EMG Review Final Vandersluis

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    Test question

    Typical EMG findings in radiculopathy include

    a) Low cmap and sensory responses; delayed / absent F wave,

    and normal needle exam

    b) Low cmap with normal sensory responses, delayed / absent F

    wave, and denervation in at least 2 related musclesc) Low cmap with normal sensory responses, enlarged F wave,

    and denervation in at least 2 related muscles

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    Components of an EMG

    Left Median Motor

    O

    P

    T

    R

    Wrist

    O

    P

    T

    R

    Elbow

    Left Median Sen Sensory

    O

    P

    T R

    2nd Digit

    O

    P

    TR

    3rd Digit

    OP

    T 4th Digit

    O

    P

    T R

    1st Digit

    EMG - Left CervPara Mid

    Nerve conduction studiesMotor nervesSensory nervesRepetitive Stimulation

    ElectromyographyQualitativeQuantitative

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    Nerve Conduction Studies

    Peripheral nerves are stimulated with a controlled

    electrical stimulus

    Responses are recorded Compound motor action potential (CMAP)

    Sensory nerve action potential (SNAP)

    F wave

    H reflex

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    Left Median Motor

    O

    P

    T

    R

    Wrist

    O

    P

    T

    R

    Elbow

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    Motor NCS Parameters Distal Latency

    determined by conduction velocity of the nerve, neuromuscular

    junction & muscle

    Amplitude

    determined by number of muscle fibersactivated

    Proximal conduction velocity

    determined by conduction velocity of the fastest fibers

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    Normal Median Motor Study

    DL CV Amp

    (msec) (m/s) (mV)

    Wrist-APB 3.2 15.0

    Elbow-Wrist 55 14.8

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    Sensory NCS Parameters

    Onset and peak latencies

    Conduction velocity

    determined by velocity of a very few fast fibers

    Amplitude determined by the number of large sensory fibers activated

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    Normal Median Sensory Study

    1 msec/div

    Latency CV Amp

    (msec) (m/s) (uV)

    Wrist-D2 2.2 58 44.1

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    CASE 1

    29 y.o. male

    Acute right foot drop 4 weeks earlier

    No trauma, no hx DM

    EXAM: MRC 2/5 rt dorsiflex toes

    4/5 rt ankle DF and eversion

    Decr pp dorsum foot

    Reflexes sym.

    No tinel

    s at fib head

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    Where is lesion

    Character (axonal, demyelinating)

    prognosis

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    .

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    CASE 2

    67 y.o. male

    buttock pain to lat thigh, exac with ambulation

    Few wks later rt foot drop

    Exam: 4/5 rt foot df, eversion, pf 5-/5

    Trace ankle reflexes

    Decr sens on dorsum foot

    SLR neg

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    F-wave study

    small late response from a short duration supramaximal stimulation.

    It initiates an ant idromicmotorresponse to the spinal cord followedby an or thodromicmotorresponse to the recording electrode.

    5% CMAP height

    The configuration and latency change with each stimulation.

    This is due to a polysynaptic response in the spinal cord, whereRenshaw cells (R) inhibit impulses from traveling the same path each

    time.

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    F Waves

    Useful to assess proximal nerve to spinal cord

    Helpful in the evaluation of:

    Radiculopathy

    Guillian-Barre Syndrome

    Peripheral neuropathy

    Other demyelinating neuropathies

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    F Waves: Normal Median

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    H- reflex study late response equivalent to achilles reflex. Stimulate tibial

    at popliteal fossa, pickup over soleus muscle

    initiated with a submax stimulus at a long duration (0.51.0 ms).

    preferentially activates the IA afferent nerve fibers(muscle spindle sensory)

    causing an or thodromicsensoryresponse to the spinalcord, and then an or thodromicmotorresponse back tothe recording electrode.

    The morphology of wave pattern and latency remainsconstant

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    Muscle SpindleIa - responsive to the rate of change in muscle length,

    as well to change in velocity

    http://en.wikipedia.org/wiki/File:MuscleSpindle.svg
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    H Reflexes

    Useful to assess proximal nerve conduction

    Criteria: 50% diff in

    amplitude)

    Helpful in the evaluation of: Polyneuropathy

    S1 radiculopathy

    Upper Motor Neuron lesions

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    Nerve Conduction Studies:Late Responses

    F Wave Latency Retrograde rebound motor impulse

    Travels full length of motor axon and back

    Information about proximal segments

    Limited sensitivity/specificity

    H Reflex Afferent Path: Sensory axons (group Ia fibers)

    Efferent Path: Motor Axons (alpha motor neurons)

    Follows muscle stretch reflex arc

    Side to side latency most valuable

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    DDX Small peroneal motor CMAPs normal sensory

    No conduction block

    Deep peroneal (spares sensory) vs L5

    Absent peroneal F points proximal

    Normal tibial CMAP + normal sural sensory

    Eliminates tibial, sciatic or plexus

    Some S1 involvement suggested

    H reflex absent with normal M response

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    Radiculopathy(Neuro-foraminal Stenosis from L-5 Disc Herniation)

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    Radiculopathy(Electrodiagnostic Features)

    Normal or low amplitude CMAP in corresponding

    dermatome

    Normal SNAP in corresponding dermatome Denervation in a segmental myotomal distribution

    (at least 2 muscles innervated by the same root

    via more than one peripheral nerve) with or

    without denervation of paraspinals

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    http://www.google.com/url?sa=i&rct=j&q=dorsal%20root%20ganglia&source=images&cd=&cad=rja&docid=QaVeUXsDVfAwBM&tbnid=5LmCVD1eXWYH1M:&ved=0CAUQjRw&url=http://otah2o.wikispaces.com/09+Nervous+System&ei=ID8NUdbjAseH0QHWnYDYBw&bvm=bv.41867550,d.dmQ&psig=AFQjCNFV3yniGkFw633fCeXH2bdUvsA_5Q&ust=1359909020796331
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    Needle Electromyography

    Needle electrode is inserted into the muscle

    Needle is disposable, single use

    Multiple muscles are accessible for examination

    Combination of muscles tested

    Dependent upon clinical question

    Level of discomfort is mild

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    Needle Electromyography

    Muscle is studied at rest and at different levels ofsustained, voluntary contraction.

    At rest, the muscle should be silent--any spontaneous

    activity may signal a nerve or muscle abnormality.

    During activity, the

    electrical shape and

    pattern of the responsecan distinguish

    between nerve and

    muscle disease.

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    http://www.google.com/url?sa=i&rct=j&q=motor+unit+diagram&source=images&cd=&cad=rja&docid=_3l8DoY7wp_G0M&tbnid=Ia2LpycbobgtqM:&ved=0CAUQjRw&url=http://www.sciencedirect.com/science/article/pii/S1047965107000897&ei=2ZYNUdzIIpKF0QHmjYGgDw&bvm=bv.41867550,d.dmQ&psig=AFQjCNH_MwRz198zFlmDmaNyLSWYCDgxHA&ust=1359931410578948
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    EMG - Motor Units

    Evaluated during early recruitment

    Morphologic parameters studied

    Amplitude

    Duration Phases

    Rule of 5s: as increase effort each unit comes in at ~5hz,

    and next added when previous firing ~10hz

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    Case 3

    53 fem, progressive weak distal L hand No neck pain, numb, loss of bowel, bladder

    PHx: dm x 8years, smoker, htn; no sig fhx

    Exam: atrophy intrinsics LH

    Brisk reflexes UE, and rt babinski present

    Normal sens, cerebellar, gait

    Init inv: mri c/s mild disk bulging. Emg lt c7-t1 radic.

    EMG IS REPEATED AT 7M

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    EMG - Denervation Recruitment is the pattern of motor unit firing when a

    muscle contracts

    Reduced - less motor units to draw upon

    Configuration size and shape:

    Large Amplitude more that normal # nerve fibers

    Large Duration nerve fibers timing is variable

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    Needle Electromyography:Neurogenic Motor Unit

    EMG - Left VastusLat

    This unit demonstrates:

    Reduced recruitment

    Increased amplitude Increased duration

    Polyphasia

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    Reinnervation collateral

    sprouting

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    Needle Electromyography:Muscle at rest

    Insertional Activity

    Burst of electrical activity as needle is inserted into

    muscle

    Due to disruption of muscle fiber membranes Prolonged with denervation, some muscle diseases

    Spontaneous Activity

    Fibrillations, positive sharp waves, fasciculations

    Hallmark of denervation, muscle membrane irritation

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    Needle Electromyography:Grading of Spontaneous Activity

    100 V 10 ms

    EMG - Left AntTibialis

    0 No Fibs/PSWs

    +/- Fibs/PSWs that are not persistent

    1+ Persistent Fibs/PSWs in at least 2 areas

    2+ Persistent Fibs/PSWs of moderate #s in three or more areas

    3+ Persistent Fibs/PSWs of large #s but not obscuring baseline

    4+ Baseline obliterated in all areas examined

    1+ 2+ 3+ 4+

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    Spontaneous Muscle Electrical Activity

    Examples:

    Fibrillation potential/positive waves

    indicates loss of muscle-nerve connection

    provides information about the chronicity of the problem

    Fasciculation

    spontaneous motor unit potential, may indicate irritability in the motor

    nerve cell

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    Fasciculation

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    Case 4

    76 healthy female, progressive LE numb / wk 1 year

    Imbalance cane walker

    Recent involvement of hands

    Exam: Motor: grip 4+, hip flex 4, dorsiflex 4-

    Sens: marked loss vib and proprioception feet

    Areflexic

    Gait wide-based; pos Romberg

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    Needle 19

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    Summary

    Sensorimotor polyneuropathy

    Cmap loss >> denervation

    Conduction blocks

    Sig slowing

    Few fibrillation potentials, some larger unit ->

    predominately chronic

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    DDX Chronic acquired demyelinating

    neuropathy CIDP +/- early HIV

    Multifocal motor NP with conduction block

    Anti MAG, monoclonal gammopathy,

    MGUS, osteosclerotic myeloma (POEMS syn)

    Multiple myeloma, Waldenstroms

    Castelmans

    Amyloidosis

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    Electrodiagnosis provides

    Confirmation of neuropathy

    Eg vib loss in np vs post cord

    Fiber type sens, motor, both

    Pathology demyel vs axonal

    Chronicity and activity

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    Test question

    Typical EMG findings in radiculopathy include

    a) Low cmap and sensory responses; delayed / absent F wave,

    and normal needle exam

    b) Low cmap with normal sensory responses, delayed / absent F

    wave, and denervation in at least 2 related musclesc) Low cmap with normal sensory responses, enlarged F wave,

    and denervation in at least 2 related muscles

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    The End

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    Limitations of NCSs/EMG

    Generally not helpful in the evaluation/diagnosis of:

    Pain from joint disease

    Fibromyalgia or myofascial pain syndromes

    Central nervous system disorders

    Disorders that do not arise from the neuromuscular system

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    What to Expect From an

    EMG Report

    A clinically and physiologically relevantinterpretation/diagnosis

    An outline of the localization, severity, and acuity of the

    process Notation of other diagnoses that are detected/excluded

    Explanation of any technical problems

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    What to Expect From an

    EMG Report

    The reason for the referral is addressed

    Pertinent information that may affect management is

    provided Need for re-evaluation in the future

    Urgent need for medical intervention

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    What to Expect From an

    EMG Report

    Data obtained during the study: (NCS)

    Amplitude

    Distal latency

    Distance

    Conduction velocity

    Normal (Reference) data

    Side-to-side comparison (when appropriate)

    Limb temperature during the study

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    What to Expect From an

    EMG Report

    Data obtained during the study: (EMG)

    Presence & type of abnormal spontaneous activity

    Motor unit recruitment

    Motor unit morphology

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    EMG Pearls

    Electrodiagnostic studies are a supplement to, and not areplacement, for the history and physical examination

    Electrodiagnostic results are often time-dependent

    Electrodiagnostic studies are not standardized

    investigations and may be modified by the practitioner toanswer the diagnostic question

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    Specialized EDX Testing

    Interference pattern analysis

    Quantitative motor unit analysis

    Single fiber analysis

    Segmentation studies

    Cranial nerve testing

    Brainstem and somatosensory evoked potentials

    Pelvic floor and respiratory muscles

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    Outline

    What conditions are commonly evaluated/diagnosed byNCSs/EMG?

    What are the technical details of these studies?

    What are some limitations of EMG studies?

    What can I expect from an EMG report?

    What are the indications for

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    What are the indications for

    electrodiagnostic

    consultation/testing?

    Suspected neuromuscular disease

    nerve root pathology

    peripheral nerve/plexus pathology

    neuromuscular junction pathology

    muscle pathology

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    What is the value of NCSs/EMG?

    Confirm the clinical impression of a neuromuscular

    disorder

    Rule out certain diagnoses

    Enhance patient care

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    Value of NCSs/EMG

    When neuromuscular disease is present,electrodiagnostic testing can:

    Clarify the type of pathology (i.e. neuropathy

    vs myopathy)

    Determine severity & extent of pathology

    Confirm site of pathology

    Estimate chronicity of pathology

    Complaints Suggestive of

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    Complaints Suggestive of

    Neuromuscular Pathology

    Numbness or Tingling

    Decreased Sensation

    Pain or Cramping

    Weakness

    Gait difficulty

    Fatigue

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    Disorders Diagnosed/Evaluated by

    NCSs/EMG Generalized Neuropathies

    Axonal

    DemyelinatingAcquired

    Acute: GBS

    Chronic: CIDP

    Hereditary

    Mixed Diabetic sensorimotor neuropathy

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    Polyneuropathies

    Polyneuropathies associated with many medicalconditions

    Multiple investigations often needed

    NCSs/EMGs: best initial test to clarify underlying

    pathophysiology (i.e., axonal vs demyelination)

    Results may help focus rest of work-up

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    Disorders Diagnosed/Evaluated by

    NCSs/EMG

    Mononeuropathy multiplex

    Vasculitic/ischemic neuropathies

    Demyelinating neuropathies

    Infectious neuropathies

    Neoplastic infiltration

    Granulomatous infiltration Compression neuropathy

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    Disorders Diagnosed/Evaluated by

    NCSs/EMG Focal Neuropathies

    Carpal Tunnel Syndrome (median neuropathy at the wrist)

    Ulnar Neuropathy Peroneal Nerve Palsy

    Others: brachial plexus lesions, tarsal

    tunnel syndrome, etc.

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    Disorders Diagnosed/Evaluated by

    NCSs/EMG Radiculopathy

    Cervical

    Lumbar

    Motor Neuron Disease

    Amyotrophic lateral sclerosis (ALS)

    Spinal muscular atrophy (SMA)

    Di d Di d/E l t d b

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    Disorders Diagnosed/Evaluated by

    NCSs/EMG Muscle Disease

    Inflammatory

    Polymyositis, Dermatomyositis Metabolic

    Hereditary or Congenital

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    Disorders Diagnosed/Evaluated by

    NCSs/EMG

    Neuromuscular Junction Disease

    Myasthenia Gravis

    Lambert Eaton Myasthenic Syndrome

    Botulism

    Medications

    Di d Di d/E l t d b

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    Disorders Diagnosed/Evaluated by

    NCSs/EMG Generalized weakness in the critical care setting

    Acute/unexplained onset of respiratory failure

    Neuromuscular cause for failure to wean from

    mechanical ventilation

    Neuromuscular diseases unique to critical care

    setting Critical illness neuropathy/myopathy

    Disorders Evaluated/Diagnosed by

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    Disorders Evaluated/Diagnosed by

    NCSs/EMG

    Specialized electrodiagnostic expertise can be useful in

    evaluation of:

    Ocular muscle weakness

    Speech difficulties due to weakness of laryngeal muscles Disorders of movement and tone from central nervous system

    disorders

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    Neuromuscular Junction Testing

    Repetitive Nerve Stimulation

    Stimulate nerve with train of supramaximal stimuli before and after

    exercise

    Record from muscle

    Attention to technical factors important

    More sensitive recording from proximal muscles

    Repetitive Nerve Stimulation:

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    3Hz stimulation

    Repetitive Nerve Stimulation:Normal

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    F-wave study (continued..)

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    This is not a reflex, because action potentials travels from the

    site of the stimulating electrode in a limb to the spinal cord and

    back to the limb in the same nerve that was stimulated. The F- waves latency can be used to derive the conduction

    velocity of nerves between the limb and spinal cord, whereas

    the motor and sensory nerve conduction study in the same

    segment of the limb. Conduction velocity is derived by measuring the limb length in

    millimeters from the stimulation site to the corresponding spinal

    segment (ex: C7 spinous process to wrist crease for median

    nerve).

    This is multiplied by 2 as it goes to the cord and returns to the

    muscle.

    Limitation: This evaluates a long neural pathway, which can

    dilute focal lesions and hinder specificity of injury location. It

    Radiculopathy

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    Radiculopathy(Spontaneous Activity)

    EMG - Right LumbPara Mid Fibrillation potentials

    Positive sharp waves

    Fasciculations

    Complex repetitive

    discharges

    Myokymia (rare)

    Myotonia (rare)

    Positive Sharp Wave

    Complex Repetitive Discharge

    Fibrillation Potential

    Needle Electromyography:

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    Needle Electromyography:Parameters Evaluated

    Motor Unit Configuration Muscle is volitionally activated at different force levels

    Single motor units are assessed

    Single motor unit: A motor axon and all its muscle fibers

    Motor Unit Configuration: Amplitude, Duration, Morphology

    Motor Unit Recruitment Pattern of motor unit activation with increasing volitional activation

    Interference Patterns Motor unit pattern with full voluntary activation

    Needle Electromyography:

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    Needle Electromyography:Parameters Evaluated

    Insertional activity

    Spontaneous activity

    Motor unit configuration

    Motor unit recruitment

    Interference pattern

    Needle Electromyography:

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    Needle Electromyography:Spontaneous Activity

    EMG - Right LumbPara Mid Fibrillation potentials

    Positive sharp waves

    Fasciculations

    Complex repetitive

    discharges

    Myokymia

    Myotonia

    Positive Sharp Wave

    Complex Repetitive Discharge

    Fibrillation Potential

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