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Hearing Evaluation in the Dispensing Practice, Part II

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HEARING EVALUATION IN THE DISPENSING PRACTICE, Part II

By Max Stanley Chartrand

(Note: Illustrations were lost during the transfer of material to this site.)

Figure 5.4 Above is an example of the aided responses of a client with a slight to moderate hearing loss as shown in Fig. 5.6.


For our purposes here we will go on to describe some other essential factors relative to speech discrimination testing, keeping in mind that, again, we are taking primarily the rehabilitative focal point:

1. Because of the prevalence of phonemic regression in many sensorineural and presbycusis cases, it is dubious at best to expect to obtain true potential aided discrim scores before adaptation to amplification. Indeed, it is widely accepted that an average of 60-90 days (or more) is required for most sufferers of this central auditory condition to overcome its effects. What has been long-forgotten must be relearned and, upon receiving the lost sounds anew, does not clearly exhibit the rehabilitative potential for improved speech discrimination at the beginning of that process. See figure 5.5 for a better illustration of a “time-based adaptation curve as shown in one recent study (Gatehouse and Killion, 1993).

2. Unless a specific pattern in the defective speech sounds is detected during discrim testing the information obtained will have little relevant information pertaining to the prescribed amplification parameters. The Duffy method is frequency-specific and is based on recognition of patterns of missed consonants, vowels, and semi-vowels.

3. For speech discrim testing to hold any validation capability it must be scientifically applicable in soundfield testing which is the only complete validation technique available to the hearing health professional. Furthermore, it must be repeatable from one evaluator to another.

4. With the introduction of noise competition such as provided in speech-in-noise (SiN) or signal-to-noise (S/N) testing, it is important for the evaluator to detect which specific speech sounds are abnormally affected.

Along with the above observations, the author recommends that the student study the phoneme recognition quick test (Duffy, 1987) and its application as a validation protocol in their hearing aid fittings. The literature is now replete with explanations, critiques, and reports to guide the specialist in the mastery of this advanced concept. For that reason we'll not provide a dialogue for the speech tests or a procedural description, with the hope that the conscientious specialist will initiate further study on the topic individually. Speech discrim testing is a most vital part of the hearing evaluation that requires the utmost skill and attention of the specialist. Furthermore, as the basis for evaluation, validation, and counseling, it will serve as an indispensable tool in the modern hearing aid practice.




Figure 5.5 Time-based speech-in-noise (SiN) score comparisons from Gatehouse (1992) in patients fitted with flat and shaped response curves. Note the significant improvements in the shaped-response patients from delivery of hearing instruments (day 1) to end of 12-week rehabilitation period. Used by permission of Gatehouse & Killion from an article on HABRAT.


Delivery and Verification
Most problems that arise from hearing aid fittings result not so much from the evaluation process, but more from (lack of) delivery protocol. It is imperative for the specialist to develop a uniform protocol for delivery and verification to assure that every point is covered, and that expectations from amplification are realistic. The more important aspects of counseling occur from this stage and beyond. Therefore, we will recommend, in the following pages, a delivery pattern for consideration, keeping in mind that this is a basic pattern that may be reproduced by all dispensers, new and experienced alike. Some of the particulars are left to the individual dispenser to utilize with their own knowledge and skills relative to the needs of their patients.

Before getting into the suggested delivery method, it must be explained that several goals are to be accomplished to make this a viable procedure:

1. Preliminary programming and quality assurance procedures are to be performed BEFORE the patient arrives.
2. By the end of the delivery, the patient should be able to:
-Insert and remove the instruments properly
-Adjust volume controls to their own voice utilizing
biofeedback methodology
-Learn how to cope with wind, background, large area
listening, etc.
-Know how to use on the telephone
-Insert & remove the battery
-Know how to care and maintain the instruments
-Understand all federal and state disclosures
3. Be given a long-range aural rehabilitation program overview, including instructions on a wearing schedule
4. The third party and patient BOTH should receive counseling in communication coping strategies, and any other assistance necessary to meet their specific needs
5. Have a post-fitting adjustment appointment date and time in hand


Explanation of the biofeedback volume control method. Since 1978, the author has utilized the “own voice first” approach to setting hearing aid controls with consistent success. At the time little research information was available to explain the neurological “markers” of the ear canal that were incited by insertion of a hearing instrument. Even to this day, with a virtual explosion in knowledge about the neuroanatomy of the ear, it seems we are still learning as an industry to respect those reflexes that nature set in place to protect the ear from “foreign objects”. Indeed, the hearing aid is a foreign object of the first order. The trigeminal nerve (Cranial V), vagus nerve (Cranial X), facial nerve (Cranial VII), glossopharyngeal nerve (Cranial IX), and a host of other, more intermediary branches of nerves course through and around the external meatus, the tympanic plexus at the TM, and around the middle ear and Eustachian tube. Non-acoustic occlusion complaints can occur in disregard of these reflexes when fitting hearing aids or earmolds (Hickock et al, 1993)(McSpaden et al, 1993).

The late Elaine Kramer (1987) introduced the author to a method she used, that developed from numerous patient reports as the best way to achieve the desired volume control level to accommodate the user’s own voice. Her methodology provided a more organized format to the author’s and has since been the subject of many continuing education lectures. But it must be said here that the concept appears to be generally regarded as illusory by normal hearing educators in the hearing instrument field, precisely because of lack of internal reference in personal experience. But the phenomenon remains for hearing impaired individuals who, in large numbers, continue have difficulty adjusting to wearing hearing aids. While its relevance to arbitrary target-gain or PB-Max may be in question, we know from experience that most users, especially men, prefer to wear their volume control at a level where they no longer experience occlusion, and where their voice resonates freely without pressure the larynx or the hollowness of the nasal area.

We know that one of the first things that must be overcome is the conductive and interaural masking effect experienced when an object touches the pinna. A related problem involving some of the same neural reflexes and conductivity arises when attempting to mask during bone conduction testing (Sanders, 1991)(Feldman, 1961). The resulting occlusion/conduction/masking effect can be as high as 25-30dB in the low frequencies (Dirks and Swindeman, 1967). Therefore, the masking stimulus must be loud enough to overcome the occlusion/conduction/masking effect that resulted from placement of an object (the earphones) over the ears. This has widely been assumed to be solely a result of closure of the ear canal. Another view of this phenomena has to do with self-monitoring of one’s own voice. Normal hearing persons hear a combination of their own voice internally, through bone conduction, and externally through the external meatus. When they hear their voice more internally than externally, they associate it with “feeling plugged”. In actuality, they are hearing a unique combination of nasality, middle ear conduction, and sinus artifact that they come to accept as “normal”. When a hearing aid is placed in their ear, this state of “normality” is upset. Some of this upset is due to high frequency information, part of it is an increase in external hearing of one’s own voice. But, when there is an increase of internal hearing of one’s own voice, there is almost immediate rejection, as it is perceived as an abnormal state. Such a condition also tends to “push down” on the larynx and pharynx, the mechanism of which we do not yet fully understand in the hearing field. An increase of volume (and sometimes a slight change in venting, externally or internally) usually relieves the downward pressure and plugged sensation---because external hearing of one’s own voice has overcome internal voice conduction. If the volume is set too loudly, complaints of hollowness, echo, and brightness are evoked.

The following sequence covers common patient reports as their volume controls are systematically manipulated to find the best position for their own voice’s resonance. In this example, the hearing aid is vented as recommended for acoustic reasons and they are reading a quotation or counting slowly to ten:

1. VC turned off, patient reports:

“feeling plugged up”
“like my head is in a barrel”
“as if I have a head cold”
“my voice sounds unnatural”


2. Volume control (VC) is turned up slightly and left at a low level, patient reports:

“pushing down in my throat”
“pressure when I speak”
“my head still feels plugged”

3. Volume control turned up to the point near best speech discrimination, they report:

“My voice sounds more natural”
“No pressure now”
“Seems to vibrate freely”
“Sounds more resonant”

4. Volume control adjusted above predicted use-gain level, report becomes:

“My voice sounds hollow”
“Kind of an echo effect”
“Too bright and loud”
“Nasally”

5. Return of the VC to the setting at #4 evokes a return to relative normality and acceptability.

By adjusting the volume control at the level best suited to the patient’s own voice, the author has found:

· Very few own voice complaints
· Proportionate hearing of external voices and sounds
· VCs adjusted near the best level of speech discrimination
· Far fewer remakes, modifications, and credit returns

It must also be kept in mind that at each programming or frequency response change that the volume control will need to be reset for the patient’s own voice. This is particularly a consideration for those with screw-set VCs or internally programmed VCs, making it particularly daunting for the specialist to assure proper readjustment of the hearing aid. Since this phenomena is especially critical for losses that begin near-normal in the lows and dropping off rapidly in the highs, careful attention to this methodology is absolutely essential. It can be safely assumed that a high percentage of shell remakes and returns for credit at the factory are due more to this one oversight/challenge than any other encountered in the industry. And while remake and credit return rates continue to plague the industry at a consistent level, it is would be safe to assume that more attention must be paid to the adjustment, and counseling of own voice complaints at the time of hearing aid delivery.

A review of the delivery procedure. If steps are skipped in this procedure some very important psychological, sociological, and physiological elements may be omitted which could weaken the success of the fitting.

1. Quality assurance, pre-programming and factory communication. Preparatory quality assurance steps should be taken before the patient arrives for delivery. In this way, there will be fewer surprises at delivery and communication with the factory can be accomplished without the pressure of a waiting patient. Pre-programming of the instruments, in programmable cases, to assure initialization and programming can be accomplished on the new instruments.

2. Listening and insertion. With the patient present, the specialist can perform a final listening and visual examination of the new instrument(s) to assure them that the instrument(s) meet the specialist's approval and expectations. Before insertion the specialist should apply a light coating of alcohol and lanolin (or other antiseptic/lubricant) on the shell portion. This will prevent gathering of the skin tissue at the entrance of the ear canal, and will allow for easy insertion. This will also prevent introduction of bacteria or fungi into the ear canal, something no new user needs added to the challenges ahead of them. Insert first, one side, asking, "How does that feel?". Upon an affirmative response, you are ready for step #3, setting the volume control.

3. Setting the volume controls. The volume control should be manipulated to the desired level in the manner described above and below, beginning the process with the instruction,

"Now, we are going to set your volume control at the point where your voice sounds just right to you. I’d like you to read the following quotation aloud, in a normal tone of voice, as we start at the bottom of your volume control taper and work my way up. You may notice a pressure sensation or stuffy feeling on your voice at first, which should clear up as I raise the volume. If I get past the best point of comfort, you may hear your voice echo or sound hollow---that means we are too loud, and we need to back off some. When I get to the point where your voice sounds just right, raise your hand. Are you ready?"

Then, hand them a card or laminated sheet with Helen Keller’s statement to read slowly and aloud:

"I am just as deaf as I am blind. Deafness is a worse misfortune, for it means the loss of the vital stimulus..." to assess their voice as the specialist raises or lowers the VC while in the ear.”

An alternative to the Helen Keller quotation is to instruct the patient to slowly count to 10 until you have adjusted the volume control to be ideal level. Remember, part of the purpose for this method is to overcome occlusion effects, both acoustic and non-acoustic. At the other extreme is to avoid over amplification of their voice, which brings the hollow effect. Since they are the closest voice to the speaker of their instruments, it is absolutely imperative that the patient uses their own voice first for quantification of comfortable loudness, instead of using another's voice. The importance of setting the volume control to the user's own voice first cannot be emphasized enough!

Adjust the other side in like manner. It is also important to note that in many cases the binaural summation effect may cause a slight over-loudness of the resulting setting, in which case a slight VC reduction on both instruments may be in order. Ascertain by again asking for a report on their own voice quality. Note: Of course, to hear high frequencies (or lack of) in one’s own voice for the first time in years can be initially very disconcerting. This must be pointed out, counseling the patient that, over time, their “new” voice should sound more normal as they become more accustomed to hearing it as others do.


4. Determining directional/localization ability. A simple test to determine directional ability of a binaural fitting is by using the handles of the two tuning forks (or other like objects) to produce sharp "clicks". The client will be instructed,

"Now, I would like you to close your eyes and point the direction from which you hear a series of clicking noises. Follow these noises with your finger."

The specialist will then begin at about 3 feet from the user's head, by clicking the fork handles near the right ear, while the user points in the direction of the sound. Next, go to the left ear and do the same until they point in that direction. Then, clicking in the center (azimuth) position, continue until they point precisely at the sound source. If there is difficulty for them to ascertain center position, a slight adjustment of the lateralized (loudest) instrument may be in order by reducing the gain slightly. Be careful that they do not turn their head or "cock their ears" for finding the signal. That will only invalidate the procedure. This is also an ear-training exercise to assist them in localization in the amplified state. For further ear-training, the specialist may also sweep from side to side, asking the patient to point (with the same hand) from where the sound is coming.

5. Noise tolerance and sensitivity.
In this section the specialist will find out whether the instruments’ output is within comfortable limits. While there are many more scientific approaches, this practical test is quick and will alert to most potential problems. Also, this constitutes excellent ear training for the patient so that THEY can determine what to expect of these kinds of sounds. Otherwise, they may be under the impression that hearing such noises in the everyday environment is something that should be adjusted out, thereby rejecting an adequate amount of amplification. The specialist will begin this test by explaining,

"I am going to make various sounds and noises to find out if they are too loud for the volume control setting that we are now on. I'd like you to tell me if these sounds bother you or sound piercing on the ear."

Then, by making sharp sounds in the following manner, one may determine not only the type of sound that may be unacceptable but the approximate frequency range of the offending noises:

1. Striking metal to metal (>700-1KHz)
2. Striking metal to glass (>1K-1.5KHz)
3. Striking glass to glass (>1.5K-2KHz)

If adjustments need to be made, the specialist may lower output slightly by use of a potentiometer or by programming. In cases where neither potentiometer or computer programmability are available the use of Knowles filters or lamb's wool (Chartrand, 1989) may be used as trial or temporary filters until more effective changes may be made by the manufacturer. The best rule of thumb is to be conservative on the use of filters. For instance, just a 2-4dB drop in peak SSPL90 can make a tremendous difference in achieving adequate “headroom” response, while not degrading necessary frequency and gain parameters significantly. An added psychological benefit of this procedure is that the patient and third party know how the patient is going to respond to those types of sounds. Rather than being startled or surprised after leaving the controlled environment of the office, they will now be more apt to subconsciously accept the sharp, extraneous noises of life once they leave the specialist's office.

6. Paper rattling. There seems to be a strong psychological component to the sound of paper rattling in new hearing aid users. The problem lies in the fact that this is a noise closely related or intermingled with the critical range of speech. Because of its prevalence in modern society, it is important to demonstrate that they can hear paper rattle without destroying their ability to function. In most cases, this is actually an ear training exercise, but there will be some legitimate situations that warrant frequency response adjustments. With the following instructions, the specialist will instruct, while rattling a thin sheet of paper in their hands,

"Now, I am going to rattle this paper and ask you to tell me if you still understand my voice over this paper rattling. Can you still separate my voice from this paper rattling?" (You may continue to talk until they have had a chance to assess your voice over the noise).

Usually the affirmative answer is an indication that the patient can subconsciously accept the sound of amplified paper rattling, and, hopefully, will not be disturbed by it next Sunday at church or at work, etc. This factor should never be overlooked or the specialist may find themselves in the formidable position of trying to appease a patient who insists they want to be completely rid of the sound of paper rattling without subduing the speech range----an impossible task at that!

Whisper test. And, finally, it is important to demonstrate that hearing sensitivity has not been sacrificed while damping, filtering, and adjusting for loud sounds. This may be accomplished in several ways, probably the most dramatic being the "whisper test". This is accomplished by the specialist leaning down near the right ear of the client and whispering,

7. "Can you hear me whisper?". Many first time patients have not heard a whisper, or at least heard it clearly, for many years. The consonant sounds that comprise a whisper are the very same sounds that we strive most to amplify with hearing aids. To help the patient get an idea of the sound of a whisper in the amplified state, and to gain confidence in hearing it, it is important to take a moment and demonstrate it. This will also help the third party appreciate the fact that improvement has been enjoyed with amplification. Going from ear to ear, in a voiceless whisper, the specialist will ask,

“Can you hear me whisper in this ear? How about over on this side, can you hear me?"

The successful response to this test will be an assurance to the client and the observing third party that indeed the potential is there for the client to hear softer speech with their new instruments. Caution should be taken in utilizing this procedure when it is not feasible, because of degree or type of hearing loss.

8. Validation by pure-tone and speech soundfield. This section can be the most important section from a validation standpoint (Chartrand, 1993), and one in which we will render a little more explanation. Keep in mind that we have adjusted the volume controls, but we have not permanently marked them or otherwise "set" them in place. We do not want the patient to touch the volume controls until we have run all tests and we have marked the VC position with the markers, which we will do at the end of this section.

We are assuming that the VCs are set at an appropriate use-gain setting. The patient's own voice sounds comfortable, various noises have been demonstrated to be tolerable, and both instruments are relatively balanced for directionality. Now, we want to use pure-tone soundfield, which this author and others (Goldberg, Duffy, etc.) advocate as an excellent comparative method with the air-conduction audiogram. While the traditional methodology has heretofore been in SPL (sound pressure level), we will herein provide a brief rendition of pure-tone soundfield in HTL-calibration so that we may superimpose the completed soundfield audiogram over the air-conduction audiogram taken earlier on the client's ears.

But first, we must explain a few things about pure-tone soundfield testing. Because we are not able, within the scope of this text, to cover the mechanics of set-up, facilities, equipment, and applied physics of sound, we will make only reference to those items that will be most pertinent to counseling for expectations from pure-tone results. It is further recommended that the student attend courses on soundfield testing and study printed materials in this regard (Speaks, 1992). Here are the considerations:

· Because of tremendously varying---and often unpredictable----suprathreshold loudness growth rates for many individuals, we cannot expect the soundfield results to show a great deal of discrete frequency correction where thresholds fall below the 70dB line of the audiogram. If, for instance, the pure-tone audiogram already indicates a threshold @2KHz of 80dB, it would be unrealistic to expect the corrected threshold to rise above the 35-40dB line of the audiogram without intruding upon the individual's discomfort level at that particular frequency. In this case, attempting to approach audiometric zero is totally unfeasible....but this may need to be explained to the client in the course of counseling. A good rule of thumb is correction of no more than 40-50dB at any given frequency for sensorineural cases, and especially for presbycusis.
· Should the patient have normal or near-normal thresholds at a given frequency (let's say, 500Hz @ 15dB), the corrected threshold should look little different than the uncorrected threshold. It is easy enough to explain that no amplification is needed in that region.
· When the pure-tone audiogram is "off the chart" in a given region (let's say @4KHz), it is possible they might respond to the mechanical noises of equipment switches instead of the tones themselves. It is important for the specialist to ascertain that possibility before recording the response. Also, a quick check for diplacusis---comparing a given pitch in one ear with the other---would be in order in cases where "off the chart" frequencies are responded to during aided soundfield.
· Generally, it is not possible and certainly not ideal, to approach "0" HTL in corrected thresholds at any frequency. A better goal is to achieve what is called the long-term spectrum of speech (Berger, Hagberg, and Rane, 1979), which presents a curve starting at a point about 25dB (on the HTL scale) in the lowest frequencies, ascending to about 10dB in the mid and high frequencies, and then gradually descending again to about 25dB in the highest frequencies. The shaping of this "curve" is reportedly the most realistic shape for most users in achieving optimum speech understanding within the inherent idiosyncrasies and limitations of hearing instruments. Especially when one considers the nature of cochlear mechanics, and the possibility of introducing cochlear distortions by over-stimulation via tectorial membrane action against the outer hair cells (OHCs). In such an event, it would be highly probable to noise-induce even more hearing loss with amplification.

Observe figures 5.6, 5.7, and 5.8 for illustrations of how pure-tone HTL soundfield scoring might be superimposed over the covered-ear air conduction audiogram. These represent typical examples of three types or patterns of losses. The small superimposed "o" and "x" marks represent binaural pure-tone responses. The stimulus may be given in pure-tones; however, warble-tones or narrow band noise is much preferable for soundfield testing. Furthermore, witness how the specialist might visually point out the expected benefits and/or limitations of a given amplification fitting to the client and interested third parties.








Figure 5.6 Typical Bilateral Presbycusis Loss: Aided HTL soundfield thresholds superimposed over TDH-39 headphone thresholds






Figure 5.7 Typical Unilateral Moderately Severe Conductive Case (left ear dead): HTL aided soundfield superimposed over TDH-39 earphone thresholds.





Figure 5.8 Typical bilateral sensorineural loss with moderate recruitment: HTL aided soundfield thresholds superimposed over unaided TDH-39 earphone thresholds.


A comparative study of an individual's aural correction which is derived by superimposing the pure-tone "aided" soundfield over the "unaided" air-conduction audiogram will allow the specialist to quantifiably and graphically assess the degree of threshold correction achieved in a given fitting in each of the four crucial frequency bands (500Hz-1KHz, 1-2KHz, 2-4KHz, 4-6KHz). We'll list here a few considerations that will assist the specialist in counseling the client and/or adjusting the instruments as a result of the pure-tone soundfield audiogram as it relates to the air-conduction audiogram by frequency region:


250Hz-1000Hz region: If there is evidence of over-amplification in this region we may expect a significantly negative signal-to-noise ratio. Adjustments to reduce the low frequency response of the instrument may be required. In fact, most losses, even "reverse slope" losses do not require a great deal of amplification below 500Hz. "Mirroring" the audiogram is definitely not the goal in the low frequency range. Otherwise, recruitment---and increased tinnitus, in some cases---may develop from noise exposure. On the other hand, if low frequency responses are deficient there may be difficulty in the patient hearing vowels, plosives, liquids, and stops; in distinguishing from men's and women's voices; and in adequate localization and spatial separation. Furthermore, there may be a "plugged" or occluded feeling if lows are too subdued. A delicate balance between not enough and too much must be achieved.

1KHz-2KHz region: Undue amplification in this range will bring discomfort and speech-masking effect in the presence of noises, such as paper rattling, dishes clinking in the cafeteria, or background music. Underamplification, on the other hand, can reduce aided speech understanding.

2KHz-4KHz region: This range is extremely critical for speech understanding, and for optimum signal-to-noise function. Coincidentally, the 2-4KHz range is also where many presbycusis cases experience a lessening of critical bandwidth sensitivity (Durrant and Lovrinic, 1985)---in such cases they may not be able to distinguish between 2.5Hz and 3KHz, which could be crucial in distinguishing various consonant sounds, particularly the letter "s". This letter is the most common and most critical consonant sound in the English language. It is also important to restore this region of frequencies without exceeding suprathreshold sensitivity (recruitment) and UCL. When unaided thresholds exceed 80dB in sensorineural cases it is unrealistic to expect more than a 35-40dB aided improvement in this region. Such threshold levels may respond to loudness growth strategies such as wide range dynamic compression.

4KHz-8KHz region: This range is also critical for speech understanding, but more importantly in difficult listening situations, and at distances. Overamplification concerns rest primarily within the UCL/difference parameters. Underamplification may cause a severe reduction in speech understanding in the presence of background noise, as well as a lessening of distance discrimination.

9. Speech Discrimination Soundfield Testing
It is not possible for a counseling textbook to adequately cover the procedures and techniques of speech discrimination testing. Again, the recommended methodology is the Duffy (1985) method or Phoneme Recognition Quick Test which utilizes comparative aided and unaided soundfield testing as its function. If, on the other hand, the situation is not within the possibility of proper equipment and environment, it is recommended that some form of comparative soundfield speech testing take place.

For instance, in cases where soundfield equipment is not available or feasible: Using the PB word list, the specialist may provide live-voice testing at 60-65dB (on the SPL meter) @ 3' with the patient facing them, eyes closed. Note: The author does not recommend the covered mouth approach because of the notable reduction high frequency speech sounds. Therefore, the facing-with-eyes-closed method is much preferable in live-voice situations, and lessens the problem of involving the examiner’s hearing acuity! This must be performed unaided first and then aided, utilizing a different list. Recording the number of correct phonemes will provide a viable basis of comparison for adjustment and counseling. Frequency response and gain adjustments may reveal an improvement in speech understanding using this method. For a more complete understanding of soundfield testing protocols, see the author's explanation in "Soundfield and Sound Control in the Dispensing Practice" (Chartrand, 1993).

Probe Microphone Measurements: A Primer. Several excellent texts have recently been published to fully explain the techniques, rationale, and equipment necessary for effective probe mic validation (Mueller et al, 1992)(Zelnick et al, 1987). At the risk of breaking continuity in the reader's understanding of the hearing aid delivery and validation procedure, however, we will spend a little time here to explain some of the facets of probe mic testing. Of course, this will be no more than a rudimental introduction, requiring the serious student to pursue further instruction elsewhere.

Probe mic measurements are an objective in situ assessment methodology to determine the following parameters:

· Real Ear Unaided Response (REUR)
· Real Ear Aided Response (REAR)
· Real Ear Insertion Response (REIR)

Other measurements, of course, can be taken, but these three fulfill the purposes for basic hearing aid validation. See Figure 5.9 for a superimposed comparison of a typical ear canal measurement using probe mic equipment.





Figure 5.9 Shown above is a composite graph of three probe mic measurements: REUR, REAR, and REIR. Also, shown is a "target gain" parameter based upon pure-tone thresholds of the user. Note the similarity between the target gain line and the Real Ear Insertion Response. Theoretically, this is an ideal match of amplification to the natural ear canal response.


Since the factory-provided electroacoustic readout on the instrument's frequency response etc. is based upon ANSI 2cc coupler specifications, there is actually little relationship between the readout it and the in situ data. Hence, probe mic testing provides data that can only be compared with itself, not with ANSI. Plus, test-retest with probe mic is much less reliable as compared to ANSI 2cc. Even the bases of parameters can be quite divergent. Probe mic data are snap-shots of the ear canal resonance properties in specific settings, which can be changed dramatically by simply opening a hearing aid vent, loosening the earmold, moving the probe tube +/- 5mm, moving away from or changing the angle of a soundfield speaker, etc. (Dirks and Kincaid, 1987)(Revit, 1987)(Ickes et al, 1991).

The Real Ear Unaided Response (REUR) is the acoustic "fingerprint" of the user's ear canal in the unaided setting (Mims, 1993). This might be considered the starting point with which all other real ear measurements relate. In fact, the REUR has nothing to do with hearing thresholds, but simply shows how sound is shaped as it passes through the user's ear canal. The next measurement is actually an output measure. In this way the Real Ear Aided Response (REAR) represents the output level of the instrument in the ear at each frequency and is shown in dBSPL.

The final, but most important measure is the Real Ear Insertion Response (REIR) which is actually a measure of in situ gain. The REIR is derived by subtracting the REUR value from the REAR value at each frequency tested by the probe mic system. The REIR, furthermore, ideally represents an approximation of "target gain" which is preprogrammed into the computerized real ear measurement system. Consequently, the differences between the "ideal" target gain and what is actually found in the REIR indicate where changes may be needed in the response of the hearing instrument. Adjustments of both gain and frequency response may be needed as shown by the results and user preferences. Keep in mind that all changes should be made while the instrument is in the user's ear. While adjustments are being made, however, it is advisable to ask the user to assess "quality" components of speech (and possibly other sounds), ascertaining that the response and peak modifications are preferable.

As a side note: It may be advisable to take probe mic measurements before administering pure-tone and speech soundfield, or, in some cases, concurrent with soundfield testing. Also, it is important to note that while real ear probe mic testing has evolved into a much-needed scientific and objective approach to hearing instrument validation, it still only measures what is taking place up to the tympanic membrane (TM)---i.e., replacement of lost canal resonance from insertion and wearing of the hearing instrument. Therefore, soundfield testing may provide a more complete and final subjective/objective profile of a given fitting. For trouble-shooting and resolution of post-fitting complaints, however, the probe mic approach is the most effective approach to-date.

10. Marking the V.C. Position. Now, after all adjustments and verification have been completed, it is time to accept the VC position as the correct one. It has taken about 30-40 minutes to arrive at this point, and the last thing one needs is to start from "square one" because the VC position was lost! Therefore, it is advisable that the specialist develop methods of removal of the instrument from the ear without moving the VC. This might entail opening the battery door, and using it as a "removal handle" or possibly carefully reaching around the concha to get a better grip of the shell. Do not let the patient remove the instrument or you will lose all that hard work!

There are two simple methods in which the VC may be marked:

· Using a ballpoint pen, the specialist may make a deep impression on the faceplate next to the dot located on the VC. Having done this, we now have two small "impressions" in which we may fill with black ink from the fine or medium point of a felt tip Exacto pen. The two "dots" should be easily seen, yet not spread over a large area, obliterating their precise setting.

· Another method is with bright red fingernail polish. Using a toothpick or other fine-pointed object, one may dip the toothpick into the bottle, careful to remove excess polish at the neck of the bottle, and apply a small "dot" in the proper positions on the faceplate and VC cap. Allow enough drying time before handling.

Now, the client is ready to be instructed on the proper setting of the VC to this effect,

"When you want to turn the instrument off, simply turn the volume control this way (demonstrate). And when you want to turn the instrument on, turn it this way (demonstrate). The point of amplification, which we've found to be best from our tests on you today, is at this point (line up the two marks for them to see). You may want it a little louder of softer than this, but we'll use this as our point of reference. Before you place the hearing aid in your ear, be sure to line up these two dots. You might hear a high-pitch whistle, but it will stop once the instrument is in position."

The client is now set to "practice" manipulating the VC in and out of their ear. By repeating insertion, removal, VC adjustment, etc. several times they will begin to feel more confidant. Of course, there will come a time when the marks will wear off. That is expected. By that time they should be able to judge the proper level of volume by listening instead of pre-setting the VCs.

11. Battery, wind-noise, and other instructions. It is also imperative that adequate time be spent practicing insertion and removal of the battery. Care and basic technical information should be covered, as well as future battery purchasing information. If there is a "battery club" or some easy-purchase system, this will be a good time to explain the program. Be sure to cover the HIA-recommended battery safety cautions.

12. Wind Noise. Wind-noise, until the advent of custom canal instruments, had been a major concern. In any event, if the specialist will talk to the patient about the probability of wind-noise, giving instructions on how to "deflect" the wind by moving the head away etc., the patient will subconsciously accept the presence of wind-noise. Wind-noise, in actuality, is not just an extraneous by-product of wearing a hearing aid. Wind generally causes bothersome sounds against the pinna of normal hearing persons, also. But one who has gone years without hearing wind at the usual level of intensity may feel that this is unnatural, or an artifact of amplification. Upon correction, the wind noise will return to the pre-loss level, and can be quite disturbing to the unsuspecting user.

13. Wearing Schedule. A viable wearing schedule is important. It must also be applicable according to each user’s experience and needs. It is not feasible for the new user to merely place the hearing aid in their ear and wear it for extended periods of time, for the lymphatic response will cause swelling and, eventually, soreness, sometimes prompting shell modifications or remakes that should not be made (Chartrand, 1999). Experienced users, though old hands with hearing aids, will also need a wearing schedule, albeit not as limited or as well-defined as the new user.

For new users, it is generally recommended:

Week one: Practice inserting and removing hearing aid(s), wearing no longer than 1-2 hours twice daily, giving the ear(s) a rest for a minimum of 2 hours. Listening should be confined to one or two people, restricting use in crowds or noisy places.

Week two: Increase wearing time to 3 hours twice daily, with at least a 2 hour rest. Listening situations may be expanded to small groups and non-intensive listening. Focus listening on one person at a time.

Week three: Increase wearing time to 4 hours twice daily with at least a 2 hour rest. Listening can now expand to larger groups, listening at Church, and other controlled situations.

Week four: Increase to wearing 6 hours per day twice daily with a 1-2 hour rest. Listening area can expand to most sound environments.

Week five: Increase wearing time to full-time use. If the ears have not completely adjusted, give them a rest at some point during the day.

Week six: Full-time wear---from rising in the morning until bedtime--- without periods of rest. But keep in mind that optimal speech understanding, especially in noise, should continue to improve over the next 8 weeks before optimal correction is available.


For experienced users it is generally recommended:

Week one: Wear 3-4 hours three times daily, giving the ear(s) a rest for at least one hour between. Avoid loud and noisy listening situations.

Week two: Wear 6 hours twice daily, giving the ear(s) a rest for at least one hour between. Minimize noise situations.

Week three: Wear full-time with a 1-hour rest break at mid-day. General listening situations of all kinds OK now.

Week four: Wear full-time without rest. Learning curve will continue, however, depending on the amount of new information being provided in the new instruments.

10. Scheduling Post Fitting Visits. It is recommended that the first post-fitting visit take place within the first three days of delivery. The second visit should occur no later than one week from the previous visit, and the third visit one week later. Visits should continue until all concerns and problems have been resolved. It would be good to make the patient aware of this so that they will not feel as if they are intruding on the specialist’s time, but instead need to continue visits as needed. In this way, the specialist may better manage the adaptation process, making adjustments as needed, pre-empting problem fitting cases, and offering ongoing counsel. This will essentially alleviate the tendency toward "mole hills" becoming "mountains". Neglecting timely post-fitting visits has caused many hearing aid failures, and hard-feelings between some patients and the specialist. Remember, we are asking them to go out into deep water, with myriad neurological, psychoacoustic, and psychosocial changes happening in a relatively short period of time in their lives. They need to know the specialist is there for them, listening and counseling them through the new challenges through which they must navigate.


11. Other Instructions. Other considerations too numerous and rudimentary to cover here should involve care, maintenance, warranties, FDA warnings and disclosures (if applicable), etc. If the patient will require compensatory training, such as speechreading, improved listening skills, use of assistive devices, considerations in the workplace, etc., this is the time to outline their program. Be ready to make referral to deaf educators, speech pathologists, or aural rehabilitation counselors in cases where overlay problems exist (CAP, aphasia, etc.). Also, consumer self-help and publications can be a vital educational and support experience for those with moderate and severe losses.


12. Third Party Counseling. Up to this point the third party has been somewhat of an observer of the proceedings. Now it is time to address their concerns directly. Here are a few areas to consider, by way of dialogue:

"Mrs. Jones, we are going to need your help to make this a successful experience with your husband. For one thing, it is going to take him some time to become reacquainted with the sounds he's been missing. In fact, for at least a period of time these sounds may even confuse him. People are going to expect him to hear perfectly, like with the flick of a light switch. But that will not happen. For even after all we can do he will still have a (slight)(mild) hearing loss."

And, continuing on, after pausing for their response...

"When you wish to speak to him, it is still important that he can see your face, when possible. Also, good lighting for speechreading will remain necessary. Please don't expect him to understand perfectly when you call him from another room of the house, especially when there is background noise present."

And....

"One very noticeable change that you will notice, however, is that the television can be turned down. He should be able to hear the phone and doorbell ring. He’ll know when you're talking to him, even though he might still misunderstand some words. It'll be easier to get his attention. Furthermore, he will be able to relax more when attending church and other meetings. He'll become more involved and feel more confident in social situations....Help him follow his wearing schedule. It may seem a little restrictive at first, but it gets better with time until he graduates to full-time wear. He is going to need your encouragement to make this a successful experience."

These instructions provide a basis for understanding the patient's probable and worst-case scenario, while, at the same time, providing hope and encouragement in the positive changes that are about to take place.

The "Ultimate" validation
Needless to say, the ultimate validation method is not a very efficient one, for it involves the final analysis of the new hearing aid user. One of the most important roles of the specialist is to remove as many extraneous obstacles, unnatural resonances, and technical barriers from the way of the user before they must make an assessment themselves. When the specialist does not do their job in a sincere and scientific manner, a great deal of frustration and failure can be experienced by all involved parties, and, hence, delay in achieving timely and effective aural rehabilitation.

Now, the path back to normality or near-normality has just begun. For most, the trek will be arduous, and will take more time and patience than they may have anticipated. By following the above considerations for delivery and validation, and then continuing on to serve in the years to come, extending long-term care and service, the specialist may be able to keep the promises made to the patient during the earlier stages of the evaluation. Further, they may be instrumental in opening new doors of opportunity and quality of life for all that are affected by the hearing impairment.







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