Professional Documents
Culture Documents
Electro-Diagnostic Tests : Erg, Eog, Ver
Electro-Diagnostic Tests : Erg, Eog, Ver
TESTS
(ERG, EOG, VER)
Dr. Ankit M. Punjabi
DOMS (final year)
Dept. of Ophthalmology, KIMS Hospital
Bangalore, Karnataka, INDIA
Email: drankitalways@gmail.com
ERG
Electric potential generated by retina in
response to stimulation of light.
First recorded by Frithiof Holmgren (1865)
In humans by Dewar (1877)
Extensive work thereafter by Riggs (1941)
ERG
ERG
a originphotoreceptors
b originMullers cells + bipolar cells.
Mainly from Mullers in response to
increase (ECF) K+ in bipolars
c origin RPE
Oscillatory potentials (small wavelets on
ascending limb of b) from amacrine cells
a wave
- Light falling Hyperpolarisation
- Outer portion of photoreceptor positive
- Inner portion - negative
- Blue dim flash - Rod ERG
- Bright red light - Cone ERG
Amplitude
Implicit time
Recording protocol
1.
Full mydriasis
2.
3.
4.
5.
Oscillatory potentials
6.
7.
8.
30 Hz flicker
ERG recording
Electrodes active, reference, ground
Ganzfeld bowl stimulator
Signal averager
Amplifier
Display monitor
Printer
ERG recording
1. Normal Waveforms Rod response /
scotopic blue / dim white are usually
smoother, dome shaped. Initial ve a wave is
not seen & is hidden by b. Longer implicit
time. Only rods contribute
ERG recording
2. Max combined response / scotopic
white flash / mesopic response is a
deep a wave with tall b. Longer
implicit, larger amplitudes. Both rods &
cones contribute
ERG recording
3. Oscillatory potentials
4. Single flash cone response / photopic
white flash small a & b waves.
Waveforms are more peaked with shorter
implicit & smaller amplitude. Cone function
5. 30 Hz flicker multiple peaked waveforms.
Cone function
4
Clinical Applications
1. Diagnosis and prognosis of retinal
disorders
a. Retinitis pigmentosa
b. Diabetic retinopathy
c. Retinal detachment
d. Vascular occlusions of retina
e. Toxic and deficiency status
Clinical Applications
2.To assess retinal function when fundus
examination is not possible
- Corneal opacities
- Dense cataract
- Vitreous haemorrhage
EOG
EOG
Measurement of resting potential of eye
Which exist between cornea and back of
the retina during fully light adapted and
Fully dark adapted conditions.
EOG
First discovered by Du Bois-Raymond (1849)
Riggs (1954) & Francois worked extensively
Arden & Fojas discovered importance of ratio
Records overall mass response only.
EOG recording
EOG recording
EOG recording
Base line. Keep lights on for 5 min
Turn off the lights. Record for 15 min in dark
adapted state
Turn on the lights. Record for 15 min in light
adapted state
Recordings sampled at 1 min intervals
Response decreases progressively during
dark adaptation
EOG
Potentials decrease progressively reaching
lowest value called dark trough in 8-12 min
Light insensitive part of EOG
Switch on record in light adapted state
Progressive increase in potential, peak is
called light peak in 69 min
Light sensitive part of EOG
EOG
Ardens ratio
Light peak / dark trough X 100
>180%
Normal
165180%
Borderline
<165%
Subnormal
2 components of EOG
A) Light sensitive [ Light peak ]
- Contributed by rods and cones
B) Light insensitive [ Dark trough ]
- Contributed by RPE , Photoreceptors
inner nuclear layer
EOG
Indications
1. Best dystrophy markedly reduced
with Arden ratio is less than 120%
2. Butterfly pattern dystrophy
3. Chloroquine toxicity
4. Stargardts dystrophy
Visually
Evoked
Potential
(Response)
VEP / VER
Types of VEP
1. Pattern VEP (checker-board
patterns on TV monitor)
2. Flash VEP (diffuse flash light for
uncooperative subjects)
VEP
Un-dilated pupils. Sit 1 meter from monitor
Electrodes in midline at forehead, vertex &
occipital lobes
2-3 different checker sizes are shown
Recording is done
VEP
Normal waveform
Pattern VEP has initial ve (N1)
+ve(P1)second ve (N2) wave
Positive wave 70 100 ms
Negative wave 100 130 ms
Positive wave - 150 200 ms
Flash VEP is complex. 2 positive & 2
negatives.
VEP Indications
a) Un-explained visual loss
b) Optic neuritis
c) Multiple sclerosis
d) Compressive ON lesions
e) Cortical blindness
f) Amblyopia
g) Glaucoma
unless