2. BAEPs
BAEPs are responses of the auditory
nerve, brainstem, and, perhaps, higher
subcortical structures to acoustic
stimulation.
Most of its components appear to arise
from multiple sources, preventing a
simple one-to-one correspondence
between potential generators and
individual BAEP waves.
3. BERA, CONTâD
The term brainstem auditory evoked potentials,â is
somewhat inappropriate in that
(1) the first component of the âbrainstem
auditory evoked potentialsâ does not arise in the
brainstem but in the auditory nerve; and
(2) the latest components may or may not
originate, at least in part, above the brainstem.
⢠Although the pathways is mainly along the
brainstem and some of the potentials are
assumed to be generated from it, so called BAEP.
4. The Auditory system
⢠In order to know about the potentials of
BAEPs one must aware about the
anatomy and physiology of auditory
system which is mainly about the
following two components.
⢠The Peripheral Auditory System (The
EAR)
⢠The Central Auditory System (The Brain)
5. 1. The Peripheral Auditory System (The
EAR).
The components are,
Outer Ear: The folds of cartilage surrounding the ear canal
are called the pinna, which amplifies the sounds .
Middle Ear: The sound wave information travels across
the air-filled middle ear cavity via a series of delicate
bones:
⢠Malleus (Hammer), Incus (Anvil) and Stapes (Stirrup)
which are mainly responsible to convert the lowerpressure eardrum sound vibrations into higher-pressure
sound vibrations at another, smaller membrane called
the oval (or elliptical) window.
7. Inner Ear
â˘
The inner ear consists of the cochlea and several non-auditory structures,
including Organ of Corti, which is located at the scala media (cochlear duct )
and transforms mechanical waves to electric signals in neurons.
â˘
Hair cell :
â˘
Hair cells are columnar cells, each with a bundle of 100-200 specialized cilia at
the top, for which they are named. There are two types of hair cells. Inner hair
cells are the mechanoreceptors for hearing: they transduce the vibration of
sound into electrical activity in nerve fibers, which is transmitted to the brain.
Outer hair cells are a motor structure. Sound energy causes changes in the
shape of these cells, which serves to amplify sound vibrations in a frequency
specific manner.
⢠Neurons (Hair cell neural connection)
â˘
Afferent neurons innervate cochlear inner hair cells, at synapses where the
neurotransmitter glutamate communicates signals from the hair cells to the
dendrites of the primary auditory neurons.
8.
9.
10. Types of AEPs
â˘
â˘
â˘
â˘
Short latency AEP
Middle latency AEP
Long latency AEP
The short latency AEP include peak of up to 10 msec
and amplitude of about 0.2uv, they are generated in
brainstem.
⢠The middle latency AEP have several variable peaks
with latency of 10-50 msec and with amplitude of about
1 uv, they probably reflect early cortical excitation.
⢠The long latency AEPs beginning after 50sec and having
peak of 1-10uv, represent later cortical excitation.
11.
12. The Central Auditory System (The Brain)
⢠The sound information, re-encoded, travels down the
vestibulo-cochlear nerve, through intermediate
stations such as the cochlear nuclei and superior
olivary complex of the brainstem and the inferior
colliculus of the midbrain, being further processed at
each waypoint. The information eventually reaches
the thalamus, and from there it is relayed to the
cortex. In the human brain, the primary auditory
cortex is located in the temporal lobe. Associated
anatomical structures include
⢠Cochlear nucleus
⢠Trapezoid body
⢠Superior olivary complex
17. GENERATORS OF WAVEFORMS FROM 1-VII
Waves
Â
Site of Neural Generator (peripheral portion of cranial nerve VIII)
I
Cochlear nerve (distal end)
II
Cochlear nerve ( proximal end)
III
Superior Olivary Complex/Nucleus
Â
IV
Lateral LeminiscusÂ
Â
V
Inferior Colliculus
VIÂ &Â VII
Presumed to be generated by the medial geniculate body and theÂ
thalamocortical pathways respectively
By
IMÂ
21. III. Stimulus Rate
⢠Stimulus rates employed vary widely from 5 to 200/s. depending on
test applications. Waves I,II, VI, and VII are particularly reduced in
amplitude at rates higher than 10/s. Thus, stimulus rates of 8-10/s
are especially suited to resolve these peaks.
⢠IV. Stimulus Intensity
⢠It is recommended that click intensity be acoustically calibrated in
âdecibels peak-equivalent sound pressure levelâ (dB pe SPL).
Stimulus intensities employed generally range between 40 and 120
dB pe SPL.( sound pressure level). Intensity of stimulus should
always be well defined to ensure :
Maximum release of neurotransmitters from the hair cells, so the
nerve fires promptly.
â˘
- Less intensity will result in increase in
Wave I latency.
22. â˘
â˘
â˘
â˘
V. Monaural Versus Binaural Stimulation
Click should be delivered monaurally, i.e., to one
ear at a time.
Contralateral Masking
It isAlthough not necessary in every situation, it is
recommended that contralateral masking be
included in the routine test protocol to avoid its
inadvertent omission when it is required.
recommended that the contralateral
(nonstimulated) ear be masked by white noise at 60
dB SPL to eliminate âcrossoverâ responses, i.e.,
bone-conducted responses originating in this ear.
23. VI. Recording.
System Bandpass
⢠The recommended system bandpass for BAEP recording is
10-30 to 2,500-3,000 Hz with a filter rolloff not exceeding
12 dB/octave for the low frequencies and 24 dB/octave for
the high frequencies. Whenever this test is performed in
the presence of irreducible EMG and mechanical artifacts,
the low-frequency cutoff may be raised to 100-200 Hz.
⢠VII. Stimulus Artifact
⢠The use of properly electrostatically and
electromagnetically shielded stimulus delivery systems is
suggested to attenuate or eliminate the stimulus artifact,
especially when using rarefaction-only or condensationonly clicks.
24. VIII. Analysis Time
⢠An analysis time of 10-15 ms from stimulus onset is
suggested. An analysis time of no less than 15 ms is
sometimes required to demonstrate extremely delayed
responses in certain pathologic conditions. Analysis times
of 15 ms are also essential for neonatal and
intraoperative recordings.
⢠IX. Filters Setting
⢠Low frequency filter setting is 10-30Hz but may be
increased to 100Hz.BAEP consist of multiple high
frequency components reaching a frequency close to
1000Hz.Thus the high frequency filter should not be less
then 2000Hz.
25. X. Number of Trials to be Averaged
⢠It is suggested that about 1,000-4,000 individual trials be averaged
until good waveform resolution has been achieved. Two or more
responses must be obtained and superimposed to demonstrate
replicability or lack of replicability of their components.
⢠XI. Electrode Placement
⢠It is recommended that recording electrodes be placed as follows:
(1) on the scalp at the vertex (Cz position of the 10-20 International
System of EEG electrode placement) and
⢠(2) over the left and right earlobes (auricular) A1 and A2 positions of
the 10-20 System) or the left and right mastoid processes (M1 and
M2).
⢠The ground electrode may be placed anywhere on the body. For
convenience, it is recommended that it be placed on the head, for
instance, on the scalp in a midline frontal location (position Fz of the
10-20 System). Electrode impedances must be < 5 KOhms.
26. XII. Montage
⢠A montage consisting of the following derivations is suggested for
BAEP recording:
⢠Channel 1: Vertex-ipsilateral earlobe or mastoid (Cz-Ai or Mi)
⢠Channel 2: Vertex-contralateral earlobe or mastoid (Cz-Ac or Mc)
⢠XIII. State of Consciousness
⢠BAEPs can be obtained during either wakefulness or sleep. Sedation
may occasionally be indicated with very young or tense patients, but
now requires special provisions in most facilities. In recording
patients who are comatose or are undergoing surgery, consideration
must be given to the fact that hypothermia may produce BAEP
alterations indistinguishable from those caused by structural lesions
of the auditory pathways
⢠XIV. Analysis of Results
⢠Records are analyzed primarily for the presence of waves I, III, and V.
27. Technical modifications to improve waveforms identification
â˘
â˘
â˘
â˘
â˘
â˘
â˘
â˘
â˘
â˘
â˘
â˘
â˘
â˘
â˘
â˘
.
1. If Stimulus artifact is too large and obscures wave I.
Decrease the impedance of recording and ground electrodes
Adjust the location of input cables and stimulus cables separate them
Decrease the stimulus intensity
Replace the ear phone
Change the polarity
2. If Wave I is not identified:
Increase stimulus intensity
Change click polarity
Decrease stimulus rate
Use ear canal electrodes
3. If Wave V is difficult to distinguish from wave IV
Decrease stimulus intensity
Use contra lateral ear reference recording
4.Wave V is difficult to differentiate from wave IV or VI:
Decrease stimulus intensity. When stimulus intensity is progressively decreased , wave V
is the last wave to remain.
28.
29. â˘
â˘
â˘
Technical modifications
Not all normal recording contain all BAEP peaks.
Wave V present most often.
Wave I and III can usually also be identified.
Wave II is often absent and wave IV may merge more of less completely with wave V.
⢠Wave I may be enhanced by increasing the stimulus intensity and decreasing the
stimulus rate.
⢠Recording a BAEP to condensation clicks in addition to to the BAEP rarefaction
clicks may help to distinguish wave I from mechanical and electrical stimulus
artifact.
⢠Wave II, although often absent in normal subjects, may be of clinical significance if
it is show prolong absolute latency of IPL I-II.
⢠Wave III may be normally splits into two peaks, its latency is then measured to the
first peak or to the middle between the two peaks. splitting may disappear if the
condensation clicks are used instead of rarefaction clicks and vice versa.
⢠Wave IV normally fuse with wave V.
⢠Wave V is the most realible peak. It may be identified by its low threashold, its
persistance during repetative stimulation up to 100/sec and by large negativity
that commonly follow it.
30. Application of BEAPS in Specific
Disorders
BEAPs are widely used for evaluation of
⢠Acoustic neuromas
⢠Degenerative diseases
⢠Brain tumor and stroke
⢠Multiple sclerosis
⢠Reversibility of comas
⢠Hearing assessment in children
31. Why Wave V
is used for Interpretation
⢠Wave V is used as the indicator in HTT because
it has
1. lowest threshold for stimulation
2.highest amplitude of BAEP waves
3.Actual & consistent later wave in all subjects
which indicates the integrity of the pathway
(peripheral to central).
32. Analysis of Results
â˘
â˘
â˘
â˘
â˘
â˘
â˘
â˘
â˘
â˘
Measurements must include the following:
(1) wave I peak latency;
(2) wave III peak latency;
(3) wave V peak latency;
(4) I-III interpeak interval;
(5) III-V interpeak interval;
(6) I-V interpeak interval;
(7) wave I amplitude;
(8) wave V amplitude; and
(9) wave IV-V/I amplitude ratio.
33. Criteria for Clinically Significant
Abnormality
⢠Abnormal BAEP measures do not necessarily imply
altered retrocochlear function. At present, criteria
for retrocochlear dysfunction include the following.
⢠1. Absence of all BAEP waves I through V.
unexplained by extreme hearing loss determined by
formal audiometric testing.
⢠2. Absence of all waves following waves I, II, or III.
⢠3. Abnormal prolongation of I-III, III-V. and I-V
interpeak intervals. I-III or III-V intervals can
sometimes be abnormally prolonged even in the face
of a normal I-V interval
34. Minimal Test Protocol
⢠It is recommended that, for neurologic
applications, minimal BAEP testing should
consist of responses to rarefaction,
condensation, or summated separate
rarefaction and condensation clicks delivered
monaurally at intensities of 90â120 dB pe
SPL, preferably 115 or 120 dB pe SPL and at
rates preferably below 25/s. The contralateral
ear should be masked by white noise at 60 dB
SPL.
35. Recording at High Stimulus Rates
⢠Recording BAEPs at stimulus rates of 50â70/s
facilitates the rapid identification of wave V in
screening studies of neonates and infants as well as
adults.
⢠4. Abnormal diminution of the IV-V/I amplitude ratio,
especially when accompanied by other abnormalities.
⢠5. Abnormally increased differences between the two
ears (interaural differences) as regards the I-III, III-V,
and I-V interpeak intervals, when not explained by
unilateral or asymmetric middle and/or ear
dysfunction determined by appropriate audiometric
tests.
36. Common Abnormal Finding
⢠Normal absolute latency of wave I but delayed
absolute latencies of corresponding waveform
⢠Prolonged interpeak latencies
⢠Prolonged absolute latency of wave I with
prolonged corresponding absolute latencies of
the remaining waveform but normal interpeak
latencies