Eyes III and IV Flashcards

1
Q

Cataracts

  • Etiology
  • Risk factors
  • Symptoms
  • PEx
  • Tx
A

Cataracts

  • Leading cause of blindness in the world
  • Opacity to natural lens of the eye
  • Often bilateral
  • Degree of opacification and extension to which lens is affected is variable

Etiology

  • Age related (senile cataracts)
  • Congenital
  • Traumatic
  • Medication related (steroids)

Risk factors

  • Sun exposure
  • Smoking

Symptoms

  • Gradual, chronic, painless loss of VA
  • Complain of glare, especially at night

PEx

  • Dec VA
  • Dec color VA
  • Opalescent changes to lens
  • Abnormal / absent red reflex
  • As cataracts mature, the retina is blurred or obscured until a normal red reflex cannot be obtained

Tx

  • Refer to ophtho
  • Rx glasses
  • CE w/ IOL
  • Prognosis is excellent
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2
Q

Strabismus

  • What is it
  • Types
  • Risk factors
  • Complications
    • Amblyopia
    • What is it
    • Types
  • PEx
  • Tx
A

Strabismus

  • Any anomly in the alignment of the eyes
  • May be intermittent or constant
  • Types:
    • Esotropia (crossing)
    • Exotropia (wandering)
    • Vertical misalignments (hypertropia)
    • Less common
      • Oblique muscle palsies
      • Duane’s syndrome (abducent nerve palsy)
      • Brown syndrome

Risk factors

  • Affects 4% of the population
  • Family hx
  • Low birth weight
  • Neurologic complications (cerebral palsy)
  • Low vision (i.e. born with optic nerve atrophy)

Complications

  • Amblyopia
    • Reduction in VA caused by disuse / misuse during the critical period of visual development
    • Visual development occurs up until the age of 6-8 years old
    • Types:
      • Strabismic
      • Anisometropic or refractive
      • Deprivational
        • Congenital cataracts
        • Ptosis
        • Blocked visual axis

PEx

  • Vision
  • EOMs
  • Corneal light reflex (Hirschberg’s test)
    • Tropia: always deviated
    • Phoria: sometimes deviated
  • Cover/uncover test
  • Alternative cover test

Tx

  • Refer to ophtho
  • Rx glasses
  • Therapeutic eye patching
  • Eye muscle sx
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3
Q

Nystagmus

  • What is it
  • Movement patterns
  • Etiology
  • Signs and symptoms
  • Tx
A

Nystagmus

  • Rhythmic regular oscillation of the eyes
  • Movement patterns
    • Jerk nystagmus (MC)
      • Consists of alternating phases of a slow drift in one direction with a quick “jerk” in the opposite direction
    • Pendular nystagmus
      • Consists of slow, “pendular” oscillations to and from
  • May be variable depending on eye movements

Etiology

  • Congenital
  • Intoxication
  • Metabolic derangements
  • Infections
  • Tumors

Signs and symptoms

  • Possible dec VA
  • Notice eye shimmering or shaking

Tx

  • Depends on underlying cause and may be managed by ophtho or neuro
    • Meds (baclofen, gabapentin)
    • Botulinum injections (Botox)
    • Prism lenses
    • Sx (Kestenbaum muscle sx)
  • Sometimes no tx is required
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4
Q

Optic neuritis

  • What is it
  • Associated with
  • Clinical presentation
  • PEx
  • Dx
  • Tx
A

Optic neuritis

  • Inflammatory demyelinating condition that results in acute vision loss in one eye
  • Strongly associated with MS and is the presenting factor in 20% of patients
  • Also associated with viral infections, such as measles, mumps, and influenza
  • Most cases occur in women between ages 20-40 (this lines up with MS)

Clinical presentation

  • Acute onset (hours to days)
  • Monocular vision loss
  • Eye pain, worse with EOMs
  • VF defects, usually central scotoma

PEx

  • Loss of color vision
  • Dec VA
  • Relative afferent pupillar defect (APD) - PERRL
  • Possible optic nerve changes
  • Most cases (2/3) are retrobulbar (behind the eye) so there may be no changes on fundus, however in some cases (1/3) the optic nerve is swollen with pallow and occasionally has flame shaped peri papillary hemorrhages

Dx

  • MRI of brain and orbit (with gadolinium contrast)
  • Also assesses risk for MS

Tx

  • Refer urgently to ophtho
  • IV methylprednisolone x 3 days, then oral taper to accelerate vision recovery
  • VA returns in 2-3 weeks
  • Optic atrophy may be seen if sufficient nerve fibers have been destroyed
  • If VA does not return, must r/o compressive lesion or tumor
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5
Q

Papilledema

  • What is it
  • Clinical presentation
  • Ddx
A

Papilledema

  • Swelling of the optic nerve head, usually in association with elevated intracranial pressure
  • Optic disk is swollen, with blurred margins, cup may be obscured due to swelling
  • The venules are dilated and tortuous
  • There may be flame hemorrhages and infarctions (white, indistinct “cotton-wool spots”) in the nerve fiber layer, and edema in the surrounding retina

Clinical presentation

  • Patients often present first with other signs & symptoms of increased intracranial pressure before papilledema is noted
  • HA (especially first thing in the morning)
  • Often with N/V
  • Transient vision changes (sometimes VA is normal in acute phase)

DDx

  • Intracranial mass lesion (tumor)
  • Cerebral edema (encephalopathy, TBI)
  • Disorders of the CSF
  • Obstructive hydrocephalus
  • Idiopathic intracranial hypertension (aka pseudotumor cerebri)

Tx

  • Urgent ophtho referral
  • MRI
  • Possible lumbar puncture
  • VF, OCT
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6
Q

Age related macular degeneration

  • What is it
  • Risk factors
  • Symptoms
  • Dry AMD
  • Wet AMD
  • PEx
  • Dx
  • Tx
A

Age related macular degeneration

  • Leading cause of adult blindness in industrialized countries
  • Degenerative dz of the macula that causes central vision loss
  • Incidence increases with each decade over 50 years old
  • Risk factors: age, female, smoking, family hx, possible genetic component

Symptoms

  • Gradual or acute painless vision loss in one or both eyes
  • Metamorphopsia (wavy/distorted vision) is one of the earliest signs of wet AMD
  • Central scotoma

​Dry AMD

  • Retinal drusen appear as discrete yellow deposits
  • Retinal pigment epithelium atrophies decreasing central vision
  • Dry AMD has better prognosis than Wet

Wet AMD

  • May be acute onset
  • Characterized by growth of abnormal vessel into the subretinal space
  • New vessels leak
  • Wet AMD accounts for 80-90 % of cases of blindness due to AMD

PEx

  • Possible dec VA
  • Amsler grid distortion
  • Dry AMD
    • Drusen, pigmented mottling
    • Geographic atrophy
  • Wet AMD
    • Subretinal fluid or blood
    • Subretinal neovascular membrane

Dx

  • Dry or wet: fundus exam with ophtho
  • Wet may require
    • Fluoresceine dye retinal angiography
    • OCT

Tx

  • Ophthalmology referral
  • Vitamins (antioxidants/zinc)
  • Smoking cessation
  • Daily Amsler Grid
  • Intravitreal anti-angiogenic injections (VEGF inhibitor)
  • Photodynamic therapy
  • Low vision aids
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7
Q

Retinal detachment

  • What is it
  • Risk factors
  • Symptoms
  • PEx
  • Tx
A

Retinal detachment

  • MC is tear in the retina - vitreous fluid can work its way under the retina causing detachment
  • Superior temporal retinal area is the most common site of detachment
  • Other causes include traction on the retina by vitreous detachment or processes such as DM
  • Can be spontaneously or secondary to trauma
  • Risk factors: age over 50 y/o, extreme myopia, previous ocular sx, or family hx

Symptoms

  • Patients often complain of an acute onset of monocular, decreased vision and may describe a “curtain coming down” over their eye
  • Other complaints include cloudy or smoky vision, “floaters”, or “flashes of light”
  • No pain or redness (no inc in IOP)

PEx

  • Afferent Pupillary Defect
  • Fundoscopic exam may reveal a billowing or tent-like elevation of the rugose retina
  • The elevated retina often appears out-of-focus and gray
  • May also notice vitreous hemorrhage

Tx

  • Urgent referral to ophtho
  • During transport patient should remain supine and with head turned to ipsilateral side to help the retina fall back into place with the aid of gravity
  • Treatment is directed at closing the tears utilizing cryosurgery or laser surgery
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8
Q

Amaurosis fugax

  • What is it
  • Dx
  • Tx
A

Amaurosis fugax

  • Amaurosis fugax (“fleeting blindness”) is usually caused by retinal emboli from ipsilateral carotid disease
  • The visual loss is usually described as a curtain passing vertically across the visual field with complete monocular visual loss lasting a few minutes, and a similar curtain effect as the episode passes
  • Workup warranted to determine cause of embolus

Dx

  • Noninvasive evaluation of the carotids can be accomplished using duplex ultrasonography and magnetic resonance angiography (MRA)
  • Emboli from cardiac sources (such as atrial fibrillation) may also be responsible, therefore EKG and echocardiography may be indicated

Tx

  • Depends on the cause
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9
Q

Central retinal artery occulsion

  • What is it
  • Symptoms
  • Signs
  • PEx
  • Tx
A

Central retinal artery occulsion

  • When amaurosis fugax lasts longer than a few minutes
  • Occlusion of retinal arteries by emboli results in decreased blood flow and hypoxia to retina
  • May have repeated transient episodes before complete loss (amaurosis fugax)

Symptoms

  • Sudden painless, total monocular vision loss
  • No eye redness

PEx

  • Often no light perception
  • Afferent pupillary defect
  • Pale retina with cherry red spot at the fovea (there is backup blood flow at the fovea)

Tx

  • Emergent referral to ophtho
  • Tx not effective unless started within a few hours of onset
  • Goal is to evaluate cause and prevent further emboli
    • Carotid plaques
    • Cardiac emboli
    • R/o temporal arteritis is pt is over than 55 y/o
  • Prognosis is poor
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10
Q

Central retinal vein occulsion

  • Symptoms
  • PEx
  • Tx
A

Central retinal vein occulsion

  • Occulsion of veins due to thrombi
  • In patients with hypercoagulable states

Symptoms

  • Symptoms often noticed first thing upon waking
  • Acute painless unilateral vision loss
  • No eye redness

PEx—

  • Signs
  • Variable visual acuity
  • +/- APD
  • Multiple hemorrhages
  • Venous dilation and tortuosity
  • “Blood and Thunder” fundus

Tx

  • Urgent referral to ophtho
  • ASA (if underlying coagulopathy)
  • Observation in most cases
  • Tx if there is macular edema
  • Evaluate cause if pt is young
    • Severe HTN
    • Hypercoagulable states
  • Prognosis: variable
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11
Q

Diabetic retinopathy

  • What is it
  • When are exams recommended
  • Symptoms
  • 2 changes to the retinal vasculature
  • Classification
  • PEx
  • Tx
A

Diabetic retinopathy

  • Leading cause of blindness in the Western world in patients less than 50 y/o
  • DM patients should have yearly dilated exam
  • Exam is recommended:
    • Type I DM within 5 years of dx
    • At first dx in Type II
    • If ocular sxs develop or if there are suspicious findings of retinopathy
  • Present in 40% of DM patients
  • Typically asymptomatic until later stages
  • Patients may complain of blurred vision due to acute increases in serum glucose, causing lens swelling and a refractive shift even in the absence of retinopathy

Many factors lead to development of clinical diabetic retinopathy which cause two basic changes to the retinal vasculature, namely:

  • Abnormal permeability of the vessels
  • Vascular occlusion leading to ischemia and subsequent neovascularization

Classification

  • Non-proliferative Diabetic Retinopathy
  • Proliferative Diabetic Retinopathy
  • Diabetic Macular Edema (can occur at any stage, with either one above)

PEx

  • Non-proliferative
    • Microaneurysms (earliest sign)
    • Dot-blot hemorrhages
    • Cotton-wool spots (ischemia)
  • Proliferative
    • All features of non-proliferative
    • Neovascularization
    • Vitreous hemorrhage
    • Traction RD
    • Prognosis worse in proliferative
  • Macular Edema
    • Can occur at any stage
    • Fundoscopic findings
      • Retinal thickening
      • Microaneurysms
      • Hard exudates

Tx

  • Control blood sugar
    • Glucose < 120
    • A1C < 7
  • Reduce comorbity
  • Ophtho referral
    • Laser photocoagulation
    • Anti angiogenic injection
    • Vitrectomy
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12
Q

Hypertensive retinopathy

  • Symptoms
  • PEx
  • Classification
  • Tx
A

Hypertensive retinopathy

  • Retinal vascular changes due to systemic HTN

Symptoms

  • Asymptomatic
  • No vision complaints

PEx

  • Systemic HTN
  • Characteristic fundoscopic findings

Classificiation

  • Mild
    • Arteriolar Narrowing (“Copper wiring”)
    • Arteriolar Sclerosis (“Silver wiring”)
    • A:V crossing changes (“A:V nicking”) - artery becomes hard and stops flow of veins, blood backs up, because they cross tightly to each other
  • Moderate
    • Cotton-wool spots
    • Retinal hemorrhages
    • Retinal edema/exudates (macular star)
  • Severe (some or all of the above, plus)
    • Disc edema (papilledema)

Tx

  • Control BP
  • Refer to ophtho
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