved 2009-08-15. 
  17. ^ "Limb Leads - ECG Lead Placement - Normal Function of the Heart - Cardiology Teaching Package - Practice Learning - Division of Nursing - The University of Nottingham". Nottingham.ac.uk. http://www.nottingham.ac.uk/nursing/practice/resources/cardiology/function/limb_leads.php. Retrieved 2009-08-15. 
  18. ^ "Lesson 1: The Standard 12 Lead ECG". Library.med.utah.edu. http://library.med.utah.edu/kw/ecg/ecg_outline/Lesson1/index.html#orientation. Retrieved 2009-08-15. 
  19. ^ http://nobelprize.org/medicine/educational/ecg/images/triangle.gif
  20. ^ e.g. Pasco Pasport EKG Sensor PS-2111, Sciencescope ECG Sensor, etc.
  21. ^ http://academic.cuesta.edu/fjohnson/PowerPoint_PDF/12leadecg.pdf
  22. ^ "Electrocardiogram Leads". CV Physiology. 2007-03-26. http://www.cvphysiology.com/Arrhythmias/A013.htm. Retrieved 2009-08-15. 
  23. ^ Watch a movie by the National Heart Lung and Blood Institute explaining the connection between an ECG and the electricity in your heart at this site http://www.nhlbi.nih.gov/health/dci/Diseases/hhw/hhw_electrical.html
  24. ^ Making sense of the ECG 3rd edition p214
  25. ^ Gan-Xin Yan; Charles Antzelevitch. Cellular Basis for the Electrocardiographic J Wave. Circulation. 1996;93:372-379. http://circ.ahajournals.org/cgi/content/full/circulationaha;93/2/372 pmid=8548912
  26. ^ Hurst JW. Current Perspective: Naming of the Waves in the ECG, With a Brief Account of Their Genesis. Circulation. 1998;98:1937-1942. http://www.circ.ahajournals.org/cgi/content/full/98/18/1937
  27. ^ thefreedictionary.com > H deflection Citing: Mosby's Medical Dictionary, 8th edition. 2009
  28. ^ thefreedictionary.com > H-V interval Citing: McGraw-Hill Concise Dictionary of Modern Medicine. 2002
  29. ^ Mark JB "Atlas of Cardiovascular Monitoring." p. 130. New York: Churchill Livingstone, 1998. ISBN 0-443-08891-8.
  30. ^ a b c d e Page 244 in: Masters, Jo; Bowden, Carole; Martin, Carole (2003). Textbook of veterinary medical nursing. Oxford: Butterworth-Heinemann. ISBN 0-7506-5171-7. 
  31. ^ Verrier, Richard L. "Dynamic Tracking of ECG Heterogeneity to Estimate Risk of Life-threatening Arrhythmias." CIMIT Forum. September 25, 2007.

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and septa

Valve repair · Valvulotomy · Mitral valve repair · Valvuloplasty (aortic, mitral) Valve replacement - Aortic valve replacement (Ross procedure, Percutaneous aortic valve replacement) · Mitral valve replacement

production of septal defect in heart: enlargement of existing septal defect (Atrial septostomy, Balloon septostomy) · creation of septal defect in heart (Blalock-Hanlon procedure)

shunt from heart chamber to blood vessel: atrium to pulmonary artery (Fontan procedure) · left ventricle to aorta (Rastelli procedure) · right ventricle to pulmonary artery (Sano shunt)

compound procedures: for transposition of great vessels (Jatene procedure, Mustard procedure) · for univentricular defect (Norwood procedure, Kawashima procedure)

shunt from blood vessel to blood vessel: systemic circulation to pulmonary artery shunt (Blalock-Taussig shunt) · SVC to the right PA (Glenn procedure)
Cardiac vessels
Other
Diagnostic
tests and
procedures
Function tests
Pacing

M: HRT

anat/phys/devp

noco/cong/tumr, sysi/epon, injr

proc, drug (C1A/1B/1C/1D), blte
Electrocardiography
Central nervous system
Peripheral nervous system
Eyes
Digestive system
Heart
Volumes
Interaction diagrams
Chamber pressure
Other
Vascular system/
Hemodynamics

M: HRT

anat/phys/devp

noco/cong/tumr, sysi/epon, injr

proc, drug (C1A/1B/1C/1D), blte

M: VAS

anat(a:h/u/t/a/l,v:h/u/t/a/l)/phys/devp/cell/prot

noco/syva/cong/lyvd/tumr, sysi/epon, injr

proc, drug(C2s+n/3/4/5/7/8/9)