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NOTES

NOTES
HEARING LOSS

GENERALLY, WHAT IS IT?


Weber
PATHOLOGY & CAUSES ▪ Distinguishes between conductive,
sensorineural hearing loss
▪ Decrease in ability to perceive sound
▪ Examiner places vibrating tuning fork
▪ Variable etiology
(128Hz) at apex of head → individual
▫ External, middle, inner ear, associated indicates loudest side
neurological input/processing structures
▫ One ear preferred/louder indicative of
possible hearing loss
SIGNS & SYMPTOMS Rinne
▪ Compares air, bone conduction of sound
▪ Hearing loss
▪ Examiner places vibrating tuning fork
▪ Balance issues, headache, tinnitus (512Hz) at mastoid process → individual
indicates when vibration heard → examiner
moves vibrating tuning fork outside of
DIAGNOSIS pinna → individual indicates if vibration
heart
OTHER DIAGNOSTICS ▫ Bone conduction (mastoid placement
▪ Bedside (otoscopy to Rinne) and formalized of tuning fork) > air conduction (i.e.
(audiogram) testing individual cannot hear vibration after
first step complete) indicative of possible
Otoscopy
hearing loss
Whisper test
Audiogram
▪ Examiner speaks in whispered voice
▪ Pure tones of varying frequencies (Hz) at
0.61m/2ft away → individual covers far
varying volume of sound
ear with hand → examiner whispers word/
phrase → individual repeats word/phrase ▪ Plot individual’s 50% correct response rate
(dependent on volume) for each frequency
Finger rub
▪ Examiner speaks closer to pinna →
individual indicates if sound heard TREATMENT
▪ Specific to underlying etiology; some
etiologies irreversible

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CONDUCTIVE HEARING LOSS


osms.it/conductive-hearing-loss
Eustachian tube dysfunction
PATHOLOGY & CAUSES ▪ Results in abnormal pressure/reflux/
clearance of middle ear contents
▪ Disability of sound waves
▪ Shorter eustachian tubes in children → ↑
▫ Unable to be amplified, transmitted by
reflux of nasopharynx contents → otitis
external/middle ear
media
▫ Higher incidence in children with
CAUSES abnormal craniofacial anatomy (e.g.
Down syndrome, Treacher Collins
Bony outgrowth syndrome)
▪ Exostoses: form at suture lines of external
auditory canal bony suture lines; associated Otitis externa
with repeated cold water exposure (e.g. ▪ AKA swimmer’s ear
swimmers) ▪ Commonly bacterial
▪ Osteomas: form at tympanosquamous ▫ Pseudomonas aeruginosa (most
suture line common pathogen)
Cerumen impaction ▪ Chronic/repeated infections → polyps (can
occlude external auditory canal)
▪ ↑ Incidence in elderly
Otitis media
Congenital
▪ Infection → effusion → poor transmittance
▪ Microtia: malformation/absence of auricle;
of sound wave in middle ear → hearing loss
1st, 2nd branchial arch derivative; mild-
moderate conductive hearing loss ▪ Highest incidence
▪ External auditory canal atresia: associated ▫ 6–18 months of age
with craniofacial diseases (e.g. Treacher ▪ Microbiology: Staphylococcus pneumoniae,
Collins syndrome, Robin sequence, Haemophilus influenzae, Moraxella
Crouzon syndrome) catarrhalis
▪ Commonly of ossicular chain (most ▪ Risk factors: daycare, bottle feeding
commonly malformation of stapes) → ▪ Complications: mastoiditis, cholesteatoma,
inability to reverberate → ↓ sound wave permanent hearing loss → deafness
transmittance to oval window

OSMOSIS.ORG 623
Otosclerosis
▪ Bony overgrowth of stapes to oval window
TREATMENT
→ inability to vibrate → inability to conduct
▪ Specific to underlying etiology
sound waves; can be autosomal dominant
with variable penetrance
MEDICATIONS
Trauma
▪ External ear
▪ Complete external auditory canal occlusion
▫ Mild: topical acidifying agent,
Tumors of middle ear glucocorticoid
▪ Cholesteatomas (most common overall) ▫ Moderate/severe: topical/oral antibiotics
▫ Desquamated, stratified, squamous ▪ Middle ear
epithelium in middle ear space ▫ Pain control (e.g. ibuprofen,
▫ Accumulation → erosion of middle acetaminophen), antibiotics
ear contents (ossicular chain) →
surrounding structures: external SURGERY
auditory canal (EAC), mastoid bone ▪ External ear
▪ Squamous cell carcinoma (most common ▫ If repeat infections/↑ size
malignant tumor)
▪ Middle ear
Tympanic membrane perforation ▫ Tissue graft
▪ Common; due to trauma/barotrauma to ear/ ▫ Surgical removal
face
OTHER INTERVENTIONS
SIGNS & SYMPTOMS ▪ External ear
▫ Cerumenolytics/irrigation/manual
▪ Decreased perception of sound removal
▫ Especially poor perception of low- ▫ Repeat infections/↑ size: EAC occlusion
frequency sound ▪ Middle ear
▫ Overcome by volume of stimulus ▫ Hearing aids

DIAGNOSIS
OTHER DIAGNOSTICS
▪ History, associated symptoms
▪ Otoscopy
▪ Special testing
▫ Weber (localization of vibration to
affected ear)
▫ Rinne (abnormal; bone conduction > air
conduction)
▪ Audiogram
▫ Universal/low-frequency deficit in pure
tone discrimination

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SENSORINEURAL HEARING LOSS
osms.it/sensorineural-hearing-loss

▪ Unilateral, episodic loss concurrent with


PATHOLOGY & CAUSES tinnitus, vertigo
▫ Pathogenesis: unknown; possible
▪ Disability of inner ear (cochlea/CN VIII)
infection, autoimmune, vascular
to transduce sound waves → viable
constriction, congenital malformation
neurologic input → brain
→ endolymphatic hydrops (e.g.
overproduction of endolymph,
CAUSES distension of endolymphatic space)

Central nervous system (CNS) Noise-induced


▪ Acoustic neuroma (CN VIII; AKA vestibular ▪ Cause: chronic exposure to loud (> 85dB)
neuroma) auditory stimuli
▫ ↑ size → compress cerebellum → ataxia ▪ Pathogenesis: overstimulation of hair cells
▪ Meningitis in organ of Corti → nitric oxide, free radical
▫ Infection (via cerebrospinal fluid) → release → damage, death of hair cells
cochlea → cochleitis → direct damage ▪ ↓ Mg2+ → ↓ Ca2+ intracellular concentration
to inner hair cells → ↑ cell damage, death
▪ Meningioma Presbycusis
▪ Acoustic nerve neuritis ▪ Most common
▫ Multiple sclerosis, syphilis ▪ Gradual, symmetric hearing loss in elderly
Congenital ▪ More significant loss with higher
▪ Spontaneous/genetic frequencies
▪ Acquired ▪ Pathogenesis: degeneration of hair cells at
base of cochlea
▫ Toxoplasmosis, other (syphilis,
varicella-zoster, parvovirus B19), Trauma
rubella, cytomegalovirus (CMV), herpes ▪ Skull fracture → injury to CN VIII/cochlea
(TORCH) infections

Drug-induced
SIGNS & SYMPTOMS
▪ Aminoglycoside antibiotics (most common);
cisplatin
▪ Decreased perception of sound (esp. high-
▪ Aspirin (high-dose 6–8g/day), quinidine, pitched sounds, speech discrimination)
loop diuretics (e.g. furosemide, ethacrynic
acid) → reversible hearing loss, tinnitus

Inner ear infection


DIAGNOSIS
▪ Labyrinthitis (inflammation, spinning,
DIAGNOSTIC IMAGING
ringing)
MRI
Menière’s disease
▪ Identifies causes such as acoustic neuroma,
▪ Rare
perilymphatic fistula

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OTHER DIAGNOSTICS ▪ Antibiotics


▪ History, associated symptoms ▫ Meninges
▪ Otoscopy
▫ Rules out causes of conductive hearing SURGERY
loss ▪ Surgical resection
▪ Special testing ▫ Acoustic nerve
▫ Weber: lateralization of sound to
unaffected ear
▫ Rinne: air, bone conduction (AC > BC)
OTHER INTERVENTIONS
▪ Hearing aids
▪ Audiogram
▫ Hair cells of organ of Corti
▫ Identifies deficit in high-pitched pure
tone discrimination ▪ Dietary changes (↓ Na+)
▫ Endolymph of labyrinthine systems
▪ Radiotherapy
TREATMENT ▫ Acoustic nerve

▪ Specific to underlying etiology

MEDICATIONS
▪ Antiemetics, vestibular suppressants (e.g.
benzodiazepines), diuretics
▫ Endolymph of labyrinthine systems

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