Short 10 Min Presentation on Speech Audiogram & Audiometry. Delivered by Abubakkar Raheel (4th Year Mbbs)
Frontier Medical College, Abbottabad, Pakistan.
Short 10 Min Presentation on Speech Audiogram & Audiometry. Delivered by Abubakkar Raheel (4th Year Mbbs)
Frontier Medical College, Abbottabad, Pakistan.
Auditory brainstem response (ABR)
Approximately 1 of every 1000 children is born deaf. Many more are born with less severe degrees of hearing impairment, while others may acquire hearing loss during early childhood.
combination of technological advances in ABR and otoacoustic emissions (OAE) testing methods are used for evaluation of hearing in newborns.
Perilymph Fistula can be difficult to diagnose as a standalone condition. Post-trauma symptoms such as dizziness, headache, etc. can be linked to other conditions like a traumatic brain injury with a concussion.
Auditory brainstem response (ABR)
Approximately 1 of every 1000 children is born deaf. Many more are born with less severe degrees of hearing impairment, while others may acquire hearing loss during early childhood.
combination of technological advances in ABR and otoacoustic emissions (OAE) testing methods are used for evaluation of hearing in newborns.
Perilymph Fistula can be difficult to diagnose as a standalone condition. Post-trauma symptoms such as dizziness, headache, etc. can be linked to other conditions like a traumatic brain injury with a concussion.
description of various audiological assessment tests at bedside and via instruments for measurement of degree of hearing loss and help in identifying cause for hearing loss and type of hearing loss.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
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Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
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TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
2. INTRODUCTION
• HEARING LOSS : Impairment of hearing
• Characterised by :
Type – Conductive, Sensorineural, Mixed
Location of cause – External ear, Middle ear, cochlea, auditory nerve,
central cause
Onset – Insidious or Sudden
Rate of progression
Degree of loss – Mild, moderate, moderately severe, severe, profound
Unilateral or Bilateral
3. CLASSIFICATION OF HEARING LOSS
HEARING LOSS
ACQUIRED
ORGANIC FUNCTIONAL
CONGENITAL
CONDUCTIVE SENSORINEURAL MIXED
7. CONGENITAL SENSORINEURAL HEARING
IMPAIRMENT
• MICHEL APLASIA : Complete lack of development of inner ear
• MONDINI DYSPLASIA : Incomplete development of bony and
membranous labyrinth
• SCHEIBE DYSPLASIA : Cochleosaccular aplasia with normal bony labyrinth
• BING – SIEBENMANN DYSPLASIA : Malformation of membranous
labyrinth with a normal osseous labyrinth
• ALEXANDER DYSPLASIA : Affects only the basal turn of membranous
cochlea. High frequencies are affected
8. ACQUIRED CAUSES OF CONDUCTIVE HEARING
LOSS
• EXTERNAL EAR :
Obstruction of EAC Wax, foreign body, furuncle, benign or malignant tumour,
atresia of canal
• MIDDLE EAR :
Perforation of tympanic membrane – Traumatic or infective
Fluid in middle ear – Acute otitis media, serous otitis media, hemotympanum
Disruption of ossicles – Trauma, CSOM, cholesteatoma
Fixation of ossicles – Otosclerosis
Eustachian tube blockage – serous otitis media, retracted tympanic membrane
9. ACQUIRED CAUSES OF SENSORINEURAL HEARING LOSS
• Infections of labyrinth – Viral, bacterial, spirochaetal
• Trauma to labyrinth or VIII nerve – Fracture of temporal bone
• Noise induced hearing loss
• Ototoxic drugs
• Presbycusis
• Meniere’s disease
• Acoustic neuroma
• Sudden hearing loss
• Familial progressive sensorineural hearing loss
• Systemic disorders – Diabetes, Hypothyroidism, autoimmune disorders,
multiple sclerosis etc.
11. EXAMINATION
• Pinna , Pre-auricular and Post-auricular regions
• External auditory canal
• Tympanic membrane
• Middle ear
• Mastoid
• Eustachean tube
• Facial nerve
12. CLINICAL TESTS OF HEARING
• FINGER FRICTION TEST : Rough method of screening. Snapping the
fingers close to the patient’s ear
• WATCH TEST : Clicking watch brought close to the ear and the distance at
which it is heard is measured. Obsolete now
• SPEECH / VOICE TESTS :
Normal person hears conversational voice -12m, whisper -6m
Test conducted in reasonably quite surroundings
Patient’s eyes are shielded
Test ear towards examiner at a distance of 6m
Distance at which conversational and whispered voice are heard is
measured
13. TUNING FORK TESTS
• RINNE’S TEST
• WEBER’S TEST
• ABSOLUTE BONE CONDUCTION TEST
• SCHWABACH’S TEST
• BING TEST
• GELLE’S TEST
14. TUNING FORK TESTS(cont.)
• Tuning fork was invented by John Shore in 1711.
• These tests are qualitative tests as these indicate the type of hearing loss.
• Tuning forks emit pure tones and allow comparison of air conduction with
bone conduction.
• Tests are done with various tuning forks, but 512 Hz is the most
commonly used as its rate of tone decay is not rapid and sound is quite
distinct from ambient noise.
• Higher frequencies decay faster and with lower frequencies, patient
perceives the vibrations more than the sound.
• The tuning fork should be held firmly by the stem and struck lightly
against resilient surface such as elbow, heel of the hand or the ‘padded’
edge of a table.
15. TUNING FORK TESTS(cont.)
• Air conduction (AC) is tested by placing the tuning fork 1/2 to 1 inch in front of
and parallel to the external acoustic meatus. It indicates the integrity of
tympano-ossicular chain. Air conduction (AC) is better termed as Ossicular
conduction. Bone conduction (BC) is tested by placing the base of tuning fork
on mastoid bone or on the forehead.
• BC signifies sound conduction through cochlea, auditory nerve and its central
connections and hence provides information about the integrity of inner ear.
a. BC signifies sound conduction through cochlea, auditory nerve and its
central connections and hence provides information about the integrity
of inner ear.
b. Sound through BC is transmitted by vibration of skull bones or through
one is own voice.
• Two different types of vibration occur, i.e.
a. Inertial type (below 800) when skull vibrates as one unit and lagging
behind of ossicles, mandible and cochlear fluid occurs due to inertia.
b. Compression type (for frequency above 800) in this the vibrations act
on the fluids of inner ear and cause its movements.
16.
17. RINNE’S TEST
• Air conduction of the ear is compared with it’s bone conduction
• A vibrating tuning fork is placed on the patient’s mastoid and when he
stops hearing, it is brought beside the meatus
• If he still hears, AC > BC
• Positive Rinnes’ (AC > BC) Normal hearing, Sensorineural hearing loss
• Negative Rinne’s (BC > AC) Conductive hearing loss
18. RINNE’S TEST(cont.)
• Prediction of air-bone gap with tuning forks of frequency 256, 512
and 1024 Hz
• Rinne negative for 256, positive for 512 AB gap of 20-30 dB
• Rinne negative for 256 and 512, positive for 1024 AB gap of 30-45 dB
• Rinne negative for all three tuning forks, 256, 512 and 1024 Hz AB gap
of 45-60 dB
19. RINNE’S TEST(cont.)
• Seen in severe unilateral sensorineural hearing loss
• Does not perceive sound by air conduction, responds to bone
conduction
• Bone conduction response from opposite ear due to transcranial
transmission of sound
• Correct diagnosis by masking the non-test ear with Barany’s noise
box
20. WEBER’S TEST
• Vibrating tuning fork placed on the middle of the forehead or vertex
• Sound travels directly to the cochlea via bone
• Patient is asked in which ear is the sound heard
• Normal – Equal on both sides
• Conductive deafness
Lateralised to worse ear
• Sensorineural deafness
Lateralised to better ear
21. ABSOLUTE BONE CONDUCTION TEST
• Patient’s bone conduction is compared with that of the examiner
• EAC of patient and examiner is occluded – to prevent ambient noise
entering through air conduction
• Conductive deafness – Bone conduction is same as that of examiner
• Sensorineural deafness – Bone conduction is reduced compared to
examiner
22. SCHWABACH’S TEST
• Bone conduction of patient compared to examiner
• EAC is not occluded
• Conductive deafness – Bone conduction equal to that of examiner
• Sensorineural deafness – Bone conduction reduced compared to
examiner
23. BING TEST
• Test of bone conduction
• Examines the effect of occlusion of ear canal on hearing
• Vibrating tuning fork placed on mastoid. The examiner alternately closes
and opens the ear canal by pressing on the tragus inwards
• Bing Positive : When sound is louder with the ear canal occluded. In
normal hearing and sensorineural hearing loss
• Bing negative : No change in loudness with the canal occluded. In
conductive hearing loss
24. GELLE’S TEST
• Test of bone conduction
• Examines the effect of increased air pressure in ear canal on hearing
• Vibrating tuning fork is placed on the mastoid. Changes in air pressure in
EAC brought about by Siegel’s speculum
• Gelle’s positive – Decreased hearing on on increased pressure. In normal
individuals and sensorineural hearing loss
• Gelle’s negative – No change in hearing on increased pressure. Seen in
ossicular chain fixation (Otosclerosis) or disruption
26. PURE TONE AUDIOMETRY
•Hearing sensitivity of a subject for pure tone sounds
•Pure tone : Sound sensation produced by the
sinusoidal wave pattern when an object vibrates in
a fixed single frequency
•Complex sound: Sound of various frequencies and
intensities – mixture of different pure tone sounds
•Audiometer: An electronic device that consists of an
audio-oscillator which generates pure tone sounds
of various frequencies
27. AIMS OF PURE TONE AUDIOMETRY
•If the subject has any definite auditory disorder
•If the hearing loss is conductive / sensorineural /
mixed
•If sensorineural, whether it is cochlear or
retrocochlear
•Degree of hearing dysfunction
28. Advantages OF PURE TONE AUDIOMETRY
•Pure tone audiometry is a reliable method of
testing the hearing acuity and gives information
about the quantity and quality of hearing loss
•In some cases, pattern of curve points towards a
disease such as otospongiosis, acoustic trauma,
Ménière’s disease and presbycusis.
•Test record is good for future reference.
•To know the degree of hearing handicap and for
prescribing a hearing aid.
•Also helps to find out speech reception threshold.
•Medicolegal purposes.
29. MASKING
• In pure tone audiometry, the exact hearing threshold by air
and bone conduction for different frequencies in each ear
should be calculated separately and individually
• When sound is presented to one ear, a part of it travels to
the other ear and stimulates it too
• To overcome the problem of cross-hearing, the non-test /
better ear should be masked
30. WHEN TO MASK
• Cross hearing should be suspected when air conduction values in
the test ear are above 40 – 45 dB (as the lower limit of interaural
attenuation is around 40 – 45 dB)
• During air conduction – contralateral ear should always be
masked if tones of 45 dB and more are used
• During bone conduction, both cochlea are stimulated equally.
Hence, the non-test ear should always be masked during bone
conduction
31. AMOUNT OF MASKING SOUND REQUIRED
•The non-test ear is masked by presenting a ‘noise’ that
is loud enough to prevent the tone from test ear
stimulating the non-test ear, but not so loud that it will
mask the sensitivity of the test ear
•Intensity of the masking sound Should neither
undermask nor overmask
32. SOUNDS USED FOR MASKING
• WHITE NOISE : Broadband or wideband noise. Equal amount of sound of
all frequencies
• NARROW BAND NOISE : More effective. Narrow band of noise centered
on the test tone frequency with 100 to 200 Hz above and below that
frequency. The masking noise varies for each frequency. The band width
which will provide the maximum effective masking for a tone of a
particular frequency at minimum intensity is called critical band width for
that particular frequency
• COMPLEX NOISE : Made up of a low frequency fundamental plus the
multiples of that frequency up to 4000 Hz
33. INTERPRETATION OF AUDIOGRAMS
• WHO classification on the basis of pure tone average of the
thresholds for frequencies 500, 1000, 2000 Hz
• DEGREE OF HEARING LOSS :
0 to 25 dB : Normal for all practical purposes
26 to 40 dB : Mild deafness
41 to 55 dB : Moderate deafness
56 to 70 dB : Moderately severe deafness
71 to 90 dB : Severe deafness
Above 90 dB: Profound deafness
34. LIMITATIONS OF PURE TONE AUDIOMETRY
• Subjective test
• Patient should understand the instructions – cannot be done in
children and psychiatric patients
• Not accurate for medico-legal purposes if malingering is suspected
• Does not evaluate the properties of supra threshold hearing, like
frequency discrimination and temporal resolution of sound
• Does not identify the exact nature of the pathology
42. BEHAVIORAL TESTS
• The portion of the auditory system from the auricle to the
cochlea – Peripheral auditory system
• The peripheral part can be assessed by different behavioural
tests namely :
1.Threshold Tone Decay Test
2.Short Increment Sensitivity Index
3.Alternate Binaural Loudness Balance test
These tests are subjective tests
43. TONE DECAY TEST
•Helps in the detection of site of pathology in the
sensorineural pathway
•Pathology in the auditory nerve causes an abnormally
rapid deterioration in the threshold of hearing of a tone
if that tone is presented continuously (as a sustained
signal) to the ear
•In TDT, the rapidity of this deterioration is measured
•Principle : Wedensky’s peripheral nerve inhibition
44. TONE DECAY TEST(cont.)
Various methods of measuring tone decay :
1.CARHART’S METHOD : Most popular
2.GREEN’S MODIFIED METHOD
3.OLSEN AND NOFFSINGER METHOD
4.ROSENBERG’S METHOD
5.SUPRATHRESHOLD ADAPTATION TEST
45. INTERPRETATION OF TONE DECAY
• Normal – if decay is 0 – 5 dB
• Mild – if decay is 10 – 15 dB
• Moderate – if decay is 20 -25 dB
• Severe – if decay is 30 dB and above
Tone decay in excess of 30 dB should arouse a
suspicion of a retro cochlear lesion and the patient should be
subjected to a detailed neuro-otological examination including :
acoustic reflex decay, brainstem evoked response audiometry,
CT and MRI.
46. RECRUITMENT
• Coined by Fowler in 1937
• Defined as abnormally steep growth of loudness with increasing
intensity and is usually associated with a sensorineural deafness
due to a cochlear pathology
• Recruitment is a normal phenomenon in high intensities of sound.
Recruitment is present in all ears when sounds of high intensity
are used – normal ear or with cochlear pathology
• Recruitment is not present in a case of retrocochlear pathology –
accounted for by the defective transmission in a diseased auditory
nerve
• Presence or absence of recruitment can be directly tested by –
ALTERNATE BINAURAL LOUDNESS BALANCE test – Described by
Fowler
• Indirect test for recruitment – SHORT INCREMENT SENSITIVITY
INDEX – First described by Jerger, Sheld and Harford in 1959
47. SHORT INCREMENT SENSITIVITY INDEX
• Determines the capacity of the patient to detect a brief 1 dB increment
in a 20 dB suprathreshold tone (carrier tone) in various frequencies
• Usually tested at 1000 and 4000 Hz, but any frequency above 250 Hz
may be used
• At intervals of 5 seconds a brief increase in the intensity of the carrier
tone occurs
• This increase in intensity may be varied from 6 dB to 1 dB
• The increase takes 50 ms, remains at the specified level for 200 ms and
returns to original carrier tone in 50 ms
• Twenty such 1 dB increments are presented to the ear and the patient is
asked to count the number of increments he could correctly identify
• This multiplied by 5 gives the percentage SISI score
• The patient is initially familiarised with increments of 6dB, 5 dB etc.
before starting the test with 1 dB increment
48. INTERPRETATION OF SISI TEST
•Scores between 70% to 100% - Positive SISI –
Indicates a cochlear lesion
•Scores between 0% to 20% - Negative SISI –
Suggests a retrocochlear pathology. But may also be
seen in ears with normal hearing or with conductive
deafness
49. ALTERNATE BINAURAL LOUDNESS BALANCE TEST
• Requires specially designed audiometers which can
alternately send two tones of the same frequency in the two
ears
• The tone stays for a duration of ½ to 1 second in each ear,
but the duration must be equal in the two ears
• Intensity is controlled by 2 separate attenuators for each ear
• The patient is instructed to indicate in which ear the sound
appears to be louder and ultimately say when the sound in
the two ears appear to be of equal loudness
• Results are plotted as a graph – poorer ear data on the
abscissa and better ear data on the ordinate
50. INTERPRETATION OF ABLB
One of the following four possibilities :
1. Absence of recruitment : Equal loudness at equal sensation levels
2. Complete recruitment : Equal loudness at equal intensities or
equal hearing levels
3. Partial recruitment : Difference in the hearing level between the
two ears for equal loudness gradually diminishes with increasing
intensities but the difference never becomes zero
4. Decruitment or Loudness reversal : When the growth in loudness
in the poorer ear is slower than in the better ear – there is
decruitment
51. LIMITATION OF ABLB
•Can be carried out when there is a substantial
difference in hearing level between the two ears
•Suitable for cases of unilateral deafness
•To overcome this, Monoaural Loudness Balance test
(MLB) was devised
•Can be done in bilateral symmetrical deafness
•Measures the growth in loudness between two
frequencies in the same ear
52. IMPEDANCE AUDIOMETRY
• The test measures the impedance of middle ear system at the
level of tympanic membrane due to changes in air pressure in
external auditory meatus.
• It consists of:
1. Tympanometry
2. Acoustic reflex audiometry.
• Advantages of Impedance Audiometry
1. Differential diagnosis of conductive and SNHL.
2. To find out the differential diagnosis of conductive hearing
loss. 3. To know the site of lesion in facial nerve palsy.
4. To test hearing acuity in infants and children.
5. To find out malingers.
6. To find out lesions of brainstem.
53. TYMPANOMETRY
• Tympanometry is an objective audiometry and measures the impedance
(means resistance) offered by the middle ear conducting apparatus such as
tympanic membrane (TM) and ossicular chain and also the compliance
(suppleness) to sound pressure transmission.
• It consists of the following:
A probe fitted into external auditory meatus connected to an oscillator,
which gives sound at 220 Hz
An air pressure pump,which is used to alter the pressure in the meatus
A microphone
• Principle : Sound strikes tympanic membrane some energy is absorbed, rest
is reflected.
• Stiffer tympanic membrane reflects more sound than a compliant one
• By changing the pressure in a sealed external auditory canal and measuring the
reflected sound energy, it is possible to find the compliance / stiffness of the
tympano-ossicular system healthy or diseased status of the middle ear
54. PATHOLOGIES WITH INCREASED COMPLIANCE
•Ossicular discontinuity
•Scarring of the tympanic membrane
•Post stapedectomy ear
•Very large tympanic membrane – very rare
55. PATHOLOGIES WITH DECREASED COMPLIANCE
•Otosclerosis
•Adhesive or secretory otitis media
•Tumours in the middle ear – glomus jugulare
•Ossicular fixations – fixed malleus syndrome
•Thickening of the tympanic membrane
56. PATHOLOGIES WITH NORMAL COMPLIANCE
•Eustachian tube obstruction only, without secretory
changes in the middle ear
•Some cases of otosclerosis
57. TYPES OF TYMPANOGRAMS
• TYPE A : Peak is near 0 pressure.
• TYPE As : Peak is at 0 but amplitude of the peak is low. Due
to incresed stiffness of the system
• TYPE Ad : Peak is around 0 but amplitude is abnormally high.
System is more compliant than normal
• TYPE B : Flat or dome shaped curve denoting that pressure
changes do not have much effect on the compliance
• TYPE C : Peak is shifted to the negative side
58. SIGNIFICANCE OF TYMPANOGRAMS
•TYPE A : Normal tympanogram
•TYPE As : Otosclerosis, tympanosclerosis, thick graft
in myringoplasty
•TYPE Ad : Ossicular discontinuity, flaccid tympanic
membrane
•TYPE B : Impacted wax, foreign body, secretory
otitis media, adhesive otitis media
•TYPE C : Retracted tympanic membrane
59.
60.
61. ACOUSTIC / STAPEDIAL REFLEX TESTS
•Objective test, non-invasive, simple to perform and
requires very little time (few minutes)
•Helps in the following :
1. Elimination of middle ear pathology
2. Differentiation of cochlear from retrocochlear pathology
3. Objective estimation of average hearing threshold level
4. Detection of non-organic hearing loss
5. Identifying the level of lesion in facial nerve paralysis
6. Hearing acuity in infants and children.
62. ACOUSTIC / STAPEDIAL REFLEX TESTS(cont.)
PRINCIPLE:
• When a loud sound reaches the ear (70 -100 dB above the
hearing threshold), the intra-aural muscles, STAPEDIUS and
TENSOR TYMPANI contract reflexly
• The net result of the contraction of the muscles leads to
stiffening of the middle ear conductive apparatus and
changing the impedance of the middle ear system
• Stapedius is innervated by branch of facial nerve. Tensor
tympani by mandibular branch of trigeminal nerve
• For all practical purposes, changes in impedance of the
middle ear are caused by contraction of stapedius muscle
only
63. ABSENCE OF ACOUSTIC REFLEX
Disorders on the afferent side :
• Disease in the ipsilateral middle ear
• Lesion in the ipsilateral cochlea or 8th cranial nerve
• Lesion in the cochlear nucleus or superior olivary complex
Disorders on the efferent side :
• Lesion in the facial nerve nucleus in brainstem
• Facial nerve palsy at a level proximal to the nerve to stapedius –
Ramsay Hunt syndrome
• Disease of stapedius muscle – myasthenia gravis
• Lesion in the middle ear – otosclerosis, ossicular discontinuity,
atelectasis
64. EUSTACHIAN TUBE FUNCTION TEST
• Physiological functions of the eustachian tube :
1.Maintenance of equality of air pressure between the middle
ear and the ambient atmosphere – VENTILATORY
FUNCTION (major)
2.Drainage of the mucous from the ear to the nasopharynx –
MUCOCILIARY CLEARANCE FUNCTION
• Muscles causing intermittent opening of the eustachian tube –
Tensor palatini and levator veli palatini – contract during
swallowing
65. EUSTACHIAN TUBE FUNCTION TEST(cont.)
Modern impedance audiometers can test eustachian
tube function by 2 methods :
1. WILLIAM’S TEST : Test of tubal function in subjects
with an intact tympanic membrane
2. TOYNBEE’S TEST : Test of tubal function in subjects
with perforated tympanic membrane
66. EUSTACHIAN TUBE FUNCTION TEST(cont.)
WILLIAM’S TEST :
• Measures middle ear pressure in 3 conditions – At the start
of the test (resting pressure), after the patient swallows
(with nose and mouth closed), after performing Valsalva
• Normally, the ambient middle ear pressure should be at or
near atmospheric pressure, should become negative on
swallowing and positive on performing Valsalva
• Any deviation from this - Abnormal
67. EUSTACHIAN TUBE FUNCTION TEST(cont.)
TOYNBEE’S TEST :
• Done in patients with perforated tympanic membrane
• The audiometer is programmed to artificially increase or
decrease the air pressure in the middle ear each time the
patient swallows
• Advantage : Can be done on a pressure differential – positive
pressure at the tympanic end of the tube and ambient
pressure at the nasopharyngeal end of the tube
• Air pressure at the middle ear end of the eustachian tube is
first changed to either +250 or -250 mmof water. Patient is
asked to swallow repeatedly. Normally, the positive or
negative pressure should be totally neutralised in 3-5
swallows. If not – impaired tubal function
68. BRAINSTEM EVOKED RESPONSE AUDIOMETRY
• Introduced by Jewitt in 1970
• Non-invasive objective audiological investigation
• PRINCIPLE : Sound waves entering cochlea are transduced to
electric potentials and transmitted via VIII nerve through
brainstem and then to the auditory cortex
• Passage of the impulse through the auditory pathway
generates an electrical activity
• These electrical responses are picked up by surface
electrodes and represented graphically
• Each wave in the graph is generated by major processing
centers of the auditory system
69. BERA
• Pure tone audiogram should preferably be done prior to
BERA because, the sound stimulus has to be presented at a
fixed suprathreshold level (usually 60 dB above threshold)
and also the interpretation of BERA is dependent on
audiometric contour
• Sound stimulus : Broad band click of 100 microseconds
duration
• Broadband click stimulated synchronously a large number of
neurons and elicits a BERA tracing which is clear, sharp and
well marked with distinctly recognisable peaks in the graph
72. WAVES IN BERA
WAVE SITE OF NEURAL GENERATOR
WAVE I Cochlear nerve (distal end)
WAVE II Cochlear nerve (proximal end)
WAVE III Cochlear nucleus
WAVE IV Superior olivary complex
WAVE V Lateral lemniscus
WAVE VI & VII Inferior colliculus
74. CLINICAL USES OF BERA
• Estimation of hearing threshold
• Diagnosis of lesions of VII cranial nerve
• Identification of nature of deafness
• Screening procedure for infants
• To diagnose brainstem pathology. Ex: multiple sclerosis or pontine
tumours
• To monitor VIII cranial nerve intraoperatively in surgery of
acoustic neuromas to preserve the function of VIII nerve
75. OTOACOUSTIC EMISSIONS
• They are low intensity sounds produced by outer hair cells of
a normal cochlea due to their biological activity
• Can be picked up, recorded and measured by placing a
microphone – receiver in the deep external meatus
• Direction of travel of OAE : Outer hair cells basilar
membrane Perilymph Oval window Ossicles
Tympanic membrane Ear canal
76. OTOACOUSTIC EMISSIONS(cont.)
Types of OAE
1. Spontaneous OAEs—arise from outer hair cells,
inhibited by ototoxic drugs.
2. Stimulus frequency OAEs—technically difficult to
record.
3. Transient evoked OAEs—elicited in response to
transient clicks.
4. Distortion product OAEs—in response to
simultaneous tones.
77. OTOACOUSTIC EMISSIONS(cont.)
Uses of OAE:
1. These are very useful in ‘screening of neonates and high risk
infants’ for hearing loss.
2. Diagnosing central processing auditory disorders, particularly
auditory neuropathy.
3. Differentiate cochlear from retrocochlear pathology.
4. Detect early changes in ototoxicity and noise induced hearing
loss.
5. To monitor Ménière’s disease.
6. Malingerers.
7. Provides objective confirmation of cochlear dysfunction in
tinnitus.
78. VESTIBULAR FUNCTION TESTS
• Derangement of vestibular system is indicated by
Vertigo and
Nystagmus, which is defined as involuntary, rhythmical,
oscillatory movements of eyes away from the
direction of gaze.
• Nystagmus of vestibular origin has 2 components:
• Slow component and quick (fast/corrective)
component and by convention, nystagmus is
named after quick component – Right or Left
• Quick component of nystagmus is eliminated when
the patient is put under anesthesia.
79. VESTIBULAR FUNCTION TESTS(cont.)
Degrees of Nystagmus
• First degree is a weak nystagmus and it is present whenthe patient
looks in the direction of quick component
• Second degree nystagmus appears when the patient is looking
straight ahead.
• Third degree nystagmus (severe) appears when the patient is looking
towards slow component.
80. VESTIBULAR FUNCTION TESTS(cont.)
Types of Nystagmus
• Central It is coarse, irregular and does not fatigue. It can be in any
direction. Vertigo is usually not present. Symptoms and signs of
intracranial disease are present.
• Ocular It is of congenital type and is pendular. Paralysis of external
rectus may simulate nystagmus.
• Vestibular It is rhythmic, has a slow and fast component, fatigues
easily, vertigo is present, duration is of less than 1 minute and
latency is 2 to 20 second. It can be spontaneous, positional or
induced.
• Spontaneous nystagmus It is horizontal, rotatory or mixed type and
does not last for more than 3 weeks and vertigo is also present.
81. VESTIBULAR FUNCTION TESTS(cont.)
Types of Nystagmus
• Positional nystagmus
• It appears and reappears when the head is put in the same
position.
• Vertigo is not much and it may be because of vestibular or
central causes
• A nystagmus, which is fatigable and short lasting is usually of
peripheral origin and the one not fatigable and with
changing direction is of central type.
• Induced nystagmus This type of nystagmus can be induced by
rotation in a chair, thermal stimuli (caloric test) or by visual
stimulation such as looking at a series of objects moving from
one side to other.
82. ASSESSING THE DEAF CHILD
Objectives :
• To ascertain whether the child has any deafness or not
• If deafness is present, whether unilateral or bilateral
• To document the degree of functional impairment for each
ear
• To establish a topographical localisation of the lesion
• To establish an etiological diagnosis
• To establish management protocols
83. ASSESSING THE DEAF CHILD(cont.)
• A detailed history is essential – Prenatal, perinatal or
postnatal causes, family history
• A detailed physical and otologic examination and
investigations depending on the cause suspected
• Suspicion of hearing loss when
a.Child sleeps through loud noises unperturbed
b.Fails to startle to loud sounds
c.Fails to develop speech at 1 – 2 years
84. ASSESSMENT OF HEARING IN INFANTS AND CHILDREN
BEHAVIOUR TESTS :
• Auditory signals presented to an infant produces a change in
behaviour – Alerting, cessation of activity, widening of eyes
or facial grimacing
• MORO’S reflex : Sudden movement of limbs and extension
of head in response to sound of 80 – 90 dB
• COCHLEOPALPEBRAL reflex : Child responds by a blink to a
loud sound
• CESSATION reflex : Child stops activity or starts crying in
response to a loud sound
85. ASSESSMENT OF HEARING IN INFANTS AND
CHILDREN(cont.)
DISTRACTION TECHNIQUES :
Used in children 6 – 7 months old.
Child turns his head to locate the source of sound
CONDITIONING TECHNIQUES :
1. Visual reinforcement audiometry
2. Play audiometry
3. Speech audiometry
86. ASSESSMENT OF HEARING IN INFANTS
AND CHILDREN(cont.)
OBJECTIVE TESTS :
• EVOKED RESPONSE AUDIOMETRY :
1.Electrocochleography
2.Brainstem Evoked Response Audiometry
• OTOACOUSTIC EMISSIONS
• IMPEDANCE AUDIOMETRY