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electromyography

 
Medical Encyclopedia: Electromyography

Definition

Electromyography (EMG) is an electrical recording of muscle activity that aids in the diagnosis of neuromuscular disease.

Description

During an EMG test, a fine needle is inserted into the muscle to be tested. This may cause some discomfort, similar to that of an injection. Recordings are made while the muscle is at rest, and then during the contraction. The person performing the test may move the limb being tested, and direct the patient to move it with various levels of force. The needle may be repositioned in the same muscle for further recording. Other muscles may be tested as well. A typical session lasts from 30–60 minutes.

A slightly different test, the nerve conduction velocity test, is often performed at the same time with the same equipment. In this test, stimulating and recording electrodes are used, and small electrical shocks are applied to measure the ability of the nerve to conduct electrical signals. This test may cause mild tingling and discomfort similar to a mild shock from static electricity. Evoked potentials may also be performed for additional diagnostic information. Nerve conduction velocity and evoked potential testing are especially helpful when pain or sensory complaints are more prominent than weakness.

— Richard Robinson



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Sci-Tech Dictionary: electromyography
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(i¦lek·trō·mī′äg·rə·fē)

(medicine) A medical specialty concerned with the production and study of electromyograms.


Neurological Disorder:

Electromyography

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Definition

Electromyography (EMG) is an electrical recording of muscle activity that aids in the diagnosis of neuromuscular disease, which affects muscle and peripheral nerves.

Purpose

Muscles are stimulated by signals from nerve cells called motor neurons. This stimulation causes electrical activity in the muscle, which in turn causes contraction. A needle electrode inserted into the muscle and connected to a recording device detects this electrical activity. Together, the electrode and recorder are called an electromyography machine. EMG can determine whether a particular muscle is responding appropriately to stimulation, and whether a muscle remains inactive when not stimulated.

EMG is performed most often to help diagnose different diseases causing weakness. Although EMG is a test of the motor system, it may help identify abnormalities of nerves or spinal nerve roots that may be associated with pain or numbness. Other symptoms for which EMG may be useful include atrophy, stiffness, fasciculation (muscle twitching), cramp, deformity, and spasticity. EMG results can help determine whether symptoms are due to a muscle disease or a neurological disorder, and, when combined with clinical findings, usually allow a confident diagnosis.

EMG can help diagnose many muscle and nerve disorders, including:

  • muscular dystrophy
  • congenital myopathies
  • mitochondrial myopathies
  • metabolic myopathies
  • myotonias
  • peripheral neuropathies
  • radiculopathies
  • nerve lesions
  • amyotrophic lateral sclerosis
  • polio
  • spinal muscular atrophy
  • Guillain-Barré syndrome ataxias
  • myasthenias
  • inflammatory myopathies

Precautions

No special precautions are needed for this test. Persons with a history of bleeding disorder should consult with their treating physician before the test. If a muscle biopsy is planned as part of the diagnostic workup, EMG should not be performed at the same site, as it may affect the microscopic appearance of the muscle. Also, persons on blood thinners should relay this information to the physician performing the EMG.

Description

During an EMG test, a fine needle is inserted into the muscle to be tested. This may cause some discomfort, similar to that of an injection. Recordings are made while the muscle is at rest, and then during the contraction. The person performing the test may move the limb being tested, and direct the patient to move it with various levels of force. The needle may be repositioned in the same muscle for further recording. Other muscles may be tested as well. A typical session lasts from 30–60 minutes, with individual muscles usually studied for a period of two to five minutes.

A slightly different test, the "nerve conduction velocity test," is often performed at the same time with the same equipment. In this test, stimulating and recording electrodes are used and small electrical shocks are applied to measure the ability of the nerve to conduct electrical signals. This test may cause mild tingling and discomfort similar to a mild shock from static electricity. Evoked potentials may also be performed for additional diagnostic information. Nerve conduction velocity and evoked potential testing are especially helpful when pain or sensory complaints are more problematic than weakness.

Preparation

No special preparation is needed. The doctor supervising and interpreting the test should be given information about the symptoms, medical conditions, suspected diagnosis, neuroimaging studies, and other test results.

Aftercare

Minor pain and bleeding may continue for several hours after the test. The muscle may be tender for a day or two.

Risks

There are no significant risks to this test, other than those associated with any needle insertion (pain, bleeding, bruising, or infection).

Normal results

There should be some brief EMG activity during needle insertion. This activity may be increased in diseases of the nerve and decreased in long-standing muscle disorders in which muscle tissue is replaced by fibrous tissue or fat. Muscle tissue normally shows no EMG activity when at rest or when moved passively by the examiner. When the patient actively contracts the muscle, spikes (motor unit action potentials) should appear on the recording screen, reflecting the electrical activity within. As the muscle is contracted more forcefully, more groups of muscle fibers are recruited or activated, causing more EMG activity.

The interpretation of EMG results is not a simple matter, requiring analysis of the onset, duration, amplitude, and other characteristics of the spike patterns.

Electrical activity at rest is abnormal; the particular pattern of firing may indicate denervation (for example, a nerve lesion, radiculopathy, or lower motor neuron degeneration), myotonia, or inflammatory myopathy.

Decreases in the amplitude and duration of spikes are associated with muscle diseases, which also show faster recruitment of other muscle fibers to compensate for weakness. Increases in the amplitude and duration of the spikes are typical of nerve diseases in which some degree of rein-nervation (repair by new nerve connections to muscle) has occurred. Recruitment is reduced in nerve disorders.

Resources

BOOKS

Basmajian, J., and C. DeLuca. Muscles Alive: Their Function Revealed by Electromyography, 5th ed. Baltimore: Williams & Wilkins, 1985.


Richard Robinson


Sci-Tech Encyclopedia: Electromyography
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The detection and recording of electrical activity generated by muscle fibers. The basic elements of motor control in the body are the motor units which comprise motor neurons in the brainstem or spinal cord, their axons, and from ten to several hundred muscle fibers supplied by each motor neuron. Motor units vary in the size and properties of their motoneurons, the sizes and conduction velocities of their axons, the morphology of their nerve muscle junctions, and the structure and physiological properties of the muscle fibers supplied by each motor neuron.

Impulses originating in single motoneurons in response to various command signals from the central nervous system conduct to the periphery of the unit, normally causing all the muscle fibers in the unit to discharge. The electrical activity generated by the more or less synchronous discharges of all the muscle fibers in the unit may be detected by recording electrodes on the skin surface or by needles inserted into the muscle. Such potentials reflect the electrical activity generated by the whole motor unit.

Diseases affecting motor neurons are sometimes accompanied by spontaneous discharges of the axons. Additionally, degeneration of motor axons may leave some muscle fibers deprived of their normal innervation, some of which spontaneously fire. Such single muscle-fiber discharges are called fibrillations and are readily detected for diagnostic purposes by needle electrodes inserted into the muscle.

Electromyography may also be used to study primary muscle diseases such as the muscular dystrophies, and a wide variety of other metabolic inflammatory and congenital myopathies affecting the muscle fibers rather than motor neurons or their axons. See also Biopotentials and ionic currents; Electrodiagnosis.


Dental Dictionary: electromyography
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(ē-lek′trō-mī-og′rə-fē)
n

The detection, recording, and interpretation of electric voltage generated by the skeletal muscles.

Medical Test: Electromyography (EMG) And Nerve Conduction Velocity (ncv)
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General information

Where It's DoneWho Does ItHow Long It TakesDiscomfort/Pain
Hospital outpatient department.Doctor or technician.Less than 1 hour for both tests.Discomfort at site of needle insertion; possible anxiety over insertion of needle electrodes.

Results Ready WhenSpecial EquipmentRisks/ComplicationsAverage Cost
Within 24 hours.Needle and surface electrodes, nerve stimulator, amplifier with filters, oscilloscope, and device to store data, such as a magnetic tape recorder.Very rare possibility of short-lived bacterial infection.$$

Other names

Electrodiagnostic study (needle exam) or latency studies.

Purpose
  • To determine the severity and exact site of nerve entrapment (in such disorders as carpal tunnel syndrome or a herniated disk).
  • To confirm diagnosis and measure the severity of peripheral nervous system disorders, such as polyneuropathies.
  • To diagnose or evaluate disorders of the muscles and motor neurons, such as amyotrophic lateral sclerosis and myasthenia gravis.
How it works

As they contract, the muscles give off a weak electrical signal that can be detected, amplified, and tracked, giving information about how well they are working. Electrical signals traveling along nerves can be measured. By measures at two points, the velocity of conduction can be measured.

Preparation
  • Avoid taking aspirin and other nonsteroidal anti-inflammatory drugs for five to seven days before the test.
  • If you take Mestinon for myasthenia gravis, stop taking it 24 hours before the test under the discretion of your physician.
  • Wear loose-fitting clothes that will allow you to expose the necessary muscles and nerves during the test. You may have to disrobe and wear a hospital gown if your hip or shoulder muscles are being tested.
  • Do not use hand cream or skin lotion before the test (so that the electrodes adhere properly).
Test procedure

You sit or lie on the examination table and expose the muscles and nerves that need to be tested. One or both of the following studies are performed.

  • The appropriate area is cleaned with alcohol, and the needle electrode (a very thin, solid needle that is similar to a pin) is inserted into the muscle.
  • The electrical activity of the muscle during relaxation, slight contraction, and forceful contraction is picked up via the electrodes, amplified, recorded on the oscilloscope, and converted to auditory signals via a speaker.
  • Several muscles or areas of muscle may be tested one by one in this manner.
  • Recording and stimulating electrodes are placed on the skin overlying a nerve supplying a muscle or muscle group.
  • A mild and brief electrical stimulus is delivered to the stimulating electrodes.
  • The response of the muscle is picked up by the recording electrodes, amplified, and displayed. The speed with which the signal generated by the muscle travels through the nerves, called nerve conduction velocity, is measured. The amplitude (strength) of the signal is also measured.
  • The maneuver is repeated on different nerves.

After the test

You are free to return to previous activities, although you should try not to strenuously exert yourself for the rest of the day. If you feel any pain, it will be a mild muscle ache, no stronger than if you had bumped yourself.

Factors affecting results
  • The position of the electrodes.
  • Muscle-relaxing and anticholinergic medications.
  • Skin temperature.
Interpretation
  • Electromyography. Normally, there is no electrical activity in the muscle when it is relaxed, only when it contracts. If the muscle is diseased, it may have electrical activity in the relaxed state; when it contracts, its electrical activity may produce abnormal patterns. By examining these abnormalities, the doctor may determine the nature of the disease and identify the nerves and muscles affected.
  • Nerve conduction studies. Nerve conduction velocity reflects the speed with which electrical impulses travel along the nerve. Various diseases can cause the impulses to slow down, or to be slower on one side of the body than on the other. The magnitude of the response to stimulation also gives clues to diagnosis and the extent of the injury.
Advantages
  • It's only mildly invasive.
  • It can help quantitate subjective symptoms.
Disadvantages

It usually provides no definitive diagnosis although it adds clues to the physical examination.

The next step
  • Treatment.
  • There may be additional laboratory testing to look for the underlying cause of a neuropathy (e.g., diabetes or hypothyroidism).

PATIENT TIP

If you take an anticoagulant (blood-thinning) medication such as Coumadin, be sure to tell your neurologist. If this is the case, it may not be necessary to have the electromyography part of the exam.

Britannica Concise Encyclopedia: electromyography
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Process of graphically recording the electrical activity of muscle, which normally generates an electric current only when contracting or when its nerve is stimulated. Electrical impulses are shown as wavelike tracings on a cathode-ray oscilloscope and recorded as an electromyogram (EMG), usually along with audible signals. The EMG can show whether muscle weakness or wasting is due to nerve impairment (as in amyotrophic lateral sclerosis and poliomyelitis) or muscle impairment or disease (myopathy).

For more information on electromyography, visit Britannica.com.

Sports Science and Medicine: electromyography
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The measurement and recording of electrical activity produced by muscle. Electromyography is used as a diagnostic tool to assess nerve conduction and muscle response in injured tissue, and to identify and measure muscle activity during a movement.

Veterinary Dictionary: electromyography
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The recording and study of the intrinsic electrical properties of skeletal muscle; abbreviated EMG.
When it is at rest, normal muscle is electrically silent, but when the muscle is active, an electrical current is generated. In electromyography the electrical impulses are picked up by needle electrodes inserted into the muscle and amplified on an oscilloscope screen in the form of wavelike tracings.

Wikipedia: Electromyography
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Electromyography (EMG) is a technique for evaluating and recording the activation signal of muscles. EMG is performed using an instrument called an electromyograph, to produce a record called an electromyogram. An electromyograph detects the electrical potential generated by muscle cells when these cells are both mechanically active and at rest. The signals can be analyzed in order to detect medical abnormalities or analyze the biomechanics of human or animal movement.

Contents

Electrical characteristics

The electrical source is the muscle membrane potential of about -90mV[1]. Measured EMG potentials range between less than 50 μV and up to 20 to 30 mV, depending on the muscle under observation.

Typical repetition rate of muscle unit firing is about 7–20 Hz, depending on the size of the muscle (eye muscles versus seat (gluteal) muscles), previous axonal damage and other factors. Damage to motor units can be expected at ranges between 450 and 780 mV[citation needed].

History

The first documented experiments dealing with EMG started with Francesco Redi’s works in 1666. Redi discovered a highly specialized muscle of the electric ray fish (Electric Eel) generated electricity. By 1773, Walsh had been able to demonstrate that the Eel fish’s muscle tissue could generate a spark of electricity. In 1792, a publication entitled "De Viribus Electricitatis in Motu Musculari Commentarius" appeared, written by Luigi Galvani, in which the author demonstrated that electricity could initiate muscle contractions. Six decades later, in 1849, Dubios-Raymond discovered that it was also possible to record electrical activity during a voluntary muscle contraction. The first actual recording of this activity was made by Marey in 1890, who also introduced the term electromyography. In 1922, Gasser and Erlanger used an oscilloscope to show the electrical signals from muscles. Because of the stochastic nature of the myoelectric signal, only rough information could be obtained from its observation. The capability of detecting electromyographic signals improved steadily from the 1930s through the 1950s, and researchers began to use improved electrodes more widely for the study of muscles. Clinical use of surface EMG (sEMG) for the treatment of more specific disorders began in the 1960s. Hardyck and his researchers were the first (1966) practitioners to use sEMG. In the early 1980s, Cram and Steger introduced a clinical method for scanning a variety of muscles using an EMG sensing device.

It is not until the middle of the 1980s that integration techniques in electrodes had sufficiently advanced to allow batch production of the required small and lightweight instrumentation and amplifiers. At present, a number of suitable amplifiers are commercially available. In the early 1980s, cables that produce artifacts in the desired microvolt range became available. During the past 15 years, research has resulted in a better understanding of the properties of surface EMG recording. In recent years, surface electromyography is increasingly used for recording from superficial muscles in clinical protocols, where intramuscular electrodes are used for deep muscle only.

There are many applications for the use of EMG. EMG is used clinically for the diagnosis of neurological and neuromuscular problems. It is used diagnostically by gait laboratories and by clinicians trained in the use of biofeedback or ergonomic assessment. EMG is also used in many types of research laboratories, including those involved in biomechanics, motor control, neuromuscular physiology, movement disorders, postural control, and physical therapy.

Procedure

There are two kinds of EMG in widespread use: surface EMG and needle (intramuscular) EMG. To perform intramuscular EMG, a needle electrode is inserted through the skin into the muscle tissue. A trained professional (most often a physiatrist, neurologist, physical therapist, or chiropractor) observes the electrical activity while inserting the electrode. The insertional activity provides valuable information about the state of the muscle and its innervating nerve. Normal muscles at rest make certain, normal electrical sounds when the needle is inserted into them. Then the electrical activity when the muscle is at rest is studied. Abnormal spontaneous activity might indicate some nerve and/or muscle damage. Then the patient is asked to contract the muscle smoothly. The shape, size and frequency of the resulting motor unit potentials is judged. Then the electrode is retracted a few millimeters, and again the activity is analyzed until at least 10-20 units have been collected. Each electrode track gives only a very local picture of the activity of the whole muscle. Because skeletal muscles differ in the inner structure, the electrode has to be placed at various locations to obtain an accurate study.

Intramuscular EMG may be considered too invasive or unnecessary in some cases. Instead, a surface electrode may be used to monitor the general picture of muscle activation, as opposed to the activity of only a few fibres as observed using a needle. This technique is used in a number of settings; for example, in the physiotherapy clinic, muscle activation is monitored using surface EMG and patients have an auditory or visual stimulus to help them know when they are activating the muscle (biofeedback).

A motor unit is defined as one motor neuron and all of the muscle fibers it innervates. When a motor unit fires, the impulse (called an action potential) is carried down the motor neuron to the muscle. The area where the nerve contacts the muscle is called the neuromuscular junction, or the motor end plate. After the action potential is transmitted across the neuromuscular junction, an action potential is elicited in all of the innervated muscle fibers of that particular motor unit. The sum of all this electrical activity is known as a motor unit action potential (MUAP). This electrophysiologic activity from multiple motor units is the signal typically evaluated during an EMG. The composition of the motor unit, the number of muscle fibres per motor unit, the metabolic type of muscle fibres and many other factors affect the shape of the motor unit potentials in the myogram.

Nerve conduction testing is also often done at the same time as an EMG in order to diagnose neurological diseases.

Some patients can find the procedure somewhat painful, whereas others experience only a small amount of discomfort when the needle is inserted. The muscle or muscles being tested may be slightly sore for a day or two after the procedure.

Normal results

Muscle tissue at rest is normally electrically inactive. After the electrical activity caused by the irritation of needle insertion subsides, the electromyograph should detect no abnormal spontaneous activity (i.e., a muscle at rest should be electrically silent, with the exception of the area of the neuromuscular junction, which is, under normal circumstances, very spontaneously active). When the muscle is voluntarily contracted, action potentials begin to appear. As the strength of the muscle contraction is increased, more and more muscle fibers produce action potentials. When the muscle is fully contracted, there should appear a disorderly group of action potentials of varying rates and amplitudes (a complete recruitment and interference pattern).

Abnormal results

EMG is used to diagnose two general categories of disease: neuropathies and myopathies.

Neuropathic disease has the following defining EMG characteristics:

Myopathic disease has these defining EMG characteristics:

  • A decrease in duration of the action potential
  • A reduction in the area to amplitude ratio of the action potential
  • A decrease in the number of motor units in the muscle (in extremely severe cases only)

Because of the individuality of each patient and disease, some of these characteristics may not appear in every case.

Abnormal results may be caused by the following medical conditions (please note this is nowhere near an exhaustive list of conditions that can result in abnormal EMG studies):

EMG signal decomposition

EMG signals are essentially made up of superimposed motor unit action potentials (MUAPs) from several motor units. For a thorough analysis, the measured EMG signals can be decomposed into their constituent MUAPs. MUAPs from different motor units tend to have different characteristic shapes, while MUAPs recorded by the same electrode from the same motor unit are typically similar. Notably MUAP size and shape depend on where the electrode is located with respect to the fibers and so can appear to be different if the electrode moves position. EMG decomposition is non-trivial, although many methods have been proposed.

Applications of EMG

EMG signals are used in many clinical and biomedical applications. EMG is used as a diagnostics tool for identifying neuromuscular diseases, assessing low-back pain, kinesiology, and disorders of motor control. EMG signals are also used as a control signal for prosthetic devices such as prosthetic hands, arms, and lower limbs.

EMG can be used to sense isometric muscular activity where no movement is produced. This enables definition of a class of subtle motionless gestures to control interfaces without being noticed and without disrupting the surrounding environment. These signals can be used to control a prosthesis or as a control signal for an electronic device such as a mobile phone or PDA.

EMG signals have been targeted as control for flight systems. The Human Senses Group at the NASA Ames Research Center at Moffett Field, CA seeks to advance man-machine interfaces by directly connecting a person to a computer. In this project, an EMG signal is used to substitute for mechanical joysticks and keyboards. EMG has also been used in research towards a "wearable cockpit," which employs EMG-based gestures to manipulate switches and control sticks necessary for flight in conjunction with a goggle-based display.

Unvoiced speech recognition recognizes speech by observing the EMG activity of muscles associated with speech. It is targeted for use in noisy environments, and may be helpful for people without vocal cords and people with aphasia.

EMG has also been used as a control signal for computers and other devices. An interface device based on EMG could be used to control moving objects, such as mobile robots or an electric wheelchair. This may be helpful for individuals that cannot operate a joystick-controlled wheelchair. Surface EMG recordings may also be a suitable control signal for some interactive video games.

See also

Notes

  1. ^ Nigg B.M., & Herzog W., 1999. Biomechanics of the Musculo-Skeletal system. Wiley. Page:349.

References

  • M. B. I. Reaz, M. S. Hussain, F. Mohd-Yasin, “Techniques of EMG Signal Analysis: Detection, Processing, Classification and Applications”, Biological Procedures Online, vol. 8, issue 1, pp. 11–35, March 2006
  • Nikias CL, Raghuveer MR. Bispectrum estimation: A digital signal processing framework. IEEE Proceedings on Communications and Radar. 1987;75(7):869–891.
  • Basmajian, JV.; de Luca, CJ. Muscles Alive - The Functions Revealed by Electromyography. The Williams & Wilkins Company; Baltimore, 1985.
  • Graupe D, Cline WK. Functional separation of EMG signals via ARMA identification methods for prosthesis control purposes. IEEE Transactions on Systems, Man and Cybernetics, 1975;5(2):252-259.
  • Kleissen RFM, Buurke JH, Harlaar J, Zilvold G. Electromyography in the biomechanical analysis of human movement and its clinical application. Gait Posture. 1998;8(2):143–158. doi: 10.1016/S0966-6362(98)00025-3. [PubMed]
  • Cram, JR.;Kasman, GS.; Holtz, J. Introduction to Surface Electromyography. Aspen Publishers Inc.; Gaithersburg, Maryland, 1998.
  • Ferguson, S.; Dunlop, G. Grasp Recognition From Myoelectric Signals. Procedures Australasian Conference Robotics and Automation 2002; pp. 78–83.
  • Stanford V. Biosignals offer potential for direct interfaces and health monitoring. Pervasive Computing, IEEE. 2004;3(1):99–103.
  • Park, DG.; Kim, HC. Muscleman: Wireless input device for a fighting action game based on the EMG signal and acceleration of the human forearm. [2]
  • Andreasen, DS.; Gabbert DG,: EMG Switch Navigation of Power Wheelchairs, RESNA 2006. [3]
  • Wheeler KR, Jorgensen CC. Gestures as input: neuroelectric joysticks and keyboards. Pervasive Computing, IEEE. 2003;2(2):56–61.
  • Manabe, H.;Hiraiwa, A.; Sugimura, T. Unvoiced Speech Recognition using EMG-Mime Speech Recognition. Conference on Human Factors in Computing Systems 2003; pp. 794–795.
  • American Association of Neuromuscular and Electrodiagnostic Medicine
  • American Board of Electrodiagnostic Medicine
  • MedlinePlus entry on EMG describes EMG
  • EMG and Nerve Conduction education, training, and expert analysis of NCV reports
  • University of Oklahoma Health Sciences Center describes the electromyograph
  • Italian website of Electromyography
  • Facial EMG

 
 

 

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