What is amblyopia?
When does it develop?
After what age is treatment rarely effective?
Amblyopia is “lazy eye”. It is a loss of visual acuity not correctable by glasses in an otherwise healthy eye.
It develops in infancy or early childhood.
Treatment is rarely effective if initiated after the age 10.
What are the 3 main types of amblyopia?
What is the cause of refractive amblyopia?
What happens when there is marked difference between the 2 eyes?
How is this disorder detected?
What is treatment?
Refractive amblyopia is due to uncorrected refractive errors.
If the refractive error is way worse in one eye, the better eye will be “preferred” and the visual pathways will not develop in the poorer eye.
Detection: eyes will look aligned so you need to detect it with the VISUAL ACUITY TEST
- visual acuity screening at 3, again when starting school
Treatment:
What is the cause of occlusion amblyopia?
How is diagnosis made?
What is treatment?
Occlusion amblyopia is when opacities of the ocular media [cataracts, corneal scarring] prevent adequate sensory input to the retina, disrupting vision development.
Diagnosis: check newborns for media opacities with red reflex
Treatment: remove media opacity [amblyopia may persist still]
What is the cause of strabismic amblyopia?
How is diagnosis made?
What is treatment?
Strabismic amblyopia occurs when the eyes are misaligned due to:
1. CN palsy affecting extraocular muscles
2. non-paralytic [more common with children]
Newborns can cross in [esotropia] or out [exotropia] and only get aligned after a few months.
Diagnosis: centration of corneal light reflex checked by pediatricians in the early months of a child’s life
Treatment:
What happens if patching is overdone when treating a child with amblyopia?
the patient may develop occlusion amblyopia in the previously good eye
How does strabismus in childhood and adulthood differ?
Childhood:
Adulthood:
Parasympathetic fibers innervating the pupillary sphincter muscle and ciliary muscle are in what location?
Where do fibers responsible for the control of extraocular muscles lie?
pupillary sphincter and ciliary muscle parasympathetic fibers wind around the periphery of CN3.
Fibers for movement of MR,SR,IR, IO, levator palpebrae lie more centrally
If a patient presents with a blown pupil and poor control of CN3 extraocular muscles, what should this be considered secondary to until proven otherwise?
What tests do you need to do to verify?
Pupil-involving CN3 palsies are assumed to be secondary to aneurysm until proven otherwise
A 50 year old patient has difficulty moving his eye inward, out and up, out and down, and in and up. The pupillary reflexes are intact.
What is the likely problem? What is this often due to?
Ischemic CN3 palsy - often due to diabetes
An adult patient presents complaining of double vision. They have esotropia.
What CN palsy do they likely have and what are the common causes of this palsy?
CN6 palsy
Esotropia means the eye goes inward, and CN6 controls the LR. If the LR does not work, the eye will go inward.
Causes:
A patient has had recent head trauma and now presents with vertical double vision. What is the most likely CN palsy?
isolated CN4 palsy [no SO function]
*vertical misalignment is frequently subtle and difficult to see on routine exam
What is the initial stage of ocular disease associated with diabetes?
What will you see on the retina?
When will patients at this initial stage experience visual loss?
Nonproliferative diabetic retinopathy
Patient will only experience vision loss at this stage if there is macular edema which thickens the retina and causes blurring
Describe the progression from non-proliferative diabetic retinopathy to proliferative retinopathy.
Describe the features in proliferative retinopathy that leads to retinal detachment and blindness
What is the best treatment for diabetic retinopathy?
Prevention!
Better diabetic control [measured by HbA1c] decreased the incidence
Get eye exams annually
What treatment is done for clinically significant macular edema from diabetes?
Focal laser photocoagulation - seals leaking microaneurysms to decrease retinal thickening
What treatment is done for proliferative diabetes?
What does prolonged systemic hypertension accelerate in the eyes?
How does this manifest on a retinal exam?
Describe normal, early, late appearance.
Prolonged hypertension causes accelerated arteriole sclerosis.
Normal = light streak is reflected by convex arteriole wall [look dark]
Early arteriole sclerosis = light streak broadens and occupies most of the width of the vessel [grey]
Late arteriole sclerosis= light reflex is obscured completely and the arteriole appears white
In addition to arteriole changes, you should also see:
What 4 ocular changes are seen with an acute rise in BP [diastolic >120]?
What change is seen in the most severe form of hypertensive retinopathy due to malignant hypertension?
Most severe = papilledema
A patient has exudate in the retina, cotton wool spots, flame-shaped hemorrhage and bilateral papilledema. This patient has malignant hypertension. How should they be treated?
BP should be lowered in a controlled way because a sudden drop in tissue perfusion can result in ischemic optic neuropathy.
What ocular changes are seen with hyperthyroidism/Graves?
Exophthalmos and lid retraction leads to exposure keratopathy [foreign body sensation, dryness of cornea]
Sarcoidosis is a chronic multisystem disease characterized histologically by ___________________________. It can affect any age, sex or race, but has a propensity for ___________________.
focal, noncaseating granulomas
black women between 20 and 40
What lab findings are associated with sarcoidosis?
What is diagnostic?
Biopsy is diagnostic.
What are the ocular manifestations of sarcoidosis?
What are the signs/manifestations of neurosarcoidosis?
Sarcoidosis is a common cause of:
Neosarcoidosis is 2x as common if fundus is involved.