Basics of Perimetry
Basics of Perimetry
PERIMETRY
Visual field
• NEGATIVE SCOTOMA - Nerve fibers pass through the sclera at the optic nerve
head, typically 10-15º nasal to fixation. At this location, no photoreceptors are
present, creating a normal absolute scotoma.[3]
• POSITIVE SCOTOMA -perceived as black spot within the field of vision
H
I
L
L
O
F
V
I
S The hill is highest at fixation, where visual sensitivity is
greatest. The height of the hill of vision declines toward
I the periphery as visual sensitivity diminishes.
O
n
EXTENT OF FIELD
BINOCULAR FIELD
measured using
Visual fields
PERIMETERS
KINETIC STATIC
Moving the test object from Stimulus remains fixed at a
a non seeing to a seeing certain location within the
area, and recording the point field, with the intensity
at which it is first seen in increased until it is seen by
relation to fixation. the subject.
Eg – Goldmann’s perimeter Eg – HFA, Octopus etc.
KINETIC PERIMETRY
(test object moves from nonseeing
to seeing area)
STATIC PERIMETRY
(measures sensitivity of retina
at a given point)
KINETIC PERIMETRY
STATIC PERIMETRY
HISTORICAL CONSIDERATIONS
AUTOMATED
MANUAL
Stimulus location is changed
Stimulus is moved by hand
by a computer, as in the
as in the Goldmann.
Humphrey visual field.
M
A
D Better examination of peripheral field.
N
E Reveal scotomas that were missed
U M between the testing point in static
A E perimetry.
L R Better in cases of central scotoma.
I Neuro-ophthalmology.
P T
S
E
R
I
M Less reliability and
reproducibility.
E Less sensitive in detecting early
T visual field defect.
E Lack of fixation monitoring.
R Lack of normative data.
S
Automated static perimetry
ADVANTAGES
DISADVANTAGES
Reproducible testing conditions.
Data storage capability. Expensive
More sensitive testing. Time consuming
Easy operation and menu driven
software - easy to learn and to use
In this stimulus is stationary and its characters
are altered till it is visible.
BRIGHTNESS
STIMULUS BACKGROUND OF
SIZE ILLUMUNATION STIMULUS
V 9.03 64
IV 4.51 16
III 2.26 4
II 1.13 1
I 0.56 0.25
0 0.28 0.0625
3 dB decrease in
measured threshold
value always means
that the eye lost approx
half of the retinal
sensitivity.
PERIMETRIC
UNIT
HARDWARE
CONTROL
COMPONENTS UNIT
OF
AUTOMATED
PERIMETER
SOFTWARE
hardware
CO
IC NT
TR
E RO
I M L
E R UN
P IT
UN IT
PERIMETRIC UNIT
STIMULUS
Size
BACKGROUND
Brightness
Illumination
Duration
Distance
The stimulus presented over a longer period of time may become
more visible, the phenomenon called temporal summation.
STIMULUS
DURATION – 0.2 sec
STIMULUS DISTANCE
– 33 cm
FIXATION TARGET
SMALL DIAMOND
LARGE DIAMOND
CENTRAL located below the central
located below the centra
target and should be
Yellow light in the center target and is used for
used if the patient cannot
of the bowl patient with central
see the central fixation
scotoma
light
CONTROL UNIT
• FIXATION CONTROL
C.C.T.V
HEIJL KRAKAU SYSTEM
EYE MOTION SENSORS
• DATA STORAGE
T
W TESTING
A STRATEGIES
R
E
TESTING
PATTERN
THRESHO SCREENIN
LD TEST G TEST
FULL SITA
THRESHOL FAST PAC STANDAR SITA FAST
D D
Determination of threshold by using
Staircase/ bracketing method – for full
threshold strategy
• Strategy: The options are
1. Full threshold: Full threshold is rarely indicated, since newer
thresholding algorithms are equally as valid and much faster.
2. Fastpac
3. SITA-standard
4. SITA- fast
• However with the newer Swedish Interactive Thresholding Algorithm
(SITA), testing is even more rapid, yet validity is protected and possibly
enhanced. SITA standard is twice as fast as full threshold and SITA-fast is
twice as fast as SITA Standard.
B
POINT
DENSITY
C
A Testing
NO. OF patterns DEGREE
TEST OF BARE
POINTS VARIABLE AREA
S
EXTENSI
ON OF
FIELD
TESTING D
30-2 CENTRAL
THRESHOLD TEST
PATTERN
A. 76
B. 6°
C. 3°
24-2 CENTRAL
THRESHOLD TEST
PATTERN
A. 54
B. 6°
C. 3°
10-2 CENTRAL
THRESHOLD TEST
PATTERN
A. 68
B. 2°
C. 1°
5° area of 10-2
central pattern
MACULAR
PROGRAMMING TEST
PATTERN
A. 16
B. 2°
C. 1°
SUMMARY
30-2 24-2 10-2 MACULAR
PROGRAMM
E
TEST POINTS 76 54 68 16
POINT 6 6 2 2
DENSITY (°)
FIELD (°) 30 24 10 5
BARE AREA 3 3 1 1
(°)
24-1 CENTRAL 24-2 CENTRAL
THRESHOLD PATTERN THRESHOLD PATTERN
14 mins
10 mins
7 mins
5 mins
EVALUATION OF HFA PRINTOUT
• Same as total deviation plot except here stat pack software has corrected the
results for the changes caused by cataract, small pupil, etc.
6.GLOBAL INDICES
PATTERN STANDARD
DEVIATION
MEAN DEVIATION
Mean difference between • Measure of variability
normative data for that age within the field
compared with collected
• Actually points out
data in db
towards localized field
Indicator for general loss
depression of field
• Identifying early defects
Worse than normal is
indicated with negative
value
7.GHT
• GHT compares 24-2 visual fields into 10
regions, with 5 inferior regions representing
mirror images of 5 corresponding superior
regions. Differences between corresponding
superior and inferior zones are compared with
the differences present in the population of
normal controls
GLAUCOMA HEMIFIELD TEST
• 5 CLUSTERS
• Not designed to
detect a temporal
defect
GHT CAN BE
GHT-Abn
GHT- ONL GHT-Borderline
sensi
Values between any sector in Values between any sector in
If the best pa
U & L zone differ to an extent U & L zone differ to an extent
depressed to a
found in 1% of the population found in 3% of the population
in <0.5% of t
D
I ESTABLISHED
GLAUCOMA
• 24-2 FULL THRESHOLD
• 24-2 SITA STANDARD
C AND FOLLOW • 24-2 FAST PAC
UP
A
• 10-2 FULL THRESHOLD
T ADVANCED • 10-2 SITA STANDARD
GLAUCOMA
I • MACULAR
PROGRAMME
THOSE WHO
O CANNOT
N WITHSTAND
LONG
• 24-2 SITA FAST
S DURATION
FEW TERMINOLOGIES
D. Advanced defect
3. Tubular vision
4. No light perception
MNEMONIC
• Isopter contraction
• Baring of blind spot
IC (see)
• Wing shaped paracentral scotoma-
BB occurs in jerrums area within central
10degree
wings &
• Siedel scotoma- comma shaped
SAD extension of blind spot
steps • Arcuate or bjerrums scotoma
• Double arcuate scotoma
Isopter contraction
IC (see) Baring of blind spot
Wing shaped paracentral scotoma-
BB occurs in jerrums area within central
wings & 10degree
Siedel scotoma- comma shaped
SAD extension of blind spot
Arcuate or bjerrums scotoma
steps Double arcuate scotoma
Roenne’s central & peripheral
NERVE FIBRE LAYER
NERVE FIBRE LAYER
GLAUCOMATOUS VISUAL FIELD LOSS
SUPERIOR ARCUATE SCOTOMA
DOUBLE ARCUATE SCOTOMA
SUPERIOR NASAL STEP
WHAT IT MAY
BE??