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Hypertension Classification




V Visual Acuity

o Purposes:

To establish a baseline

Legal reasons (drivers licenses, insurance claim, pension, and disability based on legal blindness)

Legal blindness: 20/200 or worse in better eye OR less than 30 of visual field in the widest meridian of the better eye

Monitor progression or improvement of eye disease

Guide for the rest of the exam (prediction of refractive error, correlation of data, determines additional testing)

o Always the first test performed after history

Exception: chemical burn/spill; irrigate first, then check VA

o Definition: the resolving power of the eye, or the ability to see two objects as separate

Normal resolving power is defined as the ability to detect a gap with a width of 1 min of arc

o VA is highest at the fovea and decreases with increasing retinal eccentricity

o VA best if pupil is 2-5 mm

o Types

Minimum Detectable Resolution (minimum visible): the ability to distinguish an object from its background

Minimum Separable Resolution (minimum resolvable): the ability to resolve two or more spatially separated targets

Gratings, bars, Vernier acuity, preferential looking

Recognition Resolution (minimum legible): the ability to recognize letters, numbers, and geometric forms

Snellen, Landolt C, Tumbling E

o Snellen acuity chart is the universal method of measuring VA

Snellen optotypes: width of each stroke is equal to the width of a gap on that line

Best letter is E (3 strokes and 2 gaps)

Not as good letters are T and L (no gaps)

At 20 feet, a 20 foot optotype subtends 5 min of arc

Its details each subtend 1 min of arc

20/20 letter is defined as a letter that has a height (x) such that it subtends 5 arc at 20 ft

Letter height can be altered with test distance

Details (gaps and strokes) each subtend 1 arc at 20 ft

Utilizes a folded room/operatory system

Projector with letters, 2 mirrors and a screen

Test distance= patient to mirror + mirror to screen

o MAR (minimum angle of resolution) in minutes of arc is equal to the reciprocal of the decimal acuity value or the Snellen fraction

Snellen fraction = 1/MAR

20 ft (6m) is considered optical infinity, which is defined as the distance at which no accommodation is being used

Snellen fraction = testing distance

distance at which the smallest letter read subtends an angle of 5 of arc

Also described as the distance at which a normal eye can see the smallest letter read by this patient

o Snellen equivalent is used when VA is taken at a distance other than 20 ft or when other nomenclature is used

It is better to report the actual acuity, not the equivalent

o Limitations:

Number of letters tested per line changes as you move down

Letter sizes between lines do not change by a constant ratio

Between row and between letter spacing is not proportional to the letter size

Legibility for optotypes often varies

o Standard Chart Specifications

Chart luminance: at least 10 foot lamberts

Chart contrast: at least 90%

Subdued room illumination to enhance chart contrast

Uncorrected refractive error is more likely to impact VA when pupils are slightly dilated

o Distance VA should be performed during ALL patient encounters

Procedure

Seat patient comfortably and dim lighting

VAs taken without correction(sc) and then with correction(cc)

o Minimizes chance of patient memorizing

Clean occluder with alcohol swab

Begin with full chart open and ask Which of these is the smallest line of letters that you can read?

Isolate smallest LOL that the patient can read; continue to scroll down to the next LOL and have patient read it; stop when the patient is unable to read the entire LOL

o Find the patients threshold

OBSERVE the patient (no squinting, cheating, leaning forward, etc)

o Observe the speed and degree of difficulty

Record VA as the smallest line in which not more than 2 letters were missed for OD, OS, OU

o The number at the end of each line signifies the level of acuity

o Some use several 20/20 lines to minimize memorization

o normal best-corrected VA is 20/20

Corrected visual acuity (best corrected VA) is measured with the best refractive correction in place

Habitual visual acuity is measured with patients own spectacles/CLs

o Near VA performed during full/comprehensive exam and if they have a near vision complaint

Procedure

Use full illumination: stand lamp on recording card

Done without, then with near correction

Measure the distance from the patients spectacle plane to the reading card in cm

Cover OS and instruct to Read the smallest paragraph that you are able to, switch to cover OD, and then remove to read with both eyes open

Re-measure the working distance with their correction

Record working distance (in meters!) over the smallest print read for OD, OS, OU

M system: a 1M letter subtends 5 of arc at 1 meter

Allows patient to hold card at their desired reading distance

Reduced Snellen system: gives the appearance of expressing the distance VA that is equivalent to the near VA

Should NOT be used for near VA (not appropriate to use a term that suggests a test at 20 ft when that distance is not relevant to near vision)

Jaeger system: indicates the size of the print by the letter J followed by a number

Poor system because there is no standardization of the Jaeger sizes and there is no intrinsic meaning to the J number

o Pinhole testing: a measure of potential visual acuity

Nullifies small amounts of refractive error by 1) increasing the depth of focus and 2) decreasing the size of the blur circles

Most effective diameter is 1.32 mm

If VA improves with pinhole, suggests that refractive error is probably the cause of the reduced VA

Done when entering acuities are 20/40 or worse (based on better VA)

Record PH followed by VA obtained

If no improvement, record PHNI

Super Pinhole, PAM (potential acuity measure) and laser interferometer are commonly used to determine potential VA before cataract surgery

o Brightness Acuity Test (BAT): used when you suspect acuity would be worse in a glare situation

VA with BAT is worse than without BAT for patients who have glare problems

o Alternative distance VA charts

OKN drum: cortical function only; objective test

Teller acuity cards: infants, non-responsive patients

Tumbling E: preschool, illiterate or non-verbal patients

LEA chart: children

Allen figures: children

Landolt C:

HOTV chart: amblyopes

Each letter is surrounded by crowding bars

Amblyopia: decreased VA (not correctable to 20/20) NOT due to pathology

o Snellen chart produces contour interactions (slow responses, some correct responses over a wide range of letter sizes, correct end-letter responses, out of order responses, perform better with isolated lines or letters)

Feinbloom chart: patients unable to see the 20/400 E on Snellen

Full illumination and test distance of 5 or 7 ft

Record test distance over smallest number size seen

o Alternative near VA charts (used during low vision)

Bailey-Love Chart: patients unable to see large print on other cards

Space between the letters is equal to the letter width (prevents crowding effect)

5 letters on each line

Between row spacing is equal to the height of the letters in the smaller row

Lighthouse cards

o Other measures of VA

Light perception (performed at ~ 1 ft)

LPP: light perception with projection

LPO: light perception only

NLP: no light perception

Hand motion (used as last ditch effort when Feinbloom efforts exhausted)

Count Fingers

Fix and follow: unresponsive patients

MUST ALWAYS ATTEMPT TAKING VISUAL ACUITIES

o Correlation of VA and refractive error

General rule: each 0.25DS of uncorrected refractive error accounts for ~ 1 line of Snellen VA

For cylinder, take spherical equivalent (sphere + ½ cyl)

For oblique axis, add a line for the axis

Patient must have NO accommodation or be cyclopleged

V Pupil Testing

o Pupil performs 3 primary functions

Controls entering light

Modifies depth of focus (inverse relationship)

Smaller pupil increases depth of focus

Varies optical aberrations (smaller has less aberrations)

o Should be performed during ANY patient encounter regarding eye health

Important because it is a neurological test that can detect optic nerve disease, brain mass and aneurysm

Gross examination can detect iris abnormalities, media opacities, and leukocoria

o Shape

Pupils should round and centered within the iris on optic axis

Irides should be of the same color

Abnormalities

o Corectopia: displaced or misshapen pupil

o Ectopic pupil: significantly decentered

o Polycoria: more than one pupil

o Heterochromia: iris color different between eyes or between different areas in one eye

o Aniridia: absence of iris, therefore non-existent pupil

o Size

Average of 3.5 mm in adults under normal illumination

Become smaller after adolescence due to senile miosis

Should equal one another within 1 mm

Anisocoria: unequal pupil size

20 % have physiologic anisocoria

Controlled by the autonomic nervous system

Iris dilator muscleà dilates; sympathetic innervation

Iris sphincter muscleà constricts; parasympathetic innervation

o Pupillary pathways

Afferent

Light enters pupilà impulse in retina (PR and ganglion cells)à optic nerveà optic chiasm: ½ cross, ½ ipsilateralà optic tracts to superior colliculià pretectal nuclei of hypothalamusà crossed and uncrossed fibers to EWà synapse with efferent fibers

Parasympathetic efferent

From EW nucleus travels with CN III (inferior division)à cavernous sinusà pierces globeà deviates from CN III and synapses at ciliary ganglionà postganglionic fibers reach iris sphincter via short ciliary nerves

o 97 % of the fibers control accommodation (ciliary body)

o Only 3 % innervate the sphincter

Sympathetic efferent

Hypothalamusà synapses at ciliospinal center of Budge (C8-T4)à 2nd order neurons leave spinal cord ascending close to the apex of lungà synapses at superior cervical ganglionà 3rd order neurons follow the ICAs to the globeà iris dilator via the long ciliary nerves

Sympathetic innervation reaches Mullers muscle in upper lids

o Response to light

Miosis (=constriction) occurs via parasympathetic innervation

Some latency in initial constriction is normal (depends on brightness and age)

Direct response: response that occurs in one eye while the light is shone in that eye

Consensual response: response that occurs in one eye while the light is shone in the other eye

Pupillary escape: gradual and partial re-dilation without change in light intensity

Pupillary unrest or hippus: small oscillations in pupillary diameter that occur during maintained stimulation

Due to normal fluctuation in sym/parasym equilibrium

o Response to near

Independent of retinal illumination

Near reflex is ALWAYS present when direct light reflex is intact

Near triad: pupil constriction, convergence, accommodation

o Swinging flashlight test

Compares the strength of the direct pupillary response with that of the consensual response

Detects afferent pupillary defect due to retinal abnormalities or optic nerve pathway anterior to LGN (APD or RAPD)

o Procedure

Remove spectacles and examiner positioned off to one side

Use a distant, non-accommodative target (2-3 lines above VA)

Measure pupil size under normal lighting conditions

Expected findings: should equal one another

o Size in bright: 2-4mm Size in dark: 4-8mm

If pupils are unequal, measure size in both dark and bright light

To visualize dark irides, use:

o Burton lamp: hold ~25 cm (10in) from the patients and below the patients line of sight

o Ophthalmoscope: use as a dim flashlight to illuminate both eyes simultaneously (light from below)

Judge the roundness of each pupil and describe any abnormalities

Observe pupils response to light in dim illumination

Note the magnitude of change (quantity) using scale 0-3

Note the rapidity of reaction (quality) using slow (-) or fast (+)

Expected findings

o Direct response of OD should equal direct response of OS

o Consensual response of OD should equal consensual response of OS

o Direct response of OD should equal consensual response of OD

Perform the swinging flashlight test

Expected findings

o Rate and amount of constriction should be the same for both pupils

o Direct should equal consensual for both eyes

If it is not the case for either eye: afferent pupillary defect in the eye with less constriction

Record using PERRLA (-) APD if all reflexes are normal

PE: pupils equal

R: round

RL: reactive to light (direct and consensual)

A: responsive to accommodation

(-) APD: no APD

o Afferent pupil anomalies result in an APD

Severe retinal disease, optic nerve diseases or compromise, mass/lesion behind eye compressing optic nerve or chiasm

NOT with disorders of ocular media

Afferent pupillary defect (RAPD) indicates unilateral or asymmetric damage to the anterior visual pathways

When the consensual response is greater than the direct response of one eye

If present, pupils of both eyes will constrict less when the light is directed into the affected eye

o Both eyes will constrict when light beam directed into unaffected eye

When light beam is directed in affected eye, causes less constriction in

o Affected eye: reduced direct reflex

o Unaffected eye: reduced consensual reflex

Graded from trace to 4+

o 3-4+APD: immediate dilation of the pupil, instead of initial/equal constriction

o 1-2+APD: no change in pupil size immediately, followed by dilation

o Trace APD: initial constriction, but greater escape to a larger intermediate size than when light is swung back to normal eye

Amaurotic Pupil: severe or 4+APD

Patients have an eye with NLP

Light beam directed into affected eyeà no direct response in affected eye and no consensual response in unaffected

Light beam directed into unaffected eyeà direct response in unaffected eye and consensual response in affected eye

Near reflexes will be intact

Reverse (indirect) APD

Performed when one pupil is fixed, dilated, or constricted

o ONLY observe the reactive pupil

If APD in eye with reactive pupil, that pupil will constrict more with consensual stimulation than with direct

If APD in eye with fixed pupil, the reactive pupil will constrict more with direct stimulation than with consensual

Note reverse APD (implies you used a reverse technique)

o Efferent pupil anomalies: unilateral defects/lesions will often generate anisocoria

Anisocoria: usually 2-4 mm difference in dark and light

If same degree of anisocoria in light and dark: physiologic

Big pupil problems: anisocoria greater under bright conditions due to a defect/lesion of the parasympathetic

Adies tonic pupil

o Relatively common; primarily in females 20-40

o Presentation

Unilateral semi-dilated pupil

Pupil with minimal and slow reaction to light

Pupil with reduced direct, consensual (poor constriction of sphincter) and near responses to light

May present with a reduced near vision complaint

Vermiform motion of iris: quivering motion of iris at pupillary border due to segmental palsy of sphincter

10-20% eventually affecting other eye

Reduced direct response to light bilaterally

Decreased near VA

Prolonged pupil cycle time

o Etiology

Lesion of the parasympathetic pathway (ciliary ganglion) on the side of the pupil problem

Viral

o Diagnosis

0.125% pilocarpine (wait 10-15 min)

Constriction: Adies confirmed

No constriction: either pharmacologic or 3rd nerve

o Management

Rule other orbital and ocular conditions

Cosmesis

Accommodation

Near add, sometimes unequal adds

Equalize accommodation during refraction and other near or binocular testing

Accommodation generally returns within 2 yrs

Cranial Nerve Palsy

o Presentation

EOM paresisexotropia and hypertropia (down and out) of eye affected

Ptosis

Fixed and dilated pupil, or non-reactive pupil

o Etiology

Pupil fibers are on the outside of CN III; they are involved early in a compressive lesion and are rarely involved in an ischemic infarction

Lesions that involve the pupil: tumor and aneurysm

Lesions that spare the pupil: vascular disease causing ischemia (diabetes, hypertension)

o Diagnosis

0.125% pilocarpinewill NOT constrict

1% pilocarpineWILL constrict

o Management

Presentation of acute 3rd nerve palsy with pupil involvement considered a medical emergency!

Manage diplopia and systemic cause of palsy

Pharmacologic anisocoria: dilation of one eye

o Presentation

Usually unilateral, fixed and dilated pupil

Anticholinergic substances block the action of acetylcholine on the ciliary muscle and cause mydriasis

o Etiology

Scopolamine

Jimsonweed

Antihistamine drops

Atropine, homatropine, cyclopentalate

o Diagnosis

0.125% pilocarpineWill NOT constrict

1% pilocarpineWill NOT constrict

o Management

Reassurance and patient education

Little pupil problems: anisocoria is greater in dim conditions due to a defect/lesion to the sympathetic nervous system

Horners syndrome

o Presentation

Miosis (can be mild: less than 1 mm of anisocoria)

Ptosis

Anhydrosis

***All on the same side as the lesion***

o Etiology

Interruption of the sympathetic system anywhere in its path

Congenital Horners: idiopathic or trauma at birth

Heterochromia and anhydrosis

Central lesions: stroke, MS, spinal cord cancer, neck trauma

Preganglionic lesions: pancoast tumor, trauma, thyroid enlargement or lesion

Postganglionic lesions: extracranial or intracranial cause (Raeders, ICA dissection, complicated otitis media)

o Diagnosis

Look at old photographs

History of trauma, endardectomy, thyroidectomy?

Dilation lag test

Take picture immediately after turning off lights and take another picture 15 seconds

Horners pupil has a dilation lag in the dark of ~15 sec

0.5% Apraclonidine (Iopidine) (wait 15-30 min)

Dilates: confirms diagnosis of Horners

10% Cocaine drop in affected pupil (wait 15 min)

Does NOT dilate: confirms diagnosis of Horners

o Management

Important to determine before or after the bifurcation of the carotid artery

Differentiate by testing for anhydrosis (prism bar test and corn starch under heat lamp)

Postganglionic lesions generally do not cause anhydrosis

1 % hydroxyamphetamine (done 48 hrs after cocaine test)

o Dilation: central or preganglionic lesion

o No dilation: postganglionic (fail safe affected pupil fails to dilate)

Argyll-Robertson pupil

o Presentation

Bilaterally miotic, irregular pupils

Difficult to dilate

Direct and consensual responses absent or sluggish in affected eye(s)

DOES react to near (there is light-near dissociation)

o Etiology

Midbrain lesion

Neurosyphilis or neuropathy from diabetes, alcoholism

Pharmacologic anisocoria: constriction of one eye

o Cholinergic agents: pilocarpine (glaucoma drop) and physostigmine

o Near-Light Dissociation: pupils fail to respond to light, but near response intact

Afferent pathways interrupted, efferent pathways intact

Examples of conditions that manifest near-light dissociation

Neurosyphilis: Argyll-Robertson pupil

APD or amaurotic pupil

Aberrant regenerations

o Pupil Irregularities

Aniridia: congenital absence of the iris (usually bilateral)

Iris coloboma (keyhole pupil)

Usually involves the inferior nasal portion of the iris

Wider at the pupillary margin than at the iris root

Corectopia: displaced pupil (frequently bilateral)

May be displaced in any direction

Iridectomy: surgically created sector cut of the iris

Iris atrophy

From age, inflammation, ischemia, trauma

Iris holes may form creating polycoria

May be sectoral (herpes zoster) or widespread

Iris cysts/tumors

If extensive enough, may distort pupillary margins

Laser iridotomy: hole created in iris usually located superiorly at 10:00 or 12:00

Shape of the pupil usually not affected

Persistent pupillary membrane (PPM): persistent embryolic structure

Rarely affects pupillary movement

Trauma

Tears of pupillary margin and sphincter

o Traumatic mydriasis and abnormal pupil light reflexes permanent

Iridodialysis

o Tear at the iris root; D-shaped pupil

o Monocular diplopia may occur

Posterior synechia: attachment of iris to anterior lens surface from active or history of anterior uveitis or intraocular inflammation

Iridonesis: quivering of the iris

Pupillary margins are irregular and reactivity will be reduced

Seen in aphakic patients

o Pharmacologic dilation (bilateral)

Anticholinergics

Antihistamines

CNS depressants

Sympathomimetis and CNS stimulants (bind with alpha receptors on dilator muscle to cause mydriasis)

Epinephrine, Cocaine, amphetamines

o Pharmacologic constriction (bilateral)

Barbituates

Opioids

Levodopa

Marijuana

Vitamin A

V EOM Testing

O Saccades

Rapid abrupt conjugate movement; stimulated by alternately fixating objects

Can be voluntary or reflex

O Pursuits (Versions)

Slower smooth conjugate movements; stimulated by target movements

Used to test binocular, conjugate movements of the eyes allowing the lines of sight (LOS) to move in a parallel direction (or fixed angle)

o EOM

Innervation

CN VI (abducens): LR

CN IV (trochlear): SO

CN III (oculomotor): MR, SR, IR, IO

Planes of action

LR and MR: horizontal plane

SR and IR: vertical plane, 23-25 temporal

SO and IO: vertical plane, 51-53 nasal

Muscle paresis is most obvious when the LOS is directed to move the eye in the direction of its primary action within its plane of action

Synergistic muscles: muscles in same eye that assist in an action

Antagonistic muscles: muscles in same eye that have opposite actions

Yoked muscles: neurologically paired in opposite eyes

Herings Law of Equal Innervation

o Procedure

Remove spectacles and use high illumination

Fixation target held ~40 cm from patients eyes

Instruct patient to follow light as its moved in H pattern

Make sure you test to the extreme field of gaze (limit of the EOM)

Note any overactions (+) or underactions (-); perform ductions

Ductions are monocular eye movements into the 6 cardinal positions of gaze

Identifies the faulty muscle(s)

Can test each muscle in its field/plane of action

Parks 3-step used for hyper deviations to determine faulty muscle

Record EOM: full and smooth (F and S)

FROM: full range of motion

SAFE: smooth accurate full extent

** Also record if ductions=versions, etc**

V Stereopsis

o Stereopsis: the perception of 3-D visual space due to binocular disparity cues (disparities of the two retinal images)

o 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

o 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

o 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

o 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

o Thresholds stereopsis

o Most accurate

o Two types of testing: null threshold and JND

Titmus Stereofly

o Linear polarized test

o 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

o Uses 3-D cross polarized spectacles

o 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

o Left side: modified circles (400 20), animals (400 100)

o 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

V Color Vision

o Three types of cones responsible for color vision

Each contain photopigments that maximally absorb different wavelengths

Red (long), green (middle), blue (short)

o Defects

Protan: red wavelength (L cones)

Deutan: green wavelength (M cones)

Tritan: blue wavelength (S cones)

o 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

o True color blindness (may have few cones but abnormal in shape) and poor vision

Cone

o 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

 

o Prevalence

Overall 4%

Males 8%

o Protanomaly 1% Protanopia 1%

o Deuteranolamly 5% Deutranopia 1.1%

o Tritanopia 0.002%

Females 0.5%

o Patient selection

Children at an early age

Patients at initial office visit

Unexplained decreased in VA

Report changes in color vision

Abnormal fundus findings

o Types of color vision tests

Color Naming

Color Mixing

Anomaloscope

o Assess ability to make metameric matches

o Change mixture of monochromatic red and green

Color Confusion

Pseudoisochromatic plates (PIC)

o Diagnostic plates: figure is isochromatic for one defect but not for another so it identifies type of deficiency

o Vanishing figure: normal sees, defective does not see

o Transformation: normal and defective see different figures

o Hidden digit/symbol: defective sees, normal does not see

o Screening mostly for inherited defects

HRR

o Detects inherited and acquired defects

o Can be used on illiterate patients (symbols used)

Ishihara

o Screen for inherited red/green anomalies

Color Matching (arrangement)

Detects inherited or acquired

Farnsworth D-15

o Quantifies depth of defect (mild/severe)

o Used only as diagnostic (not screener)

Farnsworth-Munsell 100-Hue

o Good for detecting/classifying early acquired color deficiencies caused by ocular disease

o Detects subtle color discrimination

Occupational

PIC, D-15, Farnsworth Lantern test (FALANT), ISCC Color Matching Aptitude test

o 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

o If ALL 6 correct: normal CV

o Only plate 5 or 6 missedà test plates 21-24: B/Y defect

o Only 1 or more plates 7-10 missedà 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

o Normal if 10/1l

o If </= 7 correct, test plates 12,13,14 to classify whether protan or deutan

Farnsworth D-15

Caps should be 45 deg to patients 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**

o Management

Rod chromatism (poor VA and photophobia)

Tinted lenses (red and amber) to obtain low scotopic luminance transmittance but decreased visibility in short wavelengths

Acquired defects should be directed to cause

Inherited defects: counseling, career limitations

V Cover Test

o Fusion: both eyes are looking at the same target at the same time

o Alignment

Orthophoria (ortho): normal, both eyes fixate on the same spot even after you break fusion

o Misalignment

Tropia (strabismus): manifest deviation of the line of sight of one eye

The LOS of one eye is directed toward the object and the LOS of the other eye is directed elsewhere

If the eye is misaligned outward it is called exotropia

o Will move in when the other eye is covered

If the eye is misaligned inward it is called esotropia

o Will move out when the other eye is covered

If the eye is misaligned upward it is called hypertropia

o Will move down when the other eye is covered

If the eye is misaligned downward it is called hypotropia

o Will move up when the other eye is covered

Patient may have symptoms such as double vision, eye strain, headaches, fatigue, and reduced stereo

Phoria: latent deviation of the LOS

Eye aligned except when fusion is disrupted

o Bruchner: observe the red reflex from the retina with the ophthalmoscope to detect leukocoria, strabismus, or anisometropia

o Hirschburg: use the transilluminator to find the corneal light reflex

To see 1 mm, patient must have 22 diopters

o Krimsky: perform Hirschburg and line up the corneal light reflex with prism

o Cover Test: objective test to determine the presence, amount, and direction of misalignment

Unilateral cover test (cover-uncover): detects tropia

Alternating cover test: to detect phoria and measure amount of tropia

o Procedure

Unilateral

Distance: patient fixates on a letter that is one line larger than the best VA of the worst eye

Near: patient uses a fixation stick with a small accommodative target

o Done at 40 cm or working distance

Important to come from the nose

Clinician covers OD and watches OS for movement; then covers OS and watches OD for movement

o Presence of movement indicates strabismus or tropia

Alternating

Patient still fixates a target

Clinician covers OD for 2 sec, then swings cover paddle from one eye to next

Do NOT allow patient to view with both eyes at the same time

o Presence of movement on alternating but not on unilateral indicates phoria

o If there is movement on both unilateral and alternating, it is a tropia (tropia trumps a phoria)

o If there is no movement on both unilateral and alternating, check with 4 BI and 4 BO and there should be equal and opposite movements

o Measuring magnitude

Prisms deviate the image towards the apex

Exos need the image sent OUT---- use base IN

Esos need the image sent IN---- use base OUT

Hypers need the image sent UP---- use base DOWN

Hypos need the image sent DOWN---- use base UP

Procedure

Put the prism behind the cover paddle and place in front of the eye at the same time

o For eso and exo, put prism in front of either eye

o For hyper and hypo, put prism in front of deviated eye

Move occluder to other eye without allowing binocular fixation

Increase prism amount without allowing binocular fixation until movement stops=neutrality

Continue to increase amount until the direction of the movement reverses

Record amount of prism that resulted in neutrality before reversal

o Recording

Orthophoria (lack of manifest or latent deviation)

Horizontally ortho

Vertically ortho

Ortho both horizontally and vertically

Magnitude: prism diopters

Direction: exo (X), eso (E), hyper, hypo*

Only name the hypo eye if it also has a horizontal constant tropia

Laterality: right (R), left (L), alternating (A)

Note the fixation preference

Frequency: constant (C) or intermittent (I)

If intermittent, write down percentage

Nature: comitant or incomitant

Use 9-gaze test or Parks 3-step test

Also note: Testing distance, cc or sc

Normal: Distance 1 XP + 2 Near 3 XP + 3

o Duanes Classifications

Basic: <8 Δ difference between distance and near

Distance vs. Near Deviations

Convergence Insufficiency

o Exo at near > distance

Convergence Excess

o Eso at near > distance

Divergence Insufficiency

o Eso at distance > near

Divergence Excess

o Exo at distance > near

V Blood Pressure

o Important to do routine BP measurements:

Elevated blood pressure increase the risk of coronary heart disease, stroke, and kidney failure

Silent killer since you cannot tell by the way you feel

Patients will often seek eye care before other health care

HTN can result in significant visual morbidity

o Risk Factors for HTN

Smoking, high cholesterol, obesity, diabetes, age (elderly), family history, race (African-Americans), gender (male) and stress

o Systolic pressure: ventricular contraction

o Diastolic pressure: ventricular relaxation

O Korotkoff Sounds

Phase 1: appearance of clear taping sounds (systolic)

Phase 2: swishing of sounds

Phase 3: increase clear sounds, increase intensity

Phase 4: abrupt muffling of sounds (diastolic I)

Phase 5: complete disappearance of sound (diastolic II)

Auscultatory gap: early, temporary disappearance of sound between phase 1 and 2 that can cause serious underestimation of systolic (or overestimation of diastolic pressure)

o Procedure

Patient should be seated and relaxed with legs uncrossed

Patients arm should be slightly bent, resting on the arm rest with palm up and unrestricted baring of arm

Palpate for systolic pressure

Place cuff ~1 above antecubital crease

Palpate the radial artery at wrist using fore finger and middle finger

Inflate cuff to ~30mmHg above level at which the pulse disappears

Note reading and deflate cuff

Place diaphragm over brachial artery between the crease and the lower edge of the cuff

Inflate cuff to 30 mmHg above systolic (determined by palpation)

Deflate at a rate of 2-3 mmHg/sec

Listen for phase 1 sound (regular tapping sound)

Note reading: systolic pressure

Continue deflation and listen for phase 5 (complete disappearance of sound)

Note reading: diastolic pressure

If sounds are too weak, ask patient to open and clench fist ~10x or inflate cuff quickly

Repeated inflation will cause venous engorgement and decrease sounds

Deflate cuff and remove

Record: systolic/ diastolic, arm used, posture, time of day, and cuff size if other than regular

o Sources of Error

Falsely High

Brachial artery below heart level

Asucultatory gap (diastolic)

Cuff too small

Anxiety or fear

Isolated sources: anxiety, stress, recent exertion, pain, caffeine

Falsely Low

Brachial artery above heart level

Asucultatory gap (systolic)

Cuff too large

Deflating too rapidly

Hypertension Classification

Pressure Normal BP Pre-hypertension Stage I Stage II
Systolic   Diastolic < 120   < 80 120-139   80-89 140-159   90-99 > 160   > 100

Referral Guidelines

Initial Screening Blood Pressure (mmHg)  
Systolic Diastolic Follow-Up Recommended
   
<130 <85 Recheck in 2 yrs
130-139 85-89 Recheck in 1 yr
140-159 90-99 Confirm within 2 months
160-179 100-109 Evaluate or refer to source of care within 1mo
180-209 110-119 Evaluate or refer to source of care within 1 wk
> 210 > 120 Evaluate or refer to source of care immediately

 





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