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Chapter 38  •  Vision Loss
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Is the loss because of a systemic disease?
Key Question
l
Do you have a chronic disease?
Chronic Disease
Diabetic retinopathy is a leading cause of vision loss. It is a progressive condition resulting from incompe­tent arterioles or microinfarctions and allowing hard exudates to leak into the retina. The risk of retinopathy increases with the duration of uncontrolled diabetes. Neurodegenerative disease and juvenile idiopathic ar­thritis can cause vision changes. Prolonged treatment with systemic steroids almost invariably results in the formation of posterior subcapsular cataracts. Marfan syndrome may cause dislocated lens.
Could this be an anatomical problem?
Key Questions (to self)
l
Do the eyes cross?
l
If a child: Does the child squint, especially in the
sun?
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Do the eyes appear symmetrical?
l
Are the eyes bulging or sunken?
Eye Alignment
Amblyopia is impaired vision in an eye that appears to be structurally normal. It is dened in one of the fol­lowing three ways:
1. Strabismic amblyopia occurs when one eye is out of alignment and the fovea of that eye receives an im­age that is different from that received in the opposite eye. The brain suppresses the image in the deviating eye to avoid diplopia and visual confusion.
2. Refractive amblyopia occurs when the refraction of each eye is so different that the child uses the eye that focuses the best, resulting in poor development of the other eye.
3. Deprivation amblyopia is anything that prevents an image from being received clearly by the retina. Conditions such as severe ptosis, congenital cata­racts, or vitreous opacity may cause this.
Squinting
Squinting blocks out the outer rays from the object, resulting in a smaller amount of distortion, and in­creases the chance of being able to perceive the image on the retina more clearly. This often occurs with strabismus. Excessive squinting in bright light may indicate glaucoma.
Exophthalmos
Bilateral exophthalmos is protrusion of the eyeballs that occurs with hyperthyroidism. Lid lag is observed on downward gaze as a lag in the falling of the lid with the globe as it moves downward. Unilateral exophthal­mos may indicate a tumor located behind the eye.
Enophthalmos
Enophthalmos is the backward displacement of the eyeball in the eye socket, leading to a sunken appear­ance. It is caused by starvation, dehydration, or trauma.
Ptosis
With ptosis, the eyelid margin is at or below the pupil. The eyelid appears to be drooping and interferes with vision. Ptosis may indicate a lesion of the oculomotor nerve (cranial nerve III), a neuromuscular weakness, or a congenital condition.
Is there a pattern to the vision loss?
Key Question
l
When does the vision loss occur?
Pattern of Vision Loss
Retinitis pigmentosa is characterized by progressive disorganization of the pigment of the retina, usually accompanied by a decrease in the number of retinal vessels and some degree of optic atrophy. Night blindness is often the rst symptom of vision loss. A progressive loss of vision may occur over decades. Dimming of vision upon standing can occur in some­one with low blood pressure or impending shock.
Individuals who are extremely myopic often expe­rience a reduction in vision at nighttime and may refer to that condition as “night blindness.” Vitamin A deciency or the result of retinotoxic drugs, such as quinine, can cause night blindness.
Can I associate the vision loss with the age of the patient?
Key Questions
l
What is your age?
l
If a child: Is there a history of developmental delay?
l
If a child: Is there a change in school performance?
Vision Loss With Aging
AMD is the leading cause of permanent blindness in older adults. The prevalence increases with each decade over 50 years to almost 35% by the age of 75.
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Chapter 38  •  Vision Loss
The majority of adults over 50 years have some degree of visual impairment. The incidence of cataracts in­creases with age. By age 80, more than half of all Americans either have a cataract or have had cataract surgery.
Developmental Delay
Decreased vision can result in developmental delays. Motor development requires good visual cues and depth perception. Poor school performance may be the rst indication of vision loss related to refractory errors and progressive myopia in some children. Craniopha­ryngiomas can compress the optic nerve system, caus­ing a decrease in visual acuity and a decrease in school performance (Box 38-1).
DIAGNOSTIC REASONING: FOCUSED PHYSICAL EXAMINATION
Children become increasingly threatened the closer the examiner comes to the face. The least-threatening assessment should be done rst.
Assess for Visual Acuity
Visual acuity for distance vision in adults and children older than 4 years is tested using the Snellen or Tum­bling E charts. Test each eye separately, with and
Box 38-1
AGE NORMAL VISION AND EYE MOVEMENTS
Birth (term) Fixation
1 mo Horizontal following to midline
2 mo Vertical following begins
3 mo Good horizontal and vertical following
6 mo Visual acuity 20/20 to 20/30
8 to 10 yr End of sensitive period for amblyopia
From Del Monte M:  The eye in  childhood,  Am Fam Physician 60:907, 
1999.
Development of Vision and Eye Movements
Poor following Intermittent strabismus frequently present Visual acuity 20/400 to 20/600
Normal alignment Visual acuity 20/300
Normal alignment Visual acuity 20/200
Normal alignment Visual acuity 20/100 Accommodation begins Binocularity detectable
Binocularity well developed
without corrective lenses. Normal visual acuity tested using a Snellen chart is 20/20 in the best eye without correction. A Snellen of 20/70 indicates visual impair­ment, and vision that cannot be corrected to better than 20/200 is legal blindness. A Rosenbaum pocket card held 15 inches from the eyes is used to test near or reading vision.
To test for central vision in infants, observe the in-
fant’s eyes as they follow large objects, such as the face or hand of the examiner, in various gazes. In children ages 1 to 3 years, use the cover/uncover test and observe the corneal light reex.
Any child who has a difference of one line between
the two eyes must be referred. Vision of 20/50 for 5-year-olds and 20/40 for children 6 years and older requires referral. Retest using the Snellen chart before referring because children tend to do better on a second examination (Table 38-1).
Assess Lids, Pupils, and Orbits
Note the position of the eyelids. Eyelids that droop (ptosis) may cause vision loss. Assess for the sym­metry of each eye and observe for a transparent cornea.
The appearance of a white pupil (leukokoria) may
indicate a cataract, retinoblastoma, persistent hyper­plastic primary vitreous retinal detachment, vitreous hemorrhage, or intraocular infection, such as by Toxocara canis, which is a roundworm that is con­tracted from dogs and invades the liver, abdomen, and eyes.
Pupil size is smaller in infants and older adults. Five
percent of people will have noticeable differences in pupil size (physiological anisocoria). However, many types of central nervous system diseases also cause differences in pupil size.
Enlargement of the pupil may be caused by ocular
injury, acute glaucoma, systemic parasympatholytic drugs, and dilating drops. Constriction of the pupil is seen in iris inammation and patients with glaucoma who are treated with pilocarpine. Irregularity of the pupil contour is invariably abnormal, occurring in iritis, syphilis of the central nervous system, trauma, and congenital defects.
Inspect for Nystagmus
On far lateral gaze, some eyes will develop a rhyth­mic twitching motion (nystagmus) in the direction of gaze followed by a drift back. This is a normal finding. However, nystagmus is a neurological sign that may indicate disease or structural changes in
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Table 38-1
Pediatric Eye Evaluation Screening Recommendations for Primary Care Providers, Nurses, Physician’s Assistants, and Trained Lay Personnel
RECOMMENDED AGE FOR SCREENING* SCREENING METHOD
Newborn to 3 mo Red reflex
Inspection Structural abnormality
6 mo to 1 yr Fix and follow with each eye
Alternate occlusion Failure to object equally to covering each 
Corneal light reflex Asymmetrical Red reflex Inspection Structural abnormality
3 yr (approximately) Visual acuity
Corneal light reflex/cover-uncover Asymmetrical ocular refixation movements Red reflex Inspection Structural abnormality
5 yr (approximately) Visual acuity
Corneal light reflex/cover-uncover Asymmetrical/ocular refixation movements Stereoacuity Red reflex Inspection Structural abnormality
Older than 5 yr Visual acuity
Corneal light reflex/cover-uncover Asymmetrical/ocular refixation movements Stereoacuity Red reflex Inspection Structural abnormality
Modified from the American  Academy of  Ophthalmology Pediatric Ophthalmology/Strabismus Panel. Preferred Practice Pattern® Guidelines. Pedi­atric Eye Evaluations. San  Francisco, CA: American  Academy  of  Ophthalmology; 2007. *Note: These recommendations are  based on expert  opinion.
Physician or nurse responsibility.
Figures, letters, “tumbling E,”  or optotypes.
§
Optional: Random Dot E  Game (RDE), Titmus Stereograms (Titmus Optical, Inc., Petersburg, VA), Randot Stereograms  (Stereo Optical Company, 
Inc., Chicago).
§
§
CRITERIA FOR REFERRAL TO AN OPHTHALMOLOGIST
Abnormal or asymmetrical
Failure to fix and follow in cooperative  
infant
eye
Abnormal or asymmetrical
20/50 or worse or two lines of difference 
between eyes
Abnormal or asymmetrical
20/40 or worse or two lines of difference 
between eyes
Failure to appreciate stereopsis Abnormal or asymmetrical
20/30 or worse or two lines of difference 
between eyes
Failure to appreciate stereopsis Abnormal or asymmetrical
EVIDENCE-BASED PRACTICE
The  purpose of this systematic review was to measure the  diagnostic  accuracy of  examination findings  and risk fac­tors  in  identifying  individuals  with  prim ary  open-a ngle  glaucoma  (POAG)  because  early  identification  ma y  pre­vent  associated  vision  loss.  The  prevalence  of  glaucoma   in  the  studies  was  2.6%  (9 5%  CI,  2.1 %-3.1%).  Myopia   of  $6  diopters  and  family  history  of  glaucoma  were  risk  factors that  had  the  strongest  association  with  glau­coma.  Demographic  factors  associated  with  an  increased 
Reference: Hollands H, Johnson D, Hollands S, Simel DL, Jinapriya D, Sharma S: Do findings on routine examination identify patients at risk for   primary open-angle glaucoma? The rational clinical examination systematic review. JAMA 309:2035, 2013.
Should Adults Have Routine Screening for Glaucoma?
risk  were  Black  race  and  increased  age  (especially  age  .80  years).  Other  risk  factors  included  an  increased  cup-to-disc  ratio  (CD R),  CDR  asymmetry,  disc  hemor­rhage,  and  increased  intraocular  pressure.  The  authors  found no studies of screening examinations  pe rformed  by  generalist  physicians  in  a  routine  setting  and  conclude  that  the  evidence  supports  examination  by  an  ophthal­mologist or optometrist as the most accurate way to detect  glaucoma.
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Chapter 38  •  Vision Loss
the vestibular-cerebellar-oculomotor system (see Chapter 13). Pathological nystagmus is seen when the movement is in the same direction, regardless of the direction of gaze. Nystagmus in the first year of life suggests bilateral vision loss until proved otherwise.
Assess Visual Fields
Testing of the visual elds assesses the function of the peripheral vision and central retina, the optic path­ways, and the cortex. The peripheral eld is damaged in glaucoma and by tumors or vascular lesions involv­ing the visual bers from the chiasm to the occipital cortex. A central vision loss is decreased visual func­tion surrounded by normal function. Hemianopsia is a visual defect in the right and left halves of the visual eld; this is caused by a lesion involving the chiasm. In homonymous hemianopsia, the same half of the visual eld of each eye is affected by a lesion posterior to the chiasm (see Figure 38-1).
Test Corneal Light Reflex
The corneal light reex test is used to detect strabis­mus. Alignment of the eyes is most easily demon­strated by observing the reection of a light on the cornea. The light should fall in each eye at the same point. An asymmetrical light reex will be present in a deviating eye or in an eye with an asymmetrical contour.
Perform a Cover/Uncover Test
Have the patient look with both eyes at a specic point. With one eye covered, watch the uncovered eye. If this eye moves to x on the point, it was not aligned before the other eye was covered and a heteropia, or deviation of an eye, is present. If the uncovered eye does not move, alignment is present and this is referred to as orthophoria. Repeat the test for the other eye.
metamorphopsia, is found in AMD or central vision loss (Figure 38-2).
Test for Extraocular Movements
Extraocular movements test six pairs of ocular muscles and three cranial nerves (III, IV, and VI). Strabismus is any condition in which the normal binocular alignment of the eyes to a single point in any and all elds of gaze is disturbed; there is an imbalance in neuromuscular sensory and motor control of the extraocular muscles. Half of patients with strabismus also have amblyopia.
Paralytic strabismus is a deviation in the direction
opposite the muscle involved. Double vision is usually a symptom but may not be present if the condition occurred at an early age and the child suppressed the vision in one eye or developed a compensatory head malposition.
Nonparalytic strabismus is present when the angle
of deviation is the same in all cardinal elds of gaze.
Obtain a Direct and Consensual Pupillary Response
In monocular blindness, the affected eye will have no direct pupil response but will react consensually to stimulation of the opposite eye. Stimulation of the blind eye, however, will not cause consensual reaction of the opposite normal eye.
Perform an Ophthalmoscopic Examination
Examination of the optic disc can rule out optic atro­phy, papilledema, and glaucoma. Death of the optic nerve bers results in disappearance of the vessels of the disc, leading to pallor or whiteness of the disc.
Perform an Alternating Cover/Uncover Test
Alternate the cover rapidly on each eye and note any movement of the eyes. Perform this test to discover a latent tendency for misalignment of the two eyes, a condition referred to as heterophoria.
Use the Amsler Grid
An Amsler grid is used to test for distortion of central vision. The patient is asked to wear reading glasses and the chart is held 15 inches from the eyes. Ask the patient to stare at the dot and tell you if the lines around the dot are curved or bent. Distortion, called
FIGURE 38-2 Example of metamorphopsia and a scotoma
projected on an Amsler grid. (From Hampton GR, Nelson PT: Age-related macular degeneration principles and practice, New York, 1992, Raven Press.)
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Observe for a red light reex, especially in the early days and months of life. If the red reexes are not equal, refer to an ophthalmologist. To obtain a red re­ex in a newborn or young infant, swaddle and then hold the child. Position the ophthalmoscope diopter at 0, direct it to the eye, and gently swing or slightly para­chute the infant. The vestibular system usually triggers the infant’s eyes to open because of the maneuver.
In older children and adults, darken the room and instruct the patient to stare at an object or a glow sticker in the distance. When the patient looks at the ophthal­moscope light, look at both red reexes simultaneously and compare them. A uniform red glow equal in color is normal. Absence of a red reex indicates that some abnormality is blocking the transmission of light through the eye.
The earliest sign of papilledema is a hyperemic disc caused by increased venous pressure. The dilated ves­sels leak their contents. The uid leak causes elevation of the disc which may spread beyond the disc margins, making the edges of the disc appear swollen or indis­tinct. In glaucoma, one sees a glaucomatous cup. The disc edge appears to be displaced slightly backward, causing a cup shape.
Hemorrhages scattered in the vitreous cavity tend to disperse and absorb light. A red reex is not seen; only darkness will be seen. This is a common nding in advanced diabetic retinopathy.
LABORATORY AND DIAGNOSTIC STUDIES
Ophthalmoscopy With Pupillary Dilation
Direct ophthalmoscopy allows a view into the retina and optic nerve. More of the peripheral posterior segment is seen when the eye is dilated with a mydriatic drug.
If the iris seems abnormally close to the cornea, dilation is contraindicated because of the risk of induc­ing acute angle-closure glaucoma.
Tonometry
A tonometer is a device that measures intraocular pressure. Intraocular pressure greater than 21 mm Hg is considered a high-risk factor for glaucoma.
Fluorescein Dye
Fluorescein dye is used to detect the presence of abra­sions or a foreign body on the corneal surface. If the corneal epithelium has been disturbed, uorescein will pool within these areas and stain the hydrophilic stoma. A stain showing a dendritic pattern indicates herpes infection.
DIFFERENTIAL DIAGNOSIS
Early detection and treatment of vision and eye dis­eases yield immense benets.
Strabismus and Amblyopia
The most common causes of vision loss in children are amblyopia and strabismus. Amblyopia, or lazy eye, is reduced visual acuity in one eye that is not correctable with lenses. It is caused by incomplete visual system development when a refractive error is not corrected in childhood. Strabismus is a condition in which the two eyes do not point in the same direction when the patient is looking at a distant object. These conditions cause vision loss in 2 out of every 100 children. The risk of the development of amblyopia is greatest during the rst 2 to 3 years of life, but the potential for recur­rence exists until visual development is complete at 9 years of age.
Refractive Errors
Refractive errors are a common visual disorder of childhood, occurring in 20% of children by 16 years of age. Permanent visual impairment may result if optical correction is not provided at an appropriate age.
Myopia (nearsightedness) is when the cornea and lens of the eye focus the image in front of the retina. Hyperopia (farsightedness) is a refractive error in which the focus of an image is behind the retina. Hyperopia can be corrected to some degree by adjustment of the natural lens (accommodation) normally done for near­focusing. The use of accommodation can cause visual fatigue, discomfort, and headache.
Astigmatism
Astigmatism is an irregularity in the refractive sys­tem of the eye that prevents light from being focused onto the retina. It can be secondary to the shape of the cornea or lens and is usually correctable with lenses.
Cataracts
A cataract is any opacity of the crystalline lens of the eye. There are many causes of cataracts and they can be dened by onset, cause, or anatomy.
Congenital cataracts are inherited in an autosomal dominant form and are associated with intrauterine infections by the TORCH complex of organisms. Cata­racts of infancy and childhood occur in 1 per 1000 live births and congenital glaucoma occurs in 1 per 10,000 live births.
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Chapter 38  •  Vision Loss
Adult cataracts are a major cause of visual impair­ment in the elderly because with time, the human lens begins to develop opacities. Cataracts can be caused by galactosemia, metabolic disorders (e.g., diabetic cata­racts), and trauma (e.g., from heat or blunt trauma); steroid-induced cataract formation is also possible. The rst signs of opacity are the inability to focus on near objects (presbyopia) and altered color vision.
Optic Neuritis
Optic neuritis occurs more often in younger adults, 20 to 50 years old, and in women; it is typically monocular. It is often idiopathic and may be associated with multiple sclerosis, after viral infection, and with granu­lomatous inammatory conditions. Vision loss occurs over a few hours to days and is extremely variable. Visual eld loss includes central scotoma in 90% of patients. In the majority of patients, pain precedes the vision loss and is worse with eye movement.
Optic Nerve Hypoplasia
This visual disorder affects the optic nerve, the bundle of bers that transmits signals from the retina to the brain. It is a nonprogressive disorder in which the optic nerve is 25% smaller than the normal size. Some chil­dren have a loss of peripheral vision although others lose central vision.
Injury
More than 100,000 eye injuries occur annually in the general population of the United States, of which 90% are preventable with the use of protective eyewear. Exposure to long periods of high heat or blunt trauma to the eye globe can result in cataracts.
Retinoblastoma
This is the most common intraocular tumor of child­hood; it occurs bilaterally in 30% of cases. A common symptom is strabismus. Retinoblastoma is inherited in an autosomal dominant manner. Early lesions are at, transparent, or white masses in the retina. The tumor can spread to the brain through the optic nerve or into the bone marrow.
have incomplete vascularization with subsequent poor vessel development and visual impairments. Infants who weigh less than 1500 g are at greatest risk.
Central Retinal Artery Occlusion
Patients with this condition have a sudden onset of severe vision loss in one eye. There is no associated pain. The loss is caused by plaque lodging at the level of the lamina cribrosa. On physical examination a few hours after occlusion, the retina becomes edematous and white or opaque. There is a reddish-orange reex from the intact choroidal vascular and foveola that creates a “cherry red spot” that contrasts with the surrounding white retina. With time, the retinal artery opens and the retinal edema clears.
Glaucoma
Glaucoma is loss of vision because of increased pres­sure in the eye. It is characterized by defects in the visual eld and optic nerve damage. Glaucoma is a leading cause of blindness in the United States. Glaucoma can be classied as primary or secondary, and as open- or closed-angle. Secondary glaucoma is associated with another ocular or nonocular event; whereas primary glaucoma is not. Closed-angle glau­coma is caused when the anterior chamber angle is narrowed, reducing the outow and removal of aque­ous humor. Open-angle glaucoma, the most common type, occurs with a normal anterior chamber angle. The condition is painless, and symptoms appear in late stages of the disease. Ophthalmic examination reveals pathological cupping of the optic disc that may be asymmetrical. Patients with intraocular pressures above 21 mm Hg should be referred to an ophthalmologist (Box 38-2).
Retinal Detachment
This condition occurs when the neurosensory retina is separated from the retinal pigment epithelium. About half of patients will have brief ashes of light (photop­sia) or oaters (entopsia). It is caused by a collection of uid beneath the neurosensory retina, traction from brovascular elements associated with diabetic
Retinopathy of Prematurity
This condition is seen in premature infants and refers to the changes of ischemia, blood vessel growth, and brosis that occur because of inadequate oxygen deliv­ery to the peripheral retina. The vessels of the retina normally complete vascularization by 40 weeks of gestation. Infants who are born before this time may
Box 38-2
Visual  acuity  should  be  assessed  intermittently  after  age   40 with no optimal interval recommended. Routine screening  for glaucoma by primary care providers is not recommended.
Adult Vision Screening
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retinopathy, or trauma. Nearly 95% of detachments are
treatable.
Macular Degeneration
AMD is the leading cause of blindness in the United
States. It may be asymptomatic or associated with
gradual loss of central vision. Risk factors include
advanced age, family history, cigarette smoking, hy-
peropia, and hypertension. There are two forms of
pathological macular degeneration, wet and dry. The
wet (exudative) form results in rapid vision loss
caused by the development of abnormal blood vessels
that grow from the choroid into the macular portion of
the retina. These new blood vessels, called choroidal
neovascularization, are very fragile and often leak
blood and uid. Blurred vision is a common early
symptom but vision loss may be rapid and severe. The
dry (nonexudative) form is associated with breakdown
of the light-sensitive macular cells and gradual loss of
central vision. Distortion upon testing with the Amsler
grid is found with dry AMD. Both types can occur in
the same eye.
Diabetic Retinopathy
Diabetic retinopathy is a retinovascular disease that
occurs in two forms. Nonproliferative retinopathy is
characterized by microaneurysms, macular edema,
lipid exudates, and intraretinal hemorrhages. In pro-
liferative retinopathy, blood vessels regenerate on
the retina. The patient may be asymptomatic or have
decreased vision or oaters. Diabetic retinopathy
progresses with the duration of diabetes.
Uveitis
Uveitis is a general term used to describe inammatory
activity of the iris, ciliary body, and choroid. Symp-
toms vary according to cause and severity, but most
patients experience some decrease in vision, light
sensitivity, and tearing. Pain may be variable. Acute
uveitis lasts less than 3 months but it may have a
chronic recurrent pattern.
infection, dry eyes, physical and chemical injury, and systemic disease. Keratitis can range from mild to se­vere and can be chronic. Diagnosis is usually made by an ophthalmologist using a slit lamp.
Optic Nerve Glioma
Optic nerve gliomas are present in two forms. In the adult, they are malignant glioblastomas; in the child, they are benign pilocytic astrocytomas. They appear in children younger than age 10 and are highly associated with neurobromatosis, a condition associated with café-au-lait lesions of the skin. In children, gliomas may appear as the rapid onset of vision loss with head­ache. Of the malignant optic nerve gliomas, nearly 75% present with unilateral, rapidly progressive vision loss with pain.
Craniopharyngioma
Craniopharyngiomas are tumors that arise from squamous epithelial cells of the brain. They are most common in the first two decades of life but also may occur in adults 50 to 70 years old. Chil­dren’s presenting symptoms include headache and visual disturbance caused by increased intracranial pressure. Nystagmus and bitemporal hemianopsia are pathognomonic for this tumor. In the older patient, visual deficit is common in the presence of normal optic discs.
Chemical or Thermal Trauma
A chemical burn is an ophthalmic emergency. Alkaline solutions denature eye proteins and lyse cell mem­branes, allowing the chemical to penetrate the eye. Acid burns can also cause severe damage, but the acid solution precipitates proteins, decreasing the amount of penetration damage.
Congenital Infection
Congenital TORCH infections can cause vision prob­lems in infants. Postnatal screening is performed to diagnose a TORCH infection.
Keratitis
Keratitis is an inammation of the cornea that creates
pain, redness, and blurred vision. It can be caused by
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DIFFERENTIAL DIAGNOSIS OF
Common Causes of Vision Loss
CONDITION HISTORY PHYSICAL FINDINGS DIAGNOSTIC STUDIES
Strabismus Family reports child’s eyes 
cross, family history
Amblyopia May have history of premature 
birth, Down syndrome, cere-
Refractive errors Sitting close to television, 
Cataracts Blurred vision, glare, distortion 
Optic neuritis History of multiple sclerosis, 
Optic nerve hypoplasia History of vision loss, may 
Injury, penetrating injury History suggesting head or eye 
Retinoblastoma
Nystagmus
Retinopathy  
of prematurity
Central retinal artery  
occlusion
Glaucoma
Retinal detachment
Macular degeneration Older than 60 yr, decreased 
Diabetic retinopathy History of diabetes, floaters, 
Uveitis
bral palsy, hydrocephalus
squinting
and change in color percep­tion, increased age, history  of infection, trauma, or  chronic disease
viral infection, pain with eye  movement, rapid vision loss
have central vision but no  peripheral vision
trauma (blunt or sharp)
Family history, child up to  
2 yr old
History of eyes moving  
repetitively, searching
Premature birth ,36 wk, 
weight 1500 g, oxygen   administered, may be a twin
Sudden onset of painless  
vision loss, may come   and go
Most often painless, gradual 
vision loss, blurring, and   halos; more common in  older adults; history of   systemic disease
Sensation of flashing light  
accompanied by shower of  floaters; history of trauma   to head or face
central vision, blue eyes,  image larger in one eye
gradual vision loss
History of  infection or chronic 
inflammation, mild to   moderate pain, photopho­bia, tearing
Extraocular movements  
abnormal, cover/uncover  test positive
Vision decreased in one eye Refer
Loss of visual acuity
Whitish appearance of pupil, 
bilateral or unilateral
Decreased visual acuity,  
reduced color perception,  afferent pupil defect and  central scotoma
Optic nerve is  one half to one 
third normal size, pale to  gray in color, surrounded  by yellow halo
Directed by history Refer
Partial or absent red reflex, 
strabismus
Rhythmic, repetitive  
oscillation of eyes
Abnormalities of retinal  
vessels
Macular edema, cherry  
red spot; may see vessel  narrowing
Decreased visual acuity; may 
have increased intraocular  pressure on palpation of  eye globe
Retina markedly elevated; 
appears gray with dark  blood vessels; may lie in  folds
Hyaline (drusen) deposits  
on retina near macula,  gray-green areas of   pigment under retina,   decreased visual acuity
Venous dilation, retinal  
hemorrhages
Findings vary according to 
cause and severity
Refer
Screen with Snellen, 
Tumbling E, or  figures; refer
Refer
Refer
Refer
Refer
Refer
Refer
Refer
Refer for tonometry
Refer
Amsler grid
Refer
Refer
Chapter 38  •  Vision Loss
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DIFFERENTIAL DIAGNOSIS OF
Common Causes of Vision Loss—cont’d
CONDITION HISTORY PHYSICAL FINDINGS DIAGNOSTIC STUDIES
Keratitis History of infection, trauma, 
mild to severe pain, blurred 
Optic nerve glioma Dimness of vision with loss of 
Craniopharyngioma
Chemical burn 
Thermal burns History of exposure to high 
Congenital infections
TORCH, Toxoplasmosis, rubella, cytomegalovirus, and herpes simplex.
vision, itching with blinking
fields; may be unilateral  rapid vision loss with pain
Unilateral vision loss, head-
ache, child or adult
History of acid or alkaline  
exposure
heat, occupational risk
TORCH, maternal exposure  
to measles
References and Readings
Bell A, Rodes M, Collier Kellar L: Childhood eye examination, Am
Fam Physician 88:241, 2013.
Harvey PT: Common eye diseases of elderly people: Identifying and
treating causes of vision loss, Gerontology 49:1, 2003.
Marx JA, Hockberger RS, Walls RM: Rosen’s emergency medicine:
Concepts & clinical practice, ed. 8, St. Louis, 2014, Elsevier.
McPhee SJ, Papadakis MA: Current medical diagnosis and treat-
ment, ed. 49, New York, 2010, McGraw-Hill.
Norton I: Practical ophthalmology: A survival guide for doctors and
optometrists, Emerg Med Australas 17:524, 2005.
Conjunctivitis Refer for evaluation 
with a slit lamp
Visual field defects, optic  
atrophy
Funduscopic examination 
may be normal
Treat first, then examine
Corneal opacities Refer
Retinitis, optic nerve  
hypoplasia
Quillen DA: Common causes of vision loss in elderly patients, Am
Fam Physician 60:99, 1999.
Thompson L, Kauffman L: The visually impaired child, Pediatr Clin
North Am 50:225, 2003.
Tingley DV: Vision screening essentials: Screening today for eye
disorders in the pediatric patient, Pediatr Rev 28:54, 2007.
Walker S, Harris Z: Detecting the serious visual disorders of
childhood, Pediatr Child Health 22:25, 2011.
World Health Organization: Visual impairment and blindness, Fact
Sheet 282, April 2011. Retrieved from www.who.int/mediacentre/
factsheets/fs282/en/print.html.
Refer
Refer
Immediate eye  
irrigation and   referral
Screen for TORCH, 
refer
CHAPTER
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Weight Loss/Gain
39
nintentional weight loss is a decrease in body
U
weight that is not voluntary. Weight loss in the adult is clinically signicant when it exceeds 5% of usual body weight over a 6- to 12-month period. Weight loss in the newborn may occur immediately after birth but weight should begin to increase by 2 weeks of age. Weight loss will occur with reduced energy (food) intake and increased metabolism or energy output. Every day individuals adjust energy balance to maintain a healthy weight through healthy eating and regular physical activity. Malignancy and endocrine disorders are the most common causes of unintentional weight loss, followed by gastrointestinal (GI), cognitive, behavioral, and functional disorders, as well as age-related changes.
Weight gain occurs when caloric intake exceeds body requirements, causing the body to store fat. Most adults do not intentionally gain weight, but as we age, a decrease in physical abilities leads to a decrease in metabolic rate (amount of energy used in a given pe­riod), which in turn contributes to weight gain. Unex­plained weight gain may be more difcult to identify, especially in the United States, where 40% of men and 28% of women are overweight, 32% of men and 36% of women are obese, and approximately 1 in 20 Amer­icans have a body mass index (BMI) .40 kg/m
The prevalence of childhood obesity is increasing. Unexplained weight gain may be endocrine-related, age-related, or associated with cognitive impairments.
(Unintentional)
2
.
DIAGNOSTIC REASONING: FOCUSED HISTORY
Unexplained Weight Loss
Has the patient lost weight? Is the weight loss really unexplained?
Key Questions
l
How do you know that you (or the child) have lost
weight?
l
How old are you?
l
How is your appetite?
l
How would you describe your typical diet and activity
patterns?
l
If an infant: If breastfeeding, how is breastfeeding
going?
l
If an infant: If feeding formula, what kind is it and
how do you prepare it?
Measuring Weight
Individuals might note that their clothes are too loose or too tight. Weight is usually measured by asking the patient to step on a balance or electric scale clothed and without shoes. Height is measured by asking the patient to stand with the back against a wall with heels touching the wall. There are several ways to classify and measure body weight, but the most commonly used method is the BMI formula, which is BMI 5 weight (kg)/height (m2). To enhance the reliability of measurement of weight changes, ask the patient to weigh himself or herself at the same time each day using the same scale.
Weight and height in infants and children is mea­sured using a scale and plotted on a National Center for Health Statistics growth chart. Infants and children should be measured in a supine position until the age of 2 years. Head circumference is also measured and plotted.
Age
Aging can be associated with both weight loss and weight gain. Normally with aging there is less lean muscle tissue, fat is deposited more in the trunk and less in the limbs, and metabolism slows. In the elderly it is especially important to assess what medications are being taken that could suppress appetite, cognitive status, and memory. Functional limitations that may impact nutrition include the ability to chew and swal­low, prepare meals, and shop for food. Social isolation can also contribute to eating less.
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