electromyography (EMG)
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Indications
- neuromuscular disease*
- peripheral nerve disease
- useful in determining the site of injury in a peripheral nerve
- can determine if neuropathy if axonal or demyelinating[3]
- useful in detecting spinal nerve root lesions
- nerve root compression
- presence of weakness, asymmetry, proximal signs, rapid course or atypical findings in a patient with peripheral neuropathy[3]
- useful in determining the site of injury in a peripheral nerve
- primary muscle diseases
- peripheral nerve disease
- spinal cord disease*
- anterior horn cell disease
- can differentiate active (inflammatory) myopathy from chronic myopathy & acute denervation from chronic denervation
* EMG can distinguish neuropathy from other neuromuscular disorders[3]
* increased activity with lower motor neuron lesion; normal with upper motor neuron lesion
Contraindications
- patients with bleeding tendencies
- patients unusually sensitive to recurrent infection[4]
Principle
- the study of electrical potentials generated by the depolarization of muscle
- EMG techniques include measurement of latencies of F-responses, H-reflexes, blink reflexes & single-fiber EMG
- the usual macro EMG techniques measure the summated electrical activity of all fibers of a motor unit
- amplitude & area are increased in re-innervation & decreased in primary muscle disease
Clinical significance
- myotonic discharges consist of rhythmic discharges lasting for long periods after the external source of excitation has come to rest.
- this may be seen in association with:
- myotonia
- polymyositis (infrequent)
- glycogen storage disease, type II
Procedure
Recording technique (4 phases of examination):[4]
- insertional activity:
- a needle electrode is placed in the muscle & electrode activity associated with its insertion is evaluated
- normal: brief activity with insertion
- lower motor neuron lesion: increased activity
- upper motor neuron lesion: normal
- myopathy: normal
- myotonia: myotonic discharges
- polymyositis: increased activity
- spontaneous activity
- the muscle is evaluated at rest, with the needle stationary in a relaxed muscle
- normal: none
- lower motor neuron lesion:
- fibrillation potential
- positive sharp waves
- upper motor neuron lesion: none
- myopathy: none
- myotonia: none
- polymyositis
- fibrillation potential
- positive sharp waves
- motor unit potentials
- muscle potentials evoked by isolated discharges of motor neurons are recorded with mild voluntary contraction of the muscle
- normal: 0.5-1.0 mV, 5-10 ms
- lower motor neuron lesion: large unit, limited recruitment
- upper motor neuron lesion: normal
- myopathy: small unit, early recruitment
- myotonia: myotonic discharge
- polymyositis: small unit, early recruitment
- recruitment & interference pattern
- the change in electrical potential is assessed as the level of muscle contraction gradually increases & eventually reaches a maximum
- normal: full
- lower motor neuron lesion: reduced, fast firing pattern
- upper motor neuron lesion: reduced, slow firing pattern
- myopathy: full, but low amplitude
- myotonia: full, but low amplitude
- polymyositis: full, but low amplitude
- repetitive stimulation protocol if myasthenia gravis suspected[3]
Interpretation
- except for end-plate noise & brief insertional activity, there are normally no electrical discharges in a relaxed muscle.
- under normal circumstances, the smallest unit of volitional contraction is a motor unit.
- fibrillation potentials & positive sharp waves are derived from single, spontaneous discharges of individual motor units.
- interference pattern:
- with greater contraction, many motor units begin to fire rapidly
- simultaneous activation of different units no longer allows recognition of individual motor unit potentials
- this summated response is referred to as the interference pattern
- it is a measure of the density or number of spikes & the amplitude of the available motor unit potentials
More general terms
More specific terms
- anal sphincter/urethral sphincter electromyography
- needle electromyography (N-EMG)
- needle oculoelectromyography
- single-fiber electromyography (EMG)
- surface electromyography (S-EMG)
Additional terms
References
- ↑ nlmpubs.nlm.nih.gov/hstat/ahcpr/
- ↑ Harrison's Principles of Internal Medicine, 13th ed. Companion Handbook, Isselbacher et al (eds), McGraw-Hill Inc. NY, 1995, pg 694-95
- ↑ 3.0 3.1 3.2 3.3 3.4 Medical Knowledge Self Assessment Program (MKSAP) 11, 18. American College of Physicians, Philadelphia 1998, 2018.
- ↑ 4.0 4.1 4.2 Electrodiagnosis in Diseases of Nerve and Muscle, Principles and Practice, Kimura, J. FA Davis, Philadelphia, 1983