eMedicine Specialties > Neurology > Electroencephalography Atlas

EEG Artifacts

Author: Selim R Benbadis, MD, Professor, Director of Comprehensive Epilepsy Program, Departments of Neurology and Neurosurgery, University of South Florida School of Medicine, Tampa General Hospital
Coauthor(s): Diego Rielo, MD, Staff Physician, Department of Neurology, Memorial Hospital West, Memorial Hospital Pembroke, Memorial Healthcare
Contributor Information and Disclosures

Updated: Sep 10, 2008

Introduction

Although EEG is designed to record cerebral activity, it also records electrical activities arising from sites other than the brain. The recorded activity that is not of cerebral origin is termed artifact and can be divided into physiologic and extraphysiologic artifacts. While physiologic artifacts are generated from the patient, they arise from sources other than the brain (ie, body). Extraphysiologic artifacts arise from outside the body (ie, equipment, environment).

Physiologic Artifacts

Muscle (electromyogram) activity

Myogenic potentials are the most common artifacts (see Media files 1-2). Frontalis and temporalis muscles (eg, clenching of jaw muscles) are common causes. Generally, the potentials generated in the muscles are of shorter duration than those generated in the brain and are identified easily on the basis of duration, morphology, and rate of firing (ie, frequency). Particular patterns of electromyogram (EMG) artifacts can occur in some movement disorders. Essential tremor and Parkinson disease can produce rhythmic 4- to 6-Hz sinusoidal artifacts that may mimic cerebral activity.

Another disorder that can produce repetitive muscle artifacts is hemifacial spasm. The photomyoclonic response is a special type of EMG artifact that occurs during intermittent photic stimulation. Some subjects contract the frontalis and orbicularis muscles. These contractions occur approximately 50-60 milliseconds after each flash, disappear after eye opening and use of paralyzers, are located mostly frontally, and have no concomitant EEG changes.

Glossokinetic artifact

In addition to muscle activity, the tongue (like the eyeball) functions as a dipole, with the tip negative with respect to the base. In this case, the tip of the tongue is the most important part because it is more mobile. The artifact produced by the tongue has a broad potential field that drops from frontal to occipital areas, although it is less steep than that produced by eye movement artifacts. The amplitude of the potentials is greater inferiorly than in parasagittal regions; the frequency is variable but usually in the delta range and occurs synchronously when the patient says "Lah-lah-lah-lah" or "Lilt-lilt-lilt-lilt," which can be verified by the technologist. Chewing and sucking can produce similar artifacts. These are commonly observed in young patients. However, they also can be observed in patients with dementia or those who are uncooperative.

Eye movements

Eye movements are observed on all EEGs and are useful in identifying sleep stages. The eyeball acts as a dipole with a positive pole oriented anteriorly (cornea) and a negative pole oriented posteriorly (retina). When the globe rotates about its axis, it generates a large-amplitude alternate current field, which is detectable by any electrodes near the eye. The other source of artifacts comes from EMG potentials from muscles in and around the orbit.

Vertical eye movements typically are observed with blinks (ie, Bell phenomenon). A blink causes the positive pole (ie, cornea) to move closer to frontopolar (Fp1-Fp2) electrodes, producing symmetric downward deflections. During downward eye movement the positive pole (ie, cornea) of the globe moves away from frontopolar electrodes, producing an upward deflection best recorded in channels 1 and 5 in the bipolar longitudinal montage.

Lateral eye movements most affect lateral frontal electrodes F7 and F8 (see Media files 3-4). During a left lateral eye movement, the positive pole of the globe moves toward F7 and away from F8. Using a bipolar longitudinal montage, maximum positivity in electrode F7 and maximum negativity in electrode F8 is recorded, and artifacts do not occur in channels 9 and 13 or 10 and 14. A so-called rectus lateralis may be present in electrode F7; it is observed best in the vertex reference montage. With right lateral eye movement, the opposite occurs.

ECG artifact

Some individual variations in the amount and persistence of ECG artifact are related to the field of the heart potentials over the surface of the scalp. Generally, people with short and wide necks have the largest ECG artifacts on their EEGs. The voltage and apparent surface of the artifact vary from derivation to derivation and, consequently, from montage to montage. The artifact is observed best in referential montages using earlobe electrodes A1 and A2.

ECG artifact is recognized easily by its rhythmicity/regularity and coincidence with the ECG tracing (each "sharp wave" equals artifact that synchronizes with each QRS complex of the ECG channel; see Media file 5). The situation becomes difficult when cerebral abnormal activity (eg, sharp waves) appears intermixed with EEG artifact, and the former may be overlooked. The EEG technologist should apply electrodes routinely to record the ECG.

Pulse

Pulse artifact occurs when an EEG electrode is placed over a pulsating vessel. The pulsation can cause slow waves that may simulate EEG activity. A direct relationship exists between ECG and the pulse waves. The QRS complex (ie, electrical component of the heart contraction) happens slightly ahead of the pulse waves (200-300 millisecond delay after ECG equals QRS complex).

Respiration artifacts

Respiration can produce 2 kinds of artifacts. One type is in the form of slow and rhythmic activity, synchronous with the body movements of respiration and mechanically affecting the impedance of (usually) one electrode. The other type can be slow or sharp waves that occur synchronously with inhalation or exhalation and involve those electrodes on which the patient is lying. Several commercially available devices to monitor respiration can be coupled to the EEG machine. As with the ECG, one channel can be dedicated to respiratory movements. The simplest way to monitor respiration is by the EEG technician making notations with a pencil (ie, upward movement of the pencil for inhalations, downward return for exhalations).

Skin artifacts

Biological processes and/or defects may alter impedance and cause artifacts. Sweat is a common cause (see Media file 6). Sodium chloride and lactic acid from sweating reacting with metals of the electrodes may produce huge slow baseline sways.

Significant asymmetry also can be observed when a collection (eg, subgaleal hematoma) is under or in the skin. In this last example, the amplitude of the background rhythm is reduced in derivations from electrodes overlying the hematoma.

Skull defects also can be the source of asymmetry. In this situation, amplitudes are greater in derivations from electrodes overlying or adjacent to skull defects.

Extraphysiologic Artifacts

Electrodes

The most common electrode artifact is the electrode popping. Morphologically this appears as single or multiple sharp waveforms due to abrupt impedance change. It is identified easily by its characteristic appearance (ie, abrupt vertical transient that does not modify the background activity) and its usual distribution, which is limited to a single electrode. In general, sharp transients that occur at a single electrode should be considered artifacts until proven otherwise (see Media file 6). At other times, the impedance change is not so abrupt, and the artifact may mimic a low-voltage arrhythmic delta wave (see Media files 7-11).

Alternating current (60-Hz) artifact

Adequate grounding on the patient has almost eliminated this type of artifact from power lines. The problem arises when the impedance of one of the active electrodes becomes significantly large between the electrodes and the ground of the amplifier. In this situation, the ground becomes an active electrode that, depending on its location, produces the 60-Hz artifact (see Media file 12). The artifact presents at exact frequency (60 Hz, as its name indicates). A better identification can be made by increasing the paper speed (ie, sweep time) to 60 mm/s and counting it (1 cycle per millimeter).

Movements in the environment

Movement of other persons around the patient can generate artifacts, usually of capacitive or electrostatic origin. Avoid this type of artifact as much as possible. If avoidance is not possible, as in the ICU and the operating room, place proper notation on the records.

Another artifact, probably due to electrostatic changes on the drops, can be introduced by a gravity-fed intravenous infusion. Morphologically this appears as spike transient potentials at fixed intervals that coincide with drops of the infusion.

With the increasing use of automatic electric infusion pumps, a new type of artifact, infusion motor artifact (IMA), has arisen. Morphologically, IMA appears as very brief spiky transients, sometimes followed by a slow component of the same polarity. Its frequency does not relate directly to drop rate. Lininger et al have suggested that this artifact arises from electromagnetic sources.1

The artifact produced by respirators varies widely in morphology and frequency. Monitoring the ventilator rate in a separate channel helps to identify this type of artifact.

Interference from high-frequency radiation from radio, television, hospital paging systems, and other electronic devices can overload EEG amplifiers. The pens may deflect upward or downward to full excursion, and no EEG can be recorded. The cutting and/or coagulating electrode used in the operating room also generates high-voltage high-frequency signals that interfere with the recording system. The best thing to do is turn off the EEG machine while using this instrument.

Patient Education

For excellent patient education resources, visit eMedicine's Procedures Center. Also, see eMedicine's patient education article Electroencephalography (EEG).

Multimedia

Electromyogram (muscle) artifact best observed in...Media file 1: Electromyogram (muscle) artifact best observed in the left temporal region. ECG artifact also is present, best observed in the posterior region.
Electromyogram (muscle) artifact best observed in...

Electromyogram (muscle) artifact best observed in the left temporal region. ECG artifact also is present, best observed in the posterior region.

Electromyogram (muscle) artifact. These waveforms...Media file 2: Electromyogram (muscle) artifact. These waveforms represent motor unit potentials as typically observed on needle electrode examination during electromyogram, with a frequency of 20-100 Hz. Distribution varies, and in this case it is more prominent on the left side. Such artifact can be diminished by the judicious use of the high-frequency filter. (This sample has the default setting of high-frequency filter 70 Hz.)
Electromyogram (muscle) artifact. These waveforms...

Electromyogram (muscle) artifact. These waveforms represent motor unit potentials as typically observed on needle electrode examination during electromyogram, with a frequency of 20-100 Hz. Distribution varies, and in this case it is more prominent on the left side. Such artifact can be diminished by the judicious use of the high-frequency filter. (This sample has the default setting of high-frequency filter 70 Hz.)

Eye movements such as these usually are observed ...Media file 3: Eye movements such as these usually are observed in frontal electrodes and not further posteriorly than the midtemporal region. The phase reversals at lateral frontal electrodes F7 and F8 are of opposite polarity, indicating lateral eye movements. Because the cornea is charged positively and the retina negatively, the side of the positivity indicates the direction of eye movement. Thus, the first one here is to the right.
Eye movements such as these usually are observed ...

Eye movements such as these usually are observed in frontal electrodes and not further posteriorly than the midtemporal region. The phase reversals at lateral frontal electrodes F7 and F8 are of opposite polarity, indicating lateral eye movements. Because the cornea is charged positively and the retina negatively, the side of the positivity indicates the direction of eye movement. Thus, the first one here is to the right.

Left frontal artifact in the fourth second. This ...Media file 4: Left frontal artifact in the fourth second. This is not limited to a single electrode and has the morphology of an eye movement, but it is unilateral. This is an eye movement in a patient who has a glass left eye.
Left frontal artifact in the fourth second. This ...

Left frontal artifact in the fourth second. This is not limited to a single electrode and has the morphology of an eye movement, but it is unilateral. This is an eye movement in a patient who has a glass left eye.

Regular (periodic) slow waves best observed at mi...Media file 5: Regular (periodic) slow waves best observed at midtemporal and posterior temporal electrodes T4-T6 and T3-T5. These clearly are related to ECG. The duration and morphology are those of pulse artifact, but as demonstrated by the marker, no delay occurs between the ECG and the artifact. Thus, this is an ECG artifact with broad QRS complexes.
Regular (periodic) slow waves best observed at mi...

Regular (periodic) slow waves best observed at midtemporal and posterior temporal electrodes T4-T6 and T3-T5. These clearly are related to ECG. The duration and morphology are those of pulse artifact, but as demonstrated by the marker, no delay occurs between the ECG and the artifact. Thus, this is an ECG artifact with broad QRS complexes.

Sweat artifact. This is characterized by very low...Media file 6: Sweat artifact. This is characterized by very low-frequency (here, 0.25- to 0.5-Hz) oscillations. The distribution here (midtemporal electrode T3 and occipital electrode O1) suggests sweat on the left side. Note that morphology and frequency are also consistent with slow rolling eye movements, but distribution is not.
Sweat artifact. This is characterized by very low...

Sweat artifact. This is characterized by very low-frequency (here, 0.25- to 0.5-Hz) oscillations. The distribution here (midtemporal electrode T3 and occipital electrode O1) suggests sweat on the left side. Note that morphology and frequency are also consistent with slow rolling eye movements, but distribution is not.

Electrode artifact at frontal pole electrode Fp1....Media file 7: Electrode artifact at frontal pole electrode Fp1. The duration is too short ("narrow") for any cerebral potential, and the distribution is limited to a single electrode (Fp1). In general, activity that affects a single electrode (ie, without the expected drop off and activity at neighboring electrodes or "plausible field") should be considered an artifact until proven otherwise.
Electrode artifact at frontal pole electrode Fp1....

Electrode artifact at frontal pole electrode Fp1. The duration is too short ("narrow") for any cerebral potential, and the distribution is limited to a single electrode (Fp1). In general, activity that affects a single electrode (ie, without the expected drop off and activity at neighboring electrodes or "plausible field") should be considered an artifact until proven otherwise.

Electrode artifact at occipital electrode O1. The...Media file 8: Electrode artifact at occipital electrode O1. The morphology is very unusual for any cerebral waveform, and the distribution is limited to a single electrode. In general, activity that affects a single electrode (ie, without the expected drop off and activity at neighboring electrodes or "plausible field") should be considered an artifact until proven otherwise.
Electrode artifact at occipital electrode O1. The...

Electrode artifact at occipital electrode O1. The morphology is very unusual for any cerebral waveform, and the distribution is limited to a single electrode. In general, activity that affects a single electrode (ie, without the expected drop off and activity at neighboring electrodes or "plausible field") should be considered an artifact until proven otherwise.

Electrode artifact at frontal electrode F3. This ...Media file 9: Electrode artifact at frontal electrode F3. This should not be misinterpreted as a spike. This sharply contoured transient clearly occurs at only one electrode, as confirmed on the referential montage.
Electrode artifact at frontal electrode F3. This ...

Electrode artifact at frontal electrode F3. This should not be misinterpreted as a spike. This sharply contoured transient clearly occurs at only one electrode, as confirmed on the referential montage.

Electrode (impedance) artifact at parietal electr...Media file 10: Electrode (impedance) artifact at parietal electrode P3. Initially, a slow artifact is followed by a more abrupt one at the seventh second. This commonly is referred to as an electrode pop. Note again the unusual morphology of the sharp component and that it is at a single electrode. Also note an eye blink in the third second and slight electromyogram artifact in the frontal regions in the first 2 seconds.
Electrode (impedance) artifact at parietal electr...

Electrode (impedance) artifact at parietal electrode P3. Initially, a slow artifact is followed by a more abrupt one at the seventh second. This commonly is referred to as an electrode pop. Note again the unusual morphology of the sharp component and that it is at a single electrode. Also note an eye blink in the third second and slight electromyogram artifact in the frontal regions in the first 2 seconds.

Just as electrode artifacts can simulate interict...Media file 11: Just as electrode artifacts can simulate interictal spikes, they also can mimic an ictal pattern. This rhythmic artifact may be mistaken for an electrographic seizure or subclinical rhythmic epileptiform discharges of adults (SREDA). However, this is confined to a single electrode (posterior temporal electrode T6), as can be confirmed on a referential montage. This artifact often is confirmed by the presence of other definite electrode pops in the same electrode.
Just as electrode artifacts can simulate interict...

Just as electrode artifacts can simulate interictal spikes, they also can mimic an ictal pattern. This rhythmic artifact may be mistaken for an electrographic seizure or subclinical rhythmic epileptiform discharges of adults (SREDA). However, this is confined to a single electrode (posterior temporal electrode T6), as can be confirmed on a referential montage. This artifact often is confirmed by the presence of other definite electrode pops in the same electrode.

Ground recording artifact. This is a somewhat les...Media file 12: Ground recording artifact. This is a somewhat less common electrode artifact, also related to accidentally high impedance. The high impedance at posterior temporal electrode T6 results in this electrode recording from the ground on the forehead, thus picking up eye movements (which normally should not be observed at T6).
Ground recording artifact. This is a somewhat les...

Ground recording artifact. This is a somewhat less common electrode artifact, also related to accidentally high impedance. The high impedance at posterior temporal electrode T6 results in this electrode recording from the ground on the forehead, thus picking up eye movements (which normally should not be observed at T6).

Keywords

electroencephalogram, electroencephalograph, electroencephalography, cerebral activity, cerebral function, muscle function, electromyogram, EMG, glossokinetic artifact, eye movement, ECG artifact, respiration artifacts, skin artifacts, electrodes, alternating current 60-Hz artifact

 


More on EEG Artifacts

References

References

  1. Lininger AW, Volow MR, Gianturco DT. Intravenous infusion motor artifact. Am J EEG Technol. Dec 1981;21(4):167-73. [Medline].

  2. Luders H, Noachtar S. Atlas and Classification of Electroencephalography. Philadelphia: WB Saunders Co; 2000.

  3. Benbadis SR. Introduction to EEG. In: Lee-Chiong T. Sleep: A Comprehensive Handbook. Hoboken, NJ: Wiley & Sons; 2006.

  4. Bickford RG, Daly D, Keith HM. Convulsive effects of light stimulation in children. AMA Am J Dis Child. Aug 1953;86(2):170-83. [Medline].

  5. Daly D, Pedley T, eds. Current Practice of Clinical Electroencephalography. 2nd ed. New York: Raven Press; 1990.

  6. Picton TW, van Roon P, Armilio ML, et al. The correction of ocular artifacts: a topographic perspective. Clin Neurophysiol. Jan 2000;111(1):53-65. [Medline].

  7. Redding FK, Wandel V, Nasser C. Intravenous infusion drop artifacts. Electroencephalogr Clin Neurophysiol. Mar 1969;26(3):318-20. [Medline].

  8. Schwab RS, Cobb S. Simultaneous EMGs and EEGs in paralysis agitans. J Neurophysiol. 1939;2:36-41.

  9. Shaffer MA. Problem record of the month. No. 3: Asymmetrical eyeblink artifact. Am J EEG Technol. 1970;10:153-6.

  10. Smith SJ. EEG in neurological conditions other than epilepsy: when does it help, what does it add?. J Neurol Neurosurg Psychiatry. Jun 2005;76 Suppl 2:ii8-12. [Medline].

  11. Smith SJ. EEG in the diagnosis, classification, and management of patients with epilepsy. J Neurol Neurosurg Psychiatry. Jun 2005;76 Suppl 2:ii2-7. [Medline].

  12. Tyner F, Knott J, Mayer Jr W, eds. Fundamentals of EEG technology. In: Basic Concepts and Methods. 1. NY: Raven Press; 1983.

  13. van de Velde M, van Erp G, Cluitmans PJ. Detection of muscle artifact in the normal human awake EEG. Electroencephalogr Clin Neurophysiol. Aug 1998;107(2):149-58. [Medline].

  14. Westmoreland BF, Espinosa RE, Klass DW. Significant prosopoglossopharyngeal movements affecting the EEG. Am J EEG Technol. 1973;13:59-70.

  15. Young GB, Campbell VC. EEG monitoring in the intensive care unit: pitfalls and caveats. J Clin Neurophysiol. Jan 1999;16(1):40-5. [Medline].

Further Reading

Keywords

electroencephalogram, electroencephalograph, electroencephalography, cerebral activity, cerebral function, muscle function, electromyogram, EMG, glossokinetic artifact, eye movement, ECG artifact, respiration artifacts, skin artifacts, electrodes, alternating current 60-Hz artifact

Contributor Information and Disclosures

Author

Selim R Benbadis, MD, Professor, Director of Comprehensive Epilepsy Program, Departments of Neurology and Neurosurgery, University of South Florida School of Medicine, Tampa General Hospital
Selim R Benbadis, MD is a member of the following medical societies: American Academy of Neurology, American Academy of Sleep Medicine, American Clinical Neurophysiology Society, American Epilepsy Society, and American Medical Association
Disclosure: Nothing to disclose.

Coauthor(s)

Diego Rielo, MD, Staff Physician, Department of Neurology, Memorial Hospital West, Memorial Hospital Pembroke, Memorial Healthcare
Diego Rielo, MD is a member of the following medical societies: American Academy of Neurology
Disclosure: Nothing to disclose.

Medical Editor

Leslie Huszar, MD, Consulting Staff, Department of Neurology, Indian River Memorial Hospital
Leslie Huszar, MD is a member of the following medical societies: American Academy of Neurology, American Association for the Advancement of Science, and American Medical Electroencephalographic Association
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Norberto Alvarez, MD, Assistant Professor, Department of Neurology, Harvard Medical School; Consulting Staff, Department of Neurology, Boston Children's Hospital
Norberto Alvarez, MD is a member of the following medical societies: American Academy of Neurology, American Epilepsy Society, and Child Neurology Society
Disclosure: Nothing to disclose.

CME Editor

Paul E Barkhaus, MD, Professor, Department of Neurology, Medical College of Wisconsin; Director of Neuromuscular Diseases, Milwaukee Veterans Administration Medical Center
Paul E Barkhaus, MD is a member of the following medical societies: American Academy of Neurology, American Association of Neuromuscular and Electrodiagnostic Medicine, and American Neurological Association
Disclosure: Nothing to disclose.

Chief Editor

Helmi L Lutsep, MD, Professor, Department of Neurology, Oregon Health and Science University; Associate Director, Oregon Stroke Center
Helmi L Lutsep, MD is a member of the following medical societies: American Academy of Neurology and American Stroke Association
Disclosure: Co-Axia Consulting fee Review panel membership; Talecris Consulting fee Review panel membership; AGA Medical Consulting fee Review panel membership; Boehringer Ingelheim Honoraria Speaking and teaching; Boston Scientific Honoraria Speaking and teaching; Concentric Medical None Review panel membership; Northstar Neuroscience  Review panel membership; ev3 Consulting fee Review panel membership

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