- •Preliminary Testing
- •Visual Acuity
- •5 Letters on each line
- •Pupil Testing
- •97 % Of the fibers control accommodation (ciliary body)
- •Independent of retinal illumination
- •If pupils are unequal, measure size in both dark and bright light
- •If it is not the case for either eye: afferent pupillary defect in the eye with less constriction
- •Reverse (indirect) apd
- •Adie’s tonic pupil
- •Cranial Nerve Palsy
- •Stereopsis
- •3 Parts: “fly” for gross stereo (3,000’’), “animal” test (400’’-100’’), Wirt circles (800’’-40’’)
- •Cover Test
- •Important to do routine bp measurements:
- •Korotkoff Sounds
- •Hypertension Classification
- •Visual field: the perceptual space available to the fixating eye
- •Important to be exactly between you and the patient so the patient’s field can be compared to yours
- •If not full, then document/draw constricted quadrant
- •Field Limits
- •Ocular Dominance
Stereopsis
Stereopsis: the perception of 3-D visual space due to binocular disparity cues (disparities of the two retinal images)
Stereoacuity: ability to discriminate very fine differences of objects in space by using binocular vision
Stereo acuity is not the same as depth perception
Must have some level of binocular vision to appreciate stereo acuity
Requires changes in both vergence and accommodation
Monocular cues to depth perception must be learned
Retinal image size, linear perspective, texture density, luminance variations, aerial perspective, overlay, motion parallax, kinetic depth, myosensory cues from muscles controlling accommodation and convergence
Each point on the retina has a local sign or directional value
Fovea: principal visual sign (straight ahead)
Corresponding retinal points: pairs of points in each eye that have the same local sign (point in one eye corresponds to an area in the other eye)
Objects that stimulate a pair of corresponding points appear to be single and located at the same position in space
Stereo Tests Designs
Local stereopsis (line or contour)
Targets have edges that are separated on background to produce disparity
Smaller separation defines better stereopsis
Howard Dolman Peg Test
Thresholds stereopsis
Most accurate
Two types of testing: null threshold and JND
Titmus Stereofly
Linear polarized test
3 Parts: “fly” for gross stereo (3,000’’), “animal” test (400’’-100’’), Wirt circles (800’’-40’’)
Stereo Reindeer
Global stereopsis
Matrix of black dots on gray background
Lateral shift in central pattern
NO monocular cues
Random Dot
Uses 3-D cross polarized spectacles
Right side: 8 random dot figures-- 500 sec of arc on top and 250 sec of arc on bottom-----must identify which cell is empty
Left side: modified circles (400’’ – 20’’), animals (400’’ – 100’’)
Procedure
Present test perpendicular to LOS at a distance of 40 cm (16 in)**
Spectacles are placed over habitual
Score last number correct after 2 errors
Record sec of arc @ test distance, test used and note cc or sc
Color Vision
Three types of cones responsible for color vision
Each contain photopigments that maximally absorb different wavelengths
Red (long), green (middle), blue (short)
Defects
Protan: red wavelength (L cones)
Deutan: green wavelength (M cones)
Tritan: blue wavelength (S cones)
Inherited color deficiencies
Anomalous trichromat (3 cone pigments)
Protananolmalous: red weak
Deutananolmalous: green weak
Tritananolmalous: blue weak
Dichromat ( 2 cone pigments)
Protanopia
Deutanopia
Tritanopia
Monochromat
Rod
True color blindness (may have few cones but abnormal in shape) and poor vision
Cone
Variation of color blindness (only one cone type present)
-
Inherited
Acquired
Permanent (not correctable)
Changes with progression or regression of primary cause
Test result relatively stable
Test results strongly influenced with changes in test conditions
Defect same in each eye in both type and severity
Severity may be greater in one eye, or one eye could be normal and the other not
More prevalent in males
Equally prevalent in males and females
Always binocular
Can affect only one eye
Almost always red/green
Most are blue/yellow
Transmitted via X chromosome
Caused by medications (plaquinel), disease, toxic effects of chemicals, aging
Prevalence
Overall 4%
Males 8%
Protanomaly 1% Protanopia 1%
Deuteranolamly 5% Deutranopia 1.1%
Tritanopia 0.002%
Females 0.5%
Patient selection
Children at an early age
Patients at initial office visit
Unexplained decreased in VA
Report changes in color vision
Abnormal fundus findings
Types of color vision tests
Color Naming
Color Mixing
Anomaloscope
Assess ability to make metameric matches
Change mixture of monochromatic red and green
Color Confusion
Pseudoisochromatic plates (PIC)
Diagnostic plates: figure is isochromatic for one defect but not for another so it identifies type of deficiency
Vanishing figure: normal sees, defective does not see
Transformation: normal and defective see different figures
Hidden digit/symbol: defective sees, normal does not see
Screening mostly for inherited defects
HRR
Detects inherited and acquired defects
Can be used on illiterate patients (symbols used)
Ishihara
Screen for inherited red/green anomalies
Color Matching (arrangement)
Detects inherited or acquired
Farnsworth D-15
Quantifies depth of defect (mild/severe)
Used only as diagnostic (not screener)
Farnsworth-Munsell 100-Hue
Good for detecting/classifying early acquired color deficiencies caused by ocular disease
Detects subtle color discrimination
Occupational
PIC, D-15, Farnsworth Lantern test (FALANT), ISCC Color Matching Aptitude test
Procedure
Use “standard” illumination “C”
MacBeth Easel Lamp
Incandescent lighting inadequate
HRR
Plates perpendicular to LOS at 75 cm
Use correction unless tinted and test monocular!
Ask patient how many symbols, what are they, and have trace where they are with brush
Time limit: 20 sec/page
Record check marks when correct for screening plates 5-10
If ALL 6 correct: normal CV
Only plate 5 or 6 missed test plates 21-24: B/Y defect
Only 1 or more plates 7-10 missed test plates 11-20: R/G defect
Ishihara
Plates perpendicular to LOS at 75 cm
Use correction unless tinted and test monocular!
Ask patient what do they see
Time limit: 3 sec/plate
Record number plates correct over number tested with pass/fail noted and the numbers said if missed
Normal if 10/1l
If </= 7 correct, test plates 12,13,14 to classify whether protan or deutan
Farnsworth D-15
Caps should be 45 deg to patient’s LOS at 50 cm
Use correction unless tinted and test monocular
Instruct patient to place caps in chromatic order
No time limit
**When recording, note the test used and if cc or sc**
