Opto 2.0 Flashcards

1
Q

What are the 7 essentials of an eye exam

What parts are examined at a minimum

A

DIPLOMA
Depth IOP Pupils Lamp Ophthalmoscopy Motility Acuity

P-DIVE
Pupil Direct ophth IOP VA EOM

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2
Q

Eyelids are AKA, seperated by ? and meet at the ?

What are their two functions

What structures do they contain

A

Palpebrae, Palpebral fissure, Canthus

Protection
Lacrimal aid- spread new/pump old

Meibomian glands

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3
Q

3 muscles located w/in the eyelid:
Function and innervation of Orbicularis Oculi muscle

Function and innervation of Levator Palpebrae Superioris muscle

Function and innervation of Mueller’s Muscle

A

Closes eyelid, CN7

Opens upper eyelid, CN 3

Opens upper/lower lid during fear/surprise via sympathetic ANS

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4
Q

What are the 3 spheres (tunics) of the globe

Define Cornea

Define Limbus

A

Fibrous Vascular Nervous

Front window of eye, 2/3 of eye refractive surface (other 1/3- lens)

Sclera and cornea junction

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5
Q

What are the two muscle of the pupil what innervates each muscle

Define Conjunctiva and the two types

Define the Ciliary Body

A

Sphincter- Parasympathetic ANS
Dilator- Sympathetic ANS

Clear membrane covering
Palpebral- eyelid
Bulbar- sclera

Produces aqueous humor
Contains ciliary muscles- alter zonular to change lens

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6
Q

What is the main function of the Ciliary Muscles

Define Choroid

What does this structure provide blood to

A

Near focus- accommodation

Pigmented and vascular layer between retina and sclera, provides blood to retina

Outer retinal layer

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7
Q

Where is the Anterior Chamber located and what does it contain

Where is the Posterior Chamber located and what is it filled with

What shape is the lens and what structures keep is suspended

A

Between cornea and iris- aqueous humor and drainage

Behind iris, in front of vitreous
Aqueous humor

Biconvex; Zonules

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8
Q

Vitreous Humor is transparent gel made of ?

What function does it perform

Retina is the ? liner and referred to as the ?

A

Collagen Protein Hyaluronic Water

Maintains structures

Neural lining, fundus

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9
Q

How many layers of the retina are there

What structures are contained here

What are the two types

A

10 layers, 9 are transparent

Photoreceptors- send signals to brain

Cones- color, visual acuity (6mill/eye)
Rods- black/white, night vision (120M/eye)

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10
Q

Define the Macula and it’s function

What is the name of the central depression in the macula

What is contained here

A

Posterior pole of retina- fine, central vision

Fovea- 4mm temporal and 0.8mm inferior to optic nerve

Mostly cones, 1/3 of all nerve fibers

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11
Q

Define the Optic Disc

What is the Disc AKA

What are the extra-ocular muscles

A

Nerve/vessels converge and leave eye

Physiologic/anatomic blind spot x 15* temporal

4 rectus (Superior Lateral Inferior Medial)
2 obliques (Superior Inferior)
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12
Q

What movements are the 6 extra-ocular muscles in charge of

What is the term that describes how these muscles work

A
IO: extortion, elevation
SO: intorsion, depression
SR: elevation
LR: abduction
IR: depression
MR: adduction

In tandem, yoked: ipsilateral opposing muscle relaxes

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13
Q

What are the 3 layers of tears from out to in and where is each layer made?

What type of pathway is the optic nerve?

What type is the oculomotor and parasympathetic?

A

Oil- outer, from meibomian glands
Water- middle, from lacrimal glands
Mucin- inner, Goblet cells

Optic= Afferent

OM+P= Efferent

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14
Q

Define Double Decussation

Where does this chiasm occur in the brain

When conducting an exam, what is the next step if vision is >20/40 and why?

A

Direct and Consensual response

Pretectal /Edinger-Westphal nuclei

Pinhole- establishes visual potential w/ or w/out glasses

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15
Q

What eye is tested first during VA

What are the next tests done if Pt can’t read chart

If Pt or chart have to be moved, what does 20/20 at 10ft equal to?

A

Right (OD), w/ correction if applicable

Count Motion Light None

20/20 at 10ft (on 20ft chart)= 20/40

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16
Q

When is Near Visual Acuity testing preferred

What distance is this method conducted at

What do abbreviations cc and sc mean?

A

Bed-ridden Pt

14-16”

cc- w/ correction
sc- w/out correction

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17
Q

What does this stand for- “DVA cc 20/20 OD, 20/40 OS”

Define Visual Impairment

Define Visual Disability

A

Distance Visual Acuity w/ correction 20/20 right eye, 20/40 left eye

Condition of the eye

Condition of individual

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18
Q
Visual Impairment to Visual Disability:
20/12 to 20/20= 
20/25 to 20/70= 
20/80 to 20/160=
20/200 to 20/400 - CF 10ft= 
CF 8ft to 4ft=
A
20/12 to 20/20= normal 
20/25 to 20/70= near normal
20/80 to 20/160= moderate low
20/200 to 20/400 - CF 10ft= severe low/legally blind
CF 8ft to 4ft= profound low
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19
Q

AF and Army flight physicals have ? many cardinal points

What are the 3 things being evaluated for

Why is dilated ophthalmoscopy not done if PT has shallow anterior chamber depth

A

AF- 6
Army- 8, add up/down

Paralysis Entrapment Weakness

Triggers angle closure glaucoma crisis

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20
Q

Medications used for dilation are called ?

What two effects do they cause

What are examples of each kind and how long they last

A

Mydriatics

Adrenergic stimulating- stimulate iris dilator
Cholinergic blocking- paralyze iris sphincter

Adrenergic: Phenylephrine- 3hrs

Cholinergic: max 20-30/45/90/45/40
Tropicamide- 2-6hrs
Cyclopentolate- 24hrs
Homatropine- 2-3 days 
Scopolamine- 4-7 days
Atropine- 1-2wks
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21
Q

When conducting ophthalmoscopy, what are the five structures being assessed

Normal IOP range

What are the two ways to measure IOP

A

Macula
Red reflex
Optic disc (physiologic cup)
Retinal circulation/background

10-21mmHg

Hand held tono-pen w/ anesthetic (latex allergy check)
Non-contact tonometry (air puff)

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22
Q

How is Anterior Chamber Depth assessed

What finding indicates a shallow chamber is present

This means Pts are at risk for ?

A

Shine light from temporal side

2/3 or more of iris in shadow= shallow chamber d/t iris bowing forward

Angle-closure glaucoma

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23
Q

Define Emmetropia

Define Hyperopia

Define Myopia

A

Normal, objects at infinity are seen clearly w/ unaccommodating eye

Far sight, axial length is short, image falls behind retina

Near sight, axial length is long, image falls before retina

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24
Q

Define Astigmatism

Define Presbyopia

What type of laser is used during SMILE eye surgery procedures

A

Elliptical, refracting power of cornea and lens different across meridians (horizontal, vertical)

Loss of accommodation, progressive lens hardening prevent focus on near objects

Femto

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25
Q

How are visual disorders Tx w/ corneal refractive surgery

Why would Intacs be placed in eyes

Corneal Cross-linking procedures use ?

A

Conductive keratoplasty
Lasers (PRK LASIK SMILE)
Radial keratotomy

Irregular cornea

Riboflavin

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26
Q

What is a surgical complication from LASIK

Folds in the flap after surgery may cause eye problems depending on ? category

What is the equation for glasses Rx

A

Flap button holes- microkeratome
Complete, De-centered, Folds

Macro/Micro-striae

(Sphere) - (Cylinder) x (Axis)

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27
Q

What is the difference in Glasses Rx sphere

What is a cylinder used to correct

What does axis mean

A

Myopia (-)
Hyperopia (+)

Astigmatism

Astigmatism orientation in eye

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28
Q

What are the 3 types of eye deviations

When a tropia is congenital, what happens with the difference of eyes

A

Orthophoria- no deviation, eyes point in same direction w/ eyes open and closed

Heterophoria (phoria)- normal deviation, not present on un/cover, seen w/ alternating cover/uncover. Covered eye deviates (fusion broken)

Heterotropia (phoria)- both eyes deviated, seen w/ un/cover test

One eye suppressed to prevent diplopia development
Deviated most will have amblyopia (worse vision)

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29
Q

Phoria and Tropia AKA while ? prefix is not used when naming phorias

Define Strabismus and how is it confirmed on PE

Define Concomitant Strabismus

A

Phoria- latent
Tropia- manifest
Hypo- reference hyper eye

Misalignment of eyes, Cover-Uncover Test or Hirschberg

Non-paralytic- misalignment equal in all directions;
Leads to amblyopia and bad VA

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30
Q

Define Incomitant Strabismus

How are these tropias induced from vasculopathic tumors identified on PE depending on the cause

A

Misaligment of eyes varies w/ direction of gaze d/t nerve/mechanical restrictions

CN3: aneurysm; R eye straight, L eye down/out and dilated
CN4: congenital/trauma; R eye horizontally abducted, L eye horizontally adducted
CN6: cranial pressure; R eye straight, L eye adducted

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31
Q

Define Nystagmus and how many are there

Many Pts w/ this will suffer from ?

Nystagmus is classified into ? two general types

A

Involuntary oscillation of eye; 45 types

Partial sightedness or legally blind

Physiological- normally evoked
Pathological- congenital (<6mon) acquired (>6mon)

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32
Q

Nystagmus can also be classified by ? two movement patterns

What is the work up process for a nystagmus

How are these Tx

A

Pendular- equally paced in each direction
Jerk- slow drift w/ rapid return to origin

Hx (Drug Infancy Vertigo ETOH TBI FamHx)
Ocular exam w/ Ophth referral
Toxin screen
CT/MRI

Alternating nystagmus= Baclofen; not for Ped Pts
Severe/disabling= retrobulbar injection w/ botulinum

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33
Q

Define Amblyopia

What are the etiologies of Amblyopia

A

Defective vision w/out anatomic damage; “Lazy Eye”

Occlusion- ptosis, incorrect patching, cataracts

Refractive- anisometropia: large refractive difference

Strabismus- deviated eye becomes amblyopic

Organic- toxin, nutrional

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34
Q

How are suspected amblyopias worked up by age of identificaiton

What is a DDx that needs to be considered and what PE finding will be poor in these Pts

What vision result is of low concern

A

<2y/o= function
2-5y/o= VA w/ picture cards
Strabismus w/ light reflex/cover test

Epicanthus
Red reflex

2-5y/o w/ VA 20/40 w/ equal eyes

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35
Q

How are amblyopias Tx

A

Refractive- hyperopia more common; place image on retina

Obstruction: ptosis/cataract/scar correction

Strabismus: atropine/patch better eye 2-6hrs/day;
>11y/o- polycarbonate contact in good eye
Surgical correction w/ eyes are equal

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36
Q

What two structures are lateral to the medial canthus?

Define Ectropion and Entropion

Both can have ? Sxs d/t ? issues

A

Canthus - Caruncle - Plica semi-lunaris

Ect: Outward turning of lid
En: Inward turning of lid

Foreign Irritation Tearing Burning
Ect: punctual malposition
En: lashes abrading globe

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37
Q

What are the etiologies of Ec/Entropions

Both are Tx w/ ?

A
Ect: 
Paralytic- CN7
Involution- lower lid lag d/t age
Cicatricial- lower lid scar
Mechanical- mass on lower lid

Ent:
Involutional- lower lid lag d/t age
Cicatricial- scarring on conjunctival surface

Tx w/ surgery

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38
Q

Define Lagophthalmos

What are the Sxs Pts present w/ and why

What signs will be seen on PE

A

Inability to close eyes

Burning Foreign Irritation Tears- failure of lacrimal pump

Inability to close eyes
Exposure keratopathy

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39
Q

What are the etiologies of Lagophthalmos

How are these Tx

A
Proptosis
Age induced lid laxity
CN7 palsy (Bells palsy)
Trauma scars
Surgical correction of ptosis/blepharoplasty

Mild: tears/gel/ointment w/ tape at bedtime
Mod-Sev: Tarsorrhaphy until definitive gold weight surgically placed in upper lid

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40
Q

Define Ptosis

What Sxs do Pts present w/

What are the etiologies of this condition

A

Drooping upper lid

Obstructions
Cosmetics
Difficulty reading
Secondary amblyopia in kids

Myasthenia gravis- worse w/ upgaze
Acquired (levator aponeurosis)
Congenital malformation (levator muscle)
Horners (Miosis Anhidrosis Ptosis)
3CN palsy w/ opthalmoplegia
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41
Q

How is Ptosis Tx

Define Blepharitis

What are the presenting Sxs

A

Tx primary condition
Congenital/Acquired- surgery tightens aponeurosis or resects levator muscle

Scaling of lid margins proximal to lashes

Burning Blurred Photophobia Irritation Epiphoria- excess tearing

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42
Q

What are the signs of blepharitis

What are the MC causes

A
Dandruff
Erythema of lid margin
Recurrent/mild conjunctivitis
Manipulated meibomian glands
Lost lashes
Scales

Demodex- mites
Meibomian dysfunction- chalazia
Seborrhea- brow/scalp dandruff
Staph- hordeola

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43
Q

How is blepharitis Tx

Hordeolums are AKA ? and present as ?

A
Daily baby shampoo lid scrubs
Warm compress x 10min w/ massage
ABX: 
Erythromycin (Staph infection)
Doxy (Meibomian dysfunction)- 1/4 dose taper over 6mon

Stye- painful nodule/pustule on lids

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44
Q

What are the signs of Hordeolums

What are the etiologies

How are these Tx

A

Erythematous nodule external to skin/internal to conjunctiva

Staph infection involving sebaceous glands

PO Doxy if w/ blepharitis
Erythromycin ointment
Warm compress w/ massage
Surgical incision- compress/ABX fail x 4wks or,
Pt requests rapid relief
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45
Q

What are the risks of performing surgical excision of hordeolum (styes)

What are the etiologies of chalazions

What are the S/Sxs

A

Scarring leading to en/ectropion

Lipogranulomatous inflammation from meibomian gland obstruction

Mildly tender, firm, demarcated lid nodule
Grayish discoloration on conjunctival surface

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46
Q

How are chalazions Tx

Define Dacryocystitis

What are the S/Sxs of Dacryocystitis

A

Warm compress w/ massage
Triamcinolone injection if persists x 4wks (c/i dark Pts)
Surgery- no resolution x 1mon= incision and curettage of meibomian gland

Inflammation of lacrimal sac

Mucopurluent d/c
Erythema
Painful tearing
Cellulitis, pre-septal

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47
Q

What are the etiologies of Dacryocystitis

How are these Tx or when is admission needed

When is surgical intervention needed and what is the name of the procedure

A

Bacterial infection
Nasolacrimal duct obstructed

Fever= IV ABX and admit
Warm compress w/ massage
Augmentin 500mg q8hrs
InD if large
Topical drops w/ PO ABX

Chronic or once acute episode is over:
Dacrycystorhinostomy- creates anastomosis between lacrimal sac and nasal mucosa via bony ostium

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48
Q

Define Dacryoadenitis

What are the S/Sxs

What is the un/common and rare etiologies

A

Inflamed lacrimal gland

Pain
Erythematous
Lateral lid swelling
Tearing

Common: Idiopathic
Uncommon: Autoimmune (Sacoidosis Vasculitis Sjogrens)
Rare: bacteria/viral (Mono/Mumps)

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49
Q

How is Dacryoadenitis worked up

How are these cases Tx

A

Autoimmune Hx
CT of orbit
Lacrimal gland biopsy

Unsure etiology= Systemic ABX w/ reassess x24hrs
Inflammation: Tx w/ PO steroids, response should be <48hrs
Infectious: Augmentin 250-500mg q8hrs or,
Cephalexin 250-500 q6hrs

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50
Q

? are the more common types of carinomas to affect the lids

Pts usually present w/ ? c/c

These are usually Tx by

A

B/SCC

ASx

Mohs removal (Basal)
Radiation- unwilling/able to have surgery
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51
Q

What are the 3 types of conjunctiva

? is a common microbe etiology for viral conjuctivitis

What are the S/Sxs

A

Palpebral- covers inner eyelid
Fornix- meeting point of bulbar and palpebral
Bulbar- overs sclera

Adenovirus

Discomfort Redness Watering Sore
Contralateral side affected 3-7d later, less severe

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52
Q

What is seen on PE of viral conjunctivitis

What is the differentiator for this Dx

Why can Pts develop decreased vision and become photosensitive

A

Follicular response- small dome shaped lymphoid nodule w/ no central blood vessel

Tender pre-auricular adenopathy

Subepithelial infiltrates from response to viral Abs

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53
Q

How is viral conjunctivitis Tx

When/why would ABX be used

What Pt education piece needs to be given

A

Self limited
Cold compress
Artificial tears
Topical steroid- if SEI/pseudo/membrane

Secondary bacterial infection concern

Highly contagious

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54
Q

Since any bacteria can cause bacterial conjunctivitis, what are the 3 MC causes

What 3 must always be considered though

If one of these other 3 considerations is the cause, ? is the next step for the Pt

A

Staph A / Strep pneumo / H influenza

C trachomatis
N gonorrheoeae
N meningitidis

Opth ASAP- risk for gonococcal corneal ulcer perf

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55
Q

What are the S/Sxs of bacterial conjunctivitis

What can give these Pts the ‘hyperacute’ appearance

How are these cases worked up if Neisseria is the suspected etiology

A

Adhesion to lid
Irritation
Redness

Mucopurulent d/c

Gram stain, Culture
Other- broad ABX

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56
Q

How is non-gonococcal conjunctivitis Tx w/ ABX

How are these Tx if Neisseria spp and Chlamydia are the cause

What is done different if corneal involvement exists w/ Neisseria spp/Chamydia etiolgies

A

Trimethoprim/Polymyxin B QID x 7d
Besi/Moxi-floxacin QID x 7d

Ceftriaxone 1gm IM (PCN allergy= Cipro 500mg x 5d)
Azithromycin 1g PO x 1 or,
Doxy 100mg bid x 7d

Admit w/ Ceftriaxone 1g IV q12-24hrs
Topical Fqn

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57
Q

Allergic conjunctivitis can be caused by ? type of hypersensitivity

What are the S/Sxs of Allergic Conjunctivitis

A

Type 1

Chemosis 
Conjunctival papillae w/ prominent central blood vessel
D/c, watery/stringy 
Intense itch
Conjunctival injections
Erythema/edema
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58
Q

How is Allergic Conjunctivitis Tx w/ topical meds depending on severity

What PO anti-histamines can be used

A

Mild- artificial tears
Moderate- Topical antihistamine/mast cell stabilizer (Olopatadine/Ketotifen)
Severe- topical steroid (Loteprednol)- q2hr x 2d, then QID x 7d, then BID x 7d

Cetirizine
Diphenhydramine
Fexofenadine

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59
Q

How do Subconjunctival Hemorrhages present

What are the six possible etiologies

What two meds need to be asked about in the Pt Hx

A

ASx in one sector, possibly whole sclera

HTN - Valsalva
Trauma - Orbital mass
Bleeding d/o - Idiopathic

Warfarin, ASA use

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60
Q

How are Sub-conjunctival Hemorrhages worked up

What are the 3 indications to get a CT to r/o masses

How are these Tx

A

BP IOP Coags EOM

Restriction EOM
Elevated IOP
Proptosis

Artificial tears for irritation
D/c ASA if elective

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61
Q

Define Pinguecula and Pterygium

What regions are these PTs commonly from

How are the two differentiated

A

White-yellow bump on conjunctiva at the 3 or 9 o’clock positions

Equitorial w/ dry/sun exposed living

Ptery- invades cornea
Ping- doe not invade

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62
Q

What S/Sxs can be seen in Pingueculas and Pterygium cases

How are these Tx

When is surgery indicated

A

Redness
ASx, typically
Dec vision

Artificial tears
Severe= topical steroids

Pterygium interferes w/ sight or close to visual axis
Excessive irritation reported

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63
Q

Define Phlyctenule

What causes these to grow

If these can’t be referred, tx at primary level w/ ? Rx combo

A

Nodule growth at limbus

Hypersensitivity to Staph proteins

Tobra and Dexameth/Lotaprednol

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64
Q

Define Conjunctival Nevus

Rarely these can progress into malignant melanoma, ? population does this occur in and what PE finding indicates it

Why would a biopsy be warranted and all suspicious lesion need ? done to them

A

ASx benign pigmented lesion, freely mobile over sclera

Middle age - elderly
Blood supply through conjuctiva

Growth/change in appearance
Resected

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65
Q

What are the 3 main concerns for Pts w/ conjunctival lacerations

What work up is done for these w/in the eye clinic

How are conjunctival lacerations Tx

A

Ruptured globe
Foreign body- intra-ocular/orbital

Fluorescein stain
Ocular exam
R/o scleral involvement
Dilated fundus 
CT consideration
<1cm= Erythromycin TID and monitor
>1cm= surgical closure
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66
Q

Thyroid Eye Dz is AKA ? and seen in ? conditions

This eye condition can precede or follow ? Dx by years

This Dx claims ? MC fact about adult health

A

Graves Ophthalmopathy- Hyper/Hypo/Euth-thyroid

Glandular Dz

MC cause of bi/uni-lateral proptosis in adults

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67
Q

What do Thyroid Eye Dz Pts present w/ as c/c early in condition

What are late c/cs

A
Photophobia
Redness
Tearing
Burning
Puffy lids in AM

Persistent swelling
Chemosis
Double vision

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68
Q

What are the sings of Thyroid Eye Dz

What is done for this condition’s work up and f/u

How is the Dz confirmed w/ imaging

A
Acuity/field loss
Lagophthalmos
Lid retraction
Exophthalmos
Swelling
Restricted motility

Thyroid panel
Normal= careful monitoring

CT

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69
Q

How is mild Thyroid Eye Dz Tx

What are the 3 classifications of conjunctivitis and predominant Sx for each

Cornea is the primary ? element of the eye, so any injury to it results in ?

A

Artificial tears
Tape eyelid
Elevate head at night

Viral: adenopathy
Bacterial: d/c
Allergic: itching

Refractive, Visual impairement

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70
Q

Define Keratitis

What are the layers of the cornea from out to in

Corneal erosions are damage to ? layer but can be stained w/ ? for evaluation

A

Inflammation of the cornea

Epithelium
Bowman's membrane
Stroma
Descements membrane
Endothelium

Epithelium, NaFl- Seidel’s sign

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71
Q

Corneal erosion is the result of ? three things?

Corneal ulcers are damage to ? layer

How does the difference in pain indicate the cause of the ulcer

A

Dryness
Inflammation
Exposure

Stromal

Bacteria/Fungal- painful and aggressive
Sterile infiltrate- minimal pain on peripheral cornea secondary to contact lens wear

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72
Q

What are the S/Sxs that corneal ulcers can present w/

What visual finding may be seen on PE

What are five facts about sterile ulcers

A
Hypopyon
D/c
Tearing
Pain
Injection
Photophobia

Focal white opacity on cornea
Dense= corneal infiltrates

Less painful
Minimal-no d/c
No iritis, corneal edema, infiltrates

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73
Q

What are the Sxs of Herpes Simplex Keratitis

What is unique about the symmetry of this condition

What will be seen if you stain Herpes Simplex Keratitis

A

Conjuctival injection
Redness
Irritation
Photophobia

98% unilateral

Epithelial dendrites
Advanced- stromal scarring/vascularization

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74
Q

How is this Herpes Simplex Keratitis Tx

Define Bacterial Keratitis

What are the 5 MC causes

A

Refer
Avoid topical steroids (possible perf)
Topical/PO anti-virals

Bacteria colonization on cornea that interrupts intact epithelium leading to proliferation and ulceration

Pseudomonas Moraxella Serratia Staph Strep

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75
Q

Bacterial Keratitis is MC seen in ? populations

What other etiologies can cause this

A

Contact lens wear especially if over night wearer

Compromised Immune defenses
Aqueous tear deficiency
Recent corneal dz
Trauma
Structure changes of eyelid
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76
Q

What are the signs of Bacterial Keratitis

What are the Sxs and are also identical w/ ? Dx

How is Bacterial Keratitis Tx

A
Ulcerated epithelium
Anterior chamber reaction
Hyperemia
Adherent exudate
Corneal infiltrate
Edema

Pain Red Photophobia D/c
Fungal keratitis

Topical Flqn
Tobra/Cipro-mycin- contact lens wear w/ d/c of wear
Refer to Opto/Ophtho for culture
Vision threatened= fortified ABX q30min

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77
Q

What causes Fungal Keratitis

What chronic/long standing condition can cause this

What is the MC and other Signs of Fungal Keratitis

A

Contact use
Outdoor eye trauma w/ vegetation
Recent surgery (cataract/refractive)
Topical CCS

Chronic keratitis secondary to ocular Dz (herpes)

Anterior chamber reaction
Conjunctiva injection
MC- Epithelial feathery white opacity

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78
Q

Fungal Keratitis can be confused w/ Bacterial Keratitis, how is fungal differentiated

How is the Fungal form Tx

What Tx needs to be avoided

A

Bacterial= yellow-white

Culture
Surgical debridement- debulking, inc ABX penetration
Topical Natamycin/Amphotericin B
PO Flu/Vori-conazole

No topical steroids

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79
Q

Corenal pigmentation is usually drug related to ? drugs

What is the good news about this Dx

How is it Tx

A

Amiodarone- whirl shaped deposits
Hydroxy/Chloroquine- corneal deposits
Indomethacin
Phenothiazine

Rarely causes vision loss

D/c drug

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80
Q

What is the etiology of Recurrent Corneal Erosions

Recurrent Corneal Erosion is commonly caused by ? and also caused by ?

How does this condition present

A

Poor epithelial adhesion

Dog claws
Degeneration/dystrophy

Middle night/morning pain-
Pain
Blurry vision
Redness
"sharp pain w/ opening eye" or "felt like eyelid was stuck onto front of eye"
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81
Q

What are early and late signs seen in Recurrent Corneal Erosions

How are these Tx

What can be done for Pt to ease accomodative spasms of the eye

A

Early: epithelial defects w/ fluorscein
Late: cornea irregularity

Tx abrasion first: Muro128 qid (hypertonic Na ointment)
Bandage contact lens if large area
Severe= laser surgery

Dilation

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82
Q

Define Keratoconus

What will Pts present w/?

Severe cases may have to be Tx w/ ?

A

Dz of unknown etiology causing thinning of central cornea

Increased myopia
Irregular astigmatism (poor vision even w/ glasses)

Corneal transplant

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83
Q

What two PE sign is associated w/ Keratoconus

Define Arcus Senilis

Since this is usually d/t age related changes, ? underlying Dx is suspected if Pt is younger

A

Munson- bulging lower lid from thinning cornea
Vogt Striae

Gray/White/yellow deposits on peripheral cornea

Abnormal hyperlipoproteinemia
<40- check systemic lipids

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84
Q

What do PTs report w/ if they have Arcus Senilis

What will be seen on PE to solidify Dx

What are the functions of the sclera

A

No effect on vision

Clear area between deposit and limbus

Protection from in/out forces
Attachment site for EOMs

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85
Q

Sclera is composed of what two layers

It is made up by what two components

How thick is it and where is it the thickest

A

Outer- episclera: loose vascular tissue w/ visible vessels
Inner- stroma

Collagen
Elastic fibers

0.3mm-1.0mm, thickest at posterior aspect

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86
Q

Episclera joins to ? capsule via strands of tissue

What is the function of this capsule

Episcleritis is more prevalent in ? population and commonly d/t ? but can be from ? d/os?

A

Tenon’s capsule- dense CT that encases globe

Sheaths for tendons at EOM insertions

Young adults, idiopathic
Herpes zoster
Rosacea
Syphilis
Collagen dz (RA, SLE)
Thyroid dz
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87
Q

How does Episcleritis present to clinic

What is absent on this presentation

How are these cases worked up

A

Hx of episodes
Acute redness w/ mild, localized pain
Normal VA
Sectorial, engorged episcleral vessels

No d/c

Hx: rash arthritis STD
External exam
Slit lamp w/ anesthesia

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88
Q

What are two findings on PE that differentiate Episcleritis as the Dx from other possibles

How is this condition Tx

Half of Scleritis cases are idiopathic and the other half are d/t CT Dzs like ?

A

Injected vessels moved w/ CTA
Phenylephrine x 15min= episcleral blanching (scleritis won’t blanch)

Refer for Dx confirmation
Mild: Tears Cold compress
Mod-Sev: Topical steroids (Fluorometholone, Loteprednol) and PO NSAID

Wegeners 
Relapsing polychondritis
AS
Polyarteritis nodosa
RA 
SLE
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89
Q

Other than the CT Dzs, what are the other RFs for developing Scleritis

On average, these Pts are different from those that get Episcleritis in what way

What is the prominent feature of this condition

A

Gout
Infection (Herpes, Zyphilis)
Trauma

Older

Severe, boring eye pain that radiates to jaw/forehead

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90
Q

Other than the prominent Sx, what other S/Sxs can Scleritis present w/

How is this condition worked up

A
Tearing
Bluish-hue (necrotizing anterior)
Decreased vision
Inflammation
Photophobia

Pheylephrine topical (won’t blanch)
Slit lamp w/ green light- avascularization indicates necrotizing
Fundus exam to r/o posterior scleritis
Skin Joints Cardio Resp

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91
Q

What are the five Scleritis classifications

A

Diffuse Anterior: widespread inflammation in anterior segment

Nodular Anterior: immovable inflamed nodules

Necrotizing Anterior w/ Inflammation: extreme pain, associated w/ systemic Dz

Necrotizing Anterior w/out Inflammation: ASx, associated w/ longer Dz, esp RA

Posterior Scleritis- unrelated to systematic Dzs

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92
Q

How is Diffuse/Nodular Scleritis Tx

What is the next step if there is no improvement

What medication is used if immuno-suppressive therapy is needed

A

All refer to Ophthalmology
NSAIDs
H2 blocker (Ranitide)

No improvement w/ NSAID= PO Prednisone

Clophosphamide

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93
Q

How is Necrotizing Scleritis Tx

Since the Tx of Posterior Scleritis is similar to Diffuse/Nodular, what are the risks associated with the therapy methods

A
Graft patch if perf present
NSAID/Prednisone
Clophosphamide
Ranitide
Refer- Rheum

Cyclophosphamide- toxicity
Rituximab- empirical
Glucocorticoids

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94
Q

What are the 3 parts of the uveal tract

Define Uveitis

What are the three types of uveitis

A

Iris- only visible part
Ciliary body- produces aqueous humor
Choroid- behind sclera and retina, blood supply to retina

Inflammation of the uveal tract

Anterior Intermediate
Posterior

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95
Q

Anterior Uveitis is synonymout w/ ? two words

What are the associated RFs for this Dx

A

Iritis and Iridocyclitis

Infection (Syphillis, TB)
Malignancy (Lymphoma)
JA
Other (Sarcoidosis Idiopathic Trauma Surgery)
Syphilis/TB
HLA-B27 pos (AS, Reiters)
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96
Q

What are the S/Sxs of Anterior Ubeitis

This condition can present with keratic precipitates, what are the two types and what etiology does each have

A
Irregular pupil
Flare- proteins in aqueous
Hypopyon- cell collection at bottom of anterior chamber
Nodules- Koeppe/Busacca
Redness
Injection/flush
Photophobia
Floating cells

Fine/white= non-granulous
Mutton Fat= granulomatous)

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97
Q

Lab work is needed during an Anterior Uveitis work up, especially during ? types

What labs are needed

A

Bilateral Granulomatous Recurrent

CXE
HLA-B27
ESR
ACE 
PPD
RPR/VDRL
FTA
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98
Q

How is Anterior Uveitis Tx depending of the severity

What topical steroid is used for Tx?

What is the prognosis for these Pts

A

Cycloplegics-
Mild-Mod: Scopolamine
Severe: Atropine

Prednisolone

First time non-granulomatous= excellent
Recurrent granulomatous= poor

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99
Q

Trifecta of what three conditions makes up Posterior Uveitis

What is the MC microbe to cause this condition in healthy/AIDS Pts

What other infections can cause this

A

Vitreitis Choroiditis Retinitis

Healthy: Toxoplasmosis
AIDS: Cytomegalovirus

Toxocariasis
TB
Syphilis

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100
Q

What are the S/Sxs of Posterior Uveitis

What is the most severe infection of the eye

Who is it seen in and what is the prognosis

A

Floaters
Inflammatory
Swelling w/ edema of disc
Hemorrhages

CMV retinitis

CD4 <100
Blindness <6mon

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101
Q

Posterior Uveitis/CMV retinitis is seen in ? other ImmComp states other than AIDS

What is uncommonly reported in Pts w/ CMV Retinitis

What Sxs may be reported

A

Transplant
Lymphoma
Leukemia

Pain/Photophobia

Dec vision
Floaters/Flashes
Scotomata

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102
Q

What is the MC sign seen in CMV Retinitis

What other signs may be seen on exam

How is this Tx

A

Cotton-wool spots

Keratic precipitates (stellate shapes)
Vitreous cells
Hemorrhages w/ retinal whitening= necrosis

W/ IDz Provider
HAART
PO Valganciclovir 900mg BID x 3wks then 1/day

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103
Q

How is Posterior Uveitis Tx

What part of the body has the highest protein concentration

However, this structure lacks ?

A

Tx systemic Dz
Anterior involvement= topical steroid w/ cycloplegic
Ophth referral

Lens

No vessels or nerves

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104
Q

What are the 3 layers of the lens and their responsibilities

A

Capsule- thin, semipermeable membrane around entire lens; Molds the lens during accommodation

Cortex - anterior and posterior; Produces fibers for life;
Held by zonules equatorially for accomodation

Nucleus

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105
Q

What is the MC RF for cataract development

What are the systemic RFs

What is the toxic RF

What are the secondary RFs for cataract development

A

Age related

DM Myotonic dystrophy NF-2

Steroids

Chronic anterior uveitis
Acute congestive angle closure
Pathological myopia
Degenerative dz (Retinitis pigmentosa)
Ionizing radiation
Ciliary body tumor
106
Q

Define Nuclear Sclerosis Cataract

What term is given for the visual changes these Pts experience

Define Posterior Subcapsular Cataracts

A

Yellow/brown discoloration of nucleus causing blurry distance vision

Second site of the aged- more myopic
Near vision improves

Opacities near posterior lens (Vacuoles, Plaque-like)
Near vision decreases

107
Q

What are common complaints in Pts w/ Posterior Subcapsular

What are the causes for this condition

A

Glare
Difficulty reading

DM
Ocular inflammation
Age <50
Steroids
High myopia
Ionizing radiation
Trauma
108
Q

Define Cortical Cataracts

What c/c do Pts present w/?

What is the MC complaint

A

Radial/spoke-like opacities (Vacuoles, Cuneiform)

ASx until central progression

Glare

109
Q

What is the MC complaint from Pts w/ cataracts

What type of vision can they develop

What benefit may these Pts report

A

Glare w/ oncoming headlights

Monocular diplopia
Decreased color perception

Thickening lens causes “second sight”

110
Q

What would prevent Pts w/ cataracts from developing “second sight”?

How are cataracts Tx

What short term relief trial can be attempted w/ these Pts

A

Posterior subcapuslr decreases near vision d/t opacity at central lens degrades visual quality

Early= Sptectacles
Small, central= pupil dilation
Large= surgery
Pt declines= refractive error correction

Mydriasis- scopolamine

111
Q

What are the indications to conduct cataract surgery

What are the biggest concerns for Pts going into surgery

A

To improve visual field
Manage ocular Dzs (Glaucoma DRetinopathy AMD Infant deprivational amblyopia)

Uncontrolled DM/HTN
Anesthesia issues
Respiratory dz
Anxiety
Tremors
Epilepsy
Recent MI/Stroke
112
Q

What is the MC cause of congenital cataracts

What are the RFs

What is the potential sole manifestation of congenital cataracts

A

Idiopathic

Familial w/ autosomal dominant
Chromosomal d/o
Galactosemia
Intrauterine infection
Rubella
Lowe syndrome

Galactosemia

113
Q

What are the different types of Congenital Cataracts

A

Coronary- deep in cortex around nucleus, like a “crown”

Lamellar

Anterior polar- flat and insignificant

Blue dot- common and innocuous

Sutural- along y-suture

114
Q

How can Congenital Cataracts present

What Hx piece is important during the work up

Why is this a Congenital Cataract in infants a surgical emergency?

A

Infant squinting/keeping eyes shut
Abnormal/absent red reflex (Leukocoria)

Maternal illness

Brain learns to see w/ macula during first 3-4mon of life
Surgery prevents irreversible deprivational amblyopia

115
Q

What are the two types of Lens Position Anomalys

A

Subluxation- partial zonular disruption; lens is decentered but partially visible in pupil apperature

Dislocation- complete disruption of zonular fibers; displaced out of neutral position in posterior chamber

116
Q

What is the MC cause of Lens Position Anomaly

What are the other RFs

A

Trauma- subluxation, 25% or > of fibers are ruptured

Marfans- superotemporal subluxation w/ retained accommodation

Homocystinuria- inferonasal subluxation/dislocation w/ lost accommodation

Other-
Acquired syphilis
High myopia
Ehlers-Danlos

117
Q

What are the S/Sxs of Lens Position Anomaly

A

Monocular diplopia
Angle closure glaucoma
Iridodonesis (iris quivers)
Decentered lens

Dec vision
Irregular astigmatism
Cataracts

Asymmetric anterior chamber
Phacodonesis (lens quivers)

118
Q

? screening test needs to be added to Lens Position Anomaly work ups?

How are Lens Position Anomalys Tx by Ophthalmologist

A

Syphilis

Dislocation into anterior chamber-
Head manipulation; risk of indenting cornea
Surgery

Dislocation into vitreous-
ASx= observation
Surgery

Subluxation-
Surgery only if Sxs

119
Q

What causes Pts to see floaters

What are the possible Dxs if these onset acutely

What causes Pts to see flashes

A

Benign vitreous opacities in vitreous cavity

Foreign body
Bleeding- DM/Sickle Cell anemia
Uveitis- intermediate/posterior
Retinal tear
Posterior vitreous detachment

Traction of vitreous on peripheral retina

120
Q

What will be seen if Pts also reports floaters while also having flashes

What two types of flashes can be reported that occur w/ migraines

A

Blood/pigment in vitreous

Scintillations
Zig-Zag lights

121
Q

What are the RFs for Posterior Vitreous Detachments

What are the S/xs of this condition

How is it Tx

A

Pesonal/FamHx of tears
Intraocular surgery
Trauma
High myopia

Sudden onset black spots/flashing lights
Floaters
Weiss ring- vitreous opacity in ring shape

Photocoagulation Cryotherapy Refer

122
Q

What are the Sxs of Vitreous Opacities

What are the RFs

What type of imaging is needed during Vitreous Opacity work up and why

A

Floaters, Dec vision

DM
Acute PVD
Retinal vein occlusion
Trauma
Vasculitis

B-scan US- excludes retinal tear/detachment

123
Q

Depending on the severity, how are Vitreous Opacities Tx

Why is the fovea darker than the surrounding retina and what reflex can be seen here

A

Vitrectomy

Lacks vascularity,
Foveolar light reflex- yellow reflex at center of fovea

124
Q

In order to view peripheral retinal structures, ? technique is needed

Where is the optic nerve viewed at when looking into eye

What is the atery/venous make up in this location

A

Indirect ophthalmoscopic

Nasal portion of retina

A:V ratio= 2:3
Arteries- thinner, orange/red
Veins- larger, crimson
A/V cross each other; V/V or A/A don’t cross

125
Q

What structures supply the retina w/ blood

The retina is mostly transparent, but it’s epithelium pigment may be called ? colors

What does the inner retina contain

A

Central retinal- inner retina
Choroid- outer wall, photo receptors (higher O2 demand)

Lightly blond/brunette

Nerve fiber layer
Ganglion cell nuclei
Retinal vasculature

126
Q

Axons from the inner retina extend though ? and into ? for ? end result

Conditions that cause ischemia will impact ? area of the eye

These condition manifest in ? layer

A

Through optic nerve/chiasm
To lateral geniculate nucleus
To midbrain for pupillary response

Inner retina

Nerve fiber layer

127
Q

Retinal artery occlusions may involve ? two structures

What type of vision loss will be experienced

Usually, ? structure will be spared meaning ? vasculature is spared

A

Central retinal artery- CRAO
Branch of retinal artery- BRAO

Horizontal hemifield loss

Macula- cilioretinal arteries arising from choroidal supply

128
Q

What are the RFs for Retinal Artery Occlusions (CRAO)

What are the S/Sxs of CRAO

What structure may show small portions of sparing

A

Giant cell arthritis
Thrombus/Embolus
Collagen-Vascular Dz (SLE)
Hypercoagulation (OCP)

Hx of Amaurosis Fugax
Opacified/white retina (BRAO too)
Painless, unilat w/ rising in AM (BRAO too)
Cherry red macula (BRAO= emoblus)
Afferent pupillary defect (not BRAO)
Box-car arterioles (BRAO too)

Cilioretinal artery- not spared in BRAO

129
Q

What is the prognosis for Pts w/ CRAO

Pts w/ CRAO need monitoring for neovascularization in ? areas

What are the S/Sxs of Branch Retinal Artery Occlusions

A

Poor d/t retinal infarction- over time, retinal cloudiness and cherry spots disappear

Retina Angle Iris Disc

Sudden altitudinal/sectoral field loss

130
Q

What is the prognosis for these Pts w/ BRAO

What is different about the future events for PTs w/ BRAO compared to CRAO

What lab work is immediately ordered for CRAO/BRAO work ups and why

A

Poor unless relieved, field defect will be permanent

CRAO- rarely have neovascularization

ESR CRP Platelets
R/o GCA if Pt >55y/o

131
Q

How are CRAO/BRAO Tx

What structures do Retinal Vein Occlusion effect and how do they present

What type of vision loss do Pts report w/

A

Paracentesis
Ophthalmic timolol
PO Acetazolamide
Ocular massage

Central Retinal Vein
Branch of Retinal Vein

Horizontal hemi-field loss w/ respect to horizontal midline

132
Q

What is the physiological reason for RVO conditions

A

Thickening arteriole compresses on vein causing stagnant blood outflow

133
Q

What are the RFs for Retinal Venous Occlusions

A

Hyperlipids
Age >65
DM

Vasculitis
HTN

Glaucoma
OCPs
Tobacco
Hypercoagulability

Platelet abnormalities
Atherosclerosis in adjacent central retinal artery
Disc edea/drusen

134
Q

What are the S/Sxs of Ischemia CRVO

What are the S/Sxs of Non-Ischemic CRVO

Of the two types, ? type is more common

A

Sudden painless unilateral loss of vision
Afferent pupil defect
Count fingers or worse

Poor VA, >20/400
Absent/mild afferent defect

Non-Ischemic

135
Q

What will be seen on fundoscopic exam of CRVO

What will be seen on fundoscopic exam if it’s Ischemic CRVO

What will be seen on fundoscopic exam if it’s non-ischemic CRVO

A

Dilated, torturous veins
Blood-and-Thunder fundus- dot, blot, flame hemorrhage w/ cotton wool spots and exudates
Dilated optic disc

Prominent cotton-wool spots
Extensive retinal hemorrhage
Neovascularization of iris/angle glaucoma

Mild fundus changes

136
Q

What are the prognosis for the CRVO types

A

Ischemic- poor, half develop neovascularization of iris but retinochoroidal veins may be spared

Non-ischemic- later develops into ischemic or chronic macular edema

137
Q

S/Sxs of BRVO

What will be seen on fundoscopic exams

What is the prognosis for these Pts

A

Sudden, painless unilateral vision loss
Superficial hemorhages affect vision but don’t cross horizontal midline

Cotton wool spots
Dilated-tortured veins
Narrowed adjacent artery
Retinal neovascularization

Good- more than half develop collateral vessels to improve VA

138
Q

What are the complications that threaten recovery from BRVOs

What is the work up for RVOs

A

Chronic macular edema
Neovascularization located other>disc
Other locations cause hemorrhages and tractional detachment of retina

BP
Ocular exam
IOP
Afferent defect to differentiate non/ischemic
Systemic Hx
Blood: CBC ESR Glucose Plasma protein electrophoresis

139
Q

How are RVOs Tx

How is RAO Tx

A
DONAD
D/c OCPs
Opth referal <72hrs
Neovasc= anti-VEGF, PRP
ASA
Dec IOP if needed
Ophtho referal then POPO:
Paracentesis
Optic Timolol
PO Acetazolamide
Ocular massage
140
Q

What is the leading cause of blindness in the US for PTs age 20-64

These Pts must have ocular eval to establish baseline w/in ? months of Dx

What is the difference in retinopathy prevalence between T1DM and T2DM when newly diagnosed

A

DM

<6mon

1- rare
2- may have
But prevalence T1>T2

141
Q

What are the RFs for DM

A
Duration- rarely starts 5yrs before/after puberty
Poor control
Pregnancy- progression linked to 1st-T 
HTN 
Nephropathy
142
Q

What two hormonal times can influence the acceleration of diabetic retinopathy

What are the two classifications of diabetic retinopathy

A

Pregnancy
Puberty

Non-proliferative- 
IRMA
Cotton-wool spots
Hemorrhages
Exudates
Mircoaneurisms

Proliferative-
Late stage, new vessels grow at disc

143
Q

What are the blood vessel changes seen during diabetic retinopathy

How does dec VA develop in these PTs

A

Microaneurysms- inc permeability
Endothelium tight junctions- blood-retina barrier

Aneurysms have incompetent blood-retina barrier
Intravascular fluids leak int retinal tissues
Accumulation occurs in fovea

144
Q

What are the 4 severity levels of Non-Proliferative Diabetic Retinopathy

A

Very Mild- microaneurysms only

Mild- Microaneurysms Exudates CWSpots

Mod-
20 med-large retinal hemorrhages in 1-3 quadrants or,
Mild IRMA

Severe- 4-2-1 Rule:
4 quadrants of severe retinal hemorrhages
2 or more quadrants of venous beading
1 or more quadrant of moderate IRMA

145
Q

Proliferative Diabetic Retinopathy results from ?

? other issue will be seen that can develop in ? locations

What are these Pts at recurrent incident risk for

A

Ischemia- dec perfusion causes angiogenic factor (VEGF) release to stimulate growth of new vessels

Neovascularization-
Iris
Disk
Retina
Into vitreous
Vascular acrades- MC

Fragile vessels= recurrent hemorrhages

146
Q

What are the Sxs associated w/ Proliferative Diabetic Retinopathy

What are the signs of this condition seen on PE

A

Unaware of changes even w/ 20/20 vision
Floaters- secondary to hemorrhages, described as shower
Scotoma

Boat shaped hemorrhages
Absent red reflex
Dot/blot hemorrhages
Lacy vessels 
CWSpots
147
Q

How is Diabetic Retinopathy worked up

A
Fasting blood glucose
A1C
CBC w/ diff
Hgb electrophoresis
CXR
Carotid US
Annual fundoscopic exam
148
Q

How is Non-Proliferative Diabetic Neuropathy Tx

What are the S/Sxs of Diabetic Macular Edema

A

Glycemic control
+Neovascular changes= Anti-VEGF , PRP

Gray/opacification of retina
ASx
Microaneurysms
Exudates- yellowish w/ discrete borders
Dot-blot hemorrhages
149
Q

Define Retinitis Pigmentosa

What is the pathophysiological reason for this condition

What do these Pts report as c/c

A

Group of retinal degenerations d/t inherited genetic defects

Lost photoreceptors, rods first
Retinal pigment epithelium changes

Night blindness (nyctalopia)
Peripheral vision loss
Photopsia
Lost color vision
Scotoma
150
Q

What may be seen on PE fo Retinitis Pigmentosa

What is done for a work up

How is Retinitis Pigmentosa Tx

A
Bone-spicule retinopathy
Anterior narrowing
Normal fundus
Golden ring sign- yellow/white halo around disc
Posterior subcapsular cataract
Optic nerve pallor

Electroretinography

Vitamin Supplements (ADEK)
Low vision aids
151
Q

Define Retinal Detachment

What are the 3 types

A

Retina seperates from pigment epithelium d/t fluid in space

Rhegmatogenous- break/tear, common in myopic eyes (higher Rx=higher risk)

Exudative- leakage w/out break; tumor below retinal layer

Tractional- contraction of fibers on retina; Proliferative Diabetic Retinopathy/Retinopathy of prematurity

152
Q

Flashes and Floaters are only seen in ? type of retinal detachment

What do Pts report during PE

How are these worked up

A

Rhegmatogenous

Curtain/shade pulled down
Metamorphopsia- wavy/distorted vision

Refer for complete dilated ocular exam
Red reflex assists w/ Dx- detachment= lighter reflex

153
Q

How are Retinal Detachments Tx

What is the MC cause of legal blindness in in PTs >60

What are the two types

A

Rhegmatogenous- Pneumatic retinopexy, Scleral buckle
Traction- Pars plana vitrectomy

ARMD

Non-exudative (dry)
Exudative (wet)

154
Q

? is the MC abnormality in ARMD

What does the abnormality change in the eye

What are the RF for developing ARMD

A

Drusen

Yellow deposits deep in retina
Limits nutritional support to photoreceptos in outter retina

Female
Lighter pigmentation
Older age
Genetics
Smoking
155
Q

S/Sxs of Dry AMD

What will be seen on fundoscopic exam

What are S/Sxs of Wet AMD

What will be seen on fundoscopic exam

A

Gradual loss of central vision

Macular drusen w/ clumps of pigment in outer retina

Metamorphopsia- distorted lines
Rapid central vision loss

Drusen
Chroidal neovascularization
Subretinal hemorrhages

156
Q

What are the RFs for progressing from Dry to Wet AMD

A

Hyperopia

Pigment clumps
HTN

FamHx
Large ill-defined drusen
Age 
Blue eyes
Smoking
157
Q

What is done for AMD work ups

A

Amsler grid test- degree of central field loss, done daily during f/u and periodic after

IV Fluorescein angiography- if sub-retinal neovascular membrane present/suspected

Macular slit-lamp eval

158
Q

How is Dry AMD Tx

How is Wet AMD Tx

A

High dose Vit C E Beta-carotene Zinc (AREDS)
Smokers= non-beta carotene

Anti-VEGF intravitreal injection
Laser photocoagulation <72hrs from angiography

159
Q

What is the hallmark of HTN Retinpathy

What does the A:V ratio change to

What two metal findings may be seen in vessels and what do they mean

A

Diffuse anteriolar narrowing causing vessel walls to be virtually invisible

1:3-1:4

Copper wire- narrowing anteriolar, yellowing of linear light reflex
Silver Wire- sclerosis of vessel

160
Q

What are the Sxs of HTN Retinopathy

What are the signs of this condition

A

Blurry/sudden dec vision
Scotoma
Double vision

Macular star- lipid exudates
CWspots
BRVO/BRAO
Retinal edema
A:V nicking
161
Q

How much Hydroxy/Chloroquine use can lead to toxicity development

What are the RFs for developing Hydroxy/Chloroquine Toxicity

A

> 5mg/kg HCQ
2.3mg/kg CQ
5yrs of use

Renal Dz
Tamoxifen use
Retinal/Macular Dzs

162
Q

What are the S/Sxs of CQ/HCQ Toxicity

What is the prognosis for these Pts

How often are eye exam screenings needed

A

S: Bulls eye maculopathy
Sxs:
Dec vision,
Abnormal color vision, Difficulty adjusting to dark

Non-reversible, may progress after stopping Rxs

Baseline- within first year
Annual- after 5yrs of use

163
Q

What is the path of aqueous humor after production

What two structures make the anterior chamber angle

Aqueous humor exits the final location via ? structure

A

Ciliary body, past lens and around iris
Into trabecular mesh (area of greatest resistance) at junction of cornea and iris

Junction of cornea and iris

Schlemms canal

164
Q

What is normal IOP levels

When is diurnal variants highest

To Dx Glaucoma, what two criteria must be met

A

10-21

AM>PM

Progressive optic nerve damage and,
Field loss

165
Q

What are the two broad categories of glaucoma

What is a rough estimate to determine if Pt has wide open or closed/narrow angle w/ potential of closure

How is this done

A

Open angle- normal structural out path, MC
Closed angle- outflow blocked

Angle assessment

Pen light near limbus on temporal side
Shine light across PTs eyes
Observe nasal portion of shadow
No shadow= wide open
Shadow= bigger shadow= narrower angle
166
Q

What is measured to assess the progression of glaucoma

What do the two parts that are assessed mean

What are the two methods to measure IOP

A

Cup to disc ratio

Smaller number- less visible cup
Larger number- bigger risk for glaucoma

Non-contact (air puff)
Applanation (tonopen, goldmann applanation**)

167
Q

? is the only factor of glaucoma that clinicians can actually adjust medically

How is ocular HTN Tx

What are the RFs that can develop into future glaucoma

A

IOP

Monitor annually

FamHx
Large C/D ratio
Age
Thin central cornea
High myopia
168
Q

What is the pathophysiological process of Primary Open Angle Glaucoma

Although the actual mechanism is not known, what are two dysfunctions that can cause POAG

What is the only modifiable RF

A

Loss of retinal fiber layers cause reduced vision

Vascular dysfunction- optic nerve ischemia
Mechanical- cribiform plate compression of axons

IOP >28mmHg= 15x more likely to develop field loss

169
Q

How is mechanical dysfunction identified on PE of POAG

What kind of decreased vision complaints may present later in Dz

What are the RFs for POAG

A

Sieve-like portion of sclera at base of disc

Parts of page are missing
Tunnel vision- late
Central fixation preserved until late
Remaining field- temporal island

FamHx- sibling (4x) offspring (2x)
Age >50
Race AfAm/Hispanic
Diabetes 2-3x

170
Q

What POAG RF has no definitive relation to ocular HTN

What is the work up for POAG

How is this Tx

A

Systemic HTN

Measure IOP
Ophthalmoscopy- C/D usually 0.6 or greater
Pupil crescent shadow= open chamber

Dec aqueous production (BBs: TLCB-olol, A2 agonist: Brim/Apracl-onidine, CA inhibitor: HADB-olamide)

Inc aqueous outflow (SympMimetic: Epi/Memantine, Prostaglandin: BULT-prost, Miotics: pilocarpine)

171
Q

What are the RF from using BBs for POAG Tx

What are the RFs from using A2 agonists for POAG Tx

What are the RF from using sympathomimetics for POAG Tx

What are the RFs from using Prostaglandin Analogs for POAG Tx

A

Dec CO, bronchoconstriction

Allergic conjunctivitis
Contact dermatitis

Exacerbation of HTN

Conjunctival hyperemia

172
Q

When is surgery indicated for POAG Tx

What are the 3 methods of surgical Tx

A

Optic neuropathy worsens
Younger/non-compliant Pts

Trabeculoplasty- argon/selective laser
Trabeculectomy- shunt, filtering bleb
Ciliary ablation- destroys ciliary epithelium

173
Q

? is a variant of POAG

What are the RFs for this variant

How are they Tx

A

Low/Normal tension glaucoma, IOP 21 or less w/ open anterior chamber
+field and nerve damage

Gender F
OSA
FamHx
Age
Thinner cornea

Same as POAG but more difficult d/t lower starting pressure

174
Q

What are the two processes that cause Acute Angle Closure Glaucoma

What are the Sxs if this develops

What are the signs seen on PE

A

Pupil Block- iris pushed forward
Non-pupil block- iris positioned anterior, often w/ inflammatory conditions

Monocular halos around lights
One eye blurry vision
Pain w/ photophobia
Frontal HA
N/V
Dilated pupil
Injections to conjunctiva
Shallow anterior chamber
Corneal edema w/ blurry light reflex
Lid edema
IOP 60-80mmHg
175
Q

What are the RFs for AACG

Define a Narrow angle

A
Gender F
Extreme dilation (walking into dark room)
Age 55-70
Race Far Eastern/Indian/Asian
Drugs (Anticholinergics, Sympathomimetics)
Short/small far sight
FamHx
Stress

Shallow central anterior chamber (space between cornea, iris) w/ no peripheral chamber

176
Q

How is AACH Tx

What can be given IV if IOP is <50

What is the TxOC

A

1 drop each w/ 5min between each:
Timolol
Apraclonidine
Predisolone/Dexamethasome

Acetazolamide

Laser Iridotomy after initial attack is broken

177
Q

What is done during a Peripheral Iridotomy

What causes Chronic Angle Closure Glaucoma to develop

What are the RFs for this to develop

A

Laser used to make hole made through iris to allow for alternate out flow path

Anterior chamber closed permanently by Peripheral Anterior Synechiae (front of iris binds to corneal epithelium)

Previous angle closures
Proliferative diabetic retinopathy
Trauma
Uveitis
Hypotony
Hx trabecular laser Tx
178
Q

What are the S/Sxs of CACG

What would be seen on gonioscopy

What is the IOP usually at

A

ASx
Dec vision/fields
Intermittend HA Eye pain Blurry vision

Broad bands of PAS
Optic nerve damage

IOP <40

179
Q

How is CACG Tx

What is the possible etiology of Congenital Glaucoma

A

Trabeculectomy/Tube shunt: areas not involved by PAS to prevent further synechial closure
Goniosynechialysis- physically strips PAS

Sturge Weber Syndrome- port wine stain

180
Q

What are the Signs of Congenital Glaucoma

What are 3 possible DDx

A

Enlarged globe and corneal diameter, >12mm before 12mon
Corneal edema
Tearing
Photophobia
Blepharospasm
Inc IOP
Inc C/D ratio- infant may regress once IOP normalizes

Megalocornea >14mm
Nasolacrimal duct obstruction

181
Q

Define Descemet’s Membrane

What can cause this to develop in infants

A

Linear tears in cornea AKA Haab striae in Congenital Glaucoma

Vertical/Oblique= Forcep delivery

182
Q

How is Congenital Glaucoma Tx non-op

What surgical procedures can be done

A

PO Acetazolamide- clear cornea prior to goniotomy
Topical Levobunolol/Timolol

Goniotomy- incises trabecular meshwork
Trabeculotomy- if clouding prevents view
Trabeculectomy/shunt

183
Q

Secondary Glaucoma is most often in ? PTs d/t ?

What causes these Pts to have neurovascular glaucoma

This neovascular glaucoma causes ? then secondary glaucoma

A

Males d/t work/sports/trauma causing angle recession

Retinal neovascularization causes iris and angle neovascularization from fibrovascular membrane

PAS

184
Q

What are the causes of Neovascular Glaucoma that can lead to Secondary Glaucoma

S/Sxs of Neovascular Glaucoma

A

Retinal artery/vein occlusion
Ocular ischemic syndrome
Diabetic retinopathy

ASx
Pain 
Red around pupil
Photophobia
Dec vision
Normal-elevated IOP
185
Q

How is Neovascular Glaucoma Tx

What can cause Steroid Response Glaucoma

How is it Tx

A

Timolol
Glaucoma filtration surgery- w/ inactive neovascularation
PRP for underlying condition

2-4wks of ophthalmic steroids
High dose skin creams
Inhalers
Nasal sprays

D/c or decrease use
Add IOP lowering med

186
Q

Glaucoma requires ? two things for Dx

Without these two, the Dx is just ?

Define Hemianopia

A

Optic nerve damage
Visual field loss

Ocular HTN

Los of half of visual field

187
Q

Define Homonymous

Define Scotoma

Define Anisocoria

A

Loss of visual field is same in both eyes

Area of reduced/absent vision w/ otherwise intact visual field

Unequal pupils >1mm

188
Q

? many photoreceptors are in the retina

The retina is where the initial ? process takes place

? many ganglion cells are there

A

126 million (120M rods, 6M cones)

Visual processing

1M, surround fovea to form optic nerve

189
Q

Path of visual signals

? is AKA the neural way station

Axons leaving here are called ?

A

Optic nerve- eye to chaism
Decussate in chiasm
Optic tract- axons leaving chiasm to lateral geniculate

Lateral geniculate body

Optic radiations

190
Q

Define Visual Cortex

What event begins here

This event is able to explain ? defect

A

Radiations converging in occipital lobe

Visual interpretation

Congruous field defects

191
Q

What are the 11 locations of optic lesions and the type of visual impairment they cause

A

1: optic nerve- monocular loss
2: optic chiasm- bilateral temporal defect
3: posterior to chiasm- homonymous, same side bilateral
4: nerve and chiasm junction- ipsilateral eye blind, contralateral temporal loss
5 and 8: homonymous hemianopic defect
6: temporal lobe- superior homonymous (pie in sky)
7: parietal- inferior homonymous
9-11: occpital lobe- congruous

192
Q

Afferent pathway is d/t ? nerve

Efferent pathway is d/t ? nerve

What are the two parts of Double Decussation

A

CN2: optic nerve, divides at chiasm, ends at EW nuclei

CN3: EW nuclei through CN3 to make pupils constrict

First: chiasm
Second: Pretectal and EW nuclei= direct/consensual responses

193
Q

Define Marcus Gunn Pupil

If this is found, it means ? but not ?

What will be seen on PE

A

Afferent path dysfunction- failure to transmit messages

Underlying d/o present
Not associated w/ particular dz

Light in abnormal eye= both pupils dilate

194
Q

What can cause Marcus Gunn Pupils w/ mild APD

What can cause severe Marcus Gunn w/ severe APD

A
BRVO/BRAO
Amblyopia
Retinal scars
Retinal detach
ARMD
Vitreous hemorrhage
Lesion in chiasm/optic tract
Optic nerve dz
Optic neuritis
Pituitary tumor
Stroke
CRA/VO
Ischemic optic neuropathy
Glaucoma
195
Q

What are the two types of Anisocoria

Define Adie’s Tonic Pupil

What will be seen on PE

A

Physiologic- same difference in dark/light rooms; benign
Pathologic- different sizes in dark/light rooms

Benign, idiopathic d/t denervation of Parasymp supply to sphincter and ciliary muscle

Slow accomodation to light
Irregular dilated
Poor reaction to light

196
Q

Adie’s Tonic Pupil is usually seen in ? population

What other abnormal PE findings may be present

If suspecting Adies Pupil, but EOMs are normal and w/out ptosis, ? Dx is suspected

A

Unilaterally in women

Dec ankle/knee DTRs

CN3 palsy

197
Q

How is Adies Tonic Pupil Dx confirmed

Define Horner’s Syndrome

What 3 PE findings is this Dx associated w/?

A

Pilocarpine in both eyes
Adies= constrict
Normal pupil= won’t constrict

Injury to sympathetic nerves of face

Ptosis- ipsilateral
Anhydrosis- facial
Miosis- anisocoria worse in dim lights

198
Q

Horner’s Syndrome can be caused by injury starting in ? runs via ? and near ?

What other etiologies may be responsible

How is a Dx confirmed

A

Starts hypothalmus
Via upper spinal cord
Near carotid artery

Brainstem stroke
Carotid artery injury
Pancoast tumor
Cluster HAs
Congenital

Topical Aproclonidine (Iopidine- a2 agonist) or Cocaine in both eyes
Horners- only small pupil will dilate
Reversal of anisocoria

199
Q

Pt w/ lack of pigmentation to iris should have ? Dx assumed based on congenital etiology

Argyll Robertson is more of a syndrome that develops d/t ? causing damage located in ?

This syndrome has ? appearance

A

Horners Syndrome

Neurosyphilis- central pupil pathway (retina to EW nucleus)

Small pupil
Light response- slow or none
Accommodates to near vision (light-near dissociation)

Bilateral and asymmetric

200
Q

Papilledema is defined as ?

This develops d/t ?

It’s finding is Dx as ? until disproven

A

Bilateral optic disc edema

Inc ICP

Intracranial mass

201
Q

What issues can impede CSF flow and cause papilledema to develop

? idiopathic etiology can cause it’s development

What are the Sxs associated w/ this Dx

A

Dural sinus thrombosis
Meningitis
Aqueductal stenosis
Trauma

Idiopathic Intracranial HTN d/t pseudotumor cerebri

HA w/ N/V
Vision loss w/ posture changes
Pulsatile tinnitus
CN6 paresis= horizontal diplopia
Secondary to intracranial mass
202
Q

What is the presentation/population Papilledema is seen in

What is always the first step in a papilledema work up

What image needs to be ordered

What is the next step if, and only if, this image is normal

A

IIH w/ obese female

Blood pressure

MRI w/ contrast

LP to measure opening pressure

203
Q

How is Papilledema Tx if it’s etiology is d/t Pseudotumor Cerebri

What is the next step if Pt continues to have visual field deterioration despite the above therapies

How does Ischemic Optic Neuropathy present

A

Furosemide
Acetazolamide
Weight loss
Neurosurgical shunt

Neurosurgical shunts

Papillitis- disc welling from inflammation

204
Q

What are the two etiologies of the papillitis seen in Ischemic Optic Neuropathy

This condition is also associated w/ ? other conditions or c/c

Pts that are >60y/o w/ Ischemic Optic Neuropathy, type AAION, probably have ? Dx compared to if the PT is middle aged they have ?

A

Sclerotic/Thrombotic artery occlusion
Severe HOTN/blood loss

DM/HTN
Carotid/Temporal artery dz
Proximal muscle/joint aches

> 60: GCA
Mid-age: NAION

205
Q

Initially, Pts w/ Ischemic Optic Neuropathy will have ?

If this is truly NAION, the optic disc pallor will resolve w/in ? time

What will the ESR be if GCA is the cause

A

Unilateral swollen optic disc

4-8wks

> 50

206
Q

What signs will be present during GCA Arteritic Anterior Ischemic Optic Neuropathy

What are the Sxs

What are the Sxs that are different during Non-Arteritic Ischemic Optic Neuropathy

A

Firm, tender temporal arteries
Mild anemia
3/4/6 palsy
Afferent pupil defect

Sudden, painless vision loss

Amaurosis Fugax- TIA
Starts during morning walks
Altered color vision w/ dec VA

207
Q

What does the work up for ION include

What are the goals of Tx for each type

How is AAIOn Tx

A

Neuroimaging
Eval for HTN DM Anemia
Westergren ESR and CRP

AAION- preserve fellow eye, worse prognosis
NAION- observe w/ ASA x 8wks

Systemic steroids-
IV Methylprednisone x 72hrs then, 
PO prednisone x 3 days then, 
50mg x 4wks or ESR/CRP normalize
Temporal artery biopsy
208
Q

What is possibly the first sign a Pt may have MS

What infectious dz could cause this

What non-infectious processes could cause this

A

Optic neuritis

Lyme Dz

Sarcoidosis
SLE

209
Q

What are the 3 variations of Optic Neuritis

What are the Sxs

What Pts is this condition more likely in and w/ ? signs

A

Retrobulbar- posterior to globe
Papillitis- edema of optic disc
Neuroretinitis- papillitis w/ inflammation of retinal nerve fibers

Unilateral vision loss w/ orbital pain, worse w/ movement
Frontal HA

30y/o average
Loss of central/altitude visual field
Dec color vision
Afferent pupil defect

210
Q

What is the work up for Optic Neuritis

How is this Tx if it’s d/t MS

A

Opthal eval
MRI w/ contrast
CBC CXR E+

One are of demyelination:
Pulsed IV steroids x 3 days then,
PO steroids x 11 days then,
4 day taper

Two or more lesions on MRI:
Same steroid regiment w/ Interferon B-1a after

211
Q

What therapy is avoided during the Tx of Optic Neuritis if d/t MS

Define Amaurosis Fugax

What is a possible physiological cause of this

A

Start therapy w/ PO Steroids- increased recurrence rate

TIA- loss of vision in one eye d/t temporary lack of blood flow to retina that resolves spontaneously

Broken clot from carotid artery

212
Q

What are the RFs for Amaurosis Fugax

What is the name of the plaque that may be seen on PE

A
Atherosclerosis
High cholesterol
DM
Heart Dz
Tobacco
HTN

Hollenhorst

213
Q

CN3 palsy will affect ? muscles

What is the etiology of this form of palsy

What are the S/Sxs of this condition

A

SR IR IO MR
Levator palpebrae
Pupil sphincter

Vasculopathic- pupil sparing (DM/HTN)
Compression- tumor, anuerysm
Trauma

Ptosis
Eye down and out w/ diplopia

214
Q

What PE finding is an ominous sign when evaluating CN3 palsy

What is the immediate next step if found

How is this Tx if no pupil involvement is present

A

Dilated pupil

Stat MRI w/ contrast to r/o aneurysm
Cerebral angiography- suspected aneurysm

Observe x 3mon, still present= image

215
Q

What is the Tertiary Action of SO nerve that would be affected during CN4 palsy

What are the etiologies for this type of palsy

A

Moves eye away from nose

Idiopathic
Trauma
Vasculopathic (DM, HTN)
Tumor

216
Q

What are the S/Sxs seen w/ CN4 palsy

MRI imaging is warranted if ? criteria are met

Other than Tx underlying d/o, what else is done for Tx

A

Vertical/oblique diplopia
Objects appear tilted
Head tilt to contralateral shoulder
Eye doesn’t depress w/ adduction

<45y/o
45-55y/o w/out RFs
Other CN involvement

Corrective lens

217
Q

CN6 Palsy affects ? nerve

What is the MC etiology

What are the other possibilities

A

Abducens innervation to LR muscle

Vasculopathic (DM, HTN)

Tumor
Idiopathic
Cavernous sinus dz
Intercranial HTN
Trauma
218
Q

What are the S/Sxs seen w/ CN6 Palsy

How are these worked up

How are these Pts Tx

A
Horizontal diplopia, worse at distance
HA
Esotropia
Abduction deficit
Head tilt toward side w/ palsy, minimizes diplopia

MRI if w/out vascular RF
Ophthalmic eval

Strabismus surgery- chronic, stable deviation
Occlusion patch for diplopia
Prism glasses- temporary

219
Q

Define Preseptal Cellulitis

This form of infection doesn’t pass ? structure

What are the two MC microbes for this Dx and Orbital Cellulitis

A

Infected inflammation of eye lid

Orbital septum

Staph A/Strep

220
Q

Pts w/ Preseptal Cellulitis may have Hx including ? 5 things

What are the Sxs

What are the four ‘NO’ signs

A
Bites, insects
Abrased skin
Sinusiits
Hordeolum
Herpes simplex/zoster

Periorbital swelling
Mild fever
Tender, red and swollen lid

No Proptosis Restricted motility Optic neuropathy Pain w/ movement

221
Q

Preseptal cellulitis lasting 6wks post-Tx needs ? three steps taken

How is this condition worked up

How are mild cases Tx

A

InD
Hot compress
IV Vanc

Ocular exam
CT scan if trauma in Hx

Mild:
PO ABX (Augmentin, Cephalexin)
222
Q

What criteris would place PT w/ Preseptal Cellulitis in Mod-sev categories

Once admitted, what ABX are used

Orbital Cellulitis is commonly secondary to ? three Dxs

A

Non-compliant
Under 5y/o
Toxic appearing

IV Vanc and Ceftriaxone

Periorbital infection
Sinusitis
Dental infection

223
Q

Pts w/ Orbital Cellulitis may have ? findings in Hx

What Sxs may be present

What sings are seen

A
Dacryocystitis
Impetigo
Conjunctivitis
Hordeolum
Rarely- septicemia

Swelling Warm lids Pain Diplopia

Fever
Inc WBC
Dec vision w/ sluggish pupil response
Proptosis
Restricted/painful ocular motility
224
Q

How is Orbital Cellulitis Tx

What is added for exposure secondary to proptosis

When is surgical drainage indicated

A

Admit
IV x 3 days then PO x 1wk: Vanc + AmpSulbactam

Erythromycin

Large abscess
No ABX response x 2-3 days

225
Q

What are 3 types of retinal tumors the eye is susceptible to

What are the Sxs of a Corneal Abrasion

What is absent on exam

A

Retinoblastoma- rare in Pts <5y/o, present as leukocoria
Astrocytoma- non-malignant tumor of CNS made of astrocytes, present as leukocoria
Malignant melanoma- ASx

Foreign body sensation
Involuntary lid closure
Tearing
Severe pain

Discharge

226
Q

What provides immediate pain relief for Pts w/ Corneal Abrasion

What needs to be carefully avoided w/ these Pts after eval and upon discharge from office?

What is a workup include

A

Topical Anesthetic- Propara/Tetra-caine

Topical anesthesia

Slit lamp w/ topical anesthetic
Lid eversion

227
Q

How are Corneal Abrasion Tx

What cycloplegic agent may be used for traumatic iritis

What also needs to be avoided depending on the etiology

A

Topical ABX if vegetative matter/contact wearer- FQN
Others- Polymyxin B/Trimethoprim

Cyclopentolate

Patching- nails or vegetative matter

228
Q

How often are Corneal Abrasion f/u w/?

Why does sleeping in contacts cause irritation

How long must these be d/c when Tx

A

Daily at first
2-3d until healed

Dec O2 to cornea= epithelium becomes hypoxic

x14 days

229
Q

If there is an abrasion associated w/ contact wear irritation, what type of coverage is needed

What ABX combo is recommended

What types of activities can lead to UV Keratitis

A

Gram-neg
Pseudomonas

Fortified Gentamicin or Tobramycin and,
Fortified Cefazolin or Vanc

Welding Tanning Snow blindness

230
Q

When are UV Keratitis Sxs worse and what may be seen on PE

How is this Tx

Most serious chemical burns to the eye are ? type

A

6-12hrs after activity
Dense punctate staining

Analgesic Cyclopentolate Erythromicin
Patch the more affected eye

Alkali-
Bleach Airbags Lye Lime Ammonia

231
Q

How long should chemical burns be washed out for

What analgesic can be used during the work up part of these burns

How are chemical burns Tx

A

30min
Wait 5-10min, measure pH in fornices w/ litmus paper
Continue irrigation until neutral pH reached

Proparacaine

Atropine
PO pain meds
IOP control/tears PRN
Erythromycin

232
Q

How are Corneal foreign bodies Tx

What ABX are recommended after removal

A
VA before any procedure
Globe penetration= Ophth referral
Superficial=
Topical anesthetic
Irrigation
CTA/Jewelers forceps

Polymyxin B/Trimethoprim
FQN

233
Q

How are Intra-ocular Foreign Bodies seen on PE

What will be seen in the foreign body has been in place for long time

What type of defect may be seen w/ Slit Lamp exam

A

Irregular pupil w/ peak at site of injury

Siderosis- deposition of Fe into tissue

Trasillumination defect- red reflex where it shouldn’t be

234
Q

How are Intraocular Foreign Bodies Tx

What are the two types of Blow-Out Fx

A

Shield eye
Tetanus
IV Vanc and Cycloplegic
Surgery always advised

Direct: involves orbital rim, extends posterior along floor
Indirect: compression of orbital soft tissue, forces transmitted to orbital walls and Fxs w/out rim involvement

235
Q

What are the Sxs of Blow-Out Fx

What do Pts need to be advised to avoid

What are the signs that may be seen

A

Pain w/ movement
Binocular vision

Sneezing/blowing nose- communication between orbit and sinus

Restricted EOMs
Enophthalmos- posterior displaced globe
Numb/tingling upper lip/cheek

236
Q

What image is used to Dx Blow-Out Fxs and what images need to be avoided for Dx

How are these Tx

Define Hyphema

A

CT
Avoid plain films for Dx

Nasal decongestants x 3days
Cephalexin
Ice packs for first 48hrs

Blood collection in anterior chamber from trauma to iris or ciliary body

237
Q

What can cause Hyphemas to spontaneously reoccur

What is the MC history

What is the next step if Pt is AfAm

A

Clotting d/o
Leukemia
Retinoblastoma
Spontaneous= abuse

Trauma

Screen for Sickle Cell

238
Q

How are Hyphemas Tx

What three Txs need to be avoided

A

Ophtha consult- mandatory
Bed rest w/ head elevation (admit if non-compliant)
Shield eye, don’t patch
Atropine BID

Patches
ASA
NSAIDs

239
Q

What needs to be evaluated during lid laceration work up

What image may be used to r/o Fxs

What muscle function needs to be assessed

A

Dilate both eyes
Eval canalicular/lacrimal system

CT

Levator muscle

240
Q

How are lid lacerations Tx

What are the indications to refer to Ophth

A

Tetanus prophylaxis
ABX if contaminated/foreign body suspected

Canalicular involvement
Ruptured glove
Intra-ocular foreign body
Levator involement (ptosis)
Visible orbital fat= orbital septum perf'd
>1/3 lid tissue lost
241
Q

Scleritis Episcleritis Conjunctivitis

Pain 
D/c
Red
Onset
SystSxs
A

Scler: Sev No Foc/Diff Insid Yes (SNFIY)

Epis: Mild No Foc Acute yes (MNFAY)

Conjunct: Min Yes Diff Days No (MYDDN)

(PDROS)

242
Q

LR6 SO4 R3

IO
SO

SR
LR
IR
MR

A

Extort/Elevate
Intort/Depress

Elevate
Abduct
Depress
Add

243
Q

Eye muscle distanced

What are the two Neuro-Significant nystagmus’

A

SR: 7.5mm
MR: 5.5mm
IR: 6.5mm
LR: 7mm

Vertical/See-saw
Brain stem lesions

244
Q

When is visual potential the greatest for amblyopia

Path from eye to nasolacrimal duct

What Sx of Blepharitis is worse in the AM

A

<8y/o d/t neuroplasticity

Punctum Caniculus Sac Duct

Epiphora

245
Q

Comitant Esotropia is AKA ? and applicable for ? ages

This can be d/t ? two things

What can cause Non-Comitant Esotropias?

A

Accommodative: 6mon-6yrs

Cataract- sensory deprivation
Tumor

EOM, CNS

246
Q

What type of Nystagmus is test for during sobriety tests

What does a See-Saw nystagmus mean

What visual issue may Pts complain of

A

Physiologic

Lesion of chiasm or 3rd venticle
Parasellar mass

Bitemporal heminopia

247
Q

What does an Upbeat Nystagmus mean

Where can the lesion be located to create this type

What finding may be noted if this is d/t drug ingestion

A

Fast phase is up

Brainstem
Vermis of cerebellum

Upward gaze

248
Q

Define Down Beat Nystagmus

This is AKA ? malformation

The lesion is usually located ?

A

Fast phase is down

Arnold-Chiari malformation

Cerebellum

249
Q

Acquired Nystagmus is AKA ?

This is usually acquired from neurological dysfunctions from ?

What do these Pts also suffer from

A

Late onset nystagmus

Stroke MS Trauma

Oscillopsia- creates vertigo effect

250
Q

What anti-seizure meds can create an acquired nystagmus

Congenital Nystagmus is AKA ?

These usually show up <6mon and can be d/t defects located where?

A

Dilantin
Phenobarbital

Early Onset

Eye, visual pathway

251
Q

Congenital Nystagmus can be a s/e of vision loss from ? eye Dzs

These PTs are less likely to suffer from ? issue

? is the MC form of conjunctivitis

A

Albinism
Cataracts
Glaucoma

Oscillopsia

Viral

252
Q

Dacryadenitis needs to have ? structures evaluated?

If this is from an infectious etiology, ? ABX are used

? is MC Sx of late onset strabismus from trauma/stroke or tumor

A

Parotid glands

Augmentin or Cephalexin

Diplopia

253
Q

? is the metabolic support system of the retina

Define the 3 criteria for Clinically Significant Macular Edema

A

Retinal pigment epithelium

Retinal edema <500um (1/3 disc diameter) of fovea center
Hard exudates <500um of fovea center
Retinal edema over 1 disc area in size and 1 disc diameter of fovea center

254
Q

CRAO PE finding

First Visual Field defect seen that could indicate possible glaucoma

A

Scattered Cotton Wool Spots

Nasal step

255
Q

? PE finding may be seen in advanced cases of POAG

Normally w/ POAG, cup:disc is ?

How is this Tx

A

Afferent defect

0.6 or >

Refer
Prostaglandin analogs

256
Q

What are Filtering Blebs associated w/

What is the name to test the angle between cornea and iris

A

POAG

Von Herrick Test

257
Q

ON

Age
Presentation
VA
VF
Disc
Pain
A
ON: 30y/o F>M w/ HA and vision loss over days
20-20/200
Central scotoma
Edema/Hyperemic
W/ eye movement
258
Q

NAION

Age
Presentation
VA
VF
Disc
Pain
A
>50
Sudden unilateral vision upon walking
20/100-20/400
Inferior altitude or variable
Edema, hemorrhage, small cup
No pain
259
Q

AAION

Age
Presentation
VA
VF
Disc
Pain
A
70y/o
F w/ HA, scalp tenderness and jaw claudication
20/400-LP
Inferior altitude
Edema, normal cup
Yes
260
Q

MC microbe to affect contact wearers

Nystagmus that causes Pt to feel like everything is moving and has vertigo is d/t ? type

Avoid steroid use during ? two Txs

A

Acanthomeobae

Acquired

HSV and Fungal keratitis

261
Q

Corneal abrasion in contact wearer needs ? ABX Rx’d

Best Dx imaging for assessing diabetic retinopathy

Gold standard test to Dx Acute Angle Closure

A

Fqn

Fluorescein angiography

Gonioscopy