Ear Anatomy and Hearing Disorders Guide
Ear Anatomy and Hearing Disorders Guide
Y
Uthuman
1
2
EAR, NOSE AND THROAT DISORDERS
Definition of Terms as used in Ear Anatomy
Acoustic
This is pertaining to sound or the sense of hearing
Cerumen
This is a yellow or brown, wax like secretion found in the
external auditory canal
Cochlea
3
This is the winding, snail-shaped bony tube that forms a portion
of the inner ear and contains the organ of Corti which is the
transducer for hearing
Cochlear (acoustic) nerve
This is the division of the eighth cranial (vestibulocochlear)
nerve which goes to the cochlea
Eustachian tube
This is a 3cm to 4cm tube that extends from the middle ear to
the nasopharynx
External auditory canal
This is the canal leading from the external auditory meatus to
the tympanic membrane and its about 2.5 cm in length
External ear
This is the portion of the ear that consists of the auricle and
external auditory canal
It is separated from the middle ear by the tympanic membrane
Incus
This is the second ear bone of the three ossicles in the middle
ear
It articulates with the malleus, stapes and the anvil
4
Inner ear
This is the portion of the ear that consists of the cochlea,
vestibule, and semicircular canals
Internal auditory canal
This is a canal in the petrous portion of the temporal bone which
houses the facial and vestibulocochlear nerves (cranial nerves
VII and VIII)
Malleus
This is the first bone (most lateral) and largest of the three
ossicles in the middle ear
It is connected to the tympanic membrane laterally and
articulates with the incus and the hammer
Middle ear
This is the small, air-filled cavity in the temporal bone that
contains the three ossicles
Organ of Corti
This is the end organ of hearing located in the cochlea
Ossicles
These are the three small bones within the middle ear ie malleus,
incus, and stapes
5
Oval window
This is a fenestra (aperture) between the vestibule of the inner
ear and the middle ear which is occupied by the base of the
stapes
Pinna
This is the outer part of the external ear which collects and
directs sound waves into the external auditory canal and the
auricle
Round window
This is a fenestra(aperture) between the middle ear and the inner
ear at the base of the cochlea which is occupied by the round
window membrane
Semicircular canals
This is the superior, posterior, and lateral bony tubes that form
part of the inner ear which contain the receptor organs for
balance
Stapes
This is the third (most medial) ossicle of the middle ear which
articulates with the incus, the stirrup and its footplate fits into
the oval window
6
Temporal bone
This is a bone on both sides of the skull at its base composed of
the squamous, mastoid, and petrous portions
Tympanic membrane
This is the membrane that separates the middle ear from the
external auditory canal and is also referred to as the eardrum
Vestibulocochlear nerve
This is a cranial nerve VIII containing the cochlear (acoustic)
nerve and vestibular nerve
7
When evaluating hearing, three characteristics are very
important ie frequency, pitch, and intensity.
Frequency is the number of sound waves emanating/
orignating from a source per second and is measured as
cycles per second, or Hertz (Hz). Its ranges from 20 to 20,000
Hz
Pitch is the term used to describe frequency ie a tone with
100 Hz is considered of low pitch and a tone of 10,000 Hz is
considered of high pitch.
The unit for measuring loudness (ie, intensity of sound) is the
decibel (dB) which is the pressure exerted by sound.
Hearing loss is measured in decibels, a logarithmic function
of intensity that is not easily converted into a percentage.
Tympanogram or impedance audiometry
This measures middle ear muscle reflex to sound stimulation
and compliance of the tympanic membrane by changing the
air pressure in a sealed ear canal. Compliance is impaired
with middle ear disease
Electronystagmography
8
This is the measurement and graphic recording of the
changes in electrical potentials created by eye movements
during spontaneous, positional, or calorically evoked
nystagmus
It is also used to assess the oculomotor and vestibular
systems and their corresponding interaction.
It helps in diagnosing conditions such as Ménières disease
and tumors of the internal auditory canal or posterior fossa
Platform posturography
This is used to investigate postural control capabilities.
Sinusoidal harmonic acceleration or a rotary chair
This is used to assess the vestibulo-ocular system by
analyzing compensatory eye movements in response to the
clockwise and counterclockwise rotation of the chair
Middle ear endoscopy
This is performed to evaluate suspected perilymphatic fistula
and new-onset conductive hearing loss, the anatomy of the
round window before transtympanic treatment of Ménières
9
disease, and the tympanic cavity before ear surgery to treat
chronic middle ear and mastoid infections
HEARING IMPAIRMENT (HEARING LOSS)
Hearing impairment and dizziness are major symptoms of
inner ear problem that can hinder communication with
others, limit social activities, and negatively impact
employment.
Hearing loss diminishes the individual aesthetic enjoyment of
major aspects of daily living and can adversely affect quality
of life
Etiology
Hearing loss is a symptom rather than a specific disease or
disorder and can be as a result of mechanical, sensory or neural
problems due to;
Trauma to the ear and head
Infections or diseases of the ear
Tumours to the ear and CNS
Advancing age (52 years)
Presence of wax in the ear
Foreign bodies in the ear
10
Ear retraction
Scarring or perforation of the tymphanic membrane
Occupation eg carpentry, plumbing and coal mining
CVA
Risk Factors for Hearing Loss
Family history of sensorineural impairment
Congenital malformations of the cranial structure (ear)
Low birth weight (<1500 g)
Use of ototoxic medications (eg, gentamicin, loop diuretics)
Recurrent ear infections eg otitis media
Bacterial meningitis
Chronic exposure to loud noises
Perforation of the tympanic membrane
Types of healing loss
Conducting Hearing Loss: Loss of the hearing from mechanical
problem
Sensorineural Hearing Loss: Loss of hearing involving the
cochlea and auditory nerve; bone and air conduction equal but
diminished.
11
Neural Hearing Loss: A sensorineural hearing loss
originating in the nerve or brainstem.
Fluctuating Hearing Loss: A sensorineural hearing loss that
varies with time.
Sensory Hearing Loss: A sensory neural hearing loss
originating in the cochlea involving the hair cells and nerve
endings.
Sudden Hearing Loss: A sensorineural hearing loss with a
sudden onset.
Central Hearing Loss: Loss of hearing from damage to the
brain auditory pathways or auditory
center.
Functional Hearing Loss: Loss of hearing for which no
organic lesion can be found.
Mixed Hearing Loss: Elements of both conduction and
sensorineural hearing loss.
Pathophysiology
Conductive Hearing Loss results from any interference with
the conduction of sound impulses through the external
auditory canal, the eardrum, or the middle ear.
12
Conductive hearing loss may be caused by anything that
blocks the external ear, such as wax, infection or a foreign
body, a chickening, retraction, scarring or perforation of the
tymphanic membrane; or any pathophysiological changes in
the middle ear affecting or fixing one or more of the ossicles.
Sensorineural Hearing Loss results from disease or trauma to
the inner ear, neural structure, or nerve pathways leading to
the brainstem.
Some of the causes of nerve deafness are infectious
diseases, (measles, mumps and meningitis), arteriosclerosis,
ototoxic drugs, neur of cranial nerve VIII, otospongiosis (form
of progressive deafness) caused by the formation of new
abnormal sponge bone in labyrinth, trauma to the head or
ear, or degeneration of the organ of corti occuring most
commonly from an advancing age (Presbycusis).
Central deafness is also known as central auditory
dysfunction, results from the inability of the CNS to interpret
normal auditory stimuli and may be due to tumour or CVA.
Clinical Manifestations
13
Early manifestations of hearing impairment and loss may
include
Tinnitus
Increasing inability to hear in groups and a need to turn up
the volume of the television
Withdrawal , suspicion, loss of self-esteem and insecurity
following advanced hearing loss
Hearing impairment can also trigger changes in attitude, the
ability to communicate, the awareness of surroundings, and
even the ability to protect oneself, affecting the persons
quality of life.
In a classroom, a student with impaired hearing may be
disinterested and inattentive and have failing grades.
Isolation while at home and may miss part of the
conversations
15
vegetable foreign bodies such as beans, maize and peas
which swell with water
Animate foreign bodies eg insects such as flies, cockroaches,
ants, fleas etc
Clinical features
Blockage of the ear and the FB may be seen
Noise in the ear if the FB is a live for example insects
Discomfort and irritation within the ear
Hearing loss when the FB occludes the external canal
Pain in the ear if the FB stays for so long in the ear
Bleeding or discharge from the ear following attempts to
remove the FB
Management
Syringe the ear with clean lukewarm water to remove the FB
if its smooth and round
If FB cannot be removed by syringing, remove the FB with a
foreign body hook under general anaesthesia for children
and sensitive adults
• Do NOT use forceps to try to grasp round objects, as this
will only push the FB further in the ear
16
If there is an edge to grab the FB, remove it with Hartmann
(crocodile) forceps
If the FB is an insect, kill it by inserting clean cooking oil or
water into the ear and then syringe it out with lukewarm
water
If the FB is a cockroach remove it using a crocodile forceps
since they have hooks on their legs that makes removal by
syringing impossible
If the FB is an impacted seed do not syringe the ear with
water as the seed may swell and block the ear but refer
immediately to ENT specialist if you cannot remove it with a
hook
Suction of the ear may also be useful for certain FBs
Complications of FBs
Hearing loss due to damage of the ear drum
Otitis media or Otitis external
17
Injury to the ear canal, ear drum and or ossicles
IMPACTED CERUMEN
This is the accumulation of wax in the external ear
Wax in the ear is normal and usually comes out naturally from
time to time.
It may accumulate to form a wax plug and cause a problem for
the patient.
Causes
Excessive and thick wax production
Small, tortuous and hairy ear canal
Use of ear pads
Clinical features
Blockage of the ears
Buzzing sound in the ears
Sometimes there is mild ear pain
Hearing loss due to blockage of the canal
Tinnitus
Vertigo
Cough
Management
18
General treatment measures
Soften the wax by inserting drops of Vegetable oil or
Glycerine or Sodium bicarbonate into the ear 3 times a day
for a few days to allow the wax fall out of the ear on its own
Syringe the ear carefully with clean Luke warm water after
insertion of cooking oil or sodium bicarbonate to soften the
wax
Cautions
Advise the patient not to poke anything into the ear in an
attempt to clean it as this may damage the eardrums eg
sticks
Do not syringe the ear if (a) there is history of ear discharge
and (b) if there is pain
OTITIS EXTERNA
This is the infection of the external ear canal which may
either be localized (furunculosis) or generalised (diffuse).
Causes
These include;
19
Bacterial infections eg staphylococci aureus and
pseudomonas spps
Fungal infections eg Aspergillus
Viral infections
Predisposing factors
These include;
Water in the ear canal (swimmers ear)
Trauma to the skin of the ear canal permitting entrance of
organisms into the tissues
Systemic conditions such as vitamin deficiency and endocrine
disorders eg diabetes mellitus
Dermatosis such as psoriasis, eczema, or seborrheic
dermatitis.
Allergic reactions to hair spray, hair dye
Clinical features
Ear pain (otalgia)
Swelling and tenderness on pulling the pinna (external ear)
Itching of the ear (especially for fungal infections)
Discharge from the external auditory canal which may be
yellow or green and foul smelling
20
Aural tenderness (usually not present in middle ear
infections)
Pruritus
Hearing loss or a feeling of fullness
Fever
Cellulitis
On otoscopic examination, the ear canal is erythematous and
edematous
In fungal infections, the hairlike black spores may even be
visible.
Investigations / diagnosis
Good history and physical examination of the external ear
Pus swab for microscopy to identify the status of the
discharge eg if the discharge is white or black it is fungal and
if yellow it is bacterial
Pus swab for culture and sensitivity to indentify the causative
organisms
Management
21
The principles of therapy are aimed at relieving the discomfort,
reducing the swelling of the ear canal, and eradicating the
infection.
The treatment options include;
Thorough cleaning of the external ear canal
Apply antibiotic ear drops, e.g. Chloramphenicol ear drops
0.5% 2 drops into the ear three times daily for 14 days
Apply topical antibiotics on the area or the ear affected eg
Neomycin or chloramphenical cream
Give analgesics to relieve ear pain e.g. NSAIDs such as
paracetamol 1g tds for 3 days
If severe administer intravenous antibiotics eg cloxacillin 500
mg 6 hourly for 5 or 7 days and children 12.5 or 25 mg/kg per
dose.
If fungal ear infection is suspected;
Syringe the ear to remove any crusting
Apply Clotrimazole solution into the ear once a week for 4-8
weeks or
Give capsules fluconazole 200 mg once daily for 10 days
22
MALIGNANT EXTERNAL OTITIS
This is a more serious external ear infection and is sometimes
called temporal bone osteomyelitis although its rare.
Its a progressive, debilitating and fatal infection of the
external auditory canal, the surrounding tissue and the base
of the skull
Its caused by Pseudomonas aeruginosa and mainly occurs in
patients with low resistance to infection eg patients with
diabetes
Clinical features
Severe stabbing otalgia
Purulent ear discharge
Granulation tissue in the floor of the external canal, at the
junction of cartilaginous part with bony part.
Investigations
23
Pus swab for culture and sensitivity to identify the
causative organism
CT scans of the temporal bone to detect and reveals skull
base destruction.
Biopsy for histopathology to exclude malignancy
Management
Successful treatment includes control of the diabetes,
administration of antibiotics (usually intravenously), and
aggressive local wound care by debridement, apply antibiotic
ear drops.
Complications
Osteomyelitis of the skull base and temporal bones
Cranial nerve palsy
OTITIS MEDIA
This is an acute or chronic infection of the middle ear
It occurs mostly in children
Acute otitis media
This is an acute infection of the middle ear, usually lasting less
than 6 weeks.
24
Causes
Bacterial infection e.g. Streptococcus pneumoniae,
Haemophilus influenza etc
The bacteria enter the middle ear after eustachian tube
dysfunction caused by obstruction related to upper
respiratory infections, inflammation of surrounding
structures (eg, sinusitis, adenoid hypertrophy), or allergic
reactions(eg, allergic rhinitis).
Bacteria can also enter the eustachian tube from
contaminated secretions in the nasopharynx and the
middle ear from a tympanic membrane perforation.
Risk factors of acute otitis media
These include
Young age
Congenital abnormalities
Immune deficiencies
Passive smoke inhalation
Eustachian tube damage from viral infections
Family history of otitis media
Recent upper respiratory infections
25
Gender mainly male
Participation in day care
Bottle feeding
Allergic rhinitis.
Clinical features
Symptoms vary with the severity of the infection;
Usually its unilateral in adults
Pain in and about the ear (otalgia), which may be intense
and relieved only after spontaneous perforation of the
eardrum or after myringotomy.
Fever
Drainage from the ear (otorrhea)
Hearing loss
Tympanic membrane is erythematous and often bulging.
Conductive hearing loss due to exudate in the middle ear.
On otoscopic examination, the external auditory canal
appears normal and the patient reports no pain with
movement of the auricle
Differential diagnosis
Foreign body in the ear
26
Otitis externa and media with effusion
Referred ear pain, e.g. from toothache
Investigations
Good history and physical examination of the ear
Pus swab for culture and sensitivity to detect and reveal
the causative micro organism
Management
The outcome of acute otitis media depends on the efficacy of
therapy (ie, the prescribed dose of an oral antibiotic and the
duration of therapy), the virulence of the bacteria, and the
physical status of the patient.
The treatment options include;
Medical treatment in case of acute infection
Give capsules Amoxicillin 500 mg every 8 hours for 5 days
Or erythromycin 500 mg every 6 hours in penicillin allergy
Give analgesics, e.g. Paracetamol to relieve pain
Apply antibiotic ear drops, 2 drops every 6 to 8 hours daily
27
Surgery mainly Myringotomy or Tympanotomy.
(Where an incision is made into the tympanic membrane to
relieve pressure and to drain serous or purulent fluid from the
middle ear)
Complications
Perforation of the tympanic membrane
Chronic otitis media.
Mastoiditis
Meningitis
Brain abscess
CHRONIC OTITIS MEDIA
This is as result of repeated episodes of acute otitis media
causing irreversible tissue pathology / infection and persistent
perforation of the tympanic membrane.
Chronic infections of the middle ear damage the tympanic
membrane, destroy the ossicles, and involve the mastoid.
Clinical features
Pus discharge from the ear (persistent or intermittent foul-
smelling otorrhea)
Healing loss
Pain in the ear in case it has involved the mastoid bone
28
Tenderness, swelling and edema of the post auricular area
Perforation of the tympanic membrane
Cholesteatoma (an in growth of the skin of the external layer
of the eardrum into the middle ear).
Management
Medical treatment
Surgery
Medical Treatment
Systemic antibiotics are NOT recommended because they
are not useful and can create resistance
Aural irrigation using hydrogen peroxide mixed with clean
lukewarm water 2-3 times daily
Drying of the ear by wicking 3 times daily until the ear is
dry
Instillation of the ear antibiotics eg ciprofloxacin ear drops
0.5% or Caf ear drop 2 - 4 drops into the ear each time
after drying or
Application of antibiotic powder in cases of otorrhea
Surgery
Surgical procedures include;
29
Tympanoplasty, to prevent recurrent infection, re -
establishe middle ear function, close the perforation, and
improve hearing.
Ossiculoplasty, to reconstruct the middle ear bones to
restore hearing.
Mastoidectomy, to remove cholesteatoma, gain access to
diseased structures, and create a dry (noninfected) and
healthy ear
Note
Refer if complications occur, e.g., meningitis, mastoid abscess
(behind the ear), infection in adjacent areas, e.g. tonsils, nose
Complications of otitis media
Cranial complications (bony skull):
Mastoiditis
Otitic labyrinthitis
Otitic facial paralysis
Intra-cranial complications (inside the intra cranial cavity):
Extra-dural abscess
Sub-dural empyema
Lateral sinus thrombosis or thrombo-phlebitis
30
Meningitis
Brain abscess (Temporal lobe or Cerebellum)
Otitic hydrocephalus
Extra-cranial complications (in the soft tissues of the head and
neck):
Otitis externa
Retropharyngeal abscess
Prevention
Health education of the public about Otitis media e.g. by
advising patients on recognizing the discharge of otitis media
(believed by some to be milk in the ear)
Early diagnosis and treatment of acute otitis media and
upper respiratory tract infections
31
Treatment of infections in adjacent area, e.g. tonsillitis
MASTOIDITIS
This is the inflammation of the mastoid bone (bone behind the
ear) resulting from an infection of the middle ear (otitis media)
Chronic otitis media may cause chronic Mastoiditis and may
lead to the formation of cholesteatoma (ingrowth of the skin of
the external layer of the eardrum into the middle ear) and if
untreated, osteomyelitis may occur
Causes
Usually is a complication of otitis media
Clinical features
Severe pain felt over the mastoid bone
Tenderness behind the ear (postauricullar tenderness)
Ear pain (otalgia)
The mastoid area may be erythematous and edematous
33
Swelling in post auricular area (pinna is pushed down and
forward)
Discharge from the middle ear (otorrhea)
Fever
Mental confusion is a grave sign of intracranial spread of
infection (Refer to ENT surgeon immediately)
Headache
Investigations / diagnosis
Diagnosis of mastoiditis is mainly by clinical features
Mastoid x-ray to detect and reveal the extent and severity of
the condition on the mastoid bone and r/o cranial
complications
Cranial CT scan to comfirm the diagnosis and r/o cranial
complications
Full blood count (CBC) to r/o leucocytosis
Pus swab for culture and sensitivity to detect and reveal the
causative agent
Management
This may be medical treatment and surgery
34
Medical treatment
Give analgesics to relieve pain eg tablets ibuprofen 400mg
tds for 5 days
Give oral antibiotics if mild eg caps ampiclox 500mg or
flucloxacillin 500mg qid for 7 days
In severe admit the patient and administer intravenous
antibiotics eg iv ceftriaxone 2g once daily and iv
metronidazole 500mg three times daily
Surgery mainly mastoidectomy to drain pus if the abscess has
formed
Complications of mastoiditis
Dizziness or vertigo as it affects the vestibular system which
maintains body balance.
35
Destruction or erosion of the mastoid bone.
Subperiosteal abscess (pus formation in the inner layer of the
bony tissue).
Cranial nerve involvement. Gradenigos syndrome Facial
nerve paralysis, deep facial pain and otitis media.
Meningitis (inflammation of membranes of the brain).
Brain abscess.
Bezold abscess (collection of pus behind the muscle of the
neck)
Moderate to severe hearing loss.
These are harmless growth that does not spread or invade other
tissues that develops in the ear
36
They do not metastasize
They do not recur after removal
If completely excised they rarely endanger life.
Their effects are due to size and site.
They are well differentiated
They have a low mitotic rate
They resemble the tissues of origin
Examples of benign masses / tumors of the ear
These include;
Exostoses
These are small, hard, bilateral bony protrusions found in the
lower posterior bony portion of the ear canal
If large, it leads to occlusion of the canal causing conductive
deafness.
Cholesteatoma
38
Complications of surgery for acoustic neuroma
These include;
• Facial nerve paralysis
• Cerebrospinal fluid leak
• Meningitis
• Cerebral edema
Sebaceous cyst
These are small sac within the ear filled with skin secretions
mainly sebum
Osteomas (bone tumors)
Keloids
This growth of excessive scar tissues with in the ear after an
injury
Clinical features of benign tumors in the ear
Early symptoms include;
Hearing loss
Tinnitus
Dizziness
Unsteadiness
39
Other symptoms develop if the tumor enlarges and
compresses other parts of the brain, the facial and trigeminal
nerves
Diagnosis
Early diagnosis is based on MRI scan and hearing test
Management
The best treatment of these tumors is by surgical removal of
the tumor and after treatment hearing usually returns to
normal.
Repeated injections of corticosteroid such as triamcinolone
or hydrocortisone for Keloids
Malignant tumours of the ear
These are harmful tumors capable of spreading and invading
other tissues far away from the site of origin (to distant areas)
Characteristics of Malignant tumours of the ear
They expand and infiltrate locally
They have no capsule or encapsulation is rare
They metastasize to other organs via blood, lymphatics or
body spaces
They endanger life if untreated.
40
They have varying degrees of differentiation from tissue of
origin,
They have a high mitotic rate.
Examples of malignant tumors of the ear
These include;
Basal cell carcinomas on the pinna
Squamous cell carcinomas in the ear canal.
These are common skin cancer that often develop on the
external ear after repeated and prolonged exposure to the
sun
They may also develop in or spread to the ear canal
If untreated, squamous cell carcinoma may spread through
the temporal bone, causing facial nerve paralysis and
hearing loss.
Ceruminoma
This is cancer of the cells that produce wax in the ear and
develops in the outer third of the ear.
Treatment is by surgical removal of the cancer and the
surrounding tissue
Melanoma
41
This is also a more rapidly spreading form of skin cancer that
can also develop in the skin of the outer ear canal
Clinical features of malignant tumors of the ear
Facial nerve paralysis
Hearing loss
Otalgia (severe ear pain)
Swelling and tenderness of the ear
Dizziness
Headache
Management
Surgery
Radiation therapy
Chemotherapy
42
Usually occurs in children <5 years and mentally retarded
persons/ adults
Common foreign objects which may be put into the nose
include;
• Seeds, e.g. bean, peas, ground nut, maize
• Piece of paper
• Foam rubber (e.g. mattress foam)
• Beads
• Stones
• Buttons
• Metal objects eg ball bearing
Predisposing factors
Curious children
Mental ill patients
Trauma
Clinical features
Usually they are inserted by the child and are mostly found in
the right-hand nasal cavity
Foreign body noticed by a child or parent may be visible or
felt
43
Nasal bleeding if object is sharp
Difficult breathing through the affected nostril
Irritation or pain in the nose
Unilateral foul-smelling discharge from the nose
Investigations
Usually not required (Clinical diagnosis is enough)
Nasal x-ray in case of metallic objects like wires or ball
bearings to r/o other nasal complications
Management
First aid
Blow through the mouth while blocking the unaffected side
of the nose
Grasp firmly and remove the paper or foam rubber with a
fine forceps e.g. Tilleys forceps
Other objects, carefully pass a blunt hook behind the object,
and then gently pull it out
If the object is visible and round encourage the patient to
blow through the nose gently to allow the FB come out
If the above fails refer to an ENT specialist
Prevention
44
Always caution children about placing objects in mouth,
nose, and ears
Complications
Sinusitis
Otitis media
Accidental migration of foreign body in the lower airway
Nasal stone or Rhinolith
46
Signs and symptoms of shock if bleeding is severe such as
hypotension, cold clammy skin, severe pallor
Signs and symptoms of predisposing cause eg hypertension
such as headache, dizziness, blurred vision, drowsiness etc
Investigations
CBC to r/o anaemia and know the patients Hb level
Blood clotting profile and platelet count to detect for blood
clotting time and platelet level
Nasal endoscopy to detect and reveal the bleeding site and
r/o other nasal complications
Nasal CT scan to r/o fractures and other complications
Management
First aid
Sit the patient up (if patient not in shock) and tilt the head
forward to avoid pooling of blood into the posterior pharynx
or aspiration of blood
Instruct patient to pinch the nose between the finger and the
thumb for 15 minutes, breathe through the mouth and spit
out any blood
47
Alternatively, apply a cotton tampon into the nose to try to
stop the bleeding.
Suction to remove excess blood and clots from the field of
inspection.
Application of anesthetics and nasal decongestants
(phenylephrine, one or two sprays) to act as vasoconstrictors
Cauterization of the visible bleeding sites with silver nitrate
or electrocautery/ diathermy
If bleeding continues:
Pack the nose with gauze and tetracycline eye ointment
using a forcep and leave the gauze in place for 24-48 hours
Administer antibiotics eg iv ceftriaxone 2g once daily
Administer analgesics eg Diclofenac 75mg three times daily
Give anti hypertensives if the cause is hypertension
Give Anti malarial if the cause is malaria
In case bleeding still continues refer the patient to the ENT
specialist
Prevention
Avoid picking the nose
Treat/control predisposing conditions
48
NASAL ALLERGY
This is an abnormal reaction of the nasal tissues to certain
allergens which tends to start in childhood
Vasomotor rhinitis starts in the 20s and 30s.21
Causes
Predisposing factors include;
Hereditary: Family history of similar or allied complaints
Infections may alter tissue permeability
Psychological and emotional factors in vasomotor rhinitis
Changes in humidity and temperature
Dust mite, infections
Certain foods
Drugs e.g. acetylsalicylic acid
Alcohol, aerosols, fumes
Clinical features
Often present in school age children
Sometimes preceded or followed by eczema or asthma. (Less
common in persons >50 years old)
Paroxysmal sneezing
49
Profuse watery nasal discharge
Nasal obstruction, variable in intensity and may alternate
from side to side
Postnasal drip (mucus dripping to the back of the nose)
Investigation
Careful history is most important
Large turbinates on examining the nose
Management
Avoid precipitating factors (most important)
Reassure the patient
Give antihistamines, e.g. Chlorphenamine 4 mg every 12
hourly for 21 days, then as required thereafter if it recurs
Apply nasal decongestants, e.g. Pseudoephedrine or
xylometazoline to relieve nasal congestion
Surgery in case of obstruction of the nose
ACUTE SINUSITIS
Inflammation of air sinuses of the skull
Causes
Allergy
50
Foreign body in the nose
Viruses, e.g. rhinovirus, often as a complication of URTI
Dental focal infection
Bacteria, e.g., Streptococcus pneumoniae, Haemophilus
influenzae, Streptococcus pyogenes
Clinical features
Rare in patients <5 years
Pain over the cheek and radiating to frontal region or teeth,
increasing with straining or bending down
Redness of nose, cheeks or eyelids
Tenderness due to pressure over the floor of the frontal
sinus immediately above the inner canthus
Referred pain to the vertex, temple or occiput
Postnasal discharge
A blocked nose/ Nasal blockage
Persistent coughing or pharyngeal irritation
Hyposmia
Fever and malaise
Investigations
51
C&S of the discharge to detect and reveal the causative
micro organism
X -ray of sinuses to detect and reveal the extent and severity
of condition to the skull sinuses and r/o other complications.
Nasal CT scan to comfirm the diagnosis and r/o other nasal
complications
Management
General measures
Steam inhalation to clear the blocked nose
Give analgesics to relieve pain eg NSAIDs
Nasal irrigation with normal saline to remove discharge
Give Antibiotics in case of infection such as Amoxicillin 500
mg 8 hourly for 7-10 days
In case of dental infection, extract the tooth and give
antibiotics such as Amoxicillin 5 00mg Metronidazole 400mg
8 hourly for 7 to 14 days
In case of FB refer immediately to the ENT specialist for
further management
Notes
52
Do NOT use antibiotics except if there are clear features of
bacterial sinusitis, e.g., persistent (> 1 week) purulent nasal
discharge, sinus tenderness, facial or periorbital swelling,
persistent fever
Complications
Chronic sinusitis
Osteomylitis
Orbital cellulitis
Orbital abscess
Meningitis
Brain abscess
Thrombophlebitis of cavernous sinus
Pharyngitis
Tonsillitis
Bronchitis and pneumonia
Otitis media
Septicemia
RHINITIS
Rhinitis refers to inflammation of the mucous membrane
of the nose.
53
It may be acute, chronic or allergic rhinitis.
All forms of rhinitis cause sneezing, nasal discharge with
nasal obstruction and headache
Acute rhinitis
This is an inflammatory condition of the mucous membrane
of the nose and accessory sinuses caused by a filterable virus.
It is spread by airborne droplet sprays emitted by the
infected person while breathing, talking, sneezing or
coughing or by direct hand contact.
Its frequency increases during winter months, when people
stay indoors and overcrowding
Other factors such as chills, fatigue, physical and emotional
stress and patient compromised immune status, may
increase susceptibility
Predisposing factors
Allergy
Environmental pollution by dust, fumes
Overuse of nasal decongestants (Rhinitis medicamentosa)
Hormone imbalances : e.g. during pregnancy, puberty
Clinical features
54
Tickling and irritation within the nose
Sneezing or dryness of the nose or nasopharynx
Copious nasal secretions
Nasal obstruction
Watery eyes
Elevated temperature,
General malaise, and
Headache
Thick and sticky mucus within a few days
Management:
Bed rest
Plenty of warm oral fluids intake
Proper nutrition
Use of home remedies such as steam, honey etc
Use of antipyretics and analgesics such as tablets
paracetamol 1g three times daily
Apply Xylometazoline 0.05% or 0.1% nose drops 2-3 drops
into each nostril 3 times daily
Causes
Its caused by allergens such as pollen of trees, grasses or weeds,
spores of molds, dustmites, and animal danders.
Clinical features
Nasal congestion
Sneezing
Watery itchy eyes and nose,
Altered sense of smell
Thin watery nasal discharge
Headache
56
Cough
Hoarseness or the recurrent need to clear throat
Management
Avoidance of the causative agents mainly allergens such as
smoke, pollens, dust mites, mold spores
Use of antihistamines such as chloropheniramine, cetrizine
or loratidine
Apply xylometazoline 0.05 or 0.1% nasal drop 2 3 drops in
each nose daily
Administer iv / im hydrocortisone 100- 200mg three times
daliy
Chronic rhinitis
This is a chronic inflammation of the mucous membrane with
increased nasal mucosa caused by repeated acute infections,
allergy and or vasomotor rhinitis.
ATROPHIC RHINITIS
This is a chronic infection of the nasal mucosa in which various
components become thinner (atrophy) due to fibrosis of the
terminal blood vessels
Cause
57
The cause is unknown but its associated with
HIV/AIDS
Poor socioeconomic status
Syphilis
Rhinoscleroma (early stages)
Clinical features
Tends to affect both nasal cavities and affects females more
than males
Foul stench not noticed by patient who cannot smell
Crusts and bleeding points in the nose
Epistaxis when crusts separate
Sensation of obstruction in the nose
Nasal airway very wide
Investigations
C&S of smear of nasal material to identify the causative
micro organisms
X-ray to detect for the extent and severity of the condition
along the nasal cavity and to r/o sinusitis
Management
58
Clean nasal cavities twice daily to remove crusts
(most important)
Syringe the nose or douche it with warm normal
saline Or sodium bicarbonate solution 5% (dissolve 1
teaspoon of powder in 100 ml cup of warm
water) then apply tetracycline eye ointment 1%
inside the nose twice daily
Give amoxicillin 500 mg every 8 hours for 14
days and in case of rhinoscleroma: Give 1 g every
8 hours for 6 weeks
In case symptoms persist refer to ENT specialist
Complications of rhinitis
Otitis media
Sinusitis
Pharyngitis
Laryngo-bronchitis
Adenoid Disease
Enlargement or inflammation of nasopharyngeal tonsil.
Common in small children.
Clinical features
59
May be due to enlargement, inflammation, or both;
Obstruction of the nose leading to mouth breathing,
difficulty eating, snoring, jaw deformities
Obstruction of Eustachian tube leading to hearing loss, which
fluctuates due to fluid in middle ear (Glue ear)
Recurrent otitis
Discharge from the nose
Recurrent cough
Physical and other developmental retardation, e.g. small size
for age
Investigations
Diagnosis is usually based on history and physical
examination
X-ray for neck soft tissue( lateral view) to detect and reveal
narrowing of the post-nasal space
Management
In mild cases manage on conservative treatment with
chlorpheniramine 1-2 mg daily (depending on age) for 7 days
Apply Topical nasal steroids if available
If moderate or severe refer to the ENT specialist
60
Adenoidectomy in cases of chronic nasal obstruction and
discharge, secretory Otitis media and sleep apnoea
Benign tumors of the nose
All areas of the nasal cavity and paranasal sinuses can be
affected, but the lateral wall, ethmoids and maxillary sinus are
the most common primary sites.
The frontal and sphenoid sinuses are rare primary sites for
reasons that are unknown.
Examples of benign tumors of the nose include;
Inverted papilloma (IP)
This is a warty, slow-growing tumour that arises from the
epithelial lining of the nasal cavity nose.
Its more common in males more than females at the ratio of
(5:1).
Its similar to a nasal polyp and causes nasal blockage.
Haemangioma
This is a soft reddish polyp on the anterior part of septum that
bleeds easily on touch and usually brings about nasal blockage.
The common types include the capillary haemangioma which is
a bleeding polypus of the nasal septum and the cavernous
haemangioma which occurs on the lateral nasal wall
Osteoma
61
This is the most common benign tumour of the nose and sinuses
commonly in frontal sinus and followed by ethmoid
The common types include the compact (ivory) osteoma which
is common in the frontal sinus and the cancellous Osteoma
which is common in the ethmoid sinuses.
Juvenile angiofibroma
This is a slow growing highly vascular tumour which arises
predominantly from the sphenopalatine region
Its common in adolescent and young adult males
The tumour is locally invasive and can cause life-threatening
epistaxis and nasal obstruction
Nasal polyps
These are the most common non-cancerous tumour of the nasal
cavity and paranasal sinuses.
They are abnormal growths of the mucosal lining of the nose
and sinuses
Nasal polyps appear most frequently near the openings to the
sinuses in the nasal passage but they can also develop anywhere
throughout the nasal passages or sinuses.
62
Causes
The exact causes of nasal polyps are not known but can be due
to the following risk factors
Sensitivity to aspirin (people with an allergic response to
aspirin or other NSAIDs (non-steroidal anti-inflammatory
drugs) are more likely to develop polyps).
Asthma.
Allergic fungal sinusitis (an allergy to airborne fungi).
Rhinitis / Rhino sinusitis (an inflammation of the nasal
passage and sinuses)
Cystic fibrosis (a chronic disease that affects organs such as
the liver, lungs, pancreas, and intestines).
Churg-Strauss syndrome (a disease that results in the
inflammation of blood vessels).
Age (occurs at any age, but young and middle-aged adults
are more at risk).
Genetics (as it may run into families).
These include;
63
Stuffy, blocked or runny nose
Loss of smell
Loss of taste
Headache
Pressure in the head
Snoring
Investigations
64
Skin prick allergy test to r/o or identify if the cause is an
allergy
Nasal biopsy to r/o cancer
Management
Medical management
Complications
Chronic sinusitis
Obstructive sleep apnea
Facial deformity
65
Prevention
66
This is the most common type of nasal cavity and paranasal
sinus cancer
Its most common in males above 40 years and
It commonly affects the lateral nasal wall, the maxillary and the
ethmoidal sinuses.
Adenocarcinoma
Malignant melanoma
This develops from cells called melanocytes that give the skin
its color and is an invasive, fast-growing cancer accounting for
about 1%
Inverting papilloma
Esthesioneuroblastoma
67
This type of cancer is related to the nerves that control the
sense of smell.
Midline granuloma
Lymphoma
Sarcoma
Others include
68
Olfactory neuroblastoma
Adenoid cystic carcinoma
Use of marijuana
Fatigue
70
A lump in the neck
Investigations / diagnosis
Good physical examination
Nasal biopsy to confirm the diagnosis
Nasal x ray to r/o nasal blockage and other nasal
complications
CT / MRI scan to detect the size of the tumor, the extent of
the disease on the nasal cavity (metastases)and r/o other
nasal complications
Management
Surgery eg excision, maxillectomy, neck dissection and
craniofacial resection
Radiation therapy
Chemotherapy
Palliation
71
T Tumor, N nodes and M- metastasis.
Primary tumor (T) in the nasal cavity and ethmoid sinus
T3: The tumor extends into the maxillary sinus or to the bone
surrounding the eye.
T4b: The tumor invades any of the following: the back of the
eye, the brain area, or the back of the head.
N (Nodes)
72
N0 (N plus zero): There is no evidence of cancer in the
regional lymph nodes.
N1: The cancer has spread to 1 lymph node on the same side
as the primary tumor. The cancer found is 3 centimeters (cm)
or smaller. It does not extend into the tissue beyond the
involved lymph node, called extranodal extension (ENE).
73
N3b: The cancer has spread to any node, and it has spread to
the tissue surrounding the lymph node (ENE).
M (metastasis)
This indicates that the cancer has spread to other parts of the
body, called distant metastasis.
Clinical features
Sudden onset of choking followed by stridor (noisy
breathing) or
Cough
Difficulty in breathing,
Wheezing
Hoarseness of voice if FB is stuck at the vocal cords
Symptoms start suddenly, some symptoms may be transient
(may disappear after a short period), but complications may
present few days later such as sudden death, intractable
pneumonia, branchiectasis, atelectasis, pneumothorax, lung
abscess
75
Upper airway obstruction as shown by flaring of the nostrils,
recession of the chest inlet and or below the ribs, rapid chest
movements and reduced air entry (usually on the right side)
Investigations
Once the history and examination are suggestive,
investigations can be omitted to save time
Chest x-ray may show lung collapse, hyperinflation,
mediastinal shift, shift of heart shadow
Management
Child
In case the child is chocking, attempt to dislodge the FB by 3
cycles of 5 back slaps or 5 chest compressions for infants or
Heimlich manoeuvre for children
Do not do blind finger sweeps
In case the foreign body is visible in the mouth, remove it
with a Magill forceps
In case the child has severe respiratory distress, refer to
higher level for airway visualization to the ENT specialist but
give oxygen if necessary
Adult
76
Dislodge large FB, e.g. chunk of meat from the pharynx by
cycles of 5 back slaps and Heimlich manoeuvre while
standing behind the patient with both arms around the
upper abdomen and give 5 thrusts. If the patient is pregnant
or very obese, perform 6-10chest thrusts while the patient is
lying on the back
In case you still suspect any FB, refer for airway visualization
to the ENT specialist for Endoscopy and extraction of the FB
under general anesthesia
Prevention
Do not give groundnuts or other small hard food items to
children <2 years
If a child is found with objects in the mouth, leave the child
alone to chew and swallow or gently persuade the child to
spit out the object (Do not struggle with/force the child)
Complications of FBs in the airway
Sudden death
Pneumonia
Branchiectasis
Atelectasis
77
Pneumothorax
Lung abscess
Foreign Body in the Food Passage / Oesophogus
This is any foreign object impacted into the oesophogus or
food passage
Causes
Accidental mainly in children and unconscious patients
Large food bolus ingestion
Types of FBs commonly involved
These include:
Fish or chicken bones often lodging in the tonsils, behind the
tongue, or in the pharynx
Coins in the esophagus especially in children.
Disc battery (is particularly dangerous and requires
immediate referral)
Clinical features
Difficulty in swallowing ( the patient winces as he attempts to
swallow)
Pain in swallowing
Drooling of saliva
78
Pointing sign (patient may point to the site where aforeign
body is stuck with a finger)
FB may be seen, e.g., in tonsil, pharynx
Investigations
Chest x-ray may reveal radio-opaque FB eg coins, fish bone
and confirm the diagnosis
Management
The approach depends upon the type of object ingested, the
location of the object, and the patients clinical status.
If the x ray is negative, no symptoms and the FB does not
belong to any dangerous category (magnets, disc batteries,
sharp long objects, etc), expectant management is advised.
If the patient is symptomatic and or the object is dangerous,
immediately refer for further management by the ENT
specialist
First Aid management
Allow the patient to take only clear fluids mainly water if able
to swallow
79
Do NOT try to dislodge or move the FB with solid food as it
may push the FB into the wall of the oesophagus causing
infection and sometimes death
Give IV infusion if unable to swallow the liquids or if oral fluid
intake is poor
If FB is visible in the pharynx or tonsil grasp and remove it
with a long forceps
If patient tried to push FB with solid food and sustained an
injury give broad-spectrum antibiotic eg capsules Amoxicillin
500 mg and tablets metronidazole 400mg three times daily
for 5 days
Prevention
Keep potential FBs out of childrens reach
Advise children to take care while eating by not taking in too
large pieces of food and chewing of food thoroughly before
swallowing
Advise the patient once a FB is stuck in the esophagus to
avoid trying to push it down with solid food as this may
sometimes be fatal
80
PHARYNGITIS (SORE THROAT)
This is the inflammation of the throat
Causes
Most cases are viral
Bacteria mainly Group A haemolytic Streptococci
Diphtheria in non-immunized children
Gonorrhoea (usually from oral sex)
Ingestion of undiluted spirits
Candida albicans in the immunosuppressed
Clinical features
Onset is abrupt
Throat pain
Pain on swallowing
Mild fever
Loss of appetite
General malaise
Nausea and vomiting, and diarrhoea in children
If the cause is viral there is presence of runny nose,
hoarseness, cough, conjunctivitis, viral rash and diarrhea
81
If cause is bacterial there is presence of tonsilar exudates,
tenderness of neck glands, high fever, and absence of cough
Differential diagnosis
Tonsillitis, epiglottitis, laryngitis
Otitis media if there is referred pain
Investigations
Throat examination with torch and tongue depressor to
reveal if inflamed
Throat swab for microscopy to reveal presence or absence of
pus
Throat swab for C&S to reveal and identify the causautive
micro organisms
CBC to r/o leukocytosis
Serological test for haemolytic streptococci (ASOT) to r/o or
confirm the causative agent
Management
Most cases are viral and do not require use of antibiotics
therefore supportive treatment include;
Keep the patient warm
82
Give the patient plenty of warm oral fluids e.g. tea or lemon
tea
Give analgesics to relieve pain e.g. tablets Paracetamol 1g 8
hourly for 3 days
Review the patient for progress after care
If the case is bacterial give antibiotics like;
Capsules Amoxyl or Ampiclox 500mg 8 hourly for 10 days or
Augmentin 625mg twice daily for 5 - 10 days if mild or
moderate
If severe admit the patient and give iv ceftriaxone 1g or 2g
once daily and injectable analgesics
Complications
Blockage of the airway (in severe cases)
Middle ear infections
Peritonsillar abscess (quinsy)
Retropharyngeal and parapharyngeal abscesses
Sinusitis
Rheumatic fever
Acute glomerulonephritis
Septicemia
83
Bronchitis
Pneumonia
Rheumatic heart disease
Septic arthritis
Notes
If not properly treated, streptococcal pharyngitis may lead to
acute rheumatic fever and retropharyngeal or peritonsillar
abscess, therefore ensure a full 10-day course of antibiotics is
completed where applicable
PHARYNGO-TONSILLITIS (tonsillitis)
This is the inflammation of the tonsils
Causes
Streptococcal infection (most common)
Viral infection (less common)
Clinical features
Onset is sudden and is most common in children
Sore throat
Fever
Shivering
Headache
84
Vomiting
Enlargement of Tonsils with exudate
Enlargement of cervical lymph nodes
Investigations
Throat swab for C&S to reveal and confirm the causative
micro organism
CBC to r/o leukocytosis
Management
Medical management
If bacterial and mild or moderate give broad spectrum
antibiotics such as capsules ampiclox 500mg 4 hourly and
analgesics such as ibuprofen 400mg 8 hourly fro 5 days
If severe admit patient and give iv ceftriaxone 1- 2g once
daily for 5 days
If patient is allergic to penicillin give Erythromycin 500 mg
every 6 hours for 10 days
If the cause is viral give analgesics mainly paracetamol 1g
three times daily and increase oral fluids
Surgery management is mainly by tonsillectomy (in cases of
chronic repetitive tonsillitis)
85
Complications
Local complications
Peritonsilar abscess (quinsy)
Cellulitis
Systemic complications
Bacterial endocarditis
Glomerulonephritis
Rheumatic fever
86
Inability to open the mouth
Salivation and dribbling
Bad mouth odour
Thickened muffled (unclear) speech
Ear pain
Enlarged cervical lymph nodes
Tonsil and soft palate reddish and oedematous
Swelling pushing the uvula to opposite side (bulging
collection of pus)
Differential diagnosis
Tumour
Tonsillitis
Abscess in the pharynx
Investigations
C&S of pus if present or after drainage to identify the causative
microorganism
Management
Medical /Conservative management
Bed rest
Oral hygiene
87
Use of antibiotics ie
• If mild, Benzyl penicillin 2 MU IV or IM every 6 hours for 48
hours then switch to amoxicillin 500 mg every 8 hours to
complete a total of 7 days
• If moderate or severe, Ceftriaxone 1 g IV once daily for 7
days, Child: 50 mg/kg IV Plus metronidazole 500 mg IV
every 8 hours Child: 10 mg/kg IV every 8 hours
Use of analgesics ie Im Diclofenac 75mg every 8 hourly daily
to relieve pain
Surgery mainly I&D to drain out pus from the abscess
TRACHEOSTOMY
Key facts
This is a surgical procedure in which an opening is made into
the trachea to relieve sudden laryngeal obstruction or for the
purpose of establishing an airway
The indwelling tube which is inserted into the trachea is
called a tracheostomy tube
Its either temporary or permanent
Indications of tracheostomy
88
To bypass an upper airway obstruction
To facilitate removal of secretions along the trachea and
bronchial or allow removal of tracheobrachial secretions
To permit long-term use of mechanical ventilation
To prevent aspiration of oral or gastric secretions in
unconscious or paralyzed patient
To replace an endotracheal tube
To Permit oral intake and speech in the patient who requires
long-term mechanical ventilation
To establish and maintain patent airway
Causes of upper air way obstruction
Upper airway obstruction is due to the following
Foreign bodies and vomitus imparted in the larynx
Acute or chronic laryngitis
Trauma
Burns of the mouth or larynx
Laryngeal edema
Laryngeal paralysis
Acute edema of the glottis
Laryngeal carcinoma
89
Peritonsillar abscess
Retrosternal goiter
Enlarged mediastinal lymph nodes
Hematoma around the upper airway
Thoracic aneurysm
Complications of tracheostomy
Complications may occur early or late in the course of
tracheostomy tube management or years after the tube has been
removed.
Early complications include
Bleeding / haemorrhage
Pneumothorax
Air embolism
Aspiration of secretions
Subcutaneous or mediastinal emphysema
Recurrent laryngeal nerve damage
Posterior tracheal wall penetration
Long-term complications include
Airway obstruction from accumulation of secretions or
protrusion of the cuff over the opening of the tube,
90
Infection
Rupture of the innominate artery
Dysphagia
Tracheoesophageal fistula,
Tracheal dilation
Tracheal ischemia and necrosis.
Tracheal stenosis after removal of the tube
Prevention of complications associated with endotracheal
and tracheostomy tubes
Complications of tracheostomy may be prevented by;
Administering adequate warmed humidity.
Maintaining the cuff around the tube.
Suction to remove secretions and prevent aspiration.
Maintaining the skin integrity by changing the tapes and
dressing prn
Auscultating the lungs for the lung sounds.
Monitoring for signs and symptoms of infection including
temperature and white blood cell count.
Administering prescribed oxygen and monitoring of the
oxygen saturation.
91
Monitoring the patient for cyanosis.
Maintaining adequate hydration of the patient.
Using sterile technique when suctioning and performing
tracheostomy care.
92
assembled, tracheostomy tray, pen, piece of paper, bell,
screen and table at the bed side.
93
Observe the tracheostomy tube to ensure its in and is held
in position by tapes tied around the patients neck and if
cuffed is inflated
Observe the NGT and urinary catheter to ensure its in
position and is continiously draining out the bladder
Take vital observations and maintain an observation chart
and thereafter they will transfer the patient from theatre to
the ward for post operative management with one nurse in
front and other behind ensuring a patent air way, privacy and
warmth respectively.
In ward
94
Proper positioning the patient in a recumbent position to
ensure a patent air way, breathing and circulation
Proper positioning of the urinary catheter and the urine bag
to ensure proper and continuous drainage.
Proper positioning of the NGT to avoid the patient from
sleeping on it and irritation of the gut
Observation of the tracheostomy tube to ensure its in situ
and properly held in position by the tapes tied around the
patients neck and its not tight.
Observation of the wound dressing for bleeding and to
ensure its in situ
Inflation of the tracheostomy tube if cuffed to minimize
pressure on tracheal wall
Oxygen therapy in case patient has difficulty in breathing to
ease breathing and maintain the SPO2 above 95%
Suction of mouth secretions present to ensure a patent air
way, ease breathing, and avoid blockage of the air way or
aspiration.
95
Administration of iv fluids (Normal saline / 5% Dextrose) as
prescribed and maintain afluid balance chart
Administration of analgesics as prescribed eg im pethidine
100mg to control pain
Taking vital observations as ordered and maintain an
observation chart
96
These will be administered to the patient as prescribed by the
ENT surgeon and a treatment chart is maintained and they
include;
98
or in case of carcinoma the tracheostomy will be permanent
and will not be removed.
Elimination
Bladder care
A urinary catheter present is maintained in situ for
continuous bladder drainage throughout the recovery period
and urine in the urine bag is observed for color and amount
and a fluid balance chart is maintained and any abnormality
detected is noted and reported to the ENT surgeon or doctor
on duty. After recovery a urinary catheter is removed as
ordered by the doctor and the patient is offered a bed pan
99
(female) or urinal ( male) prn to open the bladder throughout
the post operative period.
Bowel care
After recovery, the patient is offered a bed pan prn to open
the bowel and stool is observed for colour and amount and
any abnormality detected is and noted reported to the ENT
surgeon throughout the post operative period.
Diet
Hygiene
100
Daily bed bath and bed making to ensure patients comfort in
bed
4 hourly treatments of pressure areas to prevent
development of pressure sores.
Daily oral care to prevent oral complications such as halitosis,
stomatitis, gingivitis and to stimulate the appetite
Physiotherapy
101
Administering post medication in time and prn
Continued psychotherapy to alley anxiety
Advice on Discharge
102
To always to go or come for radiation therapy and
chemotherapy prn
103
These are caused by chronic abuse of the voice such as,
repeated yelling, shouting and strenuous singing
Symptoms include hoarseness and breathy sounds
Treatment is by surgical removal of the nodules and in
childrens it disappears with voice therapy alone
Prevetion is by stopping abusing the voice
• Laryngoceles
These are out pouching of the mucous membrane of part
of the voice box (larynx)
They may bulge inwards resulting into hoarseness and air
way obstruction or out wards producing a visual lump in
the neck
They are filled up with air and can be expanded when a
person breathes out forcefully with the mouth open and
nostril pinched shut
Treatment is by surgery
Other Benign laryngeal tumors include
Juvenile papillomas
Hemangiomas
Fibromas
104
Chondromas
Myxomas and
Neurofibromas
These may appear in any part of the larynx but Papillomas
and neurofibromas can become malignant
Symptoms of benign laryngeal tumors include;
Hoarseness
Breathy voice
Dyspnea
Aspiration
Dysphagia
Otalgia (ear pain), and
Hemoptysis
Examples of malignant throat tumors
Cancer of the larynx
Cancer of the larynx accounts for approximately half of all head
and neck cancers.
Almost all malignant tumors of the larynx arise from the surface
epithelium and are classified as squamous cell carcinoma.
105
Laryngeal carcinoma mainly affects the glottic region
accounting for 60%, supraglottic 35% and the subglottic 5%.
Its mode of spread is mainly by direct spread and lymphatic
spread according to the regions ie supraglottic, glottic and
subglottic
Risk factors of cancer of larynx
These include
Male gender
Age 60 to 70 years
Tobacco use (including smokeless
Excessive alcohol use
Vocal straining
Chronic laryngitis
Occupational exposure to carcinogens
Nutritional deficiencies (riboflavin), and
Family predisposition.
Clinical Manifestations
Early symptoms include;
Hoarseness (Dysphonia) with cancer in glottic area
Harsh, raspy, low-pitched voice
106
Persistent cough
Pain and burning in the throat when drinking hot liquids
Lump is felt in the neck.
After metastasis symptoms include:
Dysphagia
Dyspnea
Unilateral nasal obstruction or discharge
Persistent hoarseness or ulceration
Foul breath
Enlarged cervical node
Weight loss
General debilitated state
Pain radiating to the ear
Haemoptysis
Investigations / diagnosis
History and physical examination of the head and neck to r/o
neck lumps
107
Laryngeal biopsy to confirm the diagnosis
Neck CT scan to confirm the diagnosis r/o laryngeal
complications and neck involvement
Plain chest x ray to r/o chest involvement
Management
The goals of treatment of laryngeal cancer include cure,
preservation of safe effective swallowing, preservation of useful
voice, and avoidance of permanent tracheostoma.
Treatment options include;
Surgery
Radiation therapy
Chemotherapy
Combination therapy
Speech therapy eg esophageal speech, artificial larynx
(electrolarynx), or tracheoesophageal puncture.
Surgery
Depending on the location and staging of the tumor, four
different types of laryngectomy (surgical removal of part or all
of the larynx and surrounding structures) are considered:
Partial laryngectomy
108
This is recommended in the early stages of cancer in the glottic
area when only one vocal cord is involved
Supraglottic laryngectomy
This is indicated in the management of early (stage I)
supraglottic and stage II lesions, and the hyoid bone, glottis, and
false cords are removed.
Hemilaryngectomy
This is performed when the tumor extends beyond the vocal
cord but is less than 1 cm in size and is limited to the subglottic
area.
Total laryngectomy plus tracheostomy
This is performed in the most advanced stage IV laryngeal
cancer, when the tumor extends beyond the vocal cords, or for
recurrent or persistent cancer following radiation therapy.
In total laryngectomy, laryngeal structures are removed,
including the hyoid bone, epiglottis, cricoids cartilage, and two
or three rings of the trachea.
Staging of the tumours:
This is mainly based on TNM classification, to standardize
treatment method and to report the treatment results.
• Primary Tumours (T):
109
Tx: Primary tumour can't be assessed.
T0: No evidence of primary tumour.
T is: Carcinoma in situ
T1: Tumour limited to one site with normal vocal cord
mobility.
T2: Tumour extending to more than one site with normal
vocal cord mobility.
T3: Tumour limited to larynx with vocal cord fixation.
T4: Tumour extending beyond the larynx.
• Lymph Nodes (N):
N0: No clinically positive nodes.
N1: Single clinically positive ipsilateral node 3 cm or less in
diameter.
N2: Single clinically positive ipsilateral node more than 3
cm but less than 6 cm in diameter.
N3: Ipsilateral nodes equal to 6cm in diameter or bilateral
or contralateral nodes. (of any size).
• Distant Metastasis (M):
M0: No evidence of distant metastasis.
M1: Tumour with distant metastasis.
110
Post operative management of the patient after total
laryngectomy and permanent tracheostomy
Aims
To relieve symptoms that may occur during the post
operative period
To prevent complications that may occur during the post
operative period
To promote quick recovery of the patient
On Ward
111
After operation, the ward nursing team is informed and two
nurses go to theatre to collect the patient and while in
theatre they will;
Receive a verbal report from the anesthetist concerning the
general condition of the patient, any post medication and the
type of anesthesia given.
Also receive post operative instructions from the ENT
surgeon concerning the general management of the patient
during the post operative period and the type of
tracheostomy tube used (either cuffed or non cuffed).
Observe the patient for breathing by passing the back of the
palm near the patients nose and also the chest movement.
Observe the urinary catheter if present for drainage and the
drainage for colour and amount and maintain a temperature
chart
Observe the tracheostomy tube to ensure that its in situ and
is held in position by tapes tied at the sides of the patients
neck and the cuff is inflated
Observe the NGT to ensure that its in situ
112
Take vital observations and maintain an observation chart
and when satisfied, they will then transfer the patient to the
ward for further management post operatively with one
nurse in front ensuring a patent air way while the other
behind maintaining privacy and warmth.
In ward
113
Proper positioning of the NGT to avoid the patient from
sleeping on it and irritation of the gut
Observation of the tracheostomy tube to ensure that its in
situ and properly held in position by the tapes tied around
the patients neck to ensure its not tied too tight.
Observation of the wound dressing for bleeding and in case
more sterile gauze is added to arrest bleeding and
maintained in situ by strapping
Inflation of the tracheostomy tube if cuffed to minimize
pressure on tracheal wall
Administration of oxygen to ensure a patent air way and ease
breathing
Suction of secretions if present to ensure a patent air way,
ease breathing, and avoid blockage of the air way and
aspiration.
Administration of iv fluids (Normal saline / 5% Dextrose) as
prescribed to ensure fluid and electrolyte balance
Administration of analgesics as prescribed to relieve pain
such as pethidine 100mg and maintain treatment chart
114
Taking of vital observations as ordered and maintain a
temperature chart
115
IM pethidine 100mg alternating with iv paracetamol 1g three
times daily for 3days
IV fluids, Normal saline alternating with 5% Dextrose 3 litres
in 24 hours.
Oxygen therapy 4 6 litres
116
The tapes holding the tracheostomy tube in position are
changed whenever soiled with clean ones to avoid skin
irritation and sepsis or as ordered by the ENT surgeon
The tracheostomy tube is sucked as ordered to clear out the
secretions present along the air way to ensure a patent air
way and ease patient breathing.
The inner tube is removed prn or as ordered, cleaned with
sodium bicarbonate or savlon and reinserted back into the
tracheostomy tube properly.
If the tracheostomy tube is cuffed, its observed regularly ,
released and inflated prn as ordered by the surgeon
The tracheostomy tube is permanently maintain in position
as ordered by the ENT surgeon
117
Elimination
Bladder care
A urinary catheter present is maintained in situ for
continuous bladder drainage throughout the recovery period
and urine in the urine bag is observed for color, smell and
amount and a fluid balance chart is maintained. After
recovery a urinary catheter is removed as ordered by the
ENT surgeon and is offered a bed pan (female) or urinal
(male) prn to open the bladder and any abnormality
detected is noted and reported throughout the post
operative period.
Bowel care
After recovery, the patient is offered a bed pan prn to open
the bowel and stool is observed for colour, smell, texture and
amount and any abnormality detected is noted reported to
the ENT surgeon throughout the post operative period.
Diet
Hygiene
Physiotherapy
119
exercises and neck and head rotation, shoulder exercises to
prevent respiratory, circulatory complications and neck
muscle rigidity.
Advice on Discharge
120
To come back for review on the date prescribed on the
discharge form.
To always eat a light well balanced diet
To come back as early as possible in cases of any early neck
complication.
To avoid heavy lifting on the head until fully recovered
To continue caring for the trachestomy tube and the stoma
to avoid sepsis
To continue with regular exercises
To avoid alcohol consumption and smoking
To always to go or come back for radiation therapy and
chemotherapy prn
121
Tracheal crusting
Staging of cancer of larynx
This is mainly based on the TNM system
T Tumor
There are 5 main T stages for cancer of the larynx and these
include;
122
T4 Tumour has grown into body tissues outside the larynx
and has spread to the thyroid gland, windpipe (trachea) or
food pipe (oesophagus).
N Nodes
There are 4 main N stages for cancer of the larynx and these
include;
N2b Cancer cells have spread in more than one lymph node
on the same side of the neck as the cancer and all are smaller
than 6cm across.
123
N2c Cancer cells have spread to the lymph nodes on both
side of the neck from the cancer and all are less than 6cm
across.
M Metastasis
TUMORS OF NASOPHARYNX
These are tumors which affects the lower part of the nasal cavity
and the upper part of the pharynx
These may either be benign or malignant tumors
Benign tumor in the nasopharynx
Nosapharayngeal Angiofibroma
This is the commonest benign tumour of the nasopharynx
common in males only at the age 10-20 years originating from
124
the periosteum of the roof of nasopharynx or margin of the
sphenopalatine foramen in the posterior part of lateral nasal
wall.
Nasopharyngeal Angiofibroma
Clinical features
Nasal obstruction
Epistaxis
Tinnitus
Hearing loss
Facial swelling
Diplopia( double vision)
Proptosis (down ward displacement of the eye ball resulting
into amass within the orbital cavity)
Investigations / diagnosis
CT scan or MRI to detect and reveal the nature and size of
the tumor in the nasopharynx and to r/o complications
125
Management
Surgery mainly excision to remove the tumor, Transnasal
endoscopic excision, transpalatal, lateral rhinotomy or
mid-facial degloving approach,
Malignant tumors of the nasopharynx
These include;
Nasopharyngeal carcinoma
Lymphomas mainly non - Hodgkin lymphoma
Chondroma
Risk factors for nasopharyngeal carcinoma
Ingestion of salted fish
Excessive alcohol consumption
Cigarette smoking
Inhalation of industrial smoke and chemicals
Virus eg Epstain barr virus and HPV
Clinical features
Epistaxis
Nasal obstruction
Discharge from the nose
Hearing loss
126
Tinnitus
Otitis media
Horseness
Facial pain
Altered sensation of the face
Diagnosis / investigations
Facial CT scan / MRI to confirm the diagnosis
Management
Surgery
Radiation therapy
Chemotherapy
Tumors of the Laryngopharynx (Hypopharyngeal Tumors)
Benign tumors in this region are rare and the malignant tumor
which is very common is the squamous cell carcinoma
Risk factors of hypopharyngeal tumors
These include;
Cigarette smoking
Excessive alcohol consumption
Viruses eg Epstein Barr virus and HPV infection.
Clinical features
127
These include;
Dysphagia
Disphonia / hoarseness
Reffered ear pain (otalgia)
Weight loss
Enlarged neck nodes
Airway obstruction
Investigations
These include;
Barium swallow to r/ o any obstruction along the
laryngopharynx
Neck and chest x ray to detect and reveal the size of the
heart and paratracheal regions due metastasis
Neck CT MRI scan to confirm the diagnosis and r/o neck
complications due to metastasis
Management
Surgery
Radiation therapy
Chemotherapy
128
DISORDERS OF THE EYE
Terms used in ophthalmology
Accommodation
This is a process by which the eye adjusts for near distance (eg,
reading) by changing the curvature of the lens to focus a clear
image on the retina
Anterior chamber:
This is a space in the eye bordered anteriorly by the cornea and
posteriorly by the iris and pupil
Aphakia
This is absence of the natural lens
Astigmatism
This is a refractive error in which light rays are spread over a
diffuse area rather than sharply focused on the retina caused by
differences in the curvature of the cornea and lens
Binocular vision
129
This is normal ability of both eyes to focus on one object fusing
the two images into one
Blindness
This is inability to see defined by a corrected visual acuity of
20/400 or less, or a visual field of not more than 20 degrees in
the better eye
Chemosis
This is edema of the conjunctiva
Cones
These are retinal photoreceptor cells essential for visual acuity
and color discrimination
Diplopia
This is seeing one object as two or double vision
Emmetropia
This is absence of refractive error
Enucleation
This is the complete removal of the eye ball and part of the optic
nerve
Exenteration
This is the surgical removal of the entire contents of the orbit,
including the eyeball and lids
130
Evisceration
This is the removal of the intraocular contents through a corneal
or scleral incision but the optic nerve, sclera, extraocular
muscles, and the cornea are left intact
Hyperemia
This is red eye resulting from dilation of the vasculature of the
conjunctiva
Hyperopia
This means far sightedness (a refractive error in which the focus
of light rays from a distant object is behind the retina)
Hyphema
This means blood in the anterior chamber
Hypopyon
This is collection of inflammatory cells that has the appearance
of a pale layer in the inferior anterior chamber of the eye
Injection
This means congestion of blood vessels
Keratoconus
This is cone-shaped deformity of the cornea
Limbus
This is a junction of the cornea and sclera
131
Myopia
This means near sightedness (a refractive error in which the
focus of light rays from a distant object is anterior to the retina)
Nystagmus
This is involuntary oscillation of the eyeball
Papilledema
This is swelling of the optic disc due to increased intracranial
pressure
Photophobia
This is ocular pain on exposure to light
Posterior chamber
This is a space between the iris and vitreous
Proptosis
This is downward displacement of the eyeball resulting from an
inflammatory condition of the orbit or a mass within the orbital
cavity
Ptosis
This is drooping of the eyelid
Rods
This is a retinal photoreceptor cells essential for bright and dim
light
132
Scotomas
These are blind or partially blind areas in the visual field
Strabismus
This is a condition in which there is deviation from perfect
ocular alignment
Trachoma
This is a bilateral chronic follicular conjunctivitis of childhood
that leads to blindness during adulthood, if left untreated
Vitreous humor
These are gelatinous material (transparent and colorless) that
fills the eyeball behind the lens
133
pink eye) because of the sub conjunctival blood vessel
hemorrhages
Conjunctivitis may be unilateral or bilateral, but the infection
usually starts in one eye and then spreads to the other eye
by hand contact
Causes
Its caused by;
Bacteria eg chlamydia
Virus
Fungi and parasites
Eye trauma by chemicals or foreign bodies
Smoke or irritating toxic stimuli into the eye
Allergy
Pre existing ocular infection
Clinical features of conjunctivitis
Watery discharge from the eye (viral or chemicals)
Pus discharge from the eye (bacteria)
Cornea is clear and does not stain with fluorescein
Visual acuity is normal
134
Redness (usually both eyes but may start/be worse in one
usually reddest at outer edge of the eye)
Swelling and itching of the eye
Photophobia
Scratching or burning sensation of the eye
Types of conjunctivitis
Conjunctivitis is classified according to its cause and these
include;
Bacterial conjunctivitis
• This is commonly caused by bacteria eg staphylococcus
aureus, streptococcus pneumonia and Hemophilic
influenza and may be acute or chronic
• Staphylococcus aureus is the most common cause in
adults
• Its highly contagious from secretions or with contaminated
objects and surfaces.
135
• It lasts for 1 - 2 weeks and then it usually resolves
spontaneously
Signs and symptoms / clinical features of bacterial
conjunctivitis
• Eye redness and discharge which may be bilateral.
• The affected eye often is stuck shut in the morning
• Purulent eye discharge throughout the day
• Thick eye discharge which may be yellow, white or green
• Eye irritation, itching and discomfort
• Normal eye vision
• Purulent discharge at the lid margins and in the corners of
the eye
• Eye redness due to dilatation of superficial blood vessels
• Edema of the conjunctiva (chemosis)
• Swelling of the eyelids
• Corneal opacity if the cornea is involved
Viral conjunctivitis
• This is a highly contagious type of conjuctivitis spread by
direct contact with the patient and his or her secretions or
with contaminated objects & surface
136
• The common causative organisms are adenovirus and
herpes simplex virus
• It usually presents with extreme tearing, watering or
watery discharge, photophobia, eye irritation, lid edema,
ptosis conjunctival hyperemia and foreign body sensation
Allergic conjunctivitis
• This is a type of conjunctivitis caused by air borne allergy
contacting the eye.
137
• It is common in patients with history of an allergy to
pollens and other environmental allergens.
• It is more common in children and young adults and the
most affected individuals have a history of asthma or
eczema.
Signs and symptoms / clinical features include;
• Epiphora (ie, excessive secretion of tears)
• Severe photophobia
• Reddening of the eye
• Severe and persistent itching of both eyes
• Stringlike mucoid eye discharge
• No visual reduction
• Visual Acuity is normal
Chemical conjunctivitis
This is a type of conjunctivitis that may result from medications,
chlorine from swimming pools, exposure to toxic fumes among
industrial workers, or exposure to other irritants such as smoke,
hair sprays, acids, and alkalis.
Neonatal Conjunctivitis (Ophthalmia Neonatorum)
138
This is conjunctivitis in a newborn within the first 28 days
of life
Etiology / causes
Its caused by bacteria mainly gonococcus and chlamydia
resulting into profuse thin to thick purulent eye discharge
Clinical presentations
• Purulent eye discharge
• Swelling of the eye lids
• Ulcer and scarring of the eye if cornea is involved
Prevention
• Clean the eye lids with saline swabs as soon as the head is
born and before the infants eyes open.
• Apply Tetracycline eye ointment routinely whenever there
is a risk that the mother had these infections during
pregnancy.
Investigations
Clinical features are diagnostic
Pus swab for culture and sensitivity to identify and confirm
the causative micro oraganism
Management
139
Infective conjunctivitis
Instill chloramphenicol or gentamicin eye drops 2 or 3 hourly
for 2 days then reduce to 1 drop every 6 hours for 5 days
Change treatment as indicated by results of culture and
sensitivity where possible
Allergic conjunctivitis
Apply cold compresses to the eyes
Facial hygiene by thorough face washing with clean water
and soap
Instill betamethasone or hydrocortisone eye drops every 1-2
hours until inflammation is controlled then apply 2 times
daily
Viral conjunctivitis
Viral conjunctivitis is not responsive to any treatment but
may be managed by
Applying cold compresses to the eye to alleviate some
symptoms
Proper hand hygiene mainly handwashing
Avoiding sharing hand towels, face cloths, and eye drops.
Chemical conjunctivitis
140
For conjunctivitis caused by chemical irritants, the eye must
be irrigated immediately and profusely with saline or sterile
water.
Note
NB. Gonococcal conjunctivitis should be treated aggressively
and in line with management of Sexually Transmitted
Infections
Prevention
Proper personal hygiene by daily face washing using clean
water
Avoid irritants and allergen
STYE (HORDEOLUM)
This is a localized infection of the hair follicle of the eyelids
Cause
Bacteria mainly staphylococcus aureus
Clinical features
Eye itching in the early stages
Swelling of the eye
Eye pain
Eye tenderness
141
Pus formation
May burst spontaneously
Differential diagnosis
Other infections of the eyelids
Blepharitis
Management
Usually it heal spontaneously
Avoid rubbing the eye as this might spread the infection
Apply a warm / hot compress to the eye
Apply tetracycline eye ointment 1% 2-4 times daily until
symptoms disappear
Remove the eye lash when it is loose
Give analgesics to relieve pain eg tablets ibuprofen 400mg
tds for 5 days
142
Give oral antibiotic if severe eg caps flucamox 500mg qid for
5 days
I &D of pus if present
Prevention
Remove any loose eyelashes
Good personal hygiene
Early detection and medical intervation
Common ocular surgeries
These include
• Enucleation
• Exeteration
• Evisceration
Enucleation
This is the removal of the entire eye and part of the optic
nerve.
It may be performed for the following conditions:
• Severe injury resulting in prolapse of uveal tissue or loss of
light projection or perception
143
• An irritated, blind, painful, deformed, or disfigured
eye,usually caused by glaucoma, retinal detachment, or
chronic inflammation
• An eye without useful vision that is producing or has
produced sympathetic ophthalmia in the other eye
• Intraocular tumors that are untreatable by other means
Evisceration
• This is the surgical removal of the intraocular contents
through an incision or opening in the cornea or sclera.
• The optic nerve, sclera, extraocular muscles, and
sometimes, the cornea are left intact.
• The main advantage of evisceration over enucleation is
that the final cosmetic result and motility after fitting the
ocular prosthesis are enhanced
• Its main disadvantage is the high risk of sympathetic
ophthalmia
Exenteration
• This is the removal of the eyelids, the eye, and various
amounts of orbital contents.
144
• It is indicated in malignancies in the orbit that are life
threatening or when more conservative modalities of
treatment have failed or are inappropriate.
• An example is squamous cell carcinoma of the paranasal
sinuses, skin, and conjunctiva with deep orbital
involvement.
• In its most extensive form, exenteration may include the
removal of all orbital tissues and resection of the orbital
bones.
TRACHOMA
This is a chronic infection of the outer eye caused by
Chlamydia trachomatis
It is transmitted through direct personal contact, shared
towels and cloths, and flies that have come into contact with
the eyes or nose of an infected person.
Its a disease of poor hygiene and poverty
It is a common cause of blindness if not treated
Cause of trachoma
Its caused by bacteria mainly chlamydia trachomatis
Clinical features
145
In early stages symptoms include;
Reddening of eye
Discharge from the eye
Itching of the eye
Photophobia
Ocular pain
Follicles (grain-like growth) on conjunctival
Decreased visual acuity
In case of repeated untreated infections or late symptoms
include;
Scar formation on eyelids causing the upper eyelid to turn
inwards (entropion) and the eyelashes to scratch the cornea
Scarring of the cornea leading to blindness
Corneal opacities in older children and adults
Investigations
No investigation is required and done
WHO grading of trachoma
TF At least five follicles in the upper tarsal conjunctiva,
Indicates active disease and need for treatment
TI Intense inflammation, need for urgent treatment
146
TS Scarring stage, old infection now inactive
TT Trachoma trichiasis, needs surgical treatment
CO Corneal opacities. Visual loss from previous infection
Differential diagnosis
Allergic conjunctivitis (chronic)
Other chronic infections of the eye
Management
Apply tetracycline eye ointment 1% twice daily for 4-6 weeks
(until the infection / inflammation has disappeared)
Give erythromycin 500 mg every 6 hours for 14 days or
azithromycin 500mg once daily for 3 5 days.
Regular washing of the face
Good water and sanitation
If there is any complications refer for specialist management
and surgery of the entropion
GLAUCOMA
Key facts
147
Glaucoma is a group of disorders characterized by loss of
visual field associated with cupping of the optic disc and
optic nerve damage. or
Its a group of ocular conditions characterized by optic nerve
damage related to IOP caused by congestion of aqueous
humor in the eye.
In the past, it was seen more as a condition of elevated
intraocular pressure (IOP) than of optic neuropathy.
Glaucoma is the second leading causes of blindness among
adults
There is no cure for glaucoma, but the disease can be
controlled.
It is not one disease but rather group of disorders
characterized by; increased intraocular pressure and the
consequences of elevated pressure, optic nerve atrophy and
peripheral visual
The term glaucoma refers to a group of disorders such as:
Primary open angle glaucoma (POAG): Is chronic or simple
usually caused by obstruction in the trabecular meshwork.
148
Secondary open angle glaucoma (SOAG): Occur from an
abnormality in the trabecular meshwork or an increase in
venous pressure.
Primary angle-closure glaucoma (PACG): Narrow angle,
acute PACG outflow impaired as a result of narrowing or
closing of angle between iris and cornea.
Secondary angle-closure: results from ocular inflammations,
blood vessel changes and trauma.
Congenital glaucoma: Is an abnormal development of
filtration angle, can occur secondary to other systemic eye
disorders.
NB: The normal balance of production and drainage of aqueous
humor allows IOP to remain relatively constant within the
normal range of 10 to 21 mm Hg with a mean pressure of 16
mm Hg.
Etiology or causes of glaucoma
Blockage and poor drainage of aqueous humuor from the
anterior chamber of the eye
149
Raised or elevated intraocular pressure (IOP) inside the eye.
(It can also occur when this pressure is within the normal
range)20
A proper balance between the rate of aqueous production
(inflow) and the rate of aqueous reabsorption (outflow) is
essential to maintain the IOP within the normal limits.
Risk factors for glaucoma
Family history of glaucoma
Race (African American race)
Older age above 40 years
Diabetes
Cardiovascular disease
Migraine syndromes
Near or short sightedness (myopia)
Eye trauma
Prolonged use of topical and systemic corticosteroids
Raised intra-ocular pressure
Central corneal thickness
Classification of Glaucoma
Open angle glaucoma
150
Angle closure glaucoma (also called pupillary block)
Congenital glaucoma and glaucoma associated with other
conditions.
• Glaucoma can be primary or secondary, depending on
whether associated factors contribute to the rise in IOP.
• The two common clinical forms of glaucoma encountered in
adults are primary open angle glaucoma (POAG) and angle-
closure glaucoma, which are differentiated by the
mechanisms that cause impaired aqueous outflow.
• Primary open-angle glaucoma is the most common.
Types of glaucoma
Open angle glaucoma
This is usually bilateral, but one eye may be more severely
affected than the other.
In all the three types of open-angle glaucoma, the anterior
chamber angle is open and appears normal
Types of open angle glaucoma
These include;
Chronic open-angle glaucoma (COAG)
Normal tension glaucoma
151
Ocular hypertension
Closed angle glaucoma
This is due to obstruction in aqueous humor outflow due to
complete or partial closure of the angle from the forward shift of
the peripheral iris to the trabecula which results into an
increased IOP
Types of angle closure glaucoma
These include;
Acute angle-closure glaucoma (AACG)
Sub acute angle-closure glaucoma
Chronic angle-closure glaucoma
Congenital glaucoma
This is an abnormal development of filtration angle.It can occur
secondary to other systemic eye disorders.
Stages of glaucoma
Regardless of the cause of damage, glaucomatous changes
typically evolve through clearly discernible stages:
Initiating events
152
This is the first stage of glaucoma and its precipitating factors
include illness, emotional stress, congenital narrow angles, drugs
(ie long-term use of corticosteroids.
These events lead to the second stage.
Structural alterations in the aqueous outflow system
During this stage tissue and cellular changes caused by factors
that affect aqueous humor dynamics lead to structural and
functional alterations.
Functional alterations
During this stage conditions such as increased IOP or impaired
blood flow create functional changes that lead to optic nerve
damage.
Optic nerve damage
This is characterized by loss of nerve fibers and blood supply
hence visual loss
Visual loss
This is characterized by visual field defects.
Clinical features of glaucoma
Open angle glaucoma
Mostly asymptomatic
153
History of gradual loss of vision in affected eye or loss of
visual field
Often suspected after seeing cupping of optic disc on
routine fundoscopy or finding elevated intra-ocular
pressure on screening
Angle-closure glaucoma
Sudden onset of severe eye pain and redness, associated
with nausea, vomiting and headache
Difficulty adjusting of the eyes in low lighting
Loss of vision in the affected eye
Coloured halos or bright rings around lights
Hazy-looking cornea
Fixed or semi-dilated pupil
Shallow anterior chamber
Severely elevated IOP. (When palpated with a finger, the
affected eye feels hard, compared to the other eye)
If IOP rises more slowly, the patient may be asymptomatic
with gradual loss of vision
Permanent blindness due to marked increase in IOP for 24
to 48 hours.
154
Congenital Glaucoma
Enlargement of the eye
Lacrimation
Photophobia
Blepharospasm
Investigations
These include:
Visual acuity measurement with the snellens chart
Tonometry to measure IOP of the eye
Tonography to estimate the resistance in the outflow
channels by continuously recording the IOP for over 2 to 4
minutes
Ophthalmoscopy to evaluate the color and configuration
of the optic cup or to inspect the optic nerve
Visual field permietry to measure the visual function in the
central field of vision or for visual field assessment.
Gonicoscopy: to examine the angle structures of the eye,
where the iris, ciliary body and cornea meet.
Management
155
The aim of treatment is to arrest / delay progress of the
disease rather than visual improvement ie to prevent optic
nerve damage and therapy is usually life long
Angle-closure glaucoma is a medical emergency that requires
urgent reduction of intra ocular pressure
Management is both medical and surgery
Medical Treatment
Open-angle glaucoma
Instill Timolol 0.5% eye drops 1 drop to the eye12 hourly
daily for 7 days
Angle-closure glaucoma (acute)
Administer mannitol 20% IV to reduce raised IOP
Give tablets acetazolamide 500 mg single dose followed by
250 mg every 6 hours to decrease aqueous humor
production and reduce intraocular pressure
Instill timolol 0.5% eye drops 1 drop 12 hourly daily on the
eye to decrease aqueous humor production
Surgical management
This is indicated when conservative treatments fail to control the
IOP and they include;
156
Argon laser trabeculoplasty (ALT) or laser trabeculoplasty
Here laser burns are applied to the inner surface of the
trabecular meshwork to open the intratrabecular spaces
and widen the canal of Schlemm, thereby promoting
outflow of aqueous humor hence decreasing the IOP
The procedure is indicated when IOP is inadequately
controlled by medications
It is contraindicated when the trabecular meshwork
cannot be fully visualized because of narrow angles.
its complication is a transient rise in IOP (usually 2 hours
after surgery) that may become persistent.
Trabeculectomy with or without filtering implant.
This is a standard filtering technique used to remove part of the
trabecular meshwork.
Its complications include
Hemorrhage
An extremely low (hypotony) or elevated IOP
Uveitis
Cataracts
Bleb failure
157
Bleb leakage
Endophthalmitis
Laser iridotomy for pupillary block glaucoma
This is an opening made in the iris to eliminate the pupillary
blockage
It is contraindicated in patients with corneal edema, which
interferes with laser targeting and strength.
Its potential complications include;
Burns to the cornea, lens, or retina
Transient elevated IOP
Closure of the iridotomy (Pilocarpine is usually prescribed to
prevent closure of the iridotomy)
Uveitis and blurring.
Cyclocryotherapy; to destroy the ciliary body.
Filtering procedures for chronic glaucoma
These are used to create an opening or fistula in the
trabecular meshwork to drain aqueous humor from the
anterior chamber to the subconjunctival space into a bleb,
thereby bypassing the usual drainage structures.
158
This allows the aqueous humor to flow and exit by
different routes (ie, absorption by the conjunctival vessels
or mixing with tears).
Drainage implants or shunts
These are open tubes implanted in the anterior chamber
to shunt aqueous humor to an attached plate in the
conjunctival space.
A fibrous capsule develops around the episcleral plate and
filters the aqueous humor, thereby regulating the outflow
and controlling IOP.
Caution
Avoid timolol eye drops in patients with asthma, heart block
and uncontrolled heart failure
161
Corneal abrasions
Conjunctival swelling
Sub conjunctival
haemorrhages
Anterior chamber, Decreased visual acuity (this
lens, vitreous or is an indication that the
retina injury involved either the
anterior chamber, lens,
vitreous, or retina).
Poor vision
Blindness
Orbital bones Orbital bone fractures.
(Commonest is a fracture of
the ethmoid bone).
Swelling of the eye
Sunken or retracted eyeball
(depending on the site of
the fracture)
Double vision (Diplopia)
162
Proptosis if there is
haemorrhage in the orbit
Management
Assess the visual acuity, and if this is normal and there are no
signs / symptoms of orbital bone fracture;
• Instill or apply antibiotic eye drops or ointments eg
Gentamicin or chloramphenicol eye drops or tetracycline
eye ointment
• Give tablets Paracetamol 1g tds to relieve pain for 3-5 days
• Apply cold compress to avoid lid swelling
If the visual acuity is poor, pad the eye, give a pain reliever
and refer urgently the patient to a specialist as this is an
indication of injury to deeper structures
Complications of blunt eye injuries
Hyphema
• This is presence of blood in the anterior chamber.
• Its treated by putting the patient in a semi sitting up
position and early referral to the ophthalmologist for
specialized management
163
Rupture of suspensory ligaments. (This leads to the
dislocation of lens)
Delayed cataract (due to concussion damage of lens cells)
Concealed eyeball rupture
164
All perforations of the cornea or sclera are serious injuries
and may lead to blindness.
Apply an eye shield to protect the eye from direct light
Give a pain reliever eg tablets paracetamol 1g or im
Diclofenac 75mg to control pain and refer the patient
immediately to an Ophthalmologist
At secondary or tertiary level, treatment of corneal / scleral
lacerations is immediate repair with 10/0 sutures under an
operating microscope, or if the laceration is extensive, an
immediate evisceration of the eye is performed
Complication of penetrating eye injuries
Corneal scar
Cataract
Endophthalmitis (intra ocular infection)
Chemical Injuries to the Eye
Various chemicals may injure the eye when they come into
contact with the eyes or face.
The commonest are acidic and alkaline chemical products.
Acidic and Alkaline chemical products cause serious injuries
to the eye lids, cornea, and conjunctivae.
165
Management
First aid
On exposure to acid or chemical products, immediately
irrigate the eyes with copious amounts of water to reduce
its effect on the eye
At health facility
On arrival at a medical centre, continue irrigation of the eye
with normal saline to wash out the entire chemical
After irrigating of the eye, apply tetracycline eye ointment,
pad the eye, and refer to an ophthalmologist immediately
for further management
In case of tear gas, irrigate the eyes with plenty of water
since tear gas injury is usually short lived and does not
usually require treatment
Thermal injury
This is either due to direct burn from curling iron, or other
hot surface or indirect burn from ultraviolet light (e.g.
welding), sun ultraviolet burns from excessive sun exposure
(eg skiing, outdoor work, or sunbathing) or and use of heat
lamps and tanning beds.
166
Foreign Body in the Eye
This is the presence of an external object or substance in the eye.
FB in the eye is the most common eye injury and can be on the
conjunctiva or cornea
Conjunctival foreign body
Its mostly found on the upper tarsal conjunctiva
It is good to check for FB by everting the upper eye lid
Needs illumination and remove it by a cotton tip from the
eye
Irrigate the eye with normal saline or tap water if foreign
body cannot be traced in the eye
Corneal foreign body
It can be on the surface or embedded in the cornea of the
eye
Patient complains of pain and foreign body sensation within
the eye
Use adequate light to visualize it on the cornea
Causes
It may be accidental and the FB may be;
Solids such as dust, insects, metal or wood particles
167
Liquids such as splashes of irritating fluids or chemical
Clinical features
Severe eye pain
Eye tearing
Eye redness
Foreign body (FB) may be visible
Inability to open the eye
Feeling of something in the eye which may be irritating
Photophobia
Irregular pupil
Sub conjunctival haemorrhage
Differential diagnosis
Other injury or trauma
Management
Make a thin finger of moistened cotton wool, move eyelid
out of the way, and gently remove FB from the eye if visible
If this fails, apply tetracycline eye ointment 1%, pad the eye
and refer to the Eye Specialist for further management
In case of irritating fluids in the eye, wash the eye with plenty
of clean water or normal saline
168
If the cornea is damaged, apply tetracycline eye ointment
1%, cover or pad the eye, and refer to the Eye Specialist for
further management
Give tablets paracetamol 1g three times daily to relieve pain
Prevention of eye injuries
In the hospital
This is by;
Reading instructions carefully before using cleaning fluids,
detergents, ammonia, or harsh chemicals and wash hands
thoroughly after use.
Wearing special goggles to shield your eyes from fumes and
splashes when using powerful chemicals.
Use of opaque goggles to avoid burns from sunlamps
Avoiding praying with sharp objects such as surgical blades,
needles, used syringes etc
In and Around the House
This is by;
Making sure that all spray nozzles are directed away from
you before you press down on the handle.
169
Reading instructions carefully before using cleaning fluids,
detergents, ammonia, or harsh chemicals and wash hands
thoroughly after use.
Using grease shields on frying pans to decrease spattering.
Wearing special goggles to shield your eyes from fumes and
splashes when using powerful chemicals.
Using opaque goggles to avoid burns from sunlamps.
In the Workshop
This is by;
Protecting your eyes from flying fragments, fumes, dust
particles, sparks, and splashed chemicals by wearing safety
glasses
Reading instructions thoroughly before using tools and
chemicals, and follow precautions for their use
Around Children
This is by;
Paying attention to the age and maturity level of a child
when selecting toys and games by avoiding projectile toys,
such as darts and pellet guns
170
Supervising children when they are playing with toys or
games that are dangerous
Teaching children the correct way to handle potentially
dangerous items, such as scissors and pencils
In Sports
This is by;
Wearing protective safety glasses, especially for sports
such as racquetball, squash, tennis, baseball, and
basketball
Wearing protective caps, helmets, or face protectors
especially during sports such as ice hockey.
Around Fireworks
This is by;
Wearing eye glasses or safety goggles
Not using explosive fireworks.
Not allowing children to ignite fireworks.
Not standing near others when lighting fireworks.
CATARACT
Key facts
171
This is the opacity or cloudiness of the lens inside the eye
Cataracts can develop in one or both eyes and at any age.
It is the most common cause of blindness in Uganda.
Causes of cataract
These include:
Overproduction of oxidants, which are oxygen molecules
that have been chemically altered due to normal daily life
Smoking
Long-term use of steroids and other medication
Certain diseases, such as diabetes, hypoparathyroidism etc
Trauma to the eye
Radiation therapy and Ultraviolet radiation
Congenital
Other eye disorders eg uveitis, glaucoma, retinitis
pigmentosa, or detached retina.
Risk factors
Old age
Sex (slightly common in female than male)
Diabetes (high blood sugar)
Certain drugs e.g. corticosteroids
172
Eye injuries eg blunt and penetrating trauma
Cigarette smoking
Ultraviolet light and ionizing radiation exposure
Obesity
Family history of cataract
Heavy use of alcohol
Types of Cataracts
There are different types of cataracts and are classified basing on
where and how they develop in the eye
Nuclear cataract
This forms in the middle of the lens and causes the nucleus
or the center to become yellow or brown.
Cortical cataract
These are wedge-shaped and form around the edges of the
nucleus.
Posterior capsular cataract
This form is faster than th e other two types and affects the
back of the lens.
Congenital cataract
173
This is present at birth, where some babies are born with
cataract or develop it in childhood and often affects both
eyes.
They may be so small that they do not affect vision but if
they do, the lenses may need to be removed.
Secondary cataract
This is caused by disease or medications such as glaucoma,
diabetes and uveitis, use of the steroid eg prednisone
Traumatic cataract
This develops after an injury to the eye eg foreign body allow
aqueous or vitreous humor to enter the lens capsule..
Radiation cataract
This occurs after radiation treatment for cancer or exposure
to some types of radiation.
Clinical features
Reduced vision
Pupil is not a normal black colour but is grey, white,
brown, or reddish in colour
Condition is not painful unless caused by trauma
Eye is not red unless condition is caused by trauma
174
Light scattering leading to reduced contrast sensitivity,
sensitivity to glare, and reduced visual acuity.
Myopic shift (return of ability to do close work [eg, reading
fine print] without eye glasses)
Astigmatism
Monocular diplopia (double vision)
Brunescens (ie, color values shift to yellow-brown)
Reduced light transmission.
Investigations
The diagnostic tests of cataract include the following:
Visual acuity test using an eye chart to measures how well a
patient see at various distances
Ophthalmoscopy (direct or indirect).
Snellen visual acuity test
Slit lamp biomicroscopic examination (are used to establish
the degree of cataract formation)
Management
Management may involve both medical and surgical
management
Medical management
175
No non surgical treatment cures cataracts or prevents age-
related cataracts thus therefore refer the patient to the eye
specialist(ophthalmologist) for further management
Use of glasses or contact, bifocal, or magnifying lenses which
may improve vision.
Reassurance of the client
Surgical Management
In general, if reduced vision from cataract does not interfere
with normal activities, surgery may not be needed.
In deciding when cataract surgery is to be performed, the
patients functional and visual status should be a primary
consideration.
Surgical options include;
• Phacoemulsification (method of extracapsular cataract
surgery and removal of the lens)
This method of extracapsular surgery uses an ultrasonic device
that liquefies the nucleus and cortex, which are then suctioned
out through a tube but the posterior capsule is left intact.
176
• Lens replacement eg (aphakic eyeglasses, contact lenses, and
intraocular lens implants). After removal of the crystalline
lens, the patient is referred to as aphakic (ie, without lens)
177
Acute bacterial endophthalmitis: caused by Staphylococcus
epidermitus, S. aureus, Pseudomonas and Proteus species
This is characterized by marked visual loss, pain, lid
edema, hypopyon, corneal haze, and chemosis
Late Postoperative Complications
Suture-related problems
Malposition of the IOL(intraocular lens)
Chronic endophthalmitis (severe chronic inflammation
involving both the anterior and posterior segments of the
eye after intraocular surgery)
Opacification of the posterior capsule (most common late
complication of extracapsular cataract extraction)
These may result from toxic reactions or mechanical injury from
broken or loose sutures, results in astigmatism, sensitivity to
glare, or appearance of halos, persistent, low-grade inflammation
and granuloma and visual acuity is diminished.
PAEDIATRIC CATARACT
Cataract in children is unique as it may interfere with the normal
development of vision resulting in lazy eye (amblyopia).
178
Causes
Hereditary/genetic disorders
Intrauterine infections (TORCHES)
Drugs
Trauma
Metabolic diseases e.g. Diabetes
Unknown
Symptoms
A white pupil
Older children may complain of poor vision
Dancing eyes (nystagmus), squints
Investigations
If at HC2 or HC3 reassure patient and refer to hospital
Management
Condition is managed surgically under general anaesthesia
Surgery can be done as early as one month of age
Patching/occlusion therapy in case of lazy eyes (amblyopia)
Aphakic children /those less than one year who are not
implanted should be given aphakic glasses or contact lenses
Prevention
179
Wear protective goggles when hammering, sawing,
chopping, grinding, etc.
Caution children playing with sticks about risk of eye injuries
Pre and post operative management after cataract surgery
(brain storm)
CORNEAL ULCERS
This is the pitting of the cornea caused by bacteria, viruses,
fungi and or protozoan or sometimes from injury
This is an emergency
Causes
Bacteria eg staphylococci, pneumococci
Viruses
Fungi
Foreign body lodged in the eye
Vitamin A and protein deficiency
Clinical features
Eye pain
Sensitivity to light / photophobia
Reduced vision
Increased tear production / lacrimation
180
Pus discharge may appear on the cornea
Reddening of the eye
Complications of corneal ulcers
Impaired vision and scaring
Perforation of the cornea
Displacement of the iris
Destruction of the eye
Deep seated infection
Management
Apply eye drops
Use antibiotics
Surgery
KERATITIS
This is the inflammation of the cornea.
Causes
Infection eg bacterial, viral, or fungal infections leading to
corneal ulceration
Trauma by Chemical, foreign bodies
Clinical features
181
Redness and tearing of the eye
Fear of light / photophobia
Cornea is not clear and will stain with fluorescein in the case
of corneal ulcer (pattern of staining depends on the causative
agent, for example dendritic in viral keratitis)
Visual acuity is usually reduced
Condition is often unilateral
The eye is painful
Investigations (where facilities are available)
Full ocular examination to r/o ocular abnormality
Fluorescein stain to confirm diagnosis
Pus swab for gram stain, culture and sensitivity to identify
and confirm the causative micro organisms
Corneal scraping for microscopy, culture and sensitivity to
detect for and confirm the causative micro oraganism
Management
Admit the patient on eye ward
If the cause is bacterial, apply gentamicin eye drops
alternately with chloramphenicol eye drops 12 hourly until
infection is controlled
182
If viral, acyclovir eye ointment 5 times daily for herpes
simplex and viral keratitis
If fungal, natamycin ophthalmic suspension 5% or econazole
eye drops
Apply Atropine eye drops to relieve pain
Give Vitamin A capsules for children
Surgery i.e. conjunctival flap and tarsorrhaphy
Debridement (chemical/ mechanical)
Orbital Cellulitis
This is a sudden acute inflammation of the tissues around the
eye.
Causes
The cause is mainly bacteria by haemophilus influenza in
children leading to post sinus infection and Staphylococcus
aureus, Streptococcus pneumonia in adults
Risk factors
Sinus infection
Tooth extraction
Orbital trauma
Clinical features
183
Painful swelling of the eye
Pain in the eye especially on eye movements
Decreased vision
Fever and headache
Investigations
Good history and physical examination
Management
This is an emergency and needs immediate referral to the
ophthalmologist
Prevention
Prompt treatment of sinus and dental infections
Complete immunization schedule for children, more
especially Hib vaccine (included in the pentavalent DPT/
HepB/Hib vaccine)
184
the esophagus, perforate the mediastinum, or erode into
the great vessels in later stages.
Causes of Ca esophagus
Gender (male).
Race (African American).
Age (greater risk in fifth decade of life).
Geographic locale (much higher incidence in China and
northern Iran).
Chronic esophageal irritation.
Use of alcohol and tobacco.
Gastroesophageal reflux disease (GERD).
Chronic ingestion of hot liquids or foods
Nutritional deficiencies,
Poor oral hygiene
Exposure to nitrosamines in the environment or food
185
Ca esophagus in early stages is largely asymptomatic
Patient usually presents with an advanced ulcerated lesion
of the esophagus
Dysphagia
Odynophagia (steady, dull, substernal pain)
Regurgitation first with solid foods and eventually liquids.
Feeling of a lump in the throat and painful swallowing
Heartburn
Anorexia
Hemorrhage
Weight loss.
Types of Ca esophagus
Adenocarcinoma
186
It occurs anywhere in the oesophagus and is associated with
smoking, alcohol intake, diet poor in fresh fruit and
vegetables, chronic achalasia etc
Investigations
187
Radiotherapy
Chemotherapy
Palliative therapy to maintain esophageal patency by
dilation of the esophagus using a stent, balloon etc
Complications of Ca esophagus
Hemorrhage (may occur if the cancer erodes through the
esophagus and into the aorta.
Esophageal perforation with fistula formation into the lung
or trachea
Esophageal obstruction due to enlargement of the tumor.
CANCER OF THE CERVIX
Causes of Ca cervix
189
Chronic cervical infection
HIV infection
Clinical Manifestations
Cervical cancer is often asymptomatic in early stages
Irregular or intermittent vaginal bleeding after sexual
intercourse or douching
Watery, dark and foul smelling vaginal discharge because of
necrosis and infection of the tumor
Irregular vaginal bleeding between periods or after
menopause after mild trauma ie (intercourse, douching, or
defecation)
Lower abdominal pain on palpation
Enlargement of the uterus on bimanual examination
Cervical lesions like cervical ulcerations or necrotic tissues or
polypoid mass on speculum examination
Thick, hard and irregular septum on rectovaginal
examination
Rectal bleeding following rectal involvement
Edema of the extremities following metastasis
190
Excruciating pain in the back and legs due to nerve
involvement
Anemia following
Investigations
Ureteral stricture
Bladder dysfunction
Constipation
191
Altered sexual function secondary to a shortened vagina
Dyspareunia
Psychological factors eg depression
Vaginal stenosis
Fistula formation
Stage Characteristics
0 Carcinoma in situ, cervical intraepithelial lesion (CIN) 3
I Carcinoma is strictly confined to cervix (extension to
corpus should be disregarded)
192
Stage Characteristics
IA Invasion is limited to measured stromal invasion with a
maximum depth of 5 mm and no wider than 7mm
IA1 Measured invasion of stroma no greater than 3 mm in
depth and no wider than 7 mm
IA2 Measured invasion of stroma greater than 3 mm and no
greater than 5 mm in depth and no wider than 7mm
IB Clinical lesions confined to the cervix or preclinical
lesions greater than IA
IB1 Clinical lesions not greater than 4 cm in size
IB2 Clinical lesions greater than 4 cm in size
II Carcinoma extends beyond cervix but has not extended to
pelvic wall; it involves vagina, but not as far as the lower
third
IIA No obvious parametrial involvement
IIB Obvious parametrial involvement
III Carcinoma has extended to the pelvic wall; on rectal
examination there is no cancer-free space between tumor
and pelvic wall; tumor involves lower third of vagina; all
193
Stage Characteristics
cases with hydronephrosis or nonfunctioning kidney
should be included, unless they are known to be due to
another cause
IIIA No extension to pelvic wall, but involvement of lower
third of vagina
IIIB Extension to pelvic wall, or hydronephrosis or
nonfunctioning kidney due to tumor
IV Carcinoma has extended beyond true pelvis or has
clinically involved mucosa of bladder or rectum
IVA Spread of growth to adjacent pelvic organs
IVB Spread to distant organs
194