calibration
thresholds
latency / intensity functions
freq specific ABR
chirp chirp
100

what type of calibration would you use in a research environment?

electroacoustic calibration

100

what frequencies does a click evoked ABR threshold represent

2 -4 k Hz

100

normal hearing latency/intensity function

Normal hearing is a sloping curve, as intensity increases - wave V latency decreases

100
name 3 options for frequency specific ABR
  1. Tonebursts

  2. Tonebursts (or clicks) with ipsilateral masking like a notched noise or a high-pass noise

  3. Derived responses

100

who pioneered the CE Chirp

Claus Elberling

200

what is our best tool for calibration

our ears! :D

200

in what hearing loss will you not get an accurate ABR

low frequency HL

200

SNHL latency/intensity function

SNHL L/I functions are more steeply sloped than normal ones, but still follow a similar downward curve because some areas of the basal end can’t be excited when the sound is softer because of the hearing loss

200

in what instance would you use a high pass noise to increase frequency specificity 

In instances such as steeply sloping sensorineural hearing loss this is helpful because you can mask out frequencies that have better hearing. These better thresholds can be compensating for the one you’re testing for and if you ipsilaterally mask with a high-pass noise or a notched noise you’re increasing the frequency specificity of the toneburst because you’re getting it’s true response/reading. It is also helpful in finding thresholds for those better frequencies in a steeply sloping hearing loss because the worse thresholds can be pulling that threshold up, but if you mask them out you get a more frequency specific reading there as well.

200

chirp disadvantages

need norms for chirp data and no special advantage in identifying sites of lesions

300
steps of biological calibration
  1. Get at least 10 normal hearing subjects

  2. Test their puretone audiometric thresholds at 2000 Hz and 4000 Hz

  3. Take the average of all the thresholds at 2000 Hz, take the average of all the thresholds at 4000 Hz. Find the average of those two numbers.

  4. Using an ABR machine, find their behavioral thresholds to clicks (dB “on dial”)

  5. Average all their ABR behavioral thresholds.

  6. Compare the averaged puretone thresholds with the behavioral ABR thresholds. 0 dBnHL = the difference between those two averages.

300

You got your click evoked ABR threshold. How do you estimate the range of the threshold?

(click ABR threshold - 10) +- 10 dB = threshold estimation range at 2-4k Hz

300

conductive HL latency/intensity function

CHL L/I functions look similar to normal and mirror it, but they’re shifted to the right and the difference between it and a normal L/I is usually similar to the ABG

300

what are the differences in dB between toneburst ABR thresholds and the participant’s pure-tone audiometric thresholds at 500 Hz, 1000 Hz, 2000 Hz, and 4000 Hz?

500 Hz = 30 dB, 1000 Hz = 15 dB, 2000 Hz and 4000 Hz = 10 dB

300

why do chirps have a larger amplitude than clicks

Chirps utilize a time delay where each component of the basilar membrane is excited at the same time and sends synchronous signals to the brainstem. Each frequency signal reaches the brainstem at the same time, so each wave at each frequency is added together. This creates larger amplitudes, compared to a click where the frequencies’ amplitudes are measured at different times depending on when the brainstem receives the signal.

400

steps for electroacoustic calibration clicks

  1. Use an ABR machine using clicks, a coupler an SLM, and an oscilloscope. SLM reading is not meaningful. Record it’s peak amplitude and what intensity “on dial”

  2. Use a 1000 Hz reference puretone signal presented by an audiometer, coupler, SLM, and oscilloscope. Measure the dB SPL from the SLM and the amplitude. 

  3. Match the amplitude of the puretone signal to the click. If not the same, use 20log(on dial amplitude / ppe amplitude) to find the amount to add to the reading from the SLM. The ppeSPL is the missing level from the click SLM.

400

what degrees of HL can ABR not differentiate

severe / profound

400

steeply sloping SNHL latency/intensity function

Steeply sloping SNHL have an even steeper L/I function because they have good neural survival at the apex but very poor at the base

400

4 reasons frequency specific ABR doesn't guarantee place specificity

  1. ABR is an onset response, it’s so quick it’s hard to maintain frequency specificity

  2. Spread of activation in the cochlea, when intensity increases it’ll excite more of the cochlea including neurons not in your target frequency

  3. The frequency response of a transducer, inserts are okay but bone oscillators etc. aren’t too good

  4. Outer and middle ear have different resonance properties and enhance different frequencies 

400

7 advantages of chirp ABR

1. better morphology

2. shorter latencies

3. larger wave V amplitudes

4. shorter test duration

5. less sweeps

6. more accurate threshold estimation

7. maximum neural synchrony

500

advantages/disadvantages of biological calibration

advantages/disadvantages of electroacoustic calibration

biological calibration advantages: easiest to compare with an audiogram and it doesn't require expensive instrumentation to complete

biological calibration disadvantages: you rely on subjects’ responses and could be hard to replicate

electroacoustic calibration advantages: it can be verified objectively and not dependent on the number of subjects or their degree of HL to establish nHL norms

electroacoustic calibration disadvantages: it requires fancier equipment like an SLM, coupler, oscilloscope and that there’s no direct relationship between it and an audiogram

500

what type of stimulus gives best threshold estimation

chirps

500

retro cochlear pathology L/I function

looks very similar to CHL, need other testing to differentiate 

500

What stimulus and recording parameters will you use when eliciting a 500-Hz toneburst ABR? Why?

I would use rarefaction polarity, Blackman gating, 2 cycles = 4 ms, plateau at 0 ms, gain at 100,000, at a rate of 29.8 Hz, a time base at 20 ms, filter settings at 30-3000 Hz, and 2-4 replications of 2000 sweeps near threshold. 

Why?

Rarefaction polarity: alternating can get rid of peaks you want and degrade the response

Blackman gating: less ringing in the waveform than linear, cleaner peak

Gain 100,000: EEG is a small response because it’s coming from the brainstem so you need a lot of gain - makes EEGs bigger and easier for us to read waveform

Rate of 29.8 = close to 30 but avoiding integers of 60 to not have other electrical interference

Filter settings 30-3000 Hz: With tonebursts we want to focus on lower frequencies because higher frequencies are examined in clicks. This way we can filter out the higher frequencies and focus on the lows, or the specific frequency we’re looking for. 

2-4 replications of 2000 sweeps: tonebursts are noisier and have smaller responses and peaks so you have to do more sweeps than a click to get identifiable waves

500

explain rationale of the time delay of a chirp

low frequencies enter the cochlea first since this area of the BM takes the longest to reach maximum displacement high frequencies enter the cochlea last since they're the fastest to reach max displacement. this causes each frequency to reach the brain stem at the same time causing maximum neural synchrony