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• History and physical examination alone wi ll lead to the
diagnosis in most patients presenting with acute visual loss.
• The most important first step in addressing the patient
with acute monocular visual loss is to determine
whether the loss of vision is associated with pain.
• In patients with acute visual loss without pa in, suspect
centra l retinal artery occlusion (CRAO), central reti nal
vein occlusion (CRVO), or retinal detachment.
Central retinal artery occlusion ( CRAO) and central retinal
vein occlusion ( CRVO) occur most frequently in elderly
patients. About 90% of cases of CRVO occur in patients
older than 50 years. CRAO is a result of a thrombotic plaque
or more commonly an embolus of the central retinal artery,
whereas CRVO is caused by thrombosis of the retinal vein.
Optic neuritis is a painful rapid reduction of central
vision secondary to an inflammatory process of the optic
nerve. Optic neuritis occurs more commonly in women
aged 15 to 45 years. Retinal detachment results from
traction of the vitreous humor on the retina. This causes a
tear in the retina and a separation of the inner neuronal
retina from the outer pigment epithelial layer. Retinal
detachment may occur after ocular trauma, but in
atraumatic cases, this condition is more prevalent in men
>45 years old and in patients with significant myopia. The
prevalence in the United States is 0.3%.
Temporal (giant cell) arteritis is a vasculitis that results
in monocular loss of vision associated with a unilateral
temporal headache. Temporal arteritis occurs most
commonly in woman >50 years old. Whites are more
frequently affected than are other races. Temporal arteritis
• Patients with acute visual loss with associated pain may
have optic neu ritis, temporal (giant cel l) arteritis, acute
angle-closure glaucoma, or a large central cornea l abrasion or ulceration.
• An ophtha lmologist should be consulted immediately
when CRAO or acute angle-closure glaucoma are diagnosed in the emergency department.
is a vasculitis of medium and large arteries and can lead to
optic nerve infarction and blindness.
Acute angle-closure glaucoma is a sudden painful
monocular loss of vision secondary to increased pressure
in the anterior chamber. Acute angle-closure glaucoma
represents < 10% of all cases of glaucoma in the United
States. It is more common in women and is also more
common in African American and Asian populations.
Acute angle-closure glaucoma occurs in patients with
shallow (narrow) anterior chamber angles. As the pupil
dilates, the iris leaflet touches the lens. This impedes the
flow of aqueous humor from the posterior to the anterior
chamber with a subsequent increase in hydrostatic pressure.
Painless, acute loss of vision is characteristic of CRAO,
CRVO, and retinal detachment. In patients with CRAO, the
monocular vision loss is usually complete and quite
sudden. Risk factors include hypertension, carotid artery
disease, diabetes mellitus, cardiac disease (especially atrial
fibrillation and valvular disease), vasculitis, temporal
artentls, and sickle cell disease. Central retinal artery
occlusion must be considered and treated early because
irreversible visual loss occurs after 90 minutes.
The presentation of CRVO is more insidious than retinal
artery occlusion. The patient will have a sudden painless
monocular decrease in vision that is most commonly noted
on awakening. Patients may also describe a sudden decrease,
acutely imposed on a chronic gradual worsening over a
longer period of time ( eg, 1 week). Risk relates to likelihood
Patients with retinal detachment present with painless
loss of vision often described as a sensation of a curtain
moving across the visual field or a shade being pulled
down over the eye. Flashing lights, "spider webs," or "coal
dust" in the visual field may precede visual loss. Risk is
related most closely to severe myopia. Other risk factors
include trauma, previous cataract surgery, family history,
Marfan syndrome (or other inherited connective tissue
disorders), and diabetes mellitus.
Painful loss of vision is seen in patients with optic
neuritis, temporal arteritis, and acute angle closure
pain worsens with eye movement In patients without a
previous diagnosis, 25-65% will develop multiple sclerosis.
Temporal arteritis presents as a sudden monocular loss of
vision associated with a unilateral temporal headache. Eye
pain usually is not present. Risk factors include polymyalgia
rheumatica, female, Northern European descent, and
Lastly, acute angle-closure glaucoma presents as cloudy
vision associated with halos around lights. In addition, the
patient will complain of eye pain or headache along with
nausea and vomiting and possibly abdominal pain. Often
patients will have no previous history of glaucoma.
Farsighted (hyperopic) persons are at r isk secondary to the
shape of their anterior chamber; female and elderly
patients are also at increased risk.
For a full description of the physical examination of the
however, the funduscopic examination is usually most
diagnostic. To perform the funduscopic exam, allow the
patient to sit in a dark room for several minutes before
starting. When the pupil is sufficiently dilated, ask the
patient to focus on an object on the wall and ignore the
examiner. Focus the ophthalmoscope on the eye and
gradually approach the cornea from a lateral position. The
optic disc is noted medially. If only vessels are seen, the
optic disc can be located by knowing that the blood vessel's
branches "point" to the direction of the disc.
Figure 76-1 . A. Central retinal artery occlusion.
B. Central retinal vein occlusion.
Visual acuity is markedly decreased, with the patient often
only able to perceive shadows or count fingers. Initial pupil
examination may be normal; however, after 1-2 hours, the
pupil may dilate. The pupil is poorly reactive to direct light
but has a greater consensual response to light (afferent
pupillary defect). On funduscopic examination, a pale
retina with a cherry-red spotin the macular area (fovea) is
the classic finding (Figure 76-1A).
Visual acuity is variable but the deficit is usually less
severe than retinal artery occlusion. The patient may
retain the ability to see shadows or count fingers. The
veins, and disc edema, referred to as "blood and thunder"
.6. Figure 76-2. Retinal detachment on bedside
The extent of the loss of vision is dependent on the degree
of detachment. Visual field defects will be noted on con
frontation. The pupil examination is unremarkable.
Funduscopic examination reveals an undulating, dull grey,
detached retina. Ocular ultrasound is a bedside procedure
that is very helpful to making the diagnosis of retinal
Visual acuity varies from mildly reduced to no light
perception. Often the visual deficit will be limited to the
central visual field, and the patient will c omplain more of a
a dark red object with one eye and then test the other eye to
see if the object looks the same color. The affected eye will
often see the object as lighter or pink. An afferent pupillary
defect will often be present. If the fundus is normal, the
Palpation may reveal tender, tortuous, and sometimes
pulseless temporal arteries. The degree of loss of vision
depends on when the diagnosis is made. If diagnosed late,
pale, swollen optic disc will be present.
.6. Figure 76-3. A. Schititz tonometer B. Tono-Pen.
Visual acuity is markedly decreased. The patient's sclera
will be red due to ciliary injection. The cornea will be
cloudy. On gentle palpation, the eye may have a rock hard
consistency. The pupil is mid-dilated and nonreactive to
light. Funduscopic examination is difficult to perform in
the face of a cloudy cornea, but is otherwise unremarkable.
To diagnose acute angle-closure glaucoma, intraocular
When temporal arteritis is suspected, an erythrocyte
sedimentation rate (ESR) should be obtained. An ESR
.A Figure 76-4. Acute visua l loss diagnostic algorithm. ESR, erythrocyte sedimentation rate;
>50 mm/hr is almost universally present in patients with
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