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Pediatric
Eye and ENT
disorders
Amy Lalringhluani
Msc 2nd Year
CPMSCON
DISORDERS OF
THE EYE
Eye development starts in the 3-week embryo
The initial 3 years of life is the critical period for
eye development
Normal adult visual capacity develops at 3 years
of age
After the early puberty, the anterior posterior
diameter of the eye, remains unaltered in healthy
subjects
The refractive status of the eye may still change
in adults due to aging processes
Eye Development
Anatomy
&
Physiology
CHILDHOOD EYE
EXAMINATION
CHILDHOOD EYE EXAMINATION
Red Reflex
Test
Cover, Cover-
Uncover, and
Alternate Cover
Tests
Corneal
Light Reflex
Fixation and
Alignment
Pupillary
Response
External Ocular
Examination
Visual Acuity
History
History
Personal or family histories of risk factors
for eye and vision problems are assessed for
Risks include premature birth, Down
syndrome, cerebral palsy, and a family
history of strabismus, amblyopia,
retinoblastoma, childhood glaucoma,
childhood cataracts, or ocular or genetic
systemic disease
Eye Charts
Each eye to be tested independently and
opposite eye occluded to discourage peeking.
Most children do not have 20/20 vision until
after 6 years of age, but at any age, visual
acuity should be approximately equal
between the eyes.
The visual acuity test is used to determine the
smallest letters you can read on a
standardized chart (Snellen chart) or a card
held 20 feet (6 meters) away.
Visual Aquity
Eye Charts
Visual Aquity
Snellen chart
HOTV chart
Eye Charts
Visual Aquity
Lea chart
Allen chart
Visual Acuity Norms for
Children 2.5 to 6 Years of Age
Age
(months)
Norms
30 to 35 Approximately 20/60
(6/20) or better
36 to 47 20/50 (6/15) or better
48 to 59 20/40 (6/12) or better
60 to 72 Approximately 20/30
(6/10) or better
External Ocular Examination
Involves examination of the
external portion of the eye,
including
• eyelids,
• orbits,
• conjunctiva,
• sclera,
• cornea,
• iris
External Ocular Examination
Inspect for excessive tearing, watery or
purulent discharge, photosensitivity,
conjunctival infection, and gross structural
abnormalities.
Lacrimal duct obstruction is recognized
when pressure over the lacrimal sac
produces mucus in an eye.
Childhood glaucoma presents with tearing
accompanied by corneal redness, corneal
clouding, photosensitivity, and enlarged
eyes.
Pupils measured for size
and symmetry in light &
darkness
03
Assessed using
a bright light
01
Room darkened
before declaring
a response
02
Pupillary Response
Fixation and Alignment
By 2 months of age, a child should
be able to fix and follow an object.
If strong binocular fix and follow
not seen by 3 months of age, refer
Ocular alignment should be
assessed to identify strabismus
Children as young as six weeks should have
some response to an examiner’s face.
In a corneal light reflex test, the child’s
attention is attracted to a target (a light or a
brightly colored object), while a light in front
of the child is directed at the child’s eyes.
The light’s reflection will be symmetric in
each pupil by four to six months of age in
patients with normally aligned eyes.
1. Corneal Light Reflex
Hirschberg test
It gives rough objective estimate of the angle of a manifest
squint. Useful in young or uncooperative patients or when
fixation in deviating eye is poor.
Procedure:
 Patient made to fixate at point light held at a distance of
33cm .
 Deviation of corneal light reflex from the centre of pupil
noted in the squinting eye.
 1 mm of deviation ≅ 7○
. (1○
= 2 prism dioptre)
 The angle of squint is 15 ○
& 45 ○
when the corneal light
reflex falls on the border of pupil and limbus, respectively.
Hirschberg test
Normal Corneal reflex
1mm deviation ≈ 15 diopters
2mm deviation ≈ 30 diopters
3mm deviation ≈ 45 diopters
4mm deviation ≈ 60 diopters
2. Cover, Cover-Uncover, and Alternate
Cover Tests
Cover
test
Uncover
test
Cover-
Alternate
Cover
test
Cover Test
Child’s attention
is attracted to a
target
Step 1
Vision of one eye
is then occluded
Step 2
Tested (uncovered) eye is
observed for movement from
a deviated position and back
Step 3
Untested eye is
uncovered & tested
eye is observed again
for any misalignment.
Step 4
Cover-Uncover Test
A cover is placed over one eye for 1 – 2
seconds while the child’s attention is
called to the target
1
2 Cover is removed rapidly, & previously
covered eye is observed for movement
from deviated position back to fixation
on the target
Alternate Cover Tests
The cover is held over one eye for a few
seconds, then moved rapidly over the other eye
and held for a few seconds, then moved back to
cover the first eye.
This is repeated several times, and
each time the cover is moved, the
previously covered eye is observed
for any “refixation” from a deviated
to a normal position.
Step
1
Step
2
Red Reflex Test
The ophthalmoscope is used in a
darkened room
Each red reflex viewed individually
12 to 18 inches (approximately 30 to
45 cm) from the patient’s eyes
Both red reflexes simultaneously at a
distance of 2 to 3 feet (approximately
0.6 to 0.9 meters).
Red Reflex Test
A symmetric orange-red light
should reflect from each fundus.
Any abnormal finding (e.g.,
asymmetry of color or
occurrence of dark or white
spots) is a reason for referral to
an ophthalmologist.
No action
required
Referral
Referral
CONGENITAL
PROBLEMS OF
THE EYE
Infantile
hemangiomas
 Most common eyelid tumors in
infancy. Bright red or purple
appearance.
 Blanch with pressure.
 Undetected at birth.
 Enlarge in first 12 months followed by a slow
involution during the first decade.
Infantile
hemangiomas
 Vision loss is related to
amblyopia because of induced
astigmatism or visual
deprivation due to ptosis.
 Steroid treatment (intralesional
and/or oral) is the first line of
therapy.
Epibulbar
dermoids
 Choristomas (congenital dermoids)
are masses of normal tissue found in
an abnormal location
 Induce astigmatism and cause
refractive amblyopia
 May be excised to improve cosmetic
appearance and avoid amblyopia
Anophthalmia /
Microphthalmia
Anophthalmia: one or both eyes absent
Microphthalmia: one or both eyes did not
develop fully, so they are small
Often result in blindness or limited vision
Anophthalmia /
Microphthalmia
Frequently associated with secondary
orbital and ocular deformity like cataract
and genetic conditions such as trisomy 13
Colobomas
Characterized by an inferior or
ventrally located gap in one or
more tissues, extending
between the cornea and the
optic nerve
Colobomas
May be unilateral or bilateral
Clinical spectrum of
congenitally reduced ocular
size (microphthalmia), and in
severe cases, absence of one
or both eyes (anophthalmia)
Persistant fetal vasculature
(persistant hyperplastic primary
vitreus)
◙ Failure of
regression of a
component of fetal
vessels within the
eye
◙ Leads to
impairment of
vision
Crossed eyes
(strabismus),
abnormal eye
movements
(nystagmus) and
“lazy eye”
(amblyopia) are
common features
COMMON EYELID
DISEASES IN
CHILDREN
Ptosis
Drooping of upper eyelid covering >
2mm of the cornea below the upper
limbus is called ptosis
May be congenital or acquired
Can induce sensory
deprivation amblyopia
Surgical correction:
Mild cases - age of 3-4 years.
Severe cases - early surgery
required to prevent amblyopia.
Entropion
Inversion of lid margin due to congenital
or scarring
Eyelid skin and eyelashes
to rub against the eye
Friction
Discomfort and
irritation to the cornea
Entropion
Surgical entropion repair:
⁃ Eyelid tightening: This procedure
shortens the eyelid (called a lateral
tarsal strip) to tighten the lid.
⁃ Retractor reinsertion: This procedure
is used to tighten the lid retractor
(muscle that opens and closes the
lid).
Ectropion
Outward turning of the lid margin
as a result of inflammation, burns or
trauma is called ectropion
Ectropion leaves the eye too
exposed. The eye can become dry,
irritated, and even infected.
It is either congenital or acquired
Blephrospasm
▲It is the repetitive or
spastic closure of
eyelids secondary to
trichiasis, keratitis or
conjunctivitis
Blepharitis
▲Inflammation of the lid margin due to
staphylococcal or seborrheic infection
▲Characterized by itching, irritation and watering of
the eyes due to blocked meibomian glands
▲Flaky skin around the
eyes with crusty debris
covering the eyelids,
loss of eyelash
ORBITAL
INFECTIONS
IN CHILDREN
The infections occur in
two clinical forms;
Preseptal
cellulitis
Orbital
cellulitis
Causes:
Skin trauma, sinusitis, lacrimal sac
infections and rarely remote
infections
Preseptal
cellulitis
Infection of
eyelid &
surrounding
skin anterior to
the orbital
septum
Begins in superficial
to the orbital septum
and extends from the
orbital rim into the
upper and lower
eyelid
Preseptal
cellulitis
Swelling, tenderness, and
erythema of the eyelid
Swelling is confined to the
eyelid
Globe is white
Vision and ocular motility are
normal
Orbital cellulitis
Infection of the
orbital tissues
posterior to
the orbital
septum
Begins deep
to the orbital
septum
Caused by
extension of
infection from
adjacent
sinuses
Orbital cellulitis
Symptoms
 swelling & redness of eyelid
 conjunctival hyperemia &
chemosis
 pain with eye movements
 decreased visual acuity
 fever
CONJUNCTIVAL
INFECTIONS IN
CHILDREN
Ophthalmia Neonatorum
Inflammation of the conjunctiva within
the first month of life is classified as
ophthalmia neonatorum (neonatal
conjunctivitis).
Associated with catarrhal,
purulent or mucoid discharge
from one or both eyes,
conjunctival infection, edema
and erythema of the lids.
Etiology
Common causes of Ophthalmia Neonatorum with
time of onset and typical characteristics
Type Time of
onset
Characteristics
Chemical (e.g.,
silver
nitrate drops)
Within hours
of
instillation
⁃ Self-limiting, mild, serous
discharge (occasionally
purulent)
⁃ Lasts 24–36 hr
Chlamydia
trachomatis
5–14 days ⁃ Mild-moderate, thick, purulent
discharge Erythematous
conjunctiva, with palpebral
more than bulbar involvement
Common causes of Ophthalmia
Neonatorum with time of onset and typical
characteristics
Type Time of
onset
Characteristics
Neisseria
gonorrhoeae
24–48 hr ⁃ Hyperacute, copious,
purulent discharge
⁃ Lid swelling and chemosis
common
Bacterial
(nongonococcal)
After 5 days ⁃ Variable presentation,
depending on organism
Common causes of Ophthalmia
Neonatorum with time of onset and typical
characteristics
Type Time of
onset
Characteristics
Herpetic Within 2
weeks
⁃ Conjunctiva only mildly
infected
⁃ Serosanguinous discharge
⁃ Vesicular rash on lids
sometimes seen
⁃ Systemic herpetic disease
present
Mode of Infection
Intrauterine
infection
Infection during the
process of delivery
(most common)
Infection
after birth
Pathophysiology
Infection due to entry of
microorganism or
chemical
Blood vessels
dilate
Formation of new blood
vessels around the papillae
Formation of numerous
polymorphs in the
epithelium
Purulent discharge
and exudate
formation in eye
Clinical Features
Eyelids are
tense and
swollen
Conjunctiva is
congested and
swollen
Excessive tearing or turbid
and thick discharge from eyes
• Tetracycline, erythromycin
ointments or povidone-iodine
drops can be used for
prophylaxis
• Saline lavage hourly till
discharge is needed
• Systemic intravenous
antibiotics may be needed.
Treatment
Prevention
 Proper antenatal care of pregnant women.
 Treatment of infected vaginal discharge during
pregnancy.
 Use of aseptic techniques while delivery and in care
of newborn.
 Cleaning of each eye with sterile swabs dipped in
sterile water, as soon as the head is delivered and
instillation of Chloramphenicol eye drops in each eye
as a prophylactic measure.
Conjunctivitis
Conjunctivitis is inflammation of
conjunctiva characterized by red
eyes with or without discharge
and itching
Etiology is almost always
bacterial in children. It can
also be viral or allergic
Pathophysiology
Microbes enter the eye on
contact with infected object
Inflammation
of eye
Dilation of blood
vessels of eye
Swelling, redness,
exudates and
discharge
Clinical Features
Redness of eye
(hyperemia)
Tearing and
itching in eyes
Exudation
Other symptoms may include:
→Photophobia
→Pseudoptosis (drooping of
upper eyelid)
→Periorbital cellulitis
→Pain in eye
→Fever
Viral infection fever, sore
throat and runny nose
Types of conjunctivitis
Bacterial Conjunctivitis
Viral Conjunctivitis
Allergic conjunctivitis
Bacterial Conjunctivitis
• Caused by bacteria
• Causes serious damage to the eye if
left untreated
• Symptoms include redness, dryness
of eyes and skin around it and
mucoid purulent discharge.
• Topical flouroquinolone and
erythromycin may be used for
treatment
Bacterial Conjunctivitis
Types of conjunctivitis
Types of conjunctivitis
Viral Conjunctivitis
• Caused by virus like the
common cold virus
• Very contagious
• Symptoms include redness of
the eye, periodic itching and
increased lacrimation
• Clear up on its own in few days
without treatment
Viral Conjunctivitis
Allergic conjunctivitis
• Caused by irritants such as pollen and
dust
• May be seasonal or flare up year
round
• Symptoms include redness of the eye,
itching, swelling of the conjunctiva
and the eyelids
• Antihistamine drops are used to
relieve symptoms
Allergic conjunctivitis
Types of conjunctivitis
Difference between bacterial conjunctivitis
and viral/allergic conjunctivitis
Features Bacterial conjunctivitis Viral/Allergic
conjunctivitis
Symptoms Bacterial cases will
always have discharge.
Allergic cases will always
have prominent itching
Presence
and nature
of
discharge
Bacterial infections will
have a purulent,
yellow-green
discharge
Viral cases will have
serous or mucoid
discharge. Allergic cases
will have serous
discharge with excessive
tearing.
Features Bacterial
conjunctivitis
Viral/Allergic conjunctivitis
Laterality Bacterial cases
can be either
unilateral or
bilateral.
Viral and allergic conjunctivitis
occur almost always bilateral.
Systemic
associations
-
Viral conjunctivitis might be
associated with upper respiratory
infections. Allergic conjunctivitis
might be seen with upper
respiratory allergic symptoms.
Difference between bacterial conjunctivitis
and viral/allergic conjunctivitis
Features Bacterial conjunctivitis Viral/Allergic conjunctivitis
Treatment First-line therapy for
bacterial conjunctivitis is
topical flouroquinolone.
In many cases
Polysporin, erythromycin
or trimethoprim/sulfa is
effective.
Viral conjunctivitis is self-
limited.
For allergic cases topical
antihistaminic drops are
effective.
Nursing Management
Prevention
 Apply cold compress on the eye
 Reduce exposure to light
 Prevent rubbing of the eye
 Acetaminophen
 If caused by bacterial agents
− Clean eye with sterile water and cotton
swabs
− Apply antibiotic ointment or eye drops
− Use of dark glasses if photophobia present
Nursing Management
Family Teaching
Good hand washing
after touching the eye
Separate towel, sheet and
pillow case for infected child
Dropper should not touch
child’s eyes during
medication instillation
CORNEAL
DISEASES IN
CHILDREN
Congenital anomalies that
affect cornea
Megalocornea: It is
symmetric non-
progressive enlargement
of cornea. It is associated
with refractive error
Microcornea: It is a rare
condition characterized
by small isolated cornea.
It may be associated with
congenital cataract,
glaucoma, etc
Congenital anomalies
that affect cornea
Microphthalmos:
Microphthalmos is
defined as the
developmental arrest of
all ocular structures
Anophthalmos:
Anophthalmos is the
complete failure of the
eye development
Keratitis
Keratitis is an inflammation and
swelling of the cornea characterized by
oval shaped corneal infiltrations
surrounded by corneal edema,
conjunctival hyperemia, ocular pain
and photophobia
Types of Keratitis
Non-
infectious Infectious
Caused by an
eye injury, by
wearing
contact lenses
too long or by
a foreign body
in the eye
Caused by bacteria,
viruses, fungi and
parasites. Main
causative
organisms are
staph aureus, staph
epidermis & strep
pneumonia.
Signs & Symptoms
Intense pain
Red eyes
Profuse tearing
Photophobia
Corneal edema
Clouding & blurred
vision
Complications
Permanent
vision damage
Corneal
perforation
Treatment
Infectious
Mild cases - eye drops (antibiotic,
antiviral or antifungal, determined by
the cause of the infection)
Advanced infections - oral medications
Non-infectious
For mild discomfort - artificial tears.
Severe cases - a bandage contact lens
and anti-inflammatory eye medications
OPTIC
NERVE
DISEASE IN
CHILDREN
Optic neuritis
Optic neuritis is an
inflammatory, infective
or demyelinating
process affecting the
optic nerve.
DEFINITION
Etiology
Demyelinating disease
Parainfectious, infectious
Non-infectious
Sinus –related
Cat -scratch fever
Syphilis
Lyme disease
Cryptococcal meningitis
Sarcoidosis
Systemic lupus erythematosus
Polyarteritis nodosa
Classification of Optic Neuritis
Papillitis: characterized by hyperemia and
edema of the optic disc, associated with
peripapillary flame-shaped hemorrhages.
Neuroretinitis: is characterized by papillitis
in association with inflammation of the
retinal nerve fibre layer and a macular star.
Retrobulbar neuritis: the optic nerve head
is normal in retrobulbar neuritis, because
the optic nerve head is not involved
Papilloedema
Papilloedema is swelling
of the optic nerve head
secondary to raised
intracranial pressure
It is nearly always
bilateral, although it
may be asymmetrical.
Headaches, deterioration of
consciousness, nausea and
vomiting
Diplopia due to 6th
nerve palsy
SIGNS AND SYMPTOMS
RETINOPATHY
OF
PREMATURITY
Definition
Retinopathy of
prematurity (ROP) is a
vasoproliferative disorder
of the retina among
premature babies, which
was previously termed as
retrolental fibroplasia
Risk factors
Premature birth
Uncontrolled O2
therapy
Born ≤ 31 wks of GA/
wt ≤ 1500gm
Systemic problems
(sepsis, anemia, etc)
International classification of
ROP
Location
Severity
Plus disease
Category Stage/
Zone
Characteristics
Location Zone I Circle with optic
nerve at its centre
and radius of
twice the distance
from optic nerve
to macula (fovea
centralis)
Location
Category Stage/Zone Characteristics
Location Zone II Concentric circle from edge
of zone 1 to ora serrata
nasally and equator
temporally
Location
Zone II
Category Stage/
Zone
Characteristics
Location Zone III Lateral crescent
from zone 2 to
ora serrata
temporally
Location
Severity
Stage
1
Presence of thin
white demarcation
line separating
vascular from
avascular retina
Severity
Stage
2
Addition of depth
and width to the
demarcation line of
stage 1, so as the
line becomes a
ridge
Severity
Stage
3
Presence of extra
retinal fibro vascular
proliferation with
abnormal vessels
and fibrous
tissue extending
from ridge to
vitreous
Severity
Stage
4
Partial retinal
detachment not
involving macula
(4A) and
involving macula
(4B)
Severity
Stage
5
Complete retinal
detachment
Presence of dilatation and
tortuosity of retinal vessels at
posterior pole of eye.
Associated with papillary
rigidity and vitreous haze.
Plus disease frequently leads to
vessel contraction and scar
formation, which in turn, leads
to macular displacement.
Plus disease
ROP Screening
Screening is performed by an expert using
indirect ophthalmoscopy.
In India, babies with
 GA<34 weeks or Birth weight
<1700g
 Birth weight <2000g (if GA not
known)
 Sick preterm babies are screened at
the neonatologists’ discretion
To avoid confusions about the timing
of first screening it is recommended
that the first ROP screening should be
done strictly
• before “day 30” of post-natal life
• by “day 20” of life in smaller babies
(<30 weeks and/or birth weight
<1200 g).
Role of Nurses in ROP Screening
Record wt and GA at birth.
Monitor wt gain during NICU
admission.
Select babies eligible for screening.
Counsel the parents regarding
screening procedure.
Dilate eyes 1 hour before
examination using a topical agent.
Role of Nurses in ROP Screening
Keep the baby NPO one hour prior to
procedure.
Position the baby comfortably, take
adequate pain control measures.
Ensure hand washing, use sterile articles
only during procedure.
Monitor vital signs.
Documentation of procedure, fix next
appointment.
Treatment of ROP
Peripheral retinal
ablation of
avascular retina
Argon laser
photocoagulation
Follow up of the child for development
of vision, refractive status and
strabismus till preschool age
Prevention of ROP
Antenatal steroids
Judicious
oxygen therapy
Judicious use of
blood transfusions
Other
interventions
CHILDHOOD
CATARACT
Definition
Cataract is the
opacification of the
crystalline lens. A
cataract is any
cloudiness or
opacity of the
natural lens of the
eye, which is
normally crystal
clear.
Incidence
Approx 3 /10,000
children
Variable
throughout the
world.
Causes
 Intrauterine
infections (e.g.
toxoplasmosis)
 Galactosemia
 Chromosomal
anomalies (Down’s
syndrome)
 Ocular malformation
 Mental retardation
Congenital or Primary
 Trauma
 Retrolental
fibroplasia
 Uveitis
 Maternal
malnutrition
 Glaucoma
Acquired or Secondary
Classification of pediatric cataract
Congenital/Infantile
cataract
Cataract present at birth or which occurs during
the first year of life
Manifestations:
• Usually bilateral
• Visible clouding of
lens
• Varying impairment of
vision
• Maybe found with
amblyopia
Classification of pediatric cataract
Congenital/Infantile cataract
Causes:
• Prematurity
• Maternal infections - (Toxoplasmosis, rubella,
CMV, herpes simplex, measles, influenzae, etc.)
• Chromosomal disorders - (Trisomy-21, Turner’s
syndrome)
• Metabolic disorders - (Galactosemia, PKU,
cretinism mucopolysaccharidosis).
Classification of pediatric cataract
Acquired/Juvenile Cataract
Cataract that occurs after the first year of
life
Manifestations:
• Visible clouding of
lens
• Varying impairment
of vision
Classification of pediatric cataract
Acquired/Juvenile Cataract
Causes:
• Eye trauma (contusion,
foreign body and
penetrating injury)
• Child abuse
• Steroid induced
• Radiation, drug effects
(tetracyclines,
chlorpromazine)
• Hypo - and
hypervitaminosis ‘D’
• Juvenile onset
diabetes mellitus
• Hypoglycemia
• Hypocalcemia
Types of pediatric cataracts
A lamellar cataract is the opacification of a
lamella (an ovoid layer of cortex) which
causes cloudiness between the nuclear and
cortical layers of the lens
Lamellar
cataract
Types of pediatric cataracts
Nuclear
cataract
A nuclear cataract is cloudiness of the
center part of the lens. They can be dot-
like or can be quite dense. They
generally measure 2-3.5 mm and can
be associated with microphthalmia.
Types of pediatric cataracts
Posterior
sub
capsular
cataract
A posterior sub capsular cataract is a thin
layer of cloudiness that affects the back
surface of the lens cortex, just inside the
capsule. This type of cataract can often be
associated with medication use such as
steroids
Types of pediatric cataracts
Anterior polar cataract is a small, usually
central opacity of the front part of the lens
capsule. Anterior polar cataracts generally
do not grow during childhood and are
typically not visually significant. They are
often managed without surgery
Anterior
polar
cataract
Types of pediatric cataracts
A posterior polar cataract is a central
opacity at the back of the lens. In this type
of cataract, the opacity is in the capsule
itself.
Posterior
polar
cataract
Types of pediatric cataracts
Traumatic
cataract
A traumatic cataract results from either a
blunt or penetrating force that damages the
lens. The cataract can form shortly after the
trauma or months to years after the injury.
In children, traumatic anterior lens capsule
rupture quickly results in a hydrated white
cataract.
Signs and symptoms
A pupil that looks white when a flashlight is
shone into it
Eyes that aren’t in the right position
(misaligned)
Rhythmic eye movements that can't be
controlled (called nystagmus).
Cloudy or blurry vision
Trouble seeing
Lights that look too bright or have a glare
Seeing a circle of light around an object (halo)
Diagnosis
Red reflex test in
newborn
screening:
If no red reflex, or
a weak one, is
seen, it may mean
there's cloudiness
in the lens.
Vision tests for
older babies
and children:
This includes
visual acuity
tests and pupil
dilation
Management
Surgical removal of a
cataract
Restoration
of focusing
power
Contact
lenses
Intraocular
lenses
Glasses
Treat amblyopia by patching the good
eye to stimulate vision in affected eye
Antibiotic & steroid eye
ointments
Nursing Management
Preoperative Phase
 History and
physical
assessment
 Antibiotic eye
drops
 Dilating eye
drops
 Anticholinergics
: Mydriatics and
cycloplegics.
Nursing Management
Postoperative Phase
 Antibiotics and
steroid eye
ointments
 Aseptic eye care
with eye patch and
eye shield for
several days to
prevent injury
 Sedation for 24
hours to
prevent crying
 Prevention of
vomiting & ↑
IOP
Health Promotion
Wear sunglasses
Avoid unnecessary radiation –
Adequate antioxidant
vitamins
Good nutrition
Educate about disease
process and treatment options
Teach signs and symptoms of
infection
CHILDHOOD
GLAUCOMA
Definition
Glaucoma is a group of heterogenous disease
marked by high intraocular pressure (IOP) that
damages the optic nerve which can cause a
rapid loss of vision or even blindness.
Childhood glaucoma is defined by 2 of
the following features:
1.Intraocular pressure (IOP) greater
than 21 mmHg
2.Presence of optic disc cupping
3.Corneal findings of Haab striae
(breaks in Descemet's membrane
leading to scarring)
Childhood glaucoma is defined by
2 of the following features:
4. Corneal edema
5. Increased corneal diameter of
greater than 11mm in newborns,
greater than 12 mm in children less
than 1 year of age, and diameter
greater than 13 mm in any age.
Definition and Terminology
Juvenile glaucoma: Occurs after
the age of three to teenage years.
Related to age of onset
Congenital glaucoma: The glaucoma that
exists at birth, and usually before birth
Infantile glaucoma: Glaucoma that
occurs from birth until 3 years of age
Definition and Terminology
Related to development pattern
Developmental glaucoma: This term broadly
encompasses all glaucomas resulting from
abnormal development of the aqueous outflow
system. This may or may not be associated with
systemic anomaly
Definition and Terminology
Secondary developmental
glaucoma: This refers to
glaucoma resulting from
damage to aqueous outflow
system due to
maldevelopment of some
other portion of the eye, e.g.
eye with dislocated lens
Related to development pattern
Primary
developmental
glaucoma: This
is the glaucoma
resulting from
maldevelopment
of aqueous
outflow system
Incidence
More
common in
boys
1 in 10,000
births
Childhood
glaucoma is
relatively rare
Causes
• Hereditary
• Some conditions like - Axenfeld-
Reiger Syndrome, Aniridia,
Sturge -Weber Syndrome,
Neurofibromatosis
• Chronic steroid use
• Trauma
• Previous eye surgery such as
childhood cataract removal
Pathophysiology
Etiological
factors
Disturbance
in production
and
circulation of
aqueous
humour
Build-up of fluid
(aqueous humour)
↑ IOP
Damage of the
retinal layer as it
passes through the
optic nerve head
Cell
injury
& cell
death
Optic nerve
destruction
Blindness
Types of glaucoma
Glaucoma with angle-
closure
Open-Angle glaucoma
Types of glaucoma
Most prevalent type of
glaucoma is open-angle
glaucoma.
The trabecular meshwork is
partially blocked, but the
drainage angle formed by the
cornea and iris remains open.
Open-angle glaucoma
Types of glaucoma
As a result, the pressure in
the eye increases.
The optic nerve is damaged
by this pressure.
It happens so slowly that one
can lose vision before
understanding anything is
wrong.
Types of glaucoma
When the iris bulges forward,
it narrows or blocks the
drainage angle produced by
the cornea and iris, causing
angle-closure glaucoma.
Fluid cannot circulate through
the eye and pressure rises.
Angle-closure glaucoma
Types of glaucoma
People with small drainage
angles are more likely to develop
angle-closure glaucoma.
Angle-closure glaucoma can
develop quickly (acute angle-
closure glaucoma) or gradually
(progressive angle-closure
glaucoma/chronic angle-closure
glaucoma).
Classification of Childhood glaucoma
Primary glaucoma
Childhood glaucoma
Juvenile
open-angle
glaucoma
Congenital/
infantile
glaucoma
Secondary glaucoma
Associated c
̅
non-acquired
ocular
anomalies
Associated c
̅
non-acquired
systemic
disease
Associated with
an acquired
condition
After
congenital
cataract surgery
Signs and Symptoms of childhood
glaucoma
Symptoms Signs
• Photophobia • Buphthalmos (visible enlargement of
the eyeball detected at birth)
• Epiphora (excessive tearing/watering
of eyes)
• Corneal enlargement
• Blepharospasm (blinking or other
eyelid movements, like twitching, that
one can't control)
• Corneal edema
• Red eye • Breaks in Descemet’s membrane
(Haab striae)
• Irritability • Iris and pupillary abnormalities
• Cloudy cornea • Elevated intraocular pressure
• Enlarged cornea/eye • Visual impairment
• Poor vision • Myopia or astigmatism
• Asymptomatic • Optic nerve cupping
Treatment
Aim of treatment
The aim of pediatric glaucoma surgery is to reduce
IOP either by increasing the outflow of fluid from the
eye or decrease the production of fluid within the
eye.
Surgical treatments Laser
Therapy
Medical
treatments
Goniotomy
Trabeculotomy
Trabeculectomy
Medical Therapy
• The treatment for glaucoma in older children
is generally medical, i.e. eye drops initially
and if these fail, surgery is considered.
• Anti-inflammatory and antibiotic drops are
used postoperatively
• When trabeculectomy is performed in children
an antimetabolite such as 5-fluorouracil (5-FU
for short) is very often used
Nursing Care
Assessment
 Signs &
symptoms like
photophobia,
tearing, pain
and bump into
objects
 Send the patient to
assess visual
acuity, visual
fields, IOP.
Nursing Care
 Teach patient and family risks of glaucoma.
 Stress on the importance of early detection,
ophthalmologic examination.
 Administer medication to lower IOP.
 Pre and post-operative teaching of the
patient and family are to be given.
 Support for parents.
 Educate parents on use of eye medications
to alleviate pain from disease and surgery.
REFRACTIVE
DISORDERS
OF THE EYE
A refractive error occurs when the eye does not
focus light correctly and it causes blurry vision.
The presence of any of the refractive disorders is
known as ametropia
REFRACTIVE DISORDERS
Myopia
(near-sightedness)
Hyperopia
(far-sightedness)
Astigmatism
Prevalence and Incidence
 Myopia is most common refractive in the pediatric
population
 WHO estimates refractive disorders to be 2-10% worldwide.
 The prevalence is higher in the Far East.
 The prevalence of astigmatism of 1 diopter or more is 50%
in infancy.
 The prevalence decreases rapidly during the process of
emmetropization.
 Only few children develop astigmatism greater than 1
diopter by 6 years of age
MYOPIA (NEARSIGHTEDNESS)
Myopia is an eye condition in which near
objects are seen clearly, but faraway objects
appear fuzzy or blurry.
 In myopia, eye focuses incorrectly because its shape is
slightly abnormal.
 A nearsighted eyeball has a long antero posterior
diameter.
 The myopic child has excessive refractive power.
 In myopia, eye focuses light entering the eye in front of the
retina instead of onto the retina.
 According to the National Eye Institute (NEI), myopia is
usually diagnosed between the ages of 8 and 12 years when
eyes are growing at this age, so the shape of the eyes can
change.
Signs and symptoms
Blurry vision when
looking at faraway
objects
Headaches
Eyes that hurt
or feel tired
Squinting
Treatment
Corrective biconcave
lenses - Eyeglasses
and contact lenses.
Refractive
laser
surgeries
HYPEROPIA
(HYPERMETROPIA/FARSIGHTEDNESS)
Myopia is an eye condition in which far
objects are seen clearly, but near objects
appear fuzzy or blurry.
• A hyperopic eye is shorter than normal and it is caused by
insufficient refractory power.
• Light from close objects cannot focus clearly on the retina.
If cornea is too flat, eye cannot focus correctly.
• About 75% of all neonates are hyperopic; but as they have a
greater accommodative ability, they overcome the error and
see objects at a nearer range.
• In hyperopia, eyes have to work hard to see anything up
close and causes eyestrain.
Symptoms
Headache after reading or other
tasks that require focusing on
something up close.
Tension
Fatigue
Blurry vision
up close
Squinting to
see better
Aching or burning
sensation around
eyes
Treatment
Corrective biconvex
lenses - Eyeglasses
and contact lenses.
Refractive
laser
surgeries
ASTIGMATISM
When the focusing point is disrupted due to
variations in the curvature of the cornea or lens
at different meridians, the error is called
astigmatism
• Astigmatism is caused by an irregularly shaped
cornea, which causes light to refract or bend
incorrectly within the eye.
• With astigmatism, light rays do not refract (or bend)
properly as they enter the front of the eye. Vision is
blurry at near and far because light rays either fall
short of the retina or behind it. This results due to the
irregularity in curvature of the cornea which results in
different refractive power in some parts of the cornea
in comparison to other parts.
• It is possible to have astigmatism in combination with
myopia or hyperopia.
Symptoms
6 Squinting or holding
reading matter close
Eye discomfort
Blurry vision or areas
of distorted vision
Eyestrain and fatigue
Headaches
Eye rubbing to see
clearly
Treatment
Cylindrical or spherocylindrical
glasses and lenses
Corrective refractive laser
surgeries
ANISOMETROPIA
Anisometropia refers to a difference in the
refractive status of the two eyes
 It is the most important risk factor of amblyopia and
must be treated with caution
Types
Mixed anisometropia – one eye is myopic
and the other eye is hypermetropic ,it is also
called antimetropia
Simple anisometropia – one eye normal
and other eye myopic and hypermetropia
Compound anisometropia – both eye are either
hypermetropic or myopic ,but one is having higher
refractive power
Types
Simple
astigmatism
anisometropia –
one eye is
normal and
other has either
simple myopic
or
hypermetropic
astigmatism
Mixed
astigmatism
anisometropia –
One eyes has
hypermetropic
astigmatism and
the other eye has
myopic
astigmatism
Compound
astigmatism
anisometropia –
when both eyes
has astigmatic
but if unequal
degree
Symptoms
Treatment
 Glasses
 Contact lenses
 Anisometropic spectacle
 Other modalities of
treatment
− Phakic refractive lenses
− Refractive lens
exchange
PRESBYOPIA
Presbyopia is a result of changes to the eye lens, the lens
hardens or thickens and becomes less flexible, making it
unable to change its shape and focus on images
Depending on the severity of the changes to the lens, both
short and long-distance vision may be affected
Symptoms
Excess strain in the eyes post reading a book
Throbbing headaches after attempting to view objects
nearby
Feeling tired and exhausted after working with things in
close focus
Requiring much brighter light to view things that are
nearby
Inability to read the small print
Blurred vision
Frequent squinting of eyes while trying to focus on
close objects
Treatment
Refractive
laser
surgeries
Glasses and
contact lens
NURSING CARE OF A CHILD WITH
REFRACTIVE ERRORS
Assessment
 History and observation,
examination, investigation and
diagnostic procedure in eye.
 A child tilts his head, rubs eyes,
squint, and walks into objects;
he or she holds things close to
face.
NURSING CARE OF A CHILD WITH
REFRACTIVE ERRORS
Nursing Diagnosis
• Alteration in visual perception of
patient, as a result of refractive error.
• Knowledge deficit, about treatment of
refractive error.
• Altered comfort as a result of refractive
error manifested by asthenopia.
NURSING CARE OF A CHILD
WITH REFRACTIVE ERRORS
Intervention
• Refer for vision testing.
• Use corrective lenses when caring for
child.
• As preventive measure educate
parents to be aware of signs and
symptoms and their meaning.
• Encourage vision testing at early stage
STRABISMUS
The deviation of visual axis
from normal alignment is
known as strabismus. The
visual line of each eye does
not simultaneously focus on
the same object due to lack
of muscle coordination
resulting in a crossed–eye
appearance.
Definition
Incidence
Strabismus occurs in 2–3% of all children.
Approximately half of these children have a
family history for the defect.
Transient strabismus is normal in first 4–6
months of life and is attributed to
physiologic hypermetropia.
Types
Paralytic or
non-concomitant
Strabismus
Non-paralytic
or concomitant
Esotropia Exotropia Hypertropia Hypotropia
Types
Paralytic or non-concomitant
• Occurs due to
weakness or
paralysis of one or
more extra ocular
muscles.
• There is limitation in
movement of eye
and diplopia occurs
Non-paralytic or concomitant
• The movements of
individual ocular
muscles are
present, but
coordination is
lacking.
• Diplopia does not
occur in this type
Types
Diagnostic Evaluation
Cover-Uncover
test
Medical Management
Occlusion
therapy
Pharmacologic
therapy
Orthoptic
training
Surgical Management
Involves shortening,
lengthening or
repositioning of
extra ocular
muscles
Nursing Management
 Minimizing effects of vision loss
 Minimize body image disturbance
 Prevent injury.
 Promote normal growth and
development
Definition
Amblyopia is the medical term used when
the vision in one of the eyes is reduced
because the eye and the brain are not
working together properly. The eye itself
looks normal, but it is not being used
normally because the brain is favoring the
other eye. It is unrelated to an organic
cause. The condition is sometimes called
‘lazy eye’.
Incidence
Amblyopia occurs in
approximately 2–3% of
the population in
preschool age
Etiology
Organic causes-retinal
or the optic nerve
pathology
Strabismus
Anisometropia
Combined Strabismus
& Anisometropia
Ametropia
Visual/Sensory
deprivation
Risk factors
Premature
birth
Small eye
size at birth
Family
history of
lazy eye
Family history
of Refractive
Errors
Developmental
disabilities
Pathophysiology
Clinical
Features
Diagnostic
Evaluation
Infants and children
with Amblyopia often
do not display any
symptoms. They may
occasionally over reach
for an object.
Visual acquity test
Amblyopia is usually
asymptomatic because the
good eye assumes the burden
of vision and the child is
unaware that there is a
problem. The child’s eyes are
examined periodically before
the age of 7 years.
Management
Corrective
glasses and
lens
Eye
Patching
Management
RETINO
BLASTOMA
Definition
 Retinoblastoma is a
malignant glioma of the
retina.
 It may be unilateral (70%)
or bilateral (30%).
 It is a highly malignant
tumour arising from the
nuclear layer of the retina.
Incidence and
Prevalence
Predisposing
Factors
 About 90 percent
cases are found in
less than 5 years of
age.
 It is rare tumor,
though the most
common ocular
neoplasm of
childhood.
 Usually congenital
in origin but
commonly
manifests itself
between 2 to 5
years.
 Hereditary and
familial tendency
Etiology
 The disease has a genetic predisposition in
majority of the cases.
 The retinoblastoma gene is located on
chromosome 13.
 The gene carries risk of osteosarcoma and
a secondary malignancy like a pineal tumor,
the so called “trilateral retinoblastoma”.
 It usually develops in the posterior portion
of retina. About 25 per cent cases are
bilateral.
Forms of Retinoblastoma
Non-inheritable
Not passed down from
parents. This type of
retinoblastoma is caused
by mutations in the RB1
gene that occur by
chance after a child is
born. Usually unilateral
Heritable
The mutation in the RB1
gene passed from the
parent to the child, or it
may occur in the egg or
sperm before
conception or soon after
conception. Usually
bilateral
In
retinoblastoma
there is a
mutation in
the RB1 gene
Pathophysiology
B
Extension of the Tumour
When it grows towards the
choroids, it is known as
Glioma Exophytum.
When it grows towards the
vitreous humour, it is
Glioma Endophytum.
Extension of the Tumour
Quiescent Stage
Stage of Glaucoma
Stage of Extra-ocular Extension
Stage of Metastasis
Clinical features
Diagnosis
Confirmed by
fundoscopy to detect
leukocoria
CT scan to
determine the
extent of tumor
X-ray to detect
bone
involvement
CSF study, bone
marrow study to
identify the metastasis
Management
Enucleation may be
done in unilateral cases
Radiotherapy Chemotherapy Scleral plaque irradiation
Cryotherapy or
photocoagulation
ANATOMY OF EXTERNAL EAR
ANATOMY OF EXTERNAL EAR
ANATOMY OF INTERNAL EAR
ANATOMY OF INTERNAL EAR
ANATOMY AND PHYSIOLOGY OF NOSE
Frontal Sinus
Middle Turbinate
Superior Turbinate
Sphenoid Sinus
Pharyngeal tonsil
Auditory tube opening
Inferior turbinate
Vestibule
Paranasal sinus
THROAT ANATOMY AND PHYSIOLOGY
• Soft palate and vallecula
form a tongue and groove
and separates the oral
cavity from the nasal
cavity during the first 6
months of infancy when
most children are
primarily nasal breathers.
• Anterior placement of the
larynx
THROAT ANATOMY AND PHYSIOLOGY
• Shared passage for
eating and breathing.
• The tongue occupies
less of the oral cavity.
• The larynx sits lower in
the neck,
EXTERNAL EAR
DISEASE
CONDITIONS
EXTERNAL EAR
EXTERNAL OTITIS OR OTITIS EXTERNA
External otitis, or otitis
externa, refers to an
inflammation of the external
auditory canal. It is a painful
condition caused when
irritating or infective agents
come into contact with the
skin of the external ear.
Causes/Etiology
• Blockage of the
canal
• Absence of
cerumen due to
excess cleaning
• Trauma
• Alteration of pH
within the canal
Bacterial infection
Fungal infection
Pseudomonas
Aeruginosa
Staph Aureus
Aspergillus
Risk Factors
 Hot and humid climates
 Swimming
 Diabetes Mellitus
 Narrowing/obstruction of the
auditory canal
 Over-cleaning leading to a
lack of wax in the canal
 Wax build-up
 Eczema
 Trauma
Classification
Acute Otitis Externa:
• Lasts less than 6
weeks
• Typically due to
bacterial infection
Chronic Otitis Externa:
• Lasts more than 3
months
• Due to Allergies or
autoimmune diseases
Pathophysiology
Allergy, injury to external
auditory canal (EAC),
Trapped water, foreign bodies,
narrow canal, humid conditions
Retention of moisture
Multiplication and inhabitation by bacteria or fungi
Activation of inflammatory mediators and enzymes
Chemotaxis
Edema & pain Ear discharge
Clinical Manifestation
o Pain and discharge
from the EAC
o Aural tenderness
o Occasional fever
o Cellulitis
o Lymphadenopathy
o Pruritus
o Hearing loss
o Feeling of fullness in
the ear
On otoscopic
examination:
o Erythematous and
edematous ear canal
o Yellow or green, foul-
smelling discharge.
o Fungal infections –
visible hair like black
spores
Diagnostic Evaluation
Complete medical history
and physical
examination.
Otoscopic examination
Culture of the drainage
Medical Management
 Antibiotic ear drops or oral antibiotics
 Corticosteroid ear drops (to help
decrease the swelling)
 Pain medication
 Keeping the ear dry, as directed.
 Placing a wick in the ear (a piece of
sponge may be placed in the child's ear
if there is a lot of swelling. This wick
helps the antibiotic drops work more
effectively in the ear canal).
Nursing Management
 Avoid events that traumatize the external
canal such as scratching the canal with the
fingernail or other objects.
 A cotton ball can be covered in a water
insoluble gel such as petroleum jelly and
placed in the ear as a barrier to water
contamination.
 Infection can be prevented by using
antiseptic otic preparations after swimming
(eg, Swim Ear, Ear Dry).
EDUCATE
CERUMEN OR FOREIGN BODIES
Clinical Manifestation
Sensation of fullness in
the ear, with or without
hearing loss
Ear pain
Itching
Dizziness
Bleeding from
the ear
Management
 If the occluding material is cerumen, management options
include watchful waiting, manual removal, and the use of
ceruminolytic agents followed by either manual irrigation
or the use of a low-pressure, electronic, oral irrigation
device.
 The canal can be irrigated with a mixture of water and
hydrogen peroxide at body temperature.
 Insects are killed before removal unless they can be
coaxed out by a flashlight or a humming noise.
Management
 Lidocaine, a numbing agent, can be
placed in the ear canal for pain relief.
 Mineral oil or diluted alcohol instilled
into the ear can suffocate the insect,
which is then removed with ear
forceps.
 If the patient has local irritation, an
antibiotic or steroid ointment may be
applied to prevent infection and
reduce local irritation.
CONDITIONS OF
THE MIDDLE
EAR
MIDDLE EAR
ACUTE AND CHRONIC OTITIS MEDIA
 Chronic otitis media (COM): If an attack of
acute otitis media fails to heal, the
perforation and discharge may in some cases
persist. This leads to mixed infection and
further damage to the middle-ear structures,
with worsening conductive deafness
 Acute otitis media (AOM) is an acute infection of the middle ear,
usually lasting less than 6 weeks
Causative Organisms
Streptococcus
pneumoniae Haemophilus
influenzae
Moraxella
catarrhalis
Risk factors
 Crowed living conditions
 Exposure to second hand smoke
 Respiratory illness
 Close contact with siblings those
who have cold.
 Having Cleft Palate ( Abnormal
Position of muscles and tendons )
 Premature birth
Pathophysiology
c
Clinical Manifestation of Otitis
Media
Diagnosis
History, Physical
Examination
Otoscopy Tympanometry
Tympanocentesis Blood test
Hearing Test
Whisper Test, Weber Test
Rinne test
Complications
Tympanic membrane Perforation
Mastoiditis
Facial Nerve Palsy
Acute Labyrinthitis
Petrositis
Management
Analgesics Antimicrobials
Aspiration
CHRONIC SUPPURATIVE OTITIS
MEDIA (CSOM)
Chronic suppurative otitis media is defined as chronic
inflammation of the middle ear and mastoid cavity
characterized by
1) Perforation of the tympanic membrane due to acute
infection or tympanotomy tube.
2) Recurrent discharge from the middle ear (otorrhea).
3) Prolonged duration (>2 weeks).
FIG: Chronic Otitis Media with suppuration
Prevalence
Peaks around 2
years of age.
The infection is
most commonly
acquired in
children aged up
to 6 years
Classification
Tubotympanic/safe type: Atticoantral/unsafe type:
 Associated with
tympanic membrane
perforation and
recurrent / persistent ear
discharge.
 Episodes of URTI and
entry of water into the
middle ear are
precipitates
 Associated with
presence of
cholesteatoma or
granulations
 May cause life-
threatening
complications (brain
abscess, meningitis,
hydrocephalus etc.
Management
• Oral antibiotics
• Local antibiotic ear
drops
Medical
management:
• Myringotomy
• Myringoplasty
• Tympanoplasty
• Mastoidectomy
• Stapedectomy
Surgical
management:
Prevention
Preventive measures for CSOM are
described as HEAR
 H- Hygiene of the ear
 E- Early management of acute
otitis media
 A - Antiobiotics
 R - Raising awareness
TYMPANIC MEMBRANE
PERFORATION
A ruptured eardrum is a tear in the thin membrane that
separates outer ear from inner ear and when there is
abnormal opening or Perforation in tympanic membrane
Causes
Ear Infection
Insertion of objects purposefully
Concussion
Head Trauma
Barotrauma
Signs and Symptoms
 Not able to recognize at first
 Some may feel Air coming out
of their ear when they blow
nose.
 Sudden sharp pain
 Drainage from ear (Bloody,
Clear, Pus)
 Ear Noise or buzzing
 Hearing loss (Partial or
Complete)
 Facial Weakness or dizziness
Diagnosis
Audiometry Otoscopy
Tuning Fork test
Rinne test
Management
• Keep Ear Dry
• Oral or Topical Antibiotics
• Surgical
Myringoplasty
Tympanoplasty
OTOSCLEROSIS
Otosclerosis is abnormal hardening and
overgrowth of the stapes
Clinical Manifestation
 It may involve one or both ears and manifests as a
progressive conductive or mixed hearing loss.
 Bone conduction is better than air conduction on
Rinne testing.
 The audiogram confirms conductive hearing loss
or mixed loss, especially in the low frequencies.
Management
STAPEDECTOMY
MASTOIDITIS
Mastoiditis is a bacterial infection of the mastoid air
cells surrounding the inner and middle ear.
The mastoid bone, which is full of these air cells, is
part of the temporal bone of the skull.
Causes
 Middle ear infection.
 Cholesteatoma (a
growing collection of
skin cells) which blocks
ear drainage
Clinical Manifestation
Fever,
irritability,
and lethargy
Swelling of
the ear lobe
Redness and
tenderness
behind the ear
Drainage
from the ear
Bulging and
drooping of the
ear
Medical Management
• Antibiotic and steroid eardrop
for infection and inflammation,
e.g. Ciplox-D
• Ear-irrigation: For removing
purulent discharge
• Analgesics drugs: Aspirin,
Nimesulide.
Surgical Management
Mastoidectomy: It is a surgical
procedure that removes diseased
mastoid air cells
Myringotomy: It is a surgical
procedure in which a tiny incision is
created in the eardrum relieves
pressure caused by excessive
build-up of fluid or pus
Surgical Management
Mastoidectomy: It is a surgical
procedure that removes diseased
mastoid air cells
Myringotomy: It is a surgical
procedure in which a tiny incision is
created in the eardrum relieves
pressure caused by excessive
build-up of fluid or pus
Tympanoplasty: also called eardrum repair. It is the
surgical reconstruction of the perforated eardrum or the
small bones of the middle ear.
Surgical Management
Nursing Management
Nursing Diagnosis
 High risk for infection related to tissue
destruction
 Pain related to physical factors
 Altered auditory sensory perception related
to partial/total perforation of tympanic
membrane
 Impaired verbal communication related to
hearing deficit
 High risk for trauma related to impaired
balance
Nursing Management
Interventions:
• Assess pain for location, intensity etc
• Administer analgesics as prescribed to relieve
pain
• Administer antibiotics as ordered
• Administer antipyretics as prescribed
• Provide plenty of fluids
• Use cool water sponging to reduce body
temperature
• Encourage patient and family to use signs of non-
verbal communication such facial expression
HEARING
IMPAIRMENT
DISORDERS
OF THE NOSE
RHINITIS
Rhinitis is broadly defined as inflammation
of the nasal mucosa.
Classification of Rhinitis
IgE-mediated
(allergic)
Autonomic:
Drug-induced
Infectious
Idiopathic
Pathophysiology
Allergen, drugs, infections and other causes
Production of immunoglobulins (IgE) and inflammatory
mediators (histamine, thromboxane, prostaglandins)
Nerve cell irritation Loss of mucosal integrity
Sneezing, itching,
vascular
engorgement
Rhinorrhea
Symptoms
Treatment
• Avoidance of allergens.
• Non-sedating antihistamine
(loratadine, cetirizine,
fexofenadine).
• Intranasal corticosteroids.
• Oral decongestants.
• Antibiotics only if infected
rhinitis.
SINUSITIS
Sinusitis is inflammation of frontal, maxillary,
ethmoidal and sphenoidal sinuses.
Causes
Classification
Pathophysiology
Acute infection Destroys normal ciliated epithelium
Impairs drainage
from sinus
Pooling and stagnation of
secretions
Decreased mucocilliary
clearance
Inflammation, edema and
exudation
Blockage of
paranasal sinuses
Sinusitis and persistent
infection
Clinical Features
Acute bacterial sinusitis:
 Nasal or postnasal discharge (of any quality)
 Daytime cough (which may be worse at night)
 Headache
 Retro-orbital pain
 Facial pain
 Tenderness, redness and swelling of the cheek and
near inner canthus of the eye
 Fever at least 102°F (39°C).
Clinical Features
Chronic bacterial sinusitis:
 Persistent or recurrent attack of nasal or postnasal
discharge
 Low grade fever
 Malaise
 Sniffing
 Nose twitching
 Mouth breathing
 Epistaxis
 Ear discharge
Diagnosis
 Nasal examination showing
mucus or pus
 X-ray of paranasal sinus
showing air- fluid filled
levels and complete
opacification
 CT scan
 Nasal swab culture
Management
Chronic bacterial
sinusitis:
Prolonged antibiotic
therapy, nasal drops of
oxymetazoline HCI,
breathing exercise, nose
blowing and radical sinus
surgery.
Acute bacterial
sinusitis:
Antibiotic therapy with
amoxicillin,
decongestants, mucolytic
agents, nasal drops and
avoiding contacts with
URI.
EPISTAXIS
Causes
Types
Anterior
epistaxis
Posterior
Nosebleeds
Management
Non-surgical Management
• Fresh blood and clots
should be removed with
suction.
• Topical vasoconstrictors,
packing and cauterization
will stop the bleeding
effectively.
Surgical Management
• Arterial ligation,
submucosal resection
(SMR)/septoplasty
• Embolization of the
internal maxillary artery
in case of failed
surgery
Management
Preventive Measures
• To avoid nose-picking as much as possible.
• During the winter and allergic seasons, do not blow
the nose harshly but gently.
• When participating in any physical activities that can
harm the nose and head, wear a protective helmet for
safety measures.
• To avoid the consumption of excess alcohol and
smoking.
• Make use of saline nasal spray or saline nose drops
once or twice a day to keep the nose moisturized.
DISORDERS
OF THE
THROAT
PHARYNGITIS
Pharyngitis is an
inflammation of the
mucous membranes and
underlying structures of
the throat.
Etiology of Acute Pharyngitis
Rhinovirus
Adenovirus
Coronavirus
Parainfluenza virus
Bacterial Viral
Group A beta hemolytic
Streptococcus
Neisseria gonorrhoea
Corynebacterium
diphtheria.
Clinical Features
Viral pharyngitis:
• Fever
• Malaise
• Anorexia
• Sore throat
• Hoarseness of voice
• Conjunctivitis
• Coryza (inflammation of the mucous membrane in the
nose)
• Cough
• Diarrhea
Clinical Features
Bacterial pharyngitis
• Beefy, red swollen uvula
• petechiae on the palate; excoriated nares (especially in
infants) and a scarlitiniform (Scarlet fever) rash
• Sudden onset of sore throat
• Severe pain on swallowing
• Fever
• Headache
• Nausea
• Vomiting
• Abdominal pain
Diagnosis
• Streptococcal pharyngitis is
treated with oral
antimicrobial therapy
(penicillin, erythromycin or
amoxicillin) for 10-14 days.
• Supportive therapy includes
antipyretics, analgesics,
antitussives, bed rest and
saline gargles.
• Throat culture.
• Rapid antigen
detection tests.
Treatment
TONSILLITIS
Tonsillitis refers to
inflammation of the
pharyngeal tonsils – glands at
the back of the throat, usually
caused by beta hemolytic
streptococcus or viruses
Causes
Bacteria cause 15-30 percent of
pharyngotonsillitis cases
The herpes simplex virus
Streptococcus pyogenes
Epstein-Barr virus (EBV)
Cytomegalovirus (CMV)
Adenovirus
Group B Strep is the cause for most bacterial
tonsillitis – strep throat
Clinical Features
Treatment
Chronic tonsillitis:
 Tonsillectomy is indicated
when there is recurrent
infections of >7 episodes per
year, peritonsillar abscess
and severe hypertrophy of
tonsils.
Acute tonsillitis:
 Saline gargles
 Analgesics
 Antibiotics
Complications
Peritonsillar abscess.
Obstructive
sleep apnea
Tonsillar
cellulitis
ADENOIDS
Adenoids or nasopharyngeal are lymphoid tissues at the
junction of the roof and posterior wall of nasopharynx.
Clinical Features
Acute adenoiditis:
 Purulent rhinorrhea
 Nasal obstruction
 Mouth breathing
 Epistaxis
 Fever
 Associated Otitis
Media
 Nasal change in voice.
Chronic adenoiditis:
 Persistent rhinorrhea
 Postnasal drip
 Malodorous breath
 Associated otitis media >3
months
 Open mouth
 Drooling and mal-occluded
teeth (adenoid faces)
 Pulmonary hypertension.
Treatment
Surgical: Adenoidectomy if recurrent rhinosinusitis or
severe adenoid hypertrophy occurs.
Conservative treatment:
includes nasal decongestants,
antihistaminic and antibiotic
therapy.
Nursing Management
after Tonsillectomy
and Adenoidectomy
Nursing diagnosis
1. Ineffective airway clearance
related to postoperative
secretions Pain related operative
procedure.
2. Risk for deficient fluid volume
related to bleeding.
3. Deficient knowledge related to
home care.
Nursing Intervention
• Monitoring oxygen saturation especially
when they sleep. Observing bleeding for
initial 6 hours which is crucial for primary
bleeding.
• Prevention of bleeding from site of operation.
• Maintain IV access until discharge.
• Position the child in comfortable or prone
position turning the head to one side to allow
the drainage of secretions.
Nursing Intervention
• Measure and record intake and output hourly.
Assess skin turgor and moisture of mucous
membranes.
• Adequate rest and sleep.
• Soft non irritating diets and plenty of fluids.
• Avoid contacts with infected persons.
• Avoid use of straw to prevent injury to the site.
Practice nose breathing.
• Discourage excessive coughing and clearing the
throat.
RESEARCH ABSTRACTS
CONCLUSION
Eye and ENT disorders in children are very
common though most are not life threatening.
But the anatomical structures involved are
important and most may make the child
physically challenged if left untreated. So it is
the duty of the community, parents and
health care workers to actively be involved in
the care of children with these disorders
Eye and ENT.pptx

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Eye and ENT.pptx

  • 1. Pediatric Eye and ENT disorders Amy Lalringhluani Msc 2nd Year CPMSCON
  • 3. Eye development starts in the 3-week embryo The initial 3 years of life is the critical period for eye development Normal adult visual capacity develops at 3 years of age After the early puberty, the anterior posterior diameter of the eye, remains unaltered in healthy subjects The refractive status of the eye may still change in adults due to aging processes Eye Development
  • 6. CHILDHOOD EYE EXAMINATION Red Reflex Test Cover, Cover- Uncover, and Alternate Cover Tests Corneal Light Reflex Fixation and Alignment Pupillary Response External Ocular Examination Visual Acuity History
  • 7. History Personal or family histories of risk factors for eye and vision problems are assessed for Risks include premature birth, Down syndrome, cerebral palsy, and a family history of strabismus, amblyopia, retinoblastoma, childhood glaucoma, childhood cataracts, or ocular or genetic systemic disease
  • 8. Eye Charts Each eye to be tested independently and opposite eye occluded to discourage peeking. Most children do not have 20/20 vision until after 6 years of age, but at any age, visual acuity should be approximately equal between the eyes. The visual acuity test is used to determine the smallest letters you can read on a standardized chart (Snellen chart) or a card held 20 feet (6 meters) away. Visual Aquity
  • 10. Eye Charts Visual Aquity Lea chart Allen chart
  • 11. Visual Acuity Norms for Children 2.5 to 6 Years of Age Age (months) Norms 30 to 35 Approximately 20/60 (6/20) or better 36 to 47 20/50 (6/15) or better 48 to 59 20/40 (6/12) or better 60 to 72 Approximately 20/30 (6/10) or better
  • 12. External Ocular Examination Involves examination of the external portion of the eye, including • eyelids, • orbits, • conjunctiva, • sclera, • cornea, • iris
  • 13. External Ocular Examination Inspect for excessive tearing, watery or purulent discharge, photosensitivity, conjunctival infection, and gross structural abnormalities. Lacrimal duct obstruction is recognized when pressure over the lacrimal sac produces mucus in an eye. Childhood glaucoma presents with tearing accompanied by corneal redness, corneal clouding, photosensitivity, and enlarged eyes.
  • 14. Pupils measured for size and symmetry in light & darkness 03 Assessed using a bright light 01 Room darkened before declaring a response 02 Pupillary Response
  • 15. Fixation and Alignment By 2 months of age, a child should be able to fix and follow an object. If strong binocular fix and follow not seen by 3 months of age, refer Ocular alignment should be assessed to identify strabismus Children as young as six weeks should have some response to an examiner’s face.
  • 16. In a corneal light reflex test, the child’s attention is attracted to a target (a light or a brightly colored object), while a light in front of the child is directed at the child’s eyes. The light’s reflection will be symmetric in each pupil by four to six months of age in patients with normally aligned eyes. 1. Corneal Light Reflex
  • 17. Hirschberg test It gives rough objective estimate of the angle of a manifest squint. Useful in young or uncooperative patients or when fixation in deviating eye is poor. Procedure:  Patient made to fixate at point light held at a distance of 33cm .  Deviation of corneal light reflex from the centre of pupil noted in the squinting eye.  1 mm of deviation ≅ 7○ . (1○ = 2 prism dioptre)  The angle of squint is 15 ○ & 45 ○ when the corneal light reflex falls on the border of pupil and limbus, respectively.
  • 18. Hirschberg test Normal Corneal reflex 1mm deviation ≈ 15 diopters 2mm deviation ≈ 30 diopters 3mm deviation ≈ 45 diopters 4mm deviation ≈ 60 diopters
  • 19. 2. Cover, Cover-Uncover, and Alternate Cover Tests Cover test Uncover test Cover- Alternate Cover test
  • 20. Cover Test Child’s attention is attracted to a target Step 1 Vision of one eye is then occluded Step 2 Tested (uncovered) eye is observed for movement from a deviated position and back Step 3 Untested eye is uncovered & tested eye is observed again for any misalignment. Step 4
  • 21. Cover-Uncover Test A cover is placed over one eye for 1 – 2 seconds while the child’s attention is called to the target 1 2 Cover is removed rapidly, & previously covered eye is observed for movement from deviated position back to fixation on the target
  • 22.
  • 23. Alternate Cover Tests The cover is held over one eye for a few seconds, then moved rapidly over the other eye and held for a few seconds, then moved back to cover the first eye. This is repeated several times, and each time the cover is moved, the previously covered eye is observed for any “refixation” from a deviated to a normal position. Step 1 Step 2
  • 24. Red Reflex Test The ophthalmoscope is used in a darkened room Each red reflex viewed individually 12 to 18 inches (approximately 30 to 45 cm) from the patient’s eyes Both red reflexes simultaneously at a distance of 2 to 3 feet (approximately 0.6 to 0.9 meters).
  • 25. Red Reflex Test A symmetric orange-red light should reflect from each fundus. Any abnormal finding (e.g., asymmetry of color or occurrence of dark or white spots) is a reason for referral to an ophthalmologist.
  • 28. Infantile hemangiomas  Most common eyelid tumors in infancy. Bright red or purple appearance.  Blanch with pressure.  Undetected at birth.  Enlarge in first 12 months followed by a slow involution during the first decade.
  • 29. Infantile hemangiomas  Vision loss is related to amblyopia because of induced astigmatism or visual deprivation due to ptosis.  Steroid treatment (intralesional and/or oral) is the first line of therapy.
  • 30. Epibulbar dermoids  Choristomas (congenital dermoids) are masses of normal tissue found in an abnormal location  Induce astigmatism and cause refractive amblyopia  May be excised to improve cosmetic appearance and avoid amblyopia
  • 31. Anophthalmia / Microphthalmia Anophthalmia: one or both eyes absent Microphthalmia: one or both eyes did not develop fully, so they are small Often result in blindness or limited vision
  • 32. Anophthalmia / Microphthalmia Frequently associated with secondary orbital and ocular deformity like cataract and genetic conditions such as trisomy 13
  • 33. Colobomas Characterized by an inferior or ventrally located gap in one or more tissues, extending between the cornea and the optic nerve
  • 34. Colobomas May be unilateral or bilateral Clinical spectrum of congenitally reduced ocular size (microphthalmia), and in severe cases, absence of one or both eyes (anophthalmia)
  • 35. Persistant fetal vasculature (persistant hyperplastic primary vitreus) ◙ Failure of regression of a component of fetal vessels within the eye ◙ Leads to impairment of vision Crossed eyes (strabismus), abnormal eye movements (nystagmus) and “lazy eye” (amblyopia) are common features
  • 37. Ptosis Drooping of upper eyelid covering > 2mm of the cornea below the upper limbus is called ptosis May be congenital or acquired Can induce sensory deprivation amblyopia Surgical correction: Mild cases - age of 3-4 years. Severe cases - early surgery required to prevent amblyopia.
  • 38. Entropion Inversion of lid margin due to congenital or scarring Eyelid skin and eyelashes to rub against the eye Friction Discomfort and irritation to the cornea
  • 39. Entropion Surgical entropion repair: ⁃ Eyelid tightening: This procedure shortens the eyelid (called a lateral tarsal strip) to tighten the lid. ⁃ Retractor reinsertion: This procedure is used to tighten the lid retractor (muscle that opens and closes the lid).
  • 40. Ectropion Outward turning of the lid margin as a result of inflammation, burns or trauma is called ectropion Ectropion leaves the eye too exposed. The eye can become dry, irritated, and even infected. It is either congenital or acquired
  • 41. Blephrospasm ▲It is the repetitive or spastic closure of eyelids secondary to trichiasis, keratitis or conjunctivitis
  • 42. Blepharitis ▲Inflammation of the lid margin due to staphylococcal or seborrheic infection ▲Characterized by itching, irritation and watering of the eyes due to blocked meibomian glands ▲Flaky skin around the eyes with crusty debris covering the eyelids, loss of eyelash
  • 44. The infections occur in two clinical forms; Preseptal cellulitis Orbital cellulitis Causes: Skin trauma, sinusitis, lacrimal sac infections and rarely remote infections
  • 45. Preseptal cellulitis Infection of eyelid & surrounding skin anterior to the orbital septum Begins in superficial to the orbital septum and extends from the orbital rim into the upper and lower eyelid
  • 46. Preseptal cellulitis Swelling, tenderness, and erythema of the eyelid Swelling is confined to the eyelid Globe is white Vision and ocular motility are normal
  • 47. Orbital cellulitis Infection of the orbital tissues posterior to the orbital septum Begins deep to the orbital septum Caused by extension of infection from adjacent sinuses
  • 48. Orbital cellulitis Symptoms  swelling & redness of eyelid  conjunctival hyperemia & chemosis  pain with eye movements  decreased visual acuity  fever
  • 50. Ophthalmia Neonatorum Inflammation of the conjunctiva within the first month of life is classified as ophthalmia neonatorum (neonatal conjunctivitis). Associated with catarrhal, purulent or mucoid discharge from one or both eyes, conjunctival infection, edema and erythema of the lids.
  • 52. Common causes of Ophthalmia Neonatorum with time of onset and typical characteristics Type Time of onset Characteristics Chemical (e.g., silver nitrate drops) Within hours of instillation ⁃ Self-limiting, mild, serous discharge (occasionally purulent) ⁃ Lasts 24–36 hr Chlamydia trachomatis 5–14 days ⁃ Mild-moderate, thick, purulent discharge Erythematous conjunctiva, with palpebral more than bulbar involvement
  • 53. Common causes of Ophthalmia Neonatorum with time of onset and typical characteristics Type Time of onset Characteristics Neisseria gonorrhoeae 24–48 hr ⁃ Hyperacute, copious, purulent discharge ⁃ Lid swelling and chemosis common Bacterial (nongonococcal) After 5 days ⁃ Variable presentation, depending on organism
  • 54. Common causes of Ophthalmia Neonatorum with time of onset and typical characteristics Type Time of onset Characteristics Herpetic Within 2 weeks ⁃ Conjunctiva only mildly infected ⁃ Serosanguinous discharge ⁃ Vesicular rash on lids sometimes seen ⁃ Systemic herpetic disease present
  • 55. Mode of Infection Intrauterine infection Infection during the process of delivery (most common) Infection after birth
  • 56. Pathophysiology Infection due to entry of microorganism or chemical Blood vessels dilate Formation of new blood vessels around the papillae Formation of numerous polymorphs in the epithelium Purulent discharge and exudate formation in eye
  • 57. Clinical Features Eyelids are tense and swollen Conjunctiva is congested and swollen Excessive tearing or turbid and thick discharge from eyes
  • 58. • Tetracycline, erythromycin ointments or povidone-iodine drops can be used for prophylaxis • Saline lavage hourly till discharge is needed • Systemic intravenous antibiotics may be needed. Treatment
  • 59. Prevention  Proper antenatal care of pregnant women.  Treatment of infected vaginal discharge during pregnancy.  Use of aseptic techniques while delivery and in care of newborn.  Cleaning of each eye with sterile swabs dipped in sterile water, as soon as the head is delivered and instillation of Chloramphenicol eye drops in each eye as a prophylactic measure.
  • 60. Conjunctivitis Conjunctivitis is inflammation of conjunctiva characterized by red eyes with or without discharge and itching Etiology is almost always bacterial in children. It can also be viral or allergic
  • 61. Pathophysiology Microbes enter the eye on contact with infected object Inflammation of eye Dilation of blood vessels of eye Swelling, redness, exudates and discharge
  • 62. Clinical Features Redness of eye (hyperemia) Tearing and itching in eyes Exudation Other symptoms may include: →Photophobia →Pseudoptosis (drooping of upper eyelid) →Periorbital cellulitis →Pain in eye →Fever Viral infection fever, sore throat and runny nose
  • 63. Types of conjunctivitis Bacterial Conjunctivitis Viral Conjunctivitis Allergic conjunctivitis
  • 64. Bacterial Conjunctivitis • Caused by bacteria • Causes serious damage to the eye if left untreated • Symptoms include redness, dryness of eyes and skin around it and mucoid purulent discharge. • Topical flouroquinolone and erythromycin may be used for treatment Bacterial Conjunctivitis Types of conjunctivitis
  • 65. Types of conjunctivitis Viral Conjunctivitis • Caused by virus like the common cold virus • Very contagious • Symptoms include redness of the eye, periodic itching and increased lacrimation • Clear up on its own in few days without treatment Viral Conjunctivitis
  • 66. Allergic conjunctivitis • Caused by irritants such as pollen and dust • May be seasonal or flare up year round • Symptoms include redness of the eye, itching, swelling of the conjunctiva and the eyelids • Antihistamine drops are used to relieve symptoms Allergic conjunctivitis Types of conjunctivitis
  • 67. Difference between bacterial conjunctivitis and viral/allergic conjunctivitis Features Bacterial conjunctivitis Viral/Allergic conjunctivitis Symptoms Bacterial cases will always have discharge. Allergic cases will always have prominent itching Presence and nature of discharge Bacterial infections will have a purulent, yellow-green discharge Viral cases will have serous or mucoid discharge. Allergic cases will have serous discharge with excessive tearing.
  • 68. Features Bacterial conjunctivitis Viral/Allergic conjunctivitis Laterality Bacterial cases can be either unilateral or bilateral. Viral and allergic conjunctivitis occur almost always bilateral. Systemic associations - Viral conjunctivitis might be associated with upper respiratory infections. Allergic conjunctivitis might be seen with upper respiratory allergic symptoms.
  • 69. Difference between bacterial conjunctivitis and viral/allergic conjunctivitis Features Bacterial conjunctivitis Viral/Allergic conjunctivitis Treatment First-line therapy for bacterial conjunctivitis is topical flouroquinolone. In many cases Polysporin, erythromycin or trimethoprim/sulfa is effective. Viral conjunctivitis is self- limited. For allergic cases topical antihistaminic drops are effective.
  • 70. Nursing Management Prevention  Apply cold compress on the eye  Reduce exposure to light  Prevent rubbing of the eye  Acetaminophen  If caused by bacterial agents − Clean eye with sterile water and cotton swabs − Apply antibiotic ointment or eye drops − Use of dark glasses if photophobia present
  • 71. Nursing Management Family Teaching Good hand washing after touching the eye Separate towel, sheet and pillow case for infected child Dropper should not touch child’s eyes during medication instillation
  • 73. Congenital anomalies that affect cornea Megalocornea: It is symmetric non- progressive enlargement of cornea. It is associated with refractive error Microcornea: It is a rare condition characterized by small isolated cornea. It may be associated with congenital cataract, glaucoma, etc
  • 74. Congenital anomalies that affect cornea Microphthalmos: Microphthalmos is defined as the developmental arrest of all ocular structures Anophthalmos: Anophthalmos is the complete failure of the eye development
  • 75. Keratitis Keratitis is an inflammation and swelling of the cornea characterized by oval shaped corneal infiltrations surrounded by corneal edema, conjunctival hyperemia, ocular pain and photophobia
  • 76. Types of Keratitis Non- infectious Infectious Caused by an eye injury, by wearing contact lenses too long or by a foreign body in the eye Caused by bacteria, viruses, fungi and parasites. Main causative organisms are staph aureus, staph epidermis & strep pneumonia.
  • 77. Signs & Symptoms Intense pain Red eyes Profuse tearing Photophobia Corneal edema Clouding & blurred vision Complications Permanent vision damage Corneal perforation
  • 78. Treatment Infectious Mild cases - eye drops (antibiotic, antiviral or antifungal, determined by the cause of the infection) Advanced infections - oral medications Non-infectious For mild discomfort - artificial tears. Severe cases - a bandage contact lens and anti-inflammatory eye medications
  • 80. Optic neuritis Optic neuritis is an inflammatory, infective or demyelinating process affecting the optic nerve. DEFINITION
  • 81. Etiology Demyelinating disease Parainfectious, infectious Non-infectious Sinus –related Cat -scratch fever Syphilis Lyme disease Cryptococcal meningitis Sarcoidosis Systemic lupus erythematosus Polyarteritis nodosa
  • 82. Classification of Optic Neuritis Papillitis: characterized by hyperemia and edema of the optic disc, associated with peripapillary flame-shaped hemorrhages. Neuroretinitis: is characterized by papillitis in association with inflammation of the retinal nerve fibre layer and a macular star. Retrobulbar neuritis: the optic nerve head is normal in retrobulbar neuritis, because the optic nerve head is not involved
  • 83. Papilloedema Papilloedema is swelling of the optic nerve head secondary to raised intracranial pressure It is nearly always bilateral, although it may be asymmetrical. Headaches, deterioration of consciousness, nausea and vomiting Diplopia due to 6th nerve palsy SIGNS AND SYMPTOMS
  • 84.
  • 86. Definition Retinopathy of prematurity (ROP) is a vasoproliferative disorder of the retina among premature babies, which was previously termed as retrolental fibroplasia
  • 87. Risk factors Premature birth Uncontrolled O2 therapy Born ≤ 31 wks of GA/ wt ≤ 1500gm Systemic problems (sepsis, anemia, etc)
  • 88.
  • 90. Category Stage/ Zone Characteristics Location Zone I Circle with optic nerve at its centre and radius of twice the distance from optic nerve to macula (fovea centralis) Location
  • 91. Category Stage/Zone Characteristics Location Zone II Concentric circle from edge of zone 1 to ora serrata nasally and equator temporally Location
  • 93. Category Stage/ Zone Characteristics Location Zone III Lateral crescent from zone 2 to ora serrata temporally Location
  • 94. Severity Stage 1 Presence of thin white demarcation line separating vascular from avascular retina
  • 95. Severity Stage 2 Addition of depth and width to the demarcation line of stage 1, so as the line becomes a ridge
  • 96. Severity Stage 3 Presence of extra retinal fibro vascular proliferation with abnormal vessels and fibrous tissue extending from ridge to vitreous
  • 97. Severity Stage 4 Partial retinal detachment not involving macula (4A) and involving macula (4B)
  • 99. Presence of dilatation and tortuosity of retinal vessels at posterior pole of eye. Associated with papillary rigidity and vitreous haze. Plus disease frequently leads to vessel contraction and scar formation, which in turn, leads to macular displacement. Plus disease
  • 100. ROP Screening Screening is performed by an expert using indirect ophthalmoscopy.
  • 101. In India, babies with  GA<34 weeks or Birth weight <1700g  Birth weight <2000g (if GA not known)  Sick preterm babies are screened at the neonatologists’ discretion
  • 102. To avoid confusions about the timing of first screening it is recommended that the first ROP screening should be done strictly • before “day 30” of post-natal life • by “day 20” of life in smaller babies (<30 weeks and/or birth weight <1200 g).
  • 103. Role of Nurses in ROP Screening Record wt and GA at birth. Monitor wt gain during NICU admission. Select babies eligible for screening. Counsel the parents regarding screening procedure. Dilate eyes 1 hour before examination using a topical agent.
  • 104. Role of Nurses in ROP Screening Keep the baby NPO one hour prior to procedure. Position the baby comfortably, take adequate pain control measures. Ensure hand washing, use sterile articles only during procedure. Monitor vital signs. Documentation of procedure, fix next appointment.
  • 105. Treatment of ROP Peripheral retinal ablation of avascular retina Argon laser photocoagulation Follow up of the child for development of vision, refractive status and strabismus till preschool age
  • 106. Prevention of ROP Antenatal steroids Judicious oxygen therapy Judicious use of blood transfusions Other interventions
  • 108. Definition Cataract is the opacification of the crystalline lens. A cataract is any cloudiness or opacity of the natural lens of the eye, which is normally crystal clear. Incidence Approx 3 /10,000 children Variable throughout the world.
  • 109. Causes  Intrauterine infections (e.g. toxoplasmosis)  Galactosemia  Chromosomal anomalies (Down’s syndrome)  Ocular malformation  Mental retardation Congenital or Primary  Trauma  Retrolental fibroplasia  Uveitis  Maternal malnutrition  Glaucoma Acquired or Secondary
  • 110.
  • 111. Classification of pediatric cataract Congenital/Infantile cataract Cataract present at birth or which occurs during the first year of life Manifestations: • Usually bilateral • Visible clouding of lens • Varying impairment of vision • Maybe found with amblyopia
  • 112. Classification of pediatric cataract Congenital/Infantile cataract Causes: • Prematurity • Maternal infections - (Toxoplasmosis, rubella, CMV, herpes simplex, measles, influenzae, etc.) • Chromosomal disorders - (Trisomy-21, Turner’s syndrome) • Metabolic disorders - (Galactosemia, PKU, cretinism mucopolysaccharidosis).
  • 113. Classification of pediatric cataract Acquired/Juvenile Cataract Cataract that occurs after the first year of life Manifestations: • Visible clouding of lens • Varying impairment of vision
  • 114. Classification of pediatric cataract Acquired/Juvenile Cataract Causes: • Eye trauma (contusion, foreign body and penetrating injury) • Child abuse • Steroid induced • Radiation, drug effects (tetracyclines, chlorpromazine) • Hypo - and hypervitaminosis ‘D’ • Juvenile onset diabetes mellitus • Hypoglycemia • Hypocalcemia
  • 115. Types of pediatric cataracts A lamellar cataract is the opacification of a lamella (an ovoid layer of cortex) which causes cloudiness between the nuclear and cortical layers of the lens Lamellar cataract
  • 116. Types of pediatric cataracts Nuclear cataract A nuclear cataract is cloudiness of the center part of the lens. They can be dot- like or can be quite dense. They generally measure 2-3.5 mm and can be associated with microphthalmia.
  • 117. Types of pediatric cataracts Posterior sub capsular cataract A posterior sub capsular cataract is a thin layer of cloudiness that affects the back surface of the lens cortex, just inside the capsule. This type of cataract can often be associated with medication use such as steroids
  • 118. Types of pediatric cataracts Anterior polar cataract is a small, usually central opacity of the front part of the lens capsule. Anterior polar cataracts generally do not grow during childhood and are typically not visually significant. They are often managed without surgery Anterior polar cataract
  • 119. Types of pediatric cataracts A posterior polar cataract is a central opacity at the back of the lens. In this type of cataract, the opacity is in the capsule itself. Posterior polar cataract
  • 120. Types of pediatric cataracts Traumatic cataract A traumatic cataract results from either a blunt or penetrating force that damages the lens. The cataract can form shortly after the trauma or months to years after the injury. In children, traumatic anterior lens capsule rupture quickly results in a hydrated white cataract.
  • 121. Signs and symptoms A pupil that looks white when a flashlight is shone into it Eyes that aren’t in the right position (misaligned) Rhythmic eye movements that can't be controlled (called nystagmus). Cloudy or blurry vision Trouble seeing Lights that look too bright or have a glare Seeing a circle of light around an object (halo)
  • 122. Diagnosis Red reflex test in newborn screening: If no red reflex, or a weak one, is seen, it may mean there's cloudiness in the lens. Vision tests for older babies and children: This includes visual acuity tests and pupil dilation
  • 123. Management Surgical removal of a cataract Restoration of focusing power Contact lenses Intraocular lenses Glasses Treat amblyopia by patching the good eye to stimulate vision in affected eye Antibiotic & steroid eye ointments
  • 124. Nursing Management Preoperative Phase  History and physical assessment  Antibiotic eye drops  Dilating eye drops  Anticholinergics : Mydriatics and cycloplegics.
  • 125. Nursing Management Postoperative Phase  Antibiotics and steroid eye ointments  Aseptic eye care with eye patch and eye shield for several days to prevent injury  Sedation for 24 hours to prevent crying  Prevention of vomiting & ↑ IOP
  • 126. Health Promotion Wear sunglasses Avoid unnecessary radiation – Adequate antioxidant vitamins Good nutrition Educate about disease process and treatment options Teach signs and symptoms of infection
  • 128. Definition Glaucoma is a group of heterogenous disease marked by high intraocular pressure (IOP) that damages the optic nerve which can cause a rapid loss of vision or even blindness.
  • 129. Childhood glaucoma is defined by 2 of the following features: 1.Intraocular pressure (IOP) greater than 21 mmHg 2.Presence of optic disc cupping 3.Corneal findings of Haab striae (breaks in Descemet's membrane leading to scarring)
  • 130. Childhood glaucoma is defined by 2 of the following features: 4. Corneal edema 5. Increased corneal diameter of greater than 11mm in newborns, greater than 12 mm in children less than 1 year of age, and diameter greater than 13 mm in any age.
  • 131. Definition and Terminology Juvenile glaucoma: Occurs after the age of three to teenage years. Related to age of onset Congenital glaucoma: The glaucoma that exists at birth, and usually before birth Infantile glaucoma: Glaucoma that occurs from birth until 3 years of age
  • 132. Definition and Terminology Related to development pattern Developmental glaucoma: This term broadly encompasses all glaucomas resulting from abnormal development of the aqueous outflow system. This may or may not be associated with systemic anomaly
  • 133. Definition and Terminology Secondary developmental glaucoma: This refers to glaucoma resulting from damage to aqueous outflow system due to maldevelopment of some other portion of the eye, e.g. eye with dislocated lens Related to development pattern Primary developmental glaucoma: This is the glaucoma resulting from maldevelopment of aqueous outflow system
  • 134. Incidence More common in boys 1 in 10,000 births Childhood glaucoma is relatively rare
  • 135. Causes • Hereditary • Some conditions like - Axenfeld- Reiger Syndrome, Aniridia, Sturge -Weber Syndrome, Neurofibromatosis • Chronic steroid use • Trauma • Previous eye surgery such as childhood cataract removal
  • 136. Pathophysiology Etiological factors Disturbance in production and circulation of aqueous humour Build-up of fluid (aqueous humour) ↑ IOP Damage of the retinal layer as it passes through the optic nerve head Cell injury & cell death Optic nerve destruction Blindness
  • 137. Types of glaucoma Glaucoma with angle- closure Open-Angle glaucoma
  • 138. Types of glaucoma Most prevalent type of glaucoma is open-angle glaucoma. The trabecular meshwork is partially blocked, but the drainage angle formed by the cornea and iris remains open. Open-angle glaucoma
  • 139. Types of glaucoma As a result, the pressure in the eye increases. The optic nerve is damaged by this pressure. It happens so slowly that one can lose vision before understanding anything is wrong.
  • 140. Types of glaucoma When the iris bulges forward, it narrows or blocks the drainage angle produced by the cornea and iris, causing angle-closure glaucoma. Fluid cannot circulate through the eye and pressure rises. Angle-closure glaucoma
  • 141. Types of glaucoma People with small drainage angles are more likely to develop angle-closure glaucoma. Angle-closure glaucoma can develop quickly (acute angle- closure glaucoma) or gradually (progressive angle-closure glaucoma/chronic angle-closure glaucoma).
  • 142. Classification of Childhood glaucoma Primary glaucoma Childhood glaucoma Juvenile open-angle glaucoma Congenital/ infantile glaucoma Secondary glaucoma Associated c ̅ non-acquired ocular anomalies Associated c ̅ non-acquired systemic disease Associated with an acquired condition After congenital cataract surgery
  • 143. Signs and Symptoms of childhood glaucoma
  • 144. Symptoms Signs • Photophobia • Buphthalmos (visible enlargement of the eyeball detected at birth) • Epiphora (excessive tearing/watering of eyes) • Corneal enlargement • Blepharospasm (blinking or other eyelid movements, like twitching, that one can't control) • Corneal edema • Red eye • Breaks in Descemet’s membrane (Haab striae) • Irritability • Iris and pupillary abnormalities • Cloudy cornea • Elevated intraocular pressure • Enlarged cornea/eye • Visual impairment • Poor vision • Myopia or astigmatism • Asymptomatic • Optic nerve cupping
  • 145. Treatment Aim of treatment The aim of pediatric glaucoma surgery is to reduce IOP either by increasing the outflow of fluid from the eye or decrease the production of fluid within the eye. Surgical treatments Laser Therapy Medical treatments Goniotomy Trabeculotomy Trabeculectomy
  • 146.
  • 147. Medical Therapy • The treatment for glaucoma in older children is generally medical, i.e. eye drops initially and if these fail, surgery is considered. • Anti-inflammatory and antibiotic drops are used postoperatively • When trabeculectomy is performed in children an antimetabolite such as 5-fluorouracil (5-FU for short) is very often used
  • 148. Nursing Care Assessment  Signs & symptoms like photophobia, tearing, pain and bump into objects  Send the patient to assess visual acuity, visual fields, IOP.
  • 149. Nursing Care  Teach patient and family risks of glaucoma.  Stress on the importance of early detection, ophthalmologic examination.  Administer medication to lower IOP.  Pre and post-operative teaching of the patient and family are to be given.  Support for parents.  Educate parents on use of eye medications to alleviate pain from disease and surgery.
  • 151. A refractive error occurs when the eye does not focus light correctly and it causes blurry vision. The presence of any of the refractive disorders is known as ametropia REFRACTIVE DISORDERS Myopia (near-sightedness) Hyperopia (far-sightedness) Astigmatism
  • 152. Prevalence and Incidence  Myopia is most common refractive in the pediatric population  WHO estimates refractive disorders to be 2-10% worldwide.  The prevalence is higher in the Far East.  The prevalence of astigmatism of 1 diopter or more is 50% in infancy.  The prevalence decreases rapidly during the process of emmetropization.  Only few children develop astigmatism greater than 1 diopter by 6 years of age
  • 153. MYOPIA (NEARSIGHTEDNESS) Myopia is an eye condition in which near objects are seen clearly, but faraway objects appear fuzzy or blurry.
  • 154.  In myopia, eye focuses incorrectly because its shape is slightly abnormal.  A nearsighted eyeball has a long antero posterior diameter.  The myopic child has excessive refractive power.  In myopia, eye focuses light entering the eye in front of the retina instead of onto the retina.  According to the National Eye Institute (NEI), myopia is usually diagnosed between the ages of 8 and 12 years when eyes are growing at this age, so the shape of the eyes can change.
  • 155. Signs and symptoms Blurry vision when looking at faraway objects Headaches Eyes that hurt or feel tired Squinting
  • 156. Treatment Corrective biconcave lenses - Eyeglasses and contact lenses. Refractive laser surgeries
  • 157. HYPEROPIA (HYPERMETROPIA/FARSIGHTEDNESS) Myopia is an eye condition in which far objects are seen clearly, but near objects appear fuzzy or blurry.
  • 158. • A hyperopic eye is shorter than normal and it is caused by insufficient refractory power. • Light from close objects cannot focus clearly on the retina. If cornea is too flat, eye cannot focus correctly. • About 75% of all neonates are hyperopic; but as they have a greater accommodative ability, they overcome the error and see objects at a nearer range. • In hyperopia, eyes have to work hard to see anything up close and causes eyestrain.
  • 159. Symptoms Headache after reading or other tasks that require focusing on something up close. Tension Fatigue Blurry vision up close Squinting to see better Aching or burning sensation around eyes
  • 160. Treatment Corrective biconvex lenses - Eyeglasses and contact lenses. Refractive laser surgeries
  • 161. ASTIGMATISM When the focusing point is disrupted due to variations in the curvature of the cornea or lens at different meridians, the error is called astigmatism
  • 162. • Astigmatism is caused by an irregularly shaped cornea, which causes light to refract or bend incorrectly within the eye. • With astigmatism, light rays do not refract (or bend) properly as they enter the front of the eye. Vision is blurry at near and far because light rays either fall short of the retina or behind it. This results due to the irregularity in curvature of the cornea which results in different refractive power in some parts of the cornea in comparison to other parts. • It is possible to have astigmatism in combination with myopia or hyperopia.
  • 163. Symptoms 6 Squinting or holding reading matter close Eye discomfort Blurry vision or areas of distorted vision Eyestrain and fatigue Headaches Eye rubbing to see clearly
  • 164. Treatment Cylindrical or spherocylindrical glasses and lenses Corrective refractive laser surgeries
  • 165. ANISOMETROPIA Anisometropia refers to a difference in the refractive status of the two eyes  It is the most important risk factor of amblyopia and must be treated with caution
  • 166. Types Mixed anisometropia – one eye is myopic and the other eye is hypermetropic ,it is also called antimetropia Simple anisometropia – one eye normal and other eye myopic and hypermetropia Compound anisometropia – both eye are either hypermetropic or myopic ,but one is having higher refractive power
  • 167. Types Simple astigmatism anisometropia – one eye is normal and other has either simple myopic or hypermetropic astigmatism Mixed astigmatism anisometropia – One eyes has hypermetropic astigmatism and the other eye has myopic astigmatism Compound astigmatism anisometropia – when both eyes has astigmatic but if unequal degree
  • 169. Treatment  Glasses  Contact lenses  Anisometropic spectacle  Other modalities of treatment − Phakic refractive lenses − Refractive lens exchange
  • 170. PRESBYOPIA Presbyopia is a result of changes to the eye lens, the lens hardens or thickens and becomes less flexible, making it unable to change its shape and focus on images Depending on the severity of the changes to the lens, both short and long-distance vision may be affected
  • 171. Symptoms Excess strain in the eyes post reading a book Throbbing headaches after attempting to view objects nearby Feeling tired and exhausted after working with things in close focus Requiring much brighter light to view things that are nearby Inability to read the small print Blurred vision Frequent squinting of eyes while trying to focus on close objects
  • 173. NURSING CARE OF A CHILD WITH REFRACTIVE ERRORS Assessment  History and observation, examination, investigation and diagnostic procedure in eye.  A child tilts his head, rubs eyes, squint, and walks into objects; he or she holds things close to face.
  • 174. NURSING CARE OF A CHILD WITH REFRACTIVE ERRORS Nursing Diagnosis • Alteration in visual perception of patient, as a result of refractive error. • Knowledge deficit, about treatment of refractive error. • Altered comfort as a result of refractive error manifested by asthenopia.
  • 175. NURSING CARE OF A CHILD WITH REFRACTIVE ERRORS Intervention • Refer for vision testing. • Use corrective lenses when caring for child. • As preventive measure educate parents to be aware of signs and symptoms and their meaning. • Encourage vision testing at early stage
  • 177. The deviation of visual axis from normal alignment is known as strabismus. The visual line of each eye does not simultaneously focus on the same object due to lack of muscle coordination resulting in a crossed–eye appearance. Definition
  • 178. Incidence Strabismus occurs in 2–3% of all children. Approximately half of these children have a family history for the defect. Transient strabismus is normal in first 4–6 months of life and is attributed to physiologic hypermetropia.
  • 180. Types Paralytic or non-concomitant • Occurs due to weakness or paralysis of one or more extra ocular muscles. • There is limitation in movement of eye and diplopia occurs Non-paralytic or concomitant • The movements of individual ocular muscles are present, but coordination is lacking. • Diplopia does not occur in this type
  • 181. Types
  • 184. Surgical Management Involves shortening, lengthening or repositioning of extra ocular muscles
  • 185. Nursing Management  Minimizing effects of vision loss  Minimize body image disturbance  Prevent injury.  Promote normal growth and development
  • 186.
  • 187. Definition Amblyopia is the medical term used when the vision in one of the eyes is reduced because the eye and the brain are not working together properly. The eye itself looks normal, but it is not being used normally because the brain is favoring the other eye. It is unrelated to an organic cause. The condition is sometimes called ‘lazy eye’.
  • 188. Incidence Amblyopia occurs in approximately 2–3% of the population in preschool age
  • 189. Etiology Organic causes-retinal or the optic nerve pathology Strabismus Anisometropia Combined Strabismus & Anisometropia Ametropia Visual/Sensory deprivation
  • 190. Risk factors Premature birth Small eye size at birth Family history of lazy eye Family history of Refractive Errors Developmental disabilities
  • 192. Clinical Features Diagnostic Evaluation Infants and children with Amblyopia often do not display any symptoms. They may occasionally over reach for an object. Visual acquity test Amblyopia is usually asymptomatic because the good eye assumes the burden of vision and the child is unaware that there is a problem. The child’s eyes are examined periodically before the age of 7 years.
  • 196. Definition  Retinoblastoma is a malignant glioma of the retina.  It may be unilateral (70%) or bilateral (30%).  It is a highly malignant tumour arising from the nuclear layer of the retina.
  • 197. Incidence and Prevalence Predisposing Factors  About 90 percent cases are found in less than 5 years of age.  It is rare tumor, though the most common ocular neoplasm of childhood.  Usually congenital in origin but commonly manifests itself between 2 to 5 years.  Hereditary and familial tendency
  • 198. Etiology  The disease has a genetic predisposition in majority of the cases.  The retinoblastoma gene is located on chromosome 13.  The gene carries risk of osteosarcoma and a secondary malignancy like a pineal tumor, the so called “trilateral retinoblastoma”.  It usually develops in the posterior portion of retina. About 25 per cent cases are bilateral.
  • 199. Forms of Retinoblastoma Non-inheritable Not passed down from parents. This type of retinoblastoma is caused by mutations in the RB1 gene that occur by chance after a child is born. Usually unilateral Heritable The mutation in the RB1 gene passed from the parent to the child, or it may occur in the egg or sperm before conception or soon after conception. Usually bilateral In retinoblastoma there is a mutation in the RB1 gene
  • 201. Extension of the Tumour When it grows towards the choroids, it is known as Glioma Exophytum. When it grows towards the vitreous humour, it is Glioma Endophytum.
  • 202. Extension of the Tumour Quiescent Stage Stage of Glaucoma Stage of Extra-ocular Extension Stage of Metastasis
  • 203.
  • 205. Diagnosis Confirmed by fundoscopy to detect leukocoria CT scan to determine the extent of tumor X-ray to detect bone involvement CSF study, bone marrow study to identify the metastasis
  • 206. Management Enucleation may be done in unilateral cases Radiotherapy Chemotherapy Scleral plaque irradiation Cryotherapy or photocoagulation
  • 207.
  • 212. ANATOMY AND PHYSIOLOGY OF NOSE Frontal Sinus Middle Turbinate Superior Turbinate Sphenoid Sinus Pharyngeal tonsil Auditory tube opening Inferior turbinate Vestibule
  • 214. THROAT ANATOMY AND PHYSIOLOGY • Soft palate and vallecula form a tongue and groove and separates the oral cavity from the nasal cavity during the first 6 months of infancy when most children are primarily nasal breathers. • Anterior placement of the larynx
  • 215. THROAT ANATOMY AND PHYSIOLOGY • Shared passage for eating and breathing. • The tongue occupies less of the oral cavity. • The larynx sits lower in the neck,
  • 217. EXTERNAL OTITIS OR OTITIS EXTERNA External otitis, or otitis externa, refers to an inflammation of the external auditory canal. It is a painful condition caused when irritating or infective agents come into contact with the skin of the external ear.
  • 218. Causes/Etiology • Blockage of the canal • Absence of cerumen due to excess cleaning • Trauma • Alteration of pH within the canal Bacterial infection Fungal infection Pseudomonas Aeruginosa Staph Aureus Aspergillus
  • 219. Risk Factors  Hot and humid climates  Swimming  Diabetes Mellitus  Narrowing/obstruction of the auditory canal  Over-cleaning leading to a lack of wax in the canal  Wax build-up  Eczema  Trauma
  • 220. Classification Acute Otitis Externa: • Lasts less than 6 weeks • Typically due to bacterial infection Chronic Otitis Externa: • Lasts more than 3 months • Due to Allergies or autoimmune diseases
  • 221. Pathophysiology Allergy, injury to external auditory canal (EAC), Trapped water, foreign bodies, narrow canal, humid conditions Retention of moisture Multiplication and inhabitation by bacteria or fungi Activation of inflammatory mediators and enzymes Chemotaxis Edema & pain Ear discharge
  • 222. Clinical Manifestation o Pain and discharge from the EAC o Aural tenderness o Occasional fever o Cellulitis o Lymphadenopathy o Pruritus o Hearing loss o Feeling of fullness in the ear On otoscopic examination: o Erythematous and edematous ear canal o Yellow or green, foul- smelling discharge. o Fungal infections – visible hair like black spores
  • 223. Diagnostic Evaluation Complete medical history and physical examination. Otoscopic examination Culture of the drainage
  • 224. Medical Management  Antibiotic ear drops or oral antibiotics  Corticosteroid ear drops (to help decrease the swelling)  Pain medication  Keeping the ear dry, as directed.  Placing a wick in the ear (a piece of sponge may be placed in the child's ear if there is a lot of swelling. This wick helps the antibiotic drops work more effectively in the ear canal).
  • 225. Nursing Management  Avoid events that traumatize the external canal such as scratching the canal with the fingernail or other objects.  A cotton ball can be covered in a water insoluble gel such as petroleum jelly and placed in the ear as a barrier to water contamination.  Infection can be prevented by using antiseptic otic preparations after swimming (eg, Swim Ear, Ear Dry). EDUCATE
  • 227. Clinical Manifestation Sensation of fullness in the ear, with or without hearing loss Ear pain Itching Dizziness Bleeding from the ear
  • 228. Management  If the occluding material is cerumen, management options include watchful waiting, manual removal, and the use of ceruminolytic agents followed by either manual irrigation or the use of a low-pressure, electronic, oral irrigation device.  The canal can be irrigated with a mixture of water and hydrogen peroxide at body temperature.  Insects are killed before removal unless they can be coaxed out by a flashlight or a humming noise.
  • 229. Management  Lidocaine, a numbing agent, can be placed in the ear canal for pain relief.  Mineral oil or diluted alcohol instilled into the ear can suffocate the insect, which is then removed with ear forceps.  If the patient has local irritation, an antibiotic or steroid ointment may be applied to prevent infection and reduce local irritation.
  • 231. ACUTE AND CHRONIC OTITIS MEDIA  Chronic otitis media (COM): If an attack of acute otitis media fails to heal, the perforation and discharge may in some cases persist. This leads to mixed infection and further damage to the middle-ear structures, with worsening conductive deafness  Acute otitis media (AOM) is an acute infection of the middle ear, usually lasting less than 6 weeks
  • 233. Risk factors  Crowed living conditions  Exposure to second hand smoke  Respiratory illness  Close contact with siblings those who have cold.  Having Cleft Palate ( Abnormal Position of muscles and tendons )  Premature birth
  • 235. Clinical Manifestation of Otitis Media
  • 236. Diagnosis History, Physical Examination Otoscopy Tympanometry Tympanocentesis Blood test Hearing Test Whisper Test, Weber Test Rinne test
  • 237. Complications Tympanic membrane Perforation Mastoiditis Facial Nerve Palsy Acute Labyrinthitis Petrositis
  • 239. CHRONIC SUPPURATIVE OTITIS MEDIA (CSOM) Chronic suppurative otitis media is defined as chronic inflammation of the middle ear and mastoid cavity characterized by 1) Perforation of the tympanic membrane due to acute infection or tympanotomy tube. 2) Recurrent discharge from the middle ear (otorrhea). 3) Prolonged duration (>2 weeks).
  • 240. FIG: Chronic Otitis Media with suppuration
  • 241. Prevalence Peaks around 2 years of age. The infection is most commonly acquired in children aged up to 6 years
  • 242. Classification Tubotympanic/safe type: Atticoantral/unsafe type:  Associated with tympanic membrane perforation and recurrent / persistent ear discharge.  Episodes of URTI and entry of water into the middle ear are precipitates  Associated with presence of cholesteatoma or granulations  May cause life- threatening complications (brain abscess, meningitis, hydrocephalus etc.
  • 243. Management • Oral antibiotics • Local antibiotic ear drops Medical management: • Myringotomy • Myringoplasty • Tympanoplasty • Mastoidectomy • Stapedectomy Surgical management:
  • 244. Prevention Preventive measures for CSOM are described as HEAR  H- Hygiene of the ear  E- Early management of acute otitis media  A - Antiobiotics  R - Raising awareness
  • 245. TYMPANIC MEMBRANE PERFORATION A ruptured eardrum is a tear in the thin membrane that separates outer ear from inner ear and when there is abnormal opening or Perforation in tympanic membrane
  • 246. Causes Ear Infection Insertion of objects purposefully Concussion Head Trauma Barotrauma
  • 247. Signs and Symptoms  Not able to recognize at first  Some may feel Air coming out of their ear when they blow nose.  Sudden sharp pain  Drainage from ear (Bloody, Clear, Pus)  Ear Noise or buzzing  Hearing loss (Partial or Complete)  Facial Weakness or dizziness
  • 249. Management • Keep Ear Dry • Oral or Topical Antibiotics • Surgical Myringoplasty Tympanoplasty
  • 250. OTOSCLEROSIS Otosclerosis is abnormal hardening and overgrowth of the stapes
  • 251. Clinical Manifestation  It may involve one or both ears and manifests as a progressive conductive or mixed hearing loss.  Bone conduction is better than air conduction on Rinne testing.  The audiogram confirms conductive hearing loss or mixed loss, especially in the low frequencies.
  • 253. MASTOIDITIS Mastoiditis is a bacterial infection of the mastoid air cells surrounding the inner and middle ear. The mastoid bone, which is full of these air cells, is part of the temporal bone of the skull.
  • 254. Causes  Middle ear infection.  Cholesteatoma (a growing collection of skin cells) which blocks ear drainage
  • 255. Clinical Manifestation Fever, irritability, and lethargy Swelling of the ear lobe Redness and tenderness behind the ear Drainage from the ear Bulging and drooping of the ear
  • 256. Medical Management • Antibiotic and steroid eardrop for infection and inflammation, e.g. Ciplox-D • Ear-irrigation: For removing purulent discharge • Analgesics drugs: Aspirin, Nimesulide.
  • 257. Surgical Management Mastoidectomy: It is a surgical procedure that removes diseased mastoid air cells Myringotomy: It is a surgical procedure in which a tiny incision is created in the eardrum relieves pressure caused by excessive build-up of fluid or pus
  • 258. Surgical Management Mastoidectomy: It is a surgical procedure that removes diseased mastoid air cells Myringotomy: It is a surgical procedure in which a tiny incision is created in the eardrum relieves pressure caused by excessive build-up of fluid or pus
  • 259. Tympanoplasty: also called eardrum repair. It is the surgical reconstruction of the perforated eardrum or the small bones of the middle ear. Surgical Management
  • 260. Nursing Management Nursing Diagnosis  High risk for infection related to tissue destruction  Pain related to physical factors  Altered auditory sensory perception related to partial/total perforation of tympanic membrane  Impaired verbal communication related to hearing deficit  High risk for trauma related to impaired balance
  • 261. Nursing Management Interventions: • Assess pain for location, intensity etc • Administer analgesics as prescribed to relieve pain • Administer antibiotics as ordered • Administer antipyretics as prescribed • Provide plenty of fluids • Use cool water sponging to reduce body temperature • Encourage patient and family to use signs of non- verbal communication such facial expression
  • 264. RHINITIS Rhinitis is broadly defined as inflammation of the nasal mucosa.
  • 266. Pathophysiology Allergen, drugs, infections and other causes Production of immunoglobulins (IgE) and inflammatory mediators (histamine, thromboxane, prostaglandins) Nerve cell irritation Loss of mucosal integrity Sneezing, itching, vascular engorgement Rhinorrhea
  • 268. Treatment • Avoidance of allergens. • Non-sedating antihistamine (loratadine, cetirizine, fexofenadine). • Intranasal corticosteroids. • Oral decongestants. • Antibiotics only if infected rhinitis.
  • 269. SINUSITIS Sinusitis is inflammation of frontal, maxillary, ethmoidal and sphenoidal sinuses.
  • 270. Causes
  • 272. Pathophysiology Acute infection Destroys normal ciliated epithelium Impairs drainage from sinus Pooling and stagnation of secretions Decreased mucocilliary clearance Inflammation, edema and exudation Blockage of paranasal sinuses Sinusitis and persistent infection
  • 273. Clinical Features Acute bacterial sinusitis:  Nasal or postnasal discharge (of any quality)  Daytime cough (which may be worse at night)  Headache  Retro-orbital pain  Facial pain  Tenderness, redness and swelling of the cheek and near inner canthus of the eye  Fever at least 102°F (39°C).
  • 274. Clinical Features Chronic bacterial sinusitis:  Persistent or recurrent attack of nasal or postnasal discharge  Low grade fever  Malaise  Sniffing  Nose twitching  Mouth breathing  Epistaxis  Ear discharge
  • 275. Diagnosis  Nasal examination showing mucus or pus  X-ray of paranasal sinus showing air- fluid filled levels and complete opacification  CT scan  Nasal swab culture
  • 276. Management Chronic bacterial sinusitis: Prolonged antibiotic therapy, nasal drops of oxymetazoline HCI, breathing exercise, nose blowing and radical sinus surgery. Acute bacterial sinusitis: Antibiotic therapy with amoxicillin, decongestants, mucolytic agents, nasal drops and avoiding contacts with URI.
  • 278. Causes
  • 281. Non-surgical Management • Fresh blood and clots should be removed with suction. • Topical vasoconstrictors, packing and cauterization will stop the bleeding effectively. Surgical Management • Arterial ligation, submucosal resection (SMR)/septoplasty • Embolization of the internal maxillary artery in case of failed surgery Management
  • 282. Preventive Measures • To avoid nose-picking as much as possible. • During the winter and allergic seasons, do not blow the nose harshly but gently. • When participating in any physical activities that can harm the nose and head, wear a protective helmet for safety measures. • To avoid the consumption of excess alcohol and smoking. • Make use of saline nasal spray or saline nose drops once or twice a day to keep the nose moisturized.
  • 284. PHARYNGITIS Pharyngitis is an inflammation of the mucous membranes and underlying structures of the throat.
  • 285. Etiology of Acute Pharyngitis Rhinovirus Adenovirus Coronavirus Parainfluenza virus Bacterial Viral Group A beta hemolytic Streptococcus Neisseria gonorrhoea Corynebacterium diphtheria.
  • 286. Clinical Features Viral pharyngitis: • Fever • Malaise • Anorexia • Sore throat • Hoarseness of voice • Conjunctivitis • Coryza (inflammation of the mucous membrane in the nose) • Cough • Diarrhea
  • 287. Clinical Features Bacterial pharyngitis • Beefy, red swollen uvula • petechiae on the palate; excoriated nares (especially in infants) and a scarlitiniform (Scarlet fever) rash • Sudden onset of sore throat • Severe pain on swallowing • Fever • Headache • Nausea • Vomiting • Abdominal pain
  • 288. Diagnosis • Streptococcal pharyngitis is treated with oral antimicrobial therapy (penicillin, erythromycin or amoxicillin) for 10-14 days. • Supportive therapy includes antipyretics, analgesics, antitussives, bed rest and saline gargles. • Throat culture. • Rapid antigen detection tests. Treatment
  • 289. TONSILLITIS Tonsillitis refers to inflammation of the pharyngeal tonsils – glands at the back of the throat, usually caused by beta hemolytic streptococcus or viruses
  • 290. Causes Bacteria cause 15-30 percent of pharyngotonsillitis cases The herpes simplex virus Streptococcus pyogenes Epstein-Barr virus (EBV) Cytomegalovirus (CMV) Adenovirus Group B Strep is the cause for most bacterial tonsillitis – strep throat
  • 292. Treatment Chronic tonsillitis:  Tonsillectomy is indicated when there is recurrent infections of >7 episodes per year, peritonsillar abscess and severe hypertrophy of tonsils. Acute tonsillitis:  Saline gargles  Analgesics  Antibiotics
  • 294. ADENOIDS Adenoids or nasopharyngeal are lymphoid tissues at the junction of the roof and posterior wall of nasopharynx.
  • 295. Clinical Features Acute adenoiditis:  Purulent rhinorrhea  Nasal obstruction  Mouth breathing  Epistaxis  Fever  Associated Otitis Media  Nasal change in voice. Chronic adenoiditis:  Persistent rhinorrhea  Postnasal drip  Malodorous breath  Associated otitis media >3 months  Open mouth  Drooling and mal-occluded teeth (adenoid faces)  Pulmonary hypertension.
  • 296. Treatment Surgical: Adenoidectomy if recurrent rhinosinusitis or severe adenoid hypertrophy occurs. Conservative treatment: includes nasal decongestants, antihistaminic and antibiotic therapy.
  • 298. Nursing diagnosis 1. Ineffective airway clearance related to postoperative secretions Pain related operative procedure. 2. Risk for deficient fluid volume related to bleeding. 3. Deficient knowledge related to home care.
  • 299. Nursing Intervention • Monitoring oxygen saturation especially when they sleep. Observing bleeding for initial 6 hours which is crucial for primary bleeding. • Prevention of bleeding from site of operation. • Maintain IV access until discharge. • Position the child in comfortable or prone position turning the head to one side to allow the drainage of secretions.
  • 300. Nursing Intervention • Measure and record intake and output hourly. Assess skin turgor and moisture of mucous membranes. • Adequate rest and sleep. • Soft non irritating diets and plenty of fluids. • Avoid contacts with infected persons. • Avoid use of straw to prevent injury to the site. Practice nose breathing. • Discourage excessive coughing and clearing the throat.
  • 302. CONCLUSION Eye and ENT disorders in children are very common though most are not life threatening. But the anatomical structures involved are important and most may make the child physically challenged if left untreated. So it is the duty of the community, parents and health care workers to actively be involved in the care of children with these disorders