Electromyography


Electromyography is a technique for evaluating and recording the electrical activity produced by skeletal muscles. EMG is performed using an instrument called an electromyograph to produce a record called an electromyogram. An electromyograph detects the electric potential generated by muscle cells when these cells are electrically or neurologically activated. The signals can be analyzed to detect abnormalities, activation level, or recruitment order, or to analyze the biomechanics of human or animal movement. Needle EMG is an electrodiagnostic medicine technique commonly used by neurologists. Surface EMG is a non-medical procedure used to assess muscle activation by several professionals, including physiotherapists, kinesiologists and biomedical engineers. In computer science, EMG is also used as middleware in gesture recognition towards allowing the input of physical action to a computer as a form of human-computer interaction.

Clinical uses

EMG testing has a variety of clinical and biomedical applications. Needle EMG is used as a diagnostics tool for identifying neuromuscular diseases, or as a research tool for studying kinesiology, and disorders of motor control. EMG signals are sometimes used to guide botulinum toxin or phenol injections into muscles. Surface EMG is used for functional diagnosis and during instrumental motion analysis. EMG signals are also used as a control signal for prosthetic devices such as prosthetic hands, arms and lower limbs.
An acceleromyograph may be used for neuromuscular monitoring in general anesthesia with neuromuscular-blocking drugs, in order to avoid postoperative residual curarization.
Except in the case of some purely primary myopathic conditions EMG is usually performed with another electrodiagnostic medicine test that measures the conducting function of nerves. This is called nerve conduction study. Needle EMG and NCSs are typically indicated when there is pain in the limbs, weakness from spinal nerve compression, or concern about some other neurologic injury or disorder. Spinal nerve injury does not cause neck, mid back pain or low back pain, and for this reason, evidence has not shown EMG or NCS to be helpful in diagnosing causes of axial lumbar pain, thoracic pain, or cervical spine pain. Needle EMG may aid with the diagnosis of nerve compression or injury, nerve root injury, and with other problems of the muscles or nerves. Less common medical conditions include amyotrophic lateral sclerosis, myasthenia gravis, and muscular dystrophy.

Technique

Skin preparation and risks

The first step before insertion of the needle electrode is skin preparation. This typically involves simply cleaning the skin with an alcohol pad.
The actual placement of the needle electrode can be difficult and depends on a number of factors, such as specific muscle selection and the size of that muscle. Proper needle EMG placement is very important for accurate representation of the muscle of interest, although EMG is more effective on superficial muscles as it is unable to bypass the action potentials of superficial muscles and detect deeper muscles. Also, the more body fat an individual has, the weaker the EMG signal. When placing the EMG sensor, the ideal location is at the belly of the muscle: the longitudinal midline. The belly of the muscle can also be thought of as in-between the motor point of the muscle and the tendonus insertion point.
Cardiac pacemakers and implanted cardiac defibrillators are used increasingly in clinical practice, and no evidence exists indicating that performing routine electrodiagnostic studies on patients with these devices pose a safety hazard. However, there are theoretical concerns that electrical impulses of nerve conduction studies could be erroneously sensed by devices and result in unintended inhibition or triggering of output or reprogramming of the device. In general, the closer the stimulation site is to the pacemaker and pacing leads, the greater the chance for inducing a voltage of sufficient amplitude to inhibit the pacemaker. Despite such concerns, no immediate or delayed adverse effects have been reported with routine NCS.
No known contraindications exist for performing needle EMG or NCS on pregnant patients. Additionally, no complications from these procedures have been reported in the literature. Evoked potential testing, likewise, has not been reported to cause any problems when it is performed during pregnancy.
Patients with lymphedema or patients at risk for lymphedema are routinely cautioned to avoid percutaneous procedures in the affected extremity, namely venipuncture, to prevent development or worsening of lymphedema or cellulitis. Despite the potential risk, the evidence for such complications subsequent to venipuncture is limited. No published reports exist of cellulitis, infection, or other complications related to EMG performed in the setting of lymphedema or prior lymph node dissection. However, given the unknown risk of cellulitis in patients with lymphedema, reasonable caution should be exercised in performing needle examinations in lymphedematous regions to avoid complications. In patients with gross edema and taut skin, skin puncture by needle electrodes may result in chronic weeping of serous fluid. The potential bacterial media of such serous fluid and the violation of skin integrity may increase the risk of cellulitis. Before proceeding, the physician should weigh the potential risks of performing the study with the need to obtain the information gained.

Surface and intramuscular EMG recording electrodes

There are two kinds of EMG: surface EMG and intramuscular EMG. Surface EMG assesses muscle function by recording muscle activity from the surface above the muscle on the skin. Surface EMG can be recorded by a pair of electrodes or by a more complex array of multiple electrodes. More than one electrode is needed because EMG recordings display the potential difference between two separate electrodes. Limitations of this approach are the fact that surface electrode recordings are restricted to superficial muscles, are influenced by the depth of the subcutaneous tissue at the site of the recording which can be highly variable depending on the weight of a patient, and cannot reliably discriminate between the discharges of adjacent muscles. Specific electrode placements and functional tests have been developed to minimize this risk, thus providing reliable examinations.
Intramuscular EMG can be performed using a variety of different types of recording electrodes. The simplest approach is a monopolar needle electrode. This can be a fine wire inserted into a muscle with a surface electrode as a reference; or two fine wires inserted into muscle referenced to each other. Most commonly fine wire recordings are for research or kinesiology studies. Diagnostic monopolar EMG electrodes are typically insulated and stiff enough to penetrate skin, with only the tip exposed using a surface electrode for reference. Needles for injecting therapeutic botulinum toxin or phenol are typically monopolar electrodes that use a surface reference, in this case, however, the metal shaft of a hypodermic needle, insulated so that only the tip is exposed, is used both to record signals and to inject. Slightly more complex in design is the concentric needle electrode. These needles have a fine wire, embedded in a layer of insulation that fills the barrel of a hypodermic needle, that has an exposed shaft, and the shaft serves as the reference electrode. The exposed tip of the fine wire serves as the active electrode. As a result of this configuration, signals tend to be smaller when recorded from a concentric electrode than when recorded from a monopolar electrode and they are more resistant to electrical artifacts from tissue and measurements tend to be somewhat more reliable. However, because the shaft is exposed throughout its length, superficial muscle activity can contaminate the recording of deeper muscles. Single fiber EMG needle electrodes are designed to have very tiny recording areas, and allow for the discharges of individual muscle fibers to be discriminated.
To perform intramuscular EMG, typically either a monopolar or concentric needle electrode is inserted through the skin into the muscle tissue. The needle is then moved to multiple spots within a relaxed muscle to evaluate both insertional activity and resting activity in the muscle. Normal muscles exhibit a brief burst of muscle fiber activation when stimulated by needle movement, but this rarely lasts more than 100ms. The two most common pathologic types of resting activity in muscle are fasciculation and fibrillation potentials. A fasciculation potential is an involuntary activation of a motor unit within the muscle, sometimes visible with the naked eye as a muscle twitch or by surface electrodes. Fibrillations, however, are detected only by needle EMG, and represent the isolated activation of individual muscle fibers, usually as the result of nerve or muscle disease. Often, fibrillations are triggered by needle movement and persist for several seconds or more after the movement ceases.
After assessing resting and insertional activity, the electromyographer assess the activity of muscle during voluntary contraction. The shape, size, and frequency of the resulting electrical signals are judged. Then the electrode is retracted a few millimetres, and again the activity is analyzed. This is repeated, sometimes until data on 10–20 motor units have been collected in order to draw conclusions about motor unit function. 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. For the interpretation of EMG study is important to evaluate parameters of tested muscle motor units. This process may well be partially automated using appropriate software.
Single fiber electromyography assesses the delay between the contractions of individual muscle fibers within a motor unit and is a sensitive test for dysfunction of the neuromuscular junction caused by drugs, poisons, or diseases such as myasthenia gravis. The technique is complicated and typically performed only by individuals with special advanced training.
Surface EMG 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. A review of the literature on surface EMG published in 2008, concluded that surface EMG may be useful to detect the presence of neuromuscular disease, but there are insufficient data to support its utility for distinguishing between neuropathic and myopathic conditions or for the diagnosis of specific neuromuscular diseases. EMGs may be useful for additional study of fatigue associated with post-poliomyelitis syndrome and electromechanical function in myotonic dystrophy. Recently, with the rise of technology in sports, sEMG has become an area of focus for coaches to reduce the incidence of soft tissue injury and improve player performance.
Certain US states limit the performance of needle EMG by nonphysicians. New Jersey declared that it cannot be delegated to a physician's assistant. Michigan has passed legislation saying needle EMG is the practice of medicine. Special training in diagnosing medical diseases with EMG is required only in residency and fellowship programs in neurology, clinical neurophysiology, neuromuscular medicine, and physical medicine and rehabilitation. There are certain subspecialists in otolaryngology who have had selective training in performing EMG of the laryngeal muscles, and subspecialists in urology, obstetrics and gynecology who have had selective training in performing EMG of muscles controlling bowel and bladder function.