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Dr. Urfeya Mirza
Introduction
History
Indications
Types of ERG
Technical aspects
Clinical applications
Factors influencing ERG
Limitations of ERG
Commercial ERG devices
Conclusions
Electroretinography (ERG) is an electrophysiological and functional test of
the retina which provides an objective and quantitative measure of the
retinal function in response to light stimulation.
(Schaeppi and Liverani, 1987; Samuels, I. et al., 2017)
• .
It is a mainstay of clinical ophthalmic diagnostic testing which establishes
the function of the structures visualized by ophthalmoscopy, a property
that is not shared by the other electrodiagnostic techniques.
(Sims, 2000)
• .
It is a useful tool for the differential diagnosis of various ophthalmic
diseases in animals.
(Aguirre and Rubin, 1992; Aguirre, 1995; Sims, 2000; Oriá et al., 2004; Bianca Brüggen et al., 2016)
Eye
Optic Tract
Optic Chiasm
Optic Nerve
Lateral Geniculate
Nucleus
Occipital Cortex
The retina is the photosensitive lining of the posterior segment of the globe.
The retina has basically two layers: the retinal pigment epithelium and the
neuroretina.
The neuroretina is disposed in nine layers: the visual cell layer (rod and cone
layer), the outer limiting membrane, the outer nuclear layer, the outer
plexiform layer, the inner nuclear layer, the inner plexiform layer, the ganglion
cell layer, the nerve fiber layer and the inner limiting membrane.
There are 2 types of light-sensitive cells (photoreceptors): cones and rods.
The macula, composed mainly of cones, is used primarily for color vision
(photopic vision) while the remaining retina, composed mainly of rods is used
primarily for night (scotopic) vision.
Veterinary Ophthalmology (4th Ed.
2007) by Kirk N. Gelatt.
Inherited abnormalities Trauma
Metabolic disturbances Generalized infections
Tumors Blood disorders
High blood pressure Nutritional deficiencies
Electroretinogram
Multifocal Electroretinogram
Pattern Electroretinogram
Multifocal Visual Evoked
Potential
Electrooculogram
ERG mERG
pERG mVEP
EOG
Electrophysiological Tests
In small animal practice, ‘Electroretinography’ is most useful
than other diagnostic techniques for the assessment of retinal
function.
Liapis, I.C. 2004
The beginnings of visual electrophysiology date back to the 19th century when
DuBois-Reymond (1849) discovered the resting potential between the anterior
and posterior pole of the un-stimulated eye.
Holmgren (1870) demonstrated differences in the eye electrical potential
generated by light stimulation.
Einthoven and Jolly, (1908) recorded detailed records of the frog’s eye with a
string galvanometer .
Kahn and Lowenstein (1924) presented ERG wavelets recorded in humans with a
string galvanometer.
In the mid-20th century, Karpe (1945) reported that electroretinography was an
examination used to determine retinal function.
In veterinary medicine, Parry et al. (1953, 1955) were the first to perform ERG in
healthy and diseased dogs, respectively.
Rubin (1963) examined blind cats and was the first to justify the usefulness of
ERG in evaluation before cataract surgery.
Diagnosis and evaluation of retinal function in animals when the optic
system is not transparent due to cataract, glaucoma, intoxications and
progressive retinal atrophy (PRA).
Differential diagnosis between the sudden acquired retinal degeneration
(SARD) and optic neuritis.
Diagnosis of retinal diseases in cats, such as non-inflammatory
retinopathies, hereditary retinal degenerations and central retinal
degenerations due to dietary taurine deficiency.
ERG
Full field
ERG
Pattern
ERG
Focal ERG
Multifocal
ERG
Full-Field ERG:
Retinal potential elicited by a brief flash of light, recommended to be
about 5 ms in duration, that evenly illuminates the entire retina.
Pattern ERG:
It mainly represents inner retinal activity. Recorded with full correction of
refractive errors as visualization of stimulus for extended time is essential
for recording.
Focal ERG:
Used for detecting small focal lesions or pathologies. A small stimulus of 4⁰
size is projected on area of retina to be tested. Mostly used in research
setting than in clinical setting.
Multifocal ERG:
The stimuli consists densely arranged black or white hexagonal elements
displayed on CRT monitor. These hexagonal elements change from light to
dark independently and this change results into recording of mfERG.
Conducted in ambient light. Pre-exposure to strong light is
avoided. A dark-adaptation period of 1 hour is recommended.
The animal is fully anaesthetized in order to prevent artifacts
through involuntary muscle movement.
Proper oxygenation and ventilation is maintained. Body
temperature is kept stable at about 39⁰C.
Eyelids are kept open and pupils are fully dilated throughout
the examination.
Proper positioning of the pupil is maintained by the use of
sub-conjunctival stay sutures at the limbus to stabilize the
globe.
The use of full-field conditions, such as the Ganzfeld
stimulator, in order to obtain a uniform distribution of
light across the retina is recommended.
Light flashes are not more than 5 milliseconds long.
White light is used both for stimulus and background.
Neutral density filters are used in front of the light source to
attenuate the light and modify the light stimulus.
GANZFELD STIMULATION GLOBE
Reusable corneal contact lens electrodes with adequate
curvature are used.
A reference electrode is placed halfway between the
temporal canthus and the ear.
A similar subcutaneous ground electrode is placed at an
indifferent location, such as at the central top portion of
the head.
The equipment enables the amplification of the signal so
that recordings are evaluated with high accuracy.
(A)Positive electrode.
(B)Reference electrode located 1 cm caudally to the lateral eye canthus.
(C)Ground electrode positioned in the region of the occipital
protuberance.
Reusable corneal
contact lens
electrode with
adequate curvature
Electrode placement for ERG recording, with the use of Kooijman-Damhof
corneal electrodes with a built-in light source and a light diffusing contact lens.
Electrode placement for ERG recording, with the use of Jet mono-polar
corneal electrodes.
A-wave (initial negative wave) = photoreceptors
Reduced in retinitis pigmentosa (RP)
B-wave (large postive wave) = inner retinal layers
Decreased in retinoschisis, central retinal vein occlusion (CRVO),
central retinal artery occlusion (CRAO), congenital stationary night
blindness(CSNB)
Oscillatory potentials (a ripple of 3 or 4 wavelets at
the ascending limb) = amacrine cells
Attenuated in central retinal vein occlusion (CRVO), central
retinal artery occlusion (CRAO), central serous
retinopathy(CSR), congenital stationary night blindness(CSNB)
A report of the ERG recording includes the following waves:
Amacrine cells
Muller cells
and bipolar
cells
Rods and
cones
Amplitude :
a-wave measured from
the baseline to the trough
of a-wave.
b-wave measured from
the trough of a-wave to
the peak of b-wave.
Time sequences :
Latency:- time interval
between onset of stimulus and
the beginning of the a-wave
response. Normally it’s 2 ms.
Implicit time:- time from the
onset of light stimulus until
the maximum a-wave or b-wave
response.
Factors related to the conditions of the procedure:
Parameters of the stimulus
Retinal adaptation to the ambient light
Background luminance during the procedure
Type of recording electrodes
Electric properties of the stimulating and recording systems.
Factors related to the patient:
Species, breed and age of the animal
Oxygenation of the patient
Globe, eyelid or muscle movements during the procedure
Pupil size
Depth and type of anesthesia
Transparence of the refracting tissues of the eye.
Mentzer et al., 2005
Since ERG measures only the mass response of
the retina, isolated lesions like a hole
hemorrhage, a small patch of chorioretinitis or
localized area of retinal detachment can not be
detected by amplitude changes.
Disorders involving ganglion cells (e.g. Tay
sachs’ disease), optic nerve or striate cortex do
not produce any ERG abnormality.
Miller and Murphy, 2003
RETIport Animal System
Ganzfeld ERG Focal ERG
Photopic Type
Scotopic Type
ELECTRORETINOGRAPHY (in veterinary).pptx
ELECTRORETINOGRAPHY (in veterinary).pptx
ELECTRORETINOGRAPHY (in veterinary).pptx
ELECTRORETINOGRAPHY (in veterinary).pptx
ELECTRORETINOGRAPHY (in veterinary).pptx
ELECTRORETINOGRAPHY (in veterinary).pptx
ELECTRORETINOGRAPHY (in veterinary).pptx
ELECTRORETINOGRAPHY (in veterinary).pptx
ELECTRORETINOGRAPHY (in veterinary).pptx
ELECTRORETINOGRAPHY (in veterinary).pptx

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ELECTRORETINOGRAPHY (in veterinary).pptx

  • 2. Introduction History Indications Types of ERG Technical aspects Clinical applications Factors influencing ERG Limitations of ERG Commercial ERG devices Conclusions
  • 3. Electroretinography (ERG) is an electrophysiological and functional test of the retina which provides an objective and quantitative measure of the retinal function in response to light stimulation. (Schaeppi and Liverani, 1987; Samuels, I. et al., 2017) • . It is a mainstay of clinical ophthalmic diagnostic testing which establishes the function of the structures visualized by ophthalmoscopy, a property that is not shared by the other electrodiagnostic techniques. (Sims, 2000) • . It is a useful tool for the differential diagnosis of various ophthalmic diseases in animals. (Aguirre and Rubin, 1992; Aguirre, 1995; Sims, 2000; Oriá et al., 2004; Bianca Brüggen et al., 2016)
  • 4. Eye Optic Tract Optic Chiasm Optic Nerve Lateral Geniculate Nucleus Occipital Cortex
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  • 6. The retina is the photosensitive lining of the posterior segment of the globe. The retina has basically two layers: the retinal pigment epithelium and the neuroretina. The neuroretina is disposed in nine layers: the visual cell layer (rod and cone layer), the outer limiting membrane, the outer nuclear layer, the outer plexiform layer, the inner nuclear layer, the inner plexiform layer, the ganglion cell layer, the nerve fiber layer and the inner limiting membrane. There are 2 types of light-sensitive cells (photoreceptors): cones and rods. The macula, composed mainly of cones, is used primarily for color vision (photopic vision) while the remaining retina, composed mainly of rods is used primarily for night (scotopic) vision. Veterinary Ophthalmology (4th Ed. 2007) by Kirk N. Gelatt.
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  • 10. Inherited abnormalities Trauma Metabolic disturbances Generalized infections Tumors Blood disorders High blood pressure Nutritional deficiencies
  • 11. Electroretinogram Multifocal Electroretinogram Pattern Electroretinogram Multifocal Visual Evoked Potential Electrooculogram ERG mERG pERG mVEP EOG Electrophysiological Tests In small animal practice, ‘Electroretinography’ is most useful than other diagnostic techniques for the assessment of retinal function. Liapis, I.C. 2004
  • 12. The beginnings of visual electrophysiology date back to the 19th century when DuBois-Reymond (1849) discovered the resting potential between the anterior and posterior pole of the un-stimulated eye. Holmgren (1870) demonstrated differences in the eye electrical potential generated by light stimulation. Einthoven and Jolly, (1908) recorded detailed records of the frog’s eye with a string galvanometer . Kahn and Lowenstein (1924) presented ERG wavelets recorded in humans with a string galvanometer. In the mid-20th century, Karpe (1945) reported that electroretinography was an examination used to determine retinal function. In veterinary medicine, Parry et al. (1953, 1955) were the first to perform ERG in healthy and diseased dogs, respectively. Rubin (1963) examined blind cats and was the first to justify the usefulness of ERG in evaluation before cataract surgery.
  • 13. Diagnosis and evaluation of retinal function in animals when the optic system is not transparent due to cataract, glaucoma, intoxications and progressive retinal atrophy (PRA). Differential diagnosis between the sudden acquired retinal degeneration (SARD) and optic neuritis. Diagnosis of retinal diseases in cats, such as non-inflammatory retinopathies, hereditary retinal degenerations and central retinal degenerations due to dietary taurine deficiency.
  • 15. Full-Field ERG: Retinal potential elicited by a brief flash of light, recommended to be about 5 ms in duration, that evenly illuminates the entire retina. Pattern ERG: It mainly represents inner retinal activity. Recorded with full correction of refractive errors as visualization of stimulus for extended time is essential for recording. Focal ERG: Used for detecting small focal lesions or pathologies. A small stimulus of 4⁰ size is projected on area of retina to be tested. Mostly used in research setting than in clinical setting. Multifocal ERG: The stimuli consists densely arranged black or white hexagonal elements displayed on CRT monitor. These hexagonal elements change from light to dark independently and this change results into recording of mfERG.
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  • 17. Conducted in ambient light. Pre-exposure to strong light is avoided. A dark-adaptation period of 1 hour is recommended. The animal is fully anaesthetized in order to prevent artifacts through involuntary muscle movement. Proper oxygenation and ventilation is maintained. Body temperature is kept stable at about 39⁰C. Eyelids are kept open and pupils are fully dilated throughout the examination. Proper positioning of the pupil is maintained by the use of sub-conjunctival stay sutures at the limbus to stabilize the globe.
  • 18. The use of full-field conditions, such as the Ganzfeld stimulator, in order to obtain a uniform distribution of light across the retina is recommended. Light flashes are not more than 5 milliseconds long. White light is used both for stimulus and background. Neutral density filters are used in front of the light source to attenuate the light and modify the light stimulus.
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  • 21. Reusable corneal contact lens electrodes with adequate curvature are used. A reference electrode is placed halfway between the temporal canthus and the ear. A similar subcutaneous ground electrode is placed at an indifferent location, such as at the central top portion of the head. The equipment enables the amplification of the signal so that recordings are evaluated with high accuracy.
  • 22. (A)Positive electrode. (B)Reference electrode located 1 cm caudally to the lateral eye canthus. (C)Ground electrode positioned in the region of the occipital protuberance.
  • 23. Reusable corneal contact lens electrode with adequate curvature
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  • 25. Electrode placement for ERG recording, with the use of Kooijman-Damhof corneal electrodes with a built-in light source and a light diffusing contact lens.
  • 26. Electrode placement for ERG recording, with the use of Jet mono-polar corneal electrodes.
  • 27. A-wave (initial negative wave) = photoreceptors Reduced in retinitis pigmentosa (RP) B-wave (large postive wave) = inner retinal layers Decreased in retinoschisis, central retinal vein occlusion (CRVO), central retinal artery occlusion (CRAO), congenital stationary night blindness(CSNB) Oscillatory potentials (a ripple of 3 or 4 wavelets at the ascending limb) = amacrine cells Attenuated in central retinal vein occlusion (CRVO), central retinal artery occlusion (CRAO), central serous retinopathy(CSR), congenital stationary night blindness(CSNB) A report of the ERG recording includes the following waves:
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  • 29. Amacrine cells Muller cells and bipolar cells Rods and cones
  • 30. Amplitude : a-wave measured from the baseline to the trough of a-wave. b-wave measured from the trough of a-wave to the peak of b-wave. Time sequences : Latency:- time interval between onset of stimulus and the beginning of the a-wave response. Normally it’s 2 ms. Implicit time:- time from the onset of light stimulus until the maximum a-wave or b-wave response.
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  • 46. Factors related to the conditions of the procedure: Parameters of the stimulus Retinal adaptation to the ambient light Background luminance during the procedure Type of recording electrodes Electric properties of the stimulating and recording systems. Factors related to the patient: Species, breed and age of the animal Oxygenation of the patient Globe, eyelid or muscle movements during the procedure Pupil size Depth and type of anesthesia Transparence of the refracting tissues of the eye. Mentzer et al., 2005
  • 47. Since ERG measures only the mass response of the retina, isolated lesions like a hole hemorrhage, a small patch of chorioretinitis or localized area of retinal detachment can not be detected by amplitude changes. Disorders involving ganglion cells (e.g. Tay sachs’ disease), optic nerve or striate cortex do not produce any ERG abnormality. Miller and Murphy, 2003
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Editor's Notes

  1. The visual pathways start from the photoreceptor and retinal pigment epithelial (RPE) layers in the retina, proceeding through the inner retinal layers and the retinal ganglion cells. The two optic nerves meet at the optic chiasm where, in a normal, approximately 50% of the fibres project to the ipsilateral hemisphere of the brain and approximately 50% decussate to the contralateral hemisphere. From the optic chiasm the two optic tracts project to the lateral geniculate bodies of the thalami, and hence to the occipital cortex via the optic radiations.
  2. Fibrous tunic: sclera & cornea Vascular tunic: choroid layer Sensory/nervous tunic: retina
  3. Retina acts like the film in a camera - images come through the eye's lens and are focused on the retina. The retina then converts these images to electric signals and sends them via the optic nerve to the brain in order to be interpreted.
  4. Opthalmoscopic image of human Retina. The macula, composed mainly of cones, is used primarily for color vision (photopic vision) while the remaining retina, composed mainly of rods is used primarily for night (scotopic) vision.
  5. Visual electrophysiology is an extremely powerful tool to assess the functional integrity of various levels of this visual system.
  6. In veterinary ophthalmology, full-field flash ERG is most commonly used.
  7. The c-wave is a late positive potential after the b-wave. The c-wave refers to the function of RPE; however it is unusual and is not examined in most cases. RPE= Retinal pigment epithelium
  8. In every case, we test all the five responses individually.
  9. The first two responses are scotopically matched blue and red ERGs. The blue flash was dim enough that no a-wave can be discerned in a normal pAs in case of RP, the rods are affected most severely as evidenced by the extinguished response to the blue flash. Breakdown and loss of cells in the retina—which is the light sensitive tissue that lines the back of the eye.
  10. a- and b-wave ERG amplitudes attenuate proportional to degree of expression. The condition may be X-linked abnormal function of the rod system.
  11. The ERG has a specific abnormality showing a normal a-wave but no b-wave. It is a negative ERG. Retinoschisis means splitting of the eye's retina into two layers mainly due to age- at the outer plexiform layer of the retina.
  12. In contrast to retinitis pigmentosa, the ERGs of a patient with a cone dystrophy exhibit good rod b-waves that are just slower. However, the early “cone” portion (bx) of the scotopic red flash ERG is missing. The scotopic bright white ERG is fairly normal in appearance but with slow implicit times. The 30 Hz flicker and photopic white ERGs dependent upon cones are very poor.
  13. Vascular occlusions such as central retinal artery thrombosis produce a characteristic avascular appearance to select areas of the fundus and an ERG with no b-wave.
  14. In general ERG b-wave amplitudes correspond to the amount of attached healthy retina, although the detached retina may function for sometime.
  15. Attenuation of full-field ERG b-wave amplitudes can detect toxicity. Often the first indication of toxicity is reduced amplitude to 30 Hz flicker. Bull's eye maculopathy, due to cloroquine toxicity (malarial drug)
  16. reduction in ERG waveform in the affected eye Cisplatinum is most potent anti-tumour agent and interferes with dna replication causes histopathological damage in retina
  17. The ERG response was diminished in size particularly following dim scotopic flashes. Central serous chorioretinopathy (CSR) is a relatively common condition that affects the macula. In this condition, for reasons not fully understood, a pool of clear fluid accumulates under the macula forming a blister. This blister separates the retina from its supporting layers and causes vision changes.
  18. Global ERG is attenuated. Talc is a filler in prep of oral medications. It is an embolic phenomenon affecting the retinal arteries and capillaries. Some particles can clear the pulmonary capillaries to reach the ocular circulation. While circulating talc particles might occlude some small capillaries, particles that are large enough to be visible ophthalmoscopically represent an accumulation of microemboli in vessel walls.
  19. This is reflected in reduced a- and b-waves of the ERG. Deferoxamine (DFOA), sold under the brand name Desferal, is the commonest iron chelating agent used in the management of iron toxicity. Chelation of ions (iron, copper, aluminum) on the retinal pigment epithelial with resultant dysfunction or due to defective vasoregulation.
  20. The Mouse Table is a heatable examination table for small animals. It is placed in front of a Roland Consult Ganzfeld and has two free moveable electrode holders. After the animal and the electrodes are placed, the table can be slided into the Ganzfeld.
  21. Phoenix Research Labs has developed ECG 2 using laboratory animals Phoenix Research Labs’ Ganzfeld ERG System is optimized for the unique retinal response of rodent photoreceptors
  22. ERG systems specifically designed for rodent eyes
  23. Measuring Retinal Function with ERG in Rodents, ERG systems specifically designed for rodent eyes
  24. •Near infrared light allows image-guided alignment with solid contact electrode •Unique Maxwellianview allows uniform illumination of the eye •Live chart mode shows real time coupling with the cornea
  25. Handheld Multi-species Electroretinography is a portable, small and powerful – all in one device
  26. Completely portable and battery powered, Waveform and measurements are immediately viewable on the device, Easy USB connection to any PC