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Evoked Potentials.akhil

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    VISUAL

    EVOKED POTENTIALS

    AKHIL.B.S

    08/08/09

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    INTRODUCTION

    Evoked responses measure theelectrophysiological response of

    the nerve system to a variety ofstimuli.

    In clinical practice only a feware used on a routine basis.

    They are VEP,SSEP,BAEP,MEPolfactory and taste evokedresponses.

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    VI SUA L EVOK EDPO TENT IA L VEP tests the function of the

    visual pathway from the retina

    to the occipital cortex.

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    Anatomy and physiology

    of VEPThe light signal enters into the eye

    It is converted to an electrical signal

    in the retina.It travels through the optic nerves to

    the visual sensory area of the brain

    The ESG in the retina is calledelectroretinogram (ERG)

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    It passes through the lens,

    The right half retina sees the left half VF. The left half retina sees the right half VF.

    RT &LT optic nerves next to the nose

    cross at optic chiasm.

    RT &LT optic nerves next to the ear do

    not cross.

    After the optic chiasm the optic nerves

    are called optic tract.

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    It pass through lateralgeniculate body.

    Spread out and reach the visualsensory area .

    Back of brain as opticradiations.

    There are two optic radiations

    for each side. Upper half VF& lower half VF

    image.

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    The potential is generated in the

    VSA can be recorded as VEP.

    By the help of VS.

    EP is recorded from theelectrode at the same side of the

    VS.

    Main component of VEP is P100. In VEP recording the abn of the V

    Pathway can be evaluated by

    changing the VF by pattern.

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    vis ual evokedpote ntials

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    Stimulus parameters of

    VEP Two types of stimuli are used

    for recording VEP.

    They are pattern and flash(Goggle).

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    Techni cal aspe cts Checkerboard pattern or flash

    is used as stimulation.

    Responses are collected over

    Oz, O1, and O2 and with hemi

    field studies at T5 and T6electrodes using the standard

    EEG electrode placement.

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    Sedation should not be used. Impedance should be kept

    below 5k.

    Montage used in VEP is

    OL-FZ

    OR-FZ

    OZ-FZ

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    Pa ttern VEP Visual stimulation by alternating the black

    and white checkered Pattern.

    Triphasic evoked potential is recorded

    from the occipital area. It is known as pattern VEP.

    Pattern VEP has three peaks, they areN75,P100,N145.

    N75&P100 potentials are generated in thecortical visual sensory area.

    P100 with the peak latency of about

    100msec.

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    The visual angle

    =(360/2)*(w/d)=57.3*(w/d).

    Where w= horizontal screen

    size.

    Where d=distance from the pt

    &display.

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    In full vfs have the pt watch the

    centre of the screen.

    In half vfs have pt watch thenon stimulation side about

    1degree from the fixation point.

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    Stimulation settings

    Contrast ratio of w&b:50% or

    higher.

    Frequency: less than 1 HZ(b&wcounted as one cycle).

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    waveforms

    Usual waveform

    Initial negative peak ( N75)

    Large positive peak ( P100) Another negative peak (N145)

    Maximum value for P100 is 110

    milliseconds (ms) in patients < 60years

    Thereafter> 120 ms in females; 125ms in males

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    Flash VEP

    Under anesthesia and coma

    In young children

    Non cooperative patients

    When checking for integrity of

    visual pathways

    White flashes are recommended

    1 flashes/sec

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    Variable in flu encing VEP Age in flu ence the l atency of p 100. The p 100 la tency i s longer inadult ma les c ompared tofemale. Eye dominance(le ss prolonged&higher amplitu de).

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    Eye movement re ducesampli tude n o change inlatency. Visu al Acuity-wit h signifi cantreduction in acuity p100 latencycan be prolonged. Drugs can i ncreased p100latency. During me nta l activation p100la tency can decrease and theampli tude can increases.

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    Basics of VEP

    abnormalities Latency prolongation

    Amplitude reduction

    Combined latency andamplitude abn

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    The commonest prolongation of

    p100 is demyelination in the

    optic pathways.

    Axonal lose in the optic nerve

    reduces the amplitude.

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    Multiple sclerosis(10-30ms). Optic neuritis.

    Ischemic optic neuropathy.

    HIV infections. Nutritional &toxic optic

    neuropathy.

    Hereditary &degenerativediseases.

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    ABNORMAL VEP

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    SUJJET KUMAR PATHAK 27/M

    Patient with IIH

    DV 6/6 bl

    Vep -pattern

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    Shajahan.M.56y/M

    Demyelination

    DV normal

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    John lukose 52/m

    Bi optic neurotic

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    Sruthy.b 15/f

    Optic neuropathy

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    NORMAL VEP

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    Abraham .M.G 47/m

    Migraine.

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