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    OPHTHALMOLOGY DEPARTEMENT OF SRIWIJAYA UNIVERSITYM. HOESIN HOSPITAL PALEMBANG

    2014

    dr. Ristania

    Consultant

    dr. H.A.K Ansyori,Spm. Mkes.dr. Ramzi Amin, SpM.

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    ElectroretinogramLiterature reviewTuesday, Mei 30th 2014

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    Background

    Holmgren (1865)Karpe (1947)

    Research and diagnostic of retinalDiseases Record the Electroretino-graphy

    ERG

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    Aim

    To explain the function of ERG

    and how it use for the diagnosis

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    Electroretinogram (ERG)

    the Record of retinal actioncurrents produce by theretina response to light

    stimulus.

    measure the electrical responseof the light sensitive cells such as

    rods & cones

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    ERG Machine

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    Physiological Basis

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    Human Eye

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    The Structure of Retina

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    Photoreceptors

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    Distribution of Rods and cones

    The eye contains about 6.5 million cones and120 million rods.The density of the cones is greatest at the

    fovea

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    Processing of signal in retina

    LightTransduction

    Signal processingConvergen and

    divergen

    OutputGanglioncell, FireSpikes

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    Wave Origin

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    The Electroretinogram

    The a wave is produceddue to photoreceptoractivity.

    The b wave originates dueto retinal inner nuclearlayer, from Bipolar &Muller cells.

    The c wave is produced bypigmented epithelial cells.

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    Recording and Interpretation ERG

    The ISCEV Standard species ve responses

    (1) Dark-adapted 0.01 ERG(2) Dark-adapted 3.0 ERG(3) Dark-adapted 3.0

    (4) Light-adapted 3.0 ERG(5) Light-adapted 3.0 icker

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    Recording and Interpretation ERG

    Pre Adaptation of Dark

    Dark Adapted 0,01 ERG

    (Rod Response)

    Dark Adapted 3,0 ERG

    (Combine Rod-Cone Response)

    Dark Adapted 3,0

    Oscillatory potentials

    Pre Adaptation of Light

    Light Adapted 3,0 ERG

    (Single Flash Cone Response)

    Light Adapted 3,0 Flicker ERG

    (30 Hz Flicker)

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    Dark-adapted 0.01 ERG(rod response)

    The Dark-adapted 0.01 ERG isnormally the rst signal measuredafter dark adaptation

    The stimulus is a dim white ash of0.01 cd.s.m -2; with a minimuminterval of 2 s between ashes.

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    Dark-adapted 3.0 ERG (combined rod cone response)

    This is produced by a white 3.0 cd.s.m -2 ashin the dark-adapted eye. There should be aninterval of at least 10 s between stimuli.

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    Dark-adapted 3.0 oscillatory potentials

    Dark-adapted oscillatory potentials should beobtained from the dark-adapted eye, usingthe 3.0 cd.s.m -2 flash stimulus.

    The high-pass filter must be set at 75 100 Hz,and the low pass filter set at 300 Hz or above.

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    Light-adapted 3.0 ERG(single-flash cone response)

    Use a 3.0-cd.s.m -2 stimulus, withat least 0.5 s between flashes.

    To achieve stable andreproducible cone ERGs, aminimum of 10 min light

    adaptation is required,

    The background luminance should

    be 30 cd.m-2

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    Light-adapted 3.0 flicker ERG (30 Hzflicker)

    Flicker ERGs also reflect activity of the conesystem, and should be obtained with 3.0-cdsm -2 stimuli,

    Flashes should be presented at a rate ofapproximately 30 stimuli per second (30 Hz),and the rate that is chosen should be constant

    for the laboratory.

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    Interpretation eletroretinography

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    Abnormal ERG

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    Abnormal ERG

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    ERG Function

    Retinitis pigmentosa choroideremia, gyrate atrophy of the retina, Goldman-Favre syndrome, congenital stationary night blindness X-linked juvenile retinoschisis Achromatopsia cone dystrophies Usher syndrome

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    Multifocal Electro retinography(mfERG)

    Recording of multiple spatially resolved ERG

    responses from the retina over a central areaof abt 25 degrees.

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    Multifocal Electro retinography(mfERG)

    The stimulus consists ofan array of 61/102/241hexagonal elements of

    black &white color

    Multifocal Electro retinography

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    Multifocal Electro retinography(mfERG)

    N1 response offbipolar cells. P1response on bipolarpeak. N2 response onbipolar cells recovery.

    Multifocal Electro retinography

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    Multifocal Electro retinography(mfERG)

    Clinical application of mfERG It can point outlocal alterations which cannot be detected bystandard ERG.

    Excluding outer retinal diseases.Maculopathies.

    Vascular disorders. Following disease progression.

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    THANKYOU