Deafness Flashcards

1
Q

congenital causes central

A

hyperbilirubinaemia/kernicterus; hypoxia

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2
Q

congenital causes conductive

A

abnormalities of pinna, external ear canal, drum ossicles; cholesteatoma

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3
Q

congenital causes sensorineural

A

genetic- Alports, Turners; infections- CMV, syphilis, HIV; ototoxic drugs

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4
Q

perinatal and postnatal causes

A

anoxia, birth trauma, cerebral palsy, kernicterus, meningitis, ototoxic drugs, lead, skull fracture

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5
Q

what is the hearing test for new borns

A

universal newborn hearing screening- otoacoustic emissions, ABR (audiological brainstem response)

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6
Q

management childhood deafness

A

hearing aids, cochlear implants

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7
Q

how can you prevent post implant meningitis after cochlear implant

A

pneumococcal vaccine 2 weeks before cochlear implant

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8
Q

what age can you use pure tone audiogram to test the childs hearing

A

5 years

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9
Q

what type of hearing air can be used to augment bone conduction

A

BAHA- bone anchored hearing aid

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10
Q

where is the anatomy for conductive hearing loss

A

pinna to oval window, foot of the stapes

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11
Q

where is the anatomy for sensorineural hearing loss

A

oval window to auditory cortex

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12
Q

causes of conductive loss in adults

A

external canal obstruction- wax, pus, debris, FB; drum perf- trauma, barotrauma, infection; ossicular chain- otosclerosis, infection, trauma

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13
Q

causes of sensorineural loss in adults

A

ototoxic drugs, post infective (meningitis, measles, mumps, flu, herpes); Menieres, trauma

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14
Q

management deafness in adults

A

hearing aid, cochlear implant, surgery

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15
Q

what drugs are ototoxic

A

vancomycin, gentamicin, streptomycin, chloroquine, hydroxychloroquine

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16
Q

rare causes deafness in adults

A

acoustic neuroma, B12 def, MS, carcinoma in brain

17
Q

how is sensorineural sudden deafness defined

A

> 30db loss in 3 pure tone, over

18
Q

how often is cause found in sensorineural sudden deafness

A

10% of the time

19
Q

how often is a cause found in conductive sudden deafness

A

all the time- occlusion infection trauma fracture

20
Q

what is otosclerosis

A

replacement normal bone with vascular spongy bone. autosomal dominant, FHx in 50% cases.

21
Q

symptoms otosclerosis

A

conductive hearing loss. appears early adult life, worse in pregnancy, menstruation, menopause. can get tinnitus, vertigo

22
Q

signs otosclerosis

A

10% have Schwartzs- pink tinge to the drum. Caharts notch on audiogram- dip at 2kHz

23
Q

treatment otosclerosis

A

fluoride. hearing aid or surgery, cochlear implant

24
Q

what is presbyacusis

A

age related hearing loss from accumulated environmental noise toxicity

25
Q

what do you lose in presbyacusis

A

loss of high frequency sounds starts before 30years, deafness is gradual and often don’t notice for a while. hearing aids

26
Q

what should you think of in sensrineural unilateral deafness

A

acoustic neuroma

27
Q

what is an acoustic neuroma

A

benign tumour. behave as SOL

28
Q

symptoms acoustic neuroma

A

ipsilateral tinnitus and sensorineural hearing loss. giddiness common, vertigo rare

29
Q

cranial nerves at risk in acoustic neuroma

A

V, VI,VII

30
Q

tests in acoustic neuroma

A

MRI- in all with unilateral deafness/tinnitus

31
Q

DDX acoustic neuroma

A

meningioma