Definition and Overview
Nerve conduction study (NCS) is an electrophysiological test that objectively measures the electrical conduction function of peripheral nerves. When a surface electrode is attached to a nerve and electrical stimulation is applied, the stimulation propagates along the nerve and a response is recorded in the muscle (motor nerve) or sensory receptor (sensory nerve) at the end.
The functional status of the nerve is evaluated by analyzing the latency, amplitude, conduction velocity, and waveform of this response.
Inspection type
motor nerve conduction test
The motor nerve is stimulated and the compound muscle action potential (CMAP) is recorded from the muscle controlled by the nerve.
The measurement indicators are as follows. - Distal latency: conduction time from the distal stimulation site to the muscle. - CMAP amplitude: reflects the number of activated motor axons - Motor conduction velocity: Calculated by dividing the distance between two stimulation points by the momentary difference. - F wave: evaluates conduction of the proximal part of the motor nerve (up to the anterior horn cells of the spinal cord)
Sensory nerve conduction test
Stimulate sensory nerves and record sensory nerve action potential (SNAP).
- SNAP amplitude: reflects the number of activated sensory axons
- Sensory conduction velocity: The speed of conduction of sensory nerves.
- Antidromic and orthodromic tests
special inspection
- H-reflex: Assessing the afferent and efferent reflex arcs of the tibia nerve. Useful for S1 radiculopathy.
- F wave: evaluates motor nerve proximal conduction. Important in the early diagnosis of Guillain-Barre syndrome.
- Repetitive nerve stimulation test (RNS): Diagnosis of neuromuscular junction disease (myasthenia gravis)
Interpretation of results
Demyelination pattern
This is a finding that appears when myelin sheath damage is the main lesion.
- Significant decrease in conduction velocity (less than 70% of normal)
- prolonged distal latency
- Temporal dispersion: increased waveform width
- Conduction block: CMAP amplitude decreases by more than 50% compared to distal during proximal stimulation.
- Representative diseases: Guillain-Barre syndrome (AIDP), chronic inflammatory demyelinating polyneuropathy (CIDP), multifocal motor neuropathy
Axonal loss pattern
This is a finding that appears when the main lesion is damage to the axon itself.
- Decreased CMAP/SNAP amplitude (reflecting decreased axon number)
- Conduction velocity is relatively preserved (more than 70% of normal)
- Representative diseases: Diabetic polyneuropathy, alcoholic neuropathy, toxic neuropathy, axonal Guillain-Barre syndrome (AMAN)
Focal entrapment pattern
This is when a nerve is compressed in a specific anatomical area.
- Local reduction in conduction velocity through the entrapment site
- prolonged distal latency (when entrapment is distal)
- Representative diseases: Carpal tunnel syndrome (median nerve), cubital tunnel syndrome (ulnar nerve)
clinical application
carpal tunnel syndrome
Prolonged distal sensory latency and prolonged distal motor latency of the median nerve are key diagnostic findings. NCS has a sensitivity of about 85-90% and a specificity of about 95% for diagnosing carpal tunnel syndrome.
polyneuropathy
Distal predominant sensory and motor nerve conduction abnormalities are the electrophysiological characteristics of polyneuropathy. Distinguishing between axonal and demyelinating types is important in determining the cause.
Guillain-Barre Syndrome
NCS is essential for subtyping Guillain-Barre syndrome. Distinction between demyelinating type (AIDP) and axonal type (AMAN, AMSAN) is important in predicting prognosis and treatment planning. In the early stages of the disease, F-wave abnormalities may be the only finding, so repeat testing may be necessary.
radiculopathy
A pattern in which denervation is observed on electromyography while the sensory nerve conduction test is normal suggests radiculopathy. Because the dorsal root ganglion is located outside the intervertebral foramen, SNAP is preserved in lesions at the nerve root level.
Limitations of the test
- Small fibers (C fibers, Aδ fibers) cannot be evaluated. If small fiber neuropathy is suspected, additional tests such as skin biopsy and QSART are required.
- Normal values vary depending on the skin temperature of the test area (required to be maintained above 32°C), age, height, etc.
- Since Wallerian degeneration is not complete within 2 to 3 weeks after symptom onset, axonal damage may be underestimated.
