Professional Documents
Culture Documents
Notes50 - PEDIATRIC VISION OR HEARING DISORDERS
Notes50 - PEDIATRIC VISION OR HEARING DISORDERS
- light rays do not always focus onto the retina accurately as the - headache and vertigo after doing close work
child grows older > hyperopia - deceptively normal on vision screening tests
o hyperopia begins to diminish at 5 yrs of age, if hyperopia o able to see all of the numbers on a chart by tilting head
remains, child needs medical interventions
- light rays can also focus at a point in front of the retina > myopia TX: corrective lenses or contact lenses (smooths out curvature of cornea)
o tends to be familial; 10% of school-age children Nystagmus
hyperopia - rapid, irregular eye movement, either vertically or horizontally
- light rays do not always focus onto the retina accurately as the - not a disease but symptoms of underlying disease
child grows older - occurs with vision-impairing lesions (congenital cataracts)
o focusing on close objects w strong accommodation - also occurs as a neurologic sign if there is a lesion of the
o tx: glasses w convex lens cerebellum or brainstem
myopia Amblyopia
*often progresses into the teen years, when it plateaus and remains for life - subnormal vision in one eye; the child may be using only one eye
for vision while “resting” the other eye
- focuses on objects by squinting and rubbing their eyes > changes - if progresses severely: central vision fails to develop > functionally
shape of eye globe blind in one eye
o similar Ssx: tearing, red-rimmed eyes, pressing on eyes o one eye focuses more readily than the other, they come
o tx: glasses w concave lenses to depend on only the easily focused eye
- can also develop from strabismus
Therapeutic Management
Assessment: screened w preschool E chart at routine health visits
- contact lenses
o 5 year olds are capable of putting them in and taking out o 20/50 vision (normal for preschool age) in one eye, and
o 12 year olds can be relied to appropriate care for lenses the other eye shows lessened vision
- Laser in situ keratomeleusis (LASIK)
o Incision under the cornea to change the contour of the Therapeutic Management
eye globe * correctable if treated during the preschool period
o Postop: disturbed tear function for 1 or more mos →
prevent surface damage w artificial tears or ointments * prognosis for correction is considerable diminished after 6 years of age
Color Vision Deficit (Color Blindness) - inability to raise the upper eyelid normally so the eyelid always
remains slightly closed
- inability to perceive color correctly - may be congenital (frequently hereditary and bilateral) or
- one of the sets of cones of the retina that perceive red, green, or acquired (usually unilateral)
blue is absent - may be a result of injury to the third cranial nerve (neurogenic) or
o inability to distinguish red from green or blue from
to the lid or levator muscle
yellow
- always rule our myasthenia gravis
o some are unable to see any colors
- inherited as a sex-linked disorder and occurs in about 8% of boys Signs & Symptoms
- high incidence w hemophilia, congenital nystagmus, or g6pd
- no therapy for color deficit - dilated pupil
- Inability to rotate the eye globe upward, medially, or downward
- Weakness of accommodation (looking at near objects)
Structural Problems Of The Eye - tend to wrinkle their forehead and raise their eyebrows more
than usual in an attempt to lift the eyelid further
- cock their heads back to see under the lowered lid
Coloboma
Therapeutic Management
- congenital incomplete closure of the facial cleft; may involve:
o only the lower eyelid (notch in lid), - correction surgery
o iris, giving it the shape of a keyhole, rather than a circle o if ptosis obstructs vision, surgery must be done ASAP to
o ciliary body, the lens, the choroid, the retina, prevent amblyopia
o and the optic nerve
Strabismus
- Children w retina and optic nerve coloboma will have some vision
impairment in the affected eye - unequally aligned eyes (cross-eyes) caused by unbalanced muscle
control; hereditary
Hypertelorism
Signs & Symptoms
- congenital condition involving abnormally wide-spaced eyes
- associated with chromosomal abnormalities: Waardenburg’s - the resting position of one eye may be divergent (turned out) or
syndrome (also involves congenital hearing impairment) convergent (turned in)
- Detecting true hypertelorism: - One pupil may be higher than the other (vertical strabismus)
o measure distance between the pupils and compared - may be monocular (same eye deviates constantly) or alternating
with standards for the child’s age strabismus (one eye and then the other deviates)
- exotropia (eye turning out), esotropia (eye turning in), or
hypertropia (eye turning up)
Assessment - often close one eye or tilt their head to decrease the double
vision
- if infant demonstrate strabismus past 6 weeks of age - may tilt their head so much they appear to have a torticollis, or
o referred for diagnosis and treatment “wry neck”
- Infant demonstrate a constant strabismus before 6 wks of age - cannot see well and may be too young to describe what is
o need referral right away happening to them but are fussy
- detected best when children examine a nearby object
o when they read small print, they turn both eyes medially, Therapeutic Management
or converge
o if farsighted in one eye, they turn the affected eye in * eye correction for strabismus must be done before 6 years of age
more than the other (strabismus) - If the fusion mechanism is weak:
o if one eye is nearsighted, they will not need to turn o eye exercises (orthoptics)
that eye in as far as the other one (divergence) - If eyes are diverging with attempted convergence r/t hyperopia or
latent strabismus myopia:
o glasses to correct the basic visual defect
- able to maintain fusion, the strabismus is not overt - If the misalignment is caused by unequal muscle strength:
o w maintaining fusion, they experience eye strain o injection of botulinum toxin into the eye muscle
o headaches; tired, irritated eyes; nausea and vomiting o eye muscle surgery (post-op: adm antibiotics ointment
for 2 to 3 days, eye patch not required)
pseudostrabismus
Concomitant Strabismus
Paralytic strabismus
Foreign Bodies - ice pack to the eye (20 minutes on, 20 minutes off, and repeat)
o Reabsorption of hemorrhage in the tissue surrounding
- REMOVED by irrigation with a sterile normal saline solution or by the eye will take place over the next 1 to 3 wks
gentle wiping with a well-moistened, sterile, cotton-tipped
applicator after the eyelid is everted Blowout fracture
o child will blink a few times after the upper lid is returned - Limited eye movements or reports o diplopia
to its place
- fracture line is trapping intraorbital tissue and preventing the eye
o after a few minutes, child will report feeling “fine” again globe from moving freely
- If a FOREIGN BODY ADHERES TO THE CORNEA: ophthalmologist
will remove it Tx: refer to ophthalmologist; surgery
Eyelid Injuries - other surgery technique: laser therapy
- do not adm atropine sulfate before surgery
- accompany eye globe injuries or present after foreign body entry
- after surgery: restrict rough play activities for 1 week
complication: - follow up appointment for eye pressure assessment after 1 month
causes
- if ear drops cannot flow back d/t to swollen canal: cotton wick - “cold,” rhinitis, and perhaps a low-grade fever for several days >>
moistened with Burow’s solution fever of 38° C >> sharp, constant pain in one or both ears
o cotton extending out into the auricle is kept moistened - external canal is usually free of wax
by rewetting it for 24 hours with Burow’s solution - discomfort does not increase on manipulation of the auricle
o reduces swelling and further tx can be initiated - if mastoid process behind the ear feels tender to touch: infection
- ear drops containing hydrocortisone and an antibiotic or an - Infants: extremely irritable and frequently pull or tug at the
antifungal mixture (w additional alcohol base) affected ear
o Hydrocortisone: reduces inflammation - Older children can verbalize reports of pain
o antibiotic or antifungal: reduces the infection - Risk for conductive hearing loss up to 6 mos after acute infection
o alcohol base: dries external canal further o If a child still has a conductive hearing loss after 6 mos:
- if ear pain is present: acetaminophen or ibuprofen child to be examined again
- keep the ear canal dry, avoiding swimming and hair washing
Assessment
during this time
o during shower: insert ear plugs into the external meatus 1. on otoscope
Impacted Cerumen - tympanic membrane appears inflamed or reddened;
- may be seen bulging into the external canal
- light reflex of the otoscope will not be as definite as usual d/t
• Wax accumulation is rarely extensive enough to interfere w hearing
convex shape of the eardrum
• Do not clean child’s ear w cotton-tipped applicators regularly
- malleus and incus, can be visualized only poorly or not at all
o May scratch the ear canal > invasion site for 2nd infection
o Pushes accumulated cerumen father into ear canal > true 2. on pneumatic examination: decreased mobility
plugging of wax 3. tympanocentesis: obtain fluid for culture
• Never put anything smaller than an elbow in a child’s ear
Therapeutic Management
Therapeutic Management (for true plugging of cerumen)
- antibiotic therapy is unnecessary and may add to bacterial
- Commercial softeners resistance
- dilute solution of hydrogen peroxide to dissolve cerumen - analgesic and antipyretic: acetaminophen
o may be done once ion a while but not regularly > may - decongestant nose drops: to open the eustachian tubes and allow
moisten ear canal too much > external otitis air to be admitted to the middle ear { given for only 3 days )
o should be given longer than 3 days: rebound effect
acute otitis media (edema & increase in mucous membrane inflammation)
- most prevalent disease of childhood after respi tract infections - for chronic or persistent otitis media: cephalosporin (effective
- occurs most often in children 6 to 36 mos of age, again at 4 to 6 y against Staphylococcus)
- higher incidence of otitis media in formula-fed infants Otitis Media with Effusion
o fed in a more slanted position > milk enters eustachian
tube - result of chronic otitis media
- incidence higher in homes in which a parent smokes cigarettes - source of air to middle ear is shut off > middle ear epithelial cells
become secretory cells > middle ear filled w glue-like fluid
complications: permanent damage of middle ear > hearing impairment - involvement usually bilateral
- occurs most frequently in 3 to 10 y of age
Signs & Symptoms Cholesteatoma
- feeling of fullness or the sound of popping or ringing in their ears - lesion of the pars flaccida or upper portion of the tympanic
- muffled hearing and a feeling of pressure in the ear membrane > retraction cyst > necrosis w foul-smelling drainage
- drop in hearing of 20 to 40 dB o if retraction cyst is not discovered & surgically removed:
it grows gradually deeper and deeper > invades mastoid
Assessment (on ear examination) o complications: mastoiditis, meningitis, facial nerve
- level of fluid behind the tympanic membrane paralysis
o fluid line will be visible only if there is also a quantity of
air in the middle ear to contrast with
- malleus more prominent, displaced to a horizontal angle
o d/t to increasing thick fluid, eardrum retracts
- light reflex from the otoscope light becomes distorted
- w pneumatic otoscope: gentle introduction of air against the
eardrum produces no movement of the tympanic membrane
(abnormal finding)
Therapeutic Management