n. (Abbr. EKG or ECG)
The curve traced by an electrocardiograph. Also called cardiogram.
Dictionary:
e·lec·tro·car·di·o·gram (ĭ-lĕk'trō-kär'dē-ə-grăm')
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World of the Body:
electrocardiogram |
This means of studying the activity of the heart from electrical signals detectable from the body surface stemmed directly, early in the twentieth century, from the invention of the string galvanometer by the Dutch physiologist, Einthoven. Electrocardiography was demonstrated to the Royal Society in London in 1909.
The ‘ECG’ (or sometimes still ‘EKG’ in the US, from the German spelling) has become an icon representing the heart's activity. The waveform is the most familiar ‘high tech’ sign of the electrical behaviour of the heart. In various versions, its characteristic shape (see figure) reporting a healthy rhythm, or the flat line suggesting the patient's demise, is familiar to any viewer of television medical soap operas. A clever variation on the theme forms the distinctive logo for the British Heart Foundation, the largest UK charity dedicated to funding cardiovascular research.
The electrocardiogram (as a paper trace or a TV monitor display) shows the changes in the voltage, detectable during the time course of the heart beat, between pairs of electrodes placed at certain points on the skin. The basis of the ECG is that the heart, like other muscles, is triggered to contract by electrical activity. The heart is a relatively large piece of tissue, so the flow of electrical current associated with (and immediately preceding) contraction produces detectable voltages (typically a few millivolts) on the surface of the body. Electrode pairs can be placed at various positions on the body to yield information about the status of the heart. The classic ‘limb leads’ are attached to one leg and two arms; other pairings are placed at defined positions on the chest itself. Even more detail can be obtained with leads inserted in the oesophagus (the gullet) or even from within the heart itself (with the electrode introduced via a vein). Abnormal enlargement (hypertrophy) of the heart's various chambers produces characteristic distortions of the ‘ideal’ ECG form which are readily interpreted by experienced users.

The P-wave indicates the electrical activity associated with contraction of the cardiac atria, the heart's upper chambers.
The P-R interval is the delay between the beginning of activity in the atria and the ventricles (atrio-ventricular conduction time). In adults, normal P-R intervals range between 120 and 200 milliseconds, occasionally being shorter in children and slightly longer in the aged. The P-R interval shortens at high heart rates (e.g. due to exercise or to fever) and increases at lower heart rates (e.g. during sleep).
The QRS complex indicates the onset of contraction of the ventricles. The shape of the QRS complex may be modified by a number of physiological factors (e.g. body position and breathing pattern). In normal adults, the duration of the QRS complex varies between 60 and 100 milliseconds; in children it tends to be shorter.
The Q-T interval is measured from the beginning of the QRS complex to the end of the T-wave and represents the time between activation of electrical activity in the ventricles and their return to the resting state. Like the P-R interval, the Q-T interval shortens at high heart rates and increases at lower rates.
The T-wave indicates when the electrical activity associated with the cells in the cardiac ventricle returns to the resting state after electrical activation. Thus, it signals the start of relaxation of the ventricle walls. It tends to be longer lasting than QRS because the onset of relaxation across the ventricle is less tightly synchronized than that of contraction.
Some stark deviations from this classical sequence can occur, including the chaotic waves associated with ventricular fibrillation. This is the uncoordinated, apparently random electrical activity (and thus contraction) of the ventricles that can readily prove fatal without defibrillation. Heart block is a condition readily identified by ECG analysis.
There are characteristic changes in the wave pattern of the ECG in myocardial ischaemia (inadequate blood supply to the heart), which may be evident at first during exercise in sufferers from angina, and which may confirm or exclude an ischaemic episode or myocardial infarction in instances of unexplained chest pain.
— David J. Miller, Niall G. MacFarlane
See also heart; heart attack.
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A tracing on a graph of the electrical changes occurring during a heartbeat. It is one of the most useful records of heart function. It can reveal irregular heart-beats and damage to heart muscle. Specific irregularities in the trace may indicate enlargement of the heart chambers, mineral imbalances in the blood, or whether someone has had, or is having, a heart attack. ECGs are usually recorded while the subject is at rest. An exercise ECG, sometimes called a stress test, provides information about the heart's response to physical exertion.
Medical Test:
Electrocardiogram |
| Where It's Done | Who Does It | How Long It Takes | Discomfort/Pain |
| Doctor's office or clinic, or at hospital bedside. | Technician, nurse, or doctor. | 5 minutes. | None. |
| Results Ready When | Special Equipment | Risks/Complications | Average Cost |
| Immediately. | ECG machine and electrodes. | None. | $ |
Resting electrocardiogram, ECG, or EKG.
PurposeElectrodes, or leads, attached to the chest, neck, arms, and legs record the pathway of electrical impulses through the heart muscle (see figure).
To make an ECG, electrodes are attached to specific points over the heart, on the neck, and on the arm and legs.

You lie quietly on your back while the heart's electrical impulses are recorded on the graph paper.
After the testLeads are removed and gel (if used) is wiped off. Unless the test detects heart problems, you can immediately resume your normal activities.
Factors affecting resultsThe letters along the top of this ECG strip indicate readings obtained from specific leads, or sensors. For example, V-1 to V-6 are from the leads placed across the chest; the others are from leads placed on the arms and legs.

This ECG was taken during a heart attack, which is indicated by the segment labeled ST.

The segment labeled VT on this ECG shows transient ventricular tachycardia, a severe cardiac arrhythmia. In this instance, the arrhythmia stops spontaneously. If it were to continue, however, it would be potentially fatal.

Sports Science and Medicine:
electrocardiogram |
A graphical record of the electrical changes occurring during a heartbeat. A typical ECG is composed of a P wave, representing depolarization of the atria; the P-R interval, indicating the delay in conduction at the atrioventricular node; the QRS complex, produced during ventricular depolarization and contraction; and the T wave and ST segment, corresponding to ventricular repolarization. When read and interpreted by a highly skilled and experienced physician, an ECG is probably the most useful record of heart function. It can reveal the cause of irregular heart beats and damage to the heart muscle. It can also show enlargement of heart chambers, mineral imbalances in the blood, and whether someone has had or is having a heart attack. ECGs are recorded while the subject is resting or exercising. An exercise ECG, also called a stress test, can provide information on cardiorespiratory fitness and how the heart responds to strenuous exercise; it often forms part of the medical screening process of potential exercisers.

Health Dictionary:
electrocardiogram |
A written recording of the electrical activity of the heart. Electrocardiograms are used to determine the condition of the heart and to diagnose heart disease.
Veterinary Dictionary:
electrocardiogram |
The record produced by electrocardiography; a tracing representing the heart's electrical action derived by amplification of the minutely small electrical impulses normally generated by the heart. Called also ECG and EKG.
Wikipedia:
Electrocardiography |
Electrocardiography (ECG or EKG) is a transthoracic interpretation of the electrical activity of the heart over time captured and externally recorded by skin electrodes.[1] It is a noninvasive recording produced by an electrocardiographic device. The etymology of the word is derived from electro, because it is related to electrical activity, cardio, Greek for heart, and graph, a Greek root meaning "to write".
Electrical impulses in the heart originate in the sinoatrial node and travel through the intrinsic conducting system to the heart muscle. The impulses stimulate the myocardial muscle fibers to contract and thus induce systole. The electrical waves can be measured at electrodes placed at specific points on the skin. Electrodes on different sides of the heart measure the activity of different parts of the heart muscle. An ECG displays the voltage between pairs of these electrodes, and the muscle activity that they measure, from different directions, can also be understood as vectors. This display indicates the overall rhythm of the heart and weaknesses in different parts of the heart muscle. 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 ECG can identify if the heart muscle has been damaged in specific areas, though not all areas of the heart are covered.[4] The ECG cannot reliably measure the pumping ability of the heart, for which ultrasound-based (echocardiography) or nuclear medicine tests are used.
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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, The 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]
Einthoven assigned the letters P, Q, R, S and T to the various deflections, 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]
Timed interpretation of an ECG was once incumbent to a stylus and paper speed. Computational analysis now allows considerable study of heart rate variability. A typical electrocardiograph runs at a paper speed of 25 mm/s, although faster paper speeds are occasionally used. Each small block of ECG paper is 1 mm2. 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 diagnostic quality 12 lead ECG is calibrated at 10 m/V, so 1 mm translates into 0.1 mV. A calibration signal should be included with every record. A standard signal of 1 mV must move the stylus vertically 1 cm, that is two large squares on ECG paper.
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.[12]
In electrocardiography, the word lead may refer to either the electrodes attached to the patient, or, properly, (in which case, it is pronounced /lid/) to the voltage between two electrodes. The electrodes are attached to the patient's body, usually with very sticky circles of thick tape-like material (the electrode is embedded in the center of this circle), onto which cables clip.[13] ECG leads use different combinations of electrodes to produce various signals from the heart.
Ten electrodes are used for a 12-lead ECG. They are labeled and placed on the patient's body as follows:[14][15]
| Electrode label (in the USA) | Electrode placement |
|---|---|
| RA | On the right arm, avoiding bony prominences. |
| LA | In the same location that RA was placed, but on the left arm this time. |
| RL | On the right leg, avoiding bony prominences. |
| LL | In the same location that RL was placed, but on the left leg this time. |
| 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.) |
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.[17][18][19] The limb leads form the points of what is known as Einthoven's triangle.[20]
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) 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 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).
Leads aVR, aVL, and aVF are augmented limb 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" or a unipolar lead. 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.
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 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.
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 |
|---|---|---|
| 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 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. | 50 to 120ms |
| QRS complex | The QRS complex is a recording of a single heartbeat on the ECG that corresponds to the depolarization of the right and left ventricles. | 70 to 110ms |
| ST segment | The ST segment connects the QRS complex and the T wave. | 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 |
| PR interval | The PR interval is measured from the beginning of the P wave to the beginning of the QRS complex. | 120 to 200ms |
| 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. | 300 to 430ms[citation needed] |
| U wave | The U wave is not always seen. It is typically low amplitude, and, by definition, follows the T wave. |
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.[24]
| Shortened QT interval | Hypercalcemia, some drugs. |
|---|---|
| Prolonged QT interval | Hypocalcemia, some drugs. |
| Flattened or inverted T waves | Coronary ischemia, left ventricular hypertrophy, digoxin effect, some drugs. |
| Hyperacute T waves | Possibly the first manifestation of acute myocardial infarction. |
| Prominent U waves | Hypokalemia. |
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 the same anatomical area of the heart are said to be contiguous (see color coded chart).
| 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.
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| 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.
The heart's electrical axis refers to the general direction of the heart's depolarization wavefront (or mean electrical vector) in the frontal plane. 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.
| 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.
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.
There are over 350,000 cases of sudden cardiac death (SCD) in the United States each year, and over twenty percent of these cases involve people with no outward signs of serious heart disease. For decades, researchers have been attempting to come up with methods of identifying electrocardiogram (ECG) patterns that reliably precede dangerous arrhythmias. As these methods are found, devices are being created that monitor the heart in order to detect the onset of dangerous rhythms and to correct them before they cause death.
Research being conducted[25] suggests that a crescendo in ECG heterogeneity, both in the R-wave and the T-wave, often signals the start of ventricular fibrillation. In patients with coronary artery disease, exercise increases T-wave heterogeneity, but this effect is not seen in normal patients. These results, when combined with other pieces of emerging evidence, suggest that R-wave and T-wave heterogeneity both have predictive value.
In the future, researchers hope to simplify the ECG to a larger encyclopedic audience. Technology now allows deployment of temporary and permanent cardiac electrodes in a plurality of anatomic positions capable of novel ECGs unimpeded by the skin or thoracic cage. ECGs can be as variable as fingerprints to a trained observer. Patterns may be appreciated and computational analysis may illuminate the process of heterogeneity detection and to augment the clinical evidence supporting the validity of ECG heterogeneity as a predictor of arrhythmia. The electrocardiogram is fundamentally an interpretative entity but allows interventional measures, see Interventional Cardiology. Someday soon, 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.[26]
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Translations:
electrocardiogram |
Dansk (Danish)
n. - elektrokardiogram, EKG
Nederlands (Dutch)
elektrocardiogram, hartfilmpje
Français (French)
n. - électrocardiogramme
Deutsch (German)
n. - Elektrokardiogramm
Ελληνική (Greek)
n. - (ιατρ.) ηλεκτροκαρδιογράφημα
Italiano (Italian)
elettrocardiogramma
Português (Portuguese)
n. - eletrocardiograma (m) (Med.)
Русский (Russian)
электрокардиограмма
Español (Spanish)
n. - electrocardiograma
Svenska (Swedish)
n. - elektrokardiogram
中文(简体)(Chinese (Simplified))
心电图, 心动电流图
中文(繁體)(Chinese (Traditional))
n. - 心電圖, 心動電流圖
العربيه (Arabic)
(الاسم) مخطط كهربائيه القلب
עברית (Hebrew)
n. - תרשים פעולת הלב, אק"ג
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| ECG (abbreviation) |
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| What are the parts of electrocardiogram? |
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