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MUHAMMED AJMAL P,NDT,CINM
IONM TECHNOLOGIST
NEUROSURGERY.
 Needle EMG involves extracellular recording of muscle
action potentials using either monopolar or concentric needle
electrodes.
 This is a qualitative assessment
 It can distinguish myopathic from neurogenic muscle
wasting and weakness
 It can detect abnormalities such as chronic
denervation or fasciculations in clinically normal
muscle
 It can, by determining the distribution of neurogenic
abnormalities, differentiate focal nerve, plexus, or
radicular pathology
1. Insertional activity
2. Spontaneous activity
3. Recruitment Pattern
4. Interference Pattern
 Burst of high frequency positive or negative spikes
occurring
 Due to mechanical irritation/injury by the penetrating
needle
 It lasts for about few hundred milliseconds
 At least four to six brief needle movements are made in
four quadrants of each muscle to assess insertional
activity
 Its lasts longer than 300 ms
indicates increased
insertional activity
 Increased insertional
activity may be seen in both
neuropathic and myopathic
conditions
 The insertion activity can be graded as follows:
 No activity
 Decreased activity
 Normal activity
 Increased activity
 Highly increased activity
 All spontaneous activity is abnormal
 exception of potentials that occur in the
muscle endplate zone (i.e., the NMJ).
a) endplate noise
b) endplate spikes
 Physiologically, they represent MEPPs.
 It occurs with the release of acetylcholine due to
irritation of intramuscular nerve terminals by the needle
tip at the end plate region
 low-amplitude (10-50μv ), monophasic negative
potentials
 duration of 1-2ms
 Firing Rate 20-40Hz
 “seashell” sound
 It occurs due to stimulation of the single muscle fiber
by the tip of the needle at the end plate
 They are biphasic, with an initial negative deflection
 Sound like cracking, buzzing, or sputtering
 It is irregular high amplitude(100-200μv)
 Duration of 3-4ms
 Firing Rate 5-50Hz
 ABNORMAL MUSCLE FIBER POTENTIALS
1. Fibrillation Potentials
2. Positive Sharp Waves
3. Complex Repetitive Discharges (CRD)
4. Myotonic Discharges
 ABNORMAL MOTOR UNIT POTENTIALS
1. Fasciculation Potentials
2. Doublets, Triplets, and Multiplets
3. Myokymic Discharges
4. Cramp Potentials
5. Neuromyotonic Discharges
6. Rest Tremor
1. Fibrillation Potentials
 This arise from single muscle fiber.
 Active denervation.
 They typically are associated with neuropathic disorders
(i.e., neuropathies, radiculopathies, motor neuron disease)
 they also may be seen in some muscle disorders (especially
the inflammatory myopathies and dystrophies)
 rarely in severe diseases of the NMJ (especially botulism).
Morphology:
 A brief spike with an initial
positive deflection
 1 to 5 ms in duration
 low in amplitude (typically
10–100 μV).
 The firing pattern is very
regular
 0.5 to 10 Hz, occasionally
up to 30 Hz
 sound like “rain on the roof
2. Positive Sharp Waves
 spontaneous depolarization of a muscle
fiber
 active denervation.
 A brief initial positivity
followed by a long
negative phase
 sound like a dull pop
 (usually 10–100 μV,
occasionally up to 3
mV).
 Regular Pattern
 0.5-10Hz (30Hz)
 early in denervation.
 0 None present
 +1 Persistent single trains of potentials (>2–3 seconds)
in at least two areas
 +2 Moderate number of potentials in three or moreV
areas
 +3 Many potentials in all areas
 +4 Full interference pattern of potentials
3.Complex Repetitive Discharges
 depolarization of a single muscle fiber
followed by ephaptic spread to adjacent
denervated fibers
 direct spread from muscle membrane to
muscle membrane).
Pathophysiology of a complex repetitive:
discharge (CRD). A spontaneous depolarization occurs from
ephaptic transmission from one denervated muscle fiber to an
adjacent one. If the original pacemaker is reactivated, a circus
movement is formed without an intervening synapse. In neuropathic
conditions, the pathologic correlate is grouped atrophy, wherein
denervated fibers lie next to other denervated fiberS.
 high-frequency
(typically 5–100 Hz)
 repetitive discharges
 abrupt onset and
termination.
 machine-like sound
 Perfectly regular
 They occur in both
chronic neuropathic and
myopathic disorders
3.Myotonic Discharges
 spontaneous discharge of a muscle fiber
 similar to fibrillation potentials and positive sharp
waves
 waxing and waning of both amplitude and frequency
 20–150 Hz
 “revving engine” sound on EMG,
 myotonic dystrophy, myotonia congenita, and paramyotonia
congenita.
 also occur in other myopathies (acid maltasecdeficiency,
polymyositis, myotubular myopathy), hyperkalemic periodic
paralysis,
 rarely, in denervation of any cause.
 A single brief run of myotonic discharges may occur in any
denervating disorder
 1. Fasciculation Potentials
 A fasciculation potential is a single, spontaneous,
involuntary discharge of an individual motor unit
 The source generator of fasciculation potentials is the
motor neuron or its axon, prior to its terminal branches
 Stimulus can originate at any level from anterior horn
cell to axon terminal
 corn popping
 Low (0.1–10 Hz)
 generally fire very
slowly and irregularly,
2. Doublets, Triplets,
and Multiplets
 Spontaneous MUAPs
that fire in groups of
two are known as
doublets
 Same fasciculation
potentials
 Horse trotting
 Variable (1–50 Hz)
 Fasciculations are associated with numerous
disease processes affecting the lower motor
neuron
◦ Motor neuron disease, such as amyotrophic lateral
sclerosis,
◦ radiculopathies, polyneuropathies, and entrapment
neuropathies.
3. Myokymic Discharges
 The are rhythmic, grouped, spontaneous repetitive
discharges of the same motor unit (i.e., grouped
fasciculations).
 1–5 Hz (interburst)
 5–60 Hz(intraburst)
 Marching soldiers
 The origin -spontaneous depolarization of or ephaptic
transmission along demyelinated segments of nerve.
 Disorders Commonly Associated with Myokymic
Discharges:
 Radiation injury (usually brachial plexopathy)
 Guillain–Barré syndrome (facial)
 Multiple sclerosis (facial)
 Pontine tumors (facial)
 Hypocalcemia
Occasionally seen in
 Guillain–Barré syndrome (limbs)
 Chronic inflammatory demyelinating polyneuropathy
 Nerve entrapments
 Radiculopathy
 involuntary contractions
of muscle
 Cramps are painful,
 high-frequency
discharges
 usually 40–75 Hz
 Cramps may be benign
(e.g., nocturnal calf
cramps, post-exercise
cramps)
 maybe associated with a wide range of
neuropathic,endocrinologic, and metabolic
conditions.
 decrementing, repetitive discharges of a single motor unit
 high-frequency (150–250 Hz)
 “pinging” sound
 Autoimmune channelopathy
 Clinically
 Stiffness
• Hyper hidrosis
• Delayed muscle relaxation after contraction.
 Tremor is recognized as a synchronous bursting pattern
of MUAPs separated by relative silence
 Marching soldiers
 1–5 Hz (interburst)
 Bursting –synchronous bursting of many different
motor unit potentials
 The motor unit refers to
the motor neuron cell
body, motor axon, and all
innervated muscle fibres.
 The motor unit potential
(MUP ) is the sum of
activity from muscle
fibres of one motor unit
 Components:
•Amplitude
•Duration
 •Rise time
 •Phases
 It is measured from peak to
peak of the MUAP.
 amplitude100 μV- 2 mV
 MUAP amplitude reflects
only those few fibers nearest
to the needle (only 2–12
fibers).
 Measured from the
initial deflection from
the base line to the
final return to the base
line
 Duration-5 to 15 ms
 It depends primarily on
the number of muscle
fibers within the motor
unit
 Increased age -increased duration
 Decreased temperature -increased duration
 Proximal and bulbofacial muscles- shorter duration
 Polyphasia
◦ Is a measure of synchrony
◦ muscle fibers within a motor unit fire more or less
at the same time
◦ may be abnormal in both myopathic and
neuropathic disorders
◦ calculated by counting the number of baseline
crossings of the MUAP and adding one
◦ Normally, MUAPs 2-4 Phases.
◦ >4 it is called polyphasic
 also called turns
 changes in the direction
of the potential that do
not cross the baseline
 seen in early
reinnervation
 late spike distinct
from main potential
 time locked to the
main potential
 Latency can rage
from 8-32ms
 It is the time lag from
the initial positive peak
to the subsequent
negative peak of the
MUP.
 It reflects the distance
between the recording
electrode and the
muscle fibres of the
motor unit
 Rise time <500μs
 It depends on the number of muscle fibres
with in 2mm radius of the recording electrode
 Movement of the electrode has significant
effect on area
 Helps to differentiate neuropathy from
myopathy
Activation
 Refers to the ability to increase firing rate.
 This is a central process.
 Poor activation may be seen in diseases of the central
nervous system (CNS) or as a manifestation of pain,
poor cooperation, or functional disorders.
Recruitment
 the ability to add motor unit action potentials as the
firing rate increases.
 Recruitment is reduced primarily in neuropathic
diseases
 although rarely it may also be reduced in severe end-
stage myopathy
 Normal ratio of firing frequency to the number of
motor units is 5:1
 Maximum firing rate of a motor unit is about 30-50HZ
Normal recruitment:
 the pattern of recruitment is normal for that
muscle, with an adequate number of MUAPs
being recruited for the frequency of firing
present.
 If maximal effort can be obtained, a full
interference pattern is seen.
 It should obey the 5:1 Ratio
Reduced recruitment
 Reduced recruitment is characteristic of neurogenic
disorders in which axonal loss or conduction block is
the pathophysiologic mechanism
 severe or end stage myopathic disorders, reduced
recruitment may also occur due to the loss of all muscle
fibers within a motor unit.
Rapid /Early recruitment
 increased number of motor units relative to the force of
contraction
 early recruitment pattern is typically seen in muscle
disorders and in some disorders of the NMJ.
 During the maximum contraction of muscle several motor units get
activated simultaneously resulting in the over lap of MUPs creating an
interference pattern
 Equipment
 •Electrodes
 •Amplifier
 •Filter
 •Display method
 Electrodes
 For clinical Electromyography following
Needle electrodes are used
 Amplifiers
 Bioelectrical potentials recorded will be in the range of
1μV to 1mV these signals need to be amplified by
1million to thousand times for deflection of 1cm in
1v/cm recording
 Differential amplifiers increases the amplitude of the
desired response while rejecting unwanted noise
 Amplifiers ability to reject common signals is known as
its common mode rejection ratio (CMRR).
 The higher the CMRR, the better the rejection
Gain
 Amplifier gain describes the extent to which the
input signal is increased in voltage.
 Display sensitivity
 Describes the visible waveform and is expressed
as volts per division or volts per centimeter
 Usually kept at 50-200μV/cm
Filters
 They are used to selectively attenuate the noise
preserving the signal Band pass filters extending
from 10HZ to 10KHZ is
 commonly used
Preparing the patient
 Prior to the test Patient should be briefly
explained about the procedure and insertion
of needle would cause some discomfort
 Wipe the skin over the each puncture site
with spirit beforenneedle is inserted
 Though most patients tolerate the pain some
may require oral analgesic
Selecting the muscle
 It is done on the basis of clinical indication
 Ideally muscle selected should be superficial,
easily palpated, Located away from major
blood vessels and nerve trunks
Electromyography (EMG) Basics

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Electromyography (EMG) Basics

  • 1. MUHAMMED AJMAL P,NDT,CINM IONM TECHNOLOGIST NEUROSURGERY.
  • 2.  Needle EMG involves extracellular recording of muscle action potentials using either monopolar or concentric needle electrodes.  This is a qualitative assessment
  • 3.  It can distinguish myopathic from neurogenic muscle wasting and weakness  It can detect abnormalities such as chronic denervation or fasciculations in clinically normal muscle  It can, by determining the distribution of neurogenic abnormalities, differentiate focal nerve, plexus, or radicular pathology
  • 4. 1. Insertional activity 2. Spontaneous activity 3. Recruitment Pattern 4. Interference Pattern
  • 5.  Burst of high frequency positive or negative spikes occurring  Due to mechanical irritation/injury by the penetrating needle  It lasts for about few hundred milliseconds  At least four to six brief needle movements are made in four quadrants of each muscle to assess insertional activity
  • 6.  Its lasts longer than 300 ms indicates increased insertional activity  Increased insertional activity may be seen in both neuropathic and myopathic conditions
  • 7.
  • 8.  The insertion activity can be graded as follows:  No activity  Decreased activity  Normal activity  Increased activity  Highly increased activity
  • 9.  All spontaneous activity is abnormal  exception of potentials that occur in the muscle endplate zone (i.e., the NMJ). a) endplate noise b) endplate spikes
  • 10.  Physiologically, they represent MEPPs.  It occurs with the release of acetylcholine due to irritation of intramuscular nerve terminals by the needle tip at the end plate region  low-amplitude (10-50μv ), monophasic negative potentials  duration of 1-2ms  Firing Rate 20-40Hz  “seashell” sound
  • 11.
  • 12.  It occurs due to stimulation of the single muscle fiber by the tip of the needle at the end plate  They are biphasic, with an initial negative deflection  Sound like cracking, buzzing, or sputtering  It is irregular high amplitude(100-200μv)  Duration of 3-4ms  Firing Rate 5-50Hz
  • 13.
  • 14.
  • 15.  ABNORMAL MUSCLE FIBER POTENTIALS 1. Fibrillation Potentials 2. Positive Sharp Waves 3. Complex Repetitive Discharges (CRD) 4. Myotonic Discharges  ABNORMAL MOTOR UNIT POTENTIALS 1. Fasciculation Potentials 2. Doublets, Triplets, and Multiplets 3. Myokymic Discharges 4. Cramp Potentials 5. Neuromyotonic Discharges 6. Rest Tremor
  • 16. 1. Fibrillation Potentials  This arise from single muscle fiber.  Active denervation.  They typically are associated with neuropathic disorders (i.e., neuropathies, radiculopathies, motor neuron disease)  they also may be seen in some muscle disorders (especially the inflammatory myopathies and dystrophies)  rarely in severe diseases of the NMJ (especially botulism).
  • 17. Morphology:  A brief spike with an initial positive deflection  1 to 5 ms in duration  low in amplitude (typically 10–100 μV).  The firing pattern is very regular  0.5 to 10 Hz, occasionally up to 30 Hz  sound like “rain on the roof
  • 18.
  • 19. 2. Positive Sharp Waves  spontaneous depolarization of a muscle fiber  active denervation.
  • 20.  A brief initial positivity followed by a long negative phase  sound like a dull pop  (usually 10–100 μV, occasionally up to 3 mV).  Regular Pattern  0.5-10Hz (30Hz)  early in denervation.
  • 21.  0 None present  +1 Persistent single trains of potentials (>2–3 seconds) in at least two areas  +2 Moderate number of potentials in three or moreV areas  +3 Many potentials in all areas  +4 Full interference pattern of potentials
  • 22. 3.Complex Repetitive Discharges  depolarization of a single muscle fiber followed by ephaptic spread to adjacent denervated fibers  direct spread from muscle membrane to muscle membrane).
  • 23. Pathophysiology of a complex repetitive: discharge (CRD). A spontaneous depolarization occurs from ephaptic transmission from one denervated muscle fiber to an adjacent one. If the original pacemaker is reactivated, a circus movement is formed without an intervening synapse. In neuropathic conditions, the pathologic correlate is grouped atrophy, wherein denervated fibers lie next to other denervated fiberS.
  • 24.  high-frequency (typically 5–100 Hz)  repetitive discharges  abrupt onset and termination.  machine-like sound  Perfectly regular  They occur in both chronic neuropathic and myopathic disorders
  • 25.
  • 26. 3.Myotonic Discharges  spontaneous discharge of a muscle fiber  similar to fibrillation potentials and positive sharp waves  waxing and waning of both amplitude and frequency  20–150 Hz  “revving engine” sound on EMG,
  • 27.  myotonic dystrophy, myotonia congenita, and paramyotonia congenita.  also occur in other myopathies (acid maltasecdeficiency, polymyositis, myotubular myopathy), hyperkalemic periodic paralysis,  rarely, in denervation of any cause.  A single brief run of myotonic discharges may occur in any denervating disorder
  • 28.  1. Fasciculation Potentials  A fasciculation potential is a single, spontaneous, involuntary discharge of an individual motor unit  The source generator of fasciculation potentials is the motor neuron or its axon, prior to its terminal branches  Stimulus can originate at any level from anterior horn cell to axon terminal
  • 29.  corn popping  Low (0.1–10 Hz)  generally fire very slowly and irregularly,
  • 30. 2. Doublets, Triplets, and Multiplets  Spontaneous MUAPs that fire in groups of two are known as doublets  Same fasciculation potentials  Horse trotting  Variable (1–50 Hz)
  • 31.  Fasciculations are associated with numerous disease processes affecting the lower motor neuron ◦ Motor neuron disease, such as amyotrophic lateral sclerosis, ◦ radiculopathies, polyneuropathies, and entrapment neuropathies.
  • 32. 3. Myokymic Discharges  The are rhythmic, grouped, spontaneous repetitive discharges of the same motor unit (i.e., grouped fasciculations).  1–5 Hz (interburst)  5–60 Hz(intraburst)  Marching soldiers  The origin -spontaneous depolarization of or ephaptic transmission along demyelinated segments of nerve.
  • 33.
  • 34.  Disorders Commonly Associated with Myokymic Discharges:  Radiation injury (usually brachial plexopathy)  Guillain–Barré syndrome (facial)  Multiple sclerosis (facial)  Pontine tumors (facial)  Hypocalcemia Occasionally seen in  Guillain–Barré syndrome (limbs)  Chronic inflammatory demyelinating polyneuropathy  Nerve entrapments  Radiculopathy
  • 35.  involuntary contractions of muscle  Cramps are painful,  high-frequency discharges  usually 40–75 Hz  Cramps may be benign (e.g., nocturnal calf cramps, post-exercise cramps)
  • 36.  maybe associated with a wide range of neuropathic,endocrinologic, and metabolic conditions.
  • 37.
  • 38.  decrementing, repetitive discharges of a single motor unit  high-frequency (150–250 Hz)  “pinging” sound  Autoimmune channelopathy  Clinically  Stiffness • Hyper hidrosis • Delayed muscle relaxation after contraction.
  • 39.
  • 40.  Tremor is recognized as a synchronous bursting pattern of MUAPs separated by relative silence  Marching soldiers  1–5 Hz (interburst)  Bursting –synchronous bursting of many different motor unit potentials
  • 41.
  • 42.
  • 43.  The motor unit refers to the motor neuron cell body, motor axon, and all innervated muscle fibres.  The motor unit potential (MUP ) is the sum of activity from muscle fibres of one motor unit  Components: •Amplitude •Duration  •Rise time  •Phases
  • 44.
  • 45.
  • 46.  It is measured from peak to peak of the MUAP.  amplitude100 μV- 2 mV  MUAP amplitude reflects only those few fibers nearest to the needle (only 2–12 fibers).
  • 47.  Measured from the initial deflection from the base line to the final return to the base line  Duration-5 to 15 ms  It depends primarily on the number of muscle fibers within the motor unit
  • 48.  Increased age -increased duration  Decreased temperature -increased duration  Proximal and bulbofacial muscles- shorter duration
  • 49.  Polyphasia ◦ Is a measure of synchrony ◦ muscle fibers within a motor unit fire more or less at the same time ◦ may be abnormal in both myopathic and neuropathic disorders ◦ calculated by counting the number of baseline crossings of the MUAP and adding one ◦ Normally, MUAPs 2-4 Phases. ◦ >4 it is called polyphasic
  • 50.
  • 51.  also called turns  changes in the direction of the potential that do not cross the baseline
  • 52.  seen in early reinnervation  late spike distinct from main potential  time locked to the main potential  Latency can rage from 8-32ms
  • 53.  It is the time lag from the initial positive peak to the subsequent negative peak of the MUP.  It reflects the distance between the recording electrode and the muscle fibres of the motor unit  Rise time <500μs
  • 54.  It depends on the number of muscle fibres with in 2mm radius of the recording electrode  Movement of the electrode has significant effect on area  Helps to differentiate neuropathy from myopathy
  • 55. Activation  Refers to the ability to increase firing rate.  This is a central process.  Poor activation may be seen in diseases of the central nervous system (CNS) or as a manifestation of pain, poor cooperation, or functional disorders.
  • 56. Recruitment  the ability to add motor unit action potentials as the firing rate increases.  Recruitment is reduced primarily in neuropathic diseases  although rarely it may also be reduced in severe end- stage myopathy  Normal ratio of firing frequency to the number of motor units is 5:1  Maximum firing rate of a motor unit is about 30-50HZ
  • 57. Normal recruitment:  the pattern of recruitment is normal for that muscle, with an adequate number of MUAPs being recruited for the frequency of firing present.  If maximal effort can be obtained, a full interference pattern is seen.  It should obey the 5:1 Ratio
  • 58.
  • 59. Reduced recruitment  Reduced recruitment is characteristic of neurogenic disorders in which axonal loss or conduction block is the pathophysiologic mechanism  severe or end stage myopathic disorders, reduced recruitment may also occur due to the loss of all muscle fibers within a motor unit.
  • 60. Rapid /Early recruitment  increased number of motor units relative to the force of contraction  early recruitment pattern is typically seen in muscle disorders and in some disorders of the NMJ.
  • 61.  During the maximum contraction of muscle several motor units get activated simultaneously resulting in the over lap of MUPs creating an interference pattern
  • 62.
  • 63.  Equipment  •Electrodes  •Amplifier  •Filter  •Display method
  • 64.  Electrodes  For clinical Electromyography following Needle electrodes are used
  • 65.  Amplifiers  Bioelectrical potentials recorded will be in the range of 1μV to 1mV these signals need to be amplified by 1million to thousand times for deflection of 1cm in 1v/cm recording  Differential amplifiers increases the amplitude of the desired response while rejecting unwanted noise  Amplifiers ability to reject common signals is known as its common mode rejection ratio (CMRR).  The higher the CMRR, the better the rejection
  • 66. Gain  Amplifier gain describes the extent to which the input signal is increased in voltage.  Display sensitivity  Describes the visible waveform and is expressed as volts per division or volts per centimeter  Usually kept at 50-200μV/cm Filters  They are used to selectively attenuate the noise preserving the signal Band pass filters extending from 10HZ to 10KHZ is  commonly used
  • 67. Preparing the patient  Prior to the test Patient should be briefly explained about the procedure and insertion of needle would cause some discomfort  Wipe the skin over the each puncture site with spirit beforenneedle is inserted  Though most patients tolerate the pain some may require oral analgesic
  • 68. Selecting the muscle  It is done on the basis of clinical indication  Ideally muscle selected should be superficial, easily palpated, Located away from major blood vessels and nerve trunks